Incidental Mutation 'R8047:Prss23'
ID 618817
Institutional Source Beutler Lab
Gene Symbol Prss23
Ensembl Gene ENSMUSG00000039405
Gene Name serine protease 23
Synonyms 2310046G15Rik
MMRRC Submission 067484-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # R8047 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 89156991-89176395 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 89159136 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Leucine at position 311 (Q311L)
Ref Sequence ENSEMBL: ENSMUSP00000045191 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041761] [ENSMUST00000207538] [ENSMUST00000207636] [ENSMUST00000207932] [ENSMUST00000208402] [ENSMUST00000208888] [ENSMUST00000208903]
AlphaFold Q9D6X6
Predicted Effect probably damaging
Transcript: ENSMUST00000041761
AA Change: Q311L

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000045191
Gene: ENSMUSG00000039405
AA Change: Q311L

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
low complexity region 48 57 N/A INTRINSIC
Tryp_SPc 137 372 2.87e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000207538
Predicted Effect probably benign
Transcript: ENSMUST00000207636
Predicted Effect probably damaging
Transcript: ENSMUST00000207932
AA Change: Q311L

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
Predicted Effect probably benign
Transcript: ENSMUST00000208402
Predicted Effect probably benign
Transcript: ENSMUST00000208888
Predicted Effect probably benign
Transcript: ENSMUST00000208903
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a conserved member of the trypsin family of serine proteases. Mouse studies found a decrease of mRNA levels of this gene after ovulation was induced. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abce1 G A 8: 80,427,817 (GRCm39) T157I possibly damaging Het
Cd200l2 T C 16: 45,340,829 (GRCm39) I245V probably benign Het
Cdh22 G A 2: 165,012,687 (GRCm39) R133W probably damaging Het
Cep152 A T 2: 125,406,247 (GRCm39) N1428K probably benign Het
Clstn3 T A 6: 124,408,972 (GRCm39) D892V possibly damaging Het
Coch G A 12: 51,650,496 (GRCm39) probably null Het
D6Ertd527e G T 6: 87,088,454 (GRCm39) V206F unknown Het
Dnaaf9 A T 2: 130,617,019 (GRCm39) V439E probably damaging Het
Dock3 T C 9: 106,870,208 (GRCm39) I625M possibly damaging Het
Dpy19l4 A G 4: 11,317,139 (GRCm39) S20P probably benign Het
Eef1e1 T C 13: 38,830,222 (GRCm39) Q150R probably damaging Het
Eln CTCCAGCTCCGAT C 5: 134,758,003 (GRCm39) probably benign Het
Engase T C 11: 118,377,282 (GRCm39) S526P probably benign Het
Fbxo40 T A 16: 36,790,231 (GRCm39) D293V probably damaging Het
Gipc3 T A 10: 81,177,132 (GRCm39) N146I probably damaging Het
Gm11569 T C 11: 99,689,616 (GRCm39) T28A unknown Het
Gm43302 T C 5: 105,422,623 (GRCm39) I470V possibly damaging Het
Gpihbp1 A G 15: 75,469,627 (GRCm39) Q114R possibly damaging Het
Grhl2 T A 15: 37,336,465 (GRCm39) M454K probably benign Het
Gsap A T 5: 21,462,866 (GRCm39) probably null Het
Ighv6-5 T C 12: 114,380,191 (GRCm39) probably null Het
Kif1b C A 4: 149,299,379 (GRCm39) V1010L probably damaging Het
Krt8 A T 15: 101,912,406 (GRCm39) I90N probably damaging Het
Lrrc69 A T 4: 14,773,726 (GRCm39) I110N probably benign Het
Lta T C 17: 35,423,011 (GRCm39) Y104C probably damaging Het
Madd A G 2: 91,009,546 (GRCm39) Y13H probably damaging Het
Mccc2 C T 13: 100,091,181 (GRCm39) V439I probably benign Het
Mecom T A 3: 30,292,404 (GRCm39) D35V Het
Msra C T 14: 64,522,612 (GRCm39) A76T probably damaging Het
Myo18b G T 5: 112,871,681 (GRCm39) D2133E possibly damaging Het
Ncapd2 C T 6: 125,166,762 (GRCm39) V31M probably damaging Het
Npc1 A G 18: 12,346,374 (GRCm39) V274A probably benign Het
Or5m11b T C 2: 85,806,271 (GRCm39) I228T possibly damaging Het
Patz1 C T 11: 3,256,283 (GRCm39) P523L probably benign Het
