Incidental Mutation 'R5123:Prss1'
ID393397
Institutional Source Beutler Lab
Gene Symbol Prss1
Ensembl Gene ENSMUSG00000062751
Gene Nameprotease, serine 1 (trypsin 1)
SynonymsTry-1, PRSS1, Trygn16, Try1
MMRRC Submission 042711-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R5123 (G1)
Quality Score225
Status Validated
Chromosome6
Chromosomal Location41458932-41463786 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 41463197 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glycine at position 156 (D156G)
Ref Sequence ENSEMBL: ENSMUSP00000031910 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031910]
Predicted Effect possibly damaging
Transcript: ENSMUST00000031910
AA Change: D156G

PolyPhen 2 Score 0.839 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000031910
Gene: ENSMUSG00000062751
AA Change: D156G

DomainStartEndE-ValueType
low complexity region 3 16 N/A INTRINSIC
Tryp_SPc 23 239 9.87e-106 SMART
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.5%
Validation Efficiency 98% (53/54)
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 G A 17: 24,384,460 G542D possibly damaging Het
Adh6b A G 3: 138,357,689 Y343C probably damaging Het
Adsl T A 15: 80,952,294 probably null Het
Apob T A 12: 8,007,630 probably null Het
Atp6ap1l T A 13: 90,898,898 probably benign Het
Cacnb3 A G 15: 98,639,869 D74G probably damaging Het
Clca3a2 T A 3: 144,806,343 D544V probably damaging Het
Col3a1 G A 1: 45,333,596 probably benign Het
D7Ertd443e A G 7: 134,349,668 probably null Het
Dscam T C 16: 96,772,437 D775G probably damaging Het
Eif2b3 T A 4: 117,022,211 M16K probably damaging Het
Eml5 T C 12: 98,874,512 Y281C probably damaging Het
Epha2 T A 4: 141,308,865 L204Q possibly damaging Het
Filip1l A C 16: 57,570,662 I538L possibly damaging Het
Gcnt2 T A 13: 40,918,355 V158D probably damaging Het
Gnaq A G 19: 16,332,085 N162S probably benign Het
Haus5 A T 7: 30,654,226 N575K probably benign Het
Hjurp A T 1: 88,275,050 Y71N possibly damaging Het
Igsf5 A G 16: 96,373,079 D103G probably damaging Het
Myo10 A G 15: 25,726,483 D297G possibly damaging Het
Net1 C T 13: 3,886,623 R314H probably damaging Het
Olfr1273-ps C A 2: 90,296,168 R231L probably benign Het
Olfr1301 T A 2: 111,754,552 V101D probably damaging Het
Pcsk4 C A 10: 80,322,145 Q586H probably null Het
Pramef6 A T 4: 143,897,136 M156K probably benign Het
Rnf133 A T 6: 23,649,260 N266K probably damaging Het
Setd2 G T 9: 110,617,527 A2482S possibly damaging Het
Sgo2a A T 1: 58,016,567 S637C probably damaging Het
Slc2a5 C A 4: 150,139,805 S290* probably null Het
Spata6 T G 4: 111,768,795 H120Q possibly damaging Het
Stk11 G A 10: 80,127,941 V194I probably damaging Het
Tkt T C 14: 30,565,646 V199A probably benign Het
Traf3 G A 12: 111,243,518 V183M possibly damaging Het
Trappc11 T C 8: 47,513,402 Y483C probably damaging Het
Trappc9 T C 15: 72,913,366 probably benign Het
Trim59 T C 3: 69,037,734 H91R probably benign Het
Ttc21a A G 9: 119,952,212 S484G probably benign Het
Usp13 A T 3: 32,915,798 H691L probably benign Het
Vmn1r238 T C 18: 3,123,243 Y57C probably benign Het
Vmn2r111 T A 17: 22,571,143 Q294L possibly damaging Het
Vmn2r17 A G 5: 109,427,908 D215G possibly damaging Het
Wdr66 A G 5: 123,273,633 probably benign Het
Zfp280b A G 10: 76,039,349 D354G probably benign Het
Zfp607a A G 7: 27,879,098 H531R probably damaging Het
Zfp74 A T 7: 29,934,733 C517S probably damaging Het
Other mutations in Prss1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00577:Prss1 APN 6 41462711 missense possibly damaging 0.87
IGL00661:Prss1 APN 6 41462619 missense possibly damaging 0.90
IGL01780:Prss1 APN 6 41463205 missense probably damaging 0.96
IGL02350:Prss1 APN 6 41463205 missense probably damaging 0.96
IGL02357:Prss1 APN 6 41463205 missense probably damaging 0.96
R0090:Prss1 UTSW 6 41461232 missense probably benign 0.00
R0137:Prss1 UTSW 6 41462561 missense probably damaging 1.00
R0143:Prss1 UTSW 6 41463588 missense probably damaging 1.00
R0422:Prss1 UTSW 6 41463312 missense probably damaging 1.00
R0792:Prss1 UTSW 6 41458944 start codon destroyed probably null
R0939:Prss1 UTSW 6 41463588 missense probably damaging 1.00
R2762:Prss1 UTSW 6 41463281 missense possibly damaging 0.93
R2896:Prss1 UTSW 6 41463705 nonsense probably null
R2915:Prss1 UTSW 6 41462611 missense probably benign 0.11
R2959:Prss1 UTSW 6 41463238 missense probably damaging 0.99
R5587:Prss1 UTSW 6 41463265 missense possibly damaging 0.57
R5610:Prss1 UTSW 6 41461213 missense probably benign 0.07
R6521:Prss1 UTSW 6 41463681 missense probably damaging 1.00
R6788:Prss1 UTSW 6 41463720 missense possibly damaging 0.46
R7199:Prss1 UTSW 6 41462756 missense probably damaging 1.00
R7552:Prss1 UTSW 6 41462573 missense probably benign 0.05
Predicted Primers PCR Primer
(F):5'- TGAACTGATCCCCAGAATGC -3'
(R):5'- TTTGAAGCTCAACTCCCAGAAC -3'

Sequencing Primer
(F):5'- AATGCTGGCCAGGCACATG -3'
(R):5'- TCCCAGAACTGAGGTCTGCATAAG -3'
Posted On2016-06-15