Incidental Mutation 'IGL02070:Obox6'
ID 185779
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Obox6
Ensembl Gene ENSMUSG00000041583
Gene Name oocyte specific homeobox 6
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.091) question?
Stock # IGL02070
Quality Score
Status
Chromosome 7
Chromosomal Location 15567175-15573604 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 15568804 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Leucine at position 24 (S24L)
Ref Sequence ENSEMBL: ENSMUSP00000104153 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108513]
AlphaFold G3X9U1
Predicted Effect probably damaging
Transcript: ENSMUST00000108513
AA Change: S24L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000104153
Gene: ENSMUSG00000041583
AA Change: S24L

DomainStartEndE-ValueType
HOX 145 207 8.52e-21 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a null allele exhibit no detectable abnormal phenotype. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg6 A G 10: 14,343,336 (GRCm39) Y204H probably damaging Het
Akap13 C A 7: 75,316,293 (GRCm39) T583K probably benign Het
Alms1 C A 6: 85,628,385 (GRCm39) Q2948K possibly damaging Het
Auts2 C T 5: 131,499,259 (GRCm39) R327Q probably damaging Het
Card14 A C 11: 119,235,530 (GRCm39) E988A probably damaging Het
Ccl25 T C 8: 4,398,700 (GRCm39) probably benign Het
Cttnbp2nl A C 3: 104,918,582 (GRCm39) V86G probably damaging Het
Cyb5r2 G A 7: 107,350,394 (GRCm39) T213I probably damaging Het
Ear6 A G 14: 52,091,903 (GRCm39) H150R probably damaging Het
Ecm2 T C 13: 49,671,846 (GRCm39) C116R probably damaging Het
Gabrr2 G T 4: 33,095,340 (GRCm39) E385* probably null Het
Hyal5 T A 6: 24,876,961 (GRCm39) V278D probably damaging Het
Mboat1 T C 13: 30,408,380 (GRCm39) L181P probably benign Het
Mdm1 A G 10: 117,982,523 (GRCm39) I53V probably damaging Het
Mfrp T C 9: 44,015,986 (GRCm39) Y368H probably benign Het
Myo1b A G 1: 51,833,496 (GRCm39) V365A probably damaging Het
Nexmif G T X: 103,126,817 (GRCm39) H1509Q probably benign Het
Nlrp4a G T 7: 26,148,703 (GRCm39) K103N possibly damaging Het
Optc T A 1: 133,828,914 (GRCm39) I178F probably damaging Het
Or4p22 T A 2: 88,317,346 (GRCm39) I90N probably damaging Het
Or56a42-ps1 G T 7: 104,776,254 (GRCm39) L85I probably benign Het
Pcdh15 T A 10: 74,466,700 (GRCm39) N1535K probably benign Het
Pcdhb19 A T 18: 37,631,597 (GRCm39) N464I probably damaging Het
Pcsk5 C T 19: 17,416,406 (GRCm39) V1681I probably benign Het
Phf8-ps T C 17: 33,285,104 (GRCm39) E566G probably damaging Het
Pknox1 T A 17: 31,822,339 (GRCm39) probably benign Het
Ppa2 T C 3: 133,083,623 (GRCm39) F327S probably damaging Het
Rab39b G T X: 74,618,309 (GRCm39) L174M probably damaging Het
Reep5 A T 18: 34,505,526 (GRCm39) Y48* probably null Het
Rnf123 G A 9: 107,945,501 (GRCm39) R390* probably null Het
Sar1a T A 10: 61,520,673 (GRCm39) probably benign Het
Satb1 T A 17: 52,047,095 (GRCm39) D740V probably damaging Het
Sema3f G A 9: 107,569,440 (GRCm39) T128I probably damaging Het
Snx1 A T 9: 66,005,731 (GRCm39) S129R probably damaging Het
Sptb T A 12: 76,652,313 (GRCm39) K1641N possibly damaging Het
Sptbn1 T C 11: 30,095,979 (GRCm39) E305G probably damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Taar7d A T 10: 23,904,152 (GRCm39) I345F probably benign Het
Tes T C 6: 17,099,779 (GRCm39) L258P probably damaging Het
Trav9-4 A T 14: 53,913,817 (GRCm39) T24S possibly damaging Het
Utp20 A G 10: 88,657,739 (GRCm39) probably benign Het
Vcam1 T A 3: 115,919,646 (GRCm39) T207S probably benign Het
Xkrx T C X: 133,051,311 (GRCm39) S447G probably benign Het
Zfp318 T C 17: 46,707,644 (GRCm39) L234P probably damaging Het
Other mutations in Obox6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00705:Obox6 APN 7 15,567,662 (GRCm39) missense probably damaging 0.97
IGL01981:Obox6 APN 7 15,568,846 (GRCm39) missense possibly damaging 0.94
IGL02066:Obox6 APN 7 15,568,628 (GRCm39) missense probably benign 0.03
IGL02450:Obox6 APN 7 15,567,638 (GRCm39) missense probably damaging 0.99
R0091:Obox6 UTSW 7 15,568,364 (GRCm39) missense probably benign 0.38
R0512:Obox6 UTSW 7 15,567,874 (GRCm39) missense probably benign 0.42
R1686:Obox6 UTSW 7 15,567,750 (GRCm39) missense probably damaging 0.99
R1727:Obox6 UTSW 7 15,568,502 (GRCm39) missense probably benign 0.04
R1755:Obox6 UTSW 7 15,568,445 (GRCm39) missense probably damaging 0.98
R1813:Obox6 UTSW 7 15,568,770 (GRCm39) missense possibly damaging 0.65
R1896:Obox6 UTSW 7 15,568,770 (GRCm39) missense possibly damaging 0.65
R2086:Obox6 UTSW 7 15,567,532 (GRCm39) missense probably damaging 1.00
R4730:Obox6 UTSW 7 15,568,738 (GRCm39) missense possibly damaging 0.85
R4732:Obox6 UTSW 7 15,568,697 (GRCm39) missense possibly damaging 0.85
R4733:Obox6 UTSW 7 15,568,697 (GRCm39) missense possibly damaging 0.85
R4790:Obox6 UTSW 7 15,568,502 (GRCm39) missense possibly damaging 0.78
R5830:Obox6 UTSW 7 15,568,382 (GRCm39) missense possibly damaging 0.93
R6838:Obox6 UTSW 7 15,567,664 (GRCm39) missense possibly damaging 0.95
R7275:Obox6 UTSW 7 15,567,805 (GRCm39) missense probably benign 0.19
R7347:Obox6 UTSW 7 15,568,571 (GRCm39) missense possibly damaging 0.53
R7485:Obox6 UTSW 7 15,567,863 (GRCm39) missense probably damaging 1.00
R8326:Obox6 UTSW 7 15,567,481 (GRCm39) missense possibly damaging 0.95
R8438:Obox6 UTSW 7 15,567,853 (GRCm39) missense probably damaging 1.00
R8802:Obox6 UTSW 7 15,567,772 (GRCm39) missense probably damaging 0.99
R9274:Obox6 UTSW 7 15,567,766 (GRCm39) missense possibly damaging 0.83
R9340:Obox6 UTSW 7 15,567,722 (GRCm39) missense possibly damaging 0.93
R9566:Obox6 UTSW 7 15,568,352 (GRCm39) missense
R9641:Obox6 UTSW 7 15,568,742 (GRCm39) nonsense probably null
R9722:Obox6 UTSW 7 15,568,831 (GRCm39) missense probably benign 0.01
Posted On 2014-05-07