Gene Gene information from NCBI Gene database.
Entrez ID 91653
Gene name BOC cell adhesion associated, oncogene regulated
Gene symbol BOC
Synonyms (NCBI Gene)
BoiCDON2
Chromosome 3
Chromosome location 3q13.2
Summary The protein encoded by this gene is a member of the immunoglobulin/fibronectin type III repeat family. It is a component of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells, and promotes myogenic differen
miRNA miRNA information provided by mirtarbase database.
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miRTarBase ID miRNA Experiments Reference
MIRT021881 hsa-miR-128-3p Microarray 17612493
MIRT030663 hsa-miR-21-5p Microarray 18591254
MIRT539771 hsa-miR-148a-5p PAR-CLIP 21572407
MIRT539770 hsa-miR-148b-5p PAR-CLIP 21572407
MIRT539769 hsa-miR-6874-3p PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 11782431, 20519495, 21802063
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
GO:0007155 Process Cell adhesion IEA
GO:0007399 Process Nervous system development IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608708 17173 ENSG00000144857
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BWV1
Protein name Brother of CDO (Protein BOC)
Protein function Component of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells. Promotes differentiation of myogenic cells.
PDB 3N1G , 3N1M , 3N1P
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13927 Ig_3 35 109 Domain
PF00047 ig 134 213 Immunoglobulin domain Domain
PF13927 Ig_3 230 303 Domain
PF07679 I-set 323 408 Immunoglobulin I-set domain Domain
PF16625 ISET-FN3_linker 409 473 Disordered
PF00041 fn3 477 561 Fibronectin type III domain Domain
PF00041 fn3 607 693 Fibronectin type III domain Domain
PF00041 fn3 716 802 Fibronectin type III domain Domain
Tissue specificity TISSUE SPECIFICITY: Detected in skeletal muscle, heart, thymus, kidney and small intestine. Detected at lower levels in brain, placenta, lung and colon mucosa. {ECO:0000269|PubMed:11782431}.
Sequence
MLRGTMTAWRGMRPEVTLACLLLATAGCFADLNEVPQVTVQPASTVQKPGGTVILGCVVE
PPRMNVTWRLNGKELNGSDDALGVLITHGTLVITALNNHTVGRYQCVAR
MPAGAVASVPA
TVTLANLQDFKLDVQHVIEVDEGNTAVIACHLPESHPKAQVRYSVKQEWLEASRGNYLIM
PSGNLQIVNASQEDEGMYKCAAYNPVTQEVKTS
GSSDRLRVRRSTAEAARIIYPPEAQTI
IVTKGQSLILECVASGIPPPRVTWAKDGSSVTGYNKTRFLLSNLLIDTTSEEDSGTYRCM
ADN
GVGQPGAAVILYNVQVFEPPEVTMELSQLVIPWGQSAKLTCEVRGNPPPSVLWLRNA
VPLISSQRLRLSRRALRVLSMGPEDEGVYQCMAENEVGSAHAVVQLRT
SRPSITPRLWQD
AELATGTPPVSPSKLGNPEQMLRGQPALPRPPTSVGPASPQCPGEKGQGAPAE
APIILSS
PRTSKTDSYELVWRPRHEGSGRAPILYYVVKHRKVTNSSDDWTISGIPANQHRLTLTRLD
PGSLYEVEMAAYNCAGEGQTA
MVTFRTGRRPKPEIMASKEQQIQRDDPGASPQSSSQPDH
GRLSPPEAPDRPTISTASETSVYVTWIPRGNGGFPIQSFRVEYKKLKKVGDWILATSAIP
PSRLSVEITGLEKGTSYKFRVRALNMLGESEPS
APSRPYVVSGYSGRVYERPVAGPYITF
TDAVNETTIMLKWMYIPASNNNTPIHGFYIYYRPTDSDNDSDYKKDMVEGDKYWHSISHL
QPETSYDIKMQCFNEGGESEFS
NVMICETKARKSSGQPGRLPPPTLAPPQPPLPETIERP
VGTGAMVARSSDLPYLIVGVVLGSIVLIIVTFIPFCLWRAWSKQKHTTDLGFPRSALPPS
CPYTMVPLGGLPGHQASGQPYLSGISGRACANGIHMNRGCPSAAVGYPGMKPQQHCPGEL
QQQSDTSSLLRQTHLGNGYDPQSHQITRGPKSSPDEGSFLYTLPDDSTHQLLQPHHDCCQ
RQEQPAAVGQSGVRRAPDSPVLEAVWDPPFHSGPPCCLGLVPVEEVDSPDSCQVSGGDWC
PQHPVGAYVGQEPGMQLSPGPLVRVSFETPPLTI
Sequence length 1114
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Hedgehog signaling pathway
Axon guidance
  Myogenesis
Activation of SMO
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial cancer of breast Uncertain significance rs144251369 RCV005932169
Holoprosencephaly sequence Uncertain significance rs1553745274 RCV000627087
Malignant tumor of esophagus Uncertain significance rs202019169 RCV005929156
Melanoma Uncertain significance rs144251369 RCV005932172
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Basal Cell Nevus Syndrome Associate 28915250
Neoplasms Inhibit 33811245
Squamous Cell Carcinoma of Head and Neck Associate 33892811
Stomach Neoplasms Associate 33811245