Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Prl7c1 ENSRNOG00000047649

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Description

prolactin family 7, subfamily c, member 1 [Source:RGD Symbol;Acc:1593943]

Gene Synonyms

Ghd6, LOC684107

Location

Primary_assembly 17: 37,183,189-37,190,618 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 308 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000074999.4	Prl7c1-201	883	251aa	ENSRNOP00000066029.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J7Q2 M0R967	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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