Incidental Mutation 'R7313:Tex15'
| ID |
567754 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Tex15
|
| Ensembl Gene |
ENSMUSG00000009628 |
| Gene Name |
testis expressed gene 15 |
| Synonyms |
2210014E14Rik |
| MMRRC Submission |
045411-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.292)
|
| Stock # |
R7313 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
8 |
| Chromosomal Location |
34006766-34075610 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 34064845 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glutamic Acid
at position 1425
(V1425E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000009772
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000009772]
[ENSMUST00000124496]
[ENSMUST00000124501]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000009772
AA Change: V1425E
PolyPhen 2
Score 0.824 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000009772
Gene: ENSMUSG00000009628
AA Change: V1425E
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
262 |
274 |
N/A |
INTRINSIC |
|
low complexity region
|
302 |
313 |
N/A |
INTRINSIC |
|
low complexity region
|
524 |
536 |
N/A |
INTRINSIC |
|
low complexity region
|
665 |
674 |
N/A |
INTRINSIC |
|
low complexity region
|
713 |
725 |
N/A |
INTRINSIC |
|
low complexity region
|
946 |
961 |
N/A |
INTRINSIC |
|
low complexity region
|
1497 |
1508 |
N/A |
INTRINSIC |
|
Pfam:TEX15
|
1572 |
1788 |
1.3e-109 |
PFAM |
|
Pfam:TEX15
|
1901 |
2119 |
1.1e-16 |
PFAM |
|
low complexity region
|
2758 |
2770 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000124496
|
| SMART Domains |
Protein: ENSMUSP00000120744
Gene: ENSMUSG00000009628
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF3715
|
89 |
251 |
1.6e-58 |
PFAM |
|
low complexity region
|
536 |
548 |
N/A |
INTRINSIC |
|
low complexity region
|
576 |
587 |
N/A |
INTRINSIC |
|
low complexity region
|
798 |
810 |
N/A |
INTRINSIC |
|
low complexity region
|
939 |
948 |
N/A |
INTRINSIC |
|
low complexity region
|
987 |
999 |
N/A |
INTRINSIC |
|
low complexity region
|
1220 |
1235 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000124501
|
| SMART Domains |
Protein: ENSMUSP00000138070
Gene: ENSMUSG00000009628
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF3715
|
96 |
251 |
2.4e-52 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 97.8%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Male mice are infertile due to arrest of meiosis stemming from failure to repair double-strand breaks. However, female mice are fertile. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(4) : Targeted(3) Gene trapped(1)
|
| Other mutations in this stock |
Total: 110 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb1a |
A |
G |
5: 8,773,187 (GRCm39) |
N805S |
probably damaging |
Het |
| Acat2 |
A |
G |
17: 13,178,893 (GRCm39) |
V60A |
probably benign |
Het |
| Adam6b |
A |
G |
12: 113,454,754 (GRCm39) |
I524V |
probably benign |
Het |
| Adamts16 |
C |
T |
13: 70,921,074 (GRCm39) |
W590* |
probably null |
Het |
| Adamts9 |
C |
T |
6: 92,835,102 (GRCm39) |
G1257D |
probably damaging |
Het |
| Adgrf5 |
C |
T |
17: 43,755,974 (GRCm39) |
T644I |
probably benign |
Het |
| Adgrf5 |
T |
G |
17: 43,763,368 (GRCm39) |
|
probably null |
Het |
| Adgrv1 |
T |
C |
13: 81,668,634 (GRCm39) |
T2641A |
possibly damaging |
