Human (GRCh37.p13)
Description

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit s (factor B) [Source:HGNC Symbol;Acc:18799]

Gene Synonyms

ATPW, FB, HSU79253

Location

Chromosome 14: 50,779,044-50,802,276 forward strand.

GRCh37:CM000676.1

About this gene

This gene has 11 transcripts (splice variants) and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000245448.6ATP5S-0021671127aaENSP00000245448.6
 
Protein coding
CCDS32076Q99766 NM_001003805.2GENCODE basic
ENST00000311459.7ATP5S-0031292215aaENSP00000308334.7
 
Protein coding
CCDS32075Q99766 NM_001003803.2GENCODE basic
ENST00000426751.2ATP5S-0041171136aaENSP00000389246.2
 
Protein coding
CCDS45102Q99766 NM_015684.3GENCODE basic
ENST00000358473.1ATP5S-011801266aaENSP00000351258.1
 
Protein coding
Q8WXQ4 -GENCODE basic
ENST00000554204.1ATP5S-001147614aaENSP00000451583.1
 
Nonsense mediated decay
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ENST00000554438.1ATP5S-0102008No protein-
 
Processed transcript
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ENST00000555939.1ATP5S-006708No protein-
 
Processed transcript
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ENST00000554951.1ATP5S-005620No protein-
 
Processed transcript
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ENST00000557421.1ATP5S-008501No protein-
 
Processed transcript
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ENST00000553774.1ATP5S-009530No protein-
 
Retained intron
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ENST00000556962.1ATP5S-007525No protein-
 
Retained intron
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