Description

peptide YY [Source:HGNC Symbol;Acc:HGNC:9748]

Synonyms

PYY1

Location
INSDC coordinates

chromosome:GRCh38:CM000679.2:43952738:44004469:1

About this gene

This gene has 2 transcripts (splice variants), 44 orthologues, 1 paralogue, is a member of 1 Ensembl protein family and is associated with 26 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
PYY-001ENST00000360085105397aaENSP00000353198
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS32662P10082 NM_004160
NP_004151
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P2

PRINCIPAL2 - APPRIS candidate principal isoform (CCDS).

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

PYY-002ENST0000059279658090aaENSP00000467310
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-P10082 -TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS ALT1

ALTERNATIVE1 - APPRIS candidate principal isoform that is conserved in at least three tested non-primate species.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays