ORTHOLOGY: K19637
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Entry
K19637 KO
Symbol
PRCD
Name
progressive rod-cone degeneration protein
Disease
H00527
Retinitis pigmentosa
Brite
KEGG Orthology (KO) [BR:
ko00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins
K19637 PRCD; progressive rod-cone degeneration protein
Cilium and associated proteins [BR:
ko03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
K19637 PRCD; progressive rod-cone degeneration protein
BRITE hierarchy
Genes
HSA:
768206
(PRCD)
PTR:
739050
(PRCD)
PPS:
100992422
(PRCD)
PON:
100435362
(PRCD)
PPYG:
129016762
(PRCD)
NLE:
100601022
(PRCD)
HMH:
116483160
(PRCD)
SSYN:
129462302
(PRCD)
MCC:
106994137
(PRCD)
MCF:
102129771
(PRCD)
MTHB:
126939281
MNI:
105469205
(PRCD)
CSAB:
103242994
(PRCD)
PANU:
101022191
(PRCD)
TGE:
112610259
(PRCD)
MLEU:
105542653
(PRCD)
RRO:
104681270
(PRCD)
RBB:
108537438
(PRCD)
TFN:
117066727
(PRCD)
PTEH:
111542552
(PRCD)
CANG:
105517816
(PRCD)
CJC:
100407916
(PRCD)
SBQ:
101054076
(PRCD)
CIMI:
108309472
(PRCD)
ANAN:
105718093
(PRCD)
CSYR:
103251116
(PRCD)
MMUR:
105878979
(PRCD)
LCAT:
123620492
(PRCD)
PCOQ:
105824739
(PRCD)
OGA:
100965063
(PRCD)
MMU:
100038570
(Prcd)
MCAL:
110305056
(Prcd)
MPAH:
110331139
(Prcd)
RNO:
100912216
(Prcd)
MCOC:
116077596
(Prcd)
ANU:
117709914
(Prcd)
ASYL:
127694093
(Prcd)
MUN:
110566008
(Prcd)
CGE:
100755980
(Prcd)
PLEU:
114707091
(Prcd)
MORG:
121436306
(Prcd)
AAMP:
119813158
(Prcd)
NGI:
103732781
(Prcd)
HGL:
101714585
(Prcd)
CPOC:
101788669
(Prcd)
CCAN:
109685596
(Prcd)
DORD:
106003082
(Prcd)
DSP:
122128324
(Prcd)
PLOP:
125365589
(Prcd)
NCAR:
124979754
MMMA:
107157753
(Prcd)
ITI:
101975426
(Prcd)
TUP:
102467985
(PRCD)
GVR:
103604323
(PRCD)
CFA:
100049006
(PRCD)
VVP:
112920831
(PRCD)
VLG:
121473379
(PRCD)
NPO:
129514335
(PRCD)
AML:
105237917
(PRCD)
UMR:
103665767
(PRCD)
UAH:
113244592
(PRCD)
UAR:
123803210
(PRCD)
ELK:
111160271
LLV:
125087802
MPUF:
101687675
(PRCD)
MNP:
132004094
(PRCD)
MLK:
131817013
(PRCD)
NVS:
122907528
(PRCD)
EJU:
114216289
(PRCD)
ZCA:
113939635
(PRCD)
MLX:
118024233
(PRCD)
NSU:
110572586
(PRCD)
LWW:
102739141
(PRCD)
FCA:
101085163
(PRCD)
PYU:
121017959
(PRCD)
PCOO:
112864700
(PRCD)
PBG:
122486126
(PRCD)
PVIV:
125151792
(PRCD)
LRUF:
124512821
LGF:
123604054
(PRCD)
AJU:
106987786
PTG:
102954111
(PRCD)
PPAD:
109276893
(PRCD)
PUC:
125926325
PLEZ:
122206976
(PRCD)
HHV:
120228095
(PRCD)
BOM:
102280630
(PRCD)
BBUB:
102414379
(PRCD)
BBIS:
105000379
(PRCD)
CHX:
102184941
(PRCD)
OAS:
101104327
(PRCD)
CSUM:
138082718
(PRCD)
ODA:
120866783
(PRCD)
CCAD:
122437129
(PRCD)
MREE:
136149993
(PRCD)
OVR:
110152040
(PRCD)
SSC:
100516929
(PRCD)
CFR:
102509466
(PRCD)
CBAI:
105065620
(PRCD)
CDK:
105092182
(PRCD)
VPC:
102540855
(PRCD)
BACU:
103004818
(PRCD)
BMUS:
118886804
(PRCD)
LVE:
103069645
(PRCD)
OOR:
101280414
(PRCD)
LALB:
132511030
(PRCD)
DLE:
111182965
(PRCD)
PCAD:
102993619
(PRCD)
PSIU:
116745782
(PRCD)
NASI:
112410427
(PRCD)
ECB:
100051104
(PRCD)
EPZ:
103565527
(PRCD)
EAI:
123276407
(PRCD)
MYB:
102253870
(PRCD)
MYD:
102756255
(PRCD)
MLF:
102440058
(PRCD)
MDT:
132219135
(PRCD)
MYUM:
138995056
(PRCD)
PKL:
118704580
(PRCD)
EFUS:
103298391
(PRCD)
MNA:
107536585
(PRCD)
DRO:
112298740
(PRCD)
SHON:
119000072
(PRCD)
PDIC:
118502254
(PRCD)
PHAS:
123816968
(PRCD)
MMF:
118634930
(PRCD)
PPAM:
129086422
(PRCD)
HAI:
109383657
(PRCD)
RFQ:
117013058
(PRCD)
PALE:
102892010
(PRCD)
PGIG:
120599989
(PRCD)
PVP:
105293384
(PRCD)
MJV:
108398678
(PRCD)
SFUM:
130024853
(PRCD)
LAV:
100674082
(PRCD)
TMU:
101353388
ETF:
101652735
(PRCD)
DNM:
105745761
(PRCD)
CCRI:
104157711
(PRCD)
HALD:
104317788
LDI:
104350463
NNI:
104022871
PCRI:
104033853
PADL:
103921016
FGA:
104074305
DRE:
101885756
(prcd)
» show all
Taxonomy
UniProt
Reference
PMID:
23805042
Authors
Pach J, Kohl S, Gekeler F, Zobor D
Title
Identification of a novel mutation in the PRCD gene causing autosomal recessive retinitis pigmentosa in a Turkish family.
Journal
Mol Vis 19:1350-5 (2013)
Sequence
[hsa:
768206
]
Reference
PMID:
16938425
Authors
Zangerl B, Goldstein O, Philp AR, Lindauer SJ, Pearce-Kelling SE, Mullins RF, Graphodatsky AS, Ripoll D, Felix JS, Stone EM, Acland GM, Aguirre GD
Title
Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans.
Journal
Genomics 88:551-63 (2006)
DOI:
10.1016/j.ygeno.2006.07.007
Sequence
[hsa:
768206
]
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integrated database retrieval system
