Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9702
Gene name Gene Name - the full gene name approved by the HGNC.
Centrosomal protein 57
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CEP57
Synonyms (NCBI Gene) Gene synonyms aliases
MVA2, PIG8, TSP57
Disease Acronyms (UniProt) Disease acronyms from UniProt database
MVA2
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q21
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000086 Process G2/M transition of mitotic cell cycle TAS
GO:0005515 Function Protein binding IPI 15607035, 20195357, 21516116, 25416956, 31515488, 32814053
GO:0005634 Component Nucleus ISS 12954732
GO:0005794 Component Golgi apparatus IDA 10942595
GO:0005813 Component Centrosome IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607951 30794 ENSG00000166037
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial septal defect Atrial Septal Defects rs137852951, rs137852953, rs137852955, rs267607106, rs104893900, rs104893901, rs104893903, rs606231358, rs606231359, rs137852683, rs606231360, rs104893907, rs104894073, rs1585703301, rs104894074
View all (25 more)
Cafe-au-lait spot Cafe au lait spots, multiple rs1057518792, rs1555613206, rs1555608663
Cataract Cataract rs118203965, rs118203966, rs104893685, rs121908938, rs104894175, rs121909048, rs28937573, rs121909049, rs121909050, rs74315488, rs80358200, rs80358203, rs121434643, rs56141211, rs132630322
View all (150 more)
Colonic neoplasms Malignant tumor of colon rs267607789, rs774277300, rs781222233, rs1060502734, rs1060503333, rs1339238483
Unknown
Disease term Disease name Evidence References Source
Ambiguous genitalia Ambiguous Genitalia ClinVar
Mosaic Variegated Aneuploidy mosaic variegated aneuploidy syndrome GenCC
Associations from Text Mining
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