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

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Gene: SLC38A8 ENSG00000166558

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Description

solute carrier family 38, member 8 [Source:HGNC Symbol;Acc:32434]

Location

Chromosome 16: 84,043,272-84,076,241 reverse strand.

GRCh37:CM000678.1

About this gene

This gene has 4 transcripts (splice variants), 1 paralogue 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
ENST00000299709.3	SLC38A8-001	1308	435aa	ENSP00000299709.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS32495	A6NNN8 H3BP02 H3BUP5	NM_001080442.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000568178.1	SLC38A8-002	861	262aa	ENSP00000457737.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		H3BP02 H3BUP5	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000569816.1	SLC38A8-003	578	46aa	ENSP00000455085.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		H3BP02	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000568003.1	SLC38A8-004	501	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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