Incidental Mutation 'IGL01835:Gm6309'
ID 154917
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6309
Ensembl Gene ENSMUSG00000096798
Gene Name predicted gene 6309
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL01835
Quality Score
Status
Chromosome 5
Chromosomal Location 146104786-146107531 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 146105085 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Valine at position 276 (A276V)
Ref Sequence ENSEMBL: ENSMUSP00000134203 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000174320]
AlphaFold L7N481
Predicted Effect probably damaging
Transcript: ENSMUST00000174320
AA Change: A276V

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000134203
Gene: ENSMUSG00000096798
AA Change: A276V

DomainStartEndE-ValueType
RasGEFN 65 181 3.29e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik T A 12: 71,213,957 (GRCm39) M728K probably benign Het
2700049A03Rik T A 12: 71,213,955 (GRCm39) Y727* probably null Het
Adam23 T C 1: 63,582,278 (GRCm39) Y309H probably damaging Het
Ash2l C T 8: 26,329,868 (GRCm39) V97M probably damaging Het
Cyp4f13 A G 17: 33,149,588 (GRCm39) F83L probably benign Het
Dnah6 A T 6: 73,112,784 (GRCm39) S1607T probably damaging Het
Dock2 T A 11: 34,260,435 (GRCm39) M969L possibly damaging Het
Dse T A 10: 34,036,213 (GRCm39) probably benign Het
Dusp22 C T 13: 30,892,666 (GRCm39) probably null Het
F5 G A 1: 164,021,937 (GRCm39) V1471I probably benign Het
Gm14403 A T 2: 177,199,049 (GRCm39) E48D probably damaging Het
Icam4 A T 9: 20,941,086 (GRCm39) T113S probably damaging Het
Ipo5 T C 14: 121,163,650 (GRCm39) V236A probably benign Het
Mrc2 T G 11: 105,227,503 (GRCm39) F579V probably damaging Het
Myl4 T A 11: 104,468,279 (GRCm39) M1K probably null Het
Oas3 A T 5: 120,904,193 (GRCm39) C560* probably null Het
Or2w25 T C 11: 59,504,165 (GRCm39) V125A probably damaging Het
Or52e18 T C 7: 104,609,669 (GRCm39) N90S probably benign Het
Prlr G A 15: 10,329,129 (GRCm39) V535I probably damaging Het
Ptprd T C 4: 76,165,058 (GRCm39) T48A probably benign Het
Rasa4 A G 5: 136,131,461 (GRCm39) H485R possibly damaging Het
Rnf13 A T 3: 57,728,007 (GRCm39) H229L probably damaging Het
Rpap3 T C 15: 97,601,120 (GRCm39) D39G possibly damaging Het
Sec23ip T A 7: 128,357,035 (GRCm39) probably null Het
Sirpa T A 2: 129,457,484 (GRCm39) F186Y possibly damaging Het
Slc26a11 T C 11: 119,268,040 (GRCm39) Y473H probably benign Het
Slc36a2 T C 11: 55,053,559 (GRCm39) I360V probably benign Het
Spg11 G A 2: 121,918,705 (GRCm39) R975C probably benign Het
Sppl2b T A 10: 80,701,175 (GRCm39) I350N probably damaging Het
Tas2r139 A T 6: 42,118,366 (GRCm39) N166I probably benign Het
Trav14n-3 A G 14: 53,607,786 (GRCm39) T39A possibly damaging Het
Vmn2r61 A G 7: 41,950,015 (GRCm39) M812V probably benign Het
Vmn2r87 A C 10: 130,314,978 (GRCm39) F203V probably damaging Het
Vwde A C 6: 13,186,823 (GRCm39) V888G probably benign Het
Zbtb17 T C 4: 141,192,749 (GRCm39) probably null Het
Other mutations in Gm6309
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01547:Gm6309 APN 5 146,105,221 (GRCm39) missense probably benign 0.02
FR4737:Gm6309 UTSW 5 146,104,993 (GRCm39) missense probably benign
FR4976:Gm6309 UTSW 5 146,104,993 (GRCm39) missense probably benign
R1513:Gm6309 UTSW 5 146,107,393 (GRCm39) missense possibly damaging 0.83
R2022:Gm6309 UTSW 5 146,105,121 (GRCm39) missense probably benign
R2191:Gm6309 UTSW 5 146,105,681 (GRCm39) missense possibly damaging 0.93
R4735:Gm6309 UTSW 5 146,105,054 (GRCm39) missense probably damaging 0.99
R5719:Gm6309 UTSW 5 146,104,992 (GRCm39) missense probably benign 0.01
R5776:Gm6309 UTSW 5 146,105,691 (GRCm39) missense possibly damaging 0.80
R5833:Gm6309 UTSW 5 146,105,128 (GRCm39) missense probably damaging 1.00
R6246:Gm6309 UTSW 5 146,107,050 (GRCm39) missense probably damaging 1.00
R6373:Gm6309 UTSW 5 146,107,085 (GRCm39) missense probably damaging 0.97
R6873:Gm6309 UTSW 5 146,104,998 (GRCm39) missense probably damaging 0.96
R6912:Gm6309 UTSW 5 146,105,640 (GRCm39) missense probably damaging 0.97
R6954:Gm6309 UTSW 5 146,105,300 (GRCm39) missense possibly damaging 0.82
R7145:Gm6309 UTSW 5 146,107,100 (GRCm39) missense possibly damaging 0.74
R7258:Gm6309 UTSW 5 146,105,106 (GRCm39) missense probably benign 0.07
R7535:Gm6309 UTSW 5 146,105,100 (GRCm39) missense probably damaging 1.00
R8885:Gm6309 UTSW 5 146,105,103 (GRCm39) missense probably damaging 1.00
R8941:Gm6309 UTSW 5 146,107,155 (GRCm39) missense probably damaging 0.98
R9577:Gm6309 UTSW 5 146,105,700 (GRCm39) missense possibly damaging 0.74
R9668:Gm6309 UTSW 5 146,105,026 (GRCm39) missense probably benign 0.04
Posted On 2014-02-04