Homo sapiens (human): 64699
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Entry
64699 CDS
T01001
Symbol
TMPRSS3, DFNB10, DFNB8, ECHOS1, TADG12
Name
(RefSeq) transmembrane protease serine 3 isoform 1
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)
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Paralog
GFIT
Motif
Pfam:
Trypsin
SRCR_2
Nudel
Hepsin-SRCR
SRCR
Ldl_recept_a
DUF8054_C
Motif
Other DBs
NCBI-GeneID:
64699
NCBI-ProteinID:
NP_076927
OMIM:
605511
HGNC:
11877
UniProt:
P57727
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All DBs
Position
21:complement(42371890..42396052)
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AA seq
454 aa
AA seq
DB search
MGENDPPAVEAPFSFRSLFGLDDLKISPVAPDADAVAAQILSLLPLKFFPIIVIGIIALI
LALAIGLGIHFDCSGKYRCRSSFKCIELIARCDGVSDCKDGEDEYRCVRVGGQNAVLQVF
TAASWKTMCSDDWKGHYANVACAQLGFPSYVSSDNLRVSSLEGQFREEFVSIDHLLPDDK
VTALHHSVYVREGCASGHVVTLQCTACGHRRGYSSRIVGGNMSLLSQWPWQASLQFQGYH
LCGGSVITPLWIITAAHCVYDLYLPKSWTIQVGLVSLLDNPAPSHLVEKIVYHSKYKPKR
LGNDIALMKLAGPLTFNEMIQPVCLPNSEENFPDGKVCWTSGWGATEDGAGDASPVLNHA
AVPLISNKICNHRDVYGGIISPSMLCAGYLTGGVDSCQGDSGGPLVCQERRLWKLVGATS
FGIGCAEVNKPGVYTRVTSFLDWIHEQMERDLKT
NT seq
1365 nt
NT seq
+upstream
nt +downstream
nt
atgggggaaaatgatccgcctgctgttgaagcccccttctcattccgatcgctttttggc
cttgatgatttgaaaataagtcctgttgcaccagatgcagatgctgttgctgcacagatc
ctgtcactgctgccattgaagttttttccaatcatcgtcattgggatcattgcattgata
ttagcactggccattggtctgggcatccacttcgactgctcagggaagtacagatgtcgc
tcatcctttaagtgtatcgagctgatagctcgatgtgacggagtctcggattgcaaagac
ggggaggacgagtaccgctgtgtccgggtgggtggtcagaatgccgtgctccaggtgttc
acagctgcttcgtggaagaccatgtgctccgatgactggaagggtcactacgcaaatgtt
gcctgtgcccaactgggtttcccaagctatgtgagttcagataacctcagagtgagctcg
ctggaggggcagttccgggaggagtttgtgtccatcgatcacctcttgccagatgacaag
gtgactgcattacaccactcagtatatgtgagggagggatgtgcctctggccacgtggtt
accttgcagtgcacagcctgtggtcatagaaggggctacagctcacgcatcgtgggtgga
aacatgtccttgctctcgcagtggccctggcaggccagccttcagttccagggctaccac
ctgtgcgggggctctgtcatcacgcccctgtggatcatcactgctgcacactgtgtttat
gacttgtacctccccaagtcatggaccatccaggtgggtctagtttccctgttggacaat
ccagccccatcccacttggtggagaagattgtctaccacagcaagtacaagccaaagagg
ctgggcaatgacatcgcccttatgaagctggccgggccactcacgttcaatgaaatgatc
cagcctgtgtgcctgcccaactctgaagagaacttccccgatggaaaagtgtgctggacg
tcaggatggggggccacagaggatggagcaggtgacgcctcccctgtcctgaaccacgcg
gccgtccctttgatttccaacaagatctgcaaccacagggacgtgtacggtggcatcatc
tccccctccatgctctgcgcgggctacctgacgggtggcgtggacagctgccagggggac
agcggggggcccctggtgtgtcaagagaggaggctgtggaagttagtgggagcgaccagc
tttggcatcggctgcgcagaggtgaacaagcctggggtgtacacccgtgtcacctccttc
ctggactggatccacgagcagatggagagagacctaaaaacctga
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