Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
A |
T |
2: 103,539,833 (GRCm39) |
M733L |
probably benign |
Het |
Acss3 |
G |
A |
10: 106,920,717 (GRCm39) |
P131L |
probably damaging |
Het |
Adgrv1 |
T |
A |
13: 81,539,886 (GRCm39) |
I5678F |
probably benign |
Het |
Aff1 |
C |
T |
5: 103,902,586 (GRCm39) |
L6F |
possibly damaging |
Het |
Ank3 |
G |
T |
10: 69,686,006 (GRCm39) |
R273L |
probably damaging |
Het |
Anks1b |
G |
A |
10: 90,516,699 (GRCm39) |
G898D |
probably damaging |
Het |
Anxa11 |
C |
T |
14: 25,873,158 (GRCm39) |
P131S |
unknown |
Het |
Ap4e1 |
T |
A |
2: 126,889,035 (GRCm39) |
M500K |
probably benign |
Het |
Bag3 |
T |
C |
7: 128,141,922 (GRCm39) |
S138P |
probably damaging |
Het |
Capn9 |
T |
C |
8: 125,344,193 (GRCm39) |
V670A |
probably benign |
Het |
Ccne2 |
T |
A |
4: 11,199,306 (GRCm39) |
W236R |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,262,451 (GRCm39) |
Y702* |
probably null |
Het |
Chd1l |
G |
A |
3: 97,494,483 (GRCm39) |
A399V |
probably damaging |
Het |
Cit |
A |
T |
5: 116,086,124 (GRCm39) |
E896V |
probably damaging |
Het |
Cntln |
T |
A |
4: 85,014,998 (GRCm39) |
N1096K |
probably damaging |
Het |
Cntnap5c |
T |
C |
17: 58,411,747 (GRCm39) |
C544R |
probably damaging |
Het |
Csf1 |
A |
T |
3: 107,655,675 (GRCm39) |
L452Q |
possibly damaging |
Het |
Cts8 |
T |
A |
13: 61,397,037 (GRCm39) |
K294N |
possibly damaging |
Het |
Dcakd |
T |
G |
11: 102,890,618 (GRCm39) |
E56D |
possibly damaging |
Het |
Dnah17 |
T |
C |
11: 117,998,987 (GRCm39) |
I929V |
probably benign |
Het |
Dnah2 |
G |
T |
11: 69,382,467 (GRCm39) |
H1214Q |
probably benign |
Het |
Dock9 |
T |
C |
14: 121,872,006 (GRCm39) |
D536G |
probably damaging |
Het |
Drc3 |
A |
G |
11: 60,284,596 (GRCm39) |
N467S |
possibly damaging |
Het |
Dysf |
A |
G |
6: 84,084,118 (GRCm39) |
|
probably null |
Het |
Ecpas |
T |
G |
4: 58,877,157 (GRCm39) |
T93P |
probably damaging |
Het |
Evpl |
A |
T |
11: 116,121,748 (GRCm39) |
L378Q |
probably damaging |
Het |
Fer1l4 |
A |
T |
2: 155,866,660 (GRCm39) |
H1520Q |
probably damaging |
Het |
Fhod1 |
A |
T |
8: 106,063,780 (GRCm39) |
|
probably benign |
Het |
Gabra1 |
T |
A |
11: 42,073,205 (GRCm39) |
|
probably benign |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm14137 |
A |
G |
2: 119,005,572 (GRCm39) |
T44A |
possibly damaging |
Het |
H2bl1 |
T |
A |
13: 99,120,974 (GRCm39) |
R17S |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,841,013 (GRCm39) |
M3444T |
probably benign |
Het |
Igsf5 |
T |
C |
16: 96,197,648 (GRCm39) |
S208P |
possibly damaging |
Het |
Ino80b |
A |
G |
6: 83,102,066 (GRCm39) |
L12P |
possibly damaging |
Het |
Insrr |
A |
G |
3: 87,720,272 (GRCm39) |
D970G |
probably damaging |
Het |
Iqcf4 |
G |
A |
9: 106,445,874 (GRCm39) |
A91V |
probably benign |
Het |
Itga10 |
A |
G |
3: 96,564,078 (GRCm39) |
T911A |
probably benign |
Het |
Katnip |
T |
C |
7: 125,469,869 (GRCm39) |
V1446A |
probably benign |
Het |
Klhl30 |
A |
T |
1: 91,285,086 (GRCm39) |
D314V |
probably benign |
Het |
Lpcat1 |
T |
C |
13: 73,659,074 (GRCm39) |
V330A |
possibly damaging |
Het |
Myef2l |
T |
C |
3: 10,154,239 (GRCm39) |
I336T |
probably damaging |
Het |
Nhlrc3 |
A |
T |
3: 53,359,944 (GRCm39) |
D306E |
possibly damaging |
Het |
Notum |
T |
A |
11: 120,548,766 (GRCm39) |
I187F |
probably damaging |
Het |
Nphp3 |
T |
C |
9: 103,892,640 (GRCm39) |
L288P |
probably damaging |
Het |
Ntrk2 |
G |
T |
