Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
T |
11: 109,832,385 (GRCm39) |
F1309L |
possibly damaging |
Het |
Abcc6 |
C |
T |
7: 45,669,567 (GRCm39) |
A163T |
probably benign |
Het |
Adam23 |
T |
A |
1: 63,610,078 (GRCm39) |
H693Q |
probably damaging |
Het |
Afg3l2 |
A |
G |
18: 67,556,156 (GRCm39) |
F392L |
probably damaging |
Het |
Ak9 |
A |
T |
10: 41,268,724 (GRCm39) |
T1055S |
probably benign |
Het |
Ap5z1 |
T |
C |
5: 142,456,144 (GRCm39) |
|
probably benign |
Het |
Arhgef10l |
A |
G |
4: 140,338,529 (GRCm39) |
|
probably benign |
Het |
Bloc1s6 |
T |
A |
2: 122,586,141 (GRCm39) |
|
probably benign |
Het |
Caskin1 |
A |
G |
17: 24,723,870 (GRCm39) |
N886S |
probably damaging |
Het |
Celsr1 |
A |
C |
15: 85,914,963 (GRCm39) |
S1003R |
probably benign |
Het |
Cux1 |
T |
A |
5: 136,285,136 (GRCm39) |
I505F |
probably damaging |
Het |
Dcaf11 |
T |
C |
14: 55,806,767 (GRCm39) |
V490A |
probably benign |
Het |
Dscam |
A |
C |
16: 96,474,936 (GRCm39) |
W1209G |
probably damaging |
Het |
Emc8 |
A |
G |
8: 121,385,822 (GRCm39) |
|
probably benign |
Het |
Entpd6 |
A |
G |
2: 150,600,748 (GRCm39) |
K152R |
probably null |
Het |
Eps8l2 |
C |
T |
7: 140,922,884 (GRCm39) |
T49I |
probably benign |
Het |
Fcsk |
C |
T |
8: 111,620,400 (GRCm39) |
|
probably benign |
Het |
Gm12251 |
C |
A |
11: 58,283,867 (GRCm39) |
|
probably benign |
Het |
Gna11 |
A |
G |
10: 81,366,774 (GRCm39) |
M312T |
probably benign |
Het |
Hacd2 |
T |
A |
16: 34,895,997 (GRCm39) |
V105D |
probably damaging |
Het |
Il17a |
T |
A |
1: 20,803,881 (GRCm39) |
I92N |
probably damaging |
Het |
Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
Irak4 |
A |
C |
15: 94,451,753 (GRCm39) |
R115S |
probably benign |
Het |
Jarid2 |
C |
T |
13: 45,038,332 (GRCm39) |
H77Y |
probably damaging |
Het |
Kcnk6 |
A |
T |
7: 28,925,088 (GRCm39) |
L176Q |
probably damaging |
Het |
Kmt2b |
A |
T |
7: 30,276,217 (GRCm39) |
|
probably benign |
Het |
Kremen2 |
A |
C |
17: 23,962,202 (GRCm39) |
I210S |
possibly damaging |
Het |
Ldah |
T |
C |
12: 8,288,432 (GRCm39) |
|
probably benign |
Het |
Lgals9 |
A |
T |
11: 78,862,262 (GRCm39) |
|
probably benign |
Het |
Mfsd13a |
C |
T |
19: 46,354,943 (GRCm39) |
T40I |
probably benign |
Het |
Mfsd4b4 |
T |
A |
10: 39,891,097 (GRCm38) |
|
probably benign |
Het |
Msh4 |
C |
T |
3: 153,575,318 (GRCm39) |
A686T |
probably benign |
Het |
Mycbp2 |
T |
C |
14: 103,389,578 (GRCm39) |
N3411D |
probably damaging |
Het |
Myt1l |
A |
G |
12: 29,892,611 (GRCm39) |
|
probably null |
Het |
Nmbr |
A |
G |
10: 14,636,268 (GRCm39) |
N79S |
probably damaging |
Het |
Npsr1 |
A |
T |
9: 24,211,723 (GRCm39) |
I84F |
probably damaging |
Het |
Or52h1 |
G |
T |
7: 103,829,536 (GRCm39) |
H26Q |
probably benign |
Het |
Or5m10b |
C |
A |
2: 85,699,597 (GRCm39) |
Y220* |
probably null |
Het |
Or6z5 |
T |
C |
7: 6,477,679 (GRCm39) |
L190P |
probably damaging |
Het |
Prlr |
A |
G |
15: 10,328,509 (GRCm39) |
Y328C |
