Type | Description |
---|---|
Definition | ATPase, Na+/K+ transporting, alpha 3 polypeptide |
Date | Results | Publications |
---|---|---|
2020-10-10 13:00:00 | ATP1A3 mutation as a candidate cause of autosomal dominant cone-rod dystrophy. | 32440726 |
2019-10-12 12:09:00 | Na(+)/K(+)-ATPase alpha3 does not reside within the core circadian molecular clockwork, but Myk/+ mice exhibit concomitant disruption in circadian rhythms and mood. The Myshkin model demonstrates profound circadian and light-responsive behavioral alterations independent of molecular clock disruption. | 28689605 |
2019-09-21 12:07:00 | The animal model containing a E815K mutation in ATP1A3, manifests clinical and neurophysiological features of the most severe form of alternating hemiplegia of childhood. | 30071271 |
2019-03-02 11:27:00 | the neuronal specific alpha3 (alpha3)-subunit of the plasma membrane enzyme Na, K-ATPase (NKA) is a new binding partner of sAPPalpha. | 28983842 |
2018-05-19 11:36:00 | A heterozygous knock-in mouse harboring the D801Y mutation in ATP1A3 was generated. This mice displayed hyperactivity, increased sensitivity to chemically induced epileptic seizures and cognitive deficits. The findings reveal the functional significance of ATP1A3 gene in the control of spatial learning and memory and suggest a link to GABA transmission. | 27549929 |
Type | IDs |
---|---|
Synonymous | Atpa-2 |
Gene |
UniProtKB-ID:
AT1A3_MOUSE,
Q8VCE0_MOUSE,
Q8R0E8_MOUSE,
A0A0G2JGX4_MOUSE
UniprotKB:
Q6PIC6,
Q8VCE0,
Q8R0E8,
A0A0G2JGX4
UniParc:
UPI0000001528,
UPI00000E6A4E,
UPI0000F4FC6A,
UPI00000288C4
EMBL:
AC125468,
BC034645,
BC042894,
BC027000,
BC020177,
BC037206
Ensembl:
ENSMUSG00000040907
KO:
mmu:232975
|
Nucleutide sequences |
EMBL-CDS:
AAH42894.1,
AAH34645.1,
AAH37206.1,
AAH20177.1,
AAH27000.1
Ensembl_TRS:
ENSMUST00000080882,
ENSMUST00000102858,
ENSMUST00000196684
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000079691,
ENSMUSP00000099922,
ENSMUSP00000143735
RefSeq:
NP_001277398.1,
XP_011248820.1,
NP_001361556.1,
XP_011248821.1
|
Others |
UniRef100:
UniRef100_Q6PIC6,
UniRef100_Q8VCE0,
UniRef100_A0A0G2JGX4,
UniRef100_Q8R0E8
UniRef90:
UniRef90_Q6PIC6,
UniRef90_A0A286ZRK2,
UniRef90_A0A0G2JGX4,
UniRef90_Q8R0E8
UniRef50:
UniRef50_P50993,
UniRef50_P06685
UniGene:
Mm.44101
CCDS:
CCDS20969.2
|
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Refseq |
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