TMPRSS4 - transmembrane serine protease 4 Gene

Also Known as CAP2; CAPH2; MT-SP2; TMPRSS3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 56649

About TMPRSS4

Cytogenetic location: 11q23.3 Genomic coordinates (GRCh38): 11:118,077,078-118,125,505 (from NCBI)

This gene has 19 transcripts (splice variants), 148 orthologues, 12 paralogues and is associated with 1 phenotype. Biased expression in colon (RPKM 31.0), urinary bladder (RPKM 28.2) and 8 other tissues.

Summary

This gene encodes a member of the serine protease family. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified as a gene overexpressed in pancreatic carcinoma. The encoded protein is membrane bound with a N-terminal anchor sequence and a glycosylated extracellular region containing the serine protease domain. The protein has been found to promote SARS-CoV-2 entry into host cells. [provided by RefSeq, Aug 2021]

TMPRSS4 Products (6)

mRNA Protein Name
NM_001083947.2 NP_001077416.2 transmembrane protease serine 4 isoform 3
NM_001173551.2 NP_001167022.2 transmembrane protease serine 4 isoform 4
NM_001173552.2 NP_001167023.2 transmembrane protease serine 4 isoform 5
NM_001290094.2 NP_001277023.2 transmembrane protease serine 4 isoform 6
NM_001290096.2 NP_001277025.2 transmembrane protease serine 4 isoform 7
NM_019894.4 NP_063947.2 transmembrane protease serine 4 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables serine-type peptidase activity IDA
IDA: Inferred from direct assay
24434139 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within negative regulation of growth rate IDA
IDA: Inferred from direct assay
29529050 GOA
involved in positive regulation of viral entry into host cell IDA
IDA: Inferred from direct assay
32404436 GOA
involved in protein processing IDA
IDA: Inferred from direct assay
24434139 GOA
involved in proteolysis IDA
IDA: Inferred from direct assay
24434139 GOA
acts upstream of or within regulation of gene expression IDA
IDA: Inferred from direct assay
29529050 GOA
Cellular Component GO Annotation Evidence References Source
located in extracellular space IDA
IDA: Inferred from direct assay
24434139 GOA
located in secretory granule IDA
IDA: Inferred from direct assay
29529050 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TMPRSS4 Protein Structure

SRCR_2

SRCR_2: Scavenger receptor cysteine-rich domain (109 - 199)

Trypsin

Trypsin: Trypsin (206 - 429)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 437 a.a.
Protein Preferred Names Protein Names

transmembrane protease serine 4

  • channel-activating protease 2

TMPRSS4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TMPRSS4 Q9NRS4 GPX8 Homo sapiens Q8TED1 32296183
Intra
TMPRSS4 Q9NRS4 GPX8 Homo sapiens Q8TED1 32296183
Intra
TMPRSS4 Q9NRS4 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
TMPRSS4 Q9NRS4 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
TMPRSS4 Q9NRS4 RASGRP4 Homo sapiens Q8TDF6-2 32296183
Intra
TMPRSS4 Q9NRS4 RASGRP4 Homo sapiens Q8TDF6-2 32296183
Intra
TMPRSS4 Q9NRS4 CLRN1 Homo sapiens P58418 32296183
Intra
TMPRSS4 Q9NRS4 CLRN1 Homo sapiens P58418 32296183
Intra
TMPRSS4 Q9NRS4 SIGLEC12 Homo sapiens Q96PQ1 32296183
Intra
TMPRSS4 Q9NRS4 SIGLEC12 Homo sapiens Q96PQ1 32296183
Intra
TMPRSS4 Q9NRS4 ERVFRD-1 Homo sapiens P60508 32296183
Intra
TMPRSS4 Q9NRS4 ERVFRD-1 Homo sapiens P60508 32296183
Intra
TMPRSS4 Q9NRS4 SUSD3 Homo sapiens Q96L08 32296183
Intra
TMPRSS4 Q9NRS4 SUSD3 Homo sapiens Q96L08 32296183
Intra
TMPRSS4 Q9NRS4 FAM209A Homo sapiens Q5JX71 32296183
Intra
TMPRSS4 Q9NRS4 FAM209A Homo sapiens Q5JX71 32296183
Intra
TMPRSS4 Q9NRS4 KASH5 Homo sapiens Q8N6L0 25416956
Intra
TMPRSS4 Q9NRS4 BNIP3L Homo sapiens O60238 32296183
Intra
TMPRSS4 Q9NRS4 BNIP3L Homo sapiens O60238 32296183
Intra
TMPRSS4 Q9NRS4 CSNK1D Homo sapiens P48730-2 32814053
Intra
TMPRSS4 Q9NRS4 CSNK1D Homo sapiens P48730-2 32814053
Intra
TMPRSS4 Q9NRS4 CSNK1D Homo sapiens P48730-2 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

