NME8 NME/NM23 family member 8 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 51314)
Source: NCBI Gene (ID 51314)
Symbol: NME8
Full name: NME/NM23 family member 8
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: CILD6; DNAI8; HEL-S-99; NM23-H8; SPTRX2; TXNDC3; sptrx-2
Summary: This gene encodes a protein with an N-terminal thioredoxin domain and three C-terminal nucleoside diphosphate kinase (NDK) domains, but the NDK domains are thought to be catalytically inactive. The sea urchin ortholog of this gene encodes a component of sperm outer dynein arms, and the protein is implicated in ciliary function. Mutations in this gene are implicated in primary ciliary dyskinesia type 6.[provided by RefSeq, Nov 2009]
Expression: Biased expression in testis (RPKM 4.9), bone marrow (RPKM 3.6) and 3 other tissues
Orthologs: mouse
Gene size: 51801bp
Exon count: 18