Incidental Mutation 'R4601:Tdrd5'
ID 345592
Institutional Source Beutler Lab
Gene Symbol Tdrd5
Ensembl Gene ENSMUSG00000060985
Gene Name tudor domain containing 5
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.181) question?
Stock # R4601 (G1)
Quality Score 225
Status Not validated
Chromosome 1
Chromosomal Location 156082866-156131234 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 156111944 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 479 (T479S)
Ref Sequence ENSEMBL: ENSMUSP00000137298 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000121146] [ENSMUST00000167528]
AlphaFold Q5VCS6
Predicted Effect probably benign
Transcript: ENSMUST00000121146
AA Change: T479S

PolyPhen 2 Score 0.124 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000137298
Gene: ENSMUSG00000060985
AA Change: T479S

DomainStartEndE-ValueType
Pfam:OST-HTH 6 76 3.7e-11 PFAM
Pfam:OST-HTH 126 194 1.5e-10 PFAM
Pfam:OST-HTH 290 361 7.4e-10 PFAM
TUDOR 532 590 3.25e-7 SMART
low complexity region 739 753 N/A INTRINSIC
low complexity region 1001 1021 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000167528
AA Change: T402S

PolyPhen 2 Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000137182
Gene: ENSMUSG00000060985
AA Change: T402S

