Incidental Mutation 'R6346:Prss29'
ID 513973
Institutional Source Beutler Lab
Gene Symbol Prss29
Ensembl Gene ENSMUSG00000034039
Gene Name serine protease 29
Synonyms mISP-2, Isp2
MMRRC Submission 044500-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R6346 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 25537628-25541658 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 25540084 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 161 (T161A)
Ref Sequence ENSEMBL: ENSMUSP00000024993 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000024993]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000024993
AA Change: T161A

PolyPhen 2 Score 0.831 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000024993
Gene: ENSMUSG00000034039
AA Change: T161A

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
Tryp_SPc 30 271 7.11e-89 SMART
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.6%
Validation Efficiency 98% (41/42)
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap13 C T 7: 75,335,002 (GRCm39) S455L probably damaging Het
Apbb1ip T G 2: 22,757,005 (GRCm39) probably null Het
Arhgap18 A T 10: 26,722,061 (GRCm39) I11F probably damaging Het
Arl14epl A T 18: 47,059,409 (GRCm39) N8I possibly damaging Het
Atp4a T A 7: 30,414,781 (GRCm39) I190N possibly damaging Het
Bfar T C 16: 13,519,997 (GRCm39) F285S probably damaging Het
Carf C T 1: 60,180,699 (GRCm39) Q409* probably null Het
Cd244a T C 1: 171,404,889 (GRCm39) V247A probably damaging Het
Ceacam12 T A 7: 17,803,326 (GRCm39) I244K probably damaging Het
Cmya5 T C 13: 93,228,698 (GRCm39) E2130G probably damaging Het
Cyp2b23 T G 7: 26,381,150 (GRCm39) H69P probably damaging Het
Dixdc1 T C 9: 50,595,253 (GRCm39) Q183R probably damaging Het
Dock10 T A 1: 80,553,573 (GRCm39) probably null Het
Fam20c T C 5: 138,752,450 (GRCm39) F279S probably damaging Het
Hcn4 C T 9: 58,766,327 (GRCm39) T665I unknown Het
Helz2 C T 2: 180,875,260 (GRCm39) E1745K probably damaging Het
Kdm7a A T 6: 39,128,145 (GRCm39) probably null Het
Ksr1 A C 11: 78,910,490 (GRCm39) L814R possibly damaging Het
Lmnb1 A G 18: 56,876,310 (GRCm39) I473V probably benign Het
Mllt3 T C 4: 87,759,445 (GRCm39) K201R probably damaging Het
Myo1b C T 1: 51,823,666 (GRCm39) C413Y probably damaging Het
Myom3 A T 4: 135,533,362 (GRCm39) N1185I probably benign Het
Nrde2 A G 12: 100,098,565 (GRCm39) S701P probably benign Het
Ntn4 A T 10: 93,480,723 (GRCm39) D112V probably damaging Het
Nup43 T A 10: 7,550,826 (GRCm39) V232D probably damaging Het
Pcdha6 G A 18: 37,101,113 (GRCm39) C102Y probably damaging Het
Pcdhgb8 T C 18: 37,895,131 (GRCm39) L67P probably damaging Het
Pkd1l3 A G 8: 110,358,016 (GRCm39) H836R probably damaging Het
Plekha1 T A 7: 130,479,512 (GRCm39) I10N probably benign Het
Psmb5 C A 14: 54,854,130 (GRCm39) R116L probably damaging Het
Rsf1 A AGGGCGACGG 7: 97,229,111 (GRCm39) probably null Het
Secisbp2 C T 13: 51,833,923 (GRCm39) H688Y probably damaging Het
Senp5 A G 16: 31,802,665 (GRCm39) Y508H probably damaging Het
Shc3 T A 13: 51,605,651 (GRCm39) T210S possibly damaging Het
Slc27a2 G A 2: 126,429,800 (GRCm39) V467M probably damaging Het
Slc27a5 T A 7: 12,724,899 (GRCm39) E487V possibly damaging Het
Snx1 T C 9: 66,001,930 (GRCm39) T298A possibly damaging Het
Trir A G 8: 85,753,643 (GRCm39) D39G possibly damaging Het
Ubd C T 17: 37,506,242 (GRCm39) Q43* probably null Het
Ube2o T C 11: 116,432,194 (GRCm39) E924G probably damaging Het
Vps13a T C 19: 16,659,578 (GRCm39) I1650V possibly damaging Het
Xirp2 C A 2: 67,346,425 (GRCm39) R2889S probably benign Het
Zfp804b T C 5: 6,820,534 (GRCm39) E843G probably benign Het
Other mutations in Prss29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01120:Prss29 APN 17 25,541,107 (GRCm39) missense probably benign 0.05
IGL01619:Prss29 APN 17 25,540,113 (GRCm39) critical splice donor site probably null
IGL01670:Prss29 APN 17 25,541,437 (GRCm39) missense probably benign 0.03
IGL02516:Prss29 APN 17 25,539,875 (GRCm39) missense probably damaging 1.00
R1538:Prss29 UTSW 17 25,539,257 (GRCm39) start codon destroyed possibly damaging 0.93
R4285:Prss29 UTSW 17 25,541,231 (GRCm39) missense probably damaging 1.00
R5148:Prss29 UTSW 17 25,539,881 (GRCm39) missense probably benign 0.00
R5468:Prss29 UTSW 17 25,540,020 (GRCm39) missense possibly damaging 0.95
R5483:Prss29 UTSW 17 25,541,177 (GRCm39) missense probably benign 0.00
R5852:Prss29 UTSW 17 25,541,408 (GRCm39) missense probably benign 0.01
R6226:Prss29 UTSW 17 25,539,513 (GRCm39) missense possibly damaging 0.74
R7430:Prss29 UTSW 17 25,540,113 (GRCm39) critical splice donor site probably null
R7547:Prss29 UTSW 17 25,539,896 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CATCAGTCTTTCGGATCCGTG -3'
(R):5'- TACCTTAGTGCTGTGACCAGTTAG -3'

Sequencing Primer
(F):5'- TACCTCTATGGGGGCAAGG -3'
(R):5'- TGACCAGTTAGTTAGGCATGC -3'
Posted On 2018-04-27