Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot11 |
G |
C |
4: 106,606,548 (GRCm39) |
P534A |
possibly damaging |
Het |
Arhgef26 |
T |
A |
3: 62,355,626 (GRCm39) |
Y733N |
possibly damaging |
Het |
Aste1 |
G |
T |
9: 105,274,835 (GRCm39) |
M358I |
probably damaging |
Het |
B4galnt3 |
C |
T |
6: 120,209,940 (GRCm39) |
W61* |
probably null |
Het |
Brd9 |
C |
T |
13: 74,092,942 (GRCm39) |
R311W |
probably benign |
Het |
Cdkn1c |
T |
C |
7: 143,014,431 (GRCm39) |
D5G |
possibly damaging |
Het |
Cerk |
A |
G |
15: 86,043,327 (GRCm39) |
F158S |
probably damaging |
Het |
Clec2m |
C |
T |
6: 129,303,710 (GRCm39) |
R85H |
probably benign |
Het |
Cnot4 |
T |
A |
6: 35,041,941 (GRCm39) |
E235V |
probably damaging |
Het |
Crmp1 |
T |
C |
5: 37,433,624 (GRCm39) |
V275A |
possibly damaging |
Het |
Dcbld2 |
C |
A |
16: 58,285,683 (GRCm39) |
|
probably null |
Het |
Dip2a |
T |
C |
10: 76,114,394 (GRCm39) |
R1029G |
probably damaging |
Het |
Dnaaf1 |
A |
G |
8: 120,304,090 (GRCm39) |
T43A |
probably benign |
Het |
Eaf2 |
C |
T |
16: 36,648,514 (GRCm39) |
S2N |
probably benign |
Het |
Eif2b4 |
T |
C |
5: 31,348,719 (GRCm39) |
D164G |
probably benign |
Het |
Fpgs |
T |
C |
2: 32,584,005 (GRCm39) |
Y45C |
possibly damaging |
Het |
Gm1527 |
C |
T |
3: 28,968,691 (GRCm39) |
Q248* |
probably null |
Het |
Gm29666 |
C |
T |
15: 84,798,469 (GRCm39) |
A31T |
unknown |
Het |
Gmip |
C |
A |
8: 70,263,892 (GRCm39) |
A112D |
probably damaging |
Het |
Hibadh |
C |
T |
6: 52,617,197 (GRCm39) |
G13S |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,494,597 (GRCm39) |
V4164D |
probably damaging |
Het |
Kif15 |
A |
T |
9: 122,820,202 (GRCm39) |
N580I |
probably benign |
Het |
Krt25 |
G |
A |
11: 99,208,232 (GRCm39) |
T332M |
probably benign |
Het |
Krt88 |
G |
T |
15: 101,345,643 (GRCm39) |
|
probably benign |
Het |
Lrrk2 |
T |
C |
15: 91,615,858 (GRCm39) |
|
probably null |
Het |
Mapkapk5 |
A |
G |
5: 121,675,169 (GRCm39) |
|
probably benign |
Het |
Myh7b |
C |
T |
2: 155,474,460 (GRCm39) |
S1725L |
probably benign |
Het |
Nckap1l |
T |
G |
15: 103,384,526 (GRCm39) |
|
probably null |
Het |
Nphp3 |
A |
G |
9: 103,893,277 (GRCm39) |
|
probably null |
Het |
Obscn |
A |
C |
11: 58,973,185 (GRCm39) |
V1996G |
probably damaging |
Het |
Or14j8 |
T |
A |
17: 38,263,900 (GRCm39) |
N5I |
probably damaging |
Het |
Or4a66 |
A |
T |
2: 88,531,331 (GRCm39) |
V114E |
probably damaging |
Het |
Parp8 |
T |
C |
13: 117,032,307 (GRCm39) |
T289A |
probably benign |
Het |
Pcsk5 |
T |
C |
19: 17,492,577 (GRCm39) |
K932R |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,625,632 (GRCm39) |
D1322G |
probably benign |
Het |
Peli3 |
A |
T |
19: 4,985,103 (GRCm39) |
M136K |
possibly damaging |
Het |
Pgm5 |
A |
G |
19: 24,812,181 (GRCm39) |
I117T |
probably damaging |
Het |
Ppm1g |
T |
C |
5: 31,360,621 (GRCm39) |
D478G |
probably damaging |
Het |
Ppp2r5c |
A |
G |
12: 110,541,272 (GRCm39) |
T474A |
probably benign |
Het |
Ptger3 |
T |
C |
3: 157,272,764 (GRCm39) |
V37A |
probably benign |
Het |
Ptprz1 |
T |
C |
6: 23,000,906 (GRCm39) |
S999P |
probably damaging |
Het |
Pygl |
C |
T |
12: 70,274,306 (GRCm39) |
G18S |
