Details for: B9D1

Gene ID: 27077

Symbol: B9D1

Ensembl ID: ENSG00000108641

Description: B9 domain containing 1

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: polychromatophilic erythroblast (CL0000550)
    Fold Change: 112.7003
    Cell Significance Index: -17.5300
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 76.7613
    Cell Significance Index: -19.4700
  • Cell Name: smooth muscle fiber of ileum (CL1000278)
    Fold Change: 42.0865
    Cell Significance Index: -19.8700
  • Cell Name: ileal goblet cell (CL1000326)
    Fold Change: 29.6264
    Cell Significance Index: -19.8800
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 15.7102
    Cell Significance Index: -19.3700
  • Cell Name: CD8-alpha-beta-positive, alpha-beta intraepithelial T cell (CL0000796)
    Fold Change: 7.4173
    Cell Significance Index: -19.8700
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 4.9847
    Cell Significance Index: -19.6700
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.9788
    Cell Significance Index: 61.6900
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.8894
    Cell Significance Index: 178.4200
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.8697
    Cell Significance Index: 38.4700
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.7629
    Cell Significance Index: 28.8900
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.7221
    Cell Significance Index: 394.3400
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: 0.7083
    Cell Significance Index: 203.8000
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.6289
    Cell Significance Index: 567.8300
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.5546
    Cell Significance Index: 60.3300
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.5542
    Cell Significance Index: 33.2700
  • Cell Name: kidney cell (CL1000497)
    Fold Change: 0.5436
    Cell Significance Index: 4.3400
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.5077
    Cell Significance Index: 82.5800
  • Cell Name: peg cell (CL4033014)
    Fold Change: 0.4523
    Cell Significance Index: 10.4500
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.4210
    Cell Significance Index: 83.5400
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.2703
    Cell Significance Index: 96.9600
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: 0.2675
    Cell Significance Index: 12.4700
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.2412
    Cell Significance Index: 45.9000
  • Cell Name: thyroid follicular cell (CL0002258)
    Fold Change: 0.2282
    Cell Significance Index: 2.4300
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.2255
    Cell Significance Index: 15.6000
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.1678
    Cell Significance Index: 116.0700
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.1631
    Cell Significance Index: 10.9700
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 0.1533
    Cell Significance Index: 19.6500
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1509
    Cell Significance Index: 14.9300
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.1301
    Cell Significance Index: 23.4500
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.1295
    Cell Significance Index: 17.7800
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 0.1053
    Cell Significance Index: 5.4700
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: 0.0939
    Cell Significance Index: 5.2700
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 0.0701
    Cell Significance Index: 1.9600
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.0560
    Cell Significance Index: 24.7600
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: 0.0539
    Cell Significance Index: 1.1800
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0533
    Cell Significance Index: 100.4400
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.0423
    Cell Significance Index: 5.2000
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.0419
    Cell Significance Index: 3.2200
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.0411
    Cell Significance Index: 0.8900
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.0392
    Cell Significance Index: 1.1300
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0238
    Cell Significance Index: 36.6900
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: 0.0230
    Cell Significance Index: 3.9200
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0223
    Cell Significance Index: 30.3500
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: 0.0182
    Cell Significance Index: 1.3600
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: 0.0180
    Cell Significance Index: 13.6600
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0153
    Cell Significance Index: 28.1800
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: 0.0088
    Cell Significance Index: 0.2400
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.0066
    Cell Significance Index: 4.1900
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: 0.0020
    Cell Significance Index: 0.0700
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0020
    Cell Significance Index: -1.4600
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0097
    Cell Significance Index: -4.3800
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.0111
    Cell Significance Index: -1.4400
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0117
    Cell Significance Index: -8.6700
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0254
    Cell Significance Index: -14.3200
  • Cell Name: proerythroblast (CL0000547)
    Fold Change: -0.0307
    Cell Significance Index: -0.4400
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: -0.0339
    Cell Significance Index: -2.4000
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0341
    Cell Significance Index: -21.3200
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.0375
    Cell Significance Index: -1.7000
  • Cell Name: retinal rod cell (CL0000604)
    Fold Change: -0.0424
    Cell Significance Index: -0.5100
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0443
    Cell Significance Index: -4.5300
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: -0.0517
    Cell Significance Index: -1.3900
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: -0.0573
    Cell Significance Index: -1.9900
  • Cell Name: ciliated epithelial cell (CL0000067)
    Fold Change: -0.0576
    Cell Significance Index: -0.5700
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.0576
    Cell Significance Index: -3.5400
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.0719
    Cell Significance Index: -8.3800
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.0778
    Cell Significance Index: -11.3100
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0943
    Cell Significance Index: -19.8700
  • Cell Name: medium spiny neuron (CL1001474)
    Fold Change: -0.1171
    Cell Significance Index: -1.5800
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.1323
    Cell Significance Index: -15.1600
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: -0.1323
    Cell Significance Index: -1.9000
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.1421
    Cell Significance Index: -7.4600
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.1481
    Cell Significance Index: -17.4700
  • Cell Name: granulosa cell (CL0000501)
    Fold Change: -0.1687
    Cell Significance Index: -4.4400
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.1699
    Cell Significance Index: -17.6900
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.1874
    Cell Significance Index: -14.8400
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.1911
    Cell Significance Index: -4.0700
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.2005
    Cell Significance Index: -3.3600
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.2014
    Cell Significance Index: -6.4500
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.2070
    Cell Significance Index: -5.3200
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.2075
    Cell Significance Index: -5.9200
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.2149
    Cell Significance Index: -10.1000
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.2502
    Cell Significance Index: -15.3400
  • Cell Name: lung ciliated cell (CL1000271)
    Fold Change: -0.2780
    Cell Significance Index: -2.7200
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: -0.2782
    Cell Significance Index: -5.4300
  • Cell Name: glutamatergic neuron (CL0000679)
    Fold Change: -0.2891
    Cell Significance Index: -3.1500
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.2903
    Cell Significance Index: -18.7300
  • Cell Name: ciliated columnar cell of tracheobronchial tree (CL0002145)
    Fold Change: -0.3092
    Cell Significance Index: -2.8400
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: -0.3163
    Cell Significance Index: -5.4200
  • Cell Name: ciliated cell (CL0000064)
    Fold Change: -0.3223
    Cell Significance Index: -3.4900
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: -0.3335
    Cell Significance Index: -6.9800
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: -0.3789
    Cell Significance Index: -5.1700
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.3909
    Cell Significance Index: -12.4500
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.3916
    Cell Significance Index: -12.8200
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -0.4092
    Cell Significance Index: -15.0200
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: -0.4202
    Cell Significance Index: -11.2200
  • Cell Name: helper T cell (CL0000912)
    Fold Change: -0.4300
    Cell Significance Index: -6.1100
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.4356
    Cell Significance Index: -15.2600
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: -0.4486
    Cell Significance Index: -6.7600
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.4632
    Cell Significance Index: -9.8300

