Incidental Mutation 'IGL02343:Aig1'
ID 289183
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Aig1
Ensembl Gene ENSMUSG00000019806
Gene Name androgen-induced 1
Synonyms 1500031O19Rik, CGI-103
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02343
Quality Score
Status
Chromosome 10
Chromosomal Location 13522798-13744724 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 13744418 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 29 (M29V)
Ref Sequence ENSEMBL: ENSMUSP00000125366 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000019942] [ENSMUST00000105534] [ENSMUST00000162610]
AlphaFold Q9D8B1
Predicted Effect probably damaging
Transcript: ENSMUST00000019942
AA Change: M29V

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000019942
Gene: ENSMUSG00000019806
AA Change: M29V

DomainStartEndE-ValueType
Pfam:Far-17a_AIG1 12 219 5.6e-77 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000105534
AA Change: M29V

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000101174
Gene: ENSMUSG00000019806
AA Change: M29V

DomainStartEndE-ValueType
Pfam:Far-17a_AIG1 12 178 3.4e-59 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161729
Predicted Effect probably damaging
Transcript: ENSMUST00000162610
AA Change: M29V

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000125366
Gene: ENSMUSG00000019806
AA Change: M29V

DomainStartEndE-ValueType
Pfam:Far-17a_AIG1 12 219 5.4e-74 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162869
Predicted Effect noncoding transcript
Transcript: ENSMUST00000220029
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acbd5 T A 2: 22,977,507 (GRCm39) N168K possibly damaging Het
Albfm1 C A 5: 90,727,473 (GRCm39) H364N probably damaging Het
Apba2 A G 7: 64,344,894 (GRCm39) E28G probably damaging Het
Bglap3 T C 3: 88,276,423 (GRCm39) N45S possibly damaging Het
Cables2 A G 2: 179,902,072 (GRCm39) probably null Het
Cd109 A G 9: 78,596,237 (GRCm39) probably benign Het
Cdk1 T C 10: 69,176,331 (GRCm39) N259D probably benign Het
Ces1h A G 8: 94,078,654 (GRCm39) *563R probably null Het
Cfap46 C T 7: 139,262,425 (GRCm39) A115T probably damaging Het
Cry2 A T 2: 92,257,266 (GRCm39) V101E possibly damaging Het
Cyp4a31 A G 4: 115,421,026 (GRCm39) Y38C probably damaging Het
Dip2a T C 10: 76,155,312 (GRCm39) Y130C probably benign Het
Eps8l1 A G 7: 4,475,123 (GRCm39) T366A probably benign Het
Esr2 C T 12: 76,192,119 (GRCm39) R303H probably benign Het
Fbxo41 T G 6: 85,455,153 (GRCm39) L617F possibly damaging Het
Fbxw15 A T 9: 109,381,723 (GRCm39) probably benign Het
Lrriq1 T A 10: 103,070,024 (GRCm39) probably benign Het
Me1 A T 9: 86,536,694 (GRCm39) probably null Het
Moxd1 G A 10: 24,155,762 (GRCm39) V289I probably damaging Het
Muc19 T G 15: 91,778,428 (GRCm39) noncoding transcript Het
Myo15b A G 11: 115,764,226 (GRCm39) probably benign Het
Nav1 A T 1: 135,382,490 (GRCm39) L1264* probably null Het
Nhlrc4 T C 17: 26,162,335 (GRCm39) *137W probably null Het
Nrxn3 A G 12: 88,762,123 (GRCm39) T57A probably damaging Het
Or10g3 T A 14: 52,609,934 (GRCm39) D192V probably damaging Het
Orc2 A T 1: 58,508,825 (GRCm39) probably null Het
Rpap2 G A 5: 107,766,047 (GRCm39) probably null Het
S100a9 T C 3: 90,602,531 (GRCm39) H21R probably damaging Het
Spz1 T A 13: 92,712,054 (GRCm39) M141L probably benign Het
Stk40 A G 4: 126,030,695 (GRCm39) Y305C probably damaging Het
Stra6l A G 4: 45,869,588 (GRCm39) Q218R probably damaging Het
T C A 17: 8,658,732 (GRCm39) probably benign Het
Tep1 T C 14: 51,066,704 (GRCm39) D2298G probably damaging Het
Trim40 A T 17: 37,200,030 (GRCm39) L16Q probably benign Het
Tubb4a T C 17: 57,388,538 (GRCm39) I163V probably benign Het
Vwc2 T A 11: 11,066,532 (GRCm39) C207S probably damaging Het
Zfp407 A G 18: 84,227,849 (GRCm39) I1920T possibly damaging Het
Zfp429 T C 13: 67,538,844 (GRCm39) E200G probably damaging Het
Zfp451 C T 1: 33,815,574 (GRCm39) C792Y probably damaging Het
Other mutations in Aig1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02715:Aig1 APN 10 13,744,360 (GRCm39) critical splice donor site probably null
R0697:Aig1 UTSW 10 13,705,069 (GRCm39) missense probably benign 0.01
R1699:Aig1 UTSW 10 13,744,366 (GRCm39) missense possibly damaging 0.85
R1761:Aig1 UTSW 10 13,566,328 (GRCm39) missense probably damaging 1.00
R3934:Aig1 UTSW 10 13,677,656 (GRCm39) missense probably damaging 1.00
R4397:Aig1 UTSW 10 13,528,726 (GRCm39) missense probably benign 0.00
R4736:Aig1 UTSW 10 13,677,674 (GRCm39) missense probably damaging 0.97
R4767:Aig1 UTSW 10 13,677,602 (GRCm39) missense probably damaging 1.00
R5081:Aig1 UTSW 10 13,677,644 (GRCm39) missense probably benign 0.01
R5907:Aig1 UTSW 10 13,677,528 (GRCm39) intron probably benign
R7944:Aig1 UTSW 10 13,744,417 (GRCm39) missense probably damaging 1.00
R9105:Aig1 UTSW 10 13,529,339 (GRCm39) missense probably benign 0.10
R9270:Aig1 UTSW 10 13,529,505 (GRCm39) splice site probably null
R9381:Aig1 UTSW 10 13,523,417 (GRCm39) missense probably benign 0.39
R9778:Aig1 UTSW 10 13,528,757 (GRCm39) critical splice acceptor site probably null
X0018:Aig1 UTSW 10 13,566,268 (GRCm39) nonsense probably null
Posted On 2015-04-16