Incidental Mutation 'IGL02340:Tmprss11b'
ID 289043
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tmprss11b
Ensembl Gene ENSMUSG00000035861
Gene Name transmembrane protease, serine 11B
Synonyms Tmprss11bnl, 9930019B18Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02340
Quality Score
Status
Chromosome 5
Chromosomal Location 86806326-86824221 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 86810090 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 297 (I297V)
Ref Sequence ENSEMBL: ENSMUSP00000042406 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038448]
AlphaFold Q14C59
Predicted Effect probably benign
Transcript: ENSMUST00000038448
AA Change: I297V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000042406
Gene: ENSMUSG00000035861
AA Change: I297V

DomainStartEndE-ValueType
transmembrane domain 12 34 N/A INTRINSIC
Pfam:SEA 46 148 2.3e-26 PFAM
Tryp_SPc 184 410 6.19e-89 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akt2 T A 7: 27,328,824 (GRCm39) I182N probably damaging Het
Alpk3 A G 7: 80,728,255 (GRCm39) T462A probably benign Het
Amz1 A G 5: 140,738,014 (GRCm39) R425G probably damaging Het
Aoc2 A G 11: 101,217,201 (GRCm39) E428G probably damaging Het
Car4 C T 11: 84,856,593 (GRCm39) P294S probably damaging Het
Chchd6 A T 6: 89,396,762 (GRCm39) H216Q probably damaging Het
Chl1 A G 6: 103,675,086 (GRCm39) Y591C probably damaging Het
Cln8 T C 8: 14,945,178 (GRCm39) L164S probably damaging Het
Dscaml1 T C 9: 45,581,474 (GRCm39) I431T possibly damaging Het
Fam234b T C 6: 135,208,659 (GRCm39) L524P probably damaging Het
Fmo1 T C 1: 162,660,559 (GRCm39) N410S probably benign Het
Ftsj3 G A 11: 106,143,972 (GRCm39) R251* probably null Het
Greb1l A T 18: 10,515,200 (GRCm39) D555V probably damaging Het
Hcar1 G T 5: 124,017,135 (GRCm39) H185Q probably damaging Het
Kcnj12 G A 11: 60,960,319 (GRCm39) V206I probably benign Het
Lamc3 G A 2: 31,808,469 (GRCm39) G742S probably damaging Het
Lipg T C 18: 75,093,946 (GRCm39) probably null Het
Ltbp2 A G 12: 84,839,729 (GRCm39) probably null Het
Mcm3ap T G 10: 76,332,386 (GRCm39) Y1234* probably null Het
Myh6 T A 14: 55,194,612 (GRCm39) D719V possibly damaging Het
Myo9b A G 8: 71,743,689 (GRCm39) N250S probably damaging Het
Nherf1 A G 11: 115,070,858 (GRCm39) E270G probably benign Het
Notch2 G A 3: 98,054,652 (GRCm39) W2438* probably null Het
Nphp1 G A 2: 127,621,987 (GRCm39) Q47* probably null Het
Nptx2 T C 5: 144,493,056 (GRCm39) L381P probably damaging Het
Nrxn3 A G 12: 90,171,402 (GRCm39) N911S possibly damaging Het
Or10j2 A T 1: 173,097,972 (GRCm39) I77F probably benign Het
Or5d46 T C 2: 88,169,906 (GRCm39) probably benign Het
P4ha1 T A 10: 59,188,023 (GRCm39) F260Y probably benign Het
Pitpnm2 T C 5: 124,268,676 (GRCm39) D504G probably damaging Het
Prss54 A G 8: 96,292,237 (GRCm39) V114A probably benign Het
Ptprc G A 1: 137,998,957 (GRCm39) T1031M probably damaging Het
Rtf2 T C 2: 172,310,511 (GRCm39) probably benign Het
Ryr3 A G 2: 112,777,349 (GRCm39) probably benign Het
Slc14a2 C T 18: 78,206,341 (GRCm39) E492K probably damaging Het
Stab1 G T 14: 30,862,367 (GRCm39) N2322K probably damaging Het
Thsd7b A G 1: 130,087,369 (GRCm39) N1162S probably benign Het
Tnn T C 1: 159,972,775 (GRCm39) N276D probably benign Het
Trhde A T 10: 114,428,118 (GRCm39) probably benign Het
Vmn1r115 T A 7: 20,578,453 (GRCm39) H153L possibly damaging Het
Vmn1r203 T A 13: 22,708,997 (GRCm39) C259* probably null Het
Xpot T A 10: 121,451,109 (GRCm39) E97V probably damaging Het
Zbtb2 T C 10: 4,318,712 (GRCm39) D438G probably damaging Het
Other mutations in Tmprss11b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01122:Tmprss11b APN 5 86,811,376 (GRCm39) missense probably benign
IGL02500:Tmprss11b APN 5 86,815,182 (GRCm39) critical splice donor site probably null
demolished UTSW 5 86,812,173 (GRCm39) missense probably damaging 1.00
R0356:Tmprss11b UTSW 5 86,808,326 (GRCm39) makesense probably null
R0506:Tmprss11b UTSW 5 86,809,499 (GRCm39) missense probably damaging 1.00
R0528:Tmprss11b UTSW 5 86,819,753 (GRCm39) missense probably damaging 1.00
R1424:Tmprss11b UTSW 5 86,812,832 (GRCm39) missense probably benign 0.09
R1471:Tmprss11b UTSW 5 86,808,355 (GRCm39) missense possibly damaging 0.76
R1554:Tmprss11b UTSW 5 86,809,490 (GRCm39) missense probably benign 0.01
R3436:Tmprss11b UTSW 5 86,815,443 (GRCm39) nonsense probably null
R3829:Tmprss11b UTSW 5 86,809,449 (GRCm39) missense probably damaging 0.98
R4409:Tmprss11b UTSW 5 86,812,137 (GRCm39) missense probably benign 0.26
R4495:Tmprss11b UTSW 5 86,812,922 (GRCm39) nonsense probably null
R4624:Tmprss11b UTSW 5 86,812,895 (GRCm39) missense probably benign 0.04
R4834:Tmprss11b UTSW 5 86,811,418 (GRCm39) missense probably damaging 1.00
R5436:Tmprss11b UTSW 5 86,810,092 (GRCm39) missense probably benign 0.10
R5812:Tmprss11b UTSW 5 86,812,957 (GRCm39) missense possibly damaging 0.67
R6262:Tmprss11b UTSW 5 86,810,119 (GRCm39) missense probably benign 0.07
R6882:Tmprss11b UTSW 5 86,819,530 (GRCm39) splice site probably null
R6893:Tmprss11b UTSW 5 86,811,245 (GRCm39) critical splice donor site probably null
R7312:Tmprss11b UTSW 5 86,812,173 (GRCm39) missense probably damaging 1.00
R7771:Tmprss11b UTSW 5 86,809,554 (GRCm39) splice site probably null
R8101:Tmprss11b UTSW 5 86,812,821 (GRCm39) critical splice donor site probably null
X0067:Tmprss11b UTSW 5 86,810,059 (GRCm39) missense probably damaging 1.00
Z1177:Tmprss11b UTSW 5 86,809,472 (GRCm39) missense probably benign 0.13
Z1177:Tmprss11b UTSW 5 86,808,400 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16