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

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Gene: HOXC11 ENSSSCG00000028104

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Description

homeobox C11 [Source:VGNC Symbol;Acc:VGNC:103287]

Location

Primary_assembly 5: 19,178,619-19,189,013 forward strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 1 transcript (splice variant), 206 orthologues and 41 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000030009.4	HOXC11-201	2469	304aa	ENSSSCP00000025770.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1W4U9 I3LNU5	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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