NME7 (GeneID: 29922) | Homo sapiens
Description: NME/NM23 family member 7 [Source:HGNC Symbol;Acc:HGNC:20461]
Synonyms: nm23-H7, CFAP67, NDK7, MN23H7
Other ID(s): HGNC:20461, ENSG00000143156
Protein Accession Numbers: ENST00000367811, NP_932076, ENST00000525440, NP_037462, ENST00000472647, ENST00000528517
Statistics: gnomAD(325) COSMIC(436) PTM(15)
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.
ENST00000367811 You are here now! ENST00000472647 ENST00000525440 ENST00000528517 NP_037462 You are here now! NP_932076


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
PF00334 NDK Nucleoside diphosphate kinase 92-226 Homo sapiens
PF00334 NDK Nucleoside diphosphate kinase 238-375 Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Drug abuse Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Drug habituation Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Drug Use Disorders Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Organic Mental Disorders, Substance-Induced Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Situs Inversus Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.752 0.241
Substance Dependence Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Substance Use Disorders Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Substance-Related Disorders Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Gastrointestinal Stromal Tumors Neoplasms ; Digestive System Diseases ; 0.752 0.241
Substance abuse problem Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Drug Dependence Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
Gastrointestinal Stromal Sarcoma Neoplasms ; Digestive System Diseases ; 0.752 0.241
Prescription Drug Abuse Chemically-Induced Disorders ; Mental Disorders ; 0.752 0.241
NO RESULT FOUND
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