Interactions
Clinical significance
Mutations in this gene have been associated with congenital hypotonia, hypoventilation and cerebellar histopathological alterations.
Protein-coding gene in the species Homo sapiens
NME3
All data from the card 19
- Aliases
- NME3, DR-nm23, NDPK-C, NDPKC, NM23-H3, NM23H3, c371H6.2, NME/NM23 nucleoside diphosphate kinase 3
- External IDs
- OMIM: 601817; MGI: 1930182; GeneCards: NME3
- PDB
- Ortholog search: PDBe RCSB
- 2.7.4.6
- ↗
- Chr.
- Chromosome 16 (human)
- Band
- 16p13.3
- End
- 1,771,561 bp
- Chr.
- Chromosome 17 (mouse)
- Band
- 17|17 A3.3
- End
- 25,116,496 bp
- BioGPS
- More reference expression data
- Databases
- NCBI: entry; OMA: entry
- Species
- Human
- Entrez
- 4832
- Ensembl
- ENSG00000103024
- UniProt
- Q13232
- RefSeq (mRNA)
- NM_002513
- RefSeq (protein)
- NP_002504
- Location (UCSC)
- Chr 16: 1.77 – 1.77 Mb
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