Incidental Mutation 'R3864:Gm10309'
ID 276469
Institutional Source Beutler Lab
Gene Symbol Gm10309
Ensembl Gene ENSMUSG00000071036
Gene Name predicted gene 10309
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # R3864 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 86805160-86812660 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to C at 86806421 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000094874 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095186] [ENSMUST00000097274] [ENSMUST00000097275]
AlphaFold Q8C648
Predicted Effect unknown
Transcript: ENSMUST00000095186
AA Change: V31G
Predicted Effect probably benign
Transcript: ENSMUST00000097274
SMART Domains Protein: ENSMUSP00000094873
Gene: ENSMUSG00000045038

DomainStartEndE-ValueType
C2 7 114 5.78e-12 SMART
C1 170 220 4.48e-13 SMART
C1 243 292 8.29e-17 SMART
S_TKc 408 668 1.3e-104 SMART
S_TK_X 669 732 2.56e-25 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000097275
SMART Domains Protein: ENSMUSP00000094874
Gene: ENSMUSG00000045038

DomainStartEndE-ValueType
C2 7 114 5.78e-12 SMART
C1 170 220 4.48e-13 SMART
C1 243 292 8.29e-17 SMART
S_TKc 408 668 1.3e-104 SMART
S_TK_X 669 732 2.56e-25 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136986
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150486
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aanat G A 11: 116,487,642 (GRCm39) G114S probably damaging Het
Abcc4 G A 14: 118,853,827 (GRCm39) A360V probably benign Het
Catsper1 T C 19: 5,386,204 (GRCm39) S146P possibly damaging Het
Ccny A T 18: 9,449,604 (GRCm39) L23Q probably damaging Het
Chml A T 1: 175,515,810 (GRCm39) V37D probably damaging Het
Cspg4b A G 13: 113,459,485 (GRCm39) T1339A possibly damaging Het
D430041D05Rik T C 2: 104,044,522 (GRCm39) I825M possibly damaging Het
Dhx40 A T 11: 86,680,071 (GRCm39) V422E possibly damaging Het
Evi2 T A 11: 79,406,472 (GRCm39) I368F probably benign Het
Greb1 G A 12: 16,752,421 (GRCm39) R974W probably damaging Het
Grhl1 T C 12: 24,665,929 (GRCm39) *619Q probably null Het
Ighv1-7 A G 12: 114,502,266 (GRCm39) I67T probably damaging Het
Lats1 T C 10: 7,581,510 (GRCm39) V765A probably damaging Het
Lrrd1 G A 5: 3,901,248 (GRCm39) V518I probably benign Het
Ltbp3 G A 19: 5,804,050 (GRCm39) R854Q probably benign Het
Marchf11 C T 15: 26,387,952 (GRCm39) A269V probably damaging Het
Mep1b A G 18: 21,217,226 (GRCm39) N115S possibly damaging Het
Mfn1 A G 3: 32,617,241 (GRCm39) D41G possibly damaging Het
Naa25 T A 5: 121,547,260 (GRCm39) M132K probably damaging Het
Obscn T C 11: 59,022,472 (GRCm39) R758G possibly damaging Het
Pcdhb3 A G 18: 37,436,329 (GRCm39) E765G probably damaging Het
Scfd2 T G 5: 74,558,381 (GRCm39) K499Q possibly damaging Het
Tbc1d2 T C 4: 46,620,484 (GRCm39) D442G probably benign Het
Wwc1 T A 11: 35,801,143 (GRCm39) D98V probably damaging Het
Zfp426 G A 9: 20,381,382 (GRCm39) T521I possibly damaging Het
Other mutations in Gm10309
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0637:Gm10309 UTSW 17 86,806,463 (GRCm39) intron probably benign
R5426:Gm10309 UTSW 17 86,806,161 (GRCm39) intron probably benign
R5719:Gm10309 UTSW 17 86,806,421 (GRCm39) intron probably benign
R5883:Gm10309 UTSW 17 86,806,185 (GRCm39) intron probably benign
R6479:Gm10309 UTSW 17 86,812,007 (GRCm39) start codon destroyed probably null
R7474:Gm10309 UTSW 17 86,812,095 (GRCm39) intron probably benign
R9548:Gm10309 UTSW 17 86,806,161 (GRCm39) missense unknown
R9635:Gm10309 UTSW 17 86,806,494 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GAGCGTCCTGGTCGATTATG -3'
(R):5'- TCAAGTCTAGCACAAGGTCAG -3'

Sequencing Primer
(F):5'- CGTCCTGGTCGATTATGCAGAAC -3'
(R):5'- TCTAGCACAAGGTCAGAATCTG -3'
Posted On 2015-04-06