Incidental Mutation 'IGL01366:AK157302'
ID75957
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol AK157302
Ensembl Gene ENSMUSG00000078139
Gene NamecDNA sequence AK157302
Synonyms
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.944) question?
Stock #IGL01366
Quality Score
Status
Chromosome13
Chromosomal Location21495223-21497146 bp(+) (GRCm38)
Type of Mutationutr 5 prime
DNA Base Change (assembly) T to A at 21495301 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100547 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000104942]
Predicted Effect probably benign
Transcript: ENSMUST00000104942
SMART Domains Protein: ENSMUSP00000100547
Gene: ENSMUSG00000078139

DomainStartEndE-ValueType
Pfam:Fe-S_biosyn 23 125 7e-24 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310002L09Rik A T 4: 73,950,700 probably benign Het
Adamts2 T C 11: 50,796,468 Y1041H probably damaging Het
Adck5 A C 15: 76,595,616 *568C probably null Het
Bmpr2 G T 1: 59,813,677 G56W probably damaging Het
Capn11 A C 17: 45,653,200 I146S probably damaging Het
Ccdc162 A T 10: 41,580,306 D1613E possibly damaging Het
Ccdc167 T C 17: 29,705,312 E50G probably damaging Het
Col5a2 G T 1: 45,391,888 P864Q possibly damaging Het
Col7a1 C T 9: 108,977,119 probably benign Het
Crebbp T A 16: 4,126,506 H556L probably damaging Het
Dcpp1 T A 17: 23,882,736 I153N possibly damaging Het
Dgke C T 11: 89,055,386 R196H probably benign Het
Efr3a T A 15: 65,851,150 I459K probably benign Het
Espl1 T A 15: 102,319,836 C1682S probably benign Het
Exosc3 C T 4: 45,317,747 R185H probably damaging Het
Fam160b2 G A 14: 70,585,373 R688C probably damaging Het
Fgd6 T C 10: 94,043,476 V64A possibly damaging Het
Gata3 A G 2: 9,877,465 L42P probably damaging Het
Ggta1 C A 2: 35,402,450 E282* probably null Het
Ghr T C 15: 3,320,187 D503G probably damaging Het
Gls C T 1: 52,168,399 G602D probably damaging Het
Gm2058 A G 7: 39,589,234 noncoding transcript Het
Grb7 T C 11: 98,452,274 probably benign Het
Ifngr1 A T 10: 19,609,600 H449L probably damaging Het
Ighg2b T G 12: 113,307,036 D158A possibly damaging Het
Nphs2 T C 1: 156,311,035 V83A probably benign Het
Parp6 T A 9: 59,636,713 M390K possibly damaging Het
Pask T C 1: 93,310,852 K1304E probably benign Het
Scai A G 2: 39,106,961 S274P probably benign Het
Sik2 A G 9: 50,907,463 S404P probably damaging Het
Slc7a8 A T 14: 54,781,188 I47N probably damaging Het
Tas2r113 A T 6: 132,893,797 I263F probably benign Het
Tdrd1 T A 19: 56,855,302 D737E probably benign Het
Trio T C 15: 27,732,868 T2976A possibly damaging Het
Ttc28 T C 5: 111,085,171 probably null Het
Vmn1r21 A G 6: 57,843,814 I215T probably benign Het
Other mutations in AK157302
AlleleSourceChrCoordTypePredicted EffectPPH Score
Benjamin UTSW 13 21495663 missense possibly damaging 0.84
R0610:AK157302 UTSW 13 21495663 missense possibly damaging 0.84
R2155:AK157302 UTSW 13 21495657 nonsense probably null
R2378:AK157302 UTSW 13 21495562 missense possibly damaging 0.69
R4291:AK157302 UTSW 13 21495545 missense probably damaging 1.00
R4477:AK157302 UTSW 13 21495691 missense possibly damaging 0.51
R5887:AK157302 UTSW 13 21495409 missense possibly damaging 0.95
R6608:AK157302 UTSW 13 21495624 missense probably damaging 0.99
Posted On2013-10-07