Incidental Mutation 'IGL01139:Aadacl4fm5'
ID 50971
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Aadacl4fm5
Ensembl Gene ENSMUSG00000078504
Gene Name AADACL4 family member 5
Synonyms Gm438, LOC329993
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL01139
Quality Score
Status
Chromosome 4
Chromosomal Location 144503774-144513153 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 144504259 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 297 (Y297*)
Ref Sequence ENSEMBL: ENSMUSP00000101372 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105746]
AlphaFold B1ASB3
Predicted Effect probably null
Transcript: ENSMUST00000105746
AA Change: Y297*
SMART Domains Protein: ENSMUSP00000101372
Gene: ENSMUSG00000078504
AA Change: Y297*

DomainStartEndE-ValueType
transmembrane domain 3 25 N/A INTRINSIC
Pfam:Abhydrolase_3 111 270 4.9e-22 PFAM
Pfam:Abhydrolase_3 284 366 1.3e-11 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr3 A T 1: 125,333,622 (GRCm39) I215N probably damaging Het
Ambn C T 5: 88,612,376 (GRCm39) probably benign Het
Arhgef1 T A 7: 24,625,376 (GRCm39) probably benign Het
Arid1a A C 4: 133,421,308 (GRCm39) S832R unknown Het
Clca4a A T 3: 144,672,030 (GRCm39) I304N probably damaging Het
Dmxl2 G A 9: 54,366,248 (GRCm39) P274S probably damaging Het
Eif4enif1 T A 11: 3,171,143 (GRCm39) D211E probably damaging Het
Eri2 A G 7: 119,385,960 (GRCm39) probably null Het
Fhod3 C T 18: 25,199,401 (GRCm39) P691S probably benign Het
Flnb A G 14: 7,945,989 (GRCm38) S2465G probably damaging Het
Ftsj1 G A X: 8,112,831 (GRCm39) R171C probably damaging Het
Glb1l3 G A 9: 26,729,523 (GRCm39) T648I probably benign Het
Gm4222 T A 2: 89,978,889 (GRCm39) probably benign Het
Gm5475 G A 15: 100,322,096 (GRCm39) probably benign Het
Jaml C A 9: 45,012,317 (GRCm39) T268N possibly damaging Het
Kank3 G A 17: 34,036,375 (GRCm39) G81E probably damaging Het
Lrba A G 3: 86,549,969 (GRCm39) T217A possibly damaging Het
Ltn1 A G 16: 87,212,897 (GRCm39) S555P probably benign Het
Map3k15 T A X: 158,855,875 (GRCm39) M350K probably damaging Het
Mipol1 C A 12: 57,352,821 (GRCm39) Y53* probably null Het
Mn1 A G 5: 111,569,315 (GRCm39) D1095G probably damaging Het
Myh14 T C 7: 44,255,716 (GRCm39) probably benign Het
Nrn1 A G 13: 36,914,190 (GRCm39) C31R probably damaging Het
Nup210 A T 6: 91,007,079 (GRCm39) L579H possibly damaging Het
Nxf2 T C X: 133,851,145 (GRCm39) I578V probably benign Het
Obscn G A 11: 58,969,178 (GRCm39) A172V probably damaging Het
Or10h1b T A 17: 33,395,756 (GRCm39) Y123N probably damaging Het
Or9g4 T G 2: 85,504,841 (GRCm39) Y218S probably damaging Het
Phtf1 A G 3: 103,912,918 (GRCm39) D748G probably damaging Het
Psd3 A T 8: 68,361,187 (GRCm39) Y863N probably damaging Het
Psmc6 C T 14: 45,581,167 (GRCm39) T321I probably benign Het
