Homo sapiens (human): 768206
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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)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Rod_cone_degen
Motif
Other DBs
NCBI-GeneID:
768206
NCBI-ProteinID:
NP_001071088
OMIM:
610598
HGNC:
32528
Ensembl:
ENSG00000214140
UniProt:
Q00LT1
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All DBs
Position
17:76527586..76553580
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AA seq
54 aa
AA seq
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MCTTLFLLSTLAMLWRRRFANRVQPEPSDVDGAARGSSLDADPQSSGREKEPLK
NT seq
165 nt
NT seq
+upstream
nt +downstream
nt
atgtgcaccacccttttcctgctcagcaccctggccatgctctggcgccgccgatttgcc
aaccgagtccaaccagagcccagcgacgtggatggggcagctaggggcagcagcttggat
gcggaccctcagtcctcaggcagggagaaagaacctctgaagtaa
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