Description

wingless-type MMTV integration site family, member 16 [Source:HGNC Symbol;Acc:HGNC:16267]

INSDC coordinates

chromosome:GRCh38:CM000669.2:121325367:121341104:1

Transcripts

This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
WNT16-001ENST000002224623147365 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS5781Q9UBV4 NM_057168
NP_476509
TSL:1

TSL1: All splice junctions of the transcript 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 PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
WNT16-002ENST000003613011230355 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS5780E9PH60 NM_016087
NP_057171
TSL:1

TSL1: All splice junctions of the transcript 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).

Gene-based displays