1. Gene
  2. RNF5 - ring finger protein 5 Gene

RNF5 - ring finger protein 5 Gene

Homo sapiens

Also known as RMA1; RING5

Gene ID: 6048 | Gene type: protein coding

About RNF5

Cytogenetic location: 6p21.32 Genomic coordinates (GRCh38): 6:32,178,405-32,180,793 (from NCBI)

This gene has 2 transcripts (splice variants), 1 gene allele, 185 orthologues and 1 paralogue. Ubiquitous expression in kidney (RPKM 45.9), small intestine (RPKM 33.9) and 25 other tissues.

Summary

The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008]

RNF5 Products(1)

mRNA Protein Name
NM_006913.4 NP_008844.1 E3 ubiquitin-protein ligase RNF5

RNF5 Protein Structure

zf-C3HC4_2

zf-C3HC4_2: Zinc finger, C3HC4 type (RING finger) (27 - 67)

  • 0
  • 100
  • 180 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase RNF5

RING-type E3 ubiquitin transferase RNF5

Related Diseases

Diseases Alias
Cystic Fibrosis

Mucoviscidosis

CF

Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

Cystic Fibrosis Lung Disease, Modifier Of

Cystic Fibrosis Of Pancreas

Fibrocystic Disease Of Pancreas

Cf - [Cystic Fibrosis]

Cystic Fibrosis Nos

Fibrocystic Disease

Fibrocystic Disease Of The Pancreas

Mucoviscidosis Of Pancreas

Nonproliferative Fibrocystic Disease

Pancreatic Cystic Fibrosis

Inflammatory Bowel Disease 7

IBD7

Herpes Simplex Virus Keratitis

Dendritic Keratitis

Keratitis, Dendritic

Keratitis, Herpetic

Phosphoglycerate Dehydrogenase Deficiency

Phgdh Deficiency

3-Phosphoglycerate Dehydrogenase Deficiency

PHGDHD

3-Pgdh Deficiency

3-Phosphoglycerate Dehydrogenase Deficiency, Infantile/Juvenile Form

Phgdh Deficiency, Infantile/Juvenile Form

Deficiency, Phosphoglycerate Dehydrogenase

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
Macaca mulatta RNF5 VGNC VGNC:76706
Bos taurus RNF5 VGNC VGNC:34070
Felis catus RNF5 VGNC VGNC:64705
Canis familiaris RNF5 VGNC VGNC:45673
Rattus norvegicus RNF5 RGD RGD:1588458
Mus musculus RNF5 MGD MGI:1860076
Others RNF5 NCBI