Incidental Mutation 'R0165:Meiob'
ID 24138
Institutional Source Beutler Lab
Gene Symbol Meiob
Ensembl Gene ENSMUSG00000024155
Gene Name meiosis specific with OB domains
Synonyms 4930528F23Rik
MMRRC Submission 038441-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.164) question?
Stock # R0165 (G1)
Quality Score 225
Status Validated (trace)
Chromosome 17
Chromosomal Location 25023275-25058762 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 25054135 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 401 (T401A)
Ref Sequence ENSEMBL: ENSMUSP00000024972 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000024972] [ENSMUST00000164251]
AlphaFold Q9D513
Predicted Effect probably benign
Transcript: ENSMUST00000024972
AA Change: T401A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000024972
Gene: ENSMUSG00000024155
AA Change: T401A

DomainStartEndE-ValueType
SCOP:d1fgua2 167 271 2e-9 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000164251
SMART Domains Protein: ENSMUSP00000129904
Gene: ENSMUSG00000024158

DomainStartEndE-ValueType
Lactamase_B 11 173 2.61e-32 SMART
Meta Mutation Damage Score 0.0854 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.5%
  • 10x: 96.2%
  • 20x: 91.4%
Validation Efficiency 96% (81/84)
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit male and female infertility associated with germ cell apoptosis, reduced gonads and impaired meiosis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik T C 12: 71,213,924 (GRCm39) I717T possibly damaging Het
6430571L13Rik A G 9: 107,223,383 (GRCm39) probably benign Het
Abca15 T A 7: 119,950,126 (GRCm39) probably benign Het
Abca6 A G 11: 110,110,430 (GRCm39) V573A possibly damaging Het
Adgrl2 A G 3: 148,558,499 (GRCm39) probably benign Het
Agap3 A G 5: 24,684,743 (GRCm39) T544A probably damaging Het
Ahrr G A 13: 74,431,143 (GRCm39) probably benign Het
Akr1c20 T C 13: 4,573,295 (GRCm39) T7A probably benign Het
Ankrd26 A G 6: 118,517,445 (GRCm39) S459P probably benign Het
Armh4 A G 14: 50,011,243 (GRCm39) S155P probably benign Het
Ascc3 T A 10: 50,718,223 (GRCm39) probably null Het
Brd1 T C 15: 88,613,980 (GRCm39) N305S probably damaging Het
Catip T A 1: 74,407,628 (GRCm39) L320Q possibly damaging Het
Cplane1 G A 15: 8,245,866 (GRCm39) V1413M probably damaging Het
Cttnbp2 G A 6: 18,435,409 (GRCm39) Q150* probably null Het
Cyp2d22 T G 15: 82,257,481 (GRCm39) N228T probably benign Het
Dapk1 T C 13: 60,909,407 (GRCm39) V1340A probably benign Het
Dcaf4 G A 12: 83,582,762 (GRCm39) probably benign Het
Ddhd1 G A 14: 45,833,049 (GRCm39) T849M probably damaging Het
Dnah6 A G 6: 72,998,306 (GRCm39) S3987P probably benign Het
Dst C A 1: 34,193,727 (GRCm39) probably benign Het
Epha2 T C 4: 141,049,203 (GRCm39) probably null Het
Ern2 T C 7: 121,779,002 (GRCm39) T281A probably benign Het
Extl1 A G 4: 134,085,014 (GRCm39) F652S probably damaging Het
Gckr A G 5: 31,484,292 (GRCm39) S541G possibly damaging Het
Gdap1l1 A G 2: 163,293,419 (GRCm39) probably null Het
Gm7535 T C 17: 18,131,437 (GRCm39) probably benign Het
Gmps T A 3: 63,901,375 (GRCm39) I398N probably damaging Het
Igf2r A G 17: 12,917,414 (GRCm39) V1556A probably benign Het
Il3ra T A 14: 14,350,967 (GRCm38) N283K probably benign Het
Ist1 A G 8: 110,401,998 (GRCm39) probably benign Het
Lama3 A T 18: 12,657,867 (GRCm39) I1934F probably damaging Het
Lars1 A T 18: 42,335,762 (GRCm39) M1118K possibly damaging Het
Lpin2 C T 17: 71,553,514 (GRCm39) S846L probably damaging Het
Lrrc4b C A 7: 44,111,739 (GRCm39) T537K probably damaging Het
Ltn1 G A 16: 87,202,407 (GRCm39) probably benign Het
Mettl21e G A 1: 44,250,283 (GRCm39) T41M probably damaging Het
Miga1 C T 3: 151,996,480 (GRCm39) E323K probably damaging Het
Ndufs1 A T 1: 63,198,907 (GRCm39) probably null Het
Or5p62 T C 7: 107,771,882 (GRCm39) D23G probably benign Het
Otog G A 7: 45,953,655 (GRCm39) V2638M probably damaging Het
