KEGG   Homo sapiens (human): 8492
Entry
8492              CDS       T01001                                 
Symbol
PRSS12, BSSP-3, BSSP3, MRT1
Name
(RefSeq) serine protease 12
  KO
K09624  neurotrypsin [EC:3.4.21.-]
Organism
hsa  Homo sapiens (human)
Disease
H00768  Autosomal recessive intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01002 Peptidases and inhibitors [BR:hsa01002]
    8492 (PRSS12)
Peptidases and inhibitors [BR:hsa01002]
 Serine peptidases
  Family S1: chymotrypsin family
   8492 (PRSS12)
SSDB
Motif
Pfam: SRCR Trypsin SRCR_2 Kringle Trypsin_2 DUF1986
Other DBs
NCBI-GeneID: 8492
NCBI-ProteinID: NP_003610
OMIM: 606709
HGNC: 9477
Ensembl: ENSG00000164099
UniProt: P56730 Q96I80
Position
4:complement(118280038..118353003)
AA seq 875 aa
MTLARFVLALMLGALPEVVGFDSVLNDSLHHSHRHSPPAGPHYPYYLPTQQRPPRTRPPP
PLPRFPRPPRALPAQRPHALQAGHTPRPHPWGCPAGEPWVSVTDFGAPCLRWAEVPPFLE
RSPPASWAQLRGQRHNFCRSPDGAGRPWCFYGDARGKVDWGYCDCRHGSVRLRGGKNEFE
GTVEVYASGVWGTVCSSHWDDSDASVICHQLQLGGKGIAKQTPFSGLGLIPIYWSNVRCR
GDEENILLCEKDIWQGGVCPQKMAAAVTCSFSHGPTFPIIRLAGGSSVHEGRVELYHAGQ
WGTVCDDQWDDADAEVICRQLGLSGIAKAWHQAYFGEGSGPVMLDEVRCTGNELSIEQCP
KSSWGEHNCGHKEDAGVSCTPLTDGVIRLAGGKGSHEGRLEVYYRGQWGTVCDDGWTELN
TYVVCRQLGFKYGKQASANHFEESTGPIWLDDVSCSGKETRFLQCSRRQWGRHDCSHRED
VSIACYPGGEGHRLSLGFPVRLMDGENKKEGRVEVFINGQWGTICDDGWTDKDAAVICRQ
LGYKGPARARTMAYFGEGKGPIHVDNVKCTGNERSLADCIKQDIGRHNCRHSEDAGVICD
YFGKKASGNSNKESLSSVCGLRLLHRRQKRIIGGKNSLRGGWPWQVSLRLKSSHGDGRLL
CGATLLSSCWVLTAAHCFKRYGNSTRSYAVRVGDYHTLVPEEFEEEIGVQQIVIHREYRP
DRSDYDIALVRLQGPEEQCARFSSHVLPACLPLWRERPQKTASNCYITGWGDTGRAYSRT
LQQAAIPLLPKRFCEERYKGRFTGRMLCAGNLHEHKRVDSCQGDSGGPLMCERPGESWVV
YGVTSWGYGCGVKDSPGVYTKVSAFVPWIKSVTKL
NT seq 2628 nt   +upstreamnt  +downstreamnt
atgacgctcgcccgcttcgtgctagccctgatgttaggggcgctccccgaagtggtcggc
tttgattctgtcctcaatgattccctccaccacagccaccgccattcgccccctgcgggt
ccgcactacccctattaccttcccacccagcagcggcccccgaggacgcgtccgccgccg
cctctcccgcgcttcccgcgccccccgcgggcgctccctgcccagcgcccgcacgccctc
caggccgggcacacgccccggccgcacccctggggctgccccgccggcgagccatgggtc
agcgtgacggacttcggcgccccgtgtctgcggtgggcggaggtgccacccttcctggag
cggtcgcccccagcgagctgggctcagctgcgaggacagcgccacaacttttgtcggagc
cccgacggcgcgggcagaccctggtgtttctacggagacgcccgtggcaaggtggactgg
ggctactgcgactgcagacacggatcagtacgacttcgtggcggcaaaaatgagtttgaa
ggcacagtggaagtatatgcaagtggagtttggggcactgtctgtagcagccactgggat
gattctgatgcatcagtcatttgtcaccagctgcagctgggaggaaaaggaatagcaaaa
