Description

T-cell acute lymphocytic leukemia 2 [Source:HGNC Symbol;Acc:HGNC:11557]

Synonyms

bHLHa19

INSDC coordinates

chromosome:GRCh38:CM000671.2:105662457:105663112:1

About this gene

This gene has 1 transcript (splice variant), 53 orthologues, 10 paralogues, is a member of 1 Ensembl protein family and is associated with 1 phenotype.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
TAL2-001ENST00000334077656108aaENSP00000334547
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS6767Q16559 NM_005421
NP_005412
TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

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.

Gene-based displays