KEGG   Homo sapiens (human): 95681
Entry
95681             CDS       T01001                                 
Symbol
CEP41, JBTS15, TSGA14
Name
(RefSeq) centrosomal protein 41
  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
Motif
Pfam: Rhodanese
Other DBs
NCBI-GeneID: 95681
NCBI-ProteinID: NP_061188
OMIM: 610523
HGNC: 12370
Ensembl: ENSG00000106477
UniProt: Q9BYV8
Position
7:complement(130393771..130441741)
AA seq 373 aa
MSLRRHIGNPEYLMKRIPQNPRYQHIKSRLDTGNSMTKYTEKLEEIKKNYRYKKDELFKR
LKVTTFAQLIIQVASLSDQTLEVTAEEIQRLEDNDSAASDPDAETTARTNGKGNPGEQSP
SPEQFINNAGAGDSSRSTLQSVISGVGELDLDKGPVKKAEPHTKDKPYPDCPFLLLDVRD
RDSYQQCHIVGAYSYPIATLSRTMNPYSNDILEYKNAHGKIIILYDDDERLASQAATTMC
ERGFENLFMLSGGLKVLAQKFPEGLITGSLPASCQQALPPGSARKRSSPKGPPLPAENKW
RFTPEDLKKIEYYLEEEQGPADHPSRLNQANSSGRESKVPGARSAQNLPGGGPASHSNPR
SLSSGHLQGKPWK
NT seq 1122 nt   +upstreamnt  +downstreamnt
atgtccctccggaggcacattgggaaccctgagtatctgatgaaaaggataccacagaac
ccaagataccagcatatcaaatcaagactggacactggtaacagtatgactaaatatact
gagaagctcgaagagattaagaaaaattatagatacaaaaaagatgagcttttcaagaga
ctaaaagttacaacttttgcccagctgatcatccaagttgcttccctctctgatcaaaca
ctggaagtgacagctgaggagattcaaaggctggaagacaatgattctgcagcttcagac
cctgatgctgaaaccactgccaggaccaatgggaaaggaaatccaggtgagcagtcgccg
agccctgagcagttcataaacaacgcaggagcaggggactccagccgctcaactcttcag
agtgtcatcagtggtgttggggaactggatctagacaaagggccagtgaagaaagcagag
ccccataccaaagacaaaccttatcctgactgccccttcctgctgctagatgtgcgtgat
agagattcttaccagcagtgccacattgttggagcttacagttacccaattgcaactctg
tctagaacaatgaacccttattcaaatgatattcttgaatataaaaatgcccatggcaag
atcatcattctgtatgacgatgatgaaaggctggccagtcaggcggccaccaccatgtgc
gagcgtggatttgaaaacctcttcatgctttccggaggtctaaaagtcttagctcagaaa
ttcccggaaggactgattactggttccctgccagcatcttgccagcaggcccttcctcct
gggtctgcccggaaacgatccagccccaaagggccacccctaccagctgagaataaatgg
agatttaccccagaagacttaaaaaagatagaatattatctggaagaggagcaagggcct
gcagatcatcctagccgactgaaccaagctaactcctccggaagagagtccaaggtgcct
ggtgcccgaagcgctcagaatctgccaggtggcggccccgccagccactcaaacccccgc
tccctcagcagtggtcacctgcaaggcaaaccctggaagtaa

  All links  
Ontology (3)   
   KEGG BRITE (3)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (15)   
   KEGG ORTHOLOGY (1)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (16)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (14)   
DNA sequence (45)   
   RefSeq(nuc) (15)   
   GenBank (15)   
   EMBL (15)   
Protein domain (1)   
   Pfam (1)   
All databases (84)   

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