Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: Prl7b1 ENSRNOG00000016742

.

Description

prolactin family 7, subfamily B, member 1 [Source:RGD Symbol;Acc:708582]

Gene Synonyms

LOC266804, PLP-N, Prlpn

Location

Primary_assembly 17: 37,206,547-37,214,723 forward strand.

mRatBN7.2:CM026990.1

About this gene

This gene has 1 transcript (splice variant), 300 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000022447.5	Prl7b1-201	859	251aa	ENSRNOP00000022447.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UHN3 Q8CJ42	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,

.

Summary

.

.