KEGG   Homo sapiens (human): 768206
Entry
768206            CDS       T01001                                 
Symbol
PRCD, RP36
Name
(RefSeq) photoreceptor disc component
  KO
K19637  progressive rod-cone degeneration protein
Organism
hsa  Homo sapiens (human)
Disease
H00527  Retinitis pigmentosa
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    768206 (PRCD)
Cilium and associated proteins [BR:hsa03037]
 Primary cilia and associated proteins
  Other primary cilia associated proteins
   768206 (PRCD)
SSDB
Motif
Pfam: Rod_cone_degen
Other DBs
NCBI-GeneID: 768206
NCBI-ProteinID: NP_001071088
OMIM: 610598
HGNC: 32528
Ensembl: ENSG00000214140
UniProt: Q00LT1
Position
17:76527586..76553580
AA seq 54 aa
MCTTLFLLSTLAMLWRRRFANRVQPEPSDVDGAARGSSLDADPQSSGREKEPLK
NT seq 165 nt   +upstreamnt  +downstreamnt
atgtgcaccacccttttcctgctcagcaccctggccatgctctggcgccgccgatttgcc
aaccgagtccaaccagagcccagcgacgtggatggggcagctaggggcagcagcttggat
gcggaccctcagtcctcaggcagggagaaagaacctctgaagtaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (6)   
   KEGG ORTHOLOGY (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (15)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (13)   
DNA sequence (28)   
   RefSeq(nuc) (14)   
   GenBank (7)   
   EMBL (7)   
Protein domain (1)   
   Pfam (1)   
All databases (56)   

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