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: Prl2b1 ENSRNOG00000017007

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Description

prolactin family 2, subfamily B, member 1 [Source:RGD Symbol;Acc:620118]

Gene Synonyms

Ghd11, PLP-K, Prlpk

Location

Primary_assembly 17: 37,799,583-37,806,572 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 2 transcripts (splice variants), 309 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000114832.2	Prl2b1-202	807	230aa	ENSRNOP00000084002.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZWB8	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000090652.3	Prl2b1-201	801	228aa	ENSRNOP00000069833.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JWD1 A6J7S3	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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