Incidental Mutation 'R0067:Gm13941'
ID 18039
Institutional Source Beutler Lab
Gene Symbol Gm13941
Ensembl Gene ENSMUSG00000079170
Gene Name predicted gene 13941
Synonyms
MMRRC Submission 038358-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # R0067 (G1)
Quality Score
Status Validated
Chromosome 2
Chromosomal Location 110885009-110935204 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 110889761 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold A2AJ38
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136950
Coding Region Coverage
  • 1x: 87.3%
  • 3x: 82.3%
  • 10x: 64.1%
  • 20x: 35.8%
Validation Efficiency 96% (73/76)
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn4 C T 7: 28,610,995 (GRCm39) V248M possibly damaging Het
AW209491 A T 13: 14,812,328 (GRCm39) I394F probably benign Het
Cacna1d A T 14: 29,796,967 (GRCm39) probably benign Het
Cacna1i A T 15: 80,265,373 (GRCm39) I1542F probably damaging Het
Cep97 A T 16: 55,735,924 (GRCm39) N291K possibly damaging Het
Clasp2 A T 9: 113,689,209 (GRCm39) probably benign Het
Dennd1c T C 17: 57,382,465 (GRCm39) Q67R probably damaging Het
Eva1c A T 16: 90,663,305 (GRCm39) D13V possibly damaging Het
Fam151b T C 13: 92,610,504 (GRCm39) K95R probably benign Het
Gps2 C T 11: 69,805,607 (GRCm39) Q42* probably null Het
Hivep1 T A 13: 42,312,132 (GRCm39) D1457E probably benign Het
L3mbtl1 A G 2: 162,790,748 (GRCm39) K225E probably damaging Het
Limch1 A G 5: 67,131,965 (GRCm39) S143G probably damaging Het
Macf1 T C 4: 123,369,041 (GRCm39) K342E possibly damaging Het
Mc5r T G 18: 68,472,637 (GRCm39) M332R probably damaging Het
Mcf2l A G 8: 13,063,060 (GRCm39) T882A probably benign Het
Mtrex C T 13: 113,023,396 (GRCm39) V727I probably benign Het
Myf6 A T 10: 107,329,340 (GRCm39) probably null Het
Plekha5 C T 6: 140,470,629 (GRCm39) T90I probably damaging Het
Ptbp2 T C 3: 119,514,290 (GRCm39) T478A probably benign Het
Rasgrp1 C A 2: 117,125,301 (GRCm39) R246S probably damaging Het
Rflnb A T 11: 75,912,987 (GRCm39) S134T possibly damaging Het
Rnf214 A G 9: 45,778,796 (GRCm39) probably null Het
Satb1 T C 17: 52,111,364 (GRCm39) T165A probably damaging Het
Scamp1 T C 13: 94,340,658 (GRCm39) Y237C probably damaging Het
Skint10 A T 4: 112,568,753 (GRCm39) F321L probably benign Het
Slc8a1 A G 17: 81,745,188 (GRCm39) V672A probably benign Het
Spats2 C A 15: 99,110,168 (GRCm39) P522T possibly damaging Het
Stkld1 A T 2: 26,839,352 (GRCm39) E339D probably benign Het
Tbc1d9 A G 8: 83,960,872 (GRCm39) T241A probably damaging Het
Ticrr A T 7: 79,327,158 (GRCm39) D622V probably damaging Het
Trmt1l T C 1: 151,324,131 (GRCm39) V326A probably benign Het
Ube3c A G 5: 29,803,936 (GRCm39) T180A possibly damaging Het
Unc13a A C 8: 72,087,302 (GRCm39) F1482V probably damaging Het
Unc79 A G 12: 103,025,777 (GRCm39) E388G probably damaging Het
Ush2a A T 1: 188,697,043 (GRCm39) D5167V probably damaging Het
Vmn2r93 A T 17: 18,546,672 (GRCm39) H848L probably benign Het
Zcchc9 T C 13: 91,945,368 (GRCm39) I72V probably benign Het
Zfc3h1 G T 10: 115,259,379 (GRCm39) L1650F possibly damaging Het
Zzz3 A G 3: 152,134,040 (GRCm39) D366G possibly damaging Het
Other mutations in Gm13941
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00323:Gm13941 APN 2 110,935,198 (GRCm39) missense unknown
IGL00420:Gm13941 APN 2 110,922,193 (GRCm39) splice site probably benign
IGL01149:Gm13941 APN 2 110,931,482 (GRCm39) missense unknown
IGL01319:Gm13941 APN 2 110,925,150 (GRCm39) critical splice acceptor site probably null
IGL02557:Gm13941 APN 2 110,931,501 (GRCm39) missense unknown
IGL03163:Gm13941 APN 2 110,928,761 (GRCm39) missense unknown
R0918:Gm13941 UTSW 2 110,930,945 (GRCm39) missense unknown
R2315:Gm13941 UTSW 2 110,935,162 (GRCm39) missense unknown
R3847:Gm13941 UTSW 2 110,935,198 (GRCm39) missense unknown
R3848:Gm13941 UTSW 2 110,935,198 (GRCm39) missense unknown
R5416:Gm13941 UTSW 2 110,925,079 (GRCm39) missense unknown
R5574:Gm13941 UTSW 2 110,930,951 (GRCm39) missense unknown
R6389:Gm13941 UTSW 2 110,928,734 (GRCm39) missense unknown
R6616:Gm13941 UTSW 2 110,931,520 (GRCm39) missense unknown
R7056:Gm13941 UTSW 2 110,927,147 (GRCm39) missense unknown
R7455:Gm13941 UTSW 2 110,925,085 (GRCm39) missense unknown
R8197:Gm13941 UTSW 2 110,926,921 (GRCm39) splice site probably null
R9116:Gm13941 UTSW 2 110,935,146 (GRCm39) missense unknown
R9164:Gm13941 UTSW 2 110,936,324 (GRCm39) missense unknown
R9536:Gm13941 UTSW 2 110,918,861 (GRCm39) missense unknown
R9763:Gm13941 UTSW 2 110,931,518 (GRCm39) missense unknown
Z1177:Gm13941 UTSW 2 110,925,123 (GRCm39) missense unknown
Posted On 2013-03-25