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110082 Dnah5

110082

Dnah5

dynein, axonemal, heavy chain 5

protein-coding

Mus musculus

基因描述

Type Description
Definition dynein, axonemal, heavy chain 5

研究结论

Date Results Publications
2016-07-16 11:29:00 Dnah6 genetically interacts with Dnai1 and Dnah5 to cause heterotaxy and primary ciliary dyskinesia. 26918822
2010-01-21 00:00:00 Loss of function of Mdnah5 causes primary ciliary dyskinesia and hydrocephalus 11912187
2010-01-21 00:00:00 Dnahc5 is required for the specification of left-right asymmetry and suggest that the PCD-causing Dnahc5 mutation may also be associated with heterotaxy. 18037990
2010-01-21 00:00:00 These findings are consistent with studies indicating that perturbations in dynein activity can contribute to the aberrant accumulations of neurofilaments that accompany ALS/motor neuron disease. 17640622

名称对应

Type IDs
Synonymous AU022615, Dnahc5, Mdnah5, b2b1134Clo, b2b1154Clo, b2b1537Clo, b2b1565Clo, b2b3491Clo, b2b601Clo, mKIAA1603
Gene
UniProtKB-ID: DYH5_MOUSE
UniprotKB: Q8VHE6
UniParc: UPI0000435CDB
EMBL: AK052643, AC154880, AC131997, AF466704
Ensembl: ENSMUSG00000022262
KO: mmu:110082
Nucleutide sequences
EMBL-CDS: BAC35077.2, AAL69993.1
Ensembl_TRS: ENSMUST00000067048
Protein sequencees
Ensembl_PRO: ENSMUSP00000069751
RefSeq: NP_579943.3, XP_006520077.1
Others
UniRef100: UniRef100_Q8VHE6
UniRef90: UniRef90_Q8VHE6
UniRef50: UniRef50_Q8VHE6
UniGene: Mm.248464
CCDS: CCDS27404.1

全选

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研究热度

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