Incidental Mutation 'IGL01025:Gm10295'
ID 60054
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10295
Ensembl Gene ENSMUSG00000070511
Gene Name predicted gene 10295
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.157) question?
Stock # IGL01025
Quality Score
Status
Chromosome 7
Chromosomal Location 70998709-71001233 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 71000406 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 58 (D58V)
Ref Sequence ENSEMBL: ENSMUSP00000091873 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094315]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000094315
AA Change: D58V
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190004
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207237
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208757
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209171
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209182
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acap3 G A 4: 155,986,676 (GRCm39) V335M probably damaging Het
Apex1 C T 14: 51,163,711 (GRCm39) L113F possibly damaging Het
Bltp1 T A 3: 37,100,429 (GRCm39) H1218Q possibly damaging Het
Cd33 C T 7: 43,182,329 (GRCm39) V39M probably damaging Het
Chek2 A G 5: 110,996,536 (GRCm39) D166G probably damaging Het
Col2a1 T C 15: 97,874,054 (GRCm39) K1376R unknown Het
Cpd C T 11: 76,686,439 (GRCm39) R963H probably damaging Het
Cracd A G 5: 76,805,921 (GRCm39) probably benign Het
Cyp2c67 A C 19: 39,628,376 (GRCm39) Y189* probably null Het
Dock6 T C 9: 21,723,103 (GRCm39) E1606G possibly damaging Het
Dusp4 A T 8: 35,285,666 (GRCm39) E309V probably benign Het
Dync2h1 A G 9: 7,162,789 (GRCm39) I600T probably damaging Het
Fer1l4 A G 2: 155,894,105 (GRCm39) V66A probably benign Het
Fktn T C 4: 53,737,568 (GRCm39) L269P possibly damaging Het
Ftsj3 A G 11: 106,141,185 (GRCm39) I645T probably damaging Het
Fxr2 A G 11: 69,534,713 (GRCm39) H198R probably damaging Het
Fzd7 T C 1: 59,523,539 (GRCm39) V474A probably damaging Het
Hdlbp T C 1: 93,357,891 (GRCm39) I337V probably benign Het
Hydin T C 8: 111,053,033 (GRCm39) V235A probably benign Het
Igfbp4 C T 11: 98,939,069 (GRCm39) H30Y probably damaging Het
Kcna4 T C 2: 107,126,736 (GRCm39) V490A probably damaging Het
Kcnj13 T G 1: 87,314,700 (GRCm39) D174A probably benign Het
Krt7 T A 15: 101,321,302 (GRCm39) L373Q probably benign Het
Lama3 G A 18: 12,614,094 (GRCm39) V1288I probably benign Het
Mroh9 T C 1: 162,875,435 (GRCm39) D488G possibly damaging Het
Myh7 T C 14: 55,216,994 (GRCm39) E1121G probably damaging Het
Myom1 A G 17: 71,384,912 (GRCm39) N768D probably damaging Het
Naa16 T C 14: 79,622,196 (GRCm39) T48A probably damaging Het
Naglu C T 11: 100,964,773 (GRCm39) P287S probably benign Het
Nipbl A G 15: 8,379,939 (GRCm39) V951A possibly damaging Het
Nlrp3 T A 11: 59,442,713 (GRCm39) M755K probably benign Het
Nlrp4e T C 7: 23,052,586 (GRCm39) probably benign Het
Nt5dc1 C T 10: 34,283,553 (GRCm39) A79T possibly damaging Het
Or10aa3 T C 1: 173,878,251 (GRCm39) F104S probably damaging Het
Or6c205 A T 10: 129,086,609 (GRCm39) I69F possibly damaging Het
Or8b47 A G 9: 38,435,029 (GRCm39) probably benign Het
Otof A G 5: 30,541,597 (GRCm39) L774P possibly damaging Het
Phf20l1 C T 15: 66,484,981 (GRCm39) R322C probably damaging Het
Pkhd1 C T 1: 20,279,400 (GRCm39) G2973R probably benign Het
Plekhg5 G T 4: 152,192,983 (GRCm39) D613Y probably damaging Het
Ppm1h T A 10: 122,714,534 (GRCm39) probably null Het
Pramel31 T A 4: 144,089,947 (GRCm39) L329Q probably damaging Het
Prpf39 T C 12: 65,089,255 (GRCm39) probably benign Het
Rtn3 A G 19: 7,460,406 (GRCm39) S15P unknown Het
Slc22a28 G T 19: 8,094,272 (GRCm39) probably benign Het
Slc4a5 T A 6: 83,239,515 (GRCm39) L143Q probably damaging Het
Sox17 T C 1: 4,562,426 (GRCm39) D130G possibly damaging Het
Stag1 A G 9: 100,833,710 (GRCm39) T1108A possibly damaging Het
Sugp2 G A 8: 70,695,185 (GRCm39) D53N probably damaging Het
Trim33 G A 3: 103,261,234 (GRCm39) probably benign Het
Ttn A G 2: 76,629,568 (GRCm39) I14291T probably damaging Het
Ttn A G 2: 76,619,869 (GRCm39) V15933A probably damaging Het
Tulp3 A C 6: 128,302,847 (GRCm39) I324S probably damaging Het
Zfhx2 T C 14: 55,301,717 (GRCm39) E2089G probably damaging Het
Zhx1 T C 15: 57,918,075 (GRCm39) D57G probably benign Het
Other mutations in Gm10295
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01081:Gm10295 APN 7 71,000,296 (GRCm39) missense unknown
IGL02942:Gm10295 APN 7 71,000,250 (GRCm39) missense unknown
R0360:Gm10295 UTSW 7 71,000,361 (GRCm39) missense unknown
R0364:Gm10295 UTSW 7 71,000,361 (GRCm39) missense unknown
R1029:Gm10295 UTSW 7 71,000,448 (GRCm39) missense unknown
R2331:Gm10295 UTSW 7 71,000,437 (GRCm39) missense unknown
R9362:Gm10295 UTSW 7 71,000,755 (GRCm39) start gained probably benign
X0027:Gm10295 UTSW 7 71,000,253 (GRCm39) missense unknown
Posted On 2013-07-11