Details for: KMT5B

Gene ID: 51111

Symbol: KMT5B

Ensembl ID: ENSG00000110066

Description: lysine methyltransferase 5B

Associated with

Cells (max top 100)

(Cell Significance Index and respective Thresholds are uniquely calculated using our advanced thresholding algorithms to reveal cell-specific gene markers)

  • Cell Name: smooth muscle fiber of ileum (CL1000278)
    Fold Change: 124.9675
    Cell Significance Index: -59.0000
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 118.2010
    Cell Significance Index: -48.0200
  • Cell Name: peripheral blood mononuclear cell (CL2000001)
    Fold Change: 107.0987
    Cell Significance Index: -55.0900
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 50.6943
    Cell Significance Index: -48.4000
  • Cell Name: CD8-alpha-beta-positive, alpha-beta intraepithelial T cell (CL0000796)
    Fold Change: 20.4341
    Cell Significance Index: -54.7400
  • Cell Name: CD8-positive, alpha-beta regulatory T cell (CL0000795)
    Fold Change: 15.4357
    Cell Significance Index: -47.4100
  • Cell Name: epidermal Langerhans cell (CL0002457)
    Fold Change: 11.2081
    Cell Significance Index: -24.5300
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: 2.9000
    Cell Significance Index: 63.5000
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 2.7306
    Cell Significance Index: 318.2200
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: 2.0831
    Cell Significance Index: 116.8900
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 1.9026
    Cell Significance Index: 381.6500
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 1.6050
    Cell Significance Index: 318.5300
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 1.5312
    Cell Significance Index: 166.5500
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: 1.3404
    Cell Significance Index: 82.3900
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 1.2787
    Cell Significance Index: 98.1300
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 1.2358
    Cell Significance Index: 443.2600
  • Cell Name: periportal region hepatocyte (CL0019026)
    Fold Change: 1.1545
    Cell Significance Index: 17.0400
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: 1.0498
    Cell Significance Index: 20.4900
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.9167
    Cell Significance Index: 41.5500
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: 0.8210
    Cell Significance Index: 19.6900
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.7679
    Cell Significance Index: 22.1300
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 0.7564
    Cell Significance Index: 21.1400
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.7219
    Cell Significance Index: 130.1400
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.6830
    Cell Significance Index: 43.0500
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.6735
    Cell Significance Index: 82.8100
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: 0.6670
    Cell Significance Index: 31.1000
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.6387
    Cell Significance Index: 28.2500
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.5771
    Cell Significance Index: 399.1700
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.5602
    Cell Significance Index: 76.9300
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: 0.5548
    Cell Significance Index: 14.2600
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: 0.5311
    Cell Significance Index: 14.4600
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.4941
    Cell Significance Index: 218.4600
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.4883
    Cell Significance Index: 18.4900
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.4877
    Cell Significance Index: 32.8000
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.4407
    Cell Significance Index: 240.6800
  • Cell Name: fibro/adipogenic progenitor cell (CL0009099)
    Fold Change: 0.3492
    Cell Significance Index: 17.6500
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: 0.2639
    Cell Significance Index: 17.0300
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 0.1684
    Cell Significance Index: 21.5900
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.1614
    Cell Significance Index: 30.7100
  • Cell Name: retinal rod cell (CL0000604)
    Fold Change: 0.1569
    Cell Significance Index: 1.8700
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: 0.1388
    Cell Significance Index: 7.2300
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.0992
    Cell Significance Index: 1.7000
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: 0.0970
    Cell Significance Index: 4.5600
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: 0.0937
    Cell Significance Index: 42.5300
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.0824
    Cell Significance Index: 52.3400
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0661
    Cell Significance Index: 124.5000
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0645
    Cell Significance Index: 99.3300
  • Cell Name: lactocyte (CL0002325)
    Fold Change: 0.0627
    Cell Significance Index: 8.1100
