Description

solute carrier family 16, member 12 [Source:HGNC Symbol;Acc:HGNC:23094]

Synonyms

MCT12

Location
INSDC coordinates

chromosome:GRCh38:CM000672.2:89430299:89556641:1

Transcripts

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

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
SLC16A12-001ENST000003717904617516 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS7404E9PPP4 E9PSF9 Q6ZSM3
NM_213606
NP_998771
TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

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
SLC16A12-003ENST0000047568234025 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-E9PPP4 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:3

TSL3:The only support for this transcript is from a single EST.

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.

Gene-based displays