Incidental Mutation 'R8535:Gm10750'
ID 659195
Institutional Source Beutler Lab
Gene Symbol Gm10750
Ensembl Gene ENSMUSG00000074739
Gene Name predicted gene 10750
Synonyms
MMRRC Submission 068504-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R8535 (G1)
Quality Score 225.009
Status Not validated
Chromosome 2
Chromosomal Location 148857652-148859157 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 148857888 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 121 (V121A)
Ref Sequence ENSEMBL: ENSMUSP00000096872 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099266]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000099266
AA Change: V121A
SMART Domains Protein: ENSMUSP00000096872
Gene: ENSMUSG00000074739
AA Change: V121A

DomainStartEndE-ValueType
low complexity region 75 89 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 100% (34/34)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl6 A T 11: 54,229,328 (GRCm39) I362F probably damaging Het
Anks1b T A 10: 90,784,493 (GRCm39) S1154T probably benign Het
Bsn G A 9: 107,988,651 (GRCm39) A2367V probably benign Het
Chd7 T A 4: 8,859,211 (GRCm39) S2434T possibly damaging Het
Crybg2 T C 4: 133,808,514 (GRCm39) S1372P probably damaging Het
Dock5 A G 14: 68,031,425 (GRCm39) Y1002H probably benign Het
Dst T C 1: 34,225,082 (GRCm39) S1163P probably damaging Het
Fah A T 7: 84,250,305 (GRCm39) S14T probably benign Het
Gcnt7 T C 2: 172,296,466 (GRCm39) I119M possibly damaging Het
Gja10 G A 4: 32,602,274 (GRCm39) L37F probably damaging Het
Klhl25 G A 7: 75,515,843 (GRCm39) V250I probably benign Het
Kmt2a A C 9: 44,730,812 (GRCm39) S200R possibly damaging Het
Map1b T A 13: 99,571,662 (GRCm39) D353V probably damaging Het
Myh8 G A 11: 67,169,741 (GRCm39) R20Q probably damaging Het
Or4c127 G A 2: 89,833,511 (GRCm39) V254M probably benign Het
Or6c200-ps1 T C 10: 128,869,892 (GRCm39) Y273C probably damaging Het
Pcnt G A 10: 76,256,039 (GRCm39) R734W probably damaging Het
Pkn3 A T 2: 29,969,936 (GRCm39) probably null Het
Ptpn21 T A 12: 98,646,285 (GRCm39) T1058S probably damaging Het
Ryr3 A G 2: 112,779,433 (GRCm39) probably null Het
Sardh T A 2: 27,129,657 (GRCm39) I263F probably damaging Het
Scart1 G A 7: 139,804,634 (GRCm39) V546M probably benign Het
Sh3bp5 A G 14: 31,139,375 (GRCm39) V66A probably benign Het
Styxl2 T C 1: 165,928,730 (GRCm39) D294G probably benign Het
Taf4b T A 18: 14,955,195 (GRCm39) S583T probably damaging Het
Tbcb G A 7: 29,926,421 (GRCm39) P132L probably benign Het
Tcirg1 A G 19: 3,946,324 (GRCm39) I791T probably damaging Het
Tmeff2 T A 1: 51,220,985 (GRCm39) V320D probably damaging Het
Tnfrsf19 T C 14: 61,208,417 (GRCm39) E368G probably benign Het
Trdv2-1 T A 14: 54,183,972 (GRCm39) I67N probably damaging Het
Unc13c G A 9: 73,447,653 (GRCm39) T1849I probably benign Het
Vav2 G A 2: 27,161,841 (GRCm39) T655I probably damaging Het
Vps50 T C 6: 3,565,612 (GRCm39) Y517H possibly damaging Het
Wdr27 G A 17: 15,123,799 (GRCm39) T558I possibly damaging Het
Yeats2 C T 16: 19,977,926 (GRCm39) R137W probably damaging Het
Other mutations in Gm10750
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01721:Gm10750 APN 2 148,857,964 (GRCm39) missense unknown
R0107:Gm10750 UTSW 2 148,857,973 (GRCm39) missense unknown
R4283:Gm10750 UTSW 2 148,857,916 (GRCm39) missense unknown
R7935:Gm10750 UTSW 2 148,858,017 (GRCm39) missense unknown
R9294:Gm10750 UTSW 2 148,858,107 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TTTATTGGAAAGGCAGGCTCTCC -3'
(R):5'- ATGGGCTTATCCTCTGCTAGGG -3'

Sequencing Primer
(F):5'- CCAGGCTTCAACAGTGAGTC -3'
(R):5'- ATCCTCTGCTAGGGCACTGTG -3'
Posted On 2021-01-18