Type | Description |
---|---|
Definition | solute carrier family 46 member 1 |
Date | Results | Publications |
---|---|---|
2021-03-13 13:17:00 | A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation. | 32893190 |
2021-02-27 13:53:00 | Impact of hypoxia on chemoresistance of mesothelioma mediated by the proton-coupled folate transporter, and preclinical activity of new anti-LDH-A compounds. | 32493992 |
2021-02-27 13:45:00 | Decreased placental folate transporter expression and activity in first and second trimester in obese mothers. | 31926453 |
2020-10-10 13:01:00 | SLC46A1 contributes to hepatic iron metabolism by importing heme in hepatocytes. | 32621820 |
2020-05-23 12:05:00 | we report the same deep intronic mutation of c.1166-285T>G shared by four unrelated Japanese patients with hereditary folate malabsorption | 31494288 |
Type | IDs |
---|---|
Synonymous | G21, HCP1, PCFT |
Gene |
UniProtKB-ID:
PCFT_HUMAN,
A0A024QZ44_HUMAN,
A0A024QZ15_HUMAN
UniprotKB:
Q96NT5,
A0A024QZ44,
A0A024QZ15
UniParc:
UPI0000050394,
UPI00000728A8
EMBL:
AL832613,
AK074161,
AK054669,
DQ496103,
BC010691,
CH471159
Ensembl:
ENSG00000076351
KO:
hsa:113235
|
Nucleutide sequences |
EMBL-CDS:
BAB70789.1,
BAB84987.1,
AAH10691.1,
CAD89945.1,
ABF47092.1,
EAW51086.1,
EAW51089.1,
EAW51085.1,
EAW51087.1
Gene_ORFName:
hCG_31812,
hCG_31812
Ensembl_TRS:
ENST00000618626,
ENST00000612814
|
Protein sequencees |
Ensembl_PRO:
ENSP00000480703,
ENSP00000483652
RefSeq:
XP_005277843.1,
XP_016879599.1,
NP_001229295.1,
NP_542400.2
|
Others |
UniRef100:
UniRef100_Q96NT5,
UniRef100_A0A024QZ44
UniRef90:
UniRef90_A0A1U7U832,
UniRef90_Q96NT5
UniRef50:
UniRef50_Q96NT5
UniGene:
Hs.446689
CCDS:
CCDS74020.1,
CCDS74019.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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