Homo sapiens (human): 95681
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Entry
95681 CDS
T01001
Symbol
CEP41, JBTS15, TSGA14
Name
(RefSeq) centrosomal protein of 41 kDa isoform 1
KO
K16455
centrosomal protein CEP41
Organism
hsa
Homo sapiens (human)
Disease
H00530
Joubert syndrome and related disorders
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
95681 (CEP41)
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
95681 (CEP41)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Centriole proteins
95681 (CEP41)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
95681 (CEP41)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Rhodanese
Ninein_long_CC
YubE
Motif
Other DBs
NCBI-GeneID:
95681
NCBI-ProteinID:
NP_061188
OMIM:
610523
HGNC:
12370
Ensembl:
ENSP00000223208.4
UniProt:
Q9BYV8
LinkDB
All DBs
Position
7:complement(130393771..130441741)
Genome browser
AA seq
373 aa
AA seq
DB search
MSLRRHIGNPEYLMKRIPQNPRYQHIKSRLDTGNSMTKYTEKLEEIKKNYRYKKDELFKR
LKVTTFAQLIIQVASLSDQTLEVTAEEIQRLEDNDSAASDPDAETTARTNGKGNPGEQSP
SPEQFINNAGAGDSSRSTLQSVISGVGELDLDKGPVKKAEPHTKDKPYPDCPFLLLDVRD
RDSYQQCHIVGAYSYPIATLSRTMNPYSNDILEYKNAHGKIIILYDDDERLASQAATTMC
ERGFENLFMLSGGLKVLAQKFPEGLITGSLPASCQQALPPGSARKRSSPKGPPLPAENKW
RFTPEDLKKIEYYLEEEQGPADHPSRLNQANSSGRESKVPGARSAQNLPGGGPASHSNPR
SLSSGHLQGKPWK
NT seq
1122 nt
NT seq
+upstream
nt +downstream
nt
atgtccctccggaggcacattgggaaccctgagtatctgatgaaaaggataccacagaac
ccaagataccagcatatcaaatcaagactggacactggtaacagtatgactaaatatact
gagaagctcgaagagattaagaaaaattatagatacaaaaaagatgagcttttcaagaga
ctaaaagttacaacttttgcccagctgatcatccaagttgcttccctctctgatcaaaca
ctggaagtgacagctgaggagattcaaaggctggaagacaatgattctgcagcttcagac
cctgatgctgaaaccactgccaggaccaatgggaaaggaaatccaggtgagcagtcgccg
agccctgagcagttcataaacaacgcaggagcaggggactccagccgctcaactcttcag
agtgtcatcagtggtgttggggaactggatctagacaaagggccagtgaagaaagcagag
ccccataccaaagacaaaccttatcctgactgccccttcctgctgctagatgtgcgtgat
agagattcttaccagcagtgccacattgttggagcttacagttacccaattgcaactctg
tctagaacaatgaacccttattcaaatgatattcttgaatataaaaatgcccatggcaag
atcatcattctgtatgacgatgatgaaaggctggccagtcaggcggccaccaccatgtgc
gagcgtggatttgaaaacctcttcatgctttccggaggtctaaaagtcttagctcagaaa
ttcccggaaggactgattactggttccctgccagcatcttgccagcaggcccttcctcct
gggtctgcccggaaacgatccagccccaaagggccacccctaccagctgagaataaatgg
agatttaccccagaagacttaaaaaagatagaatattatctggaagaggagcaagggcct
gcagatcatcctagccgactgaaccaagctaactcctccggaagagagtccaaggtgcct
ggtgcccgaagcgctcagaatctgccaggtggcggccccgccagccactcaaacccccgc
tccctcagcagtggtcacctgcaaggcaaaccctggaagtaa
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