| Type | Description |
|---|---|
| Definition | solute carrier family 22 member 5 |
| Date | Results | Publications |
|---|---|---|
| 2021-02-02 13:27:00 | Tooth loss and adiposity: possible role of carnitine transporter (OCTN1/2) polymorphisms in women but not in men. | 32964310 |
| 2020-12-12 13:30:00 | Biochemical and genetic characteristics of 40 neonates with carnitine deficiency.", trans "40. | 33268576 |
| 2020-12-05 13:00:00 | Downregulation of OCTN2 by cytokines plays an important role in the progression of inflammatory bowel disease. | 32579962 |
| 2020-09-12 16:06:00 | [Newborn screening for primary carnitine deficiency and variant spectrum of SLC22A5 gene in Guangzhou]. | 32521959 |
| 2020-06-20 11:40:00 | High OCTN2 expression is associated with Glioblastoma Multiforme. | 30670496 |
| Type | IDs |
|---|---|
| Synonymous | CDSP, OCTN2 |
| Gene |
UniProtKB-ID:
S22A5_HUMAN
UniprotKB:
O76082
UniParc:
UPI00001C1041,
UPI0000130BB6,
UPI0000EFD9B4
EMBL:
AK128610,
BC012325,
AF057164,
CH471062,
AB291606,
AB015050,
AC118464,
AB016625,
AK313230
Ensembl:
ENSG00000197375
KO:
hsa:6584
|
| Nucleutide sequences |
EMBL-CDS:
BAC87527.1,
BAG36041.1,
EAW62338.1,
BAA29023.1,
AAH12325.1,
BAF45812.1,
BAA36712.1,
AAC24828.1,
EAW62337.1
Ensembl_TRS:
ENST00000435065,
ENST00000245407
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000402760,
ENSP00000245407
RefSeq:
NP_001295051.1,
XP_011541892.1,
XP_016865267.1,
NP_003051.1
|
| Others |
UniRef100:
UniRef100_O76082
UniRef90:
UniRef90_O76082
UniRef50:
UniRef50_O76082
UniGene:
Hs.443572
CCDS:
CCDS78058.1,
CCDS4154.1
|