Incidental Mutation 'R0594:Tdrd6'
ID |
56174 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tdrd6
|
Ensembl Gene |
ENSMUSG00000040140 |
Gene Name |
tudor domain containing 6 |
Synonyms |
|
MMRRC Submission |
038784-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0594 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
17 |
Chromosomal Location |
43926226-43941190 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 43940274 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 258
(V258A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000035338
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045717]
[ENSMUST00000168073]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000045717
AA Change: V258A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000035338 Gene: ENSMUSG00000040140 AA Change: V258A
Domain | Start | End | E-Value | Type |
Pfam:TUDOR
|
14 |
133 |
9.9e-9 |
PFAM |
low complexity region
|
166 |
187 |
N/A |
INTRINSIC |
TUDOR
|
308 |
366 |
1.14e-2 |
SMART |
low complexity region
|
452 |
463 |
N/A |
INTRINSIC |
TUDOR
|
541 |
597 |
2.68e-8 |
SMART |
TUDOR
|
817 |
877 |
2.56e-5 |
SMART |
TUDOR
|
1037 |
1090 |
5.36e-8 |
SMART |
TUDOR
|
1357 |
1415 |
2.19e-13 |
SMART |
TUDOR
|
1569 |
1628 |
3.1e-13 |
SMART |
low complexity region
|
1826 |
1842 |
N/A |
INTRINSIC |
low complexity region
|
1866 |
1876 |
N/A |
INTRINSIC |
TUDOR
|
2026 |
2083 |
9.45e-1 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000168073
AA Change: V258A
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000131277 Gene: ENSMUSG00000040140 AA Change: V258A
Domain | Start | End | E-Value | Type |
Pfam:TUDOR
|
12 |
133 |
7.2e-9 |
PFAM |
low complexity region
|
166 |
187 |
N/A |
INTRINSIC |
TUDOR
|
308 |
366 |
1.14e-2 |
SMART |
low complexity region
|
452 |
463 |
N/A |
INTRINSIC |
TUDOR
|
541 |
597 |
2.68e-8 |
SMART |
TUDOR
|
817 |
877 |
2.56e-5 |
SMART |
TUDOR
|
1037 |
1090 |
5.36e-8 |
SMART |
TUDOR
|
1357 |
1415 |
2.19e-13 |
SMART |
TUDOR
|
1569 |
1628 |
3.1e-13 |
SMART |
low complexity region
|
1826 |
1842 |
N/A |
INTRINSIC |
low complexity region
|
1866 |
1876 |
N/A |
INTRINSIC |
TUDOR
|
2027 |
2084 |
9.45e-1 |
SMART |
|
Meta Mutation Damage Score |
0.2992 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.4%
- 20x: 94.6%
|
Validation Efficiency |
99% (119/120) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a tudor domain-containing protein and component of the chromatoid body, a type of ribonucleoprotein granule present in male germ cells. Studies in rodents have demonstrated a role for the encoded protein in spermiogenesis and the nonsense mediated decay (NMD) pathway. This protein is a major autoantigen in human patients with autoimmune polyendocrine syndrome type 1 (APS1). [provided by RefSeq, Oct 2016] PHENOTYPE: Mice homozygous for a null allele exhibit male fertility associated with arrested spermatogenesis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
C |
16: 14,207,744 (GRCm39) |
V41A |
probably benign |
Het |
Acad11 |
A |
G |
9: 103,972,762 (GRCm39) |
Q367R |
probably benign |
Het |
Ackr4 |
A |
G |
9: 103,976,203 (GRCm39) |
V248A |
possibly damaging |
Het |
Adamts14 |
T |
C |
10: 61,038,666 (GRCm39) |
E945G |
probably damaging |
Het |
Ano2 |
A |
G |
6: 125,959,728 (GRCm39) |
M663V |
probably damaging |
Het |
Apc2 |
T |
A |
10: 80,142,090 (GRCm39) |
C336* |
probably null |
Het |
Arhgap17 |
A |
G |
7: 122,893,741 (GRCm39) |
S560P |
probably benign |
Het |
Arl5a |
T |
C |
2: 52,295,026 (GRCm39) |
D128G |
probably damaging |
Het |
Atp6v0a2 |
C |
A |
5: 124,795,046 (GRCm39) |
R678S |
probably benign |
Het |
B4galnt2 |
C |
A |
11: 95,782,735 (GRCm39) |
A26S |
probably benign |
Het |
C1qtnf1 |
A |
T |
11: 118,337,454 (GRCm39) |
T95S |
possibly damaging |
Het |
Ccdc188 |
T |
A |
16: 18,036,784 (GRCm39) |
F241L |
probably benign |
Het |
Cdh19 |
A |
T |
1: 110,853,597 (GRCm39) |
D281E |
probably benign |
Het |
Cdk5rap2 |
T |
C |
4: 70,273,050 (GRCm39) |
E241G |
probably damaging |
Het |
Cherp |
A |
T |
8: 73,216,246 (GRCm39) |
|
probably null |
Het |
Cpne9 |
T |
A |
6: 113,267,361 (GRCm39) |
|
probably benign |
Het |
Cthrc1 |
A |
T |
15: 38,940,537 (GRCm39) |
R47W |
possibly damaging |
Het |
Dcaf13 |
A |
G |
15: 38,986,663 (GRCm39) |
E145G |
probably benign |
Het |
Dcaf4 |
T |
A |
12: 83,584,817 (GRCm39) |
|
probably null |
Het |
Dgka |
A |
C |
10: 128,568,979 (GRCm39) |
|
probably benign |
Het |
Dhrs13 |
T |
A |
11: 77,925,351 (GRCm39) |
F157L |
probably damaging |
Het |
Dnajb5 |
A |
T |
4: 42,956,577 (GRCm39) |
Y88F |
probably damaging |
Het |
Dpp8 |
A |
G |
9: 64,944,280 (GRCm39) |
T16A |
probably damaging |
Het |
Dscc1 |
A |
T |
15: 54,952,448 (GRCm39) |
I91K |
possibly damaging |
Het |
Efemp2 |
T |
A |
19: 5,525,091 (GRCm39) |
|
probably benign |
Het |
Elf2 |
T |
C |
3: 51,163,874 (GRCm39) |
T504A |
possibly damaging |
Het |
Elk3 |
G |
A |
10: 93,101,022 (GRCm39) |
S243F |
probably damaging |
Het |
Ell2 |
A |
G |
13: 75,898,112 (GRCm39) |
D93G |
probably damaging |
Het |
Eln |
G |
T |
5: 134,741,252 (GRCm39) |
|
probably benign |
Het |
Eme1 |
C |
T |
11: 94,541,256 (GRCm39) |
D189N |
possibly damaging |
Het |
Epb41l2 |
A |
G |
10: 25,319,668 (GRCm39) |
E167G |
possibly damaging |
Het |
Exoc5 |
A |
T |
14: 49,273,544 (GRCm39) |
|
probably benign |
Het |
Fam170b |
A |
G |
14: 32,558,271 (GRCm39) |
K369E |
unknown |
Het |
Fam187b |
T |
A |
7: 30,676,579 (GRCm39) |
C29* |
probably null |
Het |
Fam20c |
T |
C |
5: 138,752,392 (GRCm39) |
S260P |
possibly damaging |
Het |
Fam216b |
G |
A |
14: 78,324,114 (GRCm39) |
A21V |
possibly damaging |
Het |
Fam98a |
A |
T |
17: 75,845,482 (GRCm39) |
Y421* |
probably null |
Het |
Farp2 |
T |
C |
1: 93,504,222 (GRCm39) |
V333A |
probably damaging |
Het |
Fcgr1 |
T |
C |
3: 96,199,628 (GRCm39) |
Y93C |
probably damaging |
Het |
Fgd2 |
A |
T |
17: 29,584,526 (GRCm39) |
I157F |
probably damaging |
Het |
Frmd4b |
T |
A |
6: 97,302,387 (GRCm39) |
|
probably benign |
Het |
Fut9 |
T |
C |
4: 25,620,526 (GRCm39) |
D96G |
possibly damaging |
Het |
Glt8d1 |
G |
A |
14: 30,732,367 (GRCm39) |
|
probably null |
Het |
Gm7579 |
T |
A |
7: 141,766,121 (GRCm39) |
C176S |
unknown |
Het |
Gmpr2 |
A |
G |
14: 55,915,445 (GRCm39) |
E272G |
probably damaging |
Het |
Grin2b |
T |
C |
6: 135,710,927 (GRCm39) |
H873R |
probably damaging |
Het |
Gtf2i |
C |
T |
5: 134,271,027 (GRCm39) |
|
probably benign |
Het |
Htr3b |
A |
T |
9: 48,858,931 (GRCm39) |
V69E |
probably benign |
Het |
Icam5 |
A |
G |
9: 20,946,894 (GRCm39) |
N474S |
probably benign |
Het |
Itgal |
T |
A |
7: 126,913,232 (GRCm39) |
S610T |
probably damaging |
Het |
Jag1 |
T |
A |
2: 136,929,000 (GRCm39) |
I819L |
probably damaging |
Het |
Kif9 |
A |
T |
9: 110,340,408 (GRCm39) |
E467V |
probably benign |
Het |
Krit1 |
T |
C |
5: 3,873,694 (GRCm39) |
L491P |
possibly damaging |
Het |
Lipo2 |
T |
G |
19: 33,724,302 (GRCm39) |
I155L |
possibly damaging |
Het |
Lmbr1 |
A |
G |
5: 29,497,207 (GRCm39) |
F65L |
possibly damaging |
Het |
Lsp1 |
G |
A |
7: 142,042,687 (GRCm39) |
|
probably benign |
Het |
Mgat5 |
T |
A |
1: 127,339,985 (GRCm39) |
D455E |
probably damaging |
Het |
Mical2 |
A |
T |
7: 111,917,657 (GRCm39) |
Y338F |
probably damaging |
Het |
Mre11a |
T |
G |
9: 14,726,505 (GRCm39) |
S396A |
probably benign |
Het |
Mrtfa |
G |
A |
15: 80,901,375 (GRCm39) |
T372I |
probably damaging |
Het |
Mtarc2 |
T |
C |
1: 184,573,536 (GRCm39) |
N121D |
probably benign |
Het |
Myo3a |
C |
T |
2: 22,436,370 (GRCm39) |
|
probably benign |
Het |
Naca |
T |
C |
10: 127,876,224 (GRCm39) |
|
probably benign |
Het |
Nav1 |
A |
T |
1: 135,395,381 (GRCm39) |
I996K |
possibly damaging |
Het |
Ncbp1 |
A |
G |
4: 46,170,551 (GRCm39) |
N742S |
probably benign |
Het |
Ndufaf3 |
G |
A |
9: 108,444,122 (GRCm39) |
A2V |
probably benign |
Het |
Niban3 |
C |
A |
8: 72,051,779 (GRCm39) |
A38E |
probably benign |
Het |
Ntn5 |
G |
T |
7: 45,336,105 (GRCm39) |
A47S |
probably damaging |
Het |
Or10ag57 |
T |
A |
2: 87,218,298 (GRCm39) |
I83N |
probably damaging |
Het |
Or1e25 |
G |
A |
11: 73,494,218 (GRCm39) |
E271K |
probably benign |
Het |
Or1e32 |
T |
C |
11: 73,705,443 (GRCm39) |
H155R |
probably benign |
Het |
Or2a7 |
T |
A |
6: 43,151,541 (GRCm39) |
V207E |
possibly damaging |
Het |
Or6c207 |
T |
C |
10: 129,105,021 (GRCm39) |
Y57C |
possibly damaging |
Het |
Or9i1 |
G |
T |
19: 13,839,643 (GRCm39) |
C162F |
probably benign |
Het |
Otud7a |
T |
A |
7: 63,377,220 (GRCm39) |
L203* |
probably null |
Het |
Pakap |
A |
G |
4: 57,856,752 (GRCm39) |
T694A |
probably benign |
Het |
Pcdhb13 |
A |
G |
18: 37,576,984 (GRCm39) |
Y454C |
probably damaging |
Het |
Pdzph1 |
C |
T |
17: 59,261,474 (GRCm39) |
V853M |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,056,453 (GRCm39) |
S4517P |
probably damaging |
Het |
Pm20d2 |
C |
T |
4: 33,181,746 (GRCm39) |
E286K |
probably damaging |
Het |
Polr2i |
T |
A |
7: 29,932,170 (GRCm39) |
|
probably null |
Het |
Ppp1r12b |
A |
G |
1: 134,704,217 (GRCm39) |
L879P |
probably damaging |
Het |
Prf1 |
C |
A |
10: 61,139,501 (GRCm39) |
Y486* |
probably null |
Het |
Qsox2 |
T |
G |
2: 26,104,056 (GRCm39) |
T325P |
probably damaging |
Het |
Rab1b |
G |
T |
19: 5,150,684 (GRCm39) |
|
probably benign |
Het |
Rbm19 |
T |
C |
5: 120,266,381 (GRCm39) |
|
probably null |
Het |
Rhobtb2 |
A |
G |
14: 70,031,397 (GRCm39) |
V576A |
probably benign |
Het |
Rnps1 |
G |
A |
17: 24,643,411 (GRCm39) |
V215M |
probably damaging |
Het |
Rps11 |
A |
G |
7: 44,773,706 (GRCm39) |
|
probably benign |
Het |
Serpinb3d |
C |
T |
1: 107,007,077 (GRCm39) |
M210I |
probably damaging |
Het |
Sgsm1 |
T |
C |
5: 113,458,428 (GRCm39) |
T17A |
probably benign |
Het |
Slc6a3 |
A |
G |
13: 73,686,761 (GRCm39) |
T43A |
probably damaging |
Het |
Sox4 |
C |
G |
13: 29,136,887 (GRCm39) |
A40P |
probably damaging |
Het |
Spry2 |
A |
T |
14: 106,130,744 (GRCm39) |
D147E |
possibly damaging |
Het |
Stpg1 |
A |
G |
4: 135,246,742 (GRCm39) |
N157D |
possibly damaging |
Het |
Sumf1 |
T |
C |
6: 108,150,375 (GRCm39) |
D152G |
probably benign |
Het |
Tbr1 |
T |
C |
2: 61,641,964 (GRCm39) |
S410P |
possibly damaging |
Het |
Tirap |
C |
T |
9: 35,100,057 (GRCm39) |
G209D |
probably damaging |
Het |
Tnfrsf8 |
A |
T |
4: 145,023,431 (GRCm39) |
V134D |
probably damaging |
Het |
Tnr |
A |
G |
1: 159,677,905 (GRCm39) |
T97A |
probably benign |
Het |
Tspan32 |
T |
A |
7: 142,569,347 (GRCm39) |
F135L |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,619,400 (GRCm39) |
K16021E |
probably damaging |
Het |
Tusc3 |
T |
A |
8: 39,564,122 (GRCm39) |
I251N |
probably damaging |
Het |
Usp38 |
A |
T |
8: 81,731,995 (GRCm39) |
I305N |
probably damaging |
Het |
Usp4 |
T |
A |
9: 108,248,080 (GRCm39) |
|
probably null |
Het |
Usp5 |
A |
T |
6: 124,794,387 (GRCm39) |
D764E |
probably damaging |
Het |
Vangl2 |
A |
T |
1: 171,832,224 (GRCm39) |
V544E |
probably damaging |
Het |
Vldlr |
G |
A |
19: 27,212,219 (GRCm39) |
V78M |
probably damaging |
Het |
Vmn1r29 |
T |
C |
6: 58,284,757 (GRCm39) |
V159A |
probably benign |
Het |
Vmn2r16 |
T |
A |
5: 109,511,762 (GRCm39) |
F656L |
probably damaging |
Het |
Wdfy3 |
T |
A |
5: 102,054,051 (GRCm39) |
I1590F |
possibly damaging |
Het |
Xpo1 |
T |
A |
11: 23,230,402 (GRCm39) |
V263E |
probably damaging |
Het |
Zbtb38 |
A |
G |
9: 96,568,007 (GRCm39) |
S1026P |
probably damaging |
Het |
Zfp407 |
A |
T |
18: 84,580,692 (GRCm39) |
D140E |
possibly damaging |
Het |
Zfp637 |
T |
A |
6: 117,822,647 (GRCm39) |
Y258* |
probably null |
Het |
Zfp951 |
T |
A |
5: 104,962,438 (GRCm39) |
Q376L |
possibly damaging |
Het |
|
Other mutations in Tdrd6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00571:Tdrd6
|
APN |
17 |
43,939,051 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00844:Tdrd6
|
APN |
17 |
43,928,087 (GRCm39) |
missense |
probably benign |
|
IGL00845:Tdrd6
|
APN |
17 |
43,937,607 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01558:Tdrd6
|
APN |
17 |
43,936,659 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01558:Tdrd6
|
APN |
17 |
43,935,657 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01575:Tdrd6
|
APN |
17 |
43,938,871 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01812:Tdrd6
|
APN |
17 |
43,936,065 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02013:Tdrd6
|
APN |
17 |
43,936,837 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02067:Tdrd6
|
APN |
17 |
43,939,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02112:Tdrd6
|
APN |
17 |
43,940,242 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02159:Tdrd6
|
APN |
17 |
43,939,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02226:Tdrd6
|
APN |
17 |
43,938,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02416:Tdrd6
|
APN |
17 |
43,935,629 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02577:Tdrd6
|
APN |
17 |
43,937,728 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02631:Tdrd6
|
APN |
17 |
43,937,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Tdrd6
|
APN |
17 |
43,931,337 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02792:Tdrd6
|
APN |
17 |
43,935,918 (GRCm39) |
missense |
probably benign |
|
IGL02929:Tdrd6
|
APN |
17 |
43,940,604 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02934:Tdrd6
|
APN |
17 |
43,938,778 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02954:Tdrd6
|
APN |
17 |
43,938,153 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02969:Tdrd6
|
APN |
17 |
43,938,440 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03006:Tdrd6
|
APN |
17 |
43,936,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Tdrd6
|
APN |
17 |
43,936,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03219:Tdrd6
|
APN |
17 |
43,938,855 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03372:Tdrd6
|
APN |
17 |
43,936,459 (GRCm39) |
missense |
probably damaging |
1.00 |
Edward
|
UTSW |
17 |
43,938,106 (GRCm39) |
missense |
probably damaging |
1.00 |
eliza
|
UTSW |
17 |
43,939,053 (GRCm39) |
missense |
possibly damaging |
0.90 |
Elizabeth
|
UTSW |
17 |
43,935,095 (GRCm39) |
missense |
probably benign |
0.00 |
henry
|
UTSW |
17 |
43,939,050 (GRCm39) |
missense |
probably damaging |
0.99 |
BB001:Tdrd6
|
UTSW |
17 |
43,938,697 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB011:Tdrd6
|
UTSW |
17 |
43,938,697 (GRCm39) |
missense |
possibly damaging |
0.94 |
G1citation:Tdrd6
|
UTSW |
17 |
43,938,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R0030:Tdrd6
|
UTSW |
17 |
43,937,482 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0057:Tdrd6
|
UTSW |
17 |
43,928,052 (GRCm39) |
splice site |
probably benign |
|
R0090:Tdrd6
|
UTSW |
17 |
43,939,132 (GRCm39) |
missense |
probably benign |
0.00 |
R0270:Tdrd6
|
UTSW |
17 |
43,935,199 (GRCm39) |
missense |
probably benign |
|
R0463:Tdrd6
|
UTSW |
17 |
43,936,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Tdrd6
|
UTSW |
17 |
43,939,050 (GRCm39) |
missense |
probably damaging |
0.99 |
R1226:Tdrd6
|
UTSW |
17 |
43,937,523 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1309:Tdrd6
|
UTSW |
17 |
43,937,512 (GRCm39) |
missense |
probably benign |
|
R1483:Tdrd6
|
UTSW |
17 |
43,938,498 (GRCm39) |
missense |
probably benign |
0.31 |
R1561:Tdrd6
|
UTSW |
17 |
43,936,515 (GRCm39) |
missense |
probably damaging |
0.96 |
R1574:Tdrd6
|
UTSW |
17 |
43,936,515 (GRCm39) |
missense |
probably damaging |
0.96 |
R1647:Tdrd6
|
UTSW |
17 |
43,938,000 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1648:Tdrd6
|
UTSW |
17 |
43,938,000 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1723:Tdrd6
|
UTSW |
17 |
43,939,218 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1786:Tdrd6
|
UTSW |
17 |
43,935,724 (GRCm39) |
missense |
probably benign |
0.01 |
R1819:Tdrd6
|
UTSW |
17 |
43,937,442 (GRCm39) |
missense |
probably benign |
0.00 |
R1836:Tdrd6
|
UTSW |
17 |
43,936,480 (GRCm39) |
missense |
probably benign |
0.03 |
R1892:Tdrd6
|
UTSW |
17 |
43,935,696 (GRCm39) |
missense |
probably benign |
0.00 |
R1911:Tdrd6
|
UTSW |
17 |
43,937,979 (GRCm39) |
missense |
probably benign |
0.21 |
R1936:Tdrd6
|
UTSW |
17 |
43,937,358 (GRCm39) |
missense |
probably damaging |
0.98 |
R2005:Tdrd6
|
UTSW |
17 |
43,939,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Tdrd6
|
UTSW |
17 |
43,939,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Tdrd6
|
UTSW |
17 |
43,935,724 (GRCm39) |
missense |
probably benign |
0.01 |
R2133:Tdrd6
|
UTSW |
17 |
43,935,724 (GRCm39) |
missense |
probably benign |
0.01 |
R3010:Tdrd6
|
UTSW |
17 |
43,938,933 (GRCm39) |
missense |
probably benign |
0.00 |
R4225:Tdrd6
|
UTSW |
17 |
43,936,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R4448:Tdrd6
|
UTSW |
17 |
43,940,626 (GRCm39) |
missense |
probably benign |
0.26 |
R4449:Tdrd6
|
UTSW |
17 |
43,940,626 (GRCm39) |
missense |
probably benign |
0.26 |
R4531:Tdrd6
|
UTSW |
17 |
43,939,645 (GRCm39) |
missense |
probably damaging |
0.98 |
R4624:Tdrd6
|
UTSW |
17 |
43,936,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R4665:Tdrd6
|
UTSW |
17 |
43,935,007 (GRCm39) |
missense |
probably benign |
|
R4676:Tdrd6
|
UTSW |
17 |
43,938,501 (GRCm39) |
missense |
probably damaging |
0.96 |
R4785:Tdrd6
|
UTSW |
17 |
43,936,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R4912:Tdrd6
|
UTSW |
17 |
43,935,218 (GRCm39) |
missense |
probably benign |
0.34 |
R5134:Tdrd6
|
UTSW |
17 |
43,937,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R5145:Tdrd6
|
UTSW |
17 |
43,936,966 (GRCm39) |
missense |
probably damaging |
0.96 |
R5623:Tdrd6
|
UTSW |
17 |
43,940,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R5712:Tdrd6
|
UTSW |
17 |
43,937,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R5897:Tdrd6
|
UTSW |
17 |
43,935,768 (GRCm39) |
missense |
probably damaging |
0.98 |
R5913:Tdrd6
|
UTSW |
17 |
43,939,302 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6142:Tdrd6
|
UTSW |
17 |
43,940,373 (GRCm39) |
missense |
probably benign |
0.01 |
R6181:Tdrd6
|
UTSW |
17 |
43,939,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Tdrd6
|
UTSW |
17 |
43,940,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6233:Tdrd6
|
UTSW |
17 |
43,940,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6289:Tdrd6
|
UTSW |
17 |
43,935,411 (GRCm39) |
missense |
probably benign |
0.01 |
R6315:Tdrd6
|
UTSW |
17 |
43,937,229 (GRCm39) |
missense |
probably benign |
0.02 |
R6578:Tdrd6
|
UTSW |
17 |
43,939,852 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6645:Tdrd6
|
UTSW |
17 |
43,935,423 (GRCm39) |
missense |
probably benign |
0.10 |
R6822:Tdrd6
|
UTSW |
17 |
43,938,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:Tdrd6
|
UTSW |
17 |
43,938,599 (GRCm39) |
missense |
probably benign |
0.28 |
R7075:Tdrd6
|
UTSW |
17 |
43,936,065 (GRCm39) |
missense |
probably benign |
0.10 |
R7107:Tdrd6
|
UTSW |
17 |
43,935,095 (GRCm39) |
missense |
probably benign |
0.00 |
R7381:Tdrd6
|
UTSW |
17 |
43,936,984 (GRCm39) |
missense |
probably benign |
0.00 |
R7458:Tdrd6
|
UTSW |
17 |
43,935,937 (GRCm39) |
missense |
probably benign |
0.02 |
R7461:Tdrd6
|
UTSW |
17 |
43,938,817 (GRCm39) |
missense |
probably benign |
0.00 |
R7505:Tdrd6
|
UTSW |
17 |
43,938,570 (GRCm39) |
missense |
not run |
|
R7583:Tdrd6
|
UTSW |
17 |
43,935,129 (GRCm39) |
missense |
probably benign |
0.29 |
R7613:Tdrd6
|
UTSW |
17 |
43,938,817 (GRCm39) |
missense |
probably benign |
0.00 |
R7723:Tdrd6
|
UTSW |
17 |
43,936,851 (GRCm39) |
missense |
probably benign |
0.09 |
R7759:Tdrd6
|
UTSW |
17 |
43,935,730 (GRCm39) |
missense |
probably benign |
0.00 |
R7924:Tdrd6
|
UTSW |
17 |
43,938,697 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8002:Tdrd6
|
UTSW |
17 |
43,940,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R8134:Tdrd6
|
UTSW |
17 |
43,937,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R8231:Tdrd6
|
UTSW |
17 |
43,933,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R8242:Tdrd6
|
UTSW |
17 |
43,939,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:Tdrd6
|
UTSW |
17 |
43,935,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Tdrd6
|
UTSW |
17 |
43,935,910 (GRCm39) |
missense |
probably benign |
0.28 |
R9100:Tdrd6
|
UTSW |
17 |
43,936,305 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9201:Tdrd6
|
UTSW |
17 |
43,936,561 (GRCm39) |
missense |
probably benign |
0.00 |
R9222:Tdrd6
|
UTSW |
17 |
43,939,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Tdrd6
|
UTSW |
17 |
43,936,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R9373:Tdrd6
|
UTSW |
17 |
43,939,053 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9384:Tdrd6
|
UTSW |
17 |
43,937,783 (GRCm39) |
missense |
probably benign |
0.26 |
R9448:Tdrd6
|
UTSW |
17 |
43,936,567 (GRCm39) |
missense |
probably benign |
|
R9534:Tdrd6
|
UTSW |
17 |
43,936,510 (GRCm39) |
missense |
probably benign |
0.19 |
R9613:Tdrd6
|
UTSW |
17 |
43,939,518 (GRCm39) |
missense |
probably damaging |
0.99 |
X0065:Tdrd6
|
UTSW |
17 |
43,936,884 (GRCm39) |
missense |
probably damaging |
0.99 |
X0065:Tdrd6
|
UTSW |
17 |
43,936,044 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1088:Tdrd6
|
UTSW |
17 |
43,937,409 (GRCm39) |
missense |
probably benign |
0.23 |
Z1177:Tdrd6
|
UTSW |
17 |
43,938,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TCCGTAATCGACGTGAAGCACC -3'
(R):5'- TGTTCGCTGCTCAAACGCTACC -3'
Sequencing Primer
(F):5'- GTACCACTGTCCGTCCAAG -3'
(R):5'- TGCTCAAACGCTACCTGACTG -3'
|
Posted On |
2013-07-11 |