DomainStartEndE-ValueType
Pfam:OST-HTH 6 75 1.4e-9 PFAM
Pfam:OST-HTH 213 284 6.4e-9 PFAM
TUDOR 455 513 3.25e-7 SMART
low complexity region 662 676 N/A INTRINSIC
low complexity region 924 944 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.1%
  • 20x: 94.5%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit male infertility associated with defective spermatid elongation, occasional arrested male meiosis, and apoptosis of male germ cells. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 91 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars2 T A 17: 45,827,847 (GRCm39) D555E probably damaging Het
Abca16 T G 7: 120,035,920 (GRCm39) F334L probably damaging Het
Abcc4 T A 14: 118,869,575 (GRCm39) M186L probably benign Het
Agap3 T C 5: 24,681,406 (GRCm39) L120P probably damaging Het
Ak7 G A 12: 105,679,834 (GRCm39) V123M probably benign Het
Aldh1a7 A T 19: 20,693,343 (GRCm39) V192D probably damaging Het
Ankrd36 A G 11: 5,520,102 (GRCm39) D59G probably benign Het
Arsi G A 18: 61,049,723 (GRCm39) G202E probably benign Het
Cacna1e A G 1: 154,347,359 (GRCm39) V936A probably benign Het
Camkv T C 9: 107,823,295 (GRCm39) V107A probably damaging Het
Camp T C 9: 109,677,730 (GRCm39) E80G probably damaging Het
Cblif A C 19: 11,729,554 (GRCm39) D171A probably damaging Het
Ccdc66 T C 14: 27,222,377 (GRCm39) N122S probably damaging Het
Cd101 G A 3: 100,901,204 (GRCm39) T960M possibly damaging Het
Cdk18 A G 1: 132,044,657 (GRCm39) V323A possibly damaging Het
Celf2 G T 2: 6,590,831 (GRCm39) N279K possibly damaging Het
Cemip T C 7: 83,600,826 (GRCm39) I932V probably damaging Het
Cep250 C A 2: 155,803,973 (GRCm39) Q28K probably benign Het
Ces2f T C 8: 105,676,596 (GRCm39) C97R probably damaging Het
Cfap126 G T 1: 170,941,627 (GRCm39) G41C possibly damaging Het
Cfap96 A T 8: 46,423,505 (GRCm39) I69N probably damaging Het
Chat T C 14: 32,146,112 (GRCm39) M354V probably benign Het
Clca4b A T 3: 144,632,945 (GRCm39) D168E possibly damaging Het
Cpxm1 T A 2: 130,235,496 (GRCm39) M499L possibly damaging Het
Dennd3 T A 15: 73,439,009 (GRCm39) W1126R probably damaging Het
Dgkb T C 12: 38,652,819 (GRCm39) S735P probably damaging Het
Dlec1 T C 9: 118,976,202 (GRCm39) probably null Het
Dnajc6 T C 4: 101,468,461 (GRCm39) F166L probably damaging Het
Dph5 A G 3: 115,693,426 (GRCm39) N115D possibly damaging Het
Ercc3 G A 18: 32,378,624 (GRCm39) A202T probably benign Het
Erich3 A T 3: 154,470,375 (GRCm39) D136V unknown Het
Exoc2 T C 13: 31,066,251 (GRCm39) N475S probably benign Het
Fam217a T C 13: 35,095,285 (GRCm39) D310G probably damaging Het
Fam53a C T 5: 33,758,007 (GRCm39) S372N probably benign Het
Fbn2 C G 18: 58,186,805 (GRCm39) G1699R probably damaging Het
Fbxo46 T C 7: 18,869,489 (GRCm39) V36A probably benign Het
Fhip1a T C 3: 85,648,487 (GRCm39) M26V probably damaging Het
G6pc1 A G 11: 101,263,567 (GRCm39) Y127C probably damaging Het
Gba2 A G 4: 43,573,810 (GRCm39) F161L probably damaging Het
Gja1 T C 10: 56,264,325 (GRCm39) L228P probably damaging Het
Gm20834 A G Y: 10,323,178 (GRCm39) V86A probably benign Het
Hmcn1 A T 1: 150,614,396 (GRCm39) C1337S probably damaging Het
Il1rl1 T A 1: 40,480,460 (GRCm39) S30T possibly damaging Het
Itgb4 A G 11: 115,896,548 (GRCm39) T1436A probably damaging Het
Itk T A 11: 46,227,342 (GRCm39) Q427L probably benign Het
Klhdc4 T C 8: 122,526,266 (GRCm39) E291G probably damaging Het
Map4 T A 9: 109,881,887 (GRCm39) S250R possibly damaging Het
Mnt T A 11: 74,727,285 (GRCm39) V57E possibly damaging Het
Mrc2 G A 11: 105,239,257 (GRCm39) probably null Het
Mslnl G A 17: 25,961,908 (GRCm39) V128M probably damaging Het
Mtcl2 T C 2: 156,881,844 (GRCm39) K736R probably benign Het
Musk A T 4: 58,301,625 (GRCm39) I128F probably damaging Het
Myh4 G A 11: 67,141,136 (GRCm39) A733T possibly damaging Het
Myo5a T A 9: 75,043,670 (GRCm39) F220I probably damaging Het
Npas3 A G 12: 54,091,361 (GRCm39) H305R probably damaging Het
Nrcam A T 12: 44,637,839 (GRCm39) Y1132F probably damaging Het
Nt5c3b A C 11: 100,323,744 (GRCm39) D189E probably benign Het
Nuf2 A G 1: 169,333,683 (GRCm39) L331P probably damaging Het
Nup214 C T 2: 31,887,977 (GRCm39) T646I probably benign Het
Or14j9 T C 17: 37,875,076 (GRCm39) N42S probably damaging Het
Pcdh18 T C 3: 49,699,174 (GRCm39) E1096G probably damaging Het
Pgm2 T A 5: 64,265,070 (GRCm39) F364I probably benign Het
Pikfyve A G 1: 65,273,421 (GRCm39) N612S probably damaging Het
Pla2g4e T G 2: 120,016,863 (GRCm39) H226P possibly damaging Het
Ppp3cb T C 14: 20,570,714 (GRCm39) N339S possibly damaging Het
Prkd2 G T 7: 16,577,573 (GRCm39) probably benign Het
Rnf133 T C 6: 23,649,041 (GRCm39) E296G possibly damaging Het
Sav1 A T 12: 70,031,095 (GRCm39) D142E probably benign Het
