Incidental Mutation 'R4707:Tex15'
| ID |
355330 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Tex15
|
| Ensembl Gene |
ENSMUSG00000009628 |
| Gene Name |
testis expressed gene 15 |
| Synonyms |
2210014E14Rik |
| MMRRC Submission |
041955-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.291)
|
| Stock # |
R4707 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
8 |
| Chromosomal Location |
34006766-34075610 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 34072525 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 2691
(T2691A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000009772
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000009772]
[ENSMUST00000124501]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000009772
AA Change: T2691A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000009772
Gene: ENSMUSG00000009628
AA Change: T2691A
| 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: 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: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.7%
|
| 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: 115 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700010I14Rik |
A |
G |
17: 9,224,544 (GRCm39) |
K450R |
probably damaging |
Het |
| Abcd2 |
T |
C |
15: 91,043,385 (GRCm39) |
D601G |
probably benign |
Het |
| Abcf3 |
A |
G |
16: 20,367,808 (GRCm39) |
K56E |
possibly damaging |
Het |
| Acaca |
T |
C |
11: 84,203,680 (GRCm39) |
V1477A |
probably damaging |
Het |
| Adamts20 |
G |
A |
15: 94,231,528 (GRCm39) |
P887L |
possibly damaging |
Het |
| Ahnak |
T |
G |
19: 8,994,099 (GRCm39) |
S5128A |
probably benign |
Het |
| Ahsa2 |
C |
A |
11: 23,443,162 (GRCm39) |
V197F |
probably benign |
Het |
| Ak9 |
C |
A |
10: 41,221,456 (GRCm39) |
H402N |
probably benign |
Het |
| Alpk1 |
G |
T |
3: 127,481,241 (GRCm39) |
N175K |
possibly damaging |
Het |
| Als2 |
A |
G |
1: 59,254,472 (GRCm39) |
V295A |
probably benign |
Het |
| Ankrd16 |
A |
G |
2: 11,783,608 (GRCm39) |
D70G |
probably damaging |
Het |
| Apob |
A |
T |
12: 8,056,205 (GRCm39) |
K1562N |
probably damaging |
Het |
| Arfgap2 |
C |
A |
2: 91,100,316 (GRCm39) |
S250R |
probably damaging |
Het |
| Arhgef10l |
C |
T |
4: 140,264,194 (GRCm39) |
M671I |
possibly damaging |
Het |
| Atrnl1 |
A |
G |
19: 57,617,590 (GRCm39) |
I122V |
probably damaging |
Het |
| B4galnt2 |
C |
T |
11: 95,766,923 (GRCm39) |
|
probably null |
Het |
| C8a |
A |
G |
4: 104,713,618 (GRCm39) |
Y171H |
probably damaging |
Het |
| Cacnb4 |
A |
G |
2: 52,364,927 (GRCm39) |
V112A |
probably benign |
Het |
| Capn9 |
G |
T |
8: 125,340,195 (GRCm39) |
C566F |
possibly damaging |
Het |
| Ccdc88a |
T |
A |
11: 29,397,956 (GRCm39) |
S230T |
probably benign |
Het |
| Cd300c2 |
A |
T |
11: 114,887,811 (GRCm39) |
F197Y |
probably benign |
Het |
| Chd5 |
A |
G |
4: 152,445,039 (GRCm39) |
Y340C |
probably damaging |
Het |
| Chrd |
A |
T |
16: 20,557,558 (GRCm39) |
I726F |
possibly damaging |
Het |
| Chrna10 |
G |
A |
7: 101,762,426 (GRCm39) |
P255S |
possibly damaging |
Het |
| Clasp1 |
T |
A |
1: 118,470,927 (GRCm39) |
Y197* |
probably null |
Het |
| Cyp2c69 |
C |
G |
19: 39,837,852 (GRCm39) |
G410A |
probably benign |
Het |
| Cyp2e1 |
G |
A |
7: 140,343,821 (GRCm39) |
V20I |
possibly damaging |
Het |
| Dapp1 |
T |
C |
3: 137,638,928 (GRCm39) |
D225G |
probably benign |
Het |
| Dnah5 |
A |
T |
15: 28,372,521 (GRCm39) |
D2924V |
probably damaging |
Het |
| Efcab12 |
A |
T |
6: 115,791,510 (GRCm39) |
