Incidental Mutation 'IGL02648:Aadacl4'
ID 302040
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Aadacl4
Ensembl Gene ENSMUSG00000070609
Gene Name arylacetamide deacetylase like 4
Synonyms Gm13177
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL02648
Quality Score
Status
Chromosome 4
Chromosomal Location 144340277-144349968 bp(+) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) A to T at 144344392 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000092087 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094510]
AlphaFold B1AVU5
Predicted Effect probably null
Transcript: ENSMUST00000094510
SMART Domains Protein: ENSMUSP00000092087
Gene: ENSMUSG00000070609

DomainStartEndE-ValueType
transmembrane domain 7 28 N/A INTRINSIC
transmembrane domain 43 60 N/A INTRINSIC
Pfam:Abhydrolase_3 115 285 9.6e-30 PFAM
Pfam:Abhydrolase_3 272 381 4.9e-11 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp4 A G 7: 43,904,414 (GRCm39) probably benign Het
Adgrv1 A T 13: 81,659,738 (GRCm39) M1997K probably benign Het
Arhgdib T C 6: 136,910,647 (GRCm39) D38G probably damaging Het
Bbox1 T G 2: 110,135,871 (GRCm39) D36A probably damaging Het
Cacna1c T C 6: 118,734,457 (GRCm39) K104R probably damaging Het
Cacna1i G A 15: 80,182,839 (GRCm39) C75Y probably damaging Het
Ccdc14 T C 16: 34,517,528 (GRCm39) L70S probably damaging Het
Ccdc88a T G 11: 29,451,051 (GRCm39) V1580G probably benign Het
Cdadc1 C A 14: 59,823,812 (GRCm39) D227Y probably damaging Het
Chd3 T C 11: 69,242,976 (GRCm39) Y1415C probably damaging Het
Cngb3 A G 4: 19,428,489 (GRCm39) N493S probably benign Het
Dock10 T A 1: 80,551,840 (GRCm39) Y665F probably damaging Het
Gm10549 C A 18: 33,597,303 (GRCm39) probably benign Het
Greb1 C T 12: 16,758,683 (GRCm39) V678M probably damaging Het
Gucy2c G A 6: 136,706,211 (GRCm39) R497* probably null Het
Itgad T C 7: 127,782,546 (GRCm39) probably benign Het
Lgr4 C A 2: 109,842,718 (GRCm39) T877K probably damaging Het
Lrig3 A G 10: 125,802,463 (GRCm39) D40G probably benign Het
Myo3b T C 2: 69,935,716 (GRCm39) probably benign Het
Neb A G 2: 52,161,093 (GRCm39) Y2193H possibly damaging Het
Or4b1 T A 2: 89,979,697 (GRCm39) I218F possibly damaging Het
Or8b3b T C 9: 38,584,312 (GRCm39) M143V probably benign Het
Pard6b A G 2: 167,940,847 (GRCm39) Q278R probably benign Het
Pate10 A T 9: 35,652,405 (GRCm39) M21L probably benign Het
Pkd2l1 T C 19: 44,143,975 (GRCm39) Y366C possibly damaging Het
Prl2c1 A G 13: 28,041,542 (GRCm39) D188G probably benign Het
Prl3a1 G T 13: 27,454,218 (GRCm39) M65I probably benign Het
Psg26 T A 7: 18,216,691 (GRCm39) E49D probably benign Het
Rapgef3 G A 15: 97,656,273 (GRCm39) R38W probably damaging Het
Rrn3 T C 16: 13,629,453 (GRCm39) F590L probably benign Het
Serpina12 T C 12: 104,004,267 (GRCm39) K122E probably benign Het
Slc39a6 T C 18: 24,715,424 (GRCm39) I699V probably damaging Het
Tmem259 G A 10: 79,813,651 (GRCm39) P443S probably damaging Het
Vmn1r75 T A 7: 11,615,091 (GRCm39) F274L probably benign Het
Other mutations in Aadacl4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02836:Aadacl4 APN 4 144,349,782 (GRCm39) missense possibly damaging 0.79
IGL02949:Aadacl4 APN 4 144,344,490 (GRCm39) missense probably damaging 1.00
IGL03253:Aadacl4 APN 4 144,349,858 (GRCm39) missense probably benign 0.05
white_rabbit UTSW 4 144,344,598 (GRCm39) missense probably benign 0.03
R0035:Aadacl4 UTSW 4 144,344,511 (GRCm39) missense probably damaging 0.98
R0268:Aadacl4 UTSW 4 144,349,565 (GRCm39) missense probably benign 0.00
R1427:Aadacl4 UTSW 4 144,349,610 (GRCm39) missense probably damaging 1.00
R1672:Aadacl4 UTSW 4 144,349,889 (GRCm39) nonsense probably null
R2220:Aadacl4 UTSW 4 144,344,572 (GRCm39) missense probably damaging 0.98
R2353:Aadacl4 UTSW 4 144,349,779 (GRCm39) missense probably damaging 1.00
R2983:Aadacl4 UTSW 4 144,349,784 (GRCm39) missense probably damaging 0.98
R4708:Aadacl4 UTSW 4 144,349,899 (GRCm39) missense probably benign 0.01
R4878:Aadacl4 UTSW 4 144,340,415 (GRCm39) missense possibly damaging 0.62
R4911:Aadacl4 UTSW 4 144,340,362 (GRCm39) missense probably damaging 1.00
R5208:Aadacl4 UTSW 4 144,344,398 (GRCm39) missense probably benign 0.04
R5237:Aadacl4 UTSW 4 144,349,850 (GRCm39) nonsense probably null
R5568:Aadacl4 UTSW 4 144,349,364 (GRCm39) missense probably benign 0.03
R5633:Aadacl4 UTSW 4 144,344,598 (GRCm39) missense probably benign 0.03
R5817:Aadacl4 UTSW 4 144,349,497 (GRCm39) missense probably benign 0.04
R5848:Aadacl4 UTSW 4 144,344,428 (GRCm39) missense probably benign 0.11
R5916:Aadacl4 UTSW 4 144,349,550 (GRCm39) missense possibly damaging 0.93
R6736:Aadacl4 UTSW 4 144,349,909 (GRCm39) missense possibly damaging 0.82
R6814:Aadacl4 UTSW 4 144,349,750 (GRCm39) missense probably benign 0.07
R6872:Aadacl4 UTSW 4 144,349,750 (GRCm39) missense probably benign 0.07
R6971:Aadacl4 UTSW 4 144,349,303 (GRCm39) missense probably damaging 1.00
R6994:Aadacl4 UTSW 4 144,349,849 (GRCm39) missense probably damaging 1.00
R7074:Aadacl4 UTSW 4 144,340,433 (GRCm39) missense probably benign
R7353:Aadacl4 UTSW 4 144,344,490 (GRCm39) missense probably damaging 1.00
R7837:Aadacl4 UTSW 4 144,344,547 (GRCm39) missense probably damaging 1.00
R7853:Aadacl4 UTSW 4 144,344,592 (GRCm39) missense probably benign 0.02
R8120:Aadacl4 UTSW 4 144,349,460 (GRCm39) missense probably benign 0.44
R8549:Aadacl4 UTSW 4 144,349,726 (GRCm39) missense probably benign
R9043:Aadacl4 UTSW 4 144,349,790 (GRCm39) missense probably damaging 1.00
R9661:Aadacl4 UTSW 4 144,340,287 (GRCm39) missense probably damaging 0.96
X0017:Aadacl4 UTSW 4 144,349,586 (GRCm39) missense probably damaging 1.00
X0065:Aadacl4 UTSW 4 144,349,679 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16