Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I06Rik |
A |
G |
14: 64,225,162 (GRCm39) |
V12A |
probably benign |
Het |
Abcc12 |
A |
G |
8: 87,243,947 (GRCm39) |
Y1069H |
probably damaging |
Het |
Abcc9 |
T |
C |
6: 142,624,977 (GRCm39) |
T473A |
probably damaging |
Het |
Acsm1 |
A |
T |
7: 119,239,868 (GRCm39) |
T271S |
probably benign |
Het |
Adh6b |
T |
C |
3: 138,055,397 (GRCm39) |
I49T |
probably benign |
Het |
Aff4 |
A |
T |
11: 53,263,231 (GRCm39) |
T84S |
probably benign |
Het |
Angptl7 |
G |
A |
4: 148,580,956 (GRCm39) |
R280* |
probably null |
Het |
Bhlhe23 |
T |
A |
2: 180,418,099 (GRCm39) |
K146N |
probably damaging |
Het |
Cacna1s |
T |
C |
1: 136,014,544 (GRCm39) |
|
probably null |
Het |
Cfap45 |
C |
G |
1: 172,372,834 (GRCm39) |
R510G |
probably damaging |
Het |
Chl1 |
A |
G |
6: 103,642,868 (GRCm39) |
Y202C |
probably damaging |
Het |
Chrna6 |
T |
A |
8: 27,896,870 (GRCm39) |
T336S |
probably benign |
Het |
Clpx |
A |
G |
9: 65,231,519 (GRCm39) |
K535E |
probably benign |
Het |
Crybg3 |
T |
C |
16: 59,376,512 (GRCm39) |
M1581V |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,758,823 (GRCm39) |
I246K |
probably benign |
Het |
F7 |
G |
T |
8: 13,078,724 (GRCm39) |
G52C |
probably damaging |
Het |
Fam186b |
T |
C |
15: 99,177,223 (GRCm39) |
Q701R |
probably benign |
Het |
Fign |
T |
A |
2: 63,809,456 (GRCm39) |
M605L |
probably benign |
Het |
Fpr2 |
T |
C |
17: 18,113,883 (GRCm39) |
F293S |
probably damaging |
Het |
Gm40460 |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
7: 141,794,171 (GRCm39) |
|
probably benign |
Het |
Gria2 |
A |
T |
3: 80,618,170 (GRCm39) |
|
probably benign |
Het |
Grid1 |
G |
A |
14: 35,043,664 (GRCm39) |
D340N |
probably damaging |
Het |
Gsto2 |
T |
C |
19: 47,873,203 (GRCm39) |
|
probably null |
Het |
Hsd3b1 |
A |
G |
3: 98,760,299 (GRCm39) |
W231R |
probably damaging |
Het |
Igflr1 |
CAGAG |
CAG |
7: 30,266,888 (GRCm39) |
|
probably null |
Het |
Ighv1-80 |
C |
T |
12: 115,876,113 (GRCm39) |
G68R |
probably damaging |
Het |
Il10ra |
A |
G |
9: 45,177,802 (GRCm39) |
V69A |
unknown |
Het |
Klhdc1 |
C |
T |
12: 69,300,537 (GRCm39) |
A159V |
probably damaging |
Het |
Krtap4-6 |
A |
G |
11: 99,556,229 (GRCm39) |
I166T |
unknown |
Het |
Lce1h |
A |
T |
3: 92,670,976 (GRCm39) |
C59S |
unknown |
Het |
Magi3 |
T |
C |
3: 103,996,748 (GRCm39) |
|
probably benign |
Het |
Map3k1 |
G |
T |
13: 111,892,837 (GRCm39) |
S806* |
probably null |
Het |
Map3k6 |
T |
A |
4: 132,979,954 (GRCm39) |
|
probably benign |
Het |
Mgam |
G |
A |
6: 40,740,137 (GRCm39) |
|
probably null |
Het |
Mtx1 |
A |
G |
3: 89,120,033 (GRCm39) |
V207A |
probably damaging |
Het |
Muc5ac |
A |
T |
7: 141,347,091 (GRCm39) |
N356Y |
probably damaging |
Het |
Myo16 |
T |
C |
8: 10,524,679 (GRCm39) |
F810S |
probably damaging |
Het |
Nlrx1 |
A |
G |
9: 44,166,761 (GRCm39) |
L774P |
probably damaging |
Het |
Nr1i2 |
C |
T |
16: 38,086,382 (GRCm39) |
V28I |
probably benign |
Het |
Or10h28 |
A |
G |
17: 33,488,589 (GRCm39) |
K297R |
probably damaging |
Het |
Or5b122 |
A |
C |
19: 13,562,860 (GRCm39) |
N64T |
probably damaging |
Het |
Pcmtd2 |
T |
C |
2: 181,496,863 (GRCm39) |
|
probably benign |
Het |
Pcnx3 |
A |
G |
19: 5,730,347 (GRCm39) |
L102P |
probably damaging |
Het |
Pnpla6 |
A |
G |
8: 3,571,319 (GRCm39) |
E114G |
possibly damaging |
Het |
Ppp4r1 |
T |
C |
17: 66,110,926 (GRCm39) |
V70A |
probably damaging |
Het |
Psd2 |
G |
A |
18: 36,121,292 (GRCm39) |
V421M |
probably damaging |
Het |
Qng1 |
C |
T |
13: 58,532,875 (GRCm39) |
A32T |
probably damaging |
Het |
