KEGG   Homo sapiens (human): 60506
Entry
60506             CDS       T01001                                 
Symbol
NYX, CLRP, CSNB1, CSNB1A, CSNB4, NBM1
Name
(RefSeq) nyctalopin
  KO
K08129  nyctalopin
Organism
hsa  Homo sapiens (human)
Disease
H00787  Congenital stationary night blindness
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00535 Proteoglycans [BR:hsa00535]
    60506 (NYX)
Proteoglycans [BR:hsa00535]
 Extracellular matrix (ECM) proteoglycans
  Small leucine-rich proteoglycan (SLRP) family
   class IV
    60506 (NYX)
SSDB
Motif
Pfam: LRR_8 LRR_4 LRR_1 LRR_5 LRR_9 LRRNT
Other DBs
NCBI-GeneID: 60506
NCBI-ProteinID: NP_072089
OMIM: 300278
HGNC: 8082
Ensembl: ENSG00000188937
UniProt: Q9GZU5
Position
X:41447343..41475652
AA seq 476 aa
MLVLLLHAVVLGLPSAWAVGACARACPAACACSTVERGCSVRCDRAGLLRVPAELPCEAV
SIDLDRNGLRFLGERAFGTLPSLRRLSLRHNNLSFITPGAFKGLPRLAELRLAHNGDLRY
LHARTFAALSRLRRLDLAACRLFSVPERLLAELPALRELAAFDNLFRRVPGALRGLANLT
HAHLERGRIEAVASSSLQGLRRLRSLSLQANRVRAVHAGAFGDCGVLEHLLLNDNLLAEL
PADAFRGLRRLRTLNLGGNALDRVARAWFADLAELELLYLDRNSIAFVEEGAFQNLSGLL
ALHLNGNRLTVLAWVAFQPGFFLGRLFLFRNPWCCDCRLEWLRDWMEGSGRVTDVPCASP
GSVAGLDLSQVTFGRSSDGLCVDPEELNLTTSSPGPSPEPAATTVSRFSSLLSKLLAPRV
PVEEAANTTGGLANASLSDSLSSRGVGGAGRQPWFLLASCLLPSVAQHVVFGLQMD
NT seq 1431 nt   +upstreamnt  +downstreamnt
atgttggtcctgcttctgcatgcggtggtcctcggcctgcccagcgcctgggccgtgggg
gcctgcgcccgcgcttgtcccgccgcctgcgcctgcagcaccgtggagcgcggctgctcg
gtgcgctgcgaccgcgcgggcctcctgcgggtgccggccgagctcccgtgcgaggcggtc
tccatcgacctggaccggaacggcctgcgcttcctgggcgagcgagccttcggcacgctg
ccgtccttgcgccgcctgtcgctgcgccacaacaacctgtccttcatcacgcccggcgcc
ttcaagggcctgccgcgcctggctgagctgcgcctggcgcacaacggcgacctgcgctac
ctgcacgcgcgcaccttcgcggcgctcagccgcctgcgccgcctagacctagcagcctgc
cgcctcttcagcgtgcccgagcgcctcctggccgaactgccggccctgcgcgaactcgcc
gccttcgacaacctgttccgccgcgtgccgggcgcgctgcgcggcctggccaacctgacg
cacgcgcacctggagcgcggccgcatcgaggcggtggcctccagctcgctgcagggcctg
cgccgcctgcgctcgctcagcctgcaggccaaccgcgtccgtgccgtgcacgctggcgcc
ttcggggactgtggcgtcctggagcatctgctgctcaacgacaacctgctggccgagctc
ccggccgacgccttccgcggcctgcggcgcctgcgcacgctcaacctgggtggcaacgcg
ctggaccgcgtggcgcgcgcctggttcgctgacctggccgagctcgagctgctctacctg
gaccgcaacagcatcgccttcgtggaggagggcgccttccagaacctctcgggtctcctc
gcgctgcacctcaacggcaaccgcctcaccgtgctcgcctgggtcgccttccagcccggc
ttcttcctgggccgcctcttcctcttccgcaacccgtggtgctgcgactgccgtctggag
tggctgagggactggatggagggctccggacgtgtcaccgacgtgccgtgcgcctccccg
ggctccgtggccggcctggacctcagccaggtgaccttcgggcgctcctccgatggcctc
tgtgtggaccccgaggagctgaacctcaccacgtccagtccaggcccgtccccagaacca
gcggccaccaccgtgagcaggttcagcagcctcctctccaagctgctggccccgagggtc
ccggtggaggaggcggccaacaccactggggggctggccaacgcctccctgtccgacagc
ctctcctcccgtggggtgggaggcgcgggccggcagccctggtttctcctcgcctcttgt
ctcctgcccagcgtggcccagcacgtggtgtttggcctgcagatggactga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (16)   
   KEGG ORTHOLOGY (1)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (8)   
   RefSeq(nuc) (2)   
   GenBank (3)   
   EMBL (3)   
Protein domain (6)   
   Pfam (6)   
All databases (40)   

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