KEGG   Homo sapiens (human): 6855
Entry
6855              CDS       T01001                                 
Symbol
SYP, MRX96, MRXSYP, XLID96
Name
(RefSeq) synaptophysin
Organism
hsa  Homo sapiens (human)
Disease
H00480  X-linked intellectual developmental disorder
SSDB
Motif
Pfam: MARVEL DUF5080 CASP_dom
Other DBs
NCBI-GeneID: 6855
NCBI-ProteinID: NP_003170
OMIM: 313475
HGNC: 11506
Ensembl: ENSG00000102003
UniProt: P08247
Position
X:complement(49187815..49200193)
AA seq 313 aa
MLLLADMDVVNQLVAGGQFRVVKEPLGFVKVLQWVFAIFAFATCGSYSGELQLSVDCANK
TESDLSIEVEFEYPFRLHQVYFDAPTCRGGTTKVFLVGDYSSSAEFFVTVAVFAFLYSMG
ALATYIFLQNKYRENNKGPMLDFLATAVFAFMWLVSSSAWAKGLSDVKMATDPENIIKEM
PVCRQTGNTCKELRDPVTSGLNTSVVFGFLNLVLWVGNLWFVFKETGWAAPFLRAPPGAP
EKQPAPGDAYGDAGYGQGPGGYGPQDSYGPQGGYQPDYGQPAGSGGSGYGPQGDYGQQGY
GPQGAPTSFSNQM
NT seq 942 nt   +upstreamnt  +downstreamnt
atgctgctgctggcggacatggacgtggtgaatcagctggtggctgggggtcagttccgg
gtggtcaaggagcccctcggctttgtgaaggtgctgcaatgggtcttcgccatcttcgcc
tttgccacatgcggcagctacagtggggagctccagctgagcgtggattgtgccaacaag
accgagagtgacctcagcatcgaggtcgagttcgagtaccccttcaggctgcaccaagtg
tactttgatgcacccacctgccgagggggcaccaccaaggtcttcttagttggggactac
tcctcgtcagccgaattctttgtcaccgtggccgtgtttgccttcctctactccatgggg
gctctggccacctacatcttcctgcagaacaagtaccgagagaataacaaagggcccatg
ctggactttctggccacggctgtgttcgccttcatgtggctagttagctcatcggcatgg
gccaaggggctgtcagatgtgaagatggccacagacccagagaacattatcaaggagatg
cctgtctgccgccagacagggaacacatgcaaggagctgagagaccctgtgacctcggga
ctcaacacctcggtggtgttcggcttcctgaacctggtgctctgggtcggcaacctgtgg
ttcgtgtttaaggagacaggctgggccgccccgttcctgcgcgcgcctcccggcgccccc
gagaaacaaccggcacccggggacgcctacggcgatgcaggctacgggcagggccccggc
gggtacgggccccaggattcctacgggcctcagggcggctaccagcctgactatggtcaa
ccagccggcagcggtggcagtggctacgggcctcagggcgactatgggcagcaaggctac
ggcccgcagggtgcacccacctccttctccaatcagatgtag

DBGET integrated database retrieval system