Loading…

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

Configure this page

Share this page

Bookmark this page

.

Gene: SLC16A12 ENSG00000152779

.

Description

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

Gene Synonyms

CJMG, MCT12

Location

Chromosome 10: 91,190,051-91,316,398 reverse strand.

GRCh37:CM000672.1

About this gene

This gene has 3 transcripts (splice variants), 11 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000341233.4	SLC16A12-201	4622	486aa	ENSP00000343022.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q6ZSM3	NM_213606.3	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000371790.4	SLC16A12-001	4617	516aa	ENSP00000360855.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS7404	E9PPP4 E9PSF9	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000475682.1	SLC16A12-003	340	25aa	ENSP00000436965.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PPP4	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

.

Summary

.

.