Incidental Mutation 'IGL01458:Eif1ad4'
ID 84867
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Eif1ad4
Ensembl Gene ENSMUSG00000113971
Gene Name eukaryotic translation initiation factor 1A domain containing 4
Synonyms Gm2022
Accession Numbers
Essential gene? Not available question?
Stock # IGL01458
Quality Score
Status
Chromosome 12
Chromosomal Location 87862140-87862574 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 87862158 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 7 (K7*)
Gene Model predicted gene model for transcript(s): [ENSMUST00000220585]
AlphaFold A0A1Y7VLT7
Predicted Effect probably null
Transcript: ENSMUST00000095510
AA Change: K7*
SMART Domains Protein: ENSMUSP00000093166
Gene: ENSMUSG00000071217
AA Change: K7*

DomainStartEndE-ValueType
low complexity region 3 25 N/A INTRINSIC
eIF1a 28 110 3.65e-46 SMART
low complexity region 125 144 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182298
Predicted Effect probably null
Transcript: ENSMUST00000220585
AA Change: K7*
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930433N12Rik A T 9: 3,134,008 (GRCm39) noncoding transcript Het
Akap12 A G 10: 4,304,060 (GRCm39) E290G probably damaging Het
Akap6 T A 12: 52,933,601 (GRCm39) C364* probably null Het
Akr1c18 A T 13: 4,187,143 (GRCm39) Y198N probably damaging Het
Aurka T C 2: 172,210,899 (GRCm39) probably benign Het
Bloc1s6 T A 2: 122,586,135 (GRCm39) probably null Het
Clca3a1 C T 3: 144,713,539 (GRCm39) M697I probably benign Het
Csn2 T C 5: 87,843,879 (GRCm39) probably benign Het
Dsc1 T C 18: 20,232,195 (GRCm39) E271G probably damaging Het
Evi5 G A 5: 107,963,513 (GRCm39) A354V probably damaging Het
Fcer2a T A 8: 3,738,151 (GRCm39) R137S probably benign Het
Fto A G 8: 92,168,344 (GRCm39) T266A probably benign Het
Fzd4 G A 7: 89,053,943 (GRCm39) V17I unknown Het
Gadd45b T C 10: 80,767,075 (GRCm39) L105P probably damaging Het
Galntl6 T C 8: 58,880,743 (GRCm39) S137G probably damaging Het
Gpr135 T C 12: 72,116,442 (GRCm39) M442V probably benign Het
Kcnq1 T A 7: 142,748,015 (GRCm39) Y330* probably null Het
Kdm5b A G 1: 134,549,724 (GRCm39) R1106G possibly damaging Het
Lrrc8e C T 8: 4,286,141 (GRCm39) R789W probably damaging Het
Myo16 T C 8: 10,485,853 (GRCm39) L644P probably damaging Het
Nbeal1 G T 1: 60,281,784 (GRCm39) probably null Het
Nlrp4c T C 7: 6,103,783 (GRCm39) C906R possibly damaging Het
Or10ag56 C T 2: 87,139,826 (GRCm39) T251I probably damaging Het
Or1e29 A T 11: 73,667,532 (GRCm39) I207N probably benign Het
Or1j15 T A 2: 36,458,754 (GRCm39) L48H probably damaging Het
Ovgp1 A G 3: 105,882,307 (GRCm39) N70D probably benign Het
Panx3 A T 9: 37,572,443 (GRCm39) M369K probably damaging Het
Plet1 A G 9: 50,406,017 (GRCm39) N52S probably benign Het
Prss1l T G 6: 41,373,621 (GRCm39) D161E probably benign Het
Psg18 A T 7: 18,088,741 (GRCm39) M1K probably null Het
Ptprz1 A T 6: 22,972,843 (GRCm39) D251V probably damaging Het
Serpinb6a A G 13: 34,114,064 (GRCm39) Y88H possibly damaging Het
Siglecf G A 7: 43,004,562 (GRCm39) R297Q possibly damaging Het
Tbx15 T C 3: 99,223,544 (GRCm39) V244A probably damaging Het
Top2a A T 11: 98,901,856 (GRCm39) L458Q probably damaging Het
Trim39 A G 17: 36,574,855 (GRCm39) probably benign Het
Vps37c T C 19: 10,687,781 (GRCm39) C81R probably damaging Het
Wdr62 A T 7: 29,941,187 (GRCm39) S744T probably benign Het
Zyg11a G A 4: 108,062,099 (GRCm39) T234I probably damaging Het
Other mutations in Eif1ad4
AlleleSourceChrCoordTypePredicted EffectPPH Score
R7361:Eif1ad4 UTSW 12 87,862,170 (GRCm39) missense unknown
R7803:Eif1ad4 UTSW 12 87,862,269 (GRCm39) missense probably benign 0.03
R9484:Eif1ad4 UTSW 12 87,862,249 (GRCm39) missense possibly damaging 0.57
R9570:Eif1ad4 UTSW 12 87,862,534 (GRCm39) missense unknown
Posted On 2013-11-11