Het |
| Agap3 |
T |
C |
5: 24,657,382 (GRCm39) |
F60L |
probably benign |
Het |
| Akap9 |
C |
A |
5: 4,054,933 (GRCm39) |
T1626K |
probably damaging |
Het |
| Ampd3 |
C |
A |
7: 110,405,261 (GRCm39) |
D603E |
probably damaging |
Het |
| Angpt4 |
T |
A |
2: 151,767,326 (GRCm39) |
V119E |
probably benign |
Het |
| Atp6v1a |
T |
C |
16: 43,934,980 (GRCm39) |
T70A |
probably benign |
Het |
| B4galt3 |
T |
A |
1: 171,100,319 (GRCm39) |
I163N |
probably damaging |
Het |
| Borcs5 |
C |
T |
6: 134,687,143 (GRCm39) |
T167M |
probably damaging |
Het |
| Btbd19 |
T |
A |
4: 116,978,616 (GRCm39) |
S156C |
probably damaging |
Het |
| Camkk2 |
C |
T |
5: 122,875,574 (GRCm39) |
R492Q |
possibly damaging |
Het |
| Casr |
T |
C |
16: 36,330,033 (GRCm39) |
I434V |
probably damaging |
Het |
| Cd4 |
G |
T |
6: 124,844,066 (GRCm39) |
T394K |
probably benign |
Het |
| Cps1 |
T |
C |
1: 67,237,517 (GRCm39) |
L1006P |
probably damaging |
Het |
| Crx |
G |
A |
7: 15,601,857 (GRCm39) |
P274S |
probably damaging |
Het |
| Crybg1 |
T |
A |
10: 43,865,107 (GRCm39) |
I1457F |
probably damaging |
Het |
| Cul4a |
C |
A |
8: 13,171,676 (GRCm39) |
|
probably benign |
Het |
| D430041D05Rik |
T |
A |
2: 104,085,910 (GRCm39) |
T196S |
probably benign |
Het |
| Dnah3 |
T |
C |
7: 119,580,567 (GRCm39) |
E1995G |
probably benign |
Het |
| Dnm1 |
T |
A |
2: 32,226,021 (GRCm39) |
T353S |
probably damaging |
Het |
| Ect2l |
T |
A |
10: 18,044,149 (GRCm39) |
T329S |
probably damaging |
Het |
| Elp2 |
T |
A |
18: 24,742,716 (GRCm39) |
S83T |
probably benign |
Het |
| Exosc7 |
A |
G |
9: 122,948,013 (GRCm39) |
T39A |
probably benign |
Het |
| Fam135a |
C |
A |
1: 24,096,473 (GRCm39) |
V91F |
probably damaging |
Het |
| Gab2 |
G |
T |
7: 96,731,005 (GRCm39) |
|
probably benign |
Het |
| Gbf1 |
A |
T |
19: 46,268,793 (GRCm39) |
I1408F |
possibly damaging |
Het |
| Glis3 |
C |
T |
19: 28,508,419 (GRCm39) |
E522K |
probably damaging |
Het |
| Gm10375 |
A |
T |
14: 43,842,314 (GRCm39) |
C139S |
possibly damaging |
Het |
| Gm26558 |
T |
C |
2: 70,492,211 (GRCm39) |
E81G |
unknown |
Het |
| Gm35315 |
C |
T |
5: 110,227,091 (GRCm39) |
C116Y |
probably benign |
Het |
| Gm3676 |
T |
A |
14: 41,366,064 (GRCm39) |
I84F |
probably damaging |
Het |
| Gm7145 |
T |
A |
1: 117,913,932 (GRCm39) |
H271Q |
probably damaging |
Het |
| Gpat2 |
T |
A |
2: 127,270,215 (GRCm39) |
I76N |
probably damaging |
Het |
| Hipk1 |
A |
T |
3: 103,685,574 (GRCm39) |
S14T |
unknown |
Het |
| Hlcs |
C |
A |
16: 94,068,362 (GRCm39) |
S286I |
probably damaging |
Het |
| Ighg1 |
A |
T |
12: 113,293,078 (GRCm39) |
F204Y |
|
Het |
| Igsf10 |
T |
C |
3: 59,236,837 (GRCm39) |
I1115V |
probably benign |
Het |
| Klk7 |
A |
T |
7: 43,462,299 (GRCm39) |
H97L |
probably damaging |
Het |
| Kmt2d |
A |
T |
15: 98,754,504 (GRCm39) |
D1605E |
unknown |
Het |
| Leng8 |
T |
A |
7: 4,142,525 (GRCm39) |
I49N |
possibly damaging |
Het |
| Lingo4 |
A |
T |
3: 94,310,451 (GRCm39) |
D463V |
possibly damaging |
Het |
| Lrp1 |
T |
A |
10: 127,389,337 (GRCm39) |
N3193I |
probably damaging |
Het |
| Lrrc7 |
T |
A |
3: 157,866,111 (GRCm39) |
Y1210F |
probably damaging |
Het |
| Mki67 |
G |
C |
7: 135,296,400 (GRCm39) |
A2878G |
probably benign |
Het |
| Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
| Mtcl3 |
T |
A |
10: 29,072,875 (GRCm39) |
