| Type | Description |
|---|---|
| Definition | family with sequence similarity 50 member A |
| Date | Results | Publications |
|---|---|---|
| 2020-09-12 16:03:00 | Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. | 32703943 |
| 2010-09-15 22:06:00 | Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) | 20628086 |
| 2010-09-15 22:06:00 | Observational study of gene-disease association. (HuGE Navigator) | 19913121 |
| Type | IDs |
|---|---|
| Synonymous | 9F, DXS9928E, HXC-26, HXC26, XAP5 |
| Gene |
UniProtKB-ID:
FA50A_HUMAN
UniprotKB:
Q14320
UniParc:
UPI0000138FCD
EMBL:
D83389,
AK293119,
BX936365,
D83260,
AD001530,
L44140,
BC000028,
AK313697,
CH471172,
BC015499
Ensembl:
ENSG00000071859
KO:
hsa:9130
|
| Nucleutide sequences |
EMBL-CDS:
AAA92649.1,
BAF85808.1,
AAB81663.1,
BAG36444.1,
AAH15499.1,
AAH00028.1,
BAA11871.1,
EAW72708.1,
BAA11907.1
Ensembl_TRS:
ENST00000393600
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000377225
RefSeq:
NP_004690.1
|
| Others |
UniRef100:
UniRef100_Q14320
UniRef90:
UniRef90_Q14320
UniRef50:
UniRef50_Q14320
UniGene:
Hs.54277
CCDS:
CCDS14751.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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