1. Gene
  2. POC5 - POC5 centriolar protein Gene

POC5 - POC5 centriolar protein Gene

Homo sapiens

Also known as C5orf37

Gene ID: 134359 | Gene type: protein coding

About POC5

Cytogenetic location: 5q13.3 Genomic coordinates (GRCh38): 5:75,674,124-75,717,437 (from NCBI)

This gene has 14 transcripts (splice variants) and 94 orthologues. Broad expression in testis (RPKM 10.4), lymph node (RPKM 4.7) and 24 other tissues.

Summary

Predicted to enable identical protein binding activity. Located in centrosome; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

POC5 Products(2)

mRNA Protein Name
NM_001099271.2 NP_001092741.1 centrosomal protein POC5 isoform 1
NM_152408.3 NP_689621.2 centrosomal protein POC5 isoform 2
Protein Preferred Names Protein Names

centrosomal protein POC5

POC5 centriolar protein homolog

Related Diseases

Diseases Alias
Syndromic Rod-Cone Dystrophy

Syndromic Retinitis Pigmentosa

Idiopathic Scoliosis

Scoliosis Idiopathic

Scoliosis
Orofaciodigital Syndrome I

OFD1

Orofaciodigital Syndrome 1

Oral-Facial-Digital Syndrome, Type I

Oral-Facial-Digital Syndrome 1

Ofds I

Papillon-Leage And Psaume Syndrome

Papillon-Leage-Psaume Syndrome

Oral-Facial-Digital Syndrome Type 1

Orofaciodigital Syndrome Type 1

Orofaciodigital Syndromes

Orofaciodigital Syndrome Type I

Oral-Facial-Digital Syndrome Type I

Ofd Syndrome 1

Ofds 1

Oral Facial Digital Syndrome 1

Oral Facial Digital Syndrome Type 1

Papillon-League-Psaume Syndrome

Ofdi

Ofdsi

Orofaciodigital Syndrome, Type I

Syringomyelia

Hydromyelia

Primary Autosomal Recessive Microcephaly

Autosomal Recessive Primary Microcephaly

Mcph

True Microcephaly

Microcephalia Vera

Microcephaly Vera

Microcephaly Primary Hereditary

Microcephaly, Primary, Autosomal Recessive

Primary Microcephaly

Bone Structure Disease
Primary Microcephaly

True Microcephaly

Microcephaly, Primary

Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus POC5 RGD RGD:1310597
Bos taurus POC5 VGNC VGNC:33100
Mus musculus POC5 MGD MGI:1914713
Canis familiaris POC5 VGNC VGNC:44762
Felis catus POC5 VGNC VGNC:64272
Macaca mulatta POC5 VGNC VGNC:76119