Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Pomc ENSRNOG00000012686

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Description

proopiomelanocortin [Source:RGD Symbol;Acc:3366]

Gene Synonyms

ACTH, Pomc1, Pomc2, alphaMSH

Location

Primary_assembly 6: 32,659,346-32,665,173 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 1 transcript (splice variant), 280 orthologues and is associated with 126 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000016976.9	Pomc-201	939	235aa	ENSRNOP00000016976.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6PTD9 Q8K422	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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