Rbak |
C |
T |
5: 143,160,025 (GRCm39) |
E343K |
possibly damaging |
Het |
Rhbdf1 |
G |
A |
11: 32,160,093 (GRCm39) |
A136V |
probably benign |
Het |
Rusc1 |
T |
A |
3: 88,995,337 (GRCm39) |
E231D |
probably benign |
Het |
Rxfp1 |
T |
C |
3: 79,552,231 (GRCm39) |
E690G |
probably damaging |
Het |
Sdr9c7 |
A |
G |
10: 127,734,776 (GRCm39) |
E88G |
probably benign |
Het |
Sec23b |
T |
C |
2: 144,411,137 (GRCm39) |
|
probably null |
Het |
Sgcb |
A |
T |
5: 73,801,661 (GRCm39) |
I68N |
probably damaging |
Het |
Sh3pxd2b |
T |
C |
11: 32,364,433 (GRCm39) |
|
probably benign |
Het |
Slc25a48 |
C |
T |
13: 56,611,519 (GRCm39) |
P209S |
probably damaging |
Het |
Slc9a3 |
C |
A |
13: 74,311,895 (GRCm39) |
H614Q |
possibly damaging |
Het |
Slurp1 |
G |
A |
15: 74,598,763 (GRCm39) |
S76L |
probably damaging |
Het |
Spen |
T |
C |
4: 141,202,969 (GRCm39) |
E1886G |
possibly damaging |
Het |
Sqor |
C |
T |
2: 122,649,549 (GRCm39) |
P151S |
possibly damaging |
Het |
Sstr4 |
C |
A |
2: 148,238,228 (GRCm39) |
L280M |
probably damaging |
Het |
Stard10 |
A |
G |
7: 100,991,847 (GRCm39) |
Y117C |
probably damaging |
Het |
Stard13 |
A |
T |
5: 150,968,574 (GRCm39) |
|
probably null |
Het |
Stim2 |
G |
T |
5: 54,262,673 (GRCm39) |
R305L |
possibly damaging |
Het |
Syt14 |
G |
A |
1: 192,612,896 (GRCm39) |
R635C |
probably damaging |
Het |
Tmcc3 |
A |
T |
10: 94,381,483 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,575,695 (GRCm39) |
N23320S |
possibly damaging |
Het |
Ugt2b34 |
A |
G |
5: 87,039,158 (GRCm39) |
L501P |
probably damaging |
Het |
Umod |
T |
C |
7: 119,068,700 (GRCm39) |
I449V |
probably damaging |
Het |
Vmn2r51 |
C |
A |
7: 9,833,953 (GRCm39) |
D362Y |
possibly damaging |
Het |
Xirp2 |
A |
C |
2: 67,346,488 (GRCm39) |
T2910P |
probably benign |
Het |
Zscan20 |
A |
G |
4: 128,498,315 (GRCm39) |
S28P |
probably benign |
Het |
|
Other mutations in Ubqln4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00941:Ubqln4
|
APN |
3 |
88,471,808 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01352:Ubqln4
|
APN |
3 |
88,471,775 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02821:Ubqln4
|
APN |
3 |
88,470,458 (GRCm39) |
missense |
probably benign |
|
IGL02852:Ubqln4
|
APN |
3 |
88,462,778 (GRCm39) |
missense |
probably damaging |
0.97 |
R0173:Ubqln4
|
UTSW |
3 |
88,462,686 (GRCm39) |
missense |
probably benign |
0.00 |
R0372:Ubqln4
|
UTSW |
3 |
88,463,276 (GRCm39) |
missense |
probably benign |
|
R1473:Ubqln4
|
UTSW |
3 |
88,473,152 (GRCm39) |
missense |
probably benign |
|
R3688:Ubqln4
|
UTSW |
3 |
88,470,466 (GRCm39) |
missense |
probably damaging |
0.97 |
R5423:Ubqln4
|
UTSW |
3 |
88,470,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R5592:Ubqln4
|
UTSW |
3 |
88,464,171 (GRCm39) |
missense |
probably damaging |
0.98 |
R5688:Ubqln4
|
UTSW |
3 |
88,472,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Ubqln4
|
UTSW |
3 |
88,462,679 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7326:Ubqln4
|
UTSW |
3 |
88,463,217 (GRCm39) |
missense |
probably benign |
|
R7572:Ubqln4
|
UTSW |
3 |
88,462,731 (GRCm39) |
unclassified |
probably benign |
|
R8134:Ubqln4
|
UTSW |
3 |
88,462,797 (GRCm39) |
critical splice donor site |
probably null |
|
R8754:Ubqln4
|
UTSW |
3 |
88,473,090 (GRCm39) |
missense |
probably benign |
0.00 |
R9447:Ubqln4
|
UTSW |
3 |
88,464,124 (GRCm39) |
missense |
probably benign |
0.17 |
R9762:Ubqln4
|
UTSW |
3 |
88,473,185 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Ubqln4
|
UTSW |
3 |
88,473,027 (GRCm39) |
missense |
probably benign |
|
|