BABAM1
BRISC and BRCA1-A complex member 1
Also known as: BABA1_HUMAN, C19orf62, FLJ20571, HSPC142, MERIT40, NBA1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NWV8
- Gene
- BABAM1
- Ensembl
- ENSG00000105393
- Chromosome
- 19
- Canonical length
- 329 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies,Cytosol
OverviewNCBI Gene
Enables identical protein binding activity. Involved in several processes, including DNA repair-dependent chromatin remodeling; mitotic G2 DNA damage checkpoint signaling; and positive regulation of DNA repair. Located in cytosol and nuclear body. Part of BRCA1-A complex and BRISC complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
329 residues, UniProt reviewed canonical sequence.
>Q9NWV8|BABAM1
1 MEVAEPSSPT EEEEEEEEHS AEPRPRTRSN PEGAEDRAVG AQASVGSRSE GEGEAASADD
61 GSLNTSGAGP KSWQVPPPAP EVQIRTPRVN CPEKVIICLD LSEEMSLPKL ESFNGSKTNA
121 LNVSQKMIEM FVRTKHKIDK SHEFALVVVN DDTAWLSGLT SDPRELCSCL YDLETASCST
181 FNLEGLFSLI QQKTELPVTE NVQTIPPPYV VRTILVYSRP PCQPQFSLTE PMKKMFQCPY
241 FFFDVVYIHN GTEEKEEEMS WKDMFAFMGS LDTKGTSYKY EVALAGPALE LHNCMAKLLA
301 HPLQRPCQSH ASYSLLEEED EAIEVEATVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BABAM1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 126 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 126 nTPM
- cerebral cortex: 95 nTPM
- tongue: 90 nTPM
- amygdala: 80 nTPM
- heart muscle: 72 nTPM
- hippocampal formation: 70 nTPM
Single-cell type
- other brain neurons: 28 nCPM
- brain excitatory neurons: 28 nCPM
- brain inhibitory neurons: 24 nCPM
- oligodendrocytes: 22 nCPM
- microglia: 20 nCPM
- oligodendrocyte progenitor cells: 20 nCPM
Immune cell
- total PBMC: 214 nTPM
- basophil: 202 nTPM
- T-reg: 181 nTPM
- eosinophil: 168 nTPM
- myeloid DC: 161 nTPM
- classical monocyte: 155 nTPM
Brain region
- cerebral cortex: 72 nTPM
- pons: 65 nTPM
- basal ganglia: 65 nTPM
- hypothalamus: 64 nTPM
- white matter: 63 nTPM
- midbrain: 60 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.32
- gnomAD pLI
- 0.96
- gnomAD missense Z
- 1.17
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell division
- DNA repair-dependent chromatin remodeling
- double-strand break repair
- hematopoietic stem cell proliferation
- mitotic G2 DNA damage checkpoint signaling
- mitotic G2/M transition checkpoint
- positive regulation of DNA repair
- regulation of DNA repair
- response to ionizing radiation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- von Willebrand factor A-like domain superfamily
- BRISC and BRCA1-A complex member 1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BABAM1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BABAM1 as an antibody target. Whether an autoantibody or antibody against BABAM1 could matter depends on whether native BABAM1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BABAM1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label BABAM1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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