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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Prl7d1 ENSRNOG00000016510

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Description

prolactin family 7, subfamily D, member 1 [Source:RGD Symbol;Acc:621307]

Gene Synonyms

PRP, Plfr

Location

Primary_assembly 17: 37,255,240-37,262,097 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 310 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000022251.8	Prl7d1-201	1281	245aa	ENSRNOP00000022251.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7F8M3 Q9R005	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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