Description

tripartite motif containing 10 [Source:HGNC Symbol;Acc:HGNC:10072]

Synonyms

HERF1, RFB30, RNF9

Location

Chromosome 6: 30,151,945-30,160,934 reverse strand.

View alleles of this gene on alternate assemblies

INSDC coordinates

chromosome:GRCh38:CM000668.2:30151945:30160934:1

About this gene

This gene has 2 transcripts (splice variants), 7 gene alleles, 49 orthologues, 13 paralogues, is a member of 1 Ensembl protein family and is associated with 67 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
TRIM10-002ENST000004497423546481aaENSP00000397073
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS34375Q9UDY6 NM_006778
NP_006769
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

TRIM10-001ENST000003767043007395aaENSP00000365894
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS4676Q9UDY6 NM_052828
NP_439893
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays