Incidental Mutation 'IGL02401:Gm9312'
ID 291877
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9312
Ensembl Gene ENSMUSG00000096279
Gene Name predicted gene 9312
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02401
Quality Score
Status
Chromosome 12
Chromosomal Location (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to C at 24302106 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: ENSMUST00000169148
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef18 C T 8: 3,487,078 (GRCm39) R266C probably damaging Het
Asb11 A T X: 163,241,753 (GRCm39) probably benign Het
Cnot1 G A 8: 96,482,761 (GRCm39) T764M possibly damaging Het
Galns A G 8: 123,331,938 (GRCm39) M59T probably damaging Het
Gm5884 A G 6: 128,622,377 (GRCm39) noncoding transcript Het
Lama3 T C 18: 12,690,784 (GRCm39) F1268S probably benign Het
Lrp5 A G 19: 3,643,585 (GRCm39) C1347R probably damaging Het
Lrrfip1 T C 1: 91,042,650 (GRCm39) S352P probably benign Het
Mcfd2 T C 17: 87,564,592 (GRCm39) T97A probably damaging Het
Mroh2b A G 15: 4,929,983 (GRCm39) N23S possibly damaging Het
Nr1i3 A T 1: 171,043,942 (GRCm39) probably benign Het
Or4c10b T C 2: 89,711,797 (GRCm39) F209S probably damaging Het
Or8b48 C T 9: 38,492,651 (GRCm39) P26L probably damaging Het
Orm2 A C 4: 63,281,568 (GRCm39) I100L probably benign Het
Pbsn A G X: 76,886,129 (GRCm39) M126T probably benign Het
Rpgr G T X: 10,024,956 (GRCm39) T1026K possibly damaging Het
Sdhaf3 C T 6: 7,038,855 (GRCm39) T59M probably benign Het
Shq1 T C 6: 100,625,208 (GRCm39) Y217C probably damaging Het
Slc17a8 A T 10: 89,412,522 (GRCm39) probably null Het
Slc6a19 A G 13: 73,848,709 (GRCm39) I15T probably damaging Het
Smarcd3 A T 5: 24,798,717 (GRCm39) V335E probably damaging Het
Sugp2 A G 8: 70,695,821 (GRCm39) T265A possibly damaging Het
Tfrc T G 16: 32,435,999 (GRCm39) S225R probably damaging Het
Vsig10l T A 7: 43,113,468 (GRCm39) L140Q probably damaging Het
Zbtb46 T A 2: 181,065,245 (GRCm39) T302S probably benign Het
Znhit1 T C 5: 137,011,513 (GRCm39) Y105C probably damaging Het
Other mutations in Gm9312
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02197:Gm9312 APN 12 24,302,163 (GRCm39) exon noncoding transcript
R1688:Gm9312 UTSW 12 24,301,920 (GRCm39) unclassified noncoding transcript
R4332:Gm9312 UTSW 12 24,302,095 (GRCm39) exon noncoding transcript
Posted On 2015-04-16