Homo sapiens (human): 10695
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Entry
10695 CDS
T01001
Symbol
CNPY3, CAG4A, DEE60, EIEE60, ERDA5, PRAT4A, TNRC5
Name
(RefSeq) protein canopy homolog 3 isoform 1 precursor
KO
K22816
protein canopy 3/4
Organism
hsa
Homo sapiens (human)
Disease
H00606
Early infantile epileptic encephalopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03110 Chaperones and folding catalysts [BR:
hsa03110
]
10695 (CNPY3)
Chaperones and folding catalysts [BR:
hsa03110
]
Other chaperones and cochaperones
Others
10695 (CNPY3)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
DUF3456
TBK1_CCD1
PTP-NADK
SapB_1
Motif
Other DBs
NCBI-GeneID:
10695
NCBI-ProteinID:
NP_006577
OMIM:
610774
HGNC:
11968
Ensembl:
ENSP00000361926.4
UniProt:
Q9BT09
LinkDB
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Position
6:42928002..42939294
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AA seq
278 aa
AA seq
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MDSMPEPASRCLLLLPLLLLLLLLLPAPELGPSQAGAEENDWVRLPSKCEVCKYVAVELK
SAFEETGKTKEVIGTGYGILDQKASGVKYTKSDLRLIEVTETICKRLLDYSLHKERTGSN
RFAKGMSETFETLHNLVHKGVKVVMDIPYELWNETSAEVADLKKQCDVLVEEFEEVIEDW
YRNHQEEDLTEFLCANHVLKGKDTSCLAEQWSGKKGDTAALGGKKSKKKSSRAKAAGGRS
SSSKQRKELGGLEGDPSPEEDEGIQKASPLTHSPPDEL
NT seq
837 nt
NT seq
+upstream
nt +downstream
nt
atggattcaatgcctgagcccgcgtcccgctgtcttctgcttcttcccttgctgctgctg
ctgctgctgctgctgccggccccggagctgggcccgagccaggccggagctgaggagaac
gactgggttcgcctgcccagcaaatgcgaagtgtgtaaatatgttgctgtggagctgaag
tcagcctttgaggaaaccggcaagaccaaggaggtgattggcacgggctatggcatcctg
gaccagaaggcctctggagtcaaatacaccaagtcggacttgcggttaatcgaagtcact
gagaccatttgcaagaggctcctggattatagcctgcacaaggagaggaccggcagcaat
cgatttgccaagggcatgtcagagacctttgagacattacacaacctggtacacaaaggg
gtcaaggtggtgatggacatcccctatgagctgtggaacgagacttctgcagaggtggct
gacctcaagaagcagtgtgatgtgctggtggaagagtttgaggaggtgatcgaggactgg
tacaggaaccaccaggaggaagacctgactgaattcctctgcgccaaccacgtgctgaag
ggaaaagacaccagttgcctggcagagcagtggtccggcaagaagggagacacagctgcc
ctgggagggaagaagtccaagaagaagagcagcagggccaaggcagcaggcggcaggagt
agcagcagcaaacaaaggaaggagctgggtggccttgagggagaccccagccccgaggag
gatgagggcatccagaaggcatcccctctcacacacagcccccctgatgagctctga
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