Type | Description |
---|---|
Definition | dynein, axonemal, heavy chain 5 |
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 |
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
|
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