Homo sapiens (human): 10491
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Entry
10491 CDS
T01001
Symbol
CRTAP, CASP, LEPREL3, OI7, P3H5
Name
(RefSeq) cartilage associated protein
KO
K19606
cartilage-associated protein
Organism
hsa
Homo sapiens (human)
Disease
H00506
Osteogenesis imperfecta
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03110 Chaperones and folding catalysts [BR:
hsa03110
]
10491 (CRTAP)
Chaperones and folding catalysts [BR:
hsa03110
]
Other chaperones and cochaperones
Others
10491 (CRTAP)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TPR_leprecan
TPR_P4H
dGTP_diPhyd_N
YfiO
Motif
Other DBs
NCBI-GeneID:
10491
NCBI-ProteinID:
NP_006362
OMIM:
605497
HGNC:
2379
Ensembl:
ENSG00000170275
UniProt:
O75718
Structure
PDB
PDBj
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All DBs
Position
3:33114014..33147773
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AA seq
401 aa
AA seq
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MEPGRRGAAALLALLCVACALRAGRAQYERYSFRSFPRDELMPLESAYRHALDKYSGEHW
AESVGYLEISLRLHRLLRDSEAFCHRNCSAAPQPEPAAGLASYPELRLFGGLLRRAHCLK
RCKQGLPAFRQSQPSREVLADFQRREPYKFLQFAYFKANNLPKAIAAAHTFLLKHPDDEM
MKRNMAYYKSLPGAEDYIKDLETKSYESLFIRAVRAYNGENWRTSITDMELALPDFFKAF
YECLAACEGSREIKDFKDFYLSIADHYVEVLECKIQCEENLTPVIGGYPVEKFVATMYHY
LQFAYYKLNDLKNAAPCAVSYLLFDQNDKVMQQNLVYYQYHRDTWGLSDEHFQPRPEAVQ
FFNVTTLQKELYDFAKENIMDDDEGEVVEYVDDLLELEETS
NT seq
1206 nt
NT seq
+upstream
nt +downstream
nt
atggagccggggcgccggggggccgcggcgctgctagcgctgctgtgcgtggcctgcgcg
ctgcgcgccgggcgcgcccaatacgaacgctacagcttccgcagcttcccacgggacgag
ctgatgccgctcgagtcggcctaccggcacgcgctggacaagtacagcggcgagcactgg
gccgagagcgtgggctacctggagatcagcctgcggctgcaccgcttgctgcgcgacagc
gaggccttctgccaccgcaactgcagcgccgcgccgcagcccgagcccgccgccggcctc
gccagctatcccgagctgcgcctcttcgggggcctgctgcgccgcgcgcactgcctcaag
cgctgcaagcagggcctgccagccttccgccagtcccagcccagccgcgaggtgctggcg
gacttccagcgccgcgagccctacaagttcctgcagttcgcttacttcaaggcaaataat
ctccccaaagccatcgccgctgctcacacctttctactgaagcatcctgatgacgaaatg
atgaagaggaacatggcatattataagagcctgcctggtgccgaggactacattaaagac
ctggaaaccaagtcatatgaaagcctgttcatccgagcagtgcgggcatacaacggtgag
aactggagaacatccatcacagacatggagctggcccttcccgacttcttcaaagccttt
tacgagtgtctcgcagcctgcgagggttccagggagatcaaggacttcaaggatttctac
ctttccatagcagatcattatgtagaagttctggaatgcaaaatacagtgtgaagagaac
ctcaccccagttataggaggctatccggttgagaaatttgtggctaccatgtatcattac
ttgcagtttgcctattataagttgaacgacctgaagaatgcagccccctgtgcagtcagc
tatctgctctttgatcagaatgacaaggtcatgcagcagaacctggtgtattaccagtac
cacagggacacttggggcctctcggatgagcacttccagcccagacctgaagcagttcag
ttctttaatgtgaccacactccagaaggagctgtatgactttgctaaggaaaatataatg
gatgatgatgagggagaagttgtggaatatgtggatgacctcttggaactggaggagacc
agctag
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