Homo sapiens (human): 4693
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Entry
4693 CDS
T01001
Symbol
NDP, EVR2, FEVR, ND
Name
(RefSeq) norrin cystine knot growth factor NDP
KO
K25688
norrin
Organism
hsa
Homo sapiens (human)
Disease
H00589
Familial exudative vitreoretinopathy
H02045
Norrie disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
4693 (NDP)
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Paralog
Gene cluster
GFIT
Motif
Pfam:
Cys_knot
DAN
Motif
Other DBs
NCBI-GeneID:
4693
NCBI-ProteinID:
NP_000257
OMIM:
300658
HGNC:
7678
Ensembl:
ENSG00000124479
UniProt:
Q00604
Structure
PDB
PDBj
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All DBs
Position
X:complement(43948776..43973390)
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AA seq
133 aa
AA seq
DB search
MRKHVLAASFSMLSLLVIMGDTDSKTDSSFIMDSDPRRCMRHHYVDSISHPLYKCSSKMV
LLARCEGHCSQASRSEPLVSFSTVLKQPFRSSCHCCRPQTSKLKALRLRCSGGMRLTATY
RYILSCHCEECNS
NT seq
402 nt
NT seq
+upstream
nt +downstream
nt
atgagaaaacatgtactagctgcatccttttctatgctctccctgctggtgataatggga
gatacagacagtaaaacggacagctcattcataatggactcggaccctcgacgctgcatg
aggcaccactatgtggattctatcagtcacccattgtacaagtgtagctcaaagatggtg
ctcctggccaggtgcgaggggcactgcagccaggcgtcacgctccgagcctttggtgtcg
ttcagcactgtcctcaagcaacccttccgttcctcctgtcactgctgccggccccagact
tccaagctgaaggcactgcggctgcgatgctcagggggcatgcgactcactgccacctac
cggtacatcctctcctgtcactgcgaggaatgcaattcctga
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