L554Q |
possibly damaging |
Het |
| Emsy |
T |
C |
7: 98,246,311 (GRCm39) |
T228A |
possibly damaging |
Het |
| Evc2 |
G |
A |
5: 37,579,204 (GRCm39) |
V1106I |
probably benign |
Het |
| Exoc8 |
G |
T |
8: 125,624,209 (GRCm39) |
Q53K |
possibly damaging |
Het |
| Fbn2 |
A |
T |
18: 58,189,344 (GRCm39) |
V1594D |
probably damaging |
Het |
| Fer1l4 |
T |
C |
2: 155,887,543 (GRCm39) |
Y551C |
possibly damaging |
Het |
| Fhip1a |
G |
T |
3: 85,595,877 (GRCm39) |
T115K |
probably damaging |
Het |
| Fmnl3 |
A |
G |
15: 99,221,362 (GRCm39) |
M481T |
probably benign |
Het |
| Fras1 |
A |
G |
5: 96,883,097 (GRCm39) |
N2543S |
probably damaging |
Het |
| Fsd2 |
T |
C |
7: 81,209,428 (GRCm39) |
D138G |
probably damaging |
Het |
| Gda |
C |
T |
19: 21,405,992 (GRCm39) |
V5I |
probably benign |
Het |
| Glt8d2 |
A |
T |
10: 82,496,583 (GRCm39) |
D158E |
probably damaging |
Het |
| Gpx6 |
C |
T |
13: 21,496,434 (GRCm39) |
Q3* |
probably null |
Het |
| Greb1l |
A |
G |
18: 10,532,922 (GRCm39) |
M830V |
probably benign |
Het |
| Hnrnpul1 |
A |
C |
7: 25,426,258 (GRCm39) |
V531G |
probably damaging |
Het |
| Ifi206 |
A |
T |
1: 173,308,432 (GRCm39) |
H521Q |
probably benign |
Het |
| Igsf3 |
G |
C |
3: 101,365,410 (GRCm39) |
R1127P |
probably benign |
Het |
| Il1rl1 |
A |
G |
1: 40,489,348 (GRCm39) |
R367G |
probably damaging |
Het |
| Islr |
T |
C |
9: 58,064,970 (GRCm39) |
D179G |
possibly damaging |
Het |
| Jcad |
G |
T |
18: 4,649,338 (GRCm39) |
E70* |
probably null |
Het |
| Kcnd2 |
T |
C |
6: 21,723,211 (GRCm39) |
I467T |
probably benign |
Het |
| Lrrc27 |
A |
G |
7: 138,822,614 (GRCm39) |
T502A |
probably benign |
Het |
| Lrrtm3 |
T |
A |
10: 63,923,781 (GRCm39) |
H462L |
probably benign |
Het |
| Mbd5 |
T |
C |
2: 49,140,168 (GRCm39) |
L44S |
probably damaging |
Het |
| Mccc1 |
C |
A |
3: 36,030,022 (GRCm39) |
M429I |
probably damaging |
Het |
| Mgam |
A |
T |
6: 40,691,566 (GRCm39) |
|
probably null |
Het |
| Mipep |
T |
A |
14: 61,109,552 (GRCm39) |
I643N |
probably damaging |
Het |
| Mmrn1 |
A |
T |
6: 60,965,457 (GRCm39) |
I1162L |
probably benign |
Het |
| Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
| Mug1 |
G |
A |
6: 121,861,600 (GRCm39) |
C1354Y |
probably damaging |
Het |
| Nbeal2 |
A |
T |
9: 110,461,123 (GRCm39) |
S1647T |
probably benign |
Het |
| Ndufaf2 |
C |
G |
13: 108,189,314 (GRCm39) |
A145P |
probably damaging |
Het |
| Nedd9 |
A |
T |
13: 41,492,051 (GRCm39) |
|
probably null |
Het |
| Nr4a2 |
T |
A |
2: 57,002,105 (GRCm39) |
H116L |
probably benign |
Het |
| Nwd2 |
A |
G |
5: 63,951,665 (GRCm39) |
Y232C |
probably damaging |
Het |
| Odf4 |
A |
G |
11: 68,817,514 (GRCm39) |
L58P |
probably damaging |
Het |
| Or2a20 |
T |
A |
6: 43,193,883 (GRCm39) |
V12D |
probably benign |
Het |
| Or4a27 |
T |
A |
2: 88,559,056 (GRCm39) |
M296L |
possibly damaging |
Het |
| Or4c116 |
A |
T |
2: 88,942,576 (GRCm39) |
F93L |
probably damaging |
Het |
| Or4g17 |
T |
A |
2: 111,209,990 (GRCm39) |
L215H |
probably damaging |
Het |
| Or7e165 |
C |
T |
9: 19,694,596 (GRCm39) |
H18Y |
probably damaging |
Het |
| Or8g24 |
A |
G |
9: 38,989,558 (GRCm39) |
V161A |
probably benign |
Het |
| Or8s5 |
G |
T |
15: 98,238,659 (GRCm39) |
H70Q |
possibly damaging |
Het |
| Orc6 |
T |
A |
8: 86,029,579 (GRCm39) |
I41K |
probably damaging |
Het |
| Pikfyve |
A |
G |
1: 65,307,005 (GRCm39) |
T1798A |
probably benign |
Het |
| Prdx6b |
T |
C |
2: 80,123,404 (GRCm39) |
L71P |
probably damaging |
Het |
| Prmt2 |
A |
