Homo sapiens (human): 10087
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Entry
10087 CDS
T01001
Symbol
CERT1, CERT, CERTL, COL4A3BP, GPBP, MRD34, NEDHSF, STARD11
Name
(RefSeq) ceramide transporter 1
KO
K08283
collagen type IV alpha-3-binding protein
Organism
hsa
Homo sapiens (human)
Disease
H00773
Autosomal dominant intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04990 Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
10087 (CERT1)
Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
Pleckstrin homology (PH) domain-containing proteins
Other PH domain-containing proteins
10087 (CERT1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
START
PH
PH_8
PH_11
SOS1_NGEF_PH
Acyl_CoA_thio
Motif
Other DBs
NCBI-GeneID:
10087
NCBI-ProteinID:
NP_005704
OMIM:
604677
HGNC:
2205
Ensembl:
ENSG00000113163
UniProt:
Q9Y5P4
Structure
PDB
PDBj
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All DBs
Position
5:complement(75368486..75511981)
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AA seq
624 aa
AA seq
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MSDNQSWNSSGSEEDPETESGPPVERCGVLSKWTNYIHGWQDRWVVLKNNALSYYKSEDE
TEYGCRGSICLSKAVITPHDFDECRFDISVNDSVWYLRAQDPDHRQQWIDAIEQHKTESG
YGSESSLRRHGSMVSLVSGASGYSATSTSSFKKGHSLREKLAEMETFRDILCRQVDTLQK
YFDACADAVSKDELQRDKVVEDDEDDFPTTRSDGDFLHSTNGNKEKLFPHVTPKGINGID
FKGEAITFKATTAGILATLSHCIELMVKREDSWQKRLDKETEKKRRTEEAYKNAMTELKK
KSHFGGPDYEEGPNSLINEEEFFDAVEAALDRQDKIEEQSQSEKVRLHWPTSLPSGDAFS
SVGTHRFVQKPYSRSSSMSSIDLVSASDDVHRFSSQVEEMVQNHMTYSLQDVGGDANWQL
VVEEGEMKVYRREVEENGIVLDPLKATHAVKGVTGHEVCNYFWNVDVRNDWETTIENFHV
VETLADNAIIIYQTHKRVWPASQRDVLYLSVIRKIPALTENDPETWIVCNFSVDHDSAPL
NNRCVRAKINVAMICQTLVSPPEGNQEISRDNILCKITYVANVNPGGWAPASVLRAVAKR
EYPKFLKRFTSYVQEKTAGKPILF
NT seq
1875 nt
NT seq
+upstream
nt +downstream
nt
atgtcggataatcagagctggaactcgtcgggctcggaggaggatccagagacggagtct
gggccgcctgtggagcgctgcggggtcctcagtaagtggacaaactacattcatgggtgg
caggatcgttgggtagttttgaaaaataatgctctgagttactacaaatctgaagatgaa
acagagtatggctgcagaggatccatctgtcttagcaaggctgtcatcacacctcacgat
tttgatgaatgtcgatttgatattagtgtaaatgatagtgtttggtatcttcgtgctcag
gatccagatcatagacagcaatggatagatgccattgaacagcacaagactgaatctgga
tatggatctgaatccagcttgcgtcgacatggctcaatggtgtccctggtgtctggagca
agtggctactctgcaacatccacctcttcattcaagaaaggccacagtttacgtgagaag
ttggctgaaatggaaacatttagagacatcttatgtagacaagttgacacgctacagaag
tactttgatgcctgtgctgatgctgtctctaaggatgaacttcaaagggataaagtggta
gaagatgatgaagatgactttcctacaacgcgttctgatggtgacttcttgcatagtacc
aacggcaataaagaaaagttatttccacatgtgacaccaaaaggaattaatggtatagac
tttaaaggggaagcgataacttttaaagcaactactgctggaatccttgcaacactttct
cattgtattgaactaatggttaaacgtgaggacagctggcagaagagactggataaggaa
actgagaagaaaagaagaacagaggaagcatataaaaatgcaatgacagaacttaagaaa
aaatcccactttggaggaccagattatgaagaaggccctaacagtctgattaatgaagaa
gagttctttgatgctgttgaagctgctcttgacagacaagataaaatagaagaacagtca
cagagtgaaaaggtgagattacattggcctacatccttgccctctggagatgccttttct
tctgtggggacacatagatttgtccaaaagccctatagtcgctcttcctccatgtcttcc
attgatctagtcagtgcctctgatgatgttcacagattcagctcccaggttgaagagatg
gtgcagaaccacatgacttactcattacaggatgtaggcggagatgccaattggcagttg
gttgtagaagaaggagaaatgaaggtatacagaagagaagtagaagaaaatgggattgtt
ctggatcctttaaaagctacccatgcagttaaaggcgtcacaggacatgaagtctgcaat
tatttctggaatgttgacgttcgcaatgactgggaaacaactatagaaaactttcatgtg
gtggaaacattagctgataatgcaatcatcatttatcaaacacacaagagggtgtggcct
gcttctcagcgagacgtattatatctttctgtcattcgaaagataccagccttgactgaa
aatgaccctgaaacttggatagtttgtaatttttctgtggatcatgacagtgctcctcta
aacaaccgatgtgtccgtgccaaaataaatgttgctatgatttgtcaaaccttggtaagc
ccaccagagggaaaccaggaaattagcagggacaacattctatgcaagattacatatgta
gctaatgtgaaccctggaggatgggcaccagcctcagtgttaagggcagtggcaaagcga
gagtatcctaaatttctaaaacgttttacttcttacgtccaagaaaaaactgcaggaaag
cctattttgttctag
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