Scn3b C A 9: 40,199,719 (GRCm39) P212T probably damaging Het
Sel1l A T 12: 91,799,827 (GRCm39) probably null Het
Septin9 A G 11: 117,251,310 (GRCm39) K543E probably damaging Het
Serpinb12 T A 1: 106,876,883 (GRCm39) D66E probably benign Het
Slc35e2 T C 4: 155,702,106 (GRCm39) F290S probably benign Het
Snrpa A G 7: 26,894,958 (GRCm39) M1T probably null Het
Sptlc3 G A 2: 139,478,600 (GRCm39) V520I probably benign Het
Srpk3 A G X: 72,818,547 (GRCm39) H79R possibly damaging Het
Stox2 A G 8: 47,645,970 (GRCm39) S497P probably damaging Het
Stradb G A 1: 59,032,731 (GRCm39) S361N probably damaging Het
Sult3a2 T C 10: 33,658,083 (GRCm39) K10R probably benign Het
Susd4 A G 1: 182,686,025 (GRCm39) N192D probably damaging Het
Tcp10a T A 17: 7,593,374 (GRCm39) D32E probably benign Het
Tdpoz4 T A 3: 93,704,339 (GRCm39) V212D probably damaging Het
Tex10 T C 4: 48,452,946 (GRCm39) D671G probably benign Het
Tex55 A G 16: 38,648,380 (GRCm39) V243A probably benign Het
Traj37 T C 14: 54,418,996 (GRCm39) probably benign Het
Ttc7b G A 12: 100,466,376 (GRCm39) R79C probably damaging Het
Vmn2r115 T A 17: 23,565,373 (GRCm39) L420Q probably benign Het
Wdr24 T A 17: 26,047,181 (GRCm39) probably null Het
Wdr81 T A 11: 75,336,484 (GRCm39) Q516L probably damaging Het
Zfp516 A G 18: 82,974,164 (GRCm39) T121A probably benign Het
Zmat1 A T X: 133,873,694 (GRCm39) S566T probably damaging Homo
Other mutations in Tdrd5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01651:Tdrd5 APN 1 156,129,397 (GRCm39) missense probably benign 0.32
IGL02441:Tdrd5 APN 1 156,087,513 (GRCm39) splice site probably benign
IGL02932:Tdrd5 APN 1 156,098,190 (GRCm39) missense possibly damaging 0.52
R0049:Tdrd5 UTSW 1 156,129,473 (GRCm39) missense probably damaging 1.00
R0416:Tdrd5 UTSW 1 156,113,051 (GRCm39) missense probably damaging 0.96
R0518:Tdrd5 UTSW 1 156,090,511 (GRCm39) missense probably damaging 0.99
R1439:Tdrd5 UTSW 1 156,105,057 (GRCm39) missense probably damaging 1.00
R1454:Tdrd5 UTSW 1 156,087,406 (GRCm39) missense probably benign 0.41
R1497:Tdrd5 UTSW 1 156,083,372 (GRCm39) missense probably benign 0.28
R1774:Tdrd5 UTSW 1 156,105,079 (GRCm39) missense probably damaging 1.00
R2101:Tdrd5 UTSW 1 156,129,209 (GRCm39) missense probably damaging 1.00
R2125:Tdrd5 UTSW 1 156,104,143 (GRCm39) missense probably damaging 0.99
R2126:Tdrd5 UTSW 1 156,104,143 (GRCm39) missense probably damaging 0.99
R2197:Tdrd5 UTSW 1 156,087,435 (GRCm39) missense probably benign 0.02
R3820:Tdrd5 UTSW 1 156,113,053 (GRCm39) missense probably benign 0.16
R3928:Tdrd5 UTSW 1 156,128,348 (GRCm39) missense probably benign 0.06
R4258:Tdrd5 UTSW 1 156,087,312 (GRCm39) missense probably benign 0.00
R4502:Tdrd5 UTSW 1 156,128,334 (GRCm39) missense probably benign 0.00
R4602:Tdrd5 UTSW 1 156,111,944 (GRCm39) missense probably benign 0.12
R4610:Tdrd5 UTSW 1 156,111,944 (GRCm39) missense probably benign 0.12
R4611:Tdrd5 UTSW 1 156,111,944 (GRCm39) missense probably benign 0.12
R4674:Tdrd5 UTSW 1 156,105,005 (GRCm39) missense probably damaging 1.00
R4722:Tdrd5 UTSW 1 156,129,945 (GRCm39) missense probably benign 0.31
R4778:Tdrd5 UTSW 1 156,083,157 (GRCm39) missense probably damaging 0.98
R5737:Tdrd5 UTSW 1 156,128,294 (GRCm39) missense probably benign 0.01
R5881:Tdrd5 UTSW 1 156,122,070 (GRCm39) missense probably damaging 0.98
R5900:Tdrd5 UTSW 1 156,105,005 (GRCm39) nonsense probably null
R6234:Tdrd5 UTSW 1 156,120,947 (GRCm39) missense possibly damaging 0.93
R6557:Tdrd5 UTSW 1 156,128,291 (GRCm39) missense probably benign 0.10
R7068:Tdrd5 UTSW 1 156,111,841 (GRCm39) missense probably damaging 1.00
R7184:Tdrd5 UTSW 1 156,087,505 (GRCm39) missense probably benign 0.30
R7199:Tdrd5 UTSW 1 156,129,293 (GRCm39) missense probably damaging 0.98
R7432:Tdrd5 UTSW 1 156,130,002 (GRCm39) missense probably damaging 1.00
R7469:Tdrd5 UTSW 1 156,090,475 (GRCm39) missense probably benign 0.00
R8030:Tdrd5 UTSW 1 156,098,165 (GRCm39) nonsense probably null
R8323:Tdrd5 UTSW 1 156,094,832 (GRCm39) missense possibly damaging 0.63
R8680:Tdrd5 UTSW 1 156,098,788 (GRCm39) missense possibly damaging 0.49
R9282:Tdrd5 UTSW 1 156,105,030 (GRCm39) missense probably benign 0.01
X0026:Tdrd5 UTSW 1 156,112,997 (GRCm39) missense probably benign 0.01
Z1176:Tdrd5 UTSW 1 156,083,269 (GRCm39) missense probably damaging 1.00
Z1177:Tdrd5 UTSW 1 156,130,158 (GRCm39) missense probably damaging 1.00
Z1177:Tdrd5 UTSW 1 156,130,156 (GRCm39) missense possibly damaging 0.95
Z1177:Tdrd5 UTSW 1 156,083,199 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTTAGGAGTCCCAAGACCAAC -3'
(R):5'- AGGGACTGCAATAAGGCTGATTC -3'

Sequencing Primer
(F):5'- CTCATCTGAGAACTCCTGATTAAAGC -3'
(R):5'- CTGCAATAAGGCTGATTCGTGAAAG -3'
Posted On 2015-09-25