Gene Gene information from NCBI Gene database.
Entrez ID 3619
Gene name Inner centromere protein
Gene symbol INCENP
Synonyms (NCBI Gene)
-
Chromosome 11
Chromosome location 11q12.3
Summary In mammalian cells, 2 broad groups of centromere-interacting proteins have been described: constitutively binding centromere proteins and `passenger,` or transiently interacting, proteins (reviewed by Choo, 1997). The constitutive proteins include CENPA (
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs61893682 G>C Likely-pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
338
miRTarBase ID miRNA Experiments Reference
MIRT021587 hsa-miR-142-3p Microarray 17612493
MIRT025087 hsa-miR-181a-5p Microarray 17612493
MIRT042486 hsa-miR-423-3p CLASH 23622248
MIRT716934 hsa-miR-216a-5p HITS-CLIP 19536157
MIRT709386 hsa-miR-24-1-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
48
GO ID Ontology Definition Evidence Reference
GO:0000278 Process Mitotic cell cycle NAS 17956729
GO:0000281 Process Mitotic cytokinesis IBA
GO:0000281 Process Mitotic cytokinesis IMP 16239925
GO:0000281 Process Mitotic cytokinesis NAS 17956729
GO:0000775 Component Chromosome, centromeric region IDA 11084331, 16239925
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604411 6058 ENSG00000149503
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NQS7
Protein name Inner centromere protein
Protein function Component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chrom
PDB 2QFA , 4AF3 , 5IEH , 5IEK , 6GR8 , 6GR9 , 6YIE , 6YIF , 6YIH , 8RUP , 9ESA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12178 INCENP_N 6 41 Chromosome passenger complex (CPC) protein INCENP N terminal Domain
PF03941 INCENP_ARK-bind 825 881 Inner centromere protein, ARK binding region Family
Sequence
MGTTAPGPIHLLELCDQKLMEFLCNMDNKDLVWLEEIQEEAERMFTREFSKEPELMPKTP
SQKNRRKKRRISYVQDENRDPIRRRLSRRKSRSSQLSSRRLRSKDSVEKLATVVGENGSV
LRRVTRAAAAAAAATMALAAPSSPTPESPTMLTKKPEDNHTQCQLVPVVEIGISERQNAE
QHVTQLMSTEPLPRTLSPTPASATAPTSQGIPTSDEESTPKKSKARILESITVSSLMATP
QDPKGQGVGTGRSASKLRIAQVSPGPRDSPAFPDSPWRERVLAPILPDNFSTPTGSRTDS
QSVRHSPIAPSSPSPQVLAQKYSLVAKQESVVRRASRRLAKKTAEEPAASGRIICHSYLE
RLLNVEVPQKVGSEQKEPPEEAEPVAAAEPEVPENNGNNSWPHNDTEIANSTPNPKPAAS
SPETPSAGQQEAKTDQADGPREPPQSARRKRSYKQAVSELDEEQHLEDEELQPPRSKTPS
SPCPASKVVRPLRTFLHTVQRNQMLMTPTSAPRSVMKSFIKRNTPLRMDPKCSFVEKERQ
RLENLRRKEEAEQLRRQKVEEDKRRRLEEVKLKREERLRKVLQARERVEQMKEEKKKQIE
QKFAQIDEKTEKAKEERLAEEKAKKKAAAKKMEEVEARRKQEEEARRLRWLQQEEEERRH
QELLQKKKEEEQERLRKAAEAKRLAEQREQERREQERREQERREQERREQERREQERQLA
EQERRREQERLQAERELQEREKALRLQKEQLQRELEEKKKKEEQQRLAERQLQEEQEKKA
KEAAGASKALNVTVDVQSPACTSYQMTPQGHRAPPKINPDNYGMDLNSDDSTDDEAHPRK
PIPTWARGTPLSQAIIHQYYHPPNLLELFGTILPLDLEDIF
KKSKPRYHKRTSSAVWNSP
PLQGARVPSSLAYSLKKH
Sequence length 918
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
Separation of Sister Chromatids
Resolution of Sister Chromatid Cohesion
SUMOylation of DNA replication proteins
RHO GTPases Activate Formins
Mitotic Prometaphase
EML4 and NUDC in mitotic spindle formation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
22
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Nephronophthisis Likely pathogenic rs61893682 RCV000662273
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs2958341, rs34441559, rs61893680 RCV005920169
RCV005923430
RCV005925121
Cervical cancer Benign rs2958341, rs34441559, rs61893680 RCV005920170
RCV005923432
RCV005925122
Cholangiocarcinoma Benign rs61893680 RCV005925127
Clear cell carcinoma of kidney Benign rs34441559 RCV005923433
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Aneuploidy Associate 18752045
Breast Neoplasms Associate 25586992
Carcinoma Hepatocellular Associate 33540684, 33830865
Ciliopathies Associate 26489029
Lymphoma B Cell Associate 18752045
Neoplasms Associate 26460953, 27432226, 31991041
Ovarian Neoplasms Associate 27432226
Pancreatic Neoplasms Associate 36401386
Prostatic Neoplasms Associate 36901944