Incidental Mutation 'R5599:Gm20767'
ID438956
Institutional Source Beutler Lab
Gene Symbol Gm20767
Ensembl Gene ENSMUSG00000096323
Gene Namepredicted gene, 20767
Synonyms
MMRRC Submission 043151-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.113) question?
Stock #R5599 (G1)
Quality Score225
Status Not validated
Chromosome13
Chromosomal Location120140246-120155335 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 120154922 bp
ZygosityHeterozygous
Amino Acid Change Glutamine to Proline at position 99 (Q99P)
Ref Sequence ENSEMBL: ENSMUSP00000152988 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000179071] [ENSMUST00000225683]
Predicted Effect probably damaging
Transcript: ENSMUST00000179071
AA Change: Q99P

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000137504
Gene: ENSMUSG00000096323
AA Change: Q99P

DomainStartEndE-ValueType
Pfam:DUF1438 7 155 3.2e-93 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000225683
AA Change: Q99P

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010300C02Rik T C 1: 37,613,343 N1128D possibly damaging Het
Abhd2 T A 7: 79,296,998 probably null Het
Agpat3 T C 10: 78,274,269 D282G probably benign Het
Ankhd1 G A 18: 36,560,807 A24T probably damaging Het
Cry1 A T 10: 85,144,250 M398K probably benign Het
Dpp10 A G 1: 123,905,076 I47T probably damaging Het
Fam208a A G 14: 27,479,929 N1427D probably benign Het
Fpr-rs6 C T 17: 20,182,113 D329N probably benign Het
Gfm2 G A 13: 97,163,151 A406T probably damaging Het
Gprc5c G T 11: 114,864,267 V257L possibly damaging Het
Gxylt1 CTCATCCGGGTCAT CTCAT 15: 93,254,317 probably benign Het
Hnrnpul1 G A 7: 25,754,672 probably benign Het
Lbx1 T A 19: 45,235,080 S50C probably damaging Het
Lims2 A G 18: 31,957,271 N183S probably benign Het
Lrp1 T C 10: 127,593,869 N444S probably damaging Het
Mast4 A T 13: 102,737,479 C1626S probably damaging Het
Mgat5 A G 1: 127,397,566 Y390C probably damaging Het
Nf2 T C 11: 4,782,269 E553G probably damaging Het
Nfatc4 A T 14: 55,832,276 T704S probably benign Het
Olfr1160 T G 2: 88,006,005 I258L probably benign Het
Olfr140 A G 2: 90,052,219 V35A probably benign Het
Olfr679 T C 7: 105,086,550 probably null Het
Olfr847 T G 9: 19,375,629 N84T possibly damaging Het
Plekha7 T A 7: 116,176,882 probably null Het
Polr1a T C 6: 71,967,362 M1271T possibly damaging Het
Ppip5k2 A G 1: 97,740,598 M595T probably damaging Het
Ppox A T 1: 171,277,460 V412D probably damaging Het
Ppp1r12b A G 1: 134,865,907 V573A probably benign Het
Prkcb T C 7: 122,582,478 Y430H probably benign Het
Psmd6 A C 14: 14,120,144 M65R probably benign Het
Rbm12 G A 2: 156,096,793 R520* probably null Het
Rin3 T C 12: 102,389,929 F830L probably damaging Het
Sema4b A G 7: 80,213,291 K104R probably benign Het
Slitrk1 T C 14: 108,911,812 D489G probably benign Het
Spef2 T C 15: 9,729,703 T110A possibly damaging Het
Sult2a6 T A 7: 14,254,704 K44* probably null Het
Tbc1d2 C T 4: 46,629,912 G252R probably benign Het
Tnxb G T 17: 34,690,202 G1445V probably damaging Het
Tnxb T C 17: 34,690,205 V1569A probably benign Het
Zcchc2 A G 1: 106,032,150 D1163G probably damaging Het
Zfp365 C T 10: 67,909,367 E194K probably damaging Het
Other mutations in Gm20767
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1004:Gm20767 UTSW 13 120155022 missense probably benign 0.00
R3753:Gm20767 UTSW 13 120154631 missense possibly damaging 0.56
R3930:Gm20767 UTSW 13 120154832 missense probably damaging 0.98
R4873:Gm20767 UTSW 13 120154670 missense probably damaging 0.98
R4875:Gm20767 UTSW 13 120154670 missense probably damaging 0.98
R5020:Gm20767 UTSW 13 120155116 missense possibly damaging 0.85
R5802:Gm20767 UTSW 13 120154913 missense possibly damaging 0.93
R6469:Gm20767 UTSW 13 120154813 missense probably damaging 1.00
R6535:Gm20767 UTSW 13 120154654 missense probably damaging 0.98
R7543:Gm20767 UTSW 13 120154754 missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- AGAACATGCACTGCCCAATG -3'
(R):5'- AGCCTAGGTGCCTGGAATTATC -3'

Sequencing Primer
(F):5'- CCTGAGTACAAGGTGTTCCAAGTC -3'
(R):5'- CCTAGGTGCCTGGAATTATCAGAAAC -3'
Posted On2016-10-26