Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam19 |
T |
C |
11: 46,029,804 (GRCm39) |
|
probably null |
Het |
Aig1 |
T |
C |
10: 13,677,602 (GRCm39) |
N130S |
probably damaging |
Het |
Alx1 |
A |
T |
10: 102,861,047 (GRCm39) |
Y160* |
probably null |
Het |
Ap4e1 |
T |
C |
2: 126,902,358 (GRCm39) |
I755T |
probably benign |
Het |
Apoc3 |
C |
A |
9: 46,145,833 (GRCm39) |
E21* |
probably null |
Het |
Atp9b |
G |
T |
18: 80,796,285 (GRCm39) |
H919Q |
probably damaging |
Het |
Cemip |
T |
G |
7: 83,622,514 (GRCm39) |
Y555S |
probably damaging |
Het |
Cic |
T |
C |
7: 24,971,025 (GRCm39) |
V252A |
possibly damaging |
Het |
Cracr2a |
A |
T |
6: 127,588,470 (GRCm39) |
N210Y |
probably damaging |
Het |
Crocc2 |
G |
A |
1: 93,130,578 (GRCm39) |
R953Q |
possibly damaging |
Het |
Csnk1d |
A |
G |
11: 120,859,954 (GRCm39) |
S318P |
probably benign |
Het |
Ddx21 |
A |
G |
10: 62,427,751 (GRCm39) |
L384P |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,270,620 (GRCm39) |
T974I |
probably benign |
Het |
Duox1 |
A |
G |
2: 122,163,922 (GRCm39) |
Y863C |
possibly damaging |
Het |
Epg5 |
C |
A |
18: 78,066,498 (GRCm39) |
P2133T |
possibly damaging |
Het |
Ephb6 |
A |
T |
6: 41,591,119 (GRCm39) |
Q92L |
possibly damaging |
Het |
Ercc4 |
C |
A |
16: 12,939,959 (GRCm39) |
A73D |
probably damaging |
Het |
Eva1c |
A |
T |
16: 90,701,235 (GRCm39) |
Y290F |
probably damaging |
Het |
Galnt5 |
T |
A |
2: 57,918,156 (GRCm39) |
V798E |
possibly damaging |
Het |
Haus4 |
T |
C |
14: 54,786,342 (GRCm39) |
E149G |
probably damaging |
Het |
Ighv1-13 |
A |
G |
12: 114,594,556 (GRCm39) |
Y86C |
unknown |
Het |
Igkv9-120 |
G |
T |
6: 68,027,351 (GRCm39) |
R88S |
possibly damaging |
Het |
Lama3 |
T |
C |
18: 12,633,620 (GRCm39) |
V1584A |
probably benign |
Het |
Lamb1 |
A |
G |
12: 31,358,010 (GRCm39) |
E1119G |
probably damaging |
Het |
Lao1 |
T |
C |
4: 118,825,185 (GRCm39) |
L335P |
probably damaging |
Het |
Mindy4 |
A |
G |
6: 55,237,550 (GRCm39) |
D375G |
probably damaging |
Het |
Myo5a |
T |
C |
9: 75,051,358 (GRCm39) |
I317T |
probably damaging |
Het |
Nhlrc2 |
G |
A |
19: 56,558,898 (GRCm39) |
V128I |
probably benign |
Het |
Nlrp2 |
C |
T |
7: 5,331,023 (GRCm39) |
D458N |
probably damaging |
Het |
Or1j18 |
A |
T |
2: 36,624,335 (GRCm39) |
M1L |
probably benign |
Het |
Or1o1 |
T |
A |
17: 37,717,091 (GRCm39) |
C217* |
probably null |
Het |
Or5a1 |
G |
T |
19: 12,097,300 (GRCm39) |
H247N |
probably damaging |
Het |
Or8g24 |
T |
C |
9: 38,989,988 (GRCm39) |
T18A |
possibly damaging |
Het |
Or9q2 |
A |
T |
19: 13,772,409 (GRCm39) |
C189S |
probably damaging |
Het |
Parp8 |
T |
C |
13: 117,005,072 (GRCm39) |
H663R |
probably damaging |
Het |
Pax6 |
T |
C |
2: 105,525,705 (GRCm39) |
S377P |
probably benign |
Het |
Pi15 |
A |
G |
1: 17,672,990 (GRCm39) |
D63G |
probably benign |
Het |
Plaa |
A |
G |
4: 94,474,495 (GRCm39) |
|
probably benign |
Het |
Rbm5 |
C |
A |
9: 107,622,412 (GRCm39) |
W546C |
probably damaging |
Het |
Rnf123 |
C |
A |
9: 107,929,288 (GRCm39) |
C1257F |
probably damaging |
Het |
Rnf185 |
A |
G |
11: 3,382,551 (GRCm39) |
