KEGG   Homo sapiens (human): 64699
Entry
64699             CDS       T01001                                 
Symbol
TMPRSS3, DFNB10, DFNB8, ECHOS1, TADG12
Name
(RefSeq) transmembrane serine protease 3
  KO
K09634  transmembrane protease serine 3 [EC:3.4.21.-]
Organism
hsa  Homo sapiens (human)
Disease
H00605  Deafness, autosomal recessive
H01705  Bilateral sudden sensorineural hearing loss
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01002 Peptidases and inhibitors [BR:hsa01002]
    64699 (TMPRSS3)
Peptidases and inhibitors [BR:hsa01002]
 Serine peptidases
  Family S1: chymotrypsin family
   64699 (TMPRSS3)
SSDB
Motif
Pfam: Trypsin SRCR_2 Hepsin-SRCR DUF1986 SRCR Ldl_recept_a
Other DBs
NCBI-GeneID: 64699
NCBI-ProteinID: NP_076927
OMIM: 605511
HGNC: 11877
Ensembl: ENSG00000160183
UniProt: P57727
Position
21:complement(42371890..42396052)
AA seq 454 aa
MGENDPPAVEAPFSFRSLFGLDDLKISPVAPDADAVAAQILSLLPLKFFPIIVIGIIALI
LALAIGLGIHFDCSGKYRCRSSFKCIELIARCDGVSDCKDGEDEYRCVRVGGQNAVLQVF
TAASWKTMCSDDWKGHYANVACAQLGFPSYVSSDNLRVSSLEGQFREEFVSIDHLLPDDK
VTALHHSVYVREGCASGHVVTLQCTACGHRRGYSSRIVGGNMSLLSQWPWQASLQFQGYH
LCGGSVITPLWIITAAHCVYDLYLPKSWTIQVGLVSLLDNPAPSHLVEKIVYHSKYKPKR
LGNDIALMKLAGPLTFNEMIQPVCLPNSEENFPDGKVCWTSGWGATEDGAGDASPVLNHA
AVPLISNKICNHRDVYGGIISPSMLCAGYLTGGVDSCQGDSGGPLVCQERRLWKLVGATS
FGIGCAEVNKPGVYTRVTSFLDWIHEQMERDLKT
NT seq 1365 nt   +upstreamnt  +downstreamnt
atgggggaaaatgatccgcctgctgttgaagcccccttctcattccgatcgctttttggc
cttgatgatttgaaaataagtcctgttgcaccagatgcagatgctgttgctgcacagatc
ctgtcactgctgccattgaagttttttccaatcatcgtcattgggatcattgcattgata
ttagcactggccattggtctgggcatccacttcgactgctcagggaagtacagatgtcgc
tcatcctttaagtgtatcgagctgatagctcgatgtgacggagtctcggattgcaaagac
ggggaggacgagtaccgctgtgtccgggtgggtggtcagaatgccgtgctccaggtgttc
acagctgcttcgtggaagaccatgtgctccgatgactggaagggtcactacgcaaatgtt
gcctgtgcccaactgggtttcccaagctatgtgagttcagataacctcagagtgagctcg
ctggaggggcagttccgggaggagtttgtgtccatcgatcacctcttgccagatgacaag
gtgactgcattacaccactcagtatatgtgagggagggatgtgcctctggccacgtggtt
accttgcagtgcacagcctgtggtcatagaaggggctacagctcacgcatcgtgggtgga
aacatgtccttgctctcgcagtggccctggcaggccagccttcagttccagggctaccac
ctgtgcgggggctctgtcatcacgcccctgtggatcatcactgctgcacactgtgtttat
gacttgtacctccccaagtcatggaccatccaggtgggtctagtttccctgttggacaat
ccagccccatcccacttggtggagaagattgtctaccacagcaagtacaagccaaagagg
ctgggcaatgacatcgcccttatgaagctggccgggccactcacgttcaatgaaatgatc
cagcctgtgtgcctgcccaactctgaagagaacttccccgatggaaaagtgtgctggacg
tcaggatggggggccacagaggatggagcaggtgacgcctcccctgtcctgaaccacgcg
gccgtccctttgatttccaacaagatctgcaaccacagggacgtgtacggtggcatcatc
tccccctccatgctctgcgcgggctacctgacgggtggcgtggacagctgccagggggac
agcggggggcccctggtgtgtcaagagaggaggctgtggaagttagtgggagcgaccagc
tttggcatcggctgcgcagaggtgaacaagcctggggtgtacacccgtgtcacctccttc
ctggactggatccacgagcagatggagagagacctaaaaacctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (2)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   KEGG ORTHOLOGY (1)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (6)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (35)   
   RefSeq(nuc) (5)   
   GenBank (15)   
   EMBL (15)   
Protein domain (6)   
   Pfam (6)   
All databases (71)   

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