Y722* |
probably null |
Het |
| Mucl2 |
C |
T |
15: 103,929,445 (GRCm39) |
|
probably null |
Het |
| Myh6 |
A |
T |
14: 55,197,727 (GRCm39) |
D470E |
probably benign |
Het |
| Myo1e |
T |
C |
9: 70,266,667 (GRCm39) |
|
probably null |
Het |
| Myo7a |
G |
A |
7: 97,713,402 (GRCm39) |
R1647W |
probably damaging |
Het |
| Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
| Nmral1 |
C |
T |
16: 4,531,660 (GRCm39) |
M198I |
probably benign |
Het |
| Nrap |
C |
A |
19: 56,330,700 (GRCm39) |
L1120F |
probably damaging |
Het |
| Nup155 |
T |
A |
15: 8,184,406 (GRCm39) |
I1267N |
probably damaging |
Het |
| Obscn |
G |
A |
11: 58,898,414 (GRCm39) |
P6616S |
unknown |
Het |
| Ocstamp |
T |
G |
2: 165,239,229 (GRCm39) |
D319A |
probably damaging |
Het |
| Ooep |
T |
C |
9: 78,285,433 (GRCm39) |
D61G |
probably damaging |
Het |
| Or10p1 |
A |
G |
10: 129,443,949 (GRCm39) |
S134P |
probably benign |
Het |
| Or1e25 |
A |
T |
11: 73,493,810 (GRCm39) |
I135F |
probably damaging |
Het |
| Or52ad1 |
A |
G |
7: 102,995,538 (GRCm39) |
V199A |
probably benign |
Het |
| Or6c5c |
T |
C |
10: 129,298,856 (GRCm39) |
S104P |
probably damaging |
Het |
| Or7g35 |
A |
G |
9: 19,495,938 (GRCm39) |
Y35C |
probably damaging |
Het |
| Otoa |
A |
G |
7: 120,701,765 (GRCm39) |
E148G |
probably benign |
Het |
| Ovgp1 |
A |
T |
3: 105,894,387 (GRCm39) |
D720V |
unknown |
Het |
| Padi2 |
T |
A |
4: 140,660,079 (GRCm39) |
F294I |
probably damaging |
Het |
| Pcdha7 |
T |
A |
18: 37,107,471 (GRCm39) |
N165K |
probably damaging |
Het |
| Pcdhb6 |
C |
A |
18: 37,468,261 (GRCm39) |
P394H |
probably damaging |
Het |
| Pcdhga6 |
T |
C |
18: 37,841,072 (GRCm39) |
V264A |
possibly damaging |
Het |
| Pik3ap1 |
G |
T |
19: 41,284,815 (GRCm39) |
D623E |
possibly damaging |
Het |
| Prdm10 |
A |
T |
9: 31,268,456 (GRCm39) |
K802* |
probably null |
Het |
| Ptgfrn |
G |
A |
3: 100,980,363 (GRCm39) |
L326F |
possibly damaging |
Het |
| Rgsl1 |
T |
G |
1: 153,683,622 (GRCm39) |
|
probably null |
Het |
| Rock1 |
T |
G |
18: 10,129,317 (GRCm39) |
T347P |
possibly damaging |
Het |
| Rprd2 |
G |
A |
3: 95,684,022 (GRCm39) |
P338S |
probably damaging |
Het |
| Sdk1 |
A |
T |
5: 141,923,377 (GRCm39) |
N333Y |
probably damaging |
Het |
| Setd4 |
T |
A |
16: 93,388,132 (GRCm39) |
H118L |
probably benign |
Het |
| Sirt3 |
G |
A |
7: 140,458,039 (GRCm39) |
P37S |
|
Het |
| Slc16a9 |
G |
T |
10: 70,119,000 (GRCm39) |
G440W |
probably damaging |
Het |
| Slc22a23 |
T |
A |
13: 34,367,161 (GRCm39) |
I616F |
probably damaging |
Het |
| Slc30a8 |
A |
C |
15: 52,180,707 (GRCm39) |
D102A |
probably damaging |
Het |
| Slc6a4 |
T |
A |
11: 76,901,527 (GRCm39) |
D87E |
possibly damaging |
Het |
| Slc9a4 |
A |
C |
1: 40,668,663 (GRCm39) |
T769P |
probably benign |
Het |
| Sspo |
A |
T |
6: 48,431,762 (GRCm39) |
Y685F |
probably damaging |
Het |
| Sspo |
C |
A |
6: 48,450,390 (GRCm39) |
Q2560K |
probably benign |
Het |
| Stpg1 |
T |
A |
4: 135,256,827 (GRCm39) |
L206Q |
probably damaging |
Het |
| Stt3b |
A |
T |
9: 115,095,183 (GRCm39) |
Y283N |
probably damaging |
Het |
| Sult4a1 |
T |
C |
15: 83,970,814 (GRCm39) |
E197G |
probably damaging |
Het |
| Syne1 |
T |
G |
10: 4,997,635 (GRCm39) |
D444A |
probably damaging |
Het |
| Tgm4 |
A |
G |
9: 122,891,556 (GRCm39) |
D557G |
probably benign |
Het |
| Tmcc3 |
A |
