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

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Gene: HOXD1 ENSSSCG00000015986

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Description

homeobox D1 [Source:VGNC Symbol;Acc:VGNC:96350]

Location

Primary_assembly 15: 81,987,769-81,990,134 forward strand.

Sscrofa11.1:CM000826.5

About this gene

This gene has 1 transcript (splice variant), 111 orthologues and 41 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000017407.4	HOXD1-201	2045	327aa	ENSSSCP00000016938.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UH02 F1RZF8	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, 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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