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Human (GRCh37.p13)
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.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000299709.3SLC38A8-0011308435aaENSP00000299709.3
 
Protein coding
CCDS32495A6NNN8 H3BP02 H3BUP5
NM_001080442.1Ensembl CanonicalGENCODE basic
ENST00000568178.1SLC38A8-002861262aaENSP00000457737.1
 
Protein coding
H3BP02 H3BUP5 -CDS 3' incomplete
ENST00000569816.1SLC38A8-00357846aaENSP00000455085.1
 
Protein coding
H3BP02 -CDS 3' incomplete
ENST00000568003.1SLC38A8-004501No protein-
 
Retained intron
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