Incidental Mutation 'R5146:Gm14415'
ID 395106
Institutional Source Beutler Lab
Gene Symbol Gm14415
Ensembl Gene ENSMUSG00000082377
Gene Name predicted gene 14415
Synonyms
MMRRC Submission 042730-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.194) question?
Stock # R5146 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 176795357-176798281 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 176796024 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: ENSMUST00000118260
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.5%
Validation Efficiency 97% (35/36)
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik A G 12: 71,289,799 (GRCm39) D1498G possibly damaging Het
Adcyap1r1 A G 6: 55,461,957 (GRCm39) I329V probably benign Het
Ahnak2 A C 12: 112,742,160 (GRCm39) H637Q probably benign Het
Carmil3 A G 14: 55,734,636 (GRCm39) D455G probably benign Het
Cdh20 A G 1: 109,922,042 (GRCm39) T45A probably damaging Het
Chil4 T A 3: 106,110,150 (GRCm39) T315S probably benign Het
Cntnap5c T C 17: 58,320,842 (GRCm39) V138A probably damaging Het
Csmd1 T C 8: 16,246,204 (GRCm39) D1065G probably damaging Het
Cspp1 C T 1: 10,145,101 (GRCm39) R296* probably null Het
Dnah17 A G 11: 118,005,005 (GRCm39) M793T probably damaging Het
Dock4 A G 12: 40,699,491 (GRCm39) probably null Het
Fgfr4 G T 13: 55,313,725 (GRCm39) L511F probably damaging Het
Gpam A G 19: 55,082,378 (GRCm39) V91A probably damaging Het
Grin2b T A 6: 135,756,340 (GRCm39) I462F probably damaging Het
Grwd1 A T 7: 45,477,258 (GRCm39) F210I probably damaging Het
H2-T9 A G 17: 36,439,907 (GRCm39) W76R probably damaging Het
Itfg1 T C 8: 86,445,497 (GRCm39) *611W probably null Het
Kcna2 T C 3: 107,012,814 (GRCm39) V465A probably benign Het
Mfng C T 15: 78,648,588 (GRCm39) R163H probably benign Het
Myo15b A G 11: 115,782,024 (GRCm39) T1444A probably benign Het
Nlgn3 G A X: 100,361,891 (GRCm39) V287I probably benign Het
Oas1c A G 5: 120,940,159 (GRCm39) S336P probably benign Het
Pirb T C 7: 3,715,620 (GRCm39) probably benign Het
Pot1b A T 17: 55,979,865 (GRCm39) Y330* probably null Het
Rnf20 A T 4: 49,651,456 (GRCm39) M641L probably benign Het
Sppl2b T C 10: 80,703,474 (GRCm39) *579Q probably null Het
Sumf1 G A 6: 108,162,271 (GRCm39) P83S probably benign Het
Tmem101 C T 11: 102,045,450 (GRCm39) R133Q probably benign Het
Ttn G A 2: 76,700,707 (GRCm39) probably benign Het
Vmn2r84 A G 10: 130,221,971 (GRCm39) Y750H probably damaging Het
Zfp873 A G 10: 81,896,058 (GRCm39) Y300C probably damaging Het
Other mutations in Gm14415
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4895:Gm14415 UTSW 2 176,796,114 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- GTGTGAAGATGACTGTTTTGTACA -3'
(R):5'- TGTACTGGAGAGCAACCCTC -3'

Sequencing Primer
(F):5'- GTAGAATGTCTTCAGAACTTTGCCG -3'
(R):5'- GCCTTTCCCAAAAGAAGTACTCTTGG -3'
Posted On 2016-06-21