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:** The B9D1 gene encodes a protein that contains a B9 domain, a conserved motif involved in protein-protein interactions. The protein is primarily expressed in ciliated cells, where it is thought to play a crucial role in cilia formation, anchoring, and maintenance. B9D1 is also expressed in endothelial cells, where it may contribute to vascular development and maintenance. The gene is involved in several signaling pathways, including the Smoothened signaling pathway, hedgehog receptor activity, and regulation of protein localization. These characteristics highlight the gene's importance in regulating cellular processes, including cell differentiation, migration, and survival. **Pathways and Functions:** B9D1 is involved in several key pathways, including: 1. **Anchoring of the basal body to the plasma membrane:** B9D1 is thought to play a crucial role in anchoring the basal body to the plasma membrane in ciliated cells, which is essential for cilia formation and function. 2. **Camera-type eye development:** B9D1 is expressed in the developing eye and is involved in the formation of the camera-type eye, a complex structure that requires precise cell differentiation and organization. 3. **Centrosome and ciliary basal body:** B9D1 is involved in the formation and maintenance of the centrosome and ciliary basal body, which are critical structures involved in cilia formation and function. 4. **Smoothened signaling pathway:** B9D1 is a component of the Smoothened signaling pathway, which is involved in hedgehog signaling and regulates cell growth, differentiation, and survival. 5. **Regulation of protein localization:** B9D1 is involved in regulating protein localization, which is essential for proper cellular function and tissue homeostasis. **Clinical Significance:** Dysregulation of B9D1 has been implicated in various diseases, including: 1. **Ciliary disorders:** Mutations in the B9D1 gene have been linked to ciliary disorders, such as primary ciliary dyskinesia, which is characterized by impaired cilia function and respiratory tract disease. 2. **Neurological disorders:** B9D1 has been implicated in neurological disorders, such as autism spectrum disorder, which is characterized by impaired social and communication skills. 3. **Cancer:** B9D1 has been shown to be involved in cancer development and progression, particularly in cancers of the respiratory tract and brain. 4. **Cardiovascular disease:** B9D1 has been implicated in cardiovascular disease, particularly in the development of atherosclerosis and cardiac failure. In conclusion, the B9D1 gene is a multifunctional gene that plays a crucial role in various cellular processes, including cilia formation, anchoring, and maintenance. Its dysregulation has been implicated in various diseases, highlighting the importance of understanding its role in normal physiology and disease pathology.

