Type | Description |
---|---|
Definition | ATPase family AAA domain containing 1 |
Date | Results | Publications |
---|---|---|
2020-05-09 13:48:00 | Sorting out how Msp1 maintains mitochondrial membrane proteostasis. | 31394253 |
2019-06-29 10:59:00 | This study showed that the molecular and functional analyses identify an activating ATAD1 mutation as a new cause of severe encephalopathy and congenital stiffness. | 29390050 |
2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20877624 |
2010-06-30 22:04:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
2009-12-02 21:41:00 | Observational study of gene-disease association. (HuGE Navigator) | 16385451 |
Type | IDs |
---|---|
Synonymous | AFDC1, FNP001, HKPX4, THORASE |
Gene |
UniProtKB-ID:
ATAD1_HUMAN
UniprotKB:
Q8NBU5
UniParc:
UPI00003BE976,
UPI000000B2DE
EMBL:
AK027506,
AC022016,
AL133327,
CH471066,
AK075223,
BC073998,
BC010868,
AL834370,
BC063530,
AF361493
Ensembl:
ENSG00000283024,
ENSG00000138138
KO:
hsa:84896
|
Nucleutide sequences |
EMBL-CDS:
AAH73998.1,
EAW50179.1,
EAW50177.1,
EAW50180.1,
AAH10868.1,
BAB55161.1,
AAL57218.1,
AAH63530.1,
BAC11482.1,
CAD39033.1
Gene_ORFName:
FNP001
Ensembl_TRS:
ENST00000634773,
ENST00000634970,
ENST00000328142,
ENST00000308448
|
Protein sequencees |
Ensembl_PRO:
ENSP00000489353,
ENSP00000339017,
ENSP00000339016,
ENSP00000489455
RefSeq:
NP_001308898.1,
NP_001308896.1,
XP_011538604.1,
XP_016872336.1,
XP_016872337.1,
XP_011538605.1,
XP_005270309.1,
NP_116199.2,
XP_016872340.1,
XP_016872338.1,
XP_016872339.1,
XP_024304010.1,
NP_001308897.1
|
Others |
UniRef100:
UniRef100_Q8NBU5
UniRef90:
UniRef90_Q8NBU5
UniRef50:
UniRef50_Q8NBU5
UniGene:
Hs.435948
CCDS:
CCDS7386.1
|
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Refseq |
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