13: 59,019,570 (GRCm39) |
E394* |
probably null |
Het |
Or6k2 |
T |
A |
1: 173,979,748 (GRCm39) |
V222D |
probably benign |
Het |
Pbld2 |
A |
G |
10: 62,874,931 (GRCm39) |
K63E |
probably benign |
Het |
Phc2 |
T |
C |
4: 128,641,982 (GRCm39) |
M768T |
possibly damaging |
Het |
Pik3c2g |
G |
A |
6: 139,603,561 (GRCm39) |
C249Y |
probably damaging |
Het |
Plod1 |
G |
A |
4: 148,000,772 (GRCm39) |
|
probably benign |
Het |
Plscr2 |
A |
T |
9: 92,172,772 (GRCm39) |
T9S |
probably benign |
Het |
Pnrc1 |
T |
A |
4: 33,246,315 (GRCm39) |
M215L |
probably benign |
Het |
Prcp |
G |
T |
7: 92,577,841 (GRCm39) |
C370F |
probably damaging |
Het |
Pter |
A |
G |
2: 12,983,205 (GRCm39) |
N70S |
probably damaging |
Het |
Ptprt |
G |
T |
2: 161,395,779 (GRCm39) |
H1131Q |
probably damaging |
Het |
Rasal2 |
T |
C |
1: 157,239,432 (GRCm39) |
D8G |
possibly damaging |
Het |
Rcn2 |
A |
C |
9: 55,960,209 (GRCm39) |
K159Q |
probably benign |
Het |
Rex2 |
T |
A |
4: 147,141,972 (GRCm39) |
C153* |
probably null |
Het |
Rps6ka2 |
T |
C |
17: 7,437,766 (GRCm39) |
F8S |
possibly damaging |
Het |
Samd9l |
A |
G |
6: 3,375,383 (GRCm39) |
L626S |
probably damaging |
Het |
Sptb |
A |
G |
12: 76,667,428 (GRCm39) |
|
probably null |
Het |
Srgap3 |
A |
T |
6: 112,793,571 (GRCm39) |
V135D |
probably damaging |
Het |
Srsf7 |
T |
C |
17: 80,514,682 (GRCm39) |
|
probably benign |
Het |
Tacc2 |
A |
G |
7: 130,228,255 (GRCm39) |
T1647A |
probably benign |
Het |
Thap12 |
G |
T |
7: 98,352,612 (GRCm39) |
A6S |
probably damaging |
Het |
Tmem33 |
T |
A |
5: 67,425,894 (GRCm39) |
L146* |
probably null |
Het |
Trip13 |
C |
A |
13: 74,084,378 (GRCm39) |
E36* |
probably null |
Het |
Vkorc1l1 |
T |
A |
5: 129,971,079 (GRCm39) |
C23S |
probably damaging |
Het |
Vmn1r20 |
G |
A |
6: 57,409,112 (GRCm39) |
R146H |
probably benign |
Het |
Vmn1r222 |
T |
A |
13: 23,416,965 (GRCm39) |
I83F |
probably benign |
Het |
Vmn2r107 |
A |
T |
17: 20,576,044 (GRCm39) |
I125F |
probably benign |
Het |
Vmn2r116 |
A |
G |
17: 23,605,736 (GRCm39) |
D216G |
probably damaging |
Het |
Vwa3a |
C |
T |
7: 120,394,874 (GRCm39) |
T898I |
probably benign |
Het |
Wdfy3 |
T |
C |
5: 102,116,812 (GRCm39) |
D76G |
probably damaging |
Het |
Wdhd1 |
T |
C |
14: 47,510,579 (GRCm39) |
D148G |
possibly damaging |
Het |
Zfp106 |
A |
T |
2: 120,353,185 (GRCm39) |
V1535D |
probably damaging |
Het |
Zfp385b |
A |
T |
2: 77,244,323 (GRCm39) |
L315Q |
possibly damaging |
Het |
Zfp458 |
T |
A |
13: 67,404,870 (GRCm39) |
H523L |
probably damaging |
Het |
Zfp712 |
T |
C |
13: 67,189,393 (GRCm39) |
H378R |
probably damaging |
Het |
Zic1 |
T |
C |
9: 91,246,556 (GRCm39) |
Y172C |
probably damaging |
Het |
|
Other mutations in Xylt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Xylt1
|
APN |
7 |
117,249,912 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01306:Xylt1
|
APN |
7 |
117,148,125 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01656:Xylt1
|
APN |
7 |
117,148,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02152:Xylt1
|
APN |
7 |
117,233,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02188:Xylt1
|
APN |
7 |
117,233,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02732:Xylt1
|
APN |
7 |
117,191,164 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02944:Xylt1
|
APN |
7 |
117,233,984 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03308:Xylt1
|
APN |
7 |
117,236,978 (GRCm39) |
nonsense |
probably null |
|
IGL03393:Xylt1
|
APN |
7 |
117,192,940 (GRCm39) |
missense |
probably damaging |
1.00 |
phloem
|
UTSW |
7 |
117,255,807 (GRCm39) |
missense |
probably damaging |
1.00 |
xylem
|
UTSW |
7 |
117,191,263 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU23:Xylt1
|
UTSW |
7 |
117,148,125 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4378001:Xylt1
|
UTSW |
7 |
117,148,100 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0023:Xylt1
|
UTSW |
7 |
117,233,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Xylt1
|
UTSW |
7 |
117,233,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0970:Xylt1
|
UTSW |
7 |
117,233,963 (GRCm39) |
missense |
probably damaging |
0.96 |
R1433:Xylt1
|
UTSW |
7 |
117,191,179 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1762:Xylt1
|
UTSW |
7 |
117,236,988 (GRCm39) |
missense |
probably benign |
0.00 |
R2169:Xylt1
|
UTSW |
7 |
117,266,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Xylt1
|
UTSW |
7 |
117,234,011 (GRCm39) |
missense |
probably benign |
0.04 |
R3024:Xylt1
|
UTSW |
7 |
117,147,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R3855:Xylt1
|
UTSW |
7 |
117,192,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R4006:Xylt1
|
UTSW |
7 |
117,074,748 (GRCm39) |
missense |
probably benign |
0.01 |
R4329:Xylt1
|
UTSW |
7 |
117,255,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4794:Xylt1
|
UTSW |
7 |
117,236,862 (GRCm39) |
missense |
probably benign |
0.07 |
R4975:Xylt1
|
UTSW |
7 |
117,266,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5225:Xylt1
|
UTSW |
7 |
117,191,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5679:Xylt1
|
UTSW |
7 |
117,242,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Xylt1
|
UTSW |
7 |
117,255,717 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5756:Xylt1
|
UTSW |
7 |
117,249,927 (GRCm39) |
missense |
probably damaging |
0.97 |
R5802:Xylt1
|
UTSW |
7 |
117,255,914 (GRCm39) |
missense |
probably benign |
0.43 |
R6057:Xylt1
|
UTSW |
7 |
117,191,135 (GRCm39) |
missense |
probably benign |
0.02 |
R6249:Xylt1
|
UTSW |
7 |
117,266,528 (GRCm39) |
missense |
probably benign |
0.11 |
R7159:Xylt1
|
UTSW |
7 |
117,236,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7198:Xylt1
|
UTSW |
7 |
117,255,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R7323:Xylt1
|
UTSW |
7 |
117,191,274 (GRCm39) |
critical splice donor site |
probably null |
|
R7449:Xylt1
|
UTSW |
7 |
117,191,232 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7545:Xylt1
|
UTSW |
7 |
117,192,812 (GRCm39) |
missense |
probably benign |
0.11 |
R7786:Xylt1
|
UTSW |
7 |
117,242,702 (GRCm39) |
splice site |
probably null |
|
R7849:Xylt1
|
UTSW |
7 |
117,255,891 (GRCm39) |
missense |
probably benign |
0.06 |
R7867:Xylt1
|
UTSW |
7 |
117,074,749 (GRCm39) |
missense |
probably benign |
0.12 |
R8169:Xylt1
|
UTSW |
7 |
117,249,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R8686:Xylt1
|
UTSW |
7 |
116,980,594 (GRCm39) |
missense |
unknown |
|
R8942:Xylt1
|
UTSW |
7 |
117,233,971 (GRCm39) |
nonsense |
probably null |
|
R9019:Xylt1
|
UTSW |
7 |
117,250,038 (GRCm39) |
critical splice donor site |
probably null |
|
R9209:Xylt1
|
UTSW |
7 |
117,255,870 (GRCm39) |
missense |
probably benign |
0.02 |
R9393:Xylt1
|
UTSW |
7 |
117,242,906 (GRCm39) |
missense |
probably benign |
|
R9721:Xylt1
|
UTSW |
7 |
117,148,255 (GRCm39) |
missense |
probably damaging |
0.99 |
|