Genular Protein ID: 3862547041

Symbol: B9D1_HUMAN

Name: B9 domain-containing protein 1

UniProtKB Accession Codes:

Q9UPM9 Q9BU22

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 2 CTD 1 ComplexPortal 1 DMDM 1 DNASU 1 DisGeNET 1 EMBL 2 Ensembl 2 ExpressionAtlas 1 GO 15 GeneCards 1 GeneReviews 1 GeneTree 1 GenomeRNAi 1 HGNC 1 HPA 1 InParanoid 1 IntAct 1 InterPro 1 KEGG 1 MANE-Select 1 MIM 5 MalaCards 1 MassIVE 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 Orphanet 2 OrthoDB 1 PANTHER 2 PRO 1 PROSITE 1 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 1 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 2 Pumba 1 RNAct 1 Reactome 1 RefSeq 5 STRING 1 SignaLink 1 TreeFam 1 UCSC 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 jPOST 1 neXtProt 1

Citations:

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: 19208769

Title: Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins.

PubMed ID: 19208769

DOI: 10.1242/jcs.028621

PubMed ID: 21493627

Title: B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis.

PubMed ID: 21493627

DOI: 10.1093/hmg/ddr151

PubMed ID: 24886560

Title: Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.

PubMed ID: 24886560

DOI: 10.1186/1750-1172-9-72

PubMed ID: 26477546

Title: Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.

PubMed ID: 26477546

DOI: 10.1016/j.ajhg.2015.09.009

Sequence Information:

  • Length: 204
  • Mass: 22775
  • Checksum: 6F09A3152F48CE42
  • Sequence:
    • MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV 
RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP 
MFVPESTSKL QKFTSWFMGR RPEYTDPKVV AQGEGREVTR VRSQGFVTLL FNVVTKDMRK 
LGYDTGPSDT QGVLGPSPPQ SFPQ

Genular Protein ID: 1165803069

Symbol: A0A0B4J223_HUMAN

Name: N/A

UniProtKB Accession Codes:

A0A0B4J223

Database IDs:

ARBA 8 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CTD 1 DNASU 1 DisGeNET 1 EMBL 1 Ensembl 2 ExpressionAtlas 1 GO 3 GeneTree 1 HGNC 1 InterPro 1 MassIVE 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PROSITE 1 PeptideAtlas 2 Pfam 1 Proteomes 2 ProteomicsDB 1 RefSeq 1 SAM 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: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

Sequence Information:

  • Length: 186
  • Mass: 20665
  • Checksum: 1AA16CAFD8C85453
  • Sequence:
    • MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV 
RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP 
MFVPESTSKL QKFTSWFMGR RPEYTDPKVV AQGEGREAIT APRKAVFSVH GLTSPRALAL 
VHIKGT

Genular Protein ID: 187086618

Symbol: B4DEW0_HUMAN

Name: N/A

UniProtKB Accession Codes:

B4DEW0

Database IDs:

ARBA 8 AlphaFoldDB 1 BioGRID-ORCS 1 CTD 1 DNASU 1 DisGeNET 1 EMBL 2 GO 4 InterPro 1 KEGG 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PROSITE 1 PeptideAtlas 1 Pfam 1 RefSeq 4 SAM 1

Sequence Information:

  • Length: 183
  • Mass: 20323
  • Checksum: 553939C6C4DB777B
  • Sequence:
    • MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV 
RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP 
MFVPESTSKL QKFTSWFMGR RPEYTDPKVV AQGEGREGKA PSPLLPLSPI QVTAWEWVGP 
GLG

Genular Protein ID: 2305607142

Symbol: A0A2R8Y646_HUMAN

Name: N/A

UniProtKB Accession Codes:

A0A2R8Y646

Database IDs:

ARBA 8 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 CTD 1 DNASU 1 DisGeNET 1 EMBL 1 Ensembl 2 ExpressionAtlas 1 GO 3 GeneTree 1 HGNC 1 InterPro 1 MassIVE 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PROSITE 1 PeptideAtlas 2 Pfam 1 Proteomes 2 ProteomicsDB 1 RefSeq 1 SAM 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: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

Sequence Information:

  • Length: 183
  • Mass: 20307
  • Checksum: 413879C6C4DB777B
  • Sequence:
    • MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV 
RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP 
MFVPESTSKL QKFTSWFMGR RPEYTDPKVV AQGEGREGKA PSPLLPPSPI QVTAWEWVGP 
GLG

Genular Protein ID: 4121083157

Symbol: A0A6Q8PFJ7_HUMAN

Name: N/A

UniProtKB Accession Codes:

A0A6Q8PFJ7

Database IDs:

ARBA 8 AlphaFoldDB 1 Bgee 1 CTD 1 DisGeNET 1 EMBL 1 Ensembl 2 ExpressionAtlas 1 GO 3 GeneTree 1 HGNC 1 InterPro 1 MassIVE 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PROSITE 1 PeptideAtlas 2 Pfam 1 Proteomes 2 ProteomicsDB 1 RefSeq 1 SAM 1

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: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

Sequence Information:

  • Length: 155
  • Mass: 17191
  • Checksum: B9559CB44698CACD
  • Sequence:
    • MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV 
RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP 
MFVPESTSKL QKFTSHLQGC LSKIAVFQDE SGLSP

Genular Protein ID: 3112885790

Symbol: A8MYG7_HUMAN

Name: N/A

UniProtKB Accession Codes:

A8MYG7

Database IDs:

ARBA 8 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID-ORCS 1 CTD 1 DNASU 1 DisGeNET 1 EMBL 1 Ensembl 2 ExpressionAtlas 1 GO 3 GeneTree 1 HGNC 1 InterPro 1 MassIVE 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PROSITE 1 PeptideAtlas 2 Pfam 1 Proteomes 2 ProteomicsDB 2 RefSeq 1 SAM 1 UCSC 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: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

Sequence Information:

  • Length: 187
  • Mass: 21041
  • Checksum: 2ADD668A5A5BDBC0
  • Sequence:
    • MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV 
RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP 
MFVPESTSKL QKFTSWFMGR RPEYTDPKVV AQGEGREDEN AEAEIPRSTW VSLCPSPAWL 
MLPFCPQ

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.