Incidental Mutation 'R6922:Tmprss4'
ID 539682
Institutional Source Beutler Lab
Gene Symbol Tmprss4
Ensembl Gene ENSMUSG00000032091
Gene Name transmembrane protease, serine 4
Synonyms
MMRRC Submission 045041-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R6922 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 45084024-45115390 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 45097220 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 15 (V15A)
Ref Sequence ENSEMBL: ENSMUSP00000131890 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034599] [ENSMUST00000165263] [ENSMUST00000170069]
AlphaFold Q8VCA5
Predicted Effect probably benign
Transcript: ENSMUST00000034599
AA Change: V15A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000034599
Gene: ENSMUSG00000032091
AA Change: V15A

DomainStartEndE-ValueType
transmembrane domain 29 51 N/A INTRINSIC
LDLa 52 92 1.55e-2 SMART
SR 102 192 2.51e-7 SMART
Tryp_SPc 202 427 9.03e-91 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000165263
AA Change: V15A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000131890
Gene: ENSMUSG00000032091
AA Change: V15A

DomainStartEndE-ValueType
transmembrane domain 29 51 N/A INTRINSIC
LDLa 52 92 1.55e-2 SMART
SR 102 192 2.51e-7 SMART
Tryp_SPc 202 335 2.26e-9 SMART
Predicted Effect unknown
Transcript: ENSMUST00000170069
AA Change: V15A
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] 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. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele appear healthy and response normally to a sodium-deficient diet. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ago2 T C 15: 72,985,601 (GRCm39) I665V probably benign Het
Aoc1l3 T G 6: 48,964,508 (GRCm39) F172C probably damaging Het
Arhgap32 A T 9: 32,063,983 (GRCm39) M74L possibly damaging Het
Asb4 T C 6: 5,398,304 (GRCm39) C90R possibly damaging Het
B3galt4 T A 17: 34,169,821 (GRCm39) D139V probably damaging Het
Camta2 A C 11: 70,564,964 (GRCm39) I852S probably benign Het
Cd200l1 A T 16: 45,264,294 (GRCm39) M88K probably benign Het
Cox4i2 G T 2: 152,599,015 (GRCm39) E57D probably benign Het
Dip2b T C 15: 100,091,724 (GRCm39) I1055T probably benign Het
Eif1ad18 T A 12: 88,050,602 (GRCm39) W46R probably benign Het
Eif4g3 C T 4: 137,824,646 (GRCm39) P284S probably damaging Het
Ephb1 C A 9: 101,806,463 (GRCm39) probably null Het
Fbxw7 A T 3: 84,879,723 (GRCm39) probably null Het
Frem1 C A 4: 82,840,506 (GRCm39) D1789Y probably damaging Het
Gm29106 A T 1: 118,127,524 (GRCm39) R405S probably damaging Het
Greb1l G A 18: 10,547,482 (GRCm39) V1567M possibly damaging Het
Hapstr1 A G 16: 8,648,553 (GRCm39) probably null Het
Heatr1 C A 13: 12,449,956 (GRCm39) D1983E probably benign Het
Lhfpl2 G T 13: 94,311,029 (GRCm39) A100S probably damaging Het
Lrp5 A T 19: 3,655,301 (GRCm39) V1073D probably damaging Het
Naip6 G A 13: 100,438,706 (GRCm39) L364F possibly damaging Het
Nek9 A G 12: 85,350,311 (GRCm39) L921P probably damaging Het
Nim1k C T 13: 120,189,263 (GRCm39) E49K probably damaging Het
