Incidental Mutation 'R5458:Gm5965'
ID432899
Institutional Source Beutler Lab
Gene Symbol Gm5965
Ensembl Gene ENSMUSG00000009047
Gene Namepredicted gene 5965
Synonyms
MMRRC Submission 043021-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.087) question?
Stock #R5458 (G1)
Quality Score225
Status Validated
Chromosome16
Chromosomal Location88777896-88778528 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 88778507 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Serine at position 189 (R189S)
Ref Sequence ENSEMBL: ENSMUSP00000009191 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000009191] [ENSMUST00000054223]
Predicted Effect probably benign
Transcript: ENSMUST00000009191
AA Change: R189S

PolyPhen 2 Score 0.093 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000009191
Gene: ENSMUSG00000009047
AA Change: R189S

DomainStartEndE-ValueType
Pfam:PMG 1 77 1e-28 PFAM
Pfam:PMG 74 196 2.3e-42 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000054223
SMART Domains Protein: ENSMUSP00000062370
Gene: ENSMUSG00000048830

DomainStartEndE-ValueType
Pfam:PMG 1 77 1.6e-28 PFAM
Pfam:PMG 74 200 7.5e-51 PFAM
Meta Mutation Damage Score 0.198 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.9%
Validation Efficiency 98% (54/55)
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acrbp A G 6: 125,050,050 probably benign Het
Acsl5 A G 19: 55,294,230 D589G probably damaging Het
Akap13 T A 7: 75,586,301 L208Q probably damaging Het
Ankfn1 C T 11: 89,434,810 R512K probably benign Het
Ankhd1 T C 18: 36,648,485 S2197P probably benign Het
Ankrd27 A G 7: 35,591,811 N11D probably damaging Het
Aspg T C 12: 112,120,002 V230A probably damaging Het
Atp2c1 A T 9: 105,414,725 Y709* probably null Het
Atp8b2 T C 3: 89,946,022 N748D probably benign Het
B4galnt3 A G 6: 120,210,385 V684A probably damaging Het
Bco2 T C 9: 50,545,344 probably null Het
Bcr T C 10: 75,154,960 V766A probably benign Het
Brca1 T C 11: 101,517,285 N1404S possibly damaging Het
Chd1 A G 17: 15,738,549 D621G probably damaging Het
Chek1 A G 9: 36,714,429 S307P probably benign Het
Dhx29 T C 13: 112,966,621 M1345T probably benign Het
Dnah6 T A 6: 73,086,185 T2697S probably damaging Het
Ephb4 T C 5: 137,369,852 V753A probably damaging Het
Fat1 T C 8: 45,013,053 Y1427H probably damaging Het
Fggy A G 4: 95,926,743 Q445R probably benign Het
Fv1 A G 4: 147,870,269 S431G probably benign Het
Gnas A G 2: 174,298,331 I98V probably benign Het
Ino80 T C 2: 119,412,429 N1086D possibly damaging Het
Lclat1 T C 17: 73,239,919 L277P probably damaging Het
Lipc T C 9: 70,852,582 probably benign Het
Myo3a T C 2: 22,245,550 I76T probably damaging Het
Nkpd1 C A 7: 19,524,276 A510E probably damaging Het
Nlgn2 G T 11: 69,827,900 Q285K possibly damaging Het
Olfr284 G A 15: 98,340,365 A208V probably benign Het
Pax5 T C 4: 44,679,526 D172G probably damaging Het
Pcdh15 T A 10: 74,504,779 V1115D probably damaging Het
Pdzd7 T C 19: 45,027,791 S964G probably benign Het
Phip G T 9: 82,926,500 P474Q probably benign Het
Pop5 C T 5: 115,240,437 probably benign Het
Ppfibp1 A T 6: 147,012,435 probably benign Het
Rdh11 C T 12: 79,188,505 A106T probably benign Het
Rin3 A G 12: 102,373,716 T642A probably damaging Het
Scmh1 C T 4: 120,505,281 probably benign Het
Skint2 A G 4: 112,624,180 H80R possibly damaging Het
Spata16 A T 3: 26,777,537 N265I probably damaging Het
Srpk1 T C 17: 28,599,472 probably null Het
Tcaf1 T C 6: 42,686,542 T135A probably benign Het
Trappc12 A G 12: 28,746,390 V381A probably damaging Het
Trim33 T A 3: 103,330,180 I184K possibly damaging Het
Unc13a C T 8: 71,664,245 V62M probably damaging Het
Vrk2 A G 11: 26,498,919 V225A probably damaging Het
Wdr66 A G 5: 123,254,445 probably benign Het
Wdr95 C T 5: 149,564,414 P171L probably damaging Het
Wsb1 T C 11: 79,248,436 T75A probably damaging Het
Other mutations in Gm5965
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00540:Gm5965 APN 16 88778340 missense probably damaging 0.99
IGL01309:Gm5965 APN 16 88778331 missense possibly damaging 0.95
R2520:Gm5965 UTSW 16 88778526 missense probably null
R5009:Gm5965 UTSW 16 88778424 missense probably benign 0.17
Predicted Primers PCR Primer
(F):5'- TGCCAGGGTACATATGCTGG -3'
(R):5'- TTCTAGACAATTTCAGGTTACCCAC -3'

Sequencing Primer
(F):5'- CAGGGTACATATGCTGGCTCTC -3'
(R):5'- GGTTACCCACTAATCTCACAATCTG -3'
Posted On2016-10-06