Homo sapiens (human): 56603
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Entry
56603 CDS
T01001
Symbol
CYP26B1, CYP26A2, P450RAI-2, P450RAI2, RHFCA
Name
(RefSeq) cytochrome P450 family 26 subfamily B member 1
KO
K12664
cytochrome P450 family 26 subfamily B [EC:1.14.14.-]
Organism
hsa
Homo sapiens (human)
Pathway
hsa00830
Retinol metabolism
hsa01100
Metabolic pathways
Disease
H02766
Radiohumeral fusions with other skeletal and craniofacial anomalies
Drug target
Talarozole:
D09385
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09108 Metabolism of cofactors and vitamins
00830 Retinol metabolism
56603 (CYP26B1)
09180 Brite Hierarchies
09181 Protein families: metabolism
00199 Cytochrome P450 [BR:
hsa00199
]
56603 (CYP26B1)
Cytochrome P450 [BR:
hsa00199
]
Cytochrome P450, animal type
CYP26 family
56603 (CYP26B1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
p450
RecA-like_ORC2
Med25
Motif
Other DBs
NCBI-GeneID:
56603
NCBI-ProteinID:
NP_063938
OMIM:
605207
HGNC:
20581
Ensembl:
ENSG00000003137
UniProt:
Q9NR63
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All DBs
Position
2:complement(72129238..72147862)
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AA seq
512 aa
AA seq
DB search
MLFEGLDLVSALATLAACLVSVTLLLAVSQQLWQLRWAATRDKSCKLPIPKGSMGFPLIG
ETGHWLLQGSGFQSSRREKYGNVFKTHLLGRPLIRVTGAENVRKILMGEHHLVSTEWPRS
TRMLLGPNTVSNSIGDIHRNKRKVFSKIFSHEALESYLPKIQLVIQDTLRAWSSHPEAIN
VYQEAQKLTFRMAIRVLLGFSIPEEDLGHLFEVYQQFVDNVFSLPVDLPFSGYRRGIQAR
QILQKGLEKAIREKLQCTQGKDYLDALDLLIESSKEHGKEMTMQELKDGTLELIFAAYAT
TASASTSLIMQLLKHPTVLEKLRDELRAHGILHSGGCPCEGTLRLDTLSGLRYLDCVIKE
VMRLFTPISGGYRTVLQTFELDGFQIPKGWSVMYSIRDTHDTAPVFKDVNVFDPDRFSQA
RSEDKDGRFHYLPFGGGVRTCLGKHLAKLFLKVLAVELASTSRFELATRTFPRITLVPVL
HPVDGLSVKFFGLDSNQNEILPETEAMLSATV
NT seq
1539 nt
NT seq
+upstream
nt +downstream
nt
atgctctttgagggcttggatctggtgtcggcgctggccaccctcgccgcgtgcctggtg
tccgtgacgctgctgctggccgtgtcgcagcagctgtggcagctgcgctgggccgccact
cgcgacaagagctgcaagctgcccatccccaagggatccatgggcttcccgctcatcgga
gagaccggccactggctgctgcagggttctggcttccagtcgtcgcggagggagaagtat
ggcaacgtgttcaagacgcatttgttggggcggccgctgatacgcgtgaccggcgcggag
aacgtgcgcaagatcctcatgggcgagcaccacctcgtgagcaccgagtggcctcgcagc
acccgcatgttgctgggccccaacacggtgtccaattccattggcgacatccaccgcaac
aagcgcaaggtcttctccaagatcttcagccacgaggccctggagagttacctgcccaag
atccagctggtgatccaggacacactgcgcgcctggagcagccaccccgaggccatcaac
gtgtaccaggaggcgcagaagctgaccttccgcatggccatccgggtgctgctgggcttc
agcatccctgaggaggaccttgggcacctctttgaggtctaccagcagtttgtggacaat
gtcttctccctgcctgtcgacctgcccttcagtggctaccggcggggcattcaggctcgg
cagatcctgcagaaggggctggagaaggccatccgggagaagctgcagtgcacacagggc
aaggactacttggacgccctggacctcctcattgagagcagcaaggagcacgggaaggag
atgaccatgcaggagctgaaggacgggaccctggagctgatctttgcggcctatgccacc
acggccagcgccagcacctcactcatcatgcagctgctgaagcaccccactgtgctggag
aagctgcgggatgagctgcgggctcatggcatcctgcacagtggcggctgcccctgcgag
ggcacactgcgcctggacacgctcagtgggctgcgctacctggactgcgtcatcaaggag
gtcatgcgcctgttcacgcccatttccggcggctaccgcactgtgctgcagaccttcgag
cttgatggtttccagatccccaaaggctggagtgtcatgtatagcatccgggacacccat
gacacagcgcccgtgttcaaagacgtgaacgtgttcgaccccgatcgcttcagccaggcg
cggagcgaggacaaggatggccgcttccattacctcccgttcggtggcggtgtccggacc
tgcctgggcaagcacctggccaagctgttcctgaaggtgctggcggtggagctggctagc
accagccgctttgagctggccacacggaccttcccccgcatcaccttggtccccgtcctg
caccccgtggatggcctcagcgtcaagttctttggcctggactccaaccagaacgagatc
ctgccggagacggaggccatgctgagcgccacagtctaa
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