NME3

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Nucleoside diphosphate kinase 3 is an enzyme that in humans is encoded by the NME3 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesNME3, DR-nm23, NDPK-C, NDPKC, NM23-H3, NM23H3, c371H6.2, NME/NM23 nucleoside diphosphate kinase 3
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NME3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNME3, DR-nm23, NDPK-C, NDPKC, NM23-H3, NM23H3, c371H6.2, NME/NM23 nucleoside diphosphate kinase 3
External IDsOMIM: 601817; MGI: 1930182; HomoloGene: 20562; GeneCards: NME3; OMA:NME3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002513

NM_019730

RefSeq (protein)

NP_002504

NP_062704

Location (UCSC)Chr 16: 1.77 – 1.77 MbChr 17: 25.12 – 25.12 Mb
PubMed search[3][4]
Wikidata
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Interactions

NME3 has been shown to interact with NME1[7][8] and NME2.[8][9]

Clinical significance

Mutations in this gene have been associated with congenital hypotonia, hypoventilation and cerebellar histopathological alterations.[10]

References

Further reading

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