CEP120 (GeneID: 153241) | Homo sapiens
Description: centrosomal protein 120 [Source:HGNC Symbol;Acc:HGNC:26690]
Synonyms: CCDC100, SRTD13
Other ID(s): HGNC:26690, ENSG00000168944
Protein Accession Numbers: ENST00000328236, NP_001362334, ENST00000513565, NP_694955, ENST00000508138, NP_001362336, ENST00000306481, NP_001159698, ENST00000510582, NP_001362338, ENST00000395431, NP_001362335, ENST00000306467, ENST00000515110, ENST00000508442, NP_001362337
Statistics: COSMIC(178) PTM(36)
Post translational modifications (PTM) by Type

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000306467 ENST00000306481 ENST00000328236 ENST00000395431 ENST00000508138 ENST00000508442 ENST00000510582 ENST00000513565 ENST00000515110 NP_001159698 NP_001362334 NP_001362335 NP_001362336 NP_001362337 NP_001362338 NP_694955


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00168 C2 C2 domain 9-114 CL0154 C2 Mus musculus
PF00168 C2 C2 domain 520-568 CL0154 C2 Mus musculus
PF12416 DUF3668 Cep120 protein 118-340 Mus musculus

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Majewski Syndrome Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.663 0.448
Saldino-Noonan Syndrome Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.663 0.448
Short Rib-Polydactyly Syndrome Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.663 0.448
Polydactyly Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.663 0.448
Jeune thoracic dystrophy Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.663 0.448
Familial aplasia of the vermis Eye Diseases ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.663 0.448
SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY N/A 0.663 0.448
Joubert syndrome with ocular defect N/A 0.663 0.448
Ciliopathies Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.663 0.448
JOUBERT SYNDROME 31 N/A 0.663 0.448
NO RESULT FOUND
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