Incidental Mutation 'IGL01722:Apol11a'
ID 105146
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Apol11a
Ensembl Gene ENSMUSG00000091650
Gene Name apolipoprotein L 11a
Synonyms EG626615
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # IGL01722
Quality Score
Status
Chromosome 15
Chromosomal Location 77392329-77402074 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 77401307 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 265 (M265L)
Ref Sequence ENSEMBL: ENSMUSP00000132565 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172191]
AlphaFold E9PZG0
Predicted Effect probably benign
Transcript: ENSMUST00000172191
AA Change: M265L

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000132565
Gene: ENSMUSG00000091650
AA Change: M265L

DomainStartEndE-ValueType
Pfam:ApoL 28 328 1e-90 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr1c T A 2: 58,173,561 (GRCm39) probably benign Het
Alb G A 5: 90,618,698 (GRCm39) probably null Het
Ankrd9 A G 12: 110,943,797 (GRCm39) V46A probably damaging Het
Ccdc158 T C 5: 92,810,598 (GRCm39) N97D possibly damaging Het
Cobl T G 11: 12,203,987 (GRCm39) H823P probably benign Het
Dnaja2 A T 8: 86,279,908 (GRCm39) H90Q probably benign Het
Dpagt1 T C 9: 44,238,899 (GRCm39) F73S possibly damaging Het
Dph3 C T 14: 31,807,417 (GRCm39) E20K possibly damaging Het
Fbxl13 G T 5: 21,695,412 (GRCm39) T660K possibly damaging Het
Gask1a G A 9: 121,794,149 (GRCm39) S101N possibly damaging Het
Glt6d1 T C 2: 25,684,431 (GRCm39) T192A probably benign Het
Mroh7 C T 4: 106,560,358 (GRCm39) V649I probably benign Het
Mta3 T C 17: 84,063,072 (GRCm39) Y4H possibly damaging Het
Myh14 A G 7: 44,292,956 (GRCm39) L369P probably damaging Het
Or2y1 G T 11: 49,385,793 (GRCm39) L144F probably damaging Het
Or4c52 T C 2: 89,845,351 (GRCm39) C26R probably benign Het
Paxx T C 2: 25,350,277 (GRCm39) D110G probably damaging Het
Pcyox1 T G 6: 86,365,735 (GRCm39) D493A probably damaging Het
Plk2 A G 13: 110,535,976 (GRCm39) E560G probably benign Het
Rnf6 A G 5: 146,147,036 (GRCm39) F661L probably benign Het
Sema4a T C 3: 88,345,491 (GRCm39) K531E probably benign Het
Svs5 T C 2: 164,079,446 (GRCm39) K154E possibly damaging Het
Tbx4 A T 11: 85,802,769 (GRCm39) Q242L probably damaging Het
Tgm3 A T 2: 129,886,488 (GRCm39) I570F probably damaging Het
Thrap3 A T 4: 126,059,322 (GRCm39) M908K possibly damaging Het
Trmo A G 4: 46,386,092 (GRCm39) probably null Het
Usp8 T A 2: 126,600,072 (GRCm39) L997Q probably damaging Het
Vmn1r202 T C 13: 22,685,890 (GRCm39) R176G probably benign Het
Vps52 T A 17: 34,180,589 (GRCm39) Y308* probably null Het
Other mutations in Apol11a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03112:Apol11a APN 15 77,401,509 (GRCm39) missense probably damaging 0.99
R1296:Apol11a UTSW 15 77,395,219 (GRCm39) splice site probably benign
R1576:Apol11a UTSW 15 77,401,131 (GRCm39) missense probably damaging 1.00
R1875:Apol11a UTSW 15 77,397,766 (GRCm39) missense possibly damaging 0.81
R2517:Apol11a UTSW 15 77,401,395 (GRCm39) missense probably benign 0.00
R4614:Apol11a UTSW 15 77,400,772 (GRCm39) missense probably benign 0.08
R4892:Apol11a UTSW 15 77,401,190 (GRCm39) nonsense probably null
R5027:Apol11a UTSW 15 77,401,153 (GRCm39) missense probably damaging 1.00
R5334:Apol11a UTSW 15 77,400,953 (GRCm39) missense probably benign 0.14
R6208:Apol11a UTSW 15 77,401,241 (GRCm39) missense probably damaging 0.99
R7883:Apol11a UTSW 15 77,400,774 (GRCm39) missense probably damaging 1.00
R8868:Apol11a UTSW 15 77,401,209 (GRCm39) missense probably damaging 1.00
R9145:Apol11a UTSW 15 77,397,778 (GRCm39) missense probably benign 0.03
R9674:Apol11a UTSW 15 77,401,347 (GRCm39) missense possibly damaging 0.85
Posted On 2014-01-21