1. Gene
  2. TRIM71 - tripartite motif containing 71 Gene

TRIM71 - tripartite motif containing 71 Gene

Homo sapiens

Also known as LIN41; HYDCC1; LIN-41

Gene ID: 131405 | Gene type: protein coding

About TRIM71

Cytogenetic location: 3p22.3 Genomic coordinates (GRCh38): 3:32,817,997-32,897,824 (from NCBI)

This gene has 1 transcript (splice variant), 213 orthologues, 80 paralogues and is associated with 2 phenotypes. Biased expression in testis (RPKM 4.2), kidney (RPKM 0.7) and 1 other tissue.

Summary

The protein encoded by this gene is an E3 ubiquitin-protein Ligase that binds with miRNAs and maintains the growth and upkeep of embryonic stem cells. This gene also is involved in the G1-S phase transition of the cell cycle. [provided by RefSeq, Dec 2015]

TRIM71 Products(1)

mRNA Protein Name
NM_001039111.3 NP_001034200.1 E3 ubiquitin-protein ligase TRIM71

TRIM71 Protein Structure

zf-B_box

zf-B_box: B-box zinc finger (276 - 312)

Filamin

Filamin: Filamin/ABP280 repeat (487 - 577)

NHL

NHL: NHL repeat (606 - 633)

NHL

NHL: NHL repeat (653 - 680)

NHL

NHL: NHL repeat (700 - 727)

NHL

NHL: NHL repeat (747 - 773)

NHL

NHL: NHL repeat (794 - 819)

NHL

NHL: NHL repeat (843 - 868)

  • 0
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  • 800
  • 868 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase TRIM71

RING-type E3 ubiquitin transferase TRIM71

Related Diseases

Diseases Alias
Hydrocephalus, Congenital Communicating, 1

HYDCC1

Congenital Communicating Hydrocephalus

Congenital Non-Obstructive Hydrocephalus

Congenital Hydrocephalus

Hydrocephalus

Hydrocephalus Adverse Event

Hydrocephalus, Nonsyndromic, Autosomal Recessive 1

Hydrocephalus In Newborn

Congenital Hydrocephaly

Hydrocephalus

Hydrocephalus, Nonsyndromic, Autosomal Recessive

Hydrocephalus, X-Linked

Hydrocephalus Adverse Event

Hydrocephaly Nos

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h

Lgmd2h

Limb-Girdle Muscular Dystrophy Due To Trim32 Deficiency

Muscular Dystrophy Hutterite Type

Sarcotubular Myopathy

Limb-Girdle Muscular Dystrophy Type 2h

Autosomal Recessive Limb-Girdle Muscular Dystrophy

Muscular Dystrophy, Limb-Girdle, Autosomal Recessive

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
Canis familiaris TRIM71 VGNC VGNC:47837
Macaca mulatta TRIM71 VGNC VGNC:79926
Felis catus TRIM71 VGNC VGNC:66553
Mus musculus TRIM71 MGD MGI:2685973
Rattus norvegicus TRIM71 RGD RGD:1566388
Bos taurus TRIM71 VGNC VGNC:57366