Type | Description |
---|---|
Definition | solute carrier family 25 member 26 |
Date | Results | Publications |
---|---|---|
2017-07-08 12:09:00 | overexpression of SLC25A26 in CaSki cells increases mitochondrial SAM availability and promotes hypermethylation of mitochondrial DNA, leading to decreased expression of key respiratory complex subunits, reduction of mitochondrial ATP and release of cytochrome c. | 28118529 |
2016-02-27 11:42:00 | SLC25A26 mutations cause various mitochondrial defects, including those affecting RNA stability, protein modification, mitochondrial translation, and the biosynthesis of CoQ10 and lipoic acid. | 26522469 |
2013-07-02 10:28:00 | Compares and contrasts all the known human SLC25A* genes and includes functional information. | 23266187 |
2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20877624 |
2010-01-21 00:00:00 | SAMC was expressed in mitochondria of all human tissues examined. The role of SAMC is probably to exchange cytosolic SAM for mitochondrial S-adenosylhomocysteine. This is the 1st report of identification & characterization of the human SAMC & its gene. | 14674884 |
Type | IDs |
---|---|
Synonymous | COXPD28, SAMC |
Gene |
UniProtKB-ID:
SAMC_HUMAN
UniprotKB:
Q70HW3
UniParc:
UPI00001A92F4,
UPI000003615A,
UPI00001A92DA
EMBL:
AC170165,
BC003399,
CH471055,
AK096876,
AC145425,
AC170801,
AK291873,
AC092034,
AJ580932,
AEKP01024816,
BC012852,
AK092495,
AC235952
Ensembl:
ENSG00000144741,
ENSG00000282739
KO:
hsa:115286
|
Nucleutide sequences |
EMBL-CDS:
EAW65449.1,
BAF84562.1,
CAE45652.1,
BAG53388.1,
AAH12852.2,
EAW65451.1,
BAG52559.1
Ensembl_TRS:
ENST00000632575,
ENST00000354883,
ENST00000633701,
ENST00000336733
|
Protein sequencees |
Ensembl_PRO:
ENSP00000488659,
ENSP00000346955,
ENSP00000336801,
ENSP00000488865
RefSeq:
NP_001337922.1,
XP_024309103.1,
NP_775742.4,
NP_001158268.1,
NP_001337921.1,
NP_001366139.1,
XP_016861163.1,
XP_011531630.1,
XP_011531629.1,
NP_001337920.1,
XP_006713019.1
|
Others |
UniRef100:
UniRef100_Q70HW3
UniRef90:
UniRef90_Q70HW3
UniRef50:
UniRef50_Q70HW3
UniGene:
Hs.379386
CCDS:
CCDS2905.2,
CCDS54604.1
|
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Refseq |
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