Type | Description |
---|---|
Definition | HYDIN, axonemal central pair apparatus protein |
Date | Results | Publications |
---|---|---|
2019-03-30 12:53:00 | It plays a role in sperm motility. | 30089752 |
2015-01-10 10:19:00 | Hydin is identified as a novel pain gene in mouse model. | 24700285 |
2010-01-21 00:00:00 | We conclude that hydrocephalus in hydin mutants is caused by a central pair defect impairing ciliary motility and fluid transport in the brain. | 18250199 |
2010-01-21 00:00:00 | A domain with homology to caldesmon, an actin-binding protein, suggests an interaction with the cytoskeleton. | 12719380 |
2010-01-21 00:00:00 | data provide the first evidence of Hydin's role within the trypanosome axoneme, and reveal central pair anomalies and thus impairment of ependymal ciliary motility as the likely cause of the hydrocephalus observed in the hy3 mouse | 17683645 |
Type | IDs |
---|---|
Synonymous | 1700034M11Rik, 4930545D19Rik, 4932703P14, 672398, A830061H17, AC069308.21gm4, Gm9558, hy-3, hy3, hyrh |
Gene |
UniProtKB-ID:
HYDIN_MOUSE
UniprotKB:
Q80W93
UniParc:
UPI0000F50933,
UPI00001F8927,
UPI00000276D2
EMBL:
AK142981,
BB664150,
AY173049,
BB641870,
AK043971,
AK030144,
BC080316
Ensembl:
ENSMUSG00000059854
KO:
mmu:244653
|
Nucleutide sequences |
EMBL-CDS:
AAO44953.1,
BAE25238.1,
BAC31720.1,
BAC26807.1,
AAH80316.1
Ensembl_TRS:
ENSMUST00000043141
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000046204
RefSeq:
XP_030099421.1,
XP_030099414.1,
NP_766504.3,
XP_030099418.1,
XP_030099416.1,
XP_030099417.1,
XP_030099412.1,
XP_030099413.1,
XP_030099419.1,
XP_030099420.1,
XP_030099415.1
|
Others |
UniRef100:
UniRef100_Q80W93
UniRef90:
UniRef90_Q80W93
UniRef50:
UniRef50_Q4G0P3
UniGene:
Mm.444803,
Mm.488112
CCDS:
CCDS40476.1
|
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