Incidental Mutation 'R2331:Gm10295'
ID 245874
Institutional Source Beutler Lab
Gene Symbol Gm10295
Ensembl Gene ENSMUSG00000070511
Gene Name predicted gene 10295
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # R2331 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 70998709-71001233 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 71000437 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Alanine at position 48 (S48A)
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: S48A
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
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aff3 C T 1: 38,243,971 (GRCm39) probably null Het
Cadps A G 14: 12,603,692 (GRCm38) I376T probably damaging Het
Crygs C T 16: 22,624,301 (GRCm39) G102D possibly damaging Het
Gstcd A G 3: 132,704,641 (GRCm39) C538R probably damaging Het
Hcn3 A T 3: 89,055,397 (GRCm39) S617T probably benign Het
Hectd4 A G 5: 121,458,089 (GRCm39) I752V probably benign Het
Itgb7 G T 15: 102,131,983 (GRCm39) T200K probably damaging Het
Lcn11 C A 2: 25,670,188 (GRCm39) T177K possibly damaging Het
Lsm14a A G 7: 34,056,915 (GRCm39) V241A probably benign Het
Magi1 T C 6: 93,662,543 (GRCm39) K1075E probably damaging Het
Or4c111 T C 2: 88,844,265 (GRCm39) I48V probably benign Het
Or4d10c C A 19: 12,065,522 (GRCm39) L211F probably benign Het
P4hb T C 11: 120,459,106 (GRCm39) N129S probably benign Het
Piezo1 C T 8: 123,214,005 (GRCm39) probably null Het
Ppp3ca T C 3: 136,503,580 (GRCm39) M51T probably benign Het
Sema6d T C 2: 124,499,983 (GRCm39) V353A probably damaging Het
Setx GTGGCT GT 2: 29,044,073 (GRCm39) 1814 probably null Het
Sh3rf1 C T 8: 61,679,321 (GRCm39) P121L probably benign Het
Sh3rf2 T C 18: 42,186,928 (GRCm39) F16L probably benign Het
Sparcl1 A G 5: 104,233,660 (GRCm39) L563P probably damaging Het
Stra6l T C 4: 45,858,224 (GRCm39) probably null Het
Sult2a6 A T 7: 13,959,795 (GRCm39) M246K possibly damaging Het
Trpv5 A G 6: 41,636,902 (GRCm39) S399P probably damaging Het
Uggt2 A T 14: 119,264,011 (GRCm39) F1006L possibly damaging Het
Uhrf1 C A 17: 56,617,671 (GRCm39) probably null Het
Wdr72 A G 9: 74,055,608 (GRCm39) Y279C probably damaging Het
Other mutations in Gm10295
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01025:Gm10295 APN 7 71,000,406 (GRCm39) missense unknown
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
R9362:Gm10295 UTSW 7 71,000,755 (GRCm39) start gained probably benign
X0027:Gm10295 UTSW 7 71,000,253 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CTTGGCAGTAAGTCTCAAACTC -3'
(R):5'- CCATTCGGTGTAGAGTGTCC -3'

Sequencing Primer
(F):5'- GCAGTAAGTCTCAAACTCTGCTC -3'
(R):5'- CGGTGTAGAGTGTCCTTTTAAAACTC -3'
Posted On 2014-10-30