caaaccccgttttctggactgggccttattcccatttattggagcaatgtccgttgccga
ggagatgaagaaaatatactgctttgtgaaaaagacatctggcagggtggggtgtgtcct
cagaagatggcagctgctgtcacgtgtagcttttcccatggcccaacgttccccatcatt
cgccttgctggaggcagcagtgtgcatgaaggccgggtggagctctaccatgctggccag
tggggaaccgtttgtgatgaccaatgggatgatgccgatgcagaagtgatctgcaggcag
ctgggcctcagtggcattgccaaagcatggcatcaggcatattttggggaagggtctggc
ccagttatgttggatgaagtacgctgcactgggaatgagctttcaattgagcagtgtcca
aagagctcctggggagagcataactgtggccataaagaagatgctggagtgtcctgtacc
cctctaacagatggggtcatcagacttgcaggtgggaaaggcagccatgagggtcgcttg
gaggtatattacagaggccagtggggaactgtctgtgatgatggctggactgagctgaat
acatacgtggtttgtcgacaattgggatttaaatatggtaaacaagcatctgccaaccat
tttgaagaaagcacagggcccatatggttggatgacgtcagctgctcaggaaaggaaacc
agatttcttcagtgttccaggcgacagtggggaaggcatgactgcagccaccgcgaagat
gttagcattgcctgctaccctggcggcgagggacacaggctctctctgggttttcctgtc
agactgatggatggagaaaataagaaagaaggacgagtggaggtttttatcaatggccag
tggggaacaatctgtgatgatggatggactgataaggatgcagctgtgatctgtcgtcag
cttggctacaagggtcctgccagagcaagaaccatggcttactttggagaaggaaaagga
cccatccatgtggataatgtgaagtgcacaggaaatgagaggtccttggctgactgtatc
aagcaagatattggaagacacaactgccgccacagtgaagatgcaggagttatttgtgat
tattttggcaagaaggcctcaggtaacagtaataaagagtccctctcatctgtttgtggc
ttgagattactgcaccgtcggcagaagcggatcattggtgggaaaaattctttaaggggt
ggttggccttggcaggtttccctccggctgaagtcatcccatggagatggcaggctcctc
tgcggggctacgctcctgagtagctgctgggtcctcacagcagcacactgtttcaagagg
tatggcaacagcactaggagctatgctgttagggttggagattatcatactctggtacca
gaggagtttgaggaagaaattggagttcaacagattgtgattcatcgggagtatcgaccc
gaccgcagtgattatgacatagccctggttagattacaaggaccagaagagcaatgtgcc
agattcagcagccatgttttgccagcctgtttaccactctggagagagaggccacagaaa
acagcatccaactgttacataacaggatggggtgacacaggacgagcctattcaagaaca
ctacaacaagcagccattcccttacttcctaaaaggttttgtgaagaacgttataagggt
cggtttacagggagaatgctttgtgctggaaacctccatgaacacaaacgcgtggacagc
tgccagggagacagcggaggaccactcatgtgtgaacggcccggagagagctgggtggtg
tatggggtgacctcctgggggtatggctgtggagtcaaggattctcctggtgtttatacc
aaagtctcagcctttgtaccttggataaaaagtgtcaccaaactgtaa

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (38)   
   KEGG ORTHOLOGY (1)   
   RefGene (28)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (8)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (13)   
   RefSeq(nuc) (5)   
   GenBank (4)   
   EMBL (4)   
Protein domain (6)   
   Pfam (6)   
All databases (71)   

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