TMPRSS4 Antibodies

Cat. No. Product Name Application Reactivity
HY-P89692 TMPRSS4 Antibody (YA9036) WB, ICC/IF, IF-Tissue, IP, ELISA human

Related Diseases

Diseases Alias
Autosomal Recessive Cerebral Atrophy
Deafness, Autosomal Recessive 8
  • Neurosensory Nonsyndromic Recessive Deafness 8

  • DFNB8

  • Dfnb10

  • Deafness, Autosomal Recessive 10

  • Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8

  • Nsrd8

  • Autosomal Recessive Nonsyndromic Deafness 8

  • Deafness, Autosomal Recessive 8/10

  • Autosomal Recessive Deafness 10

  • Autosomal Recessive Deafness 8

  • Childhood-Onset Neurosensory Autosomal Recessive Deafness 8

  • Nrsd8

  • Deafness, Autosomal Recessive, 8

  • Childhood-Onset Neurosensory Deafness Autosomal Recessive 8

  • Deafness Autosomal Recessive 10

  • Deafness Autosomal Recessive 8/10

  • Deafness Neurosensory Autosomal Recessive 8

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 8

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 8

  • Deafness, Autosomal Recessive, Type 8/10

Covid-19
  • 2019 Novel Coronavirus

  • 2019-Ncov Infection

  • Covid19

  • Sars-Cov-2 Infection

  • Wuhan Coronavirus Infection

  • Wuhan Seafood Market Pneumonia Virus Infection

Colorectal Cancer, Hereditary Nonpolyposis, Type 8
  • HNPCC8

  • Hereditary Nonpolyposis Colorectal Cancer Type 8

  • Hereditary Non-Polyposis Colorectal Cancer 8

  • Cancer, Colorectal, Nonpolyposis, Hereditary, Type 8

Deafness, Autosomal Recessive 98
  • DFNB98

  • Autosomal Recessive Nonsyndromic Deafness 98

  • Autosomal Recessive Deafness 98

  • Deafness, Autosomal Recessive, 98

  • Deafness, Autosomal Recessive, Type 98

Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct
  • Enlarged Vestibular Aqueduct

