Homo sapiens (human): 4884
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Entry
4884 CDS
T01001
Symbol
NPTX1, NP1, SCA50
Name
(RefSeq) neuronal pentraxin 1
KO
K25709
neuronal pentraxin
Organism
hsa
Homo sapiens (human)
Disease
H00063
Spinocerebellar ataxia (SCA)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
4884 (NPTX1)
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Gene cluster
GFIT
Motif
Pfam:
Pentaxin
Laminin_G_3
Laminin_G_2
MRP-S27
DUF6626
DUF16
SlyX
Gp58
Motif
Other DBs
NCBI-GeneID:
4884
NCBI-ProteinID:
NP_002513
OMIM:
602367
HGNC:
7952
Ensembl:
ENSG00000171246
UniProt:
Q15818
Structure
PDB
PDBj
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All DBs
Position
17:complement(80466834..80476607)
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AA seq
432 aa
AA seq
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MPAGRAARTCALLALCLLGAGAQDFGPTRFICTSVPVDADMCAASVAAGGAEELRSSVLQ
LRETVLQQKETILSQKETIRELTAKLGRCESQSTLDPGAGEARAGGGRKQPGSGKNTMGD
LSRTPAAETLSQLGQTLQSLKTRLENLEQYSRLNSSSQTNSLKDLLQSKIDELERQVLSR
VNTLEEGKGGPRNDTEERVKIETALTSLHQRISELEKGQKDNRPGDKFQLTFPLRTNYMY
AKVKKSLPEMYAFTVCMWLKSSATPGVGTPFSYAVPGQANELVLIEWGNNPMEILINDKV
AKLPFVINDGKWHHICVTWTTRDGVWEAYQDGTQGGSGENLAPYHPIKPQGVLVLGQEQD
TLGGGFDATQAFVGELAHFNIWDRKLTPGEVYNLATCSTKALSGNVIAWAESHIEIYGGA
TKWTFEACRQIN
NT seq
1299 nt
NT seq
+upstream
nt +downstream
nt
atgccggccggccgcgccgcgcgcacctgtgcgctgctcgccctctgcctcctgggcgcc
ggggcccaggatttcgggccgacgcgcttcatctgcacctcggtgcccgtggacgccgac
atgtgcgccgcgtccgtggccgccggcggcgccgaggagctccggagcagcgtgctgcag
ctccgcgagacggtgctgcagcagaaggagaccatcctgagccagaaggagaccatccgc
gagctgaccgccaagctgggccgctgcgagagccagagcacgctggaccccggagccggc
gaggcccgggcgggcggcggccgcaagcagcccggctcgggcaagaacaccatgggcgac
ctgtcccggacaccggccgccgagacgctcagccaactcgggcaaactttgcaatcgctc
aaaacccgcctggagaacctcgagcagtacagccgcctcaattcctccagccagaccaac
agcctcaaggatctgctgcagagcaagatcgatgagctggagaggcaggtgctgtcccgg
gtgaacaccctggaggagggcaaggggggccccaggaacgacaccgaggagagggtcaag
atcgagaccgccctgacctccctgcaccagcggatcagcgagctcgagaaaggtcagaaa
gacaaccgccctggagacaagttccagctcacattcccactgcggaccaactatatgtat
gccaaggtgaagaagagcctgccagagatgtacgccttcactgtctgcatgtggctcaag
tccagcgccacgccaggtgtgggcacgcccttctcctacgctgtgcccggccaggccaac
gagctggtcctcattgagtggggcaacaaccccatggagatcctcatcaatgacaaggtg
gccaagttgccttttgtcatcaatgatggcaagtggcaccacatctgtgtcacctggacc
acccgggacggggtctgggaggcctaccaggatggcacgcagggtggcagtggcgagaac
ttggcgccctatcaccccatcaagccccagggcgtgctggtgctgggccaggagcaggac
actctgggtggtgggtttgatgccacccaggcatttgtgggtgagctggcccacttcaac
atctgggaccgcaagctgacccccggggaggtgtacaacctggccacctgcagcaccaag
gctctgtccggcaatgtcatcgcctgggctgaatcccacatcgagatctacggaggggcc
accaagtggaccttcgaggcctgtcgccagatcaactga
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