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Results for the Protein: NP_001010932
58533170
HGF

hepatocyte growth factor isoform 3 precursor [Homo sapiens]

Known Diseases associated with this Protein:
  DEAFNESS, AUTOSOMAL RECESSIVE 39
1
3
1
3
0
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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Default View:

PAN_1 - pfam00024
PAN_AP - smart00473
PAN_AP_HGF - cd01099
PAN_APPLE - cd00129
KR - cd00108
KR - smart00130
Kringle - pfam00051
Tryp_SPc - smart00020
Trypsin - pfam00089
Tryp_SPc - cd00190




Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
PAN_APPLEcd001294.1e-4439122
PAN_AP_HGFcd010997.5e-1939122
KRcd001081.9e-44125202
KRcd001081e-48203284
KRcd001081.2e-45297378
KRcd001081.3e-40383465
Tryp_SPccd001903.5e-64490714
PAN_1pfam000243.2e-1334121
Kringlepfam000511.1e-44128201
Kringlepfam000511.3e-50206283
Kringlepfam000512.5e-51300378
Kringlepfam000511.8e-43386464
Trypsinpfam000894.5e-63490711
PAN_APsmart004737.5e-1637122
KRsmart001307.2e-45126203
KRsmart001302e-48204285
KRsmart001303.1e-49298380
KRsmart001305e-41384466
Tryp_SPcsmart000202.2e-64489711

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs5745688 Polymorphismp.ASP325TYRN/A
dbSNPrs5745687 Polymorphismp.GLU299LYSN/A
dbSNPrs17566 Polymorphismp.SER153ILEN/A
OMIM142409.0001 Diseasep.SER1SERDEAFNESS, AUTOSOMAL RECESSIVE 39



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