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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ANHX ENSG00000227059

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Description

anomalous homeobox [Source:HGNC Symbol;Acc:40024]

Location

Chromosome 12: 133,794,898-133,812,681 reverse strand.

GRCh37:CM000674.1

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000545940.1	ANHX-001	3452	379aa	ENSP00000439513.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS53855	E9PGG2	-	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,
ENST00000419717.1	ANHX-201	1757	379aa	ENSP00000409950.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS53855	E9PGG2	NM_001191054.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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