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NPM1 information


NPM1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNPM1, B23, NPM, nucleophosmin (nucleolar phosphoprotein B23, numatrin), nucleophosmin, nucleophosmin 1
External IDsOMIM: 164040; MGI: 106184; HomoloGene: 81697; GeneCards: NPM1; OMA:NPM1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001252260
NM_001252261
NM_008722

RefSeq (protein)

NP_001239189
NP_001239190
NP_032748

Location (UCSC)Chr 5: 171.39 – 171.41 MbChr 11: 33.1 – 33.11 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Nucleophosmin (NPM), also known as nucleolar phosphoprotein B23 or numatrin, is a protein that in humans is encoded by the NPM1 gene.[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000181163 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000057113 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Liu QR, Chan PK (March 1993). "Characterization of seven processed pseudogenes of nucleophosmin/B23 in the human genome". DNA and Cell Biology. 12 (2): 149–156. doi:10.1089/dna.1993.12.149. PMID 8471164.
  6. ^ Morris SW, Kirstein MN, Valentine MB, Dittmer KG, Shapiro DN, Saltman DL, Look AT (March 1994). "Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin's lymphoma". Science. 263 (5151): 1281–1284. Bibcode:1994Sci...263.1281M. doi:10.1126/science.8122112. PMID 8122112.

and 25 Related for: NPM1 information

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NPM1

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or numatrin, is a protein that in humans is encoded by the NPM1 gene. In humans, the NPM1 gene is located on the long arm of chromosome 5 (5q35). The...

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B23

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B23 may refer to: A human nucleolar protein also known as NPM1 The 2.3L, pre-revision variant of the Volvo Redblock engine Bundesstraße 23, federal highway...

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Down syndrome

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lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22...

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Acute myeloid leukemia

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under study for their prognostic impact in AML. However, only FLT3-ITD, NPM1, CEBPA and c-KIT are currently included in validated international risk stratification...

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Birth defect

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lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22...

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Turner syndrome

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lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22...

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Tumors of the hematopoietic and lymphoid tissues

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with t(1;22)(p13.3;q13.1); RBM15-MKL1 AML with BCR-ABL1 AML with mutated NPM1 AML with biallelic mutation of CEBPA AML with mutated RUNX1 AML with myelodysplasia-related...

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Miscarriage

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lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22...

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Chromosomal translocation

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1;q14.3) Schizophrenia t(2;5)(p23;q35) Anaplastic large cell lymphoma ALK NPM1 t(11;22)(q24;q11.2-12) Ewing's sarcoma FLI1 EWS t(17;22) DFSP Collagen I...

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Brunangelo Falini

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genomic studies on AML and hairy cell leukemia (HCL). His discoveries of NPM1 mutations in AML and BRAF-V600E in HCL, identified new mechanisms of leukemogenesis...

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SOX2

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transcription of all pluripotency circuitry proteins in the LIF pathway. NPM1, a transcriptional regulator involved in cell proliferation, individually...

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SENP3

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yeast and localize to nucleolus through B23/NPM1. SENP3 is associated and regulated by B23/nucleophosmin/NPM1 and involved in the regulation of ribosome...

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BRCA1

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H2AFX JUNB JunD LMO4 MAP3K3 MED17 MED21 MRE11A MSH2 MSH3 MSH6 Myc NBN NMI NPM1 NCOA2 NUFIP1 P53 PALB2 POLR2A PPP1CA Rad50 RAD51 RBBP4 RBBP7 RBBP8 RELA RB1...

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MicroRNA sequencing

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miR-127, miR-299-5p, miR-323 with t(8;21) or inv(16) let-7b/c, miR-127 with NPM1 mutations miR-10a/b, let-7, miR-29, miR-204, miR-128a, miR-196a/b with FLT3...

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Nucleoplasmin

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Humans express three members of the nucleoplasmin family: Nucleophosmin (NPM1) Nucleoplasmin 2 (NPM2) Nucleoplasmin 3 (NPM3) Dingwall C, Laskey RA (February...

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Miscarriage and mental disorders

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lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22...

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Gene signature

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Delwel R, Löwenberg B, Valk PJ (December 2005). "Mutations in nucleophosmin (NPM1) in acute myeloid leukemia (AML): association with other gene abnormalities...

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AKT1

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ILK, KRT10, MAP2K4, MAP3K11, MAP3K8, MAPK14, MAPKAPK2, MARK2, MTCP1, MTOR, NPM1, NR4A1, NR3C4, PKN2, PRKCQ, PDPK1, PLXNA1, TCL1A, TRIB3, TSC1, TSC2, and...

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PTPN11

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mutations (24%) were detected by next-generation sequencing in a cohort of NPM1-mutated acute myeloid leukemia patients, although the prognostic significance...

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Minimal residual disease

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t(15;17) PML-RARA, t(8;21) AML1-RUNX1T1 (AML-ETO), inv(16), BCL2, FLT3, IDH1/2, NPM1. Uses: Chromosomal translocation MRD detection widely used as a standard...

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Chronic myelomonocytic leukemia

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in 10% of cases. Mutations in transcription factors such as RUNX1, CEBPA, NPM1 and WT1 have been found in up to 30% of cases. Mutations of CBL are found...

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Miscarriage risks

Last Update:

lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22...

Word Count : 1923

Polysomy

Last Update:

lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large-cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22...

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Nucleolin

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has been shown to interact with: MTDH, CSNK2A2, Centaurin, alpha 1, HuR, NPM1, P53, PPP1CB, S100A11, Sjögren syndrome antigen B, TOP1, and Telomerase reverse...

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Blastic plasmacytoid dendritic cell neoplasm

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32–67% of all BPDCN cases and often accompanied by mutations in either the NPM1 or SRSF2 gene. Numerous other genetic abnormalities are associated with the...

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