Incidental Mutation 'IGL02895:Odam'
ID 363373
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Odam
Ensembl Gene ENSMUSG00000009580
Gene Name odontogenic, ameloblast asssociated
Synonyms 2310011G06Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.108) question?
Stock # IGL02895
Quality Score
Status
Chromosome 5
Chromosomal Location 88032888-88042033 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 88033723 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Arginine at position 21 (Q21R)
Ref Sequence ENSEMBL: ENSMUSP00000117898 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113274] [ENSMUST00000129757]
AlphaFold A1E960
Predicted Effect probably benign
Transcript: ENSMUST00000113274
AA Change: Q21R

PolyPhen 2 Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000108899
Gene: ENSMUSG00000009580
AA Change: Q21R

DomainStartEndE-ValueType
Pfam:ODAM 16 273 1.4e-128 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000129757
AA Change: Q21R

PolyPhen 2 Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000117898
Gene: ENSMUSG00000009580
AA Change: Q21R

DomainStartEndE-ValueType
Pfam:ODAM 16 273 5.1e-132 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahctf1 C T 1: 179,621,376 (GRCm39) E130K probably damaging Het
Atf7ip C A 6: 136,537,686 (GRCm39) S306R probably damaging Het
Cpd A G 11: 76,676,029 (GRCm39) V1208A probably benign Het
Cplane1 A G 15: 8,261,591 (GRCm39) probably benign Het
Ctsl C T 13: 64,514,326 (GRCm39) A195T probably damaging Het
Dennd2c T C 3: 103,044,519 (GRCm39) Y367H possibly damaging Het
Endod1 T A 9: 14,268,166 (GRCm39) T440S probably benign Het
Gm12695 T C 4: 96,612,186 (GRCm39) R526G probably damaging Het
Ighv1-39 T C 12: 114,878,302 (GRCm39) T90A probably damaging Het
Kdm2a G A 19: 4,412,930 (GRCm39) R19C probably damaging Het
Klra1 C T 6: 130,352,203 (GRCm39) E180K possibly damaging Het
Or4c11c A G 2: 88,661,986 (GRCm39) Y175C probably damaging Het
Or8b8 G A 9: 37,809,278 (GRCm39) V193I probably benign Het
Plk1 A G 7: 121,768,389 (GRCm39) E504G possibly damaging Het
Rtl3 T C X: 105,883,150 (GRCm39) I37M possibly damaging Het
Srebf2 A G 15: 82,031,668 (GRCm39) E22G possibly damaging Het
Tmem74b A G 2: 151,548,311 (GRCm39) S13G probably benign Het
Utp14b T C 1: 78,642,324 (GRCm39) V74A possibly damaging Het
Znrf3 T C 11: 5,239,085 (GRCm39) M93V probably damaging Het
Other mutations in Odam
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00970:Odam APN 5 88,034,467 (GRCm39) splice site probably benign
IGL01339:Odam APN 5 88,033,755 (GRCm39) critical splice donor site probably null
IGL01940:Odam APN 5 88,035,192 (GRCm39) missense possibly damaging 0.87
IGL03051:Odam APN 5 88,040,335 (GRCm39) splice site probably benign
IGL03118:Odam APN 5 88,033,613 (GRCm39) missense unknown
BB005:Odam UTSW 5 88,035,269 (GRCm39) missense possibly damaging 0.95
BB015:Odam UTSW 5 88,035,269 (GRCm39) missense possibly damaging 0.95
R1816:Odam UTSW 5 88,037,329 (GRCm39) splice site probably null
R2033:Odam UTSW 5 88,040,278 (GRCm39) missense probably benign
R4965:Odam UTSW 5 88,037,967 (GRCm39) nonsense probably null
R7257:Odam UTSW 5 88,035,404 (GRCm39) missense probably benign 0.14
R7682:Odam UTSW 5 88,040,287 (GRCm39) missense possibly damaging 0.71
R7928:Odam UTSW 5 88,035,269 (GRCm39) missense possibly damaging 0.95
R8099:Odam UTSW 5 88,040,299 (GRCm39) missense possibly damaging 0.52
R8844:Odam UTSW 5 88,037,322 (GRCm39) missense probably damaging 0.98
R8872:Odam UTSW 5 88,035,797 (GRCm39) critical splice acceptor site probably null
R9006:Odam UTSW 5 88,040,298 (GRCm39) missense probably benign 0.16
R9227:Odam UTSW 5 88,034,457 (GRCm39) missense probably benign 0.32
R9230:Odam UTSW 5 88,034,457 (GRCm39) missense probably benign 0.32
R9705:Odam UTSW 5 88,037,228 (GRCm39) missense probably benign 0.06
R9779:Odam UTSW 5 88,037,327 (GRCm39) critical splice donor site probably null
Posted On 2015-12-18