Incidental Mutation 'R3158:Gm7853'
ID 263597
Institutional Source Beutler Lab
Gene Symbol Gm7853
Ensembl Gene ENSMUSG00000072616
Gene Name predicted gene 7853
Synonyms
MMRRC Submission 040609-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # R3158 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 35811316-35812773 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 35811358 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: ENSMUST00000100708
SMART Domains Protein: ENSMUSP00000098274
Gene: ENSMUSG00000072616

DomainStartEndE-ValueType
RasGEFN 7 128 4.76e-7 SMART
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.4%
Validation Efficiency 97% (35/36)
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aoc2 A T 11: 101,220,102 (GRCm39) N696I probably damaging Het
Ccr4 G T 9: 114,321,350 (GRCm39) N238K probably benign Het
Cd300e A C 11: 114,952,849 (GRCm39) M1R probably null Het
Cep95 A G 11: 106,700,013 (GRCm39) probably benign Het
Cfap54 T C 10: 92,834,918 (GRCm39) I1096V probably benign Het
Clca4b C A 3: 144,617,878 (GRCm39) V742L probably benign Het
Diaph3 A T 14: 86,893,892 (GRCm39) I39N possibly damaging Het
Dll3 A T 7: 27,993,520 (GRCm39) D566E possibly damaging Het
Dmpk A G 7: 18,826,944 (GRCm39) T579A probably benign Het
E330034G19Rik A T 14: 24,346,965 (GRCm39) Y84F possibly damaging Het
Eya1 G A 1: 14,374,691 (GRCm39) probably benign Het
Fat4 A G 3: 38,944,940 (GRCm39) T1278A possibly damaging Het
Galnt12 A G 4: 47,104,264 (GRCm39) D174G probably damaging Het
Gm20939 T A 17: 95,184,721 (GRCm39) H456Q probably damaging Het
Hsd3b5 G A 3: 98,529,375 (GRCm39) A85V probably benign Het
Itga11 A G 9: 62,676,560 (GRCm39) K916R probably benign Het
Kcnh8 GAGACCAACGAGCAGCTGATGCTTCAGA GAGA 17: 53,032,934 (GRCm39) 74 probably benign Het
Krt6a T C 15: 101,599,801 (GRCm39) Y437C probably damaging Het
Lrp5 A G 19: 3,665,849 (GRCm39) S707P probably damaging Het
Med14 G A X: 12,550,330 (GRCm39) probably benign Het
Mmp11 C T 10: 75,762,948 (GRCm39) probably benign Het
Mtus2 A G 5: 148,168,637 (GRCm39) H950R probably damaging Het
Myo1g G T 11: 6,464,527 (GRCm39) T511K possibly damaging Het
Myo7a A G 7: 97,701,499 (GRCm39) F2154S probably damaging Het
Or11h4 A G 14: 50,974,271 (GRCm39) V116A probably benign Het
Or5b101 G C 19: 13,005,411 (GRCm39) A94G probably benign Het
Or8h8 C T 2: 86,752,950 (GRCm39) E309K probably benign Het
Prss52 G T 14: 64,350,992 (GRCm39) W259L probably damaging Het
Sbk2 G A 7: 4,960,526 (GRCm39) R215* probably null Het
Sectm1a A G 11: 120,959,603 (GRCm39) I175T probably benign Het
Smu1 T A 4: 40,754,529 (GRCm39) R123S possibly damaging Het
Stk3 A G 15: 35,008,387 (GRCm39) S178P possibly damaging Het
Tle6 T C 10: 81,431,038 (GRCm39) probably null Het
Vmn2r37 C T 7: 9,220,713 (GRCm39) M383I probably benign Het
Other mutations in Gm7853
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1476:Gm7853 UTSW 14 35,811,540 (GRCm39) exon noncoding transcript
R2229:Gm7853 UTSW 14 35,811,484 (GRCm39) exon noncoding transcript
R2314:Gm7853 UTSW 14 35,811,621 (GRCm39) splice site noncoding transcript
R5009:Gm7853 UTSW 14 35,811,466 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- CACTGTATCTACCAGCATGCTG -3'
(R):5'- CTGAGGACTTTTGTGACCCC -3'

Sequencing Primer
(F):5'- CAGGTTACACAGCTGCTATCAGG -3'
(R):5'- GAGGACTTTTGTGACCCCTCAGAC -3'
Posted On 2015-02-05