Incidental Mutation 'IGL01845:Prss28'
ID 178167
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prss28
Ensembl Gene ENSMUSG00000024171
Gene Name serine protease 28
Synonyms mIsp-1, Isp1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.084) question?
Stock # IGL01845
Quality Score
Status
Chromosome 17
Chromosomal Location 25527620-25530850 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 25529011 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 117 (N117K)
Ref Sequence ENSEMBL: ENSMUSP00000015267 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000015267]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000015267
AA Change: N117K

PolyPhen 2 Score 0.895 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000015267
Gene: ENSMUSG00000024171
AA Change: N117K

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Tryp_SPc 30 269 8.58e-74 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000158305
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600012H06Rik T C 17: 15,164,380 (GRCm39) L169P probably damaging Het
4933405L10Rik C A 8: 106,435,567 (GRCm39) A75E probably benign Het
Abca1 A G 4: 53,090,297 (GRCm39) L384P probably damaging Het
Acox2 C A 14: 8,251,617 (GRCm38) M293I probably damaging Het
Acp6 A G 3: 97,081,123 (GRCm39) S288G probably benign Het
Arhgef12 T A 9: 42,934,137 (GRCm39) H127L possibly damaging Het
Arid2 T G 15: 96,254,678 (GRCm39) F175V probably damaging Het
Ccdc15 G A 9: 37,226,532 (GRCm39) Q468* probably null Het
Ccdc93 T C 1: 121,390,859 (GRCm39) I277T probably damaging Het
Cdh8 T C 8: 99,825,586 (GRCm39) probably benign Het
Cdipt T C 7: 126,578,725 (GRCm39) S145P possibly damaging Het
Cfap206 T C 4: 34,719,610 (GRCm39) N268S possibly damaging Het
Clcn3 A T 8: 61,366,129 (GRCm39) N814K probably benign Het
Col6a3 T C 1: 90,724,293 (GRCm39) D2019G probably damaging Het
Corin C A 5: 72,511,282 (GRCm39) G432C probably damaging Het
Crppa A G 12: 36,597,918 (GRCm39) R350G probably benign Het
Cyld C T 8: 89,432,403 (GRCm39) Q134* probably null Het
Dhh C A 15: 98,795,864 (GRCm39) R97L probably damaging Het
Dnah5 T C 15: 28,449,315 (GRCm39) V4239A probably benign Het
Dock2 T C 11: 34,599,692 (GRCm39) I296V probably benign Het
Gabbr1 T C 17: 37,359,306 (GRCm39) probably benign Het
Gbp10 T C 5: 105,367,815 (GRCm39) probably null Het
Itgam T A 7: 127,711,644 (GRCm39) L753Q probably damaging Het
Kbtbd12 A G 6: 88,590,922 (GRCm39) V430A probably benign Het
Kdm4a A G 4: 118,017,656 (GRCm39) V470A possibly damaging Het
Larp1b A T 3: 40,924,960 (GRCm39) T146S probably benign Het
Lrrfip2 T A 9: 111,028,728 (GRCm39) probably benign Het
Mier2 A T 10: 79,385,418 (GRCm39) C137S possibly damaging Het
Morc3 A G 16: 93,657,455 (GRCm39) Y393C probably damaging Het
Ms4a7 A T 19: 11,299,751 (GRCm39) M217K possibly damaging Het
Msl1 A G 11: 98,696,191 (GRCm39) probably null Het
Myh2 A G 11: 67,083,860 (GRCm39) E1546G probably benign Het
Nlgn2 A G 11: 69,716,675 (GRCm39) L622P possibly damaging Het
Oga T A 19: 45,756,301 (GRCm39) E447D probably benign Het
Or10q3 A G 19: 11,847,888 (GRCm39) S231P probably benign Het
Or1e33 A G 11: 73,738,298 (GRCm39) Y218H probably damaging Het
Or1j11 A C 2: 36,312,105 (GRCm39) K232Q probably benign Het
Or56b1b T A 7: 108,164,343 (GRCm39) I220L possibly damaging Het
Or5k17 T C 16: 58,746,929 (GRCm39) M2V probably benign Het
Phf20 C A 2: 156,118,577 (GRCm39) S427* probably null Het
Pirt G A 11: 66,816,794 (GRCm39) S35N probably damaging Het
Rbbp8nl A G 2: 179,925,104 (GRCm39) C34R probably damaging Het
Rtn3 A T 19: 7,435,241 (GRCm39) D231E probably damaging Het
Sema5a T C 15: 32,474,514 (GRCm39) probably benign Het
Sh3bp2 T A 5: 34,713,347 (GRCm39) L196Q probably damaging Het
Slc26a9 G T 1: 131,685,256 (GRCm39) D325Y probably damaging Het
Slc4a1 A G 11: 102,244,729 (GRCm39) V622A probably benign Het
Thbd A G 2: 148,249,016 (GRCm39) V284A probably benign Het
Tmc5 T C 7: 118,251,733 (GRCm39) F609L possibly damaging Het
Tnr T C 1: 159,695,576 (GRCm39) probably benign Het
Ttc17 A T 2: 94,163,177 (GRCm39) Y881* probably null Het
Ttc41 A T 10: 86,612,488 (GRCm39) T1254S probably benign Het
Ttn C T 2: 76,640,347 (GRCm39) D13754N probably damaging Het
Vmn2r16 T A 5: 109,511,762 (GRCm39) F656L probably damaging Het
Wdr19 A G 5: 65,382,709 (GRCm39) I478V probably damaging Het
Zan T C 5: 137,379,116 (GRCm39) probably benign Het
Zp2 T A 7: 119,737,414 (GRCm39) D258V probably damaging Het
Other mutations in Prss28
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03357:Prss28 APN 17 25,528,669 (GRCm39) missense probably benign 0.03
R0144:Prss28 UTSW 17 25,528,424 (GRCm39) missense probably damaging 0.97
R1171:Prss28 UTSW 17 25,529,029 (GRCm39) missense possibly damaging 0.61
R4577:Prss28 UTSW 17 25,529,079 (GRCm39) missense probably damaging 0.99
R4979:Prss28 UTSW 17 25,528,711 (GRCm39) missense probably damaging 1.00
R5941:Prss28 UTSW 17 25,528,717 (GRCm39) missense probably damaging 0.99
R6457:Prss28 UTSW 17 25,530,331 (GRCm39) missense probably benign 0.02
R8811:Prss28 UTSW 17 25,528,627 (GRCm39) missense probably benign 0.34
R8987:Prss28 UTSW 17 25,528,395 (GRCm39) missense probably damaging 1.00
R9441:Prss28 UTSW 17 25,530,215 (GRCm39) missense probably benign 0.41
R9564:Prss28 UTSW 17 25,528,911 (GRCm39) missense probably damaging 0.99
Z1177:Prss28 UTSW 17 25,530,625 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07