Type | Description |
---|---|
Definition | family with sequence similarity 13 member A |
Date | Results | Publications |
---|---|---|
2020-11-21 13:30:00 | Loss of Family with Sequence Similarity 13, Member A Exacerbates Pulmonary Fibrosis Potentially by Promoting Epithelial to Mesenchymal Transition. | 32029695 |
2020-07-18 10:25:00 | GWAS-associated variants within the FAM13A locus alter adipose FAM13A expression, which in turn, regulates adipocyte differentiation and contribute to changes in body fat distribution. | 32193374 |
2020-04-25 12:44:00 | Our results suggest that FAM13A is dispensable for adipose development and insulin sensitivity. Yet the expression of FAM13A needs to be tightly controlled in adipose precursor cells for their proper survival and downstream adipogenesis. These data provide novel insights into the link between FAM13A and obesity. | 30301961 |
2019-12-07 12:00:00 | Variant genotypes of rs9224 in the FAM13A 3'UTR may modify Lung squamous carcinoma (LUSQ) susceptibility by affecting the binding of miRNA-22-5p and predict a poor prognosis of patients with LUSQ. | 31539274 |
2019-11-16 12:58:00 | Data show that FAM13A is a modifier gene of Cystic Fibrosis lung phenotype regulating RhoA activity, actin cytoskeleton dynamics and epithelial-mesenchymal transition. | 29239766 |
Type | IDs |
---|---|
Synonymous | ARHGAP48, FAM13A1 |
Gene |
UniProtKB-ID:
FA13A_HUMAN
UniprotKB:
O94988
UniParc:
UPI0000481AF3,
UPI0001D14750,
UPI000004EC64,
UPI000018DB8B,
UPI000020B1AB
EMBL:
AC021183,
AB020721,
AC108065,
AK296932,
AK091328,
BN000265,
AK027138,
BC086875
Ensembl:
ENSG00000138640
KO:
hsa:10144
|
Nucleutide sequences |
EMBL-CDS:
BAG59483.1,
BAC03636.1,
AAH86875.1,
BAA74937.3,
CAE18110.1
Ensembl_TRS:
ENST00000395002,
ENST00000503556,
ENST00000264344,
ENST00000508369,
ENST00000513837
|
Protein sequencees |
Ensembl_PRO:
ENSP00000421562,
ENSP00000427189,
ENSP00000264344,
ENSP00000423252,
ENSP00000378450
RefSeq:
XP_016863116.1,
XP_005262740.1,
XP_016863119.1,
XP_005262741.1,
XP_011529818.1,
NP_001252509.1,
XP_016863121.1,
XP_011529820.1,
XP_006714120.1,
NP_001252507.1,
XP_016863122.1,
XP_011529819.1,
XP_005262738.1,
XP_005262739.1,
XP_016863113.1,
NP_001015045.1,
XP_016863115.1,
XP_011529821.1,
XP_016863117.1,
XP_016863118.1,
XP_016863114.1,
NP_055698.2,
XP_024309638.1,
XP_016863120.1,
NP_001252508.1,
XP_016863123.1
|
Others |
UniRef100:
UniRef100_O94988
UniRef90:
UniRef90_O94988
UniRef50:
UniRef50_O94988
UniGene:
Hs.97270,
Hs.714536
CCDS:
CCDS43251.1,
CCDS58911.1,
CCDS58912.1,
CCDS58913.1,
CCDS34029.1
|
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Refseq |
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