Incidental Mutation 'IGL03118:Odam'
ID409859
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Odam
Ensembl Gene ENSMUSG00000009580
Gene Nameodontogenic, ameloblast asssociated
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.092) question?
Stock #IGL03118
Quality Score
Status
Chromosome5
Chromosomal Location87885029-87894174 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 87885754 bp
ZygosityHeterozygous
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]
Predicted Effect unknown
Transcript: ENSMUST00000113274
AA Change: S15P
SMART Domains Protein: ENSMUSP00000108899
Gene: ENSMUSG00000009580
AA Change: S15P

DomainStartEndE-ValueType
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

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: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 G A 17: 24,400,450 G921S probably benign Het
Abca8b T C 11: 109,947,181 T1082A possibly damaging Het
AF366264 C T 8: 13,838,096 probably benign Het
B9d2 T C 7: 25,681,476 probably null Het
Bfsp1 T C 2: 143,827,333 E442G possibly damaging Het
Bpifb5 C T 2: 154,236,753 probably benign Het
Ccl1 A G 11: 82,178,070 I47T probably damaging Het
Cln3 T C 7: 126,575,397 I285V probably null Het
Cyp4a12b G T 4: 115,432,976 R242I possibly damaging Het
Dcc T C 18: 71,420,273 T771A probably benign Het
Erbb4 T C 1: 68,042,719 D1052G probably benign Het
Fcnb T C 2: 28,076,618 N301S probably benign Het
Gm28043 A C 17: 29,634,731 E403A probably damaging Het
Gria4 A G 9: 4,793,804 probably benign Het
Ighv5-12 T A 12: 113,702,578 M1L probably benign Het
Il17rd A G 14: 27,093,395 probably null Het
Kcnn3 T A 3: 89,667,161 L660Q probably damaging Het
Lcor C T 19: 41,558,369 P131S probably damaging Het
Leng1 T C 7: 3,665,410 N13S probably damaging Het
Loxhd1 T C 18: 77,380,464 V827A probably damaging Het
Mapk13 A G 17: 28,777,735 Y208C probably benign Het
Mybpc3 T C 2: 91,124,503 V453A probably damaging Het
Olfr26 A T 9: 38,855,230 H56L probably damaging Het
Olfr323 A T 11: 58,625,443 V201D probably damaging Het
Pcdhb19 T C 18: 37,499,565 probably benign Het
Per2 G T 1: 91,444,619 Y244* probably null Het
Pik3ca A T 3: 32,459,935 I857F probably damaging Het
Pold1 T A 7: 44,539,400 I447F probably benign Het
Ppm1f T A 16: 16,914,078 W131R probably null Het
Ppp2r2c A G 5: 36,926,316 Y67C probably damaging Het
Psmb10 A T 8: 105,936,900 H155Q probably damaging Het
Ptbp3 G A 4: 59,501,470 A149V probably benign Het
Pygb T A 2: 150,820,811 V566E probably benign Het
Rictor G A 15: 6,759,518 R205Q possibly damaging Het
Ryr1 T A 7: 29,015,786 R4638W unknown Het
Sept3 G A 15: 82,284,514 probably null Het
Serpina3b A T 12: 104,131,054 D198V probably benign Het
Slc27a6 C A 18: 58,556,743 H94N probably benign Het
Taf2 C T 15: 55,052,163 V456M probably damaging Het
Tbpl2 T C 2: 24,087,289 E238G probably benign Het
Ttn C T 2: 76,754,207 V20440I possibly damaging Het
Zfp638 T A 6: 83,935,018 probably benign Het
Zfp865 T C 7: 5,034,645 probably benign Het
Other mutations in Odam
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00970:Odam APN 5 87886608 splice site probably benign
IGL01339:Odam APN 5 87885896 critical splice donor site probably null
IGL01940:Odam APN 5 87887333 missense possibly damaging 0.87
IGL02895:Odam APN 5 87885864 missense probably benign 0.32
IGL03051:Odam APN 5 87892476 splice site probably benign
BB005:Odam UTSW 5 87887410 missense possibly damaging 0.95
BB015:Odam UTSW 5 87887410 missense possibly damaging 0.95
R1816:Odam UTSW 5 87889470 splice site probably null
R2033:Odam UTSW 5 87892419 missense probably benign
R4965:Odam UTSW 5 87890108 nonsense probably null
R7257:Odam UTSW 5 87887545 missense probably benign 0.14
R7682:Odam UTSW 5 87892428 missense possibly damaging 0.71
R7928:Odam UTSW 5 87887410 missense possibly damaging 0.95
R8099:Odam UTSW 5 87892440 missense possibly damaging 0.52
Posted On2016-08-02