Homo sapiens (human): 340665
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Entry
340665 CDS
T01001
Symbol
CYP26C1, FFDD4
Name
(RefSeq) cytochrome P450 family 26 subfamily C member 1
KO
K12665
cytochrome P450 family 26 subfamily C [EC:1.14.14.-]
Organism
hsa
Homo sapiens (human)
Pathway
hsa00830
Retinol metabolism
hsa01100
Metabolic pathways
Disease
H02083
Focal facial dermal dysplasia
Drug target
Talarozole:
D09385
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09108 Metabolism of cofactors and vitamins
00830 Retinol metabolism
340665 (CYP26C1)
09180 Brite Hierarchies
09181 Protein families: metabolism
00199 Cytochrome P450 [BR:
hsa00199
]
340665 (CYP26C1)
Cytochrome P450 [BR:
hsa00199
]
Cytochrome P450, animal type
CYP26 family
340665 (CYP26C1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
p450
Motif
Other DBs
NCBI-GeneID:
340665
NCBI-ProteinID:
NP_899230
OMIM:
608428
HGNC:
20577
Ensembl:
ENSG00000187553
UniProt:
Q6V0L0
LinkDB
All DBs
Position
10:93060798..93069540
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AA seq
522 aa
AA seq
DB search
MFPWGLSCLSVLGAAGTALLCAGLLLSLAQHLWTLRWMLSRDRASTLPLPKGSMGWPFFG
ETLHWLVQGSRFHSSRRERYGTVFKTHLLGRPVIRVSGAENVRTILLGEHRLVRSQWPQS
AHILLGSHTLLGAVGEPHRRRRKVLARVFSRAALERYVPRLQGALRHEVRSWCAAGGPVS
VYDASKALTFRMAARILLGLRLDEAQCATLARTFEQLVENLFSLPLDVPFSGLRKGIRAR
DQLHRHLEGAISEKLHEDKAAEPGDALDLIIHSARELGHEPSMQELKESAVELLFAAFFT
TASASTSLVLLLLQHPAAIAKIREELVAQGLGRACGCAPGAAGGSEGPPPDCGCEPDLSL
AALGRLRYVDCVVKEVLRLLPPVSGGYRTALRTFELDGYQIPKGWSVMYSIRDTHETAAV
YRSPPEGFDPERFGAAREDSRGASSRFHYIPFGGGARSCLGQELAQAVLQLLAVELVRTA
RWELATPAFPAMQTVPIVHPVDGLRLFFHPLTPSVAGNGLCL
NT seq
1569 nt
NT seq
+upstream
nt +downstream
nt
atgttcccttgggggctgagctgcctgtcagtgctgggggcggcgggcactgctctcctg
tgcgcgggcctgctgctcagcctggcccagcacctctggaccctccgctggatgctgagc
cgggaccgggcctccaccctgcctctgcccaagggctccatggggtggcccttcttcggc
gaaacgctgcactggttagttcagggctcgcgcttccacagttctcgccgagagcgctat
gggacagtgttcaagacgcacctgctgggcaggccagtgatccgcgtgagcggcgcggag
aacgtgcgcaccatcctgctgggcgagcaccgcctggtgcgcagccagtggccgcagagt
gcgcacatcctgctgggctcgcacacactgctaggtgcggtcggcgagccgcaccggcgg
cggcgcaaggtcctggcgcgcgtgttcagccgcgccgcgctggagcgctacgtgccgcgc
ctgcagggggcgctgcggcatgaggtgcgctcctggtgcgcggcgggcgggccggtctca
gtctacgacgcctccaaagcgctcaccttccgcatggccgcgcgcatcctgctggggttg
cggctggacgaggcgcagtgcgccacgctggcccggaccttcgagcagctcgtggagaac
ctcttctcactgcctctggacgttcccttcagtggcctacgcaagggcatccgggcaagg
gaccagctgcatcggcacctggagggggccatttctgagaagcttcacgaggacaaggct
gcagagccgggtgatgccctcgacctaatcattcacagtgcaagggagctgggccatgag
ccctccatgcaggagctgaaggagtcggctgtggagctcctcttcgccgccttcttcacc
acggccagtgccagcacctcgctcgtcctgctgctactgcagcatccggcggccatcgcc
aagattcgggaggagctggtggcgcaggggctggggcgcgcgtgcggctgcgcgcccggg
gccgctgggggcagcgaggggcccccgcccgactgcggctgcgagcccgacctcagcctc
gcggcgctgggccgtctgcgctacgtcgactgcgtggtcaaggaggtgctgcgcctcctg
ccgccagtgtccgggggctaccgcaccgccctgcgcaccttcgagctcgacggctaccag
atccccaagggctggagcgtgatgtatagcatccgggacacgcacgagacggctgcggtg
taccgcagccctcccgaaggcttcgatccagagcgcttcggcgcagcgcgcgaagattcc
cggggcgcctccagccgcttccattacatcccgttcggcggcggtgcgcgcagctgcctc
ggccaggagctggcgcaagccgtgctccagctgctagctgtggagctagtgcgcaccgcg
cgctgggaactggccacacccgccttccccgccatgcagacggtgcccatcgtgcaccca
gtggacgggctgcggctctttttccaccccctcacgccttcggttgcggggaatgggcta
tgcctctga
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