probably damaging |
Het |
Rasal3 |
A |
G |
17: 32,610,357 (GRCm39) |
S977P |
probably benign |
Het |
Ros1 |
C |
T |
10: 52,056,287 (GRCm39) |
V68I |
probably benign |
Het |
Shmt2 |
G |
A |
10: 127,356,917 (GRCm39) |
T31M |
possibly damaging |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Snrnp200 |
C |
G |
2: 127,079,827 (GRCm39) |
L1899V |
probably damaging |
Het |
Snrnp48 |
T |
A |
13: 38,400,356 (GRCm39) |
C154* |
probably null |
Het |
Tdrd6 |
G |
A |
17: 43,928,052 (GRCm39) |
|
probably benign |
Het |
Tmem175 |
C |
T |
5: 108,787,428 (GRCm39) |
H92Y |
probably damaging |
Het |
Tom1l1 |
G |
A |
11: 90,575,975 (GRCm39) |
|
probably benign |
Het |
Top3a |
C |
T |
11: 60,631,510 (GRCm39) |
A951T |
probably benign |
Het |
Tram2 |
C |
T |
1: 21,076,378 (GRCm39) |
R184Q |
probably damaging |
Het |
Trpc4ap |
T |
C |
2: 155,482,406 (GRCm39) |
E528G |
possibly damaging |
Het |
Vwa7 |
G |
A |
17: 35,243,523 (GRCm39) |
S710N |
possibly damaging |
Het |
Zfa-ps |
A |
T |
10: 52,421,202 (GRCm39) |
|
noncoding transcript |
Het |
Zfp770 |
T |
A |
2: 114,027,713 (GRCm39) |
R119* |
probably null |
Het |
|
Other mutations in Ctse |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02151:Ctse
|
APN |
1 |
131,600,273 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02492:Ctse
|
APN |
1 |
131,595,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Ctse
|
UTSW |
1 |
131,591,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Ctse
|
UTSW |
1 |
131,602,516 (GRCm39) |
splice site |
probably benign |
|
R2198:Ctse
|
UTSW |
1 |
131,600,185 (GRCm39) |
nonsense |
probably null |
|
R4190:Ctse
|
UTSW |
1 |
131,590,479 (GRCm39) |
missense |
probably benign |
0.02 |
R4668:Ctse
|
UTSW |
1 |
131,590,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Ctse
|
UTSW |
1 |
131,592,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Ctse
|
UTSW |
1 |
131,595,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R5499:Ctse
|
UTSW |
1 |
131,600,251 (GRCm39) |
nonsense |
probably null |
|
R5705:Ctse
|
UTSW |
1 |
131,592,112 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7207:Ctse
|
UTSW |
1 |
131,592,112 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7828:Ctse
|
UTSW |
1 |
131,590,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Ctse
|
UTSW |
1 |
131,600,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Ctse
|
UTSW |
1 |
131,590,467 (GRCm39) |
missense |
probably benign |
0.01 |
R8270:Ctse
|
UTSW |
1 |
131,595,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R8496:Ctse
|
UTSW |
1 |
131,592,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Ctse
|
UTSW |
1 |
131,595,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R9349:Ctse
|
UTSW |
1 |
131,592,111 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Ctse
|
UTSW |
1 |
131,598,510 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ctse
|
UTSW |
1 |
131,600,182 (GRCm39) |
critical splice acceptor site |
probably null |
|
|