Incidental Mutation 'IGL02604:Obox7'
ID300161
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Obox7
Ensembl Gene ENSMUSG00000055942
Gene Nameoocyte specific homeobox 7
SynonymsGm4745
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.291) question?
Stock #IGL02604
Quality Score
Status
Chromosome7
Chromosomal Location14659496-14665996 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 14665368 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Glycine at position 173 (E173G)
Ref Sequence ENSEMBL: ENSMUSP00000138932 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000069740] [ENSMUST00000183424] [ENSMUST00000183788]
Predicted Effect probably benign
Transcript: ENSMUST00000069740
AA Change: E173G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000069239
Gene: ENSMUSG00000055942
AA Change: E173G

DomainStartEndE-ValueType
HOX 94 156 1.89e-13 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000183424
SMART Domains Protein: ENSMUSP00000138871
Gene: ENSMUSG00000055942

DomainStartEndE-ValueType
Pfam:Homeobox 95 137 7.8e-8 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000183788
AA Change: E173G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000138932
Gene: ENSMUSG00000055942
AA Change: E173G

DomainStartEndE-ValueType
HOX 94 156 1.89e-13 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2300002M23Rik T C 17: 35,567,948 V61A probably benign Het
Arfgef1 G A 1: 10,181,050 probably benign Het
Arhgef4 T A 1: 34,811,723 L594* probably null Het
Cacna2d3 T C 14: 29,293,109 T375A possibly damaging Het
Calb2 A C 8: 110,148,528 Y155D probably damaging Het
Camkmt A G 17: 85,096,625 T92A possibly damaging Het
Chsy3 A G 18: 59,409,115 S442G probably benign Het
Cyp4f13 T C 17: 32,932,421 I173V probably benign Het
Dapk1 A G 13: 60,748,320 T741A probably benign Het
Dennd3 T C 15: 73,556,403 I866T probably damaging Het
Dhrs2 A T 14: 55,237,321 I138F possibly damaging Het
Dscaml1 C T 9: 45,744,328 probably benign Het
Fsbp A G 4: 11,584,147 E282G probably damaging Het
Hpgds A T 6: 65,123,610 L128Q probably damaging Het
Hspa9 A G 18: 34,954,213 V13A unknown Het
Itgb3 A G 11: 104,662,443 E709G probably damaging Het
Jarid2 T C 13: 44,874,401 S148P probably damaging Het
Kcna6 C T 6: 126,739,204 G241R probably benign Het
Kdm5a T A 6: 120,431,980 N1541K probably benign Het
Kel C A 6: 41,687,582 E640D probably damaging Het
Lcp1 A T 14: 75,224,126 I520F probably benign Het
Lgr4 A G 2: 110,011,313 I524V probably damaging Het
Maats1 A G 16: 38,321,559 probably benign Het
Mup20 A C 4: 62,051,904 Y139D probably damaging Het
Notch4 T C 17: 34,565,388 probably null Het
Olfr1502 T A 19: 13,861,806 N4K probably benign Het
Olfr153 A T 2: 87,532,605 T191S probably damaging Het
Olfr447 T A 6: 42,912,058 C178* probably null Het
Olfr517 T A 7: 108,868,650 Y168F probably benign Het
Olfr889 C T 9: 38,115,852 Q19* probably null Het
Patl2 T G 2: 122,125,333 T241P possibly damaging Het
Pip5k1c C A 10: 81,317,321 probably null Het
Plekhg6 T C 6: 125,377,379 probably benign Het
Pon1 C A 6: 5,168,375 G344V probably damaging Het
Ppp1r21 G T 17: 88,572,743 K529N probably benign Het
Prdm15 A G 16: 97,821,942 S203P probably benign Het
Psmc2 T A 5: 21,795,100 probably null Het
Ptn T C 6: 36,715,718 M166V unknown Het
Ptpn13 A G 5: 103,501,903 N391D probably benign Het
Rnf214 A G 9: 45,869,543 S383P probably damaging Het
Rufy4 T A 1: 74,134,189 L438H probably damaging Het
Scarf2 A G 16: 17,803,744 T353A probably damaging Het
Serpinb9e A C 13: 33,257,759 I225L probably benign Het
Slc25a40 T C 5: 8,453,219 V312A probably benign Het
Tmc3 A G 7: 83,622,619 Y993C possibly damaging Het
Trim56 A C 5: 137,113,076 C529G probably damaging Het
Trim8 T C 19: 46,515,478 S490P probably damaging Het
Trmt6 A T 2: 132,810,437 Y147* probably null Het
Vmn2r109 T A 17: 20,540,701 H798L probably damaging Het
Vps35 A G 8: 85,286,389 L153P probably damaging Het
Wdr82 T C 9: 106,183,681 I131T probably damaging Het
Zfp69 A T 4: 120,931,463 D218E probably benign Het
Other mutations in Obox7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00597:Obox7 APN 7 14664032 utr 5 prime probably benign
R0058:Obox7 UTSW 7 14664388 missense probably benign 0.30
R1656:Obox7 UTSW 7 14665421 missense probably benign 0.01
R1977:Obox7 UTSW 7 14664398 missense probably damaging 1.00
R3708:Obox7 UTSW 7 14664197 nonsense probably null
R3939:Obox7 UTSW 7 14664047 missense probably benign 0.05
R4178:Obox7 UTSW 7 14664106 missense probably damaging 0.99
R4178:Obox7 UTSW 7 14664107 missense probably damaging 0.99
R4496:Obox7 UTSW 7 14665374 missense probably benign 0.19
R4818:Obox7 UTSW 7 14664485 missense probably damaging 1.00
R7839:Obox7 UTSW 7 14665425 missense probably benign 0.01
R7922:Obox7 UTSW 7 14665425 missense probably benign 0.01
Posted On2015-04-16