Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
A |
6: 128,536,032 (GRCm39) |
H720L |
probably benign |
Het |
Abca15 |
T |
C |
7: 119,987,388 (GRCm39) |
Y1225H |
probably benign |
Het |
Adck1 |
C |
A |
12: 88,335,193 (GRCm39) |
N26K |
probably benign |
Het |
Adcy3 |
A |
G |
12: 4,245,208 (GRCm39) |
D382G |
probably damaging |
Het |
Ahi1 |
T |
A |
10: 20,876,488 (GRCm39) |
C800S |
probably benign |
Het |
Ahnak |
G |
T |
19: 8,992,287 (GRCm39) |
V4524L |
probably benign |
Het |
Aoc1l1 |
C |
A |
6: 48,952,890 (GRCm39) |
R272S |
probably benign |
Het |
Arid1a |
T |
C |
4: 133,421,214 (GRCm39) |
M479V |
unknown |
Het |
Atp13a2 |
T |
A |
4: 140,724,056 (GRCm39) |
C324S |
probably damaging |
Het |
C2cd2 |
T |
G |
16: 97,677,486 (GRCm39) |
T413P |
probably damaging |
Het |
Cct5 |
A |
C |
15: 31,591,107 (GRCm39) |
D531E |
|
Het |
Chst1 |
A |
T |
2: 92,444,523 (GRCm39) |
I332F |
probably damaging |
Het |
Col12a1 |
A |
T |
9: 79,527,344 (GRCm39) |
V2662D |
probably benign |
Het |
Cts3 |
A |
G |
13: 61,712,800 (GRCm39) |
Y307H |
probably benign |
Het |
D630023F18Rik |
G |
A |
1: 65,160,371 (GRCm39) |
|
probably benign |
Het |
Dhx9 |
A |
G |
1: 153,336,826 (GRCm39) |
I807T |
probably damaging |
Het |
Exoc3l4 |
T |
C |
12: 111,388,586 (GRCm39) |
L25P |
probably benign |
Het |
Ggcx |
T |
A |
6: 72,402,905 (GRCm39) |
C288S |
probably benign |
Het |
Gjb3 |
A |
G |
4: 127,220,140 (GRCm39) |
Y131H |
probably damaging |
Het |
Hdhd3 |
A |
G |
4: 62,417,574 (GRCm39) |
S201P |
probably benign |
Het |
Helz2 |
A |
T |
2: 180,881,848 (GRCm39) |
V315E |
probably damaging |
Het |
Hsp90aa1 |
A |
G |
12: 110,662,684 (GRCm39) |
|
probably null |
Het |
Ift70a1 |
A |
T |
2: 75,810,423 (GRCm39) |
Y553* |
probably null |
Het |
Il12a |
C |
T |
3: 68,598,875 (GRCm39) |
R19W |
unknown |
Het |
Isoc1 |
C |
T |
18: 58,806,347 (GRCm39) |
A219V |
possibly damaging |
Het |
Jup |
T |
A |
11: 100,269,124 (GRCm39) |
T430S |
probably benign |
Het |
Klra5 |
C |
T |
6: 129,886,911 (GRCm39) |
C39Y |
probably benign |
Het |
Map4 |
A |
T |
9: 109,855,268 (GRCm39) |
Q131L |
probably damaging |
Het |
Mau2 |
T |
A |
8: 70,480,165 (GRCm39) |
K314M |
probably damaging |
Het |
Mga |
A |
G |
2: 119,794,493 (GRCm39) |
M2726V |
probably benign |
Het |
Mgme1 |
G |
A |
2: 144,114,405 (GRCm39) |
|
probably null |
Het |
Msrb2 |
A |
G |
2: 19,399,066 (GRCm39) |
E143G |
probably benign |
Het |
Muc5b |
G |
T |
7: 141,411,350 (GRCm39) |
C1432F |
unknown |
Het |
Naglu |
T |
C |
11: 100,961,940 (GRCm39) |
Y138H |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nlrp1b |
A |
G |
11: 71,109,193 (GRCm39) |
Y103H |
probably benign |
Het |
Nodal |
A |
G |
10: 61,259,459 (GRCm39) |
N299D |
probably damaging |
Het |
Notch1 |
T |
C |
2: 26,349,587 (GRCm39) |
T2518A |
probably benign |
Het |
Nr2e1 |
A |
C |
10: 42,448,948 (GRCm39) |
S97A |
probably benign |
Het |
