Type | Description |
---|---|
Definition | ATPase, class V, type 10A |
Date | Results | Publications |
---|---|---|
2010-07-19 11:28:00 | Data report that Atp10a is biallelically expressed in both the newborn and adult brain, and Atp10a allelic expression is insensitive to deletion or mutation of the PWS imprinting center. | 19894069 |
2010-01-21 00:00:00 | report the generation of the complete genomic structure | 12105293 |
2010-01-21 00:00:00 | Atp10a was biallelically expressed in all tissues examined. Furthermore, there was no differential methylation in the CpG island and no antisense transcripts of the gene. These findings suggest that the mouse Atp10a gene escapes genomic imprinting. | 12782135 |
2010-01-21 00:00:00 | data suggest that heterozygous deletion along with an unusual pattern of maternal inheritance of the chromosomal region containing the single gene, Atp10c, causes obesity, type 2 diabetes, and nonalcoholic fatty liver disease in these mice | 15051828 |
2010-01-21 00:00:00 | A putative phospholipid transporter, is the only coding unit between Gabrb3 and Ube3a. | 15620220 |
Type | IDs |
---|---|
Synonymous | Atp10c, pfatp |
Gene |
UniProtKB-ID:
AT10A_MOUSE,
Q3V1Y7_MOUSE,
Q6A046_MOUSE
UniprotKB:
O54827,
Q3V1Y7,
Q6A046
UniParc:
UPI00003FEF23,
UPI00001F4EDF
EMBL:
BC138356,
AK172972,
AF372979,
AF011337,
AF156549,
BC138357,
BC025643,
AK132174
Ensembl:
ENSMUSG00000025324
KO:
mmu:11982
|
Nucleutide sequences |
EMBL-CDS:
AAC02902.1,
AAH25643.1,
AAM20894.1,
AAF09447.1,
AAI38357.1,
BAE21012.1,
AAI38358.1,
BAD32250.1
Ensembl_TRS:
ENSMUST00000168747
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000129811
RefSeq:
XP_036008505.1,
XP_017177441.1,
NP_033858.2,
XP_006540644.1,
XP_006540643.1,
XP_006540646.1
|
Others |
UniRef100:
UniRef100_A0A140LHF0,
UniRef100_O54827
UniRef90:
UniRef90_O54827
UniRef50:
UniRef50_O60312
UniGene:
Mm.135129
CCDS:
CCDS39972.1
|
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