Incidental Mutation 'IGL03118:Odam'
ID 409859
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 # IGL03118
Quality Score
Chromosome 5
Chromosomal Location 88032888-88042033 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 88033613 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 15 (S15P)
Ref Sequence ENSEMBL: ENSMUSP00000117898 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113274] [ENSMUST00000129757]
AlphaFold A1E960
Predicted Effect unknown
Transcript: ENSMUST00000113274
AA Change: S15P
SMART Domains Protein: ENSMUSP00000108899
Gene: ENSMUSG00000009580
AA Change: S15P

Pfam:ODAM 16 273 1.4e-128 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000129757
AA Change: S15P
SMART Domains Protein: ENSMUSP00000117898
Gene: ENSMUSG00000009580
AA Change: S15P

Pfam:ODAM 16 273 5.1e-132 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 G A 17: 24,619,424 (GRCm39) G921S probably benign Het
Abca8b T C 11: 109,838,007 (GRCm39) T1082A possibly damaging Het
B9d2 T C 7: 25,380,901 (GRCm39) probably null Het
Bfsp1 T C 2: 143,669,253 (GRCm39) E442G possibly damaging Het
Bpifb5 C T 2: 154,078,673 (GRCm39) probably benign Het
Ccl1 A G 11: 82,068,896 (GRCm39) I47T probably damaging Het
Cln3 T C 7: 126,174,569 (GRCm39) I285V probably null Het
Cyp4a12b G T 4: 115,290,173 (GRCm39) R242I possibly damaging Het
Dcc T C 18: 71,553,344 (GRCm39) T771A probably benign Het
Erbb4 T C 1: 68,081,878 (GRCm39) D1052G probably benign Het
Fcnb T C 2: 27,966,630 (GRCm39) N301S probably benign Het
Gm28043 A C 17: 29,853,705 (GRCm39) E403A probably damaging Het
Gria4 A G 9: 4,793,804 (GRCm39) probably benign Het
Ighv5-12 T A 12: 113,666,198 (GRCm39) M1L probably benign Het
Il17rd A G 14: 26,815,352 (GRCm39) probably null Het
Kcnn3 T A 3: 89,574,468 (GRCm39) L660Q probably damaging Het
Lcor C T 19: 41,546,808 (GRCm39) P131S probably damaging Het
Leng1 T C 7: 3,668,409 (GRCm39) N13S probably damaging Het
Loxhd1 T C 18: 77,468,160 (GRCm39) V827A probably damaging Het
Mapk13 A G 17: 28,996,709 (GRCm39) Y208C probably benign Het
Mybpc3 T C 2: 90,954,848 (GRCm39) V453A probably damaging Het
Or11l3 A T 11: 58,516,269 (GRCm39) V201D probably damaging Het
Or8d1 A T 9: 38,766,526 (GRCm39) H56L probably damaging Het
Pcdhb19 T C 18: 37,632,618 (GRCm39) probably benign Het
Per2 G T 1: 91,372,341 (GRCm39) Y244* probably null Het
Pik3ca A T 3: 32,514,084 (GRCm39) I857F probably damaging Het
Pold1 T A 7: 44,188,824 (GRCm39) I447F probably benign Het
Ppm1f T A 16: 16,731,942 (GRCm39) W131R probably null Het
Ppp2r2c A G 5: 37,083,660 (GRCm39) Y67C probably damaging Het
Psmb10 A T 8: 106,663,532 (GRCm39) H155Q probably damaging Het
Ptbp3 G A 4: 59,501,470 (GRCm39) A149V probably benign Het
Pygb T A 2: 150,662,731 (GRCm39) V566E probably benign Het
Rictor G A 15: 6,788,999 (GRCm39) R205Q possibly damaging Het
Ryr1 T A 7: 28,715,211 (GRCm39) R4638W unknown Het
Semp2l2a C T 8: 13,888,096 (GRCm39) probably benign Het
Septin3 G A 15: 82,168,715 (GRCm39) probably null Het
Serpina3b A T 12: 104,097,313 (GRCm39) D198V probably benign Het
Slc27a6 C A 18: 58,689,815 (GRCm39) H94N probably benign Het
Taf2 C T 15: 54,915,559 (GRCm39) V456M probably damaging Het
Tbpl2 T C 2: 23,977,301 (GRCm39) E238G probably benign Het
Ttn C T 2: 76,584,551 (GRCm39) V20440I possibly damaging Het
Zfp638 T A 6: 83,912,000 (GRCm39) probably benign Het
Zfp865 T C 7: 5,037,644 (GRCm39) probably benign 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
IGL02895:Odam APN 5 88,033,723 (GRCm39) missense probably benign 0.32
IGL03051:Odam APN 5 88,040,335 (GRCm39) splice site probably benign
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 2016-08-02