Incidental Mutation 'R4407:Tdpoz6'
ID 327698
Institutional Source Beutler Lab
Gene Symbol Tdpoz6
Ensembl Gene ENSMUSG00000103350
Gene Name TD and POZ domain containing 6
Synonyms Gm9107, Gm37596
MMRRC Submission 041689-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.375) question?
Stock # R4407 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 93599357-93600377 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 93599419 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Leucine at position 317 (V317L)
Ref Sequence ENSEMBL: ENSMUSP00000142038 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000193565]
AlphaFold A0A0A6YXL2
Predicted Effect noncoding transcript
Transcript: ENSMUST00000192747
Predicted Effect probably benign
Transcript: ENSMUST00000193565
AA Change: V317L

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000142038
Gene: ENSMUSG00000103350
AA Change: V317L

DomainStartEndE-ValueType
MATH 20 126 5.8e-4 SMART
BTB 184 283 5.8e-26 SMART
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency 100% (61/61)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830035A12Rik T C 11: 107,422,881 (GRCm39) noncoding transcript Het
Bbs10 A G 10: 111,135,720 (GRCm39) T278A probably benign Het
Bcl6b A G 11: 70,116,929 (GRCm39) L450P probably damaging Het
Braf T G 6: 39,592,654 (GRCm39) K674Q probably damaging Het
Cep112 C T 11: 108,410,027 (GRCm39) T481I possibly damaging Het
Cep135 T A 5: 76,772,514 (GRCm39) M633K probably benign Het
Cpped1 T C 16: 11,623,285 (GRCm39) Y278C probably damaging Het
Depdc5 T A 5: 33,061,878 (GRCm39) probably null Het
Dolpp1 C T 2: 30,286,464 (GRCm39) A128V possibly damaging Het
E2f5 T A 3: 14,668,823 (GRCm39) D238E probably benign Het
Fat4 A T 3: 39,012,689 (GRCm39) D2328V probably benign Het
Fbln1 T A 15: 85,115,757 (GRCm39) probably null Het
Fkbp3 T C 12: 65,116,778 (GRCm39) T53A probably damaging Het
Flg2 G T 3: 93,122,176 (GRCm39) G1449C unknown Het
G530012D18Rik G C 1: 85,504,923 (GRCm39) probably benign Het
Glyctk A T 9: 106,034,307 (GRCm39) probably benign Het
Gm6430 T C 1: 96,953,297 (GRCm39) noncoding transcript Het
Golga1 C A 2: 38,909,653 (GRCm39) probably null Het
Gucy2g A T 19: 55,226,269 (GRCm39) F216I probably benign Het
L3mbtl3 A G 10: 26,189,782 (GRCm39) V494A unknown Het
Lama2 AATCAGACAGGAG A 10: 27,088,124 (GRCm39) probably benign Het
Lemd3 A T 10: 120,761,335 (GRCm39) L907Q possibly damaging Het
Lrp2 A T 2: 69,332,861 (GRCm39) V1552D probably damaging Het
Map3k12 T C 15: 102,413,837 (GRCm39) T45A probably damaging Het
Mycbp2 A T 14: 103,524,664 (GRCm39) D665E probably damaging Het
Myof A G 19: 37,911,426 (GRCm39) S1502P probably damaging Het
Or4p7 A T 2: 88,222,427 (GRCm39) M279L probably benign Het
Pcdhac2 G T 18: 37,277,499 (GRCm39) V160L probably benign Het
Pcnt T C 10: 76,210,704 (GRCm39) E2473G possibly damaging Het
Pitpnm2 T A 5: 124,290,678 (GRCm39) I3L possibly damaging Het
Prkd3 C A 17: 79,290,987 (GRCm39) W176L probably damaging Het
Prpf39 C T 12: 65,103,040 (GRCm39) A438V probably damaging Het
Rpgrip1 T A 14: 52,384,856 (GRCm39) F655I probably damaging Het
Rrp12 T C 19: 41,880,990 (GRCm39) Y147C probably damaging Het
Sec23b A T 2: 144,416,638 (GRCm39) N429Y possibly damaging Het
Slc2a10 T A 2: 165,356,684 (GRCm39) S115T probably damaging Het
Spg11 A C 2: 121,905,813 (GRCm39) D1277E probably benign Het
Sspo A G 6: 48,437,454 (GRCm39) D1279G probably damaging Het
St18 T C 1: 6,898,061 (GRCm39) I621T probably benign Het
Tbc1d31 T A 15: 57,783,438 (GRCm39) D112E possibly damaging Het
Tgm4 A T 9: 122,885,595 (GRCm39) D379V probably damaging Het
Thyn1 A T 9: 26,914,893 (GRCm39) D15V possibly damaging Het
Timd6 A G 11: 46,468,207 (GRCm39) T94A probably damaging Het
Tm4sf19 T C 16: 32,226,712 (GRCm39) V167A possibly damaging Het
Trim38 A C 13: 23,975,474 (GRCm39) Q471P probably benign Het
Trmt1 T A 8: 85,424,384 (GRCm39) probably benign Het
Ubqlnl C T 7: 103,798,925 (GRCm39) V191M probably benign Het
Usp9y T C Y: 1,336,375 (GRCm39) I1500V probably benign Het
Vgll4 C T 6: 114,867,573 (GRCm39) probably null Het
Vmn1r173 T A 7: 23,402,441 (GRCm39) N225K probably damaging Het
Vmn2r22 C T 6: 123,614,913 (GRCm39) G226R probably damaging Het
Wnk3 C A X: 150,016,209 (GRCm39) P555Q probably benign Het
Yes1 T G 5: 32,797,929 (GRCm39) Y83D possibly damaging Het
Zdhhc15 G A X: 103,604,294 (GRCm39) R322* probably null Het
Other mutations in Tdpoz6
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4665:Tdpoz6 UTSW 3 93,599,776 (GRCm39) missense probably damaging 1.00
R4815:Tdpoz6 UTSW 3 93,599,593 (GRCm39) missense probably benign 0.44
R5664:Tdpoz6 UTSW 3 93,599,994 (GRCm39) missense probably benign 0.15
R6465:Tdpoz6 UTSW 3 93,600,303 (GRCm39) missense probably damaging 1.00
R6937:Tdpoz6 UTSW 3 93,599,523 (GRCm39) missense probably benign 0.04
R7467:Tdpoz6 UTSW 3 93,600,265 (GRCm39) missense probably benign
R7943:Tdpoz6 UTSW 3 93,600,070 (GRCm39) missense probably benign 0.00
R8132:Tdpoz6 UTSW 3 93,599,452 (GRCm39) nonsense probably null
R8927:Tdpoz6 UTSW 3 93,599,950 (GRCm39) missense probably benign 0.20
R8928:Tdpoz6 UTSW 3 93,599,950 (GRCm39) missense probably benign 0.20
R9023:Tdpoz6 UTSW 3 93,599,742 (GRCm39) missense probably damaging 1.00
R9033:Tdpoz6 UTSW 3 93,600,168 (GRCm39) missense probably damaging 1.00
R9355:Tdpoz6 UTSW 3 93,600,307 (GRCm39) missense possibly damaging 0.58
R9728:Tdpoz6 UTSW 3 93,599,807 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- TGTACTCTAACCAGAAATCAGTGG -3'
(R):5'- ACTCCATGGCCACTGATGTG -3'

Sequencing Primer
(F):5'- CAACACTGGTTATACCTGTTGGAAG -3'
(R):5'- ATGGCCACTGATGTGCTGAC -3'
Posted On 2015-07-07