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: Prl2c1 ENSRNOG00000039058

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Description

prolactin family 2, subfamily C, member 1 [Source:RGD Symbol;Acc:1562878]

Gene Synonyms

Ghd4, LOC502122, RGD1562878

Location

Primary_assembly 17: 37,089,507-37,097,827 reverse strand.

GRCr8:CM070407.1

About this gene

This gene has 2 transcripts (splice variants), 317 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000059738.6	Prl2c1-201	744	227aa	ENSRNOP00000056493.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1KZI0	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,
ENSRNOT00000119514.2	Prl2c1-202	636	191aa	ENSRNOP00000081386.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZRV4	-

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Summary

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