Incidental Mutation 'IGL01959:Gm3298'
ID 182303
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm3298
Ensembl Gene ENSMUSG00000079383
Gene Name predicted gene 3298
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01959
Quality Score
Status
Chromosome 14
Chromosomal Location 17451096-17453882 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 5018731 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Leucine to Serine at position 162 (L162S)
Ref Sequence ENSEMBL: ENSMUSP00000131718 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165289] [ENSMUST00000172110]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000165289
SMART Domains Protein: ENSMUSP00000126766
Gene: ENSMUSG00000079383

DomainStartEndE-ValueType
Pfam:Takusan 46 129 1.5e-32 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000172110
AA Change: L162S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000131718
Gene: ENSMUSG00000079383
AA Change: L162S

DomainStartEndE-ValueType
Pfam:Takusan 48 128 3.9e-23 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9230009I02Rik T C 11: 50,982,645 (GRCm39) noncoding transcript Het
Aip A G 19: 4,171,397 (GRCm39) I13T probably damaging Het
Cacna2d1 C T 5: 16,417,895 (GRCm39) P140S probably benign Het
Cald1 A G 6: 34,730,403 (GRCm39) D40G probably damaging Het
Cep250 T A 2: 155,825,279 (GRCm39) V1052E possibly damaging Het
Chd1 A G 17: 15,962,435 (GRCm39) N731D probably damaging Het
Chml C T 1: 175,515,166 (GRCm39) V252I probably benign Het
Cog8 T C 8: 107,783,010 (GRCm39) Y93C probably damaging Het
Creld1 G A 6: 113,469,794 (GRCm39) A399T probably damaging Het
Cyp2a4 T A 7: 26,007,133 (GRCm39) V80E probably damaging Het
Cyp2c37 T A 19: 39,984,277 (GRCm39) L255* probably null Het
Cyp2d12 C A 15: 82,439,545 (GRCm39) probably benign Het
Dimt1 A G 13: 107,089,963 (GRCm39) I229V probably benign Het
Dsc1 G A 18: 20,230,282 (GRCm39) T341I probably damaging Het
Ercc3 T A 18: 32,390,411 (GRCm39) F567I probably damaging Het
Espl1 C A 15: 102,214,097 (GRCm39) probably benign Het
Fcrl2 T C 3: 87,166,939 (GRCm39) D18G probably damaging Het
Fnip1 T A 11: 54,381,738 (GRCm39) S296R possibly damaging Het
Fzd5 C A 1: 64,775,105 (GRCm39) A219S possibly damaging Het
Gbp7 A G 3: 142,247,108 (GRCm39) probably benign Het
Hspa1l A G 17: 35,196,111 (GRCm39) E50G probably damaging Het
Ipo9 T C 1: 135,348,093 (GRCm39) probably null Het
Kazn A G 4: 141,878,195 (GRCm39) L185P probably damaging Het
Kcnh8 T C 17: 53,141,635 (GRCm39) S293P probably damaging Het
Lrp1b T C 2: 41,202,539 (GRCm39) T1191A probably damaging Het
Mnat1 A G 12: 73,228,705 (GRCm39) probably benign Het
Msx2 C T 13: 53,622,638 (GRCm39) probably benign Het
Ndufs2 T G 1: 171,064,798 (GRCm39) I317L probably benign Het
Nms T C 1: 38,981,006 (GRCm39) probably benign Het
Oosp3 T A 19: 11,678,286 (GRCm39) F87L probably benign Het
Pask A G 1: 93,262,329 (GRCm39) V177A probably benign Het
Poldip2 G T 11: 78,403,133 (GRCm39) probably benign Het
Prr14l A T 5: 32,987,549 (GRCm39) S649T possibly damaging Het
Slc6a18 T A 13: 73,825,984 (GRCm39) N22I probably damaging Het
Smco2 T A 6: 146,763,208 (GRCm39) S228T probably benign Het
Speer4a1 G A 5: 26,240,902 (GRCm39) Q197* probably null Het
Speg A G 1: 75,367,734 (GRCm39) K641R probably damaging Het
Strip2 G A 6: 29,928,553 (GRCm39) V286M probably damaging Het
Tnfrsf22 C T 7: 143,197,012 (GRCm39) probably null Het
Tnpo3 A G 6: 29,589,019 (GRCm39) probably benign Het
Top2b T A 14: 16,422,695 (GRCm38) N1377K probably benign Het
Trmt1 T A 8: 85,418,005 (GRCm39) probably null Het
Trpm1 A G 7: 63,858,723 (GRCm39) M266V possibly damaging Het
Vmn1r199 A G 13: 22,567,290 (GRCm39) T195A probably benign Het
Vmn2r10 A G 5: 109,145,571 (GRCm39) V512A probably benign Het
Zfp777 A G 6: 48,021,275 (GRCm39) F116L probably benign Het
Zp3r T A 1: 130,519,188 (GRCm39) K253* probably null Het
Other mutations in Gm3298
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02394:Gm3298 APN 14 5,018,778 (GRCm38) missense probably benign 0.06
Posted On 2014-05-07