  • DFNB4

  • Neurosensory Nonsyndromic Recessive Deafness 4

  • Enlarged Vestibular Aqueduct Syndrome

  • Nsrd4

  • Autosomal Recessive Nonsyndromic Deafness 4

  • Dilated Vestibular Aqueduct

  • Dva

  • Enlarged Vestibular Aqueduct, Digenic

  • Autosomal Recessive Deafness 4 With Enlarged Vestibular Aqueduct

  • Large Vestibular Aqueduct Syndrome

  • Deafness, Autosomal Recessive, 4

  • Deafness Neurosensory Autosomal Recessive 4

  • Eva

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 4

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 4

  • Deafness, Autosomal Recessive, Type 4 , With Enlarged Vestibular Aqueduct

Deafness, Autosomal Recessive 39
  • DFNB39

  • Autosomal Recessive Nonsyndromic Deafness 39

  • Autosomal Recessive Deafness 39

  • Deafness, Autosomal Recessive, 39

  • Congenital Neurosensory Deafness Autosomal Recessive 39

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 39

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 39

  • Deafness, Autosomal Recessive, Type 39

Deafness, Autosomal Recessive 83
  • DFNB83

  • Autosomal Recessive Nonsyndromic Deafness 83

  • Autosomal Recessive Deafness 83

Deafness, Autosomal Recessive 77
  • DFNB77

  • Autosomal Recessive Nonsyndromic Deafness 77

  • Autosomal Recessive Deafness 77

  • Deafness, Autosomal Recessive, 77

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 77

  • Deafness, Autosomal Recessive, Type 77

Petroclival Meningioma
Deafness, Autosomal Recessive 61
  • DFNB61

  • Autosomal Recessive Nonsyndromic Deafness 61

  • Autosomal Recessive Deafness 61

  • Deafness, Autosomal Recessive, 61

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 61

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 61

  • Deafness, Autosomal Recessive, Type 61

Deafness, Autosomal Recessive 42
  • DFNB42

  • Autosomal Recessive Nonsyndromic Deafness 42

  • Autosomal Recessive Deafness 42

  • Deafness, Autosomal Recessive, 42

  • Congenital Neurosensory Deafness Autosomal Recessive 42

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 42

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 42

  • Deafness, Autosomal Recessive, Type 42

Auditory System Disease
  • Ear Diseases

  • Ear And Mastoid Disease

Deafness, Autosomal Recessive 12
  • DFNB12

  • Deafness, Autosomal Recessive 12, Modifier Of

  • Autosomal Recessive Nonsyndromic Deafness 12

  • Autosomal Recessive Deafness 12

  • Deafness, Autosomal Recessive, 12

  • Congenital Neurosensory Deafness Autosomal Recessive 12

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 12

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 12

  • Deafness, Autosomal Recessive, Type 12

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Autosomal Recessive Nonsyndromic Deafness
  • Deafness, Autosomal Recessive, Nonsyndromic

Cataract 44
  • CTRCT44

  • Total Early-Onset Cataract

  • Cataract 44 And Hypotrichosis

  • Cataract And Hypotrichosis

  • Cataract, Type 44

Autosomal Dominant Nonsyndromic Deafness
  • Autosomal Dominant Deafness

Usher Syndrome Type 2
  • Ush2

  • Usher Syndrome Type Ii

Usher Syndrome
  • Deafness-Retinitis Pigmentosa Syndrome

  • Dystrophia Retinae Pigmentosa-Dysostosis Syndrome

  • Graefe-Usher Syndrome

  • Hallgren Syndrome

  • Usher'S Syndrome

  • Retinitis Pigmentosa-Deafness Syndrome

  • Retinitis Pigmentosa-Hearing Loss Syndrome

  • Ush

  • Usher Syndromes

Sensorineural Hearing Loss
  • Sensory Hearing Loss

  • Sensorineural Deafness

  • Sensorineural Hearing Loss Disorder

  • Hearing Loss, Sensorineural

  • Central Hearing Loss

  • High Frequency Deafness

  • High Frequency Hearing Loss

  • High-Frequency Hearing Loss

  • Perceptive Deafness

  • Perceptive Hearing Loss

  • Perceptive Hearing Loss Or Deafness

  • Hearing Loss Sensorineural

  • Deafness Sensorineural

  • Hearing Loss High-Frequency

  • Hearing Loss, Central

  • Hearing Loss, High-Frequency

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris TMPRSS4 VGNC VGNC:47634
Felis catus TMPRSS4 VGNC VGNC:66387
Bos taurus TMPRSS4 VGNC VGNC:36142
Macaca mulatta TMPRSS4 VGNC VGNC:78577
Rattus norvegicus TMPRSS4 RGD RGD:1305033
Mus musculus TMPRSS4 MGD MGI:2384877
Others TMPRSS4 NCBI