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

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Gene: HOXC13 ENSSSCG00000000279

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Description

homeobox C13 [Source:VGNC Symbol;Acc:VGNC:88951]

Location

Primary_assembly 5: 19,151,084-19,158,646 forward strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 1 transcript (splice variant), 205 orthologues, 41 paralogues and is associated with 1 phenotype.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000000300.5	HOXC13-201	2085	332aa	ENSSSCP00000000295.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1WBW3 F1SFN9	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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Orthologues

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