Incidental Mutation 'R2406:Gm10650'
ID 247996
Institutional Source Beutler Lab
Gene Symbol Gm10650
Ensembl Gene ENSMUSG00000074237
Gene Name predicted gene 10650
Synonyms
MMRRC Submission 040372-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.133) question?
Stock # R2406 (G1)
Quality Score 216
Status Validated
Chromosome 3
Chromosomal Location 127832342-127834310 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 127833530 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000098625
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196581
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.9%
  • 20x: 93.9%
Validation Efficiency 95% (42/44)
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2300002M23Rik T A 17: 35,879,352 (GRCm39) V230E probably damaging Het
Adam22 A T 5: 8,230,064 (GRCm39) probably benign Het
AW554918 A G 18: 25,473,344 (GRCm39) I180V possibly damaging Het
C9 T C 15: 6,512,780 (GRCm39) S301P possibly damaging Het
Cdc42bpb T C 12: 111,268,558 (GRCm39) Q1214R probably benign Het
Chaf1b T C 16: 93,697,043 (GRCm39) I351T probably damaging Het
Clip1 T C 5: 123,741,723 (GRCm39) E1177G probably damaging Het
Colgalt1 G A 8: 72,070,312 (GRCm39) C198Y probably damaging Het
Dennd4b C T 3: 90,182,795 (GRCm39) R871C probably damaging Het
Efcab3 A T 11: 104,611,457 (GRCm39) D433V probably benign Het
Eif4ebp1 A G 8: 27,763,362 (GRCm39) I52V probably damaging Het
Fbxw5 T C 2: 25,394,195 (GRCm39) I86T probably damaging Het
Helz G A 11: 107,577,378 (GRCm39) A1910T unknown Het
Hsf2 C T 10: 57,373,642 (GRCm39) T70I probably damaging Het
Ifih1 A G 2: 62,437,447 (GRCm39) probably benign Het
Kdm2a T C 19: 4,372,546 (GRCm39) D933G probably damaging Het
Macc1 T C 12: 119,429,346 (GRCm39) I832T probably damaging Het
Mapk15 T C 15: 75,870,697 (GRCm39) S512P possibly damaging Het
Mybpc2 A T 7: 44,171,149 (GRCm39) I134N possibly damaging Het
Myh4 A G 11: 67,150,000 (GRCm39) E1853G probably damaging Het
Ncoa3 T C 2: 165,897,279 (GRCm39) V690A probably damaging Het
Nsf C T 11: 103,821,578 (GRCm39) E26K possibly damaging Het
Or5b97 A G 19: 12,878,991 (GRCm39) V51A probably benign Het
Pacsin2 A T 15: 83,269,313 (GRCm39) probably benign Het
Piezo2 A T 18: 63,155,596 (GRCm39) L2416Q probably damaging Het
Pip5k1c T A 10: 81,144,858 (GRCm39) I233N probably damaging Het
Ptcd3 T C 6: 71,865,631 (GRCm39) D428G probably damaging Het
Ptprf T C 4: 118,126,501 (GRCm39) D84G possibly damaging Het
Rasgrf2 T C 13: 92,120,359 (GRCm39) D798G probably benign Het
Setd7 A G 3: 51,450,097 (GRCm39) Y110H probably damaging Het
Sgta T C 10: 80,887,081 (GRCm39) I61M possibly damaging Het
Shank1 A G 7: 44,006,376 (GRCm39) D2031G possibly damaging Het
Skint5 A G 4: 113,799,864 (GRCm39) Y88H probably damaging Het
Spata31f1a A T 4: 42,851,696 (GRCm39) D153E probably benign Het
Stox1 T C 10: 62,499,945 (GRCm39) I872V probably benign Het
Tmc4 A G 7: 3,674,025 (GRCm39) F385L probably benign Het
Top3a A G 11: 60,646,838 (GRCm39) F258L probably damaging Het
Ttn T C 2: 76,780,499 (GRCm39) Y1084C probably damaging Het
Ubtf A T 11: 102,199,528 (GRCm39) Y504* probably null Het
Wdfy3 T C 5: 102,036,125 (GRCm39) T2098A probably damaging Het
Wnk2 G T 13: 49,214,964 (GRCm39) T1194K possibly damaging Het
Zbtb40 T A 4: 136,725,879 (GRCm39) E560V probably benign Het
Other mutations in Gm10650
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02222:Gm10650 APN 3 127,833,789 (GRCm39) exon noncoding transcript
R2230:Gm10650 UTSW 3 127,833,412 (GRCm39) exon noncoding transcript
R5061:Gm10650 UTSW 3 127,833,666 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- ACAGCTTCCTTGTCTGTGTAG -3'
(R):5'- AGGCTAGCATACAAACGGCC -3'

Sequencing Primer
(F):5'- CCTATGCTGCAACATTAAAGTTCTC -3'
(R):5'- ATACAAACGGCCCCGGGTG -3'
Posted On 2014-11-11