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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

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Gene: SLC25A42 ENSG00000181035

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Description

solute carrier family 25, member 42 [Source:HGNC Symbol;Acc:28380]

Gene Synonyms

MGC26694

Location

Chromosome 19: 19,174,808-19,223,697 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 6 transcripts (splice variants), 6 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000318596.7	SLC25A42-001	3120	318aa	ENSP00000326693.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS32966	Q86VD7	NM_178526.4	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000600275.1	SLC25A42-006	318	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-
ENST00000594070.1	SLC25A42-002	1228	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000596819.1	SLC25A42-005	753	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000597661.1	SLC25A42-003	519	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000600251.1	SLC25A42-004	414	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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