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

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Gene: HIGD1A ENSBTAG00000038640

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Description

HIG1 hypoxia inducible domain family member 1A [Source:NCBI gene (formerly Entrezgene);Acc:768057]

Gene Synonyms

HIGD1D

Location

Primary_assembly 22: 14,883,951-14,891,253 reverse strand.

ARS-UCD1.3:CM008189.2

About this gene

This gene has 2 transcripts (splice variants), 237 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000054347.4	HIGD1A-202	1447	102aa	ENSBTAP00000047644.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3X833	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,
ENSBTAT00000123195.1	HIGD1A-201	1472	93aa	ENSBTAP00000103399.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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