1. Gene
  2. URM1 - ubiquitin related modifier 1 Gene

URM1 - ubiquitin related modifier 1 Gene

Homo sapiens

Also known as C9orf74

Gene ID: 81605 | Gene type: protein coding

About URM1

Cytogenetic location: 9q34.11 Genomic coordinates (GRCh38): 9:128,371,319-128,392,016 (from NCBI)

This gene has 5 transcripts (splice variants) and 181 orthologues. Ubiquitous expression in spleen (RPKM 8.1), lymph node (RPKM 7.6) and 25 other tissues.

Summary

Enables sulfur carrier activity. Involved in tRNA thio-modification and tRNA wobble uridine modification. Predicted to be located in cytosol. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

URM1 Products(3)

mRNA Protein Name
NM_001135947.2 NP_001129419.1 ubiquitin-related modifier 1 isoform b
NM_001265582.1 NP_001252511.1 ubiquitin-related modifier 1 isoform c
NM_030914.4 NP_112176.1 ubiquitin-related modifier 1 isoform a

URM1 Protein Structure

Urm1

Urm1: Urm1 (Ubiquitin related modifier) (6 - 101)

  • 0
  • 101 a.a.
Protein Preferred Names Protein Names

ubiquitin-related modifier 1

ubiquitin-related modifier 1 homolog

Related Diseases

Diseases Alias
Neuropathy, Hereditary Sensory And Autonomic, Type Iii

Familial Dysautonomia

Riley-Day Syndrome

Dysautonomia, Familial

HSAN3

Hsan Iii

Fd

Hereditary Sensory And Autonomic Neuropathy Type Iii

Dys

Hereditary Sensory And Autonomic Neuropathy 3

Riley Day Syndrome

Familial Autonomic Nervous Dysfunction

Hereditary Sensory Autonomic Neuropathy Type Iii

Hsan 3

Hsn 3

Hereditary Sensory Neuropathy Type 3

Hsan Type Iii

Hsn-Iii

Hereditary Sensory And Autonomic Neuropathy Type 3

Neuropathy, Hereditary Sensory And Autonomic, 3

Hsn Iii

Dysautonomia Familial

Neuropathy, Sensory And Autonomic, Hereditary, Type Iii

Hsan3 - [Hereditary Sensory And Autonomic Neuropathy Type 3]

Benign Epilepsy With Centrotemporal Spikes

Rolandic Epilepsy

Benign Rolandic Epilepsy

Epilepsy, Rolandic

Bcects

Benign Childhood Epilepsy With Centrotemporal Spike

Sylvan Seizures

Becrs

Bects

Bre

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Benign Familial Epilepsy Of Childhood With Rolandic Spikes

Centrotemporal Epilepsy

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 URM1 VGNC VGNC:79704
Bos taurus URM1 VGNC VGNC:36699
Mus musculus URM1 MGD MGI:1915455
Rattus norvegicus URM1 RGD RGD:1306599
Felis catus URM1 VGNC VGNC:66854
Canis familiaris URM1 VGNC VGNC:48167
Others URM1 NCBI