Incidental Mutation 'IGL02578:Gm9892'
ID 299246
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9892
Ensembl Gene ENSMUSG00000052825
Gene Name predicted gene 9892
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.226) question?
Stock # IGL02578
Quality Score
Status
Chromosome 8
Chromosomal Location 52649100-52650091 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 52649328 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: ENSMUST00000182415
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 G A 7: 120,023,179 (GRCm39) probably null Het
Ago1 T A 4: 126,333,324 (GRCm39) D545V probably benign Het
Arid2 T C 15: 96,270,116 (GRCm39) S1410P probably benign Het
Cbfa2t3 T A 8: 123,360,187 (GRCm39) D488V possibly damaging Het
Cdx2 T C 5: 147,240,094 (GRCm39) D194G probably damaging Het
Cyp4a32 A G 4: 115,466,939 (GRCm39) Q208R possibly damaging Het
Degs1 A C 1: 182,106,592 (GRCm39) Y222* probably null Het
Dnah7a T A 1: 53,472,074 (GRCm39) E3564D probably benign Het
Dsg4 A T 18: 20,604,250 (GRCm39) I906F possibly damaging Het
Elovl3 A G 19: 46,123,132 (GRCm39) H236R possibly damaging Het
Foxp2 A G 6: 15,376,814 (GRCm39) probably benign Het
Herc2 A G 7: 55,756,283 (GRCm39) probably null Het
Hhat A G 1: 192,376,221 (GRCm39) V304A probably damaging Het
Il16 C T 7: 83,327,194 (GRCm39) probably null Het
Kansl1l G A 1: 66,840,848 (GRCm39) Q151* probably null Het
Kmt2c G T 5: 25,571,198 (GRCm39) probably benign Het
Krt39 T C 11: 99,412,032 (GRCm39) N18S probably benign Het
Lcor G T 19: 41,547,589 (GRCm39) G391V probably damaging Het
Mical2 A T 7: 111,950,580 (GRCm39) T845S probably benign Het
Mon1b G T 8: 114,365,455 (GRCm39) R261L possibly damaging Het
Mphosph8 C T 14: 56,911,667 (GRCm39) A230V probably benign Het
Myh2 T A 11: 67,077,517 (GRCm39) M884K probably benign Het
Nlrp3 T C 11: 59,439,227 (GRCm39) L268P probably damaging Het
Ntng1 T A 3: 110,042,710 (GRCm39) T39S probably benign Het
Or10ag58 T A 2: 87,265,401 (GRCm39) I190K probably damaging Het
Or1j14 A C 2: 36,418,156 (GRCm39) H244P probably damaging Het
Or5al7 A T 2: 85,993,073 (GRCm39) Y73* probably null Het
Pde4b T A 4: 102,112,494 (GRCm39) M26K possibly damaging Het
Polh G A 17: 46,505,218 (GRCm39) Q133* probably null Het
Postn A T 3: 54,284,625 (GRCm39) N647I possibly damaging Het
Scimp T A 11: 70,682,387 (GRCm39) I110F possibly damaging Het
Sell A G 1: 163,893,165 (GRCm39) D127G probably damaging Het
Serpinb12 G A 1: 106,883,220 (GRCm39) probably null Het
She A G 3: 89,739,373 (GRCm39) E188G probably damaging Het
Shisal2a C T 4: 108,225,225 (GRCm39) M112I probably benign Het
Slc22a1 T C 17: 12,886,126 (GRCm39) Y169C probably damaging Het
Slco2a1 C T 9: 102,923,957 (GRCm39) T57I probably damaging Het
Sox2 A T 3: 34,704,745 (GRCm39) M61L probably benign Het
Sra1 G A 18: 36,803,150 (GRCm39) Q32* probably null Het
Syne2 T A 12: 76,069,053 (GRCm39) S4340T possibly damaging Het
Ucn A C 5: 31,295,738 (GRCm39) W43G possibly damaging Het
Xdh C T 17: 74,213,241 (GRCm39) M836I probably damaging Het
Xirp2 T A 2: 67,341,591 (GRCm39) D1277E probably damaging Het
Other mutations in Gm9892
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02318:Gm9892 APN 8 52,649,260 (GRCm39) exon noncoding transcript
IGL02372:Gm9892 APN 8 52,649,871 (GRCm39) exon noncoding transcript
R0637:Gm9892 UTSW 8 52,649,860 (GRCm39) nonsense probably null
R1342:Gm9892 UTSW 8 52,649,458 (GRCm39) missense probably benign 0.20
R1473:Gm9892 UTSW 8 52,649,649 (GRCm39) missense possibly damaging 0.67
R4244:Gm9892 UTSW 8 52,649,435 (GRCm39) exon noncoding transcript
R5296:Gm9892 UTSW 8 52,649,964 (GRCm39) exon noncoding transcript
Posted On 2015-04-16