Description

retina and anterior neural fold homeobox 2 [Source:HGNC Symbol;Acc:HGNC:18286]

Synonyms

ARMD6, CORD11, MGC15631, RAXL1

Location
INSDC coordinates

chromosome:GRCh38:CM000681.2:3769089:3772221:1

About this gene

This gene has 2 transcripts (splice variants), 31 orthologues, 14 paralogues, is a member of 1 Ensembl protein family and is associated with 3 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
RAX2-001ENST000005556332414184aaENSP00000450456
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS12112Q96IS3 -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.

RAX2-003ENST000005559782145184aaENSP00000450687
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS12112Q96IS3 NM_032753
NP_116142
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.

Gene-based displays