Nsun5 A C 5: 135,399,046 (GRCm39) N32T probably damaging Het
Nuggc T C 14: 65,855,092 (GRCm39) S325P probably damaging Het
Or2d36 A G 7: 106,747,290 (GRCm39) I256V probably damaging Het
Or5w12 T A 2: 87,501,797 (GRCm39) K305* probably null Het
Pcdhga7 A G 18: 37,848,710 (GRCm39) D239G probably damaging Het
Pld2 A G 11: 70,444,273 (GRCm39) D523G probably benign Het
Prokr1 C A 6: 87,565,455 (GRCm39) W130L probably damaging Het
Prpf8 A G 11: 75,381,562 (GRCm39) N266S probably damaging Het
Rdh10 T C 1: 16,176,255 (GRCm39) V5A probably benign Het
Rp1l1 T C 14: 64,267,834 (GRCm39) L1140P possibly damaging Het
Sacs A G 14: 61,448,874 (GRCm39) D3640G probably damaging Het
Smarca2 A G 19: 26,668,749 (GRCm39) E916G probably damaging Het
Steap3 A T 1: 120,171,624 (GRCm39) H160Q probably damaging Het
Tlk2 T C 11: 105,147,779 (GRCm39) probably null Het
Togaram2 T C 17: 72,014,129 (GRCm39) L559P probably damaging Het
Topbp1 T A 9: 103,213,045 (GRCm39) L990H probably damaging Het
Ttll7 A G 3: 146,615,369 (GRCm39) T278A possibly damaging Het
Ttn G A 2: 76,604,780 (GRCm39) L18385F probably damaging Het
Upf3a G T 8: 13,841,911 (GRCm39) A149S probably damaging Het
Vmn2r111 T C 17: 22,778,032 (GRCm39) N549S possibly damaging Het
Zfp316 A T 5: 143,239,280 (GRCm39) F913Y probably damaging Het
Other mutations in Tmprss4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01936:Tmprss4 APN 9 45,090,718 (GRCm39) missense probably damaging 1.00
R0153:Tmprss4 UTSW 9 45,095,634 (GRCm39) missense probably benign 0.01
R1445:Tmprss4 UTSW 9 45,095,683 (GRCm39) missense possibly damaging 0.59
R2359:Tmprss4 UTSW 9 45,097,130 (GRCm39) missense probably benign
R3918:Tmprss4 UTSW 9 45,091,964 (GRCm39) missense probably benign 0.13
R3919:Tmprss4 UTSW 9 45,091,964 (GRCm39) missense probably benign 0.13
R4655:Tmprss4 UTSW 9 45,087,702 (GRCm39) missense probably benign
R4949:Tmprss4 UTSW 9 45,086,841 (GRCm39) missense possibly damaging 0.92
R4976:Tmprss4 UTSW 9 45,084,706 (GRCm39) missense possibly damaging 0.86
R5177:Tmprss4 UTSW 9 45,085,260 (GRCm39) missense probably benign 0.09
R5918:Tmprss4 UTSW 9 45,086,414 (GRCm39) nonsense probably null
R7091:Tmprss4 UTSW 9 45,095,571 (GRCm39) missense probably damaging 0.97
R7488:Tmprss4 UTSW 9 45,086,853 (GRCm39) missense probably benign 0.03
R8431:Tmprss4 UTSW 9 45,095,661 (GRCm39) missense probably benign 0.35
R8781:Tmprss4 UTSW 9 45,087,740 (GRCm39) missense possibly damaging 0.96
R9654:Tmprss4 UTSW 9 45,090,700 (GRCm39) critical splice donor site probably null
X0058:Tmprss4 UTSW 9 45,089,131 (GRCm39) missense probably damaging 1.00
Z1088:Tmprss4 UTSW 9 45,086,763 (GRCm39) missense probably damaging 0.98
Z1177:Tmprss4 UTSW 9 45,095,539 (GRCm39) missense possibly damaging 0.47
Z1177:Tmprss4 UTSW 9 45,087,817 (GRCm39) missense probably benign 0.44
Predicted Primers PCR Primer
(F):5'- ATCACTGTGCATGGGAGGAC -3'
(R):5'- GATAGGTGAATCCGGTCGAG -3'

Sequencing Primer
(F):5'- CATGGGAGGACTGGTGCATG -3'
(R):5'- GGGAGGAAAGGTTCTTAAAGCTC -3'
Posted On 2018-11-06