Incidental Mutation 'R0789:Omt2b'
ID 76400
Institutional Source Beutler Lab
Gene Symbol Omt2b
Ensembl Gene ENSMUSG00000038750
Gene Name oocyte maturation, beta
Synonyms OM2b
MMRRC Submission 038969-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R0789 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 78235312-78236902 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to T at 78235447 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000034902] [ENSMUST00000043734] [ENSMUST00000125479] [ENSMUST00000129247] [ENSMUST00000186336] [ENSMUST00000187667]
AlphaFold D3YX29
Predicted Effect probably benign
Transcript: ENSMUST00000034902
SMART Domains Protein: ENSMUSP00000034902
Gene: ENSMUSG00000057933

DomainStartEndE-ValueType
Pfam:GST_N 5 77 5.1e-23 PFAM
Pfam:GST_C 99 192 8.9e-21 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000043734
AA Change: G10C
SMART Domains Protein: ENSMUSP00000036132
Gene: ENSMUSG00000038750
AA Change: G10C

DomainStartEndE-ValueType
transmembrane domain 69 91 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000125479
SMART Domains Protein: ENSMUSP00000115517
Gene: ENSMUSG00000057933

DomainStartEndE-ValueType
Pfam:GST_N 5 77 1.1e-21 PFAM
Pfam:GST_C 78 182 1.1e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000129247
SMART Domains Protein: ENSMUSP00000117101
Gene: ENSMUSG00000057933

DomainStartEndE-ValueType
Pfam:GST_N 5 77 1.1e-21 PFAM
Pfam:GST_C 78 179 1.2e-13 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000186336
AA Change: G10C
Predicted Effect unknown
Transcript: ENSMUST00000187667
AA Change: G10C
SMART Domains Protein: ENSMUSP00000139767
Gene: ENSMUSG00000038750
AA Change: G10C

DomainStartEndE-ValueType
transmembrane domain 69 91 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187890
Predicted Effect probably benign
Transcript: ENSMUST00000189243
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.6%
  • 3x: 98.9%
  • 10x: 96.7%
  • 20x: 91.7%
Validation Efficiency 98% (45/46)
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Asb10 T C 5: 24,744,862 (GRCm39) T111A probably damaging Het
BC024139 T C 15: 76,005,283 (GRCm39) I526M possibly damaging Het
Cacnb4 C T 2: 52,341,895 (GRCm39) V335I probably damaging Het
Ccdc33 C T 9: 58,024,497 (GRCm39) probably benign Het
Cfap58 T G 19: 47,943,748 (GRCm39) I316S probably benign Het
Chpf A T 1: 75,452,407 (GRCm39) L349Q probably damaging Het
Cntnap1 A G 11: 101,072,210 (GRCm39) probably benign Het
Col4a4 G A 1: 82,502,717 (GRCm39) P356S unknown Het
Dnah1 T C 14: 31,026,548 (GRCm39) I777V probably benign Het
Dnah11 A G 12: 117,874,967 (GRCm39) V3966A probably damaging Het
Fbxo38 G A 18: 62,648,570 (GRCm39) S656F possibly damaging Het
Fgf10 T A 13: 118,925,741 (GRCm39) N173K probably benign Het
Flt1 C T 5: 147,576,293 (GRCm39) E572K probably damaging Het
Gabra6 C A 11: 42,205,844 (GRCm39) R336S probably benign Het
Glt8d2 T C 10: 82,500,519 (GRCm39) N77S probably damaging Het
Grem1 C A 2: 113,580,056 (GRCm39) K148N probably benign Het
Hat1 G A 2: 71,252,088 (GRCm39) probably benign Het
Hydin A T 8: 111,293,603 (GRCm39) I3517F possibly damaging Het
Immt A G 6: 71,838,051 (GRCm39) K253R probably damaging Het
Klk1b8 A C 7: 43,595,151 (GRCm39) probably benign Het
Krt39 T C 11: 99,411,888 (GRCm39) Y66C probably benign Het
Mrgprb1 T C 7: 48,105,932 (GRCm39) probably benign Het
Nrp2 A G 1: 62,784,609 (GRCm39) M253V probably benign Het
Or5as1 T C 2: 86,980,171 (GRCm39) Y278C probably damaging Het
Or7g32 C A 9: 19,408,458 (GRCm39) P138H possibly damaging Het
Pcdh20 T C 14: 88,706,226 (GRCm39) Y358C probably damaging Het
Pik3r4 T C 9: 105,562,366 (GRCm39) M1215T probably benign Het
Polr1has T C 17: 37,275,852 (GRCm39) Y145H probably damaging Het
Rasal2 T C 1: 156,984,891 (GRCm39) E927G probably damaging Het
Ryr3 A G 2: 112,611,318 (GRCm39) probably null Het
Scaf8 T C 17: 3,247,112 (GRCm39) C812R possibly damaging Het
Scart2 G T 7: 139,828,133 (GRCm39) G114W probably damaging Het
Smpd4 T C 16: 17,443,690 (GRCm39) V78A probably benign Het
Sp2 A T 11: 96,852,202 (GRCm39) S241T probably benign Het
Tsga10 A T 1: 37,840,868 (GRCm39) I446N possibly damaging Het
Ubr4 G A 4: 139,137,582 (GRCm39) probably null Het
Usp44 T C 10: 93,683,082 (GRCm39) probably benign Het
Usp54 A T 14: 20,612,225 (GRCm39) S864T probably benign Het
Vmn2r56 A G 7: 12,466,762 (GRCm39) Y91H probably damaging Het
Vmn2r96 T C 17: 18,802,738 (GRCm39) V216A possibly damaging Het
Wdr17 A T 8: 55,112,607 (GRCm39) probably benign Het
Zmym6 A G 4: 127,016,615 (GRCm39) T799A possibly damaging Het
Other mutations in Omt2b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02325:Omt2b APN 9 78,235,854 (GRCm39) missense possibly damaging 0.66
R0497:Omt2b UTSW 9 78,235,513 (GRCm39) unclassified probably benign
R1526:Omt2b UTSW 9 78,235,420 (GRCm39) unclassified probably benign
R2191:Omt2b UTSW 9 78,235,457 (GRCm39) unclassified probably benign
R2192:Omt2b UTSW 9 78,235,457 (GRCm39) unclassified probably benign
R4568:Omt2b UTSW 9 78,235,529 (GRCm39) unclassified probably benign
R5884:Omt2b UTSW 9 78,235,839 (GRCm39) missense probably benign 0.00
R6287:Omt2b UTSW 9 78,235,543 (GRCm39) missense possibly damaging 0.92
R7409:Omt2b UTSW 9 78,235,894 (GRCm39) missense probably benign 0.03
R9077:Omt2b UTSW 9 78,235,548 (GRCm39) critical splice donor site probably null
Z1176:Omt2b UTSW 9 78,236,612 (GRCm39) missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- CAGTGAGCCTGGAACCATAGTGTG -3'
(R):5'- GCCAGCAGTAGCAGCAGCAATAATC -3'

Sequencing Primer
(F):5'- CTGGAACCATAGTGTGCCTTG -3'
(R):5'- GTCCACCTAGACAGAGCTGATG -3'
Posted On 2013-10-16