Type | Description |
---|---|
Definition | deoxyguanosine kinase |
Date | Results | Publications |
---|---|---|
2018-03-31 10:26:00 | DGUOK deficiency and mutation is associated with mitochondrial DNA depletion syndromes. | 28493820 |
2017-07-22 13:36:00 | rare homozygous p.N46S mutation associated with idiopathic noncirrhotic portal hypertension | 26874653 |
2016-12-17 11:28:00 | The goals of this work are to characterize the DGUOK rat in terms of mitochondrial dysfunction and pathological outcome, and to evaluate EPR as a new and additional technique in an integrated characterization of mitochondrial disease . | 26773591 |
2016-09-17 12:09:00 | sequencing results showed that the patient was a compound heterozygote for c.679G>A and c.817delT in the DGUOK gene | 27324545 |
2015-02-21 10:47:00 | thymidine kinase 2 but not deoxyguanosine kinase is up-regulated during the stationary growth phase of cultured cells | 24940680 |
Type | IDs |
---|---|
Synonymous | MTDPS3, NCPH, PEOB4, dGK |
Gene |
UniProtKB-ID:
DGUOK_HUMAN,
D6W5I0_HUMAN,
E5KSL6_HUMAN,
E5KSL5_HUMAN
UniprotKB:
Q16854,
D6W5I0,
E5KSL6,
E5KSL5
UniParc:
UPI000002A7DD,
UPI000012921F,
UPI000002A7DE,
UPI000002A7DC,
UPI0000EE25F8,
UPI000002A7DF,
UPI0000072129
EMBL:
HQ206042,
HQ206033,
HQ206053,
HQ206031,
HQ206026,
HQ206044,
HQ206056,
HQ206063,
HQ206032,
HQ206061,
KU178023,
AC073046,
HQ206050,
HQ206059,
BC024019,
HQ206062,
HQ206065,
HQ206034,
HQ206054,
HQ206035,
U41668,
HQ206057,
HQ206028,
HQ206045,
HQ206046,
HQ206027,
HQ206049,
U81499,
HQ206041,
CH471053,
X97386,
HQ206055,
HQ206036,
HQ206047,
HQ206029,
HQ206038,
HQ206040,
HQ206064,
HQ206030,
HQ206058,
HQ206039,
HQ206037,
HQ206060,
BC015757,
HQ206048,
HQ206052,
HQ206043,
HQ206051
Ensembl:
ENSG00000114956
KO:
hsa:1716
|
Nucleutide sequences |
EMBL-CDS:
AAH24019.1,
AAC50624.1,
AAX88910.1,
EAW99704.1,
EAW99707.1,
AAB39858.1,
AAH15757.1,
EAW99709.1,
CAA66054.1,
EAW99706.1,
EAW99711.1,
ADP91947.1,
ADP91961.1,
ADP91895.1,
ADP91957.1,
ADP91931.1,
ADP91915.1,
ADP91967.1,
ADP91953.1,
ADP91945.1,
ADP91943.1,
ADP91937.1,
ADP91909.1,
ADP91917.1,
ADP91929.1,
EAW99710.1,
ADP91935.1,
ADP91933.1,
ADP91905.1,
ADP91919.1,
ADP91959.1,
ADP91973.1,
ADP91925.1,
ADP91913.1,
ADP91927.1,
ADP91963.1,
ADP91901.1,
ADP91969.1,
ADP91941.1,
ADP91923.1,
ADP91965.1,
ADP91921.1,
ADP91911.1,
ADP91903.1,
ADP91955.1,
ADP91899.1,
ADP91939.1,
ADP91971.1,
ADP91907.1,
ADP91897.1,
ADP91949.1,
ADP91951.1,
ADP91896.1,
ADP91894.1,
ADP91898.1,
ADP91970.1,
ADP91946.1,
ADP91958.1,
ADP91948.1,
ADP91940.1,
ADP91930.1,
ADP91922.1,
ADP91928.1,
ADP91914.1,
ADP91960.1,
ADP91908.1,
ADP91936.1,
ADP91920.1,
ADP91972.1,
ADP91956.1,
ADP91902.1,
ADP91938.1,
ADP91918.1,
ADP91904.1,
ADP91924.1,
ADP91952.1,
ADP91916.1,
ADP91964.1,
ADP91942.1,
ADP91932.1,
ADP91950.1,
ADP91912.1,
ADP91944.1,
ADP91906.1,
ADP91910.1,
ADP91966.1,
ALQ33481.1,
ADP91900.1,
ADP91954.1,
ADP91926.1,
ADP91934.1,
ADP91968.1,
ADP91962.1
Gene_ORFName:
hCG_40733,
hCG_40733
Ensembl_TRS:
ENST00000348222,
ENST00000629438,
ENST00000264093,
ENST00000418996
|
Protein sequencees |
Ensembl_PRO:
ENSP00000408209,
ENSP00000306964,
ENSP00000264093,
ENSP00000487122
RefSeq:
NP_001305792.1,
XP_024308507.1,
NP_550438.1,
XP_011530949.1,
NP_001305788.1,
NP_001305789.1,
NP_550440.1,
NP_001305791.1,
NP_001305790.1
|
Others |
UniRef100:
UniRef100_Q16854,
UniRef100_E5KSL6
UniRef90:
UniRef90_A0A2I3HF78,
UniRef90_Q16854
UniRef50:
UniRef50_Q16854,
UniRef50_A0A2I3HF78
UniGene:
Hs.469022
CCDS:
CCDS1931.1,
CCDS1932.1
|
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---|---|---|---|---|---|---|---|---|
Refseq |
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