Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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11116 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Centrosomal protein 43 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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CEP43 |
SynonymsGene synonyms aliases
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FGFR1OP, FOP |
ChromosomeChromosome number
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6 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6q27 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a largely hydrophilic centrosomal protein that is required for anchoring microtubules to subcellular structures. A t(6;8)(q27;p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has |
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
O95684 |
Protein name |
Centrosomal protein 43 (FGFR1 oncogene partner) |
Protein function |
Required for anchoring microtubules to the centrosomes (PubMed:16314388, PubMed:28659385). Required for ciliation (PubMed:28625565, PubMed:28659385). |
PDB |
2D68
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF09398 |
FOP_dimer |
54 → 134 |
FOP N terminal dimerisation domain |
Domain |
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Sequence |
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Sequence length |
399 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Asthma |
Asthma |
rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283 |
21150878 |
Multiple sclerosis |
Multiple Sclerosis |
rs104895219, rs483353022, rs483353023, rs483353028, rs483353029, rs483353024, rs483353030, rs3207617, rs483353031, rs483353032, rs483353033, rs483353034, rs483353035, rs483353036, rs483353039, rs483353038, rs61731956, rs568165874, rs767480544 |
22190364 |
Psoriasis |
Psoriasis |
rs281875215, rs587777763, rs281875213, rs281875212 |
26974007 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Ankylosing spondylitis |
Ankylosing spondylitis |
|
26974007 |
Cholangitis |
Cholangitis, Sclerosing |
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26974007 |
Crohn disease |
Crohn Disease |
rs2066847, rs2066844, rs886052047, rs5743265, rs111608429, rs104895438 |
18587394, 26974007, 20570966 |
Graves disease |
Graves Disease |
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22922229, 21841780 |
Ulcerative colitis |
Ulcerative Colitis |
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26974007 |
Vitiligo |
Vitiligo |
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20526339, 22561518 |
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