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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: PRY2 ENSG00000169807

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Description

PTPN13-like, Y-linked 2 [Source:HGNC Symbol;Acc:21504]

Gene Synonyms

PRY1, PTPN13LY, PTPN13LY2

Location

Chromosome Y: 24,217,903-24,242,154 reverse strand.

GRCh37:CM000686.1

About this gene

This gene has 3 transcripts (splice variants) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000303804.1	PRY2-001	1238	147aa	ENSP00000303300.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS35482	O14603	NM_001002758.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000341740.2	PRY2-201	443	71aa	ENSP00000341879.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		O14603	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000472391.1	PRY2-002	1353	71aa	ENSP00000474545.1	Nonsense mediated decay		O14603	-	-

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Summary

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