Incidental Mutation 'R5201:Prss46'
ID400805
Institutional Source Beutler Lab
Gene Symbol Prss46
Ensembl Gene ENSMUSG00000049719
Gene Nameprotease, serine 46
Synonyms1700112C13Rik
MMRRC Submission 042776-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.054) question?
Stock #R5201 (G1)
Quality Score214
Status Not validated
Chromosome9
Chromosomal Location110844506-110856522 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 110851475 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Stop codon at position 229 (C229*)
Ref Sequence ENSEMBL: ENSMUSP00000135787 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000119427] [ENSMUST00000176403]
Predicted Effect probably null
Transcript: ENSMUST00000119427
AA Change: C226*
SMART Domains Protein: ENSMUSP00000112855
Gene: ENSMUSG00000049719
AA Change: C226*

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
Tryp_SPc 40 273 1.62e-60 SMART
transmembrane domain 288 310 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000176403
AA Change: C229*
SMART Domains Protein: ENSMUSP00000135787
Gene: ENSMUSG00000049719
AA Change: C229*

DomainStartEndE-ValueType
Tryp_SPc 43 276 1.62e-60 SMART
transmembrane domain 291 313 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930407I10Rik C A 15: 82,062,544 T214N probably benign Het
Actn4 A T 7: 28,916,255 probably null Het
Arap2 T C 5: 62,683,489 E678G probably damaging Het
Atl2 T C 17: 79,865,151 N130S probably benign Het
Ccdc129 T C 6: 55,968,006 S571P probably benign Het
Cyp2b10 A G 7: 25,916,994 D342G probably damaging Het
Dnah6 A G 6: 73,195,732 Y248H possibly damaging Het
Drd5 A T 5: 38,320,023 M120L probably damaging Het
Duox1 A G 2: 122,327,922 R629G probably benign Het
Dyrk1b A G 7: 28,185,096 Y279C probably damaging Het
Efemp1 A T 11: 28,914,590 I215L probably benign Het
Enpp6 C A 8: 47,065,451 Q205K probably damaging Het
Fam170a A T 18: 50,282,126 T280S probably benign Het
Fam222a G A 5: 114,611,066 A108T possibly damaging Het
Fgd3 G T 13: 49,296,378 P132T probably benign Het
Fzr1 A T 10: 81,367,528 L399H probably damaging Het
Galnt15 G A 14: 32,049,865 R289Q probably damaging Het
Hira T C 16: 18,952,115 V834A probably damaging Het
Ilf3 T C 9: 21,389,383 L93P probably damaging Het
Itgae G A 11: 73,110,556 R71Q probably benign Het
Kif14 T A 1: 136,503,407 S1181T probably benign Het
Lrig3 C A 10: 126,013,151 P946Q possibly damaging Het
Macf1 A T 4: 123,475,945 C1674* probably null Het
Malt1 A G 18: 65,476,055 K710R probably benign Het
Man1a2 A T 3: 100,617,012 N373K probably benign Het
Mkl2 A C 16: 13,401,592 T701P probably benign Het
Mpped2 A G 2: 106,699,502 N32S possibly damaging Het
Myh10 A T 11: 68,783,195 T652S probably damaging Het
Nfia A G 4: 98,111,225 Y485C probably damaging Het
Olfml2b A T 1: 170,668,864 T355S probably benign Het
Olfr1419 A T 19: 11,870,631 I195K probably benign Het
Otx1 C A 11: 21,997,037 A91S probably damaging Het
Pcdh1 A T 18: 38,198,918 V344D probably damaging Het
Plekhn1 C A 4: 156,230,527 V558L probably benign Het
Prr14l A G 5: 32,830,247 S635P possibly damaging Het
Rad50 A G 11: 53,698,820 probably null Het
Slc27a3 A T 3: 90,389,219 L191Q probably benign Het
Spert A G 14: 75,584,009 V101A probably damaging Het
Surf4 A G 2: 26,933,766 probably benign Het
Taf3 A G 2: 9,952,184 S391P probably damaging Het
Tep1 A C 14: 50,868,110 L151R probably benign Het
Tmprss11d A C 5: 86,309,355 N148K possibly damaging Het
Tpd52l2 G A 2: 181,515,086 V172I probably benign Het
Vmn2r77 A G 7: 86,811,638 D724G probably damaging Het
Wdr75 T A 1: 45,823,359 D779E probably benign Het
Zfp943 A T 17: 21,992,813 K293N probably damaging Het
Other mutations in Prss46
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03324:Prss46 APN 9 110849679 missense probably benign 0.01
PIT4508001:Prss46 UTSW 9 110851416 missense probably damaging 0.99
PIT4677001:Prss46 UTSW 9 110856030 missense probably benign 0.00
R0013:Prss46 UTSW 9 110850055 missense probably damaging 0.96
R0013:Prss46 UTSW 9 110850055 missense probably damaging 0.96
R0827:Prss46 UTSW 9 110851432 missense probably benign 0.21
R1521:Prss46 UTSW 9 110849635 missense probably benign 0.00
R1532:Prss46 UTSW 9 110850168 missense probably benign 0.00
R4888:Prss46 UTSW 9 110844550 start codon destroyed possibly damaging 0.75
R5246:Prss46 UTSW 9 110850034 missense probably damaging 1.00
R7196:Prss46 UTSW 9 110851465 missense probably benign 0.38
R7446:Prss46 UTSW 9 110850121 missense probably damaging 1.00
R7704:Prss46 UTSW 9 110849997 missense probably damaging 1.00
R8005:Prss46 UTSW 9 110856076 missense probably benign
Predicted Primers PCR Primer
(F):5'- AGATCTTTCTCTCCATAGGGCAC -3'
(R):5'- TCTCTGATGGTCACATGCAAAAG -3'

Sequencing Primer
(F):5'- GGCACCCAAAGACTCCCTATAGTG -3'
(R):5'- GACCTGAGAATGTTGCACAC -3'
Posted On2016-07-06