Incidental Mutation 'IGL01605:Eif1ad5'
ID 278749
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Eif1ad5
Ensembl Gene ENSMUSG00000079030
Gene Name eukaryotic translation initiation factor 1A domain containing 5
Synonyms Gm2046
Accession Numbers
Essential gene? Not available question?
Stock # IGL01605
Quality Score
Status
Chromosome 12
Chromosomal Location 87937598-87947001 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 87940530 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
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: 85,952,830 (GRCm39) T984S possibly damaging Het
Cdh17 T C 4: 11,795,670 (GRCm39) Y417H probably damaging Het
Chd7 T A 4: 8,833,834 (GRCm39) I1196N probably damaging Het
Cyp3a57 T C 5: 145,323,854 (GRCm39) F447S probably damaging Het
Dock8 C T 19: 25,067,252 (GRCm39) probably benign Het
Fam163b A G 2: 27,002,688 (GRCm39) F103S probably damaging Het
G0s2 A G 1: 192,954,964 (GRCm39) L40P probably damaging Het
Gucy1b1 C T 3: 81,942,660 (GRCm39) R494Q probably benign Het
Hsd17b1 T C 11: 100,969,755 (GRCm39) V89A probably damaging Het
Iqcg T C 16: 32,837,348 (GRCm39) probably benign Het
Lmo7 T C 14: 102,148,192 (GRCm39) probably benign Het
Mmp17 A G 5: 129,679,008 (GRCm39) D331G probably benign Het
Mnx1 T C 5: 29,682,591 (GRCm39) D228G unknown Het
Msh2 T C 17: 88,003,917 (GRCm39) probably benign Het
Pabpc1 A G 15: 36,599,550 (GRCm39) Y382H probably benign Het
Prl7b1 A G 13: 27,786,027 (GRCm39) S214P possibly damaging Het
Ptk2 C T 15: 73,136,188 (GRCm39) probably benign Het
Rbpj-ps3 T C 6: 46,507,025 (GRCm39) probably benign Het
Sgsm1 A T 5: 113,433,531 (GRCm39) M162K possibly damaging Het
Skint2 A G 4: 112,483,191 (GRCm39) T199A probably benign Het
Stim1 A G 7: 102,035,322 (GRCm39) D100G possibly damaging Het
Taar5 C T 10: 23,846,962 (GRCm39) T120I probably benign Het
Trhde A G 10: 114,623,848 (GRCm39) V352A probably benign Het
Ubap2 T A 4: 41,227,237 (GRCm39) D160V probably damaging Het
Vmn2r18 A G 5: 151,510,106 (GRCm39) V89A possibly damaging Het
Wbp1l A G 19: 46,642,839 (GRCm39) D264G possibly damaging Het
Other mutations in Eif1ad5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01602:Eif1ad5 APN 12 87,940,530 (GRCm39) unclassified noncoding transcript
R1298:Eif1ad5 UTSW 12 87,946,853 (GRCm39) missense probably benign 0.00
R2337:Eif1ad5 UTSW 12 87,946,948 (GRCm39) missense unknown
R4641:Eif1ad5 UTSW 12 87,946,852 (GRCm39) missense probably benign 0.03
R8185:Eif1ad5 UTSW 12 87,940,433 (GRCm39) missense noncoding transcript
R8234:Eif1ad5 UTSW 12 87,940,508 (GRCm39) missense noncoding transcript
Posted On 2015-04-16