NOL3 (GeneID: 8996) | Homo sapiens
Description: nucleolar protein 3 [Source:HGNC Symbol;Acc:HGNC:7869]
Synonyms: NOP, ARC, MYP, NOP30, FCM
Other ID(s): HGNC:7869, ENSG00000140939
Protein Accession Numbers: ENST00000565560, NP_001263248, ENST00000564053, NP_001263238, ENST00000432069, ENST00000568146, ENST00000564992, NP_001263241, ENST00000563439, NP_001263236, ENST00000268605, ENST00000566871, NP_003937, ENST00000564860, NP_001263240, ENST00000563258, NP_001171986
Statistics: ClinVar(5) gnomAD(324) COSMIC(54) PTM(8)
ClinVar Pathogenicity of Variations help

∙ 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.
ENST00000268605 ENST00000432069 ENST00000563258 ENST00000563439 ENST00000564053 You are here now! ENST00000564860 ENST00000564992 ENST00000565560 ENST00000566871 ENST00000568146 NP_001171986 NP_001263236 NP_001263238 NP_001263240 NP_001263241 NP_001263248 You are here now! NP_003937


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
PF00619 CARD Caspase recruitment domain 9-96 CL0041 Death Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Mitochondrial Diseases Nutritional and Metabolic Diseases ; 0.667 0.552
Electron Transport Chain Deficiencies, Mitochondrial Nutritional and Metabolic Diseases ; 0.667 0.552
Oxidative Phosphorylation Deficiencies Nutritional and Metabolic Diseases ; 0.667 0.552
Mitochondrial Respiratory Chain Deficiencies Nutritional and Metabolic Diseases ; 0.667 0.552
MYOCLONUS, FAMILIAL CORTICAL N/A 0.667 0.552
NO RESULT FOUND
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