Incidental Mutation 'IGL02677:Tmprss11g'
ID 303202
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tmprss11g
Ensembl Gene ENSMUSG00000079451
Gene Name transmembrane protease, serine 11g
Synonyms Desc4, 9930032O22Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # IGL02677
Quality Score
Status
Chromosome 5
Chromosomal Location 86633736-86666459 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 86640149 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 160 (D160G)
Ref Sequence ENSEMBL: ENSMUSP00000115540 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000134179] [ENSMUST00000140095]
AlphaFold Q8BZ10
Predicted Effect probably benign
Transcript: ENSMUST00000134179
AA Change: D173G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000122709
Gene: ENSMUSG00000079451
AA Change: D173G

DomainStartEndE-ValueType
transmembrane domain 21 43 N/A INTRINSIC
Pfam:SEA 48 150 1.5e-25 PFAM
Tryp_SPc 185 411 1.39e-82 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000140095
AA Change: D160G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000115540
Gene: ENSMUSG00000079451
AA Change: D160G

DomainStartEndE-ValueType
transmembrane domain 21 43 N/A INTRINSIC
Pfam:SEA 45 154 1.3e-19 PFAM
Tryp_SPc 172 398 1.39e-82 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199703
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931406B18Rik G T 7: 43,150,519 (GRCm39) Y84* probably null Het
Adam5 A G 8: 25,302,395 (GRCm39) probably benign Het
Aipl1 T C 11: 71,920,222 (GRCm39) E282G possibly damaging Het
Akp3 A G 1: 87,052,994 (GRCm39) D61G probably damaging Het
Anpep A G 7: 79,488,478 (GRCm39) S451P probably damaging Het
Csnka2ip A G 16: 64,298,675 (GRCm39) L119P probably damaging Het
Ddx19a T C 8: 111,716,241 (GRCm39) E53G probably benign Het
Ddx50 C T 10: 62,452,072 (GRCm39) R116Q unknown Het
Ddx60 A T 8: 62,441,166 (GRCm39) E1078D probably damaging Het
Dpy19l1 T C 9: 24,396,368 (GRCm39) D116G probably damaging Het
Dsg4 A G 18: 20,597,933 (GRCm39) T668A possibly damaging Het
Dspp A G 5: 104,323,843 (GRCm39) T329A possibly damaging Het
Eftud2 T C 11: 102,737,440 (GRCm39) T554A probably damaging Het
Enpp1 T C 10: 24,555,083 (GRCm39) probably benign Het
Ext2 A T 2: 93,537,590 (GRCm39) F599I probably damaging Het
Fahd1 A T 17: 25,068,504 (GRCm39) I191N probably damaging Het
Fcrl2 A T 3: 87,166,694 (GRCm39) S100T probably benign Het
Fras1 T A 5: 96,692,883 (GRCm39) C181S probably damaging Het
Garre1 T A 7: 33,941,834 (GRCm39) probably benign Het
Gcnt4 A G 13: 97,083,741 (GRCm39) I346V probably benign Het
Gfra1 G A 19: 58,441,787 (GRCm39) T48I probably damaging Het
Kcnma1 A G 14: 23,513,224 (GRCm39) Y392H probably damaging Het
Klc2 T C 19: 5,161,696 (GRCm39) Y298C probably damaging Het
Lamb3 G A 1: 193,021,830 (GRCm39) V1011I probably benign Het
Ldb1 T C 19: 46,024,594 (GRCm39) probably benign Het
Mcph1 A G 8: 18,675,609 (GRCm39) K11E probably damaging Het
Myc A G 15: 61,861,513 (GRCm39) H374R probably damaging Het
Myom1 A G 17: 71,391,344 (GRCm39) Y853C probably damaging Het
Or4k38 A T 2: 111,166,147 (GRCm39) I92N probably damaging Het
Pakap C T 4: 57,856,263 (GRCm39) P572S probably benign Het
Pclo A G 5: 14,726,943 (GRCm39) probably benign Het
Pde3a G A 6: 141,350,898 (GRCm39) probably benign Het
Per1 T C 11: 68,997,486 (GRCm39) V887A probably benign Het
Prokr1 G A 6: 87,565,350 (GRCm39) probably benign Het
Rb1cc1 A G 1: 6,319,643 (GRCm39) I1021V probably benign Het
Ryr1 T C 7: 28,810,033 (GRCm39) E344G probably benign Het
Sec24c A T 14: 20,739,710 (GRCm39) D529V probably damaging Het
