Incidental Mutation 'IGL02505:Aldoa'
ID296253
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Aldoa
Ensembl Gene ENSMUSG00000114515
Gene Name
SynonymsAldo-1, Aldo1
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #IGL02505
Quality Score
Status
Chromosome7
Chromosomal Location126800790-126809108 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 126795994 bp
ZygosityHeterozygous
Amino Acid Change Alanine to Glutamic Acid at position 252 (A252E)
Ref Sequence ENSEMBL: ENSMUSP00000101955 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032934] [ENSMUST00000032936] [ENSMUST00000087566] [ENSMUST00000106348] [ENSMUST00000133514] [ENSMUST00000141355] [ENSMUST00000151137] [ENSMUST00000153686] [ENSMUST00000205324] [ENSMUST00000205336] [ENSMUST00000205890] [ENSMUST00000205935] [ENSMUST00000206570] [ENSMUST00000207534]
Predicted Effect probably damaging
Transcript: ENSMUST00000032934
AA Change: A252E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000032934
Gene: ENSMUSG00000030695
AA Change: A252E

DomainStartEndE-ValueType
Pfam:Glycolytic 15 364 1.2e-179 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000032936
SMART Domains Protein: ENSMUSP00000032936
Gene: ENSMUSG00000030697

DomainStartEndE-ValueType
PP2Ac 20 290 4.04e-147 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000087566
AA Change: A306E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000084846
Gene: ENSMUSG00000030695
AA Change: A306E

DomainStartEndE-ValueType
signal peptide 1 29 N/A INTRINSIC
Pfam:Glycolytic 69 418 2.8e-193 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000106348
AA Change: A252E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000101955
Gene: ENSMUSG00000030695
AA Change: A252E

DomainStartEndE-ValueType
Pfam:Glycolytic 15 364 1.2e-179 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000133514
SMART Domains Protein: ENSMUSP00000114587
Gene: ENSMUSG00000030695

DomainStartEndE-ValueType
signal peptide 1 29 N/A INTRINSIC
Pfam:Glycolytic 69 193 5.4e-59 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135707
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139657
Predicted Effect probably benign
Transcript: ENSMUST00000141355
SMART Domains Protein: ENSMUSP00000117349
Gene: ENSMUSG00000030695

DomainStartEndE-ValueType
Pfam:Glycolytic 15 131 7.5e-53 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143509
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147748
Predicted Effect probably benign
Transcript: ENSMUST00000151137
SMART Domains Protein: ENSMUSP00000118417
Gene: ENSMUSG00000030695

