Incidental Mutation 'IGL01605:Gm2046'
ID278749
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm2046
Ensembl Gene ENSMUSG00000079030
Gene Namepredicted gene 2046
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01605
Quality Score
Status
Chromosome12
Chromosomal Location87973528-87980224 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to T at 87973760 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect
SMART Domains Protein: ENSMUSP00000105775
Gene: ENSMUSG00000079030

DomainStartEndE-ValueType
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