Gene Gene information from NCBI Gene database.
Entrez ID 9702
Gene name Centrosomal protein 57
Gene symbol CEP57
Synonyms (NCBI Gene)
MVA2PIG8TSP57
Chromosome 11
Chromosome location 11q21
Summary This gene encodes a cytoplasmic protein called Translokin. This protein localizes to the centrosome and has a function in microtubular stabilization. The N-terminal half of this protein is required for its centrosome localization and for its multimerizati
SNPs SNP information provided by dbSNP.
7
SNP ID Visualize variation Clinical significance Consequence
rs387906977 C>A,T Pathogenic Synonymous variant, stop gained, coding sequence variant, non coding transcript variant
rs577173144 G>A,C,T Likely-pathogenic, uncertain-significance Coding sequence variant, missense variant, non coding transcript variant
rs771182933 C>A,G,T Pathogenic, likely-benign Coding sequence variant, non coding transcript variant, synonymous variant, stop gained, missense variant
rs1166323407 ->CAATGTTCAGC Pathogenic Coding sequence variant, non coding transcript variant, frameshift variant
rs1555052278 A>- Pathogenic Coding sequence variant, non coding transcript variant, frameshift variant, intron variant
miRNA miRNA information provided by mirtarbase database.
231
miRTarBase ID miRNA Experiments Reference
MIRT039373 hsa-miR-421 CLASH 23622248
MIRT247082 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT247079 hsa-miR-20a-5p HITS-CLIP 22473208
MIRT247082 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT247078 hsa-miR-17-5p HITS-CLIP 22473208
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 15607035, 20195357, 21516116, 25416956, 27107012, 31515488, 32296183, 32814053, 33961781, 35709258
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus ISS 12954732
GO:0005737 Component Cytoplasm IEA
GO:0005794 Component Golgi apparatus IDA 10942595
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607951 30794 ENSG00000166037
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86XR8
Protein name Centrosomal protein of 57 kDa (Cep57) (FGF2-interacting protein) (Testis-specific protein 57) (Translokin)
Protein function Centrosomal protein which may be required for microtubule attachment to centrosomes. May act by forming ring-like structures around microtubules. Mediates nuclear translocation and mitogenic activity of the internalized growth factor FGF2, but t
PDB 4L0R , 8IBH
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14073 Cep57_CLD 68 245 Centrosome localisation domain of Cep57 Coiled-coil
PF06657 Cep57_MT_bd 348 421 Centrosome microtubule-binding domain of Cep57 Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:12717444}.
Sequence
MAAASVSAASGSHLSNSFAEPSRSNGSMVRHSSSPYVVYPSDKPFLNSDLRRSPSKPTLA
YPESNSRAIFSALKNLQDKIRRLELERIQAEESVKTLSRETIEYKKVLDEQIQERENSKN
EESKHNQELTSQLLAAENKCNLLEKQLEYMRNMIKHAEMERTSVLEKQVSLERERQHDQT
HVQSQLEKLDLLEQEYNKLTTMQALAEKKMQELEAKLHEEEQERKRMQAKAAELQTGLET
NRLIF
EDKATPCVPNARRIKKKKSKPPEKKSSRNYFGAQPHYRLCLGDMPFVAGKSTSPS
HAVVANVQLVLHLMKQHSKALCNDRVINSIPLAKQVSSRGGKSKKLSVTPPSSNGINEEL
SEVLQTLQDEFGQMSFDHQQLAKLIQESPTVELKDKLECELEALVGRMEAKANQITKVRK
Y
QAQLEKQKLEKQKKELKATKKTLDEERNSSSRSGITGTTNKKDFMKLRPGEKRRKNLQL
LKDMQSIQNSLQSSSLCWDY
Sequence length 500
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Regulation of PLK1 Activity at G2/M Transition
Loss of Nlp from mitotic centrosomes
Recruitment of mitotic centrosome proteins and complexes
Loss of proteins required for interphase microtubule organization from the centrosome
Recruitment of NuMA to mitotic centrosomes
Anchoring of the basal body to the plasma membrane
AURKA Activation by TPX2
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
436
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Mosaic variegated aneuploidy syndrome Pathogenic rs1555052278 RCV000498788
Mosaic variegated aneuploidy syndrome 1 Pathogenic rs1166323407 RCV000656492
Mosaic variegated aneuploidy syndrome 2 Pathogenic; Likely pathogenic rs1399711421, rs775752088, rs1284736469, rs2496049330, rs2496263182, rs2496221057, rs1452779317, rs1565326373, rs1166323407, rs387906977, rs1565334264, rs1590962541, rs771182933, rs773014425, rs1862141371 RCV001331873
RCV001923710
RCV003078596
RCV003085098
RCV003641647
RCV003640709
RCV003640818
RCV000023668
RCV000023669
RCV000023670
RCV000696209
RCV000791171
RCV000797548
RCV001205462
RCV001255701
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
CEP57-related disorder Likely benign; Benign; Conflicting classifications of pathogenicity rs1390672128, rs117602509, rs61903295, rs143711180, rs768269976 RCV003962008
RCV003942541
RCV004730948
RCV003935493
RCV003955597
Colon adenocarcinoma Conflicting classifications of pathogenicity rs202115720 RCV005908973
Sarcoma Likely benign rs150303764 RCV005926186
Uterine corpus endometrial carcinoma Likely benign rs150303764 RCV005926187
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Aneuploidy Associate 21552266
Arthritis Rheumatoid Associate 32831971
Brachydactyly Associate 35434947
Carcinoma Associate 28553959
Genetic Diseases Inborn Associate 29659569
Growth Disorders Associate 35434947
Microcephalic Osteodysplastic Primordial Dwarfism Type II Associate 30804344
Microcephaly Associate 35434947
Mosaic variegated aneuploidy syndrome Associate 21552266, 30804344, 31943948, 35434947
Neoplasms Associate 29659569