G |
10: 94,266,434 (GRCm39) |
|
probably benign |
Het |
| Tnfrsf8 |
T |
A |
4: 145,000,952 (GRCm39) |
N385Y |
probably benign |
Het |
| Ttc4 |
T |
C |
4: 106,536,017 (GRCm39) |
D15G |
possibly damaging |
Het |
| Tut1 |
A |
G |
19: 8,941,413 (GRCm39) |
N400S |
probably benign |
Het |
| Usp39 |
T |
C |
6: 72,313,413 (GRCm39) |
K259R |
probably benign |
Het |
| Vmn1r215 |
C |
T |
13: 23,260,484 (GRCm39) |
H175Y |
probably benign |
Het |
| Vmn1r36 |
A |
T |
6: 66,693,107 (GRCm39) |
M256K |
probably benign |
Het |
| Zfp128 |
T |
A |
7: 12,624,461 (GRCm39) |
H276Q |
possibly damaging |
Het |
| Zfp276 |
T |
C |
8: 123,994,562 (GRCm39) |
M543T |
probably damaging |
Het |
| Zfp354c |
A |
T |
11: 50,705,483 (GRCm39) |
Y531N |
probably damaging |
Het |
| Zfp532 |
T |
A |
18: 65,756,076 (GRCm39) |
M3K |
probably damaging |
Het |
| Zfp64 |
T |
G |
2: 168,741,810 (GRCm39) |
K373Q |
probably damaging |
Het |
| Zfp764l1 |
C |
T |
7: 126,990,856 (GRCm39) |
S377N |
probably benign |
Het |
| Zfp983 |
T |
G |
17: 21,880,413 (GRCm39) |
S114A |
probably damaging |
Het |
| Zranb1 |
G |
A |
7: 132,584,481 (GRCm39) |
R583K |
probably damaging |
Het |
|
| Other mutations in Tex15 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00639:Tex15
|
APN |
8 |
34,065,339 (GRCm39) |
missense |
probably benign |
0.18 |
|
IGL00705:Tex15
|
APN |
8 |
34,071,620 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00820:Tex15
|
APN |
8 |
34,069,034 (GRCm39) |
splice site |
probably benign |
|
|
IGL01288:Tex15
|
APN |
8 |
34,061,412 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01328:Tex15
|
APN |
8 |
34,061,424 (GRCm39) |
nonsense |
probably null |
|
|
IGL01359:Tex15
|
APN |
8 |
34,071,926 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01603:Tex15
|
APN |
8 |
34,063,575 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL01861:Tex15
|
APN |
8 |
34,060,717 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02052:Tex15
|
APN |
8 |
34,072,493 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL02560:Tex15
|
APN |
8 |
34,071,779 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02677:Tex15
|
APN |
8 |
34,061,108 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02739:Tex15
|
APN |
8 |
34,071,721 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
Big_gulp
|
UTSW |
8 |
34,071,762 (GRCm39) |
missense |
probably damaging |
1.00 |
|
P0005:Tex15
|
UTSW |
8 |
34,060,896 (GRCm39) |
missense |
probably benign |
0.00 |
|
P0037:Tex15
|
UTSW |
8 |
34,071,608 (GRCm39) |
missense |
probably benign |
0.00 |
|
PIT4377001:Tex15
|
UTSW |
8 |
34,061,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0056:Tex15
|
UTSW |
8 |
34,072,055 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0056:Tex15
|
UTSW |
8 |
34,072,055 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0058:Tex15
|
UTSW |
8 |
34,071,530 (GRCm39) |
splice site |
probably benign |
|
|
R0058:Tex15
|
UTSW |
8 |
34,071,530 (GRCm39) |
splice site |
probably benign |
|
|
R0595:Tex15
|
UTSW |
8 |
34,062,645 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0646:Tex15
|
UTSW |
8 |
34,072,354 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R0688:Tex15
|
UTSW |
8 |
34,063,528 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0842:Tex15
|
UTSW |
8 |
34,061,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0987:Tex15