Nuak1 |
A |
T |
10: 84,210,587 (GRCm39) |
S500R |
probably benign |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Nyap1 |
T |
C |
5: 137,736,175 (GRCm39) |
E104G |
probably benign |
Het |
Or3a1b |
C |
T |
11: 74,012,526 (GRCm39) |
T137I |
probably benign |
Het |
Or52e18 |
T |
A |
7: 104,609,204 (GRCm39) |
H245L |
probably damaging |
Het |
Palld |
T |
C |
8: 62,330,107 (GRCm39) |
T257A |
probably benign |
Het |
Pcnx4 |
C |
T |
12: 72,603,043 (GRCm39) |
P435L |
probably damaging |
Het |
Piezo1 |
T |
C |
8: 123,208,753 (GRCm39) |
T2538A |
unknown |
Het |
Plagl1 |
T |
C |
10: 13,003,872 (GRCm39) |
L380P |
unknown |
Het |
Polrmt |
G |
T |
10: 79,576,415 (GRCm39) |
Q514K |
probably benign |
Het |
Psg17 |
T |
G |
7: 18,553,851 (GRCm39) |
D133A |
probably benign |
Het |
Rab3b |
G |
A |
4: 108,797,903 (GRCm39) |
D185N |
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,291,736 (GRCm39) |
S248T |
probably benign |
Het |
Rdh10 |
C |
A |
1: 16,199,430 (GRCm39) |
A212D |
probably damaging |
Het |
Rinl |
A |
G |
7: 28,495,089 (GRCm39) |
H154R |
|
Het |
Selenbp1 |
T |
C |
3: 94,851,414 (GRCm39) |
M389T |
probably benign |
Het |
Serpina1c |
T |
A |
12: 103,862,400 (GRCm39) |
H305L |
possibly damaging |
Het |
Sh3rf2 |
T |
A |
18: 42,282,746 (GRCm39) |
S467T |
|
Het |
Sipa1l1 |
A |
G |
12: 82,443,335 (GRCm39) |
D875G |
probably benign |
Het |
Slc10a6 |
A |
T |
5: 103,776,800 (GRCm39) |
V100D |
probably damaging |
Het |
Slc13a4 |
T |
C |
6: 35,247,290 (GRCm39) |
I577V |
possibly damaging |
Het |
Slc20a2 |
T |
C |
8: 23,030,447 (GRCm39) |
F168L |
probably benign |
Het |
Slc25a1 |
A |
T |
16: 17,745,108 (GRCm39) |
|
probably null |
Het |
Slc5a12 |
A |
G |
2: 110,471,242 (GRCm39) |
S495G |
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,677,028 (GRCm39) |
D42G |
possibly damaging |
Het |
Spag16 |
G |
C |
1: 70,420,459 (GRCm39) |
L482F |
probably damaging |
Het |
Susd5 |
G |
A |
9: 113,925,289 (GRCm39) |
G391R |
probably damaging |
Het |
Sync |
G |
T |
4: 129,187,618 (GRCm39) |
A217S |
|
Het |
Tha1 |
T |
A |
11: 117,759,512 (GRCm39) |
N326Y |
probably damaging |
Het |
Tjp1 |
A |
T |
7: 64,952,564 (GRCm39) |
F1590Y |
probably benign |
Het |
Tle4 |
T |
C |
19: 14,445,583 (GRCm39) |
N221S |
probably benign |
Het |
Tln1 |
T |
C |
4: 43,536,024 (GRCm39) |
T2054A |
probably damaging |
Het |
Ttll4 |
A |
G |
1: 74,718,949 (GRCm39) |
K267E |
probably benign |
Het |
Usp32 |
C |
T |
11: 84,913,118 (GRCm39) |
G930D |
probably damaging |
Het |
Vmn2r75 |
T |
C |
7: 85,813,447 (GRCm39) |
N452D |
probably damaging |
Het |
Vmn2r81 |
T |
C |
10: 79,104,028 (GRCm39) |
L217P |
possibly damaging |
Het |
Wnt2 |
T |
A |
6: 18,030,397 (GRCm39) |
|
probably benign |
Het |
Zfp459 |
C |
T |
13: 67,556,735 (GRCm39) |
S116N |
probably benign |
Het |
Zfp981 |
C |
A |
4: 146,622,410 (GRCm39) |
T445N |
possibly damaging |
Het |
|