NPM1 (GeneID: 4869) | Homo sapiens
Description: nucleophosmin 1 [Source:HGNC Symbol;Acc:HGNC:7910]
Synonyms: B23, NPM
Other ID(s): HGNC:7910, ENSG00000181163
Protein Accession Numbers: ENST00000351986, NP_001341939, NP_001032827, ENST00000517671, NP_954654, ENST00000296930.5, NP_001341938, ENST00000523622, ENST00000393820, NP_002511, ENST00000296930, NP_001341935, ENST00000521672
Statistics: ClinVar(4)
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.
ENST00000296930 ENST00000351986 ENST00000393820 ENST00000517671 ENST00000521672 ENST00000523622 NP_001032827 NP_001341935 NP_001341938 NP_001341939 NP_002511 NP_954654


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
NO DOMAINS EXIST

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Cytopenia N/A 0.496 0.69
Leukemia, Myelocytic, Acute Neoplasms ; 0.496 0.69
Acute Promyelocytic Leukemia Neoplasms ; 0.496 0.69
Lymphoma, Non-Hodgkin Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.496 0.69
Malignant neoplasm of stomach Neoplasms ; Digestive System Diseases ; 0.496 0.69
Acute Myeloid Leukemia, M1 Neoplasms ; 0.496 0.69
Stomach Neoplasms Neoplasms ; Digestive System Diseases ; 0.496 0.69
Adenocarcinoma of lung (disorder) Neoplasms ; Respiratory Tract Diseases ; 0.496 0.69
Congenital anemia N/A 0.496 0.69
Lymphomatoid Papulosis Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.496 0.69
Primary Cutaneous Anaplastic Large Cell Lymphoma Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.496 0.69
Hereditary Diffuse Gastric Cancer Neoplasms ; Digestive System Diseases ; 0.496 0.69
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.496 0.69
NO RESULT FOUND
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