|
UTSW |
8 |
34,066,875 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1084:Tex15
|
UTSW |
8 |
34,067,032 (GRCm39) |
missense |
probably benign |
0.28 |
|
R1183:Tex15
|
UTSW |
8 |
34,064,893 (GRCm39) |
missense |
probably benign |
0.35 |
|
R1186:Tex15
|
UTSW |
8 |
34,061,661 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1378:Tex15
|
UTSW |
8 |
34,065,244 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1500:Tex15
|
UTSW |
8 |
34,065,120 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1508:Tex15
|
UTSW |
8 |
34,066,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1597:Tex15
|
UTSW |
8 |
34,061,511 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1636:Tex15
|
UTSW |
8 |
34,066,415 (GRCm39) |
nonsense |
probably null |
|
|
R1639:Tex15
|
UTSW |
8 |
34,060,845 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1809:Tex15
|
UTSW |
8 |
34,064,262 (GRCm39) |
missense |
probably benign |
|
|
R1843:Tex15
|
UTSW |
8 |
34,066,682 (GRCm39) |
missense |
probably benign |
0.27 |
|
R2029:Tex15
|
UTSW |
8 |
34,061,302 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2228:Tex15
|
UTSW |
8 |
34,061,265 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2229:Tex15
|
UTSW |
8 |
34,061,265 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2245:Tex15
|
UTSW |
8 |
34,061,524 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R2246:Tex15
|
UTSW |
8 |
34,072,540 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R2880:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
|
R2881:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
|
R2882:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
|
R3001:Tex15
|
UTSW |
8 |
34,064,556 (GRCm39) |
missense |
probably benign |
0.15 |
|
R3002:Tex15
|
UTSW |
8 |
34,064,556 (GRCm39) |
missense |
probably benign |
0.15 |
|
R3020:Tex15
|
UTSW |
8 |
34,066,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3084:Tex15
|
UTSW |
8 |
34,064,913 (GRCm39) |
missense |
probably benign |
0.11 |
|
R3085:Tex15
|
UTSW |
8 |
34,064,913 (GRCm39) |
missense |
probably benign |
0.11 |
|
R3701:Tex15
|
UTSW |
8 |
34,064,194 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3702:Tex15
|
UTSW |
8 |
34,064,194 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3752:Tex15
|
UTSW |
8 |
34,061,443 (GRCm39) |
missense |
probably benign |
|
|
R4162:Tex15
|
UTSW |
8 |
34,071,586 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4231:Tex15
|
UTSW |
8 |
34,062,165 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4589:Tex15
|
UTSW |
8 |
34,047,401 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4707:Tex15
|
UTSW |
8 |
34,072,525 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4773:Tex15
|
UTSW |
8 |
34,072,760 (GRCm39) |
missense |
probably benign |
0.42 |
|
R4967:Tex15
|
UTSW |
8 |
34,064,498 (GRCm39) |
missense |
probably benign |
0.34 |
|
R5063:Tex15
|
UTSW |
8 |
34,072,638 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R5121:Tex15
|
UTSW |
8 |
34,061,794 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5147:Tex15
|
UTSW |
8 |
34,062,340 (GRCm39) |
nonsense |
probably null |
|
|
R5166:Tex15
|
UTSW |
8 |
34,066,420 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5173:Tex15
|
UTSW |
8 |
34,061,768 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5439:Tex15