probably benign |
Het |
Rest |
T |
C |
5: 77,428,976 (GRCm39) |
V465A |
probably benign |
Het |
Sart1 |
T |
C |
19: 5,433,231 (GRCm39) |
D422G |
probably damaging |
Het |
Sgk1 |
A |
G |
10: 21,869,972 (GRCm39) |
M4V |
probably benign |
Het |
Slc33a1 |
A |
G |
3: 63,855,075 (GRCm39) |
V395A |
possibly damaging |
Het |
Slc4a2 |
T |
A |
5: 24,634,713 (GRCm39) |
S76T |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,132,341 (GRCm39) |
D223G |
unknown |
Het |
Ssc4d |
T |
A |
5: 135,994,965 (GRCm39) |
S184C |
probably damaging |
Het |
Tspoap1 |
A |
G |
11: 87,669,347 (GRCm39) |
Y1540C |
probably benign |
Het |
Ube3a |
T |
A |
7: 58,926,383 (GRCm39) |
L408Q |
probably damaging |
Het |
Usp43 |
C |
A |
11: 67,767,155 (GRCm39) |
|
probably null |
Het |
Zan |
A |
C |
5: 137,385,232 (GRCm39) |
V5067G |
unknown |
Het |
Zfp180 |
C |
A |
7: 23,804,915 (GRCm39) |
L445I |
probably damaging |
Het |
|
Other mutations in Slc38a11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00668:Slc38a11
|
APN |
2 |
65,184,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01467:Slc38a11
|
APN |
2 |
65,147,200 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02585:Slc38a11
|
APN |
2 |
65,166,135 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03001:Slc38a11
|
APN |
2 |
65,184,159 (GRCm39) |
missense |
probably damaging |
0.97 |
R0458:Slc38a11
|
UTSW |
2 |
65,193,813 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0514:Slc38a11
|
UTSW |
2 |
65,147,209 (GRCm39) |
missense |
probably benign |
0.08 |
R0815:Slc38a11
|
UTSW |
2 |
65,184,124 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1695:Slc38a11
|
UTSW |
2 |
65,147,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Slc38a11
|
UTSW |
2 |
65,180,452 (GRCm39) |
missense |
probably benign |
0.44 |
R1760:Slc38a11
|
UTSW |
2 |
65,185,663 (GRCm39) |
splice site |
probably null |
|
R1854:Slc38a11
|
UTSW |
2 |
65,193,860 (GRCm39) |
splice site |
probably null |
|
R1961:Slc38a11
|
UTSW |
2 |
65,160,683 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1991:Slc38a11
|
UTSW |
2 |
65,160,683 (GRCm39) |
missense |
probably benign |
0.22 |
R2046:Slc38a11
|
UTSW |
2 |
65,188,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R2078:Slc38a11
|
UTSW |
2 |
65,160,728 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2103:Slc38a11
|
UTSW |
2 |
65,160,683 (GRCm39) |
missense |
probably benign |
0.22 |
R3154:Slc38a11
|
UTSW |
2 |
65,160,679 (GRCm39) |
missense |
probably damaging |
0.98 |
R4358:Slc38a11
|
UTSW |
2 |
65,188,460 (GRCm39) |
missense |
probably benign |
0.01 |
R5635:Slc38a11
|
UTSW |
2 |
65,191,747 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5729:Slc38a11
|
UTSW |
2 |
65,147,365 (GRCm39) |
missense |
probably benign |
0.00 |
R6059:Slc38a11
|
UTSW |
2 |
65,165,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6755:Slc38a11
|
UTSW |
2 |
65,194,235 (GRCm39) |
missense |
probably benign |
|
R7339:Slc38a11
|
UTSW |
2 |
65,156,914 (GRCm39) |
missense |
probably benign |
|
R8397:Slc38a11
|
UTSW |
2 |
65,160,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Slc38a11
|
UTSW |
2 |
65,188,484 (GRCm39) |
missense |
probably benign |
0.17 |
|