Pbx2 T C 17: 34,814,262 (GRCm39) S350P probably benign Het
Plk4 T C 3: 40,760,187 (GRCm39) I361T probably benign Het
Ppat G T 5: 77,073,557 (GRCm39) N122K probably damaging Het
Psg26 G T 7: 18,212,474 (GRCm39) Q294K possibly damaging Het
Rab3il1 G T 19: 10,011,166 (GRCm39) R285L probably benign Het
Radil A G 5: 142,480,695 (GRCm39) C587R probably damaging Het
Rd3 A T 1: 191,709,620 (GRCm39) probably benign Het
Reck T C 4: 43,927,221 (GRCm39) L504P probably damaging Het
Rmc1 C T 18: 12,313,586 (GRCm39) T233M possibly damaging Het
Selenov A C 7: 27,990,108 (GRCm39) L132R probably benign Het
Spag16 A T 1: 69,882,155 (GRCm39) D49V probably damaging Het
Ston2 C T 12: 91,608,617 (GRCm39) V828I probably damaging Het
Tiam1 A G 16: 89,694,672 (GRCm39) S262P probably benign Het
Tlnrd1 A T 7: 83,532,069 (GRCm39) S121T probably damaging Het
Unc13c T A 9: 73,719,636 (GRCm39) K1011* probably null Het
Vmn2r89 T A 14: 51,692,549 (GRCm39) D117E probably benign Het
Zbtb7c A C 18: 76,270,221 (GRCm39) N103T probably damaging Het
Zfp764 T C 7: 127,005,412 (GRCm39) E75G probably damaging Het
Other mutations in Prss23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01296:Prss23 APN 7 89,159,095 (GRCm39) missense possibly damaging 0.83
IGL03308:Prss23 APN 7 89,158,938 (GRCm39) missense probably benign 0.09
IGL03349:Prss23 APN 7 89,159,065 (GRCm39) missense probably benign 0.09
IGL03378:Prss23 APN 7 89,159,352 (GRCm39) missense probably damaging 0.99
R0394:Prss23 UTSW 7 89,159,055 (GRCm39) missense probably damaging 1.00
R1026:Prss23 UTSW 7 89,159,166 (GRCm39) missense probably benign 0.01
R1417:Prss23 UTSW 7 89,159,392 (GRCm39) missense probably damaging 1.00
R1467:Prss23 UTSW 7 89,159,217 (GRCm39) missense probably damaging 1.00
R1467:Prss23 UTSW 7 89,159,217 (GRCm39) missense probably damaging 1.00
R1691:Prss23 UTSW 7 89,159,922 (GRCm39) missense probably benign 0.18
R1806:Prss23 UTSW 7 89,159,599 (GRCm39) missense probably damaging 1.00
R2153:Prss23 UTSW 7 89,159,119 (GRCm39) missense probably damaging 1.00
R3420:Prss23 UTSW 7 89,159,107 (GRCm39) missense possibly damaging 0.91
R3849:Prss23 UTSW 7 89,158,959 (GRCm39) missense probably damaging 1.00
R4567:Prss23 UTSW 7 89,160,074 (GRCm39) utr 5 prime probably benign
R4828:Prss23 UTSW 7 89,159,108 (GRCm39) nonsense probably null
R5010:Prss23 UTSW 7 89,159,422 (GRCm39) missense probably benign 0.25
R5251:Prss23 UTSW 7 89,159,530 (GRCm39) missense probably damaging 1.00
R5399:Prss23 UTSW 7 89,159,174 (GRCm39) missense probably benign 0.02
R5629:Prss23 UTSW 7 89,159,400 (GRCm39) missense probably damaging 1.00
R5697:Prss23 UTSW 7 89,159,190 (GRCm39) missense probably damaging 0.99
R6378:Prss23 UTSW 7 89,159,241 (GRCm39) missense probably damaging 1.00
R6716:Prss23 UTSW 7 89,159,055 (GRCm39) missense probably damaging 1.00
R6880:Prss23 UTSW 7 89,160,033 (GRCm39) missense probably benign 0.03
R7097:Prss23 UTSW 7 89,159,392 (GRCm39) missense probably damaging 1.00
R7362:Prss23 UTSW 7 89,158,972 (GRCm39) missense probably damaging 1.00
R7563:Prss23 UTSW 7 89,159,038 (GRCm39) missense probably damaging 1.00
R7637:Prss23 UTSW 7 89,159,454 (GRCm39) missense probably benign 0.00
R7815:Prss23 UTSW 7 89,159,253 (GRCm39) missense probably damaging 0.99
R8548:Prss23 UTSW 7 89,159,416 (GRCm39) missense probably benign 0.21
R8869:Prss23 UTSW 7 89,159,887 (GRCm39) missense probably benign 0.00
R8914:Prss23 UTSW 7 89,159,854 (GRCm39) missense probably benign
R9310:Prss23 UTSW 7 89,159,142 (GRCm39) missense probably damaging 1.00
R9729:Prss23 UTSW 7 89,159,931 (GRCm39) missense probably benign
R9762:Prss23 UTSW 7 89,159,683 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGGCAAGAAGACGCATGTC -3'
(R):5'- TGCTGGAACTCAAGAAACCC -3'

Sequencing Primer
(F):5'- CCTTTAATCCAATAGCAAATCTGGGC -3'
(R):5'- CCACAAAAGACAGTTCATGAAGATTG -3'
Posted On 2020-01-23