Type | Description |
---|---|
Definition | cytochrome P450 family 7 subfamily B member 1 |
Date | Results | Publications |
---|---|---|
2020-08-22 15:29:00 | AKR1D1 and CYP7B1 mutations in patients with inborn errors of bile acid metabolism: Possibly underdiagnosed diseases. | 31337596 |
2019-11-23 10:47:00 | This study provides evidence for CYP7B1 as a key regulator of three vital intracellular regulatory oxysterol levels. | 30710743 |
2017-07-29 11:06:00 | SPG11 and CYP7B1 were the most common cause of autosomal recessive hereditary spastic paraplegia in Greece. | 26374131 |
2017-03-11 11:43:00 | miR17 induces epithelial-mesenchymal transition consistent with the cancer stem cell phenotype by regulating CYP7B1 expression in colon cancer. | 27278684 |
2016-12-17 10:20:00 | The two novel variants cosegregated with pyramidal signs and autoimmune diseases suggesting that they might be susceptibility factors. | 26370385 |
Type | IDs |
---|---|
Synonymous | CBAS3, CP7B, SPG5A |
Gene |
UniProtKB-ID:
CP7B1_HUMAN,
Q05C57_HUMAN
UniprotKB:
O75881,
Q05C57
UniParc:
UPI0000128218,
UPI0000D49BAA
EMBL:
AF176801,
BC136574,
BC029155,
AF176803,
AF176805,
AF127090,
AF176802,
AF176804,
AF029403,
AF176800,
CH471068
Ensembl:
ENSG00000172817
KO:
hsa:9420
|
Nucleutide sequences |
EMBL-CDS:
AAK11850.1,
AAC95426.1,
AAI36575.1,
AAD20021.1,
EAW86877.1,
AAH29155.1
Ensembl_TRS:
ENST00000310193
|
Protein sequencees |
Ensembl_PRO:
ENSP00000310721
RefSeq:
XP_016869491.1,
NP_001311041.1,
NP_004811.1
|
Others |
UniRef100:
UniRef100_Q05C57,
UniRef100_O75881
UniRef90:
UniRef90_O75881
UniRef50:
UniRef50_O75881
UniGene:
Hs.667720
CCDS:
CCDS6180.1
|
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Refseq |
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