NME5 (NME/NM23 family member 5)

2012-08-01  

Identity

HGNC
LOCATION
5q31.2
LOCUSID
ALIAS
NM23-H5,NM23H5,RSPH23

Other Information

Locus ID:

NCBI: 8382
MIM: 603575
HGNC: 7853
Ensembl: ENSG00000112981

Variants:

dbSNP: 8382
ClinVar: 8382
TCGA: ENSG00000112981
COSMIC: NME5

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000112981ENST00000265191P56597
ENSG00000112981ENST00000265191A0A0S2Z4L9

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
321857942020A nonsense variant in NME5 causes human primary ciliary dyskinesia with radial spoke defects.17
321857942020A nonsense variant in NME5 causes human primary ciliary dyskinesia with radial spoke defects.17
225647042012Transactivation of the human NME5 gene by Sp1 in pancreatic cancer cells.7
225647042012Transactivation of the human NME5 gene by Sp1 in pancreatic cancer cells.7
144996302003Nm23/NDP kinases in human male germ cells: role in spermiogenesis and sperm motility?15
144996302003Nm23/NDP kinases in human male germ cells: role in spermiogenesis and sperm motility?15

Citation

Dessen P

NME5 (NME/NM23 family member 5)

Atlas Genet Cytogenet Oncol Haematol. 2012-08-01

Online version: http://atlasgeneticsoncology.org/gene/52826/nme5