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0423
    Cell Significance Index: 77.9700
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0285
    Cell Significance Index: 38.8000
  • Cell Name: decidual cell (CL2000002)
    Fold Change: 0.0274
    Cell Significance Index: 0.4400
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: 0.0161
    Cell Significance Index: 1.1400
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 0.0150
    Cell Significance Index: 0.7800
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.0032
    Cell Significance Index: 0.3200
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0191
    Cell Significance Index: -14.0100
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.0392
    Cell Significance Index: -0.8500
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0397
    Cell Significance Index: -29.4100
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: -0.0566
    Cell Significance Index: -1.5100
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0573
    Cell Significance Index: -43.3500
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0692
    Cell Significance Index: -11.8200
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: -0.0721
    Cell Significance Index: -11.7200
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0922
    Cell Significance Index: -52.0200
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.1059
    Cell Significance Index: -66.1100
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.1466
    Cell Significance Index: -21.3100
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.1546
    Cell Significance Index: -8.1200
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.1721
    Cell Significance Index: -49.5300
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.1795
    Cell Significance Index: -18.3400
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.2145
    Cell Significance Index: -15.9900
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.2304
    Cell Significance Index: -27.1700
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.2681
    Cell Significance Index: -3.3300
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.2719
    Cell Significance Index: -57.2600
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.2835
    Cell Significance Index: -32.4800
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: -0.3019
    Cell Significance Index: -10.4900
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: -0.3238
    Cell Significance Index: -4.7800
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.3721
    Cell Significance Index: -10.6200
  • Cell Name: granulosa cell (CL0000501)
    Fold Change: -0.3738
    Cell Significance Index: -9.8300
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.4087
    Cell Significance Index: -6.8400
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.4277
    Cell Significance Index: -13.7000
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.4757
    Cell Significance Index: -49.5300
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.5736
    Cell Significance Index: -45.4300
  • Cell Name: peg cell (CL4033014)
    Fold Change: -0.5800
    Cell Significance Index: -13.4000
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: -0.6109
    Cell Significance Index: -15.2700
  • Cell Name: centrilobular region hepatocyte (CL0019029)
    Fold Change: -0.6426
    Cell Significance Index: -10.8300
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: -0.7725
    Cell Significance Index: -10.5400
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.8594
    Cell Significance Index: -52.6900
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.9228
    Cell Significance Index: -29.3900
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.9249
    Cell Significance Index: -30.2800
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: -0.9523
    Cell Significance Index: -13.6800
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: -0.9868
    Cell Significance Index: -20.6600
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -1.0106
    Cell Significance Index: -21.4500
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: -1.0393
    Cell Significance Index: -20.5500
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -1.1032
    Cell Significance Index: -23.5000
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: -1.1339
    Cell Significance Index: -32.5100
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -1.2348
    Cell Significance Index: -24.7900
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -1.2449
    Cell Significance Index: -43.6100
  • Cell Name: cardiac endothelial cell (CL0010008)
    Fold Change: -1.2682
    Cell Significance Index: -18.2400
  • Cell Name: umbrella cell of urothelium (CL4030056)
    Fold Change: -1.2901
    Cell Significance Index: -11.8800
  • Cell Name: corneal epithelial cell (CL0000575)
    Fold Change: -1.3007
    Cell Significance Index: -18.5200
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -1.3411
    Cell Significance Index: -49.2300
  • Cell Name: kidney epithelial cell (CL0002518)
    Fold Change: -1.3835
    Cell Significance Index: -40.7500

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this specific cell.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Other Information

**Key Characteristics:** KMT5B is a member of the lysine methyltransferase family and exhibits a conserved catalytic domain. It is characterized by its ability to specifically methylate histone H4 lysines, particularly H4K20, which is a crucial epigenetic mark involved in various cellular processes. KMT5B is highly expressed in multiple cell types, including smooth muscle fibers, mucosal type mast cells, and immune cells such as T cells and dendritic cells. **Pathways and Functions:** KMT5B is involved in several key pathways, including: 1. **Chromatin remodeling**: KMT5B plays a crucial role in the regulation of chromatin structure and function by modifying histone H4 lysines, which in turn affects gene expression and cell differentiation. 2. **Histone modification**: KMT5B is a histone methyltransferase that specifically methylates histone H4 lysines, which is essential for the regulation of gene expression and cell differentiation. 3. **DNA repair**: KMT5B is involved in the positive regulation of double-strand break repair via nonhomologous end joining, which is a critical mechanism for maintaining genome stability. 4. **Immune system regulation**: KMT5B is highly expressed in immune cells and plays a crucial role in the regulation of immune responses, including positive regulation of isotype switching and positive regulation of double-strand break repair. **Clinical Significance:** KMT5B has been implicated in various diseases, including: 1. **Immunodeficiency**: Mutations in KMT5B have been associated with immunodeficiency, including severe combined immunodeficiency (SCID) and X-linked lymphoproliferative disease (XLP). 2. **Cancer**: KMT5B has been implicated in the development and progression of various cancers, including leukemia, lymphoma, and solid tumors. 3. **Neurological disorders**: KMT5B has been associated with neurological disorders, including autism spectrum disorder and schizophrenia. 4. **Muscle disorders**: KMT5B has been implicated in muscle disorders, including muscular dystrophy and myotonic dystrophy. In conclusion, KMT5B is a critical gene involved in various biological processes, including chromatin remodeling, histone modification, and immune system regulation. Its dysregulation has been implicated in various diseases, highlighting the importance of further research into the role of KMT5B in human health and disease.

Genular Protein ID: 4235737196

Symbol: KMT5B_HUMAN

Name: Lysine N-methyltransferase 5B

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 11401438

Title: The sequence and gene characterization of a 400-kb candidate region for IDDM4 on chromosome 11q13.

PubMed ID: 11401438

DOI: 10.1006/geno.2000.6492

PubMed ID: 10810093

Title: Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics.

PubMed ID: 10810093

DOI: 10.1101/gr.10.5.703

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 17974005

Title: The full-ORF clone resource of the German cDNA consortium.

PubMed ID: 17974005

DOI: 10.1186/1471-2164-8-399

PubMed ID: 16322686

Title: Loss of DNA methylation and histone H4 lysine 20 trimethylation in human breast cancer cells is associated with aberrant expression of DNA methyltransferase 1, Suv4-20h2 histone methyltransferase and methyl-binding proteins.

PubMed ID: 16322686

DOI: 10.4161/cbt.5.1.2288

PubMed ID: 23720823

Title: FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.

PubMed ID: 23720823

DOI: 10.1093/jmcb/mjt018

PubMed ID: 25218447

Title: Uncovering global SUMOylation signaling networks in a site-specific manner.

PubMed ID: 25218447

DOI: 10.1038/nsmb.2890

PubMed ID: 25772364

Title: SUMO-2 orchestrates chromatin modifiers in response to DNA damage.

PubMed ID: 25772364

DOI: 10.1016/j.celrep.2015.02.033

PubMed ID: 28112733

Title: Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation.

PubMed ID: 28112733

DOI: 10.1038/nsmb.3366

PubMed ID: 24396869

Title: Crystal structures of the human histone H4K20 methyltransferases SUV420H1 and SUV420H2.

PubMed ID: 24396869

DOI: 10.1016/j.febslet.2013.10.020

PubMed ID: 28114273

Title: The SUV4-20 inhibitor A-196 verifies a role for epigenetics in genomic integrity.

PubMed ID: 28114273

DOI: 10.1038/nchembio.2282

PubMed ID: 28191889

Title: Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.

PubMed ID: 28191889

DOI: 10.1038/ng.3792

PubMed ID: 29276005

Title: Histone lysine methylases and demethylases in the landscape of human developmental disorders.

PubMed ID: 29276005

DOI: 10.1016/j.ajhg.2017.11.013

Sequence Information:

  • Length: 885
  • Mass: 99188
  • Checksum: 13B0B6E35F751F48
  • Sequence:
  • MKWLGESKNM VVNGRRNGGK LSNDHQQNQS KLQHTGKDTL KAGKNAVERR SNRCNGNSGF 
    EGQSRYVPSS GMSAKELCEN DDLATSLVLD PYLGFQTHKM NTSAFPSRSS RHFSKSDSFS 
    HNNPVRFRPI KGRQEELKEV IERFKKDEHL EKAFKCLTSG EWARHYFLNK NKMQEKLFKE 
    HVFIYLRMFA TDSGFEILPC NRYSSEQNGA KIVATKEWKR NDKIELLVGC IAELSEIEEN 
    MLLRHGENDF SVMYSTRKNC AQLWLGPAAF INHDCRPNCK FVSTGRDTAC VKALRDIEPG 
    EEISCYYGDG FFGENNEFCE CYTCERRGTG AFKSRVGLPA PAPVINSKYG LRETDKRLNR 
    LKKLGDSSKN SDSQSVSSNT DADTTQEKNN ATSNRKSSVG VKKNSKSRTL TRQSMSRIPA 
    SSNSTSSKLT HINNSRVPKK LKKPAKPLLS KIKLRNHCKR LEQKNASRKL EMGNLVLKEP 
    KVVLYKNLPI KKDKEPEGPA QAAVASGCLT RHAAREHRQN PVRGAHSQGE SSPCTYITRR 
    SVRTRTNLKE ASDIKLEPNT LNGYKSSVTE PCPDSGEQLQ PAPVLQEEEL AHETAQKGEA 
    KCHKSDTGMS KKKSRQGKLV KQFAKIEEST PVHDSPGKDD AVPDLMGPHS DQGEHSGTVG 
    VPVSYTDCAP SPVGCSVVTS DSFKTKDSFR TAKSKKKRRI TRYDAQLILE NNSGIPKLTL 
    RRRHDSSSKT NDQENDGMNS SKISIKLSKD HDNDNNLYVA KLNNGFNSGS GSSSTKLKIQ 
    LKRDEENRGS YTEGLHENGV CCSDPLSLLE SRMEVDDYSQ YEEESTDDSS SSEGDEEEDD 
    YDDDFEDDFI PLPPAKRLRL IVGKDSIDID ISSRRREDQS LRLNA

Genular Protein ID: 4153679324

Symbol: B7Z5N2_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 370
  • Mass: 42030
  • Checksum: 1B092FDC6418B85E
  • Sequence:
  • MKWLGESKNM VVNGRRNGGK LSNDHQQNQS KLQHTGKDTL KAGKNAVERR SNRCNGNSGF 
    EGQSRYVPSS GMSAKELCEN DDLATSLVLD PYLGFQTHTM NTRFRPIKGR QEELKEVIER 
    FKKDEHLEKA FKCLTSGEWA RHYFLNKNKM QEKLFKEHVF IYLRMFATDS GFEILPCNRY 
    SSEQNGAKIV ATKEWKRNDK IELLVGCIAE LSEIEENMLL RHGENDFSVM YSTRKNCAQL 
    WLGPAAFINH DCRPNCKFVS TGRDTACVKA LRDIEPGEEI SCYYGDGFFG ENNEFCECYT 
    CERRGTGAFK SRVGLPAPAP VINSKYGLRE TDKRLNRLKK LGDSSKNSDS QSVSSNTDAD 
    TTQEKNNASK

Genular Protein ID: 3956902830

Symbol: A0A8V8TQB9_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

Sequence Information:

  • Length: 713
  • Mass: 79529
  • Checksum: AA54AAD0449C8D92
  • Sequence:
  • MQEKLFKEHV FIYLRMFATD SGFEILPCNR YSSEQNGAKI VATKEWKRND KIELLVGCIA 
    ELSEIEENML LRHGENDFSV MYSTRKNCAQ LWLGPAAFIN HDCRPNCKFV STGRDTACVK 
    ALRDIEPGEE ISCYYGDGFF GENNEFCECY TCERRGTGAF KSRVGLPAPA PVINSKYGLR 
    ETDKRLNRLK KLGDSSKNSD SQSVSSNTDA DTTQEKNNAT SNRKSSVGVK KNSKSRTLTR 
    QSMSRIPASS NSTSSKLTHI NNSRVPKKLK KPAKPLLSKI KLRNHCKRLE QKNASRKLEM 
    GNLVLKEPKV VLYKNLPIKK DKEPEGPAQA AVASGCLTRH AAREHRQNPV RGAHSQGESS 
    PCTYITRRSV RTRTNLKEAS DIKLEPNTLN GYKSSVTEPC PDSGEQLQPA PVLQEEELAH 
    ETAQKGEAKC HKSDTGMSKK KSRQGKLVKQ FAKIEESTPV HDSPGKDDAV PDLMGPHSDQ 
    GEHSGTVGVP VSYTDCAPSP VGCSVVTSDS FKTKDSFRTA KSKKKRRITR YDAQLILENN 
    SGIPKLTLRR RHDSSSKTND QENDGMNSSK ISIKLSKDHD NDNNLYVAKL NNGFNSGSGS 
    SSTKLKIQLK RDEENRGSYT EGLHENGVCC SDPLSLLESR MEVDDYSQYE EESTDDSSSS 
    EGDEEEDDYD DDFEDDFIPL PPAKRLRLIV GKDSIDIDIS SRRREDQSLR LNA

Genular Protein ID: 2074561460

Symbol: B7WNX0_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

Sequence Information:

  • Length: 370
  • Mass: 42057
  • Checksum: 6FE2BFD4F927B858
  • Sequence:
  • MKWLGESKNM VVNGRRNGGK LSNDHQQNQS KLQHTGKDTL KAGKNAVERR SNRCNGNSGF 
    EGQSRYVPSS GMSAKELCEN DDLATSLVLD PYLGFQTHKM NTRFRPIKGR QEELKEVIER 
    FKKDEHLEKA FKCLTSGEWA RHYFLNKNKM QEKLFKEHVF IYLRMFATDS GFEILPCNRY 
    SSEQNGAKIV ATKEWKRNDK IELLVGCIAE LSEIEENMLL RHGENDFSVM YSTRKNCAQL 
    WLGPAAFINH DCRPNCKFVS TGRDTACVKA LRDIEPGEEI SCYYGDGFFG ENNEFCECYT 
    CERRGTGAFK SRVGLPAPAP VINSKYGLRE TDKRLNRLKK LGDSSKNSDS QSVSSNTDAD 
    TTQEKNNASK

Genular Protein ID: 1779247368

Symbol: C9J6S5_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

Sequence Information:

  • Length: 814
  • Mass: 91374
  • Checksum: D1DD8F64D9C6B008
  • Sequence:
  • MSAKELCEND DLATSLVLDP YLGFQTHKMN TSAFPSRSSR HFSKSDSFSH NNPVRFRPIK 
    GRQEELKEVI ERFKKDEHLE KAFKCLTSGE WARHYFLNKN KMQEKLFKEH VFIYLRMFAT 
    DSGFEILPCN RYSSEQNGAK IVATKEWKRN DKIELLVGCI AELSEIEENM LLRHGENDFS 
    VMYSTRKNCA QLWLGPAAFI NHDCRPNCKF VSTGRDTACV KALRDIEPGE EISCYYGDGF 
    FGENNEFCEC YTCERRGTGA FKSRVGLPAP APVINSKYGL RETDKRLNRL KKLGDSSKNS 
    DSQSVSSNTD ADTTQEKNNA TSNRKSSVGV KKNSKSRTLT RQSMSRIPAS SNSTSSKLTH 
    INNSRVPKKL KKPAKPLLSK IKLRNHCKRL EQKNASRKLE MGNLVLKEPK VVLYKNLPIK 
    KDKEPEGPAQ AAVASGCLTR HAAREHRQNP VRGAHSQGES SPCTYITRRS VRTRTNLKEA 
    SDIKLEPNTL NGYKSSVTEP CPDSGEQLQP APVLQEEELA HETAQKGEAK CHKSDTGMSK 
    KKSRQGKLVK QFAKIEESTP VHDSPGKDDA VPDLMGPHSD QGEHSGTVGV PVSYTDCAPS 
    PVGCSVVTSD SFKTKDSFRT AKSKKKRRIT RYDAQLILEN NSGIPKLTLR RRHDSSSKTN 
    DQENDGMNSS KISIKLSKDH DNDNNLYVAK LNNGFNSGSG SSSTKLKIQL KRDEENRGSY 
    TEGLHENGVC CSDPLSLLES RMEVDDYSQY EEESTDDSSS SEGDEEEDDY DDDFEDDFIP 
    LPPAKRLRLI VGKDSIDIDI SSRRREDQSL RLNA

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.