Incidental Mutation 'IGL01625:Prss3b'
ID 92735
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prss3b
Ensembl Gene ENSMUSG00000029882
Gene Name serine protease 3B
Synonyms 2210010C04Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # IGL01625
Quality Score
Status
Chromosome 6
Chromosomal Location 41007202-41012443 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 41009882 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Alanine at position 151 (S151A)
Ref Sequence ENSEMBL: ENSMUSP00000031931 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031931]
AlphaFold Q9CPN9
Predicted Effect probably benign
Transcript: ENSMUST00000031931
AA Change: S151A

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000031931
Gene: ENSMUSG00000029882
AA Change: S151A

DomainStartEndE-ValueType
Tryp_SPc 24 240 3.52e-102 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik T A 5: 144,979,957 (GRCm39) H37Q possibly damaging Het
Akr1c19 T A 13: 4,283,816 (GRCm39) I16N probably damaging Het
Arpc1b T C 5: 145,058,555 (GRCm39) probably null Het
Bzw1 A G 1: 58,440,599 (GRCm39) T191A probably benign Het
Cacna1h G A 17: 25,604,686 (GRCm39) T1209I possibly damaging Het
Cacna1h T C 17: 25,602,459 (GRCm39) D1523G probably damaging Het
Cdc20b T C 13: 113,196,319 (GRCm39) L148P possibly damaging Het
Cubn A G 2: 13,311,085 (GRCm39) F3147L possibly damaging Het
Dagla A G 19: 10,228,566 (GRCm39) probably benign Het
Dnah9 T C 11: 65,935,471 (GRCm39) N1983D probably damaging Het
Fbxw10 G A 11: 62,750,853 (GRCm39) D479N probably damaging Het
Fer A T 17: 64,344,621 (GRCm39) Q630L probably damaging Het
Gbp5 A G 3: 142,208,789 (GRCm39) N111D probably damaging Het
Gm8127 T G 14: 43,148,520 (GRCm39) probably benign Het
Heatr1 T A 13: 12,428,409 (GRCm39) N814K probably damaging Het
Iba57 G A 11: 59,049,775 (GRCm39) R191W probably damaging Het
Itgae C A 11: 73,010,263 (GRCm39) F584L probably benign Het
Kdm5b A G 1: 134,545,706 (GRCm39) K956E possibly damaging Het
Muc4 C T 16: 32,575,918 (GRCm39) probably benign Het
Mybpc2 T C 7: 44,166,337 (GRCm39) K218E possibly damaging Het
Pcdh10 T C 3: 45,333,832 (GRCm39) S49P probably damaging Het
Rai14 T C 15: 10,572,460 (GRCm39) D889G probably benign Het
Rbpjl A G 2: 164,249,705 (GRCm39) K102R possibly damaging Het
Retreg2 A G 1: 75,121,359 (GRCm39) probably benign Het
Rfc4 A T 16: 22,934,573 (GRCm39) L149Q probably damaging Het
Rft1 T A 14: 30,398,853 (GRCm39) D274E possibly damaging Het
Rlf A T 4: 121,045,457 (GRCm39) S143R possibly damaging Het
Rptn T A 3: 93,305,201 (GRCm39) S845T probably benign Het
Slamf8 C A 1: 172,410,049 (GRCm39) D267Y probably damaging Het
Smoc2 C T 17: 14,545,876 (GRCm39) S55L probably damaging Het
Sptan1 C T 2: 29,916,126 (GRCm39) A2038V probably damaging Het
Stx17 C A 4: 48,181,526 (GRCm39) P210T probably damaging Het
Tbc1d5 A G 17: 51,224,601 (GRCm39) Y317H probably benign Het
Tenm4 C A 7: 96,534,565 (GRCm39) T1737N probably damaging Het
Tesk2 T C 4: 116,628,998 (GRCm39) F116L possibly damaging Het
Tln2 T C 9: 67,277,905 (GRCm39) S370G probably damaging Het
Tm6sf2 G T 8: 70,528,733 (GRCm39) G162C probably null Het
Togaram2 A C 17: 72,021,693 (GRCm39) E718D probably benign Het
Ttn A C 2: 76,578,327 (GRCm39) F15862V probably damaging Het
Uba6 T A 5: 86,268,388 (GRCm39) R916* probably null Het
Umodl1 A G 17: 31,215,229 (GRCm39) M1018V probably benign Het
Wdr26 G A 1: 181,019,381 (GRCm39) T332I possibly damaging Het
Xdh A T 17: 74,223,781 (GRCm39) probably null Het
Other mutations in Prss3b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01120:Prss3b APN 6 41,008,607 (GRCm39) missense probably damaging 1.00
IGL02159:Prss3b APN 6 41,009,891 (GRCm39) missense probably benign 0.34
IGL03161:Prss3b APN 6 41,011,240 (GRCm39) missense probably damaging 0.96
R0419:Prss3b UTSW 6 41,011,281 (GRCm39) missense probably benign 0.05
R1715:Prss3b UTSW 6 41,009,870 (GRCm39) splice site probably null
R2057:Prss3b UTSW 6 41,009,315 (GRCm39) missense probably benign 0.06
R2059:Prss3b UTSW 6 41,009,315 (GRCm39) missense probably benign 0.06
R2136:Prss3b UTSW 6 41,012,396 (GRCm39) missense probably benign 0.28
R2446:Prss3b UTSW 6 41,008,582 (GRCm39) missense probably benign 0.15
R4862:Prss3b UTSW 6 41,009,345 (GRCm39) missense possibly damaging 0.74
R5068:Prss3b UTSW 6 41,009,370 (GRCm39) missense probably benign 0.35
R5369:Prss3b UTSW 6 41,009,940 (GRCm39) missense probably benign 0.00
R6392:Prss3b UTSW 6 41,009,306 (GRCm39) missense probably damaging 1.00
R7010:Prss3b UTSW 6 41,009,247 (GRCm39) missense probably benign 0.42
R7567:Prss3b UTSW 6 41,010,127 (GRCm39) missense probably benign 0.04
R7727:Prss3b UTSW 6 41,010,127 (GRCm39) missense probably benign 0.04
R7962:Prss3b UTSW 6 41,012,387 (GRCm39) missense probably benign 0.01
R8373:Prss3b UTSW 6 41,008,622 (GRCm39) missense possibly damaging 0.53
R8529:Prss3b UTSW 6 41,009,369 (GRCm39) missense probably benign 0.00
R8883:Prss3b UTSW 6 41,009,305 (GRCm39) nonsense probably null
R8916:Prss3b UTSW 6 41,010,103 (GRCm39) missense probably damaging 1.00
R9066:Prss3b UTSW 6 41,008,640 (GRCm39) missense probably benign 0.41
R9095:Prss3b UTSW 6 41,010,038 (GRCm39) missense possibly damaging 0.76
R9180:Prss3b UTSW 6 41,008,681 (GRCm39) missense probably damaging 1.00
R9389:Prss3b UTSW 6 41,010,079 (GRCm39) missense probably benign 0.02
Posted On 2013-12-09