Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bcl7b |
G |
T |
5: 135,208,879 (GRCm39) |
S114I |
probably damaging |
Het |
Cct8 |
A |
T |
16: 87,284,566 (GRCm39) |
M207K |
probably benign |
Het |
Cnga1 |
A |
G |
5: 72,769,702 (GRCm39) |
|
probably null |
Het |
Cst13 |
T |
C |
2: 148,670,111 (GRCm39) |
C94R |
probably damaging |
Het |
Cyp8b1 |
G |
T |
9: 121,744,864 (GRCm39) |
S156* |
probably null |
Het |
Dip2b |
T |
C |
15: 100,049,157 (GRCm39) |
S184P |
probably damaging |
Het |
Dmbt1 |
T |
C |
7: 130,659,984 (GRCm39) |
W516