Slc1a6 T C 10: 78,624,898 (GRCm39) V101A probably damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Tap2 G A 17: 34,431,021 (GRCm39) V374M probably benign Het
Tex15 T A 8: 34,061,108 (GRCm39) D179E probably benign Het
Tmem8b T C 4: 43,686,092 (GRCm39) L241P probably damaging Het
Trim30a C T 7: 104,085,120 (GRCm39) C30Y probably damaging Het
Ttn A G 2: 76,601,840 (GRCm39) probably benign Het
Ush2a A G 1: 188,466,882 (GRCm39) R2849G probably damaging Het
Usp5 A G 6: 124,796,389 (GRCm39) V570A probably damaging Het
Vipr1 T C 9: 121,489,349 (GRCm39) probably benign Het
Zc2hc1c A C 12: 85,336,850 (GRCm39) D169A probably benign Het
Other mutations in Tmprss11g
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00423:Tmprss11g APN 5 86,640,050 (GRCm39) missense probably benign 0.00
IGL01611:Tmprss11g APN 5 86,638,640 (GRCm39) missense probably benign 0.02
IGL02417:Tmprss11g APN 5 86,638,750 (GRCm39) missense probably benign 0.25
IGL02832:Tmprss11g APN 5 86,645,128 (GRCm39) missense probably benign 0.23
IGL02887:Tmprss11g APN 5 86,645,188 (GRCm39) splice site probably benign
R0377:Tmprss11g UTSW 5 86,638,610 (GRCm39) missense probably damaging 0.98
R0847:Tmprss11g UTSW 5 86,638,585 (GRCm39) missense probably benign 0.01
R1037:Tmprss11g UTSW 5 86,638,606 (GRCm39) missense probably damaging 1.00
R1507:Tmprss11g UTSW 5 86,647,470 (GRCm39) missense probably benign 0.09
R1617:Tmprss11g UTSW 5 86,647,422 (GRCm39) missense probably damaging 0.99
R1955:Tmprss11g UTSW 5 86,646,391 (GRCm39) missense probably damaging 0.99
R2094:Tmprss11g UTSW 5 86,647,415 (GRCm39) missense probably damaging 1.00
R2906:Tmprss11g UTSW 5 86,640,661 (GRCm39) intron probably benign
R4730:Tmprss11g UTSW 5 86,637,092 (GRCm39) missense probably damaging 1.00
R4730:Tmprss11g UTSW 5 86,637,091 (GRCm39) nonsense probably null
R4934:Tmprss11g UTSW 5 86,644,401 (GRCm39) missense probably benign
R4982:Tmprss11g UTSW 5 86,640,674 (GRCm39) missense probably damaging 1.00
R5086:Tmprss11g UTSW 5 86,644,377 (GRCm39) missense possibly damaging 0.65
R5606:Tmprss11g UTSW 5 86,635,269 (GRCm39) missense probably damaging 1.00
R5825:Tmprss11g UTSW 5 86,646,392 (GRCm39) missense probably damaging 0.98
R6291:Tmprss11g UTSW 5 86,635,281 (GRCm39) missense probably damaging 1.00
R6481:Tmprss11g UTSW 5 86,640,015 (GRCm39) missense probably benign 0.20
R6849:Tmprss11g UTSW 5 86,644,491 (GRCm39) missense probably benign 0.01
R6925:Tmprss11g UTSW 5 86,635,295 (GRCm39) missense probably benign 0.00
R6925:Tmprss11g UTSW 5 86,635,285 (GRCm39) missense probably benign 0.09
R7084:Tmprss11g UTSW 5 86,640,059 (GRCm39) missense probably damaging 1.00
R7089:Tmprss11g UTSW 5 86,637,150 (GRCm39) missense probably damaging 0.97
R7190:Tmprss11g UTSW 5 86,644,491 (GRCm39) missense probably benign 0.18
R7352:Tmprss11g UTSW 5 86,644,401 (GRCm39) missense not run
R7432:Tmprss11g UTSW 5 86,644,366 (GRCm39) missense possibly damaging 0.71
R7514:Tmprss11g UTSW 5 86,645,176 (GRCm39) missense probably damaging 1.00
R8198:Tmprss11g UTSW 5 86,646,352 (GRCm39) missense probably benign
R8490:Tmprss11g UTSW 5 86,639,976 (GRCm39) critical splice donor site probably null
R8495:Tmprss11g UTSW 5 86,640,119 (GRCm39) missense probably benign 0.07
R8706:Tmprss11g UTSW 5 86,644,404 (GRCm39) missense probably damaging 1.00
R8730:Tmprss11g UTSW 5 86,638,837 (GRCm39) critical splice acceptor site probably null
R9158:Tmprss11g UTSW 5 86,637,166 (GRCm39) missense probably damaging 1.00
R9224:Tmprss11g UTSW 5 86,640,003 (GRCm39) missense probably benign
Posted On 2015-04-16