|
UTSW |
8 |
34,064,199 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R5537:Tex15
|
UTSW |
8 |
34,061,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5580:Tex15
|
UTSW |
8 |
34,062,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5588:Tex15
|
UTSW |
8 |
34,067,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5696:Tex15
|
UTSW |
8 |
34,063,220 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5734:Tex15
|
UTSW |
8 |
34,036,364 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5756:Tex15
|
UTSW |
8 |
34,065,861 (GRCm39) |
missense |
probably benign |
0.17 |
|
R5823:Tex15
|
UTSW |
8 |
34,060,962 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R6126:Tex15
|
UTSW |
8 |
34,063,591 (GRCm39) |
missense |
probably benign |
0.19 |
|
R6129:Tex15
|
UTSW |
8 |
34,064,158 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6276:Tex15
|
UTSW |
8 |
34,067,217 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6374:Tex15
|
UTSW |
8 |
34,065,940 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6430:Tex15
|
UTSW |
8 |
34,061,329 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6452:Tex15
|
UTSW |
8 |
34,062,844 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6471:Tex15
|
UTSW |
8 |
34,071,762 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6700:Tex15
|
UTSW |
8 |
34,064,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6918:Tex15
|
UTSW |
8 |
34,063,212 (GRCm39) |
missense |
probably benign |
0.27 |
|
R6958:Tex15
|
UTSW |
8 |
34,060,899 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6970:Tex15
|
UTSW |
8 |
34,047,456 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7059:Tex15
|
UTSW |
8 |
34,064,758 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R7069:Tex15
|
UTSW |
8 |
34,060,748 (GRCm39) |
missense |
probably benign |
|
|
R7072:Tex15
|
UTSW |
8 |
34,065,459 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7212:Tex15
|
UTSW |
8 |
34,063,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7212:Tex15
|
UTSW |
8 |
34,060,854 (GRCm39) |
nonsense |
probably null |
|
|
R7216:Tex15
|
UTSW |
8 |
34,063,014 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7219:Tex15
|
UTSW |
8 |
34,036,268 (GRCm39) |
missense |
probably benign |
0.40 |
|
R7315:Tex15
|
UTSW |
8 |
34,071,544 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7444:Tex15
|
UTSW |
8 |
34,066,590 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7455:Tex15
|
UTSW |
8 |
34,067,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7643:Tex15
|
UTSW |
8 |
34,065,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7644:Tex15
|
UTSW |
8 |
34,064,445 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7724:Tex15
|
UTSW |
8 |
34,036,291 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R7779:Tex15
|
UTSW |
8 |
34,065,309 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7798:Tex15
|
UTSW |
8 |
34,071,875 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R7816:Tex15
|
UTSW |
8 |
34,071,683 (GRCm39) |
missense |
probably benign |
0.14 |
|
R7820:Tex15
|
UTSW |
8 |
34,065,090 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8041:Tex15
|
UTSW |
8 |
34,065,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8150:Tex15
|
UTSW |
8 |
34,063,534 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8152:Tex15
|
UTSW |
8 |
34,062,921 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8237:Tex15
|
UTSW |
8 |
34,067,427 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R8250:Tex15
|
UTSW |
8 |
34,055,233 (GRCm39) |
missense |
probably null |
0.27 |
|
R8264:Tex15
|
UTSW |
8 |
34,072,390 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8279:Tex15
|
UTSW |
8 |
34,061,765 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8353:Tex15
|
UTSW |
8 |
34,066,899 (GRCm39) |
nonsense |
probably null |
|
|
R8388:Tex15
|
UTSW |
8 |
34,065,237 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8432:Tex15
|
UTSW |
8 |
34,066,572 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8453:Tex15
|
UTSW |
8 |
34,066,899 (GRCm39) |
nonsense |
probably null |
|
|
R8489:Tex15
|
UTSW |
8 |
34,067,574 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8670:Tex15
|
UTSW |
8 |
34,064,746 (GRCm39) |
missense |
probably benign |
0.19 |
|
R8703:Tex15
|
UTSW |
8 |
34,062,724 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8871:Tex15
|
UTSW |
8 |
34,066,992 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R8945:Tex15
|
UTSW |
8 |
34,064,724 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9104:Tex15
|
UTSW |
8 |
34,060,950 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R9132:Tex15
|
UTSW |
8 |
34,067,554 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R9207:Tex15
|
UTSW |
8 |
34,065,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9210:Tex15
|
UTSW |
8 |
34,064,319 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R9330:Tex15
|
UTSW |
8 |
34,065,143 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9354:Tex15
|
UTSW |
8 |
34,063,344 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R9365:Tex15
|
UTSW |
8 |
34,064,564 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R9440:Tex15
|
UTSW |
8 |
34,072,273 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9534:Tex15
|
UTSW |
8 |
34,060,999 (GRCm39) |
missense |
probably benign |
0.45 |
|
R9570:Tex15
|
UTSW |
8 |
34,067,309 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9574:Tex15
|
UTSW |
8 |
34,064,509 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9618:Tex15
|
UTSW |
8 |
34,062,397 (GRCm39) |
missense |
probably benign |
0.35 |
|
R9655:Tex15
|
UTSW |
8 |
34,066,784 (GRCm39) |
nonsense |
probably null |
|
|
R9786:Tex15
|
UTSW |
8 |
34,062,457 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9798:Tex15
|
UTSW |
8 |
34,062,721 (GRCm39) |
missense |
probably damaging |
0.98 |
|
RF005:Tex15
|
UTSW |
8 |
34,066,705 (GRCm39) |
missense |
probably benign |
0.05 |
|
X0020:Tex15
|
UTSW |
8 |
34,066,607 (GRCm39) |
missense |
probably benign |
0.03 |
|
X0065:Tex15
|
UTSW |
8 |
34,065,545 (GRCm39) |
nonsense |
probably null |
|
|
Z1088:Tex15
|
UTSW |
8 |
34,061,343 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
Z1088:Tex15
|
UTSW |
8 |
34,064,898 (GRCm39) |
missense |
probably benign |
|
|
Z1088:Tex15
|
UTSW |
8 |
34,061,838 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
Z1176:Tex15
|
UTSW |
8 |
34,064,754 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGTTCTCTGTGAAAGCAATCCAGTG -3'
(R):5'- TTGAAGGACCCGTTATATTCTCC -3'
Sequencing Primer
(F):5'- TTCAAATTGTAAAGCCAACACTGAC -3'
(R):5'- GACCCGTTATATTCTCCTTTAATAGC -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation