Incidental Mutation 'IGL01605:Gm2046'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm2046
Ensembl Gene ENSMUSG00000079030
Gene Namepredicted gene 2046
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01605
Quality Score
Chromosomal Location87973528-87980224 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to T at 87973760 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect
SMART Domains Protein: ENSMUSP00000105775
Gene: ENSMUSG00000079030

low complexity region 3 25 N/A INTRINSIC
eIF1a 28 110 6.82e-46 SMART
low complexity region 125 144 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222774
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Brip1 T A 11: 86,062,004 T984S possibly damaging Het
Cdh17 T C 4: 11,795,670 Y417H probably damaging Het
Chd7 T A 4: 8,833,834 I1196N probably damaging Het
Cyp3a57 T C 5: 145,387,044 F447S probably damaging Het
Dock8 C T 19: 25,089,888 probably benign Het
Fam163b A G 2: 27,112,676 F103S probably damaging Het
G0s2 A G 1: 193,272,656 L40P probably damaging Het
Gucy1b1 C T 3: 82,035,353 R494Q probably benign Het
Hsd17b1 T C 11: 101,078,929 V89A probably damaging Het
Iqcg T C 16: 33,016,978 probably benign Het
Lmo7 T C 14: 101,910,756 probably benign Het
Mmp17 A G 5: 129,601,944 D331G probably benign Het
Mnx1 T C 5: 29,477,593 D228G unknown Het
Msh2 T C 17: 87,696,489 probably benign Het
Pabpc1 A G 15: 36,599,306 Y382H probably benign Het
Prl7b1 A G 13: 27,602,044 S214P possibly damaging Het
Ptk2 C T 15: 73,264,339 probably benign Het
Rbpj-ps3 T C 6: 46,530,091 probably benign Het
Sgsm1 A T 5: 113,285,665 M162K possibly damaging Het
Skint2 A G 4: 112,625,994 T199A probably benign Het
Stim1 A G 7: 102,386,115 D100G possibly damaging Het
Taar5 C T 10: 23,971,064 T120I probably benign Het
Trhde A G 10: 114,787,943 V352A probably benign Het
Ubap2 T A 4: 41,227,237 D160V probably damaging Het
Vmn2r18 A G 5: 151,586,641 V89A possibly damaging Het
Wbp1l A G 19: 46,654,400 D264G possibly damaging Het
Other mutations in Gm2046
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01602:Gm2046 APN 12 87973760 unclassified noncoding transcript
R1298:Gm2046 UTSW 12 87980083 missense probably benign 0.00
R2337:Gm2046 UTSW 12 87980178 missense unknown
R4641:Gm2046 UTSW 12 87980082 missense probably benign 0.03
R8185:Gm2046 UTSW 12 87973663 missense noncoding transcript
R8234:Gm2046 UTSW 12 87973738 missense noncoding transcript
Posted On2015-04-16