BCAS3
BCAS3 microtubule associated cell migration factor
Also known as: BCAS3_HUMAN, FLJ20128, PHAF2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H6U6
- Gene
- BCAS3
- Ensembl
- ENSG00000141376
- Chromosome
- 17
- Canonical length
- 928 aa
- Protein class
- Disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoli
OverviewNCBI Gene
Enables several functions, including acetyltransferase activator activity; beta-tubulin binding activity; and histone acetyltransferase binding activity. Involved in cellular response to estrogen stimulus; positive regulation of catalytic activity; and positive regulation of transcription by RNA polymerase II. Located in euchromatin; nucleus; and phagophore assembly site. Implicated in Hengel-Maroofian-Schols syndrome. Biomarker of breast cancer. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
928 residues, UniProt reviewed canonical sequence.
>Q9H6U6|BCAS3
1 MNEAMATDSP RRPSRCTGGV VVRPQAVTEQ SYMESVVTFL QDVVPQAYSG TPLTEEKEKI
61 VWVRFENADL NDTSRNLEFH EIHSTGNEPP LLIMIGYSDG MQVWSIPISG EAQELFSVRH
121 GPIRAARILP APQFGAQKCD NFAEKRPLLG VCKSIGSSGT SPPYCCVDLY SLRTGEMVKS
181 IQFKTPIYDL HCNKRILVVV LQEKIAAFDS CTFTKKFFVT SCYPCPGPNM NPIALGSRWL
241 AYAENKLIRC HQSRGGACGD NIQSYTATVI SAAKTLKSGL TMVGKVVTQL TGTLPSGVTE
301 DDVAIHSNSR RSPLVPGIIT VIDTETVGEG QVLVSEDSDS DGIVAHFPAH EKPVCCMAFN
361 TSGMLLVTTD TLGHDFHVFQ ILTHPWSSSQ CAVHHLYTLH RGETEAKVQD ICFSHDCRWV
421 VVSTLRGTSH VFPINPYGGQ PCVRTHMSPR VVNRMSRFQK SAGLEEIEQE LTSKQGGRCS
481 PVPGLSSSPS GSPLHGKLNS QDSYNNFTNN NPGNPRLSPL PSLMVVMPLA QIKQPMTLGT
541 ITKRTGPYLF GAGCFSIKAP CKVKPPPQIS PSKSMGGEFC VAAIFGTSRS WFANNAGLKR
601 EKDQSKQVVV ESLYIISCYG TLVEHMMEPR PLSTAPKISD DTPLEMMTSP RASWTLVRTP
661 QWNELQPPFN ANHPLLLAAD AVQYYQFLLA GLVPPGSPGP ITRHGSYDSL ASDHSGQEDE
721 EWLSQVEIVT HTGPHRRLWM GPQFQFKTIH PSGQTTVISS SSSVLQSHGP SDTPQPLLDF
781 DTDDLDLNSL RIQPVRSDPV SMPGSSRPVS DRRGVSTVID AASGTFDRSV TLLEVCGSWP
841 EGFGLRHMSS MEHTEEGLRE RLADAMAESP SRDVVGSGTE LQREGSIETL SNSSGSTSGS
901 IPRNFDGYRS PLPTNESQPL SLFPTGFPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BCAS3 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)
- 0.43
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 17 nTPM
- blood vessel: 17 nTPM
- skeletal muscle: 16 nTPM
- retina: 16 nTPM
- parathyroid gland: 14 nTPM
- skin: 14 nTPM
Single-cell type
- respiratory ciliated cells: 1,157 nCPM
- neutrophils: 1,099 nCPM
- renal connecting tubule cells: 795 nCPM
- renal collecting duct principal cells: 790 nCPM
- myonuclei: 769 nCPM
- oligodendrocytes: 689 nCPM
Immune cell
- neutrophil: 35 nTPM
- basophil: 27 nTPM
- T-reg: 18 nTPM
- eosinophil: 16 nTPM
- NK-cell: 15 nTPM
- gdT-cell: 15 nTPM
Brain region
- white matter: 63 nTPM
- pons: 51 nTPM
- cerebral cortex: 50 nTPM
- basal ganglia: 47 nTPM
- medulla oblongata: 47 nTPM
- cerebellum: 46 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about BCAS3.
Disease | AllUniProt
Conditions BCAS3 is implicated in, by any mechanism.
- Hengel-Maroofian-Schols syndrome (HEMARS) MIM:619641
Disease | GeneticClinVar
16 pathogenic / likely-pathogenic of 171 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Global developmental delay
- Hengel-Maroofian-Schols syndrome
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)
- 0.47
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.6
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- angiogenesis
- autophagy
- cell-cell signaling
- cellular response to estrogen stimulus
- positive regulation of catalytic activity
- positive regulation of endothelial cell migration
- positive regulation of transcription by RNA polymerase II
- regulation of actin cytoskeleton organization
- response to estrogen
- response to starvation
Molecular functions
- acetyltransferase activator activity
- beta-tubulin binding
- chromatin binding
- histone acetyltransferase binding
- histone binding
- nuclear receptor binding
- phosphatidylinositol binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- WD40/YVTN repeat-like-containing domain superfamily
- WD40-repeat-containing domain superfamily
- BCAS3 domain
- BCAS3-like
- BCAS3, WD40 domain
- BCAS3 microtubule associated cell migration factor, C-terminal
- BCAS3, WD40 repeat
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BCAS3 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 BCAS3 as an antibody target. Whether an autoantibody or antibody against BCAS3 could matter depends on whether native BCAS3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BCAS3 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 BCAS3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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