Rassf6 T C 5: 90,756,825 (GRCm39) *31W probably null Het
Rictor A C 15: 6,807,749 (GRCm39) K791Q probably damaging Het
Slc12a9 C T 5: 137,321,104 (GRCm39) M470I probably damaging Het
Tex28 A T X: 73,194,830 (GRCm39) M367K possibly damaging Het
Thnsl2 A T 6: 71,115,718 (GRCm39) V163D probably damaging Het
Tmco3 G A 8: 13,369,887 (GRCm39) R633Q possibly damaging Het
Trf A T 9: 103,100,803 (GRCm39) V224D probably damaging Het
Ttc8 C T 12: 98,930,804 (GRCm39) Q273* probably null Het
Usp9x A G X: 12,970,815 (GRCm39) probably benign Het
Vmn2r117 A G 17: 23,696,778 (GRCm39) W210R probably damaging Het
Vmn2r5 A G 3: 64,398,826 (GRCm39) S718P probably benign Het
Vps13a T C 19: 16,617,989 (GRCm39) D2932G probably damaging Het
Whamm T C 7: 81,245,662 (GRCm39) L706P probably damaging Het
Yeats2 G A 16: 20,033,143 (GRCm39) V45I probably damaging Het
Yipf3 G A 17: 46,561,383 (GRCm39) probably null Het
Zeb1 T C 18: 5,705,061 (GRCm39) V26A possibly damaging Het
Other mutations in Aadacl4fm5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01293:Aadacl4fm5 APN 4 144,504,159 (GRCm39) missense probably benign 0.00
IGL01678:Aadacl4fm5 APN 4 144,504,443 (GRCm39) missense probably benign 0.20
IGL02609:Aadacl4fm5 APN 4 144,506,307 (GRCm39) missense probably damaging 1.00
IGL02684:Aadacl4fm5 APN 4 144,504,755 (GRCm39) splice site probably benign
IGL02734:Aadacl4fm5 APN 4 144,506,349 (GRCm39) missense probably damaging 1.00
IGL02869:Aadacl4fm5 APN 4 144,512,938 (GRCm39) missense probably benign 0.01
IGL02988:Aadacl4fm5 APN 4 144,513,100 (GRCm39) utr 5 prime probably benign
R0553:Aadacl4fm5 UTSW 4 144,503,985 (GRCm39) missense possibly damaging 0.57
R1514:Aadacl4fm5 UTSW 4 144,504,329 (GRCm39) missense probably damaging 1.00
R1856:Aadacl4fm5 UTSW 4 144,504,453 (GRCm39) missense probably benign
R1957:Aadacl4fm5 UTSW 4 144,504,389 (GRCm39) missense possibly damaging 0.94
R2014:Aadacl4fm5 UTSW 4 144,506,295 (GRCm39) missense probably damaging 1.00
R2243:Aadacl4fm5 UTSW 4 144,503,991 (GRCm39) missense probably benign
R4943:Aadacl4fm5 UTSW 4 144,504,290 (GRCm39) missense probably benign 0.07
R5439:Aadacl4fm5 UTSW 4 144,504,683 (GRCm39) missense probably damaging 1.00
R5520:Aadacl4fm5 UTSW 4 144,504,594 (GRCm39) missense probably benign 0.00
R6414:Aadacl4fm5 UTSW 4 144,503,985 (GRCm39) missense possibly damaging 0.57
R6664:Aadacl4fm5 UTSW 4 144,503,969 (GRCm39) makesense probably null
R6869:Aadacl4fm5 UTSW 4 144,507,042 (GRCm39) critical splice donor site probably null
R7384:Aadacl4fm5 UTSW 4 144,507,191 (GRCm39) missense possibly damaging 0.89
R7439:Aadacl4fm5 UTSW 4 144,504,332 (GRCm39) missense probably damaging 1.00
R7484:Aadacl4fm5 UTSW 4 144,504,521 (GRCm39) missense probably damaging 0.97
R9284:Aadacl4fm5 UTSW 4 144,504,191 (GRCm39) missense probably damaging 1.00
Posted On 2013-06-21