Incidental Mutation 'IGL00815:Adal'
ID 8565
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Adal
Ensembl Gene ENSMUSG00000027259
Gene Name adenosine deaminase-like
Synonyms 4930578F03Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00815
Quality Score
Status
Chromosome 2
Chromosomal Location 120970909-120987161 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 120981699 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000113052 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028702] [ENSMUST00000066155] [ENSMUST00000110662] [ENSMUST00000110665] [ENSMUST00000119031]
AlphaFold Q80SY6
Predicted Effect probably benign
Transcript: ENSMUST00000028702
SMART Domains Protein: ENSMUSP00000028702
Gene: ENSMUSG00000027259

DomainStartEndE-ValueType
Pfam:A_deaminase 1 276 1.8e-37 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000066155
SMART Domains Protein: ENSMUSP00000067133
Gene: ENSMUSG00000027259

DomainStartEndE-ValueType
Pfam:A_deaminase 16 343 1.6e-36 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000110662
SMART Domains Protein: ENSMUSP00000106290
Gene: ENSMUSG00000027259

DomainStartEndE-ValueType
Pfam:A_deaminase 2 200 1.1e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000110665
SMART Domains Protein: ENSMUSP00000106293
Gene: ENSMUSG00000027259

DomainStartEndE-ValueType
Pfam:A_deaminase 2 236 4.3e-24 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000119031
SMART Domains Protein: ENSMUSP00000113052
Gene: ENSMUSG00000027259

DomainStartEndE-ValueType
Pfam:A_deaminase 16 343 3e-44 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147271
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152164
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156132
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap20 A G 9: 51,760,713 (GRCm39) N819D probably benign Het
Cenpe A G 3: 134,965,112 (GRCm39) I2061V probably benign Het
Chrna4 T C 2: 180,671,184 (GRCm39) I191V probably benign Het
Crim1 A G 17: 78,677,520 (GRCm39) E907G probably damaging Het
Cyp2d9 T A 15: 82,340,576 (GRCm39) D175E possibly damaging Het
Eml4 A G 17: 83,758,219 (GRCm39) probably benign Het
Faim G A 9: 98,874,218 (GRCm39) G15R probably damaging Het
Fam3c A T 6: 22,318,947 (GRCm39) D151E probably damaging Het
Far1 G A 7: 113,139,896 (GRCm39) V115I probably benign Het
Gfap T C 11: 102,779,516 (GRCm39) D427G possibly damaging Het
Hdac5 A G 11: 102,088,168 (GRCm39) F934S probably damaging Het
Hyou1 A G 9: 44,296,443 (GRCm39) E456G probably benign Het
Kl G A 5: 150,904,315 (GRCm39) E356K possibly damaging Het
Morc1 T C 16: 48,281,055 (GRCm39) I198T possibly damaging Het
Mroh9 C T 1: 162,866,700 (GRCm39) V679M probably damaging Het
Pigr T A 1: 130,762,167 (GRCm39) M1K probably null Het
Pkn3 C A 2: 29,971,212 (GRCm39) P260T possibly damaging Het
Pld5 T G 1: 175,967,585 (GRCm39) D28A probably damaging Het
Plekhg2 G A 7: 28,060,294 (GRCm39) Q1012* probably null Het
Ppp1ca A G 19: 4,243,143 (GRCm39) I104V probably benign Het
Rad21l A G 2: 151,509,909 (GRCm39) V64A probably damaging Het
Rbm20 A G 19: 53,803,948 (GRCm39) D427G probably damaging Het
Rev3l A G 10: 39,735,149 (GRCm39) I2792V possibly damaging Het
Sec23a C T 12: 59,039,068 (GRCm39) C248Y possibly damaging Het
Sf3b1 A T 1: 55,036,090 (GRCm39) probably benign Het
Slc30a1 A G 1: 191,641,191 (GRCm39) N279S probably damaging Het
Slit2 G A 5: 48,146,493 (GRCm39) E95K possibly damaging Het
Spic T C 10: 88,511,729 (GRCm39) N176D probably damaging Het
Tlk2 C T 11: 105,137,621 (GRCm39) Q184* probably null Het
Tpm4 T C 8: 72,897,347 (GRCm39) I107T probably benign Het
Ttll11 A T 2: 35,792,732 (GRCm39) C186* probably null Het
Txlnb A T 10: 17,718,711 (GRCm39) H514L probably damaging Het
Zfpm2 T A 15: 40,962,887 (GRCm39) M183K probably benign Het
Other mutations in Adal
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01917:Adal APN 2 120,973,035 (GRCm39) missense possibly damaging 0.88
IGL02487:Adal APN 2 120,985,877 (GRCm39) missense probably benign 0.12
R0004:Adal UTSW 2 120,982,966 (GRCm39) missense probably damaging 1.00
R0234:Adal UTSW 2 120,978,798 (GRCm39) missense probably benign 0.01
R0234:Adal UTSW 2 120,978,798 (GRCm39) missense probably benign 0.01
R1376:Adal UTSW 2 120,983,011 (GRCm39) missense probably damaging 1.00
R1376:Adal UTSW 2 120,983,011 (GRCm39) missense probably damaging 1.00
R4989:Adal UTSW 2 120,986,030 (GRCm39) utr 3 prime probably benign
R6532:Adal UTSW 2 120,976,604 (GRCm39) splice site probably null
R6606:Adal UTSW 2 120,980,769 (GRCm39) missense probably damaging 1.00
R6750:Adal UTSW 2 120,973,130 (GRCm39) missense probably damaging 1.00
R6819:Adal UTSW 2 120,978,794 (GRCm39) missense probably damaging 0.99
R7035:Adal UTSW 2 120,985,942 (GRCm39) missense probably benign 0.00
R8210:Adal UTSW 2 120,985,236 (GRCm39) missense possibly damaging 0.91
R9373:Adal UTSW 2 120,980,703 (GRCm39) missense probably benign 0.21
R9446:Adal UTSW 2 120,976,530 (GRCm39) missense probably null 0.99
Posted On 2012-12-06