Loading…

Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: ISL2 ENSG00000159556

.

Description

ISL LIM homeobox 2 [Source:HGNC Symbol;Acc:18524]

Gene Synonyms

FLJ10160

Location

Chromosome 15: 76,629,065-76,634,817 forward strand.

GRCh37:CM000677.1

About this gene

This gene has 3 transcripts (splice variants) and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000290759.4	ISL2-001	1881	359aa	ENSP00000290759.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS10290	Q96A47	NM_145805.1	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000558656.1	ISL2-002	1446	195aa	ENSP00000453837.1	Nonsense mediated decay		H0YN25	-	-
ENST00000558437.1	ISL2-003	793	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

.

Summary

.

.