Incidental Mutation 'R3910:Gm7104'
ID 309349
Institutional Source Beutler Lab
Gene Symbol Gm7104
Ensembl Gene ENSMUSG00000094635
Gene Name predicted gene 7104
Synonyms
MMRRC Submission 040815-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.398) question?
Stock # R3910 (G1)
Quality Score 172
Status Validated
Chromosome 12
Chromosomal Location 88251308-88253839 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to T at 88251364 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: ENSMUST00000179741
SMART Domains Protein: ENSMUSP00000136935
Gene: ENSMUSG00000094635

DomainStartEndE-ValueType
Pfam:EloA-BP1 80 248 1.6e-64 PFAM
EXOIII 345 504 5.07e-38 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223359
Meta Mutation Damage Score 0.4666 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency 97% (36/37)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bod1l T C 5: 41,974,441 (GRCm39) E2291G probably damaging Het
Cchcr1 T C 17: 35,836,233 (GRCm39) V341A probably damaging Het
Cimip3 AC A 17: 47,744,348 (GRCm39) probably benign Het
Dsg1c T C 18: 20,399,253 (GRCm39) V119A possibly damaging Het
Fap A G 2: 62,386,448 (GRCm39) S58P probably damaging Het
Flnc A T 6: 29,459,426 (GRCm39) T2509S probably damaging Het
Fnip2 A T 3: 79,386,812 (GRCm39) D971E possibly damaging Het
Gab2 A G 7: 96,948,280 (GRCm39) Y290C probably damaging Het
Ints10 T A 8: 69,266,272 (GRCm39) S478T probably damaging Het
Iqca1l A T 5: 24,750,440 (GRCm39) probably benign Het
Kirrel1 C T 3: 86,996,458 (GRCm39) M380I probably null Het
Krt90 G A 15: 101,471,218 (GRCm39) R15W probably damaging Het
Lgr5 A G 10: 115,423,368 (GRCm39) S11P possibly damaging Het
Mycn T A 12: 12,987,281 (GRCm39) N372I probably damaging Het
Or2ag18 A T 7: 106,405,072 (GRCm39) V199D probably damaging Het
Or9a2 A G 6: 41,749,083 (GRCm39) V50A probably benign Het
Paxbp1 T A 16: 90,839,569 (GRCm39) E117V probably damaging Het
Phc2 T C 4: 128,637,351 (GRCm39) probably null Het
Prr5 T A 15: 84,587,345 (GRCm39) V365E probably benign Het
Rev3l A G 10: 39,696,552 (GRCm39) I521M probably damaging Het
Robo3 A T 9: 37,330,591 (GRCm39) Y1002N probably damaging Het
Svep1 A T 4: 58,145,156 (GRCm39) probably null Het
Thsd7a A G 6: 12,331,548 (GRCm39) V1342A probably damaging Het
Tmtc3 A C 10: 100,284,888 (GRCm39) N582K probably damaging Het
Tnfrsf11b G A 15: 54,119,578 (GRCm39) probably benign Het
Trim30a A G 7: 104,060,348 (GRCm39) V476A probably damaging Het
Ugt1a8 A G 1: 88,015,770 (GRCm39) E61G possibly damaging Het
Vmn1r75 A T 7: 11,614,757 (GRCm39) N163I possibly damaging Het
Vps35l A G 7: 118,345,613 (GRCm39) T49A possibly damaging Het
Zfp119a G A 17: 56,173,520 (GRCm39) L108F probably benign Het
Other mutations in Gm7104
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0630:Gm7104 UTSW 12 88,252,479 (GRCm39) unclassified noncoding transcript
R1485:Gm7104 UTSW 12 88,252,333 (GRCm39) unclassified noncoding transcript
R2044:Gm7104 UTSW 12 88,252,551 (GRCm39) unclassified noncoding transcript
R2567:Gm7104 UTSW 12 88,252,242 (GRCm39) unclassified noncoding transcript
R3177:Gm7104 UTSW 12 88,252,498 (GRCm39) unclassified noncoding transcript
R3277:Gm7104 UTSW 12 88,252,498 (GRCm39) unclassified noncoding transcript
R3778:Gm7104 UTSW 12 88,252,441 (GRCm39) unclassified noncoding transcript
R3946:Gm7104 UTSW 12 88,252,812 (GRCm39) unclassified noncoding transcript
R4754:Gm7104 UTSW 12 88,252,765 (GRCm39) unclassified noncoding transcript
R5022:Gm7104 UTSW 12 88,252,529 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- ACCTGAAGCAAAAGCTCTGG -3'
(R):5'- TCATTGGACACAGCCTGGAG -3'

Sequencing Primer
(F):5'- AGGCATGTGGTCAGCTATCAC -3'
(R):5'- GAGCGACCTACTGGCTCTCAAAG -3'
Posted On 2015-04-17