Parp6 T C 9: 59,540,208 (GRCm39) Y274H probably damaging Het
Prom2 A T 2: 127,381,434 (GRCm39) probably benign Het
Prune2 T A 19: 17,099,974 (GRCm39) M1826K probably benign Het
Qki T A 17: 10,457,892 (GRCm39) D159V probably damaging Het
Rab12 A T 17: 66,807,312 (GRCm39) I139N probably damaging Het
Rab25 T A 3: 88,455,362 (GRCm39) E7D probably benign Het
Rala A T 13: 18,063,174 (GRCm39) V139E probably benign Het
Ralgapa2 A G 2: 146,230,407 (GRCm39) probably benign Het
Rbl2 T A 8: 91,800,804 (GRCm39) Y89N probably damaging Het
Rho A T 6: 115,909,188 (GRCm39) I75F probably damaging Het
Slc38a4 C A 15: 96,906,830 (GRCm39) A303S probably benign Het
Slc6a15 A G 10: 103,245,670 (GRCm39) D551G probably null Het
Smyd3 T C 1: 178,871,437 (GRCm39) N314S probably benign Het
Speer4f1 T A 5: 17,684,512 (GRCm39) L180* probably null Het
Stat6 T C 10: 127,493,096 (GRCm39) V576A probably damaging Het
Strn T C 17: 78,984,803 (GRCm39) D127G possibly damaging Het
Syne1 T C 10: 4,983,096 (GRCm39) R8610G probably benign Het
Tbc1d7 A C 13: 43,306,678 (GRCm39) probably null Het
Tcf3 C T 10: 80,248,831 (GRCm39) R548Q probably damaging Het
Tlr9 C A 9: 106,103,286 (GRCm39) A859D probably benign Het
Tmem106c T A 15: 97,866,020 (GRCm39) probably benign Het
Tmprss11c A T 5: 86,379,786 (GRCm39) probably benign Het
Tnfsf18 A G 1: 161,322,300 (GRCm39) R7G probably benign Het
Tnrc6b T A 15: 80,742,871 (GRCm39) probably null Het
Trpm7 A T 2: 126,639,433 (GRCm39) F1684I probably damaging Het
Ttbk1 C A 17: 46,789,864 (GRCm39) R133L possibly damaging Het
Ttn A G 2: 76,551,686 (GRCm39) S22962P probably damaging Het
Ube2q1 T A 3: 89,683,460 (GRCm39) L135Q probably damaging Het
Vmn1r28 G A 6: 58,242,702 (GRCm39) A182T probably benign Het
Vwce T C 19: 10,637,337 (GRCm39) probably benign Het
Wdhd1 A G 14: 47,504,525 (GRCm39) S350P probably benign Het
Zbtb21 A G 16: 97,752,604 (GRCm39) S560P probably damaging Het
Other mutations in Meiob
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00090:Meiob APN 17 25,042,603 (GRCm39) missense probably benign 0.00
IGL01830:Meiob APN 17 25,054,105 (GRCm39) missense probably benign 0.45
IGL01838:Meiob APN 17 25,042,643 (GRCm39) missense possibly damaging 0.68
R0605:Meiob UTSW 17 25,037,236 (GRCm39) splice site probably benign
R1170:Meiob UTSW 17 25,055,458 (GRCm39) missense probably damaging 1.00
R1496:Meiob UTSW 17 25,032,026 (GRCm39) missense possibly damaging 0.93
R1721:Meiob UTSW 17 25,053,021 (GRCm39) missense probably damaging 1.00
R1857:Meiob UTSW 17 25,042,544 (GRCm39) missense probably damaging 1.00
R1858:Meiob UTSW 17 25,042,544 (GRCm39) missense probably damaging 1.00
R1937:Meiob UTSW 17 25,037,305 (GRCm39) missense probably benign 0.34
R2066:Meiob UTSW 17 25,037,290 (GRCm39) missense probably damaging 1.00
R2510:Meiob UTSW 17 25,035,571 (GRCm39) splice site probably benign
R3433:Meiob UTSW 17 25,035,571 (GRCm39) splice site probably benign
R3906:Meiob UTSW 17 25,046,922 (GRCm39) missense probably benign 0.00
R4967:Meiob UTSW 17 25,037,353 (GRCm39) missense probably damaging 1.00
R5707:Meiob UTSW 17 25,054,025 (GRCm39) missense probably benign
R6109:Meiob UTSW 17 25,031,993 (GRCm39) missense probably benign
R6524:Meiob UTSW 17 25,051,491 (GRCm39) missense probably benign
R6756:Meiob UTSW 17 25,058,506 (GRCm39) missense possibly damaging 0.94
R7167:Meiob UTSW 17 25,055,419 (GRCm39) missense probably damaging 1.00
R8382:Meiob UTSW 17 25,046,913 (GRCm39) missense possibly damaging 0.79
R8440:Meiob UTSW 17 25,037,302 (GRCm39) missense probably benign
R8751:Meiob UTSW 17 25,047,008 (GRCm39) critical splice donor site probably null
R9000:Meiob UTSW 17 25,047,916 (GRCm39) splice site probably benign
R9799:Meiob UTSW 17 25,042,574 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GGTCCTCTCAGCCACGCTCC -3'
(R):5'- GCCTGACCAACATCTCCACTATGTTTT -3'

Sequencing Primer
(F):5'- ACCTGTGGTATTTTAGAGCACC -3'
(R):5'- ctcataaccatctttaactccagttc -3'
Posted On 2013-04-16