S45P |
possibly damaging |
Het |
Sh3bp1 |
T |
C |
15: 78,788,697 (GRCm39) |
S241P |
possibly damaging |
Het |
Slfn8 |
G |
A |
11: 82,894,023 (GRCm39) |
A872V |
possibly damaging |
Het |
Smoc1 |
G |
A |
12: 81,151,547 (GRCm39) |
|
probably null |
Het |
Sox14 |
A |
T |
9: 99,757,686 (GRCm39) |
W18R |
probably damaging |
Het |
Spata31d1a |
T |
C |
13: 59,848,969 (GRCm39) |
E1053G |
probably benign |
Het |
Syne1 |
T |
A |
10: 5,294,866 (GRCm39) |
K1246* |
probably null |
Het |
Tbrg4 |
A |
C |
11: 6,570,909 (GRCm39) |
S188A |
probably benign |
Het |
Thnsl2 |
A |
T |
6: 71,111,279 (GRCm39) |
D196E |
probably damaging |
Het |
Tmem266 |
C |
T |
9: 55,288,025 (GRCm39) |
T34I |
probably damaging |
Het |
Tmem59l |
C |
A |
8: 70,938,748 (GRCm39) |
R111L |
probably benign |
Het |
Tpr |
T |
C |
1: 150,306,280 (GRCm39) |
|
probably benign |
Het |
Trpc6 |
T |
C |
9: 8,643,687 (GRCm39) |
S491P |
probably damaging |
Het |
Tspan10 |
A |
T |
11: 120,336,992 (GRCm39) |
N254I |
probably damaging |
Het |
Vmn1r183 |
TATCCATC |
TATC |
7: 23,754,531 (GRCm39) |
|
probably null |
Het |
Vmn2r4 |
C |
T |
3: 64,298,397 (GRCm39) |
C577Y |
probably damaging |
Het |
Vmn2r86 |
A |
T |
10: 130,291,606 (GRCm39) |
M53K |
probably benign |
Het |
Zfp948 |
T |
A |
17: 21,808,569 (GRCm39) |
I587N |
possibly damaging |
Het |
|
Other mutations in Ubox5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00538:Ubox5
|
APN |
2 |
130,441,808 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01947:Ubox5
|
APN |
2 |
130,442,579 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01978:Ubox5
|
APN |
2 |
130,442,372 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02252:Ubox5
|
APN |
2 |
130,441,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02994:Ubox5
|
APN |
2 |
130,442,237 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03150:Ubox5
|
APN |
2 |
130,442,060 (GRCm39) |
missense |
probably benign |
0.44 |
PIT4403001:Ubox5
|
UTSW |
2 |
130,442,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R0792:Ubox5
|
UTSW |
2 |
130,442,630 (GRCm39) |
missense |
probably damaging |
0.99 |
R1344:Ubox5
|
UTSW |
2 |
130,442,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Ubox5
|
UTSW |
2 |
130,442,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1436:Ubox5
|
UTSW |
2 |
130,439,213 (GRCm39) |
unclassified |
probably benign |
|
R1608:Ubox5
|
UTSW |
2 |
130,439,376 (GRCm39) |
missense |
probably benign |
0.04 |
R1650:Ubox5
|
UTSW |
2 |
130,442,345 (GRCm39) |
missense |
probably benign |
0.03 |
R1772:Ubox5
|
UTSW |
2 |
130,433,794 (GRCm39) |
missense |
probably benign |
0.24 |
R2495:Ubox5
|
UTSW |
2 |
130,441,441 (GRCm39) |
nonsense |
probably null |
|
R5107:Ubox5
|
UTSW |
2 |
130,441,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Ubox5
|
UTSW |
2 |
130,441,629 (GRCm39) |
missense |
probably benign |
|
R8290:Ubox5
|
UTSW |
2 |
130,442,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R9330:Ubox5
|
UTSW |
2 |
130,442,165 (GRCm39) |
missense |
probably benign |
0.00 |
R9599:Ubox5
|
UTSW |
2 |
130,441,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|