G |
10: 76,062,055 (GRCm39) |
I50T |
probably damaging |
Het |
| Ptdss1 |
T |
C |
13: 67,143,482 (GRCm39) |
|
probably null |
Het |
| Pygl |
T |
C |
12: 70,254,532 (GRCm39) |
T138A |
possibly damaging |
Het |
| Rab3c |
T |
C |
13: 110,198,434 (GRCm39) |
E198G |
probably benign |
Het |
| Rbl2 |
A |
G |
8: 91,812,196 (GRCm39) |
Y255C |
probably damaging |
Het |
| Rev3l |
T |
A |
10: 39,699,393 (GRCm39) |
S1297T |
probably damaging |
Het |
| Rgma |
C |
A |
7: 73,067,564 (GRCm39) |
T367K |
probably damaging |
Het |
| Rps6ka5 |
C |
T |
12: 100,564,144 (GRCm39) |
|
probably null |
Het |
| Rslcan18 |
A |
T |
13: 67,246,590 (GRCm39) |
C217S |
probably damaging |
Het |
| Rtp3 |
A |
G |
9: 110,815,279 (GRCm39) |
|
probably benign |
Het |
| Ryr1 |
A |
T |
7: 28,745,087 (GRCm39) |
N3848K |
probably damaging |
Het |
| Sema6a |
T |
A |
18: 47,381,779 (GRCm39) |
T923S |
probably benign |
Het |
| Serpinb6d |
A |
T |
13: 33,855,336 (GRCm39) |
T337S |
possibly damaging |
Het |
| Sf3b1 |
G |
A |
1: 55,029,666 (GRCm39) |
T1112M |
probably damaging |
Het |
| Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
| Sidt1 |
A |
T |
16: 44,090,221 (GRCm39) |
Y369* |
probably null |
Het |
| Slc16a6 |
A |
G |
11: 109,354,193 (GRCm39) |
S59P |
probably benign |
Het |
| Slc25a17 |
A |
C |
15: 81,211,527 (GRCm39) |
L163W |
probably damaging |
Het |
| Slc44a3 |
T |
C |
3: 121,320,723 (GRCm39) |
T93A |
possibly damaging |
Het |
| Sptbn1 |
T |
C |
11: 30,087,197 (GRCm39) |
T1081A |
possibly damaging |
Het |
| Sptbn4 |
T |
C |
7: 27,116,431 (GRCm39) |
D456G |
probably benign |
Het |
| Sycp1 |
C |
A |
3: 102,760,805 (GRCm39) |
A703S |
possibly damaging |
Het |
| Tas2r118 |
T |
A |
6: 23,969,225 (GRCm39) |
M279L |
probably benign |
Het |
| Tc2n |
T |
G |
12: 101,660,832 (GRCm39) |
Q133H |
probably benign |
Het |
| Tctn1 |
A |
G |
5: 122,399,468 (GRCm39) |
|
probably null |
Het |
| Tenm4 |
A |
C |
7: 96,423,253 (GRCm39) |
K683Q |
probably damaging |
Het |
| Tex10 |
A |
T |
4: 48,468,984 (GRCm39) |
S64T |
probably benign |
Het |
| Tmem175 |
A |
T |
5: 108,790,016 (GRCm39) |
T123S |
probably damaging |
Het |
| Tsc1 |
C |
A |
2: 28,562,419 (GRCm39) |
S348R |
probably damaging |
Het |
| Ttll4 |
A |
T |
1: 74,718,166 (GRCm39) |
T6S |
possibly damaging |
Het |
| Ttll8 |
A |
T |
15: 88,801,293 (GRCm39) |
I465N |
probably damaging |
Het |
| Ubr3 |
A |
G |
2: 69,768,714 (GRCm39) |
|
probably benign |
Het |
| Ugdh |
A |
T |
5: 65,580,695 (GRCm39) |
|
probably null |
Het |
| Usp34 |
T |
C |
11: 23,437,215 (GRCm39) |
L3326S |
probably damaging |
Het |
| Vmn2r125 |
A |
T |
4: 156,702,276 (GRCm39) |
I21F |
probably damaging |
Het |
| Vps9d1 |
G |
A |
8: 123,975,351 (GRCm39) |
|
probably benign |
Het |
| Xab2 |
G |
A |
8: 3,668,117 (GRCm39) |
R154C |
possibly damaging |
Het |
| Zbtb12 |
T |
C |
17: 35,114,475 (GRCm39) |
S87P |
probably damaging |
Het |
| Zc3h12a |
A |
G |
4: 125,014,686 (GRCm39) |
M266T |
probably damaging |
Het |
| Zfp108 |
G |
A |
7: 23,959,837 (GRCm39) |
A143T |
probably benign |
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 |
|
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 |
|
R7313:Tex15
|
UTSW |
8 |
34,064,845 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
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'- GTCCTGACTCAGAAAGTTGGC -3'
(R):5'- CTGGTTGATGAGAAGCAAACTG -3'
Sequencing Primer
(F):5'- TGACTCAGAAAGTTGGCACATC -3'
(R):5'- GCAAACTGTGAATAAACTGGTTG -3'
|
| Posted On |
2015-10-21 |
Incidental Mutation