Details for: NFIX

Gene ID: 4784

Symbol: NFIX

Ensembl ID: ENSG00000008441

Description: nuclear factor I X

Associated with

  • Gene expression (transcription)
    (R-HSA-74160)
  • Rna polymerase iii abortive and retractive initiation
    (R-HSA-749476)
  • Rna polymerase iii transcription
    (R-HSA-74158)
  • Rna polymerase iii transcription termination
    (R-HSA-73980)
  • Chromatin
    (GO:0000785)
  • Dna-binding transcription factor activity
    (GO:0003700)
  • Dna-binding transcription factor activity, rna polymerase ii-specific
    (GO:0000981)
  • Dna replication
    (GO:0006260)
  • Negative regulation of transcription by rna polymerase ii
    (GO:0000122)
  • Nucleus
    (GO:0005634)
  • Positive regulation of transcription by rna polymerase ii
    (GO:0045944)
  • Protein binding
    (GO:0005515)
  • Regulation of transcription by rna polymerase ii
    (GO:0006357)
  • Rna polymerase ii cis-regulatory region sequence-specific dna binding
    (GO:0000978)
  • Sequence-specific double-stranded dna binding
    (GO:1990837)
  • Transcription by rna polymerase ii
    (GO:0006366)

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: polychromatophilic erythroblast (CL0000550)
    Fold Change: 364.7814
    Cell Significance Index: -56.7400
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 242.8212
    Cell Significance Index: -61.5900
  • Cell Name: smooth muscle fiber of ileum (CL1000278)
    Fold Change: 125.0099
    Cell Significance Index: -59.0200
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 117.5610
    Cell Significance Index: -47.7600
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 49.9401
    Cell Significance Index: -47.6800
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 43.3511
    Cell Significance Index: -53.4500
  • Cell Name: CD8-positive, alpha-beta regulatory T cell (CL0000795)
    Fold Change: 21.4361
    Cell Significance Index: -65.8400
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 15.9172
    Cell Significance Index: -62.8100
  • Cell Name: epidermal Langerhans cell (CL0002457)
    Fold Change: 15.5214
    Cell Significance Index: -33.9700
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 2.5177
    Cell Significance Index: 70.3600
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 2.3081
    Cell Significance Index: 463.0100
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 1.7637
    Cell Significance Index: 632.6000
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 1.5818
    Cell Significance Index: 699.3600
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: 1.5473
    Cell Significance Index: 109.4300
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 1.5216
    Cell Significance Index: 1373.8600
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: 1.4855
    Cell Significance Index: 69.2600
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: 1.4001
    Cell Significance Index: 86.0600
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 1.0162
    Cell Significance Index: 68.3300
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.9199
    Cell Significance Index: 100.0600
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: 0.6959
    Cell Significance Index: 16.6900
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.6842
    Cell Significance Index: 93.9600
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.6250
    Cell Significance Index: 37.5200
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: 0.6074
    Cell Significance Index: 31.6400
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.5461
    Cell Significance Index: 108.3800
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: 0.5349
    Cell Significance Index: 13.7500
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: 0.5204
    Cell Significance Index: 14.8500
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: 0.4488
    Cell Significance Index: 8.7600
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.4144
    Cell Significance Index: 637.9400
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: 0.3982
    Cell Significance Index: 6.0000
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.3976
    Cell Significance Index: 9.9400
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.3381
    Cell Significance Index: 23.3800
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.3131
    Cell Significance Index: 216.5500
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.3099
    Cell Significance Index: 8.9300
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.2618
    Cell Significance Index: 482.9000
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.2357
    Cell Significance Index: 4.0400
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: 0.1836
    Cell Significance Index: 83.3500
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.1798
    Cell Significance Index: 13.8000
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.1777
    Cell Significance Index: 8.0600
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1726
    Cell Significance Index: 17.0700
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: 0.1687
    Cell Significance Index: 7.9300
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.1432
    Cell Significance Index: 194.6500
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: 0.1025
    Cell Significance Index: 5.3800
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.1022
    Cell Significance Index: 64.9200
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.1013
    Cell Significance Index: 190.8000
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.0451
    Cell Significance Index: 24.6200
  • Cell Name: lactocyte (CL0002325)
    Fold Change: 0.0382
    Cell Significance Index: 4.9400
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: 0.0342
    Cell Significance Index: 0.9800
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.0240
    Cell Significance Index: 4.3200
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.0076
    Cell Significance Index: 0.9400
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0031
    Cell Significance Index: -1.9300
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0092
    Cell Significance Index: -6.9500
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: -0.0395
    Cell Significance Index: -7.5100
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0505
    Cell Significance Index: -37.3900
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0650
    Cell Significance Index: -47.6800
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0755
    Cell Significance Index: -42.6000
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0789
    Cell Significance Index: -13.4700
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: -0.1000
    Cell Significance Index: -16.2600
  • Cell Name: odontoblast (CL0000060)
    Fold Change: -0.1085
    Cell Significance Index: -13.9100
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.1645
    Cell Significance Index: -5.7800
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.1981
    Cell Significance Index: -57.0000
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.2343
    Cell Significance Index: -34.0600
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.2666
    Cell Significance Index: -5.5300
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.2887
    Cell Significance Index: -60.8200
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.3066
    Cell Significance Index: -35.7300
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.3085
    Cell Significance Index: -31.5100
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.3625
    Cell Significance Index: -41.5300
  • Cell Name: pancreatic endocrine cell (CL0008024)
    Fold Change: -0.4710
    Cell Significance Index: -53.7600
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.4996
    Cell Significance Index: -52.0200
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.5013
    Cell Significance Index: -10.8600
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.5046
    Cell Significance Index: -59.5100
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.5099
    Cell Significance Index: -38.0000
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.5789
    Cell Significance Index: -18.5400
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.6589
    Cell Significance Index: -42.5100
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.6689
    Cell Significance Index: -52.9800
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.6707
    Cell Significance Index: -14.2900
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.7265
    Cell Significance Index: -40.7700
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: -0.7476
    Cell Significance Index: -10.2000
  • Cell Name: peg cell (CL4033014)
    Fold Change: -0.7826
    Cell Significance Index: -18.0800
  • Cell Name: fallopian tube secretory epithelial cell (CL4030006)
    Fold Change: -0.7957
    Cell Significance Index: -12.3100
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.8310
    Cell Significance Index: -50.9500
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: -0.9056
    Cell Significance Index: -24.6500
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -1.0040
    Cell Significance Index: -32.8700
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -1.0349
    Cell Significance Index: -32.9600
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -1.1240
    Cell Significance Index: -70.8400
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -1.1325
    Cell Significance Index: -58.8300
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -1.1574
    Cell Significance Index: -19.3700
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -1.2019
    Cell Significance Index: -24.1300
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -1.2920
    Cell Significance Index: -45.2600
  • Cell Name: leptomeningeal cell (CL0000708)
    Fold Change: -1.2994
    Cell Significance Index: -27.7800
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: -1.3920
    Cell Significance Index: -61.5700
  • Cell Name: hippocampal astrocyte (CL0002604)
    Fold Change: -1.4102
    Cell Significance Index: -19.7200
  • Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
    Fold Change: -1.4408
    Cell Significance Index: -31.1300
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -1.4604
    Cell Significance Index: -53.6100
  • Cell Name: astrocyte of the cerebral cortex (CL0002605)
    Fold Change: -1.5396
    Cell Significance Index: -26.6200
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: -1.6407
    Cell Significance Index: -62.1300
  • Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
    Fold Change: -1.7120
    Cell Significance Index: -42.7100
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: -1.9147
    Cell Significance Index: -27.5000
  • Cell Name: keratinocyte (CL0000312)
    Fold Change: -1.9659
    Cell Significance Index: -49.1000
  • Cell Name: neutrophil progenitor cell (CL0000834)
    Fold Change: -1.9720
    Cell Significance Index: -52.7500
  • Cell Name: pro-T cell (CL0000827)
    Fold Change: -2.0163
    Cell Significance Index: -51.5100

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:** 1. **Transcriptional Regulation:** NFIX acts as a transcription factor, binding to specific DNA sequences and modulating the expression of target genes. 2. **Chromatin Association:** NFIX interacts with chromatin components, influencing DNA replication, transcription, and termination. 3. **Cell Type-Specific Expression:** NFIX is highly expressed in cells involved in neuronal development, muscle growth, and lens function, underscoring its role in tissue-specific gene regulation. 4. **Diverse Binding Specificities:** NFIX exhibits specificity for different DNA sequences, enabling it to regulate a wide range of genes involved in various cellular processes. **Pathways and Functions:** 1. **RNA Polymerase II-Regulated Transcription:** NFIX interacts with RNA polymerase II, a key enzyme responsible for transcriptional initiation and elongation. 2. **Chromatin Remodeling:** NFIX contributes to chromatin remodeling, facilitating the accessibility of transcription factors and other regulatory proteins to specific DNA sequences. 3. **DNA Replication and Termination:** NFIX influences DNA replication and termination by interacting with enzymes involved in these processes, such as DNA polymerase and RNA polymerase III. 4. **Gene Expression Regulation:** NFIX modulates the expression of target genes by regulating transcriptional initiation, elongation, and termination. **Clinical Significance:** 1. **Neurological Disorders:** Abnormalities in NFIX expression have been linked to neurological disorders, such as autism, schizophrenia, and epilepsy, highlighting its potential role in neurodevelopmental diseases. 2. **Muscular Dystrophy:** NFIX mutations have been identified in patients with muscular dystrophy, emphasizing its importance in muscle development and function. 3. **Lens Disorders:** NFIX expression is critical for lens function, and its dysregulation may contribute to lens-related disorders, such as cataracts and glaucoma. 4. **Cancer:** NFIX may play a role in cancer development and progression, as alterations in its expression have been observed in various cancer types. In conclusion, NFIX is a vital transcription factor that regulates gene expression in diverse cell types, influencing chromatin structure, DNA replication, transcription, and termination. Its dysregulation has been implicated in various diseases, including neurological disorders, muscular dystrophy, lens disorders, and cancer. Further investigation into the mechanisms of NFIX action and its role in disease will provide valuable insights into the development of novel therapeutic strategies.

Genular Protein ID: 2449051213

Symbol: NFIX_HUMAN

Name: Nuclear factor 1 X-type

UniProtKB Accession Codes:

Q14938 B4DM25 O60413 Q0VG09 Q12859 Q13050 Q13052 Q5U094 Q9UPH1 Q9Y6R8

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 5 CTD 1 ChiTaRS 1 DMDM 1 DNASU 1 DisGeNET 1 EMBL 12 Ensembl 5 ExpressionAtlas 1 GO 11 GeneCards 1 GeneTree 1 GeneWiki 1 GenomeRNAi 1 GlyCosmos 1 GlyGen 1 HGNC 1 HPA 1 InParanoid 1 IntAct 1 InterPro 5 KEGG 1 MANE-Select 1 MIM 5 MINT 1 MalaCards 1 MassIVE 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 Orphanet 3 OrthoDB 1 PANTHER 2 PDB 2 PDBsum 2 PIR 1 PRO 1 PROSITE 2 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 3 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 5 Pumba 1 RNAct 1 Reactome 2 RefSeq 3 SIGNOR 1 SMART 1 SMR 1 STRING 1 SignaLink 1 SwissPalm 1 TreeFam 1 UCSC 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 jPOST 1 neXtProt 1

Citations:

PubMed ID: 7937100

Title: Cloning and functional analysis of spliced isoforms of human nuclear factor I-X: interference with transcriptional activation by NFI/CTF in a cell-type specific manner.

PubMed ID: 7937100

DOI: 10.1093/nar/22.19.3825

PubMed ID: 8799200

Title: Expression of multiple classes of the nuclear factor-1 family in the developing human brain: differential expression of two classes of NF-1 genes.

PubMed ID: 8799200

DOI: 10.3109/13550289609146542

PubMed ID: 14702039

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

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15057824

Title: The DNA sequence and biology of human chromosome 19.

PubMed ID: 15057824

DOI: 10.1038/nature02399

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: 7590749

Title: Chromosomal localization of the four genes (NFIA, B, C, and X) for the human transcription factor nuclear factor I by FISH.

PubMed ID: 7590749

DOI: 10.1006/geno.1995.1107

PubMed ID: 19690332

Title: Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.

PubMed ID: 19690332

DOI: 10.1126/scisignal.2000007

PubMed ID: 20673863

Title: Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.

PubMed ID: 20673863

DOI: 10.1016/j.ajhg.2010.07.001

PubMed ID: 23186163

Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

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: 31375868

Title: The evolution of the 9aaTAD domain in Sp2 proteins: inactivation with valines and intron reservoirs.

PubMed ID: 31375868

DOI: 10.1007/s00018-019-03251-w

PubMed ID: 22301465

Title: Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features.

PubMed ID: 22301465

DOI: 10.1038/jhg.2012.7

PubMed ID: 26193383

Title: NFIX mutations affecting the DNA-binding domain cause a peculiar overgrowth syndrome (Malan syndrome): a new patients series.

PubMed ID: 26193383

DOI: 10.1016/j.ejmg.2015.06.009

PubMed ID: 26200704

Title: Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes.

PubMed ID: 26200704

DOI: 10.1038/pr.2015.135

Sequence Information:

  • Length: 502
  • Mass: 55098
  • Checksum: 55B40A7DC505EA21
  • Sequence:
    • MYSPYCLTQD EFHPFIEALL PHVRAFSYTW FNLQARKRKY FKKHEKRMSK DEERAVKDEL 
LGEKPEIKQK WASRLLAKLR KDIRPEFRED FVLTITGKKP PCCVLSNPDQ KGKIRRIDCL 
RQADKVWRLD LVMVILFKGI PLESTDGERL YKSPQCSNPG LCVQPHHIGV TIKELDLYLA 
YFVHTPESGQ SDSSNQQGDA DIKPLPNGHL SFQDCFVTSG VWNVTELVRV SQTPVATASG 
PNFSLADLES PSYYNINQVT LGRRSITSPP STSTTKRPKS IDDSEMESPV DDVFYPGTGR 
SPAAGSSQSS GWPNDVDAGP ASLKKSGKLD FCSALSSQGS SPRMAFTHHP LPVLAGVRPG 
SPRATASALH FPSTSIIQQS SPYFTHPTIR YHHHHGQDSL KEFVQFVCSD GSGQATGQPN 
GSGQGKVPGS FLLPPPPPVA RPVPLPMPDS KSTSTAPDGA ALTPPSPSFA TTGASSANRF 
VSIGPRDGNF LNIPQQSQSW FL

Genular Protein ID: 4170111697

Symbol: B4DHW2_HUMAN

Name: N/A

UniProtKB Accession Codes:

B4DHW2

Database IDs:

ARBA 9 Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CTD 1 DNASU 1 DisGeNET 1 EMBL 6 Ensembl 2 GO 5 GeneTree 1 HGNC 1 InterPro 5 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PROSITE 3 PeptideAtlas 1 Pfam 3 Proteomes 2 ProteomicsDB 1 RefSeq 1 RuleBase 1 SAM 1 SMART 1 VEuPathDB 1

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15057824

Title: The DNA sequence and biology of human chromosome 19.

PubMed ID: 15057824

DOI: 10.1038/nature02399

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

Sequence Information:

  • Length: 510
  • Mass: 55815
  • Checksum: 650EB017A1F99EB3
  • Sequence:
    • MEMSWARQSL AGIPAACDEF HPFIEALLPH VRAFSYTWFN LQARKRKYFK KHEKRMSKDE 
ERAVKDELLG EKPEIKQKWA SRLLAKLRKD IRPEFREDFV LTITGKKPPC CVLSNPDQKG 
KIRRIDCLRQ ADKVWRLDLV MVILFKGIPL ESTDGERLYK SPQCSNPGLC VQPHHIGVTI 
KELDLYLAYF VHTPESGQSD SSNQQGDADI KPLPNGHLSF QDCFVTSGVW NVTELVRVSQ 
TPVATASGPN FSLADLESPS YYNINQVTLG RRSITSPPST STTKRPKSID DSEMESPVDD 
VFYPGTGRSP AAGSSQSSGW PNDVDAGPAS LKKSGKLDFC SALSSQGSSP RMAFTHHPLP 
VLAGVRPGSP RATASALHFP STSIIQQSSP YFTHPTIRYH HHHGQDSLKE FVQFVCSDGS 
GQATGQPNGS GQGKVPGSFL LPPPPPVARP VPLPMPDSKS TSTAPDGAAL TPPSPSFATT 
GASSANRFVS IGPRDGNFLN IPQQSQSWFL

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.