DomainStartEndE-ValueType
Pfam:Glycolytic 15 237 6.9e-121 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000153686
Predicted Effect probably benign
Transcript: ENSMUST00000205324
Predicted Effect probably benign
Transcript: ENSMUST00000205336
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205862
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205879
Predicted Effect probably benign
Transcript: ENSMUST00000205890
Predicted Effect probably benign
Transcript: ENSMUST00000205935
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205950
Predicted Effect probably benign
Transcript: ENSMUST00000206334
Predicted Effect probably benign
Transcript: ENSMUST00000206570
Predicted Effect probably benign
Transcript: ENSMUST00000207534
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10. [provided by RefSeq, Aug 2011]
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aagab C A 9: 63,616,814 L68M probably damaging Het
Abca13 T G 11: 9,581,498 L4575W probably damaging Het
Abcb11 A T 2: 69,245,761 V1201D probably damaging Het
Ap1b1 C T 11: 5,031,700 A536V probably benign Het
Arhgef3 A G 14: 27,394,000 H233R possibly damaging Het
Arhgef40 A T 14: 52,000,863 E1266D probably damaging Het
Atp1a4 C T 1: 172,235,075 V622M probably damaging Het
Aup1 A G 6: 83,055,277 T142A probably benign Het
Bcl6 A T 16: 23,977,569 I36N probably damaging Het
Best1 A G 19: 9,989,150 S358P probably damaging Het
Cadps T G 14: 12,449,759 Q1150P probably damaging Het
Capn5 T A 7: 98,131,196 E322D possibly damaging Het
Ccdc94 G T 17: 55,962,051 G53V probably damaging Het
Cd300ld2 A T 11: 115,013,687 M118K probably benign Het
Cdh9 T C 15: 16,855,989 L705P probably damaging Het
Cep170b T G 12: 112,743,070 N436K probably damaging Het
Chil6 T A 3: 106,405,962 I24F probably benign Het
Chmp2a T A 7: 13,033,855 K48* probably null Het
Col19a1 C T 1: 24,300,584 probably benign Het
Cops7b C A 1: 86,592,321 Q65K probably benign Het
Cyp2e1 T A 7: 140,769,156 L133H probably damaging Het
Dirc2 G T 16: 35,735,558 D177E probably benign Het
Dkc1 T C X: 75,108,733 probably benign Het
Erlec1 A G 11: 30,950,767 Y134H probably damaging Het
F8 C A X: 75,379,598 probably benign Het
Fus G A 7: 127,981,507 R252Q possibly damaging Het
Fzd3 A T 14: 65,253,106 D9E probably benign Het
Gm15821 T C 17: 34,214,285 probably benign Het
Gm5117 C A 8: 31,738,316 noncoding transcript Het
H2afy A G 13: 56,074,330 V336A probably damaging Het
H2-Q6 A G 17: 35,425,176 I45V probably benign Het
Hectd1 A G 12: 51,800,713 probably null Het
Ifi204 T C 1: 173,755,654 K333E probably benign Het
Ildr1 G A 16: 36,716,164 G185D probably damaging Het
Itgb2 G A 10: 77,547,218 D141N probably damaging Het
Kdm1b G T 13: 47,060,855 D226Y probably damaging Het
Krt77 A G 15: 101,860,946 L460P probably damaging Het
Lamp3 A G 16: 19,655,457 I389T possibly damaging Het
Mars C A 10: 127,304,244 E414* probably null Het
Mpg T C 11: 32,230,042 V190A probably damaging Het
Myh15 A G 16: 49,117,263 I742M possibly damaging Het
Nell2 A T 15: 95,296,263 probably benign Het
Nmur1 T C 1: 86,386,335 D370G probably benign Het
Npsr1 A G 9: 24,098,282 E28G probably benign Het
Olfr569 T C 7: 102,887,607 E182G probably damaging Het
Olfr679 A T 7: 105,086,333 I206L probably benign Het
Olfr8 G T 10: 78,955,933 V243F probably benign Het
Olfr876 G A 9: 37,804,331 C140Y probably benign Het
Pdzrn3 T C 6: 101,151,938 N589S possibly damaging Het
Pkd1l3 T C 8: 109,633,216 L901P probably damaging Het
Plekhg1 G T 10: 3,957,139 K685N probably damaging Het
Prim1 T A 10: 128,029,783 *419R probably null Het
Ptk2b G T 14: 66,154,243 N905K probably damaging Het
Rbm34 T C 8: 126,949,321 I395V probably benign Het
Rfx1 A G 8: 84,095,809 E912G possibly damaging Het
Rngtt T C 4: 33,337,936 V253A possibly damaging Het
Slc2a9 A G 5: 38,436,659 Y169H possibly damaging Het
Susd4 C A 1: 182,892,080 T420K probably benign Het
Tdrd3 G A 14: 87,511,682 G676D probably damaging Het
Tec T C 5: 72,789,244 K47E probably damaging Het
Tenm2 C A 11: 36,051,916 G1308* probably null Het
Tmprss15 A T 16: 78,987,741 D675E probably benign Het
Vmn1r84 A G 7: 12,362,419 C104R probably damaging Het
Vmn2r49 T A 7: 9,976,451 M785L probably benign Het
Vmn2r85 G T 10: 130,425,580 T296K probably damaging Het
Wdr3 C T 3: 100,151,974 S343N probably benign Het
Zfp143 A T 7: 110,091,786 M515L possibly damaging Het
Zfp735 A G 11: 73,689,800 I42V probably benign Het
Zswim5 A T 4: 116,962,552 M385L probably benign Het
Other mutations in Aldoa
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01090:Aldoa APN 7 126796035 missense probably benign 0.22
IGL01743:Aldoa APN 7 126796703 missense probably damaging 0.97
R2079:Aldoa UTSW 7 126796904 missense probably null 1.00
R2141:Aldoa UTSW 7 126797642 critical splice donor site probably null
R4650:Aldoa UTSW 7 126797707 missense possibly damaging 0.95
R7144:Aldoa UTSW 7 126796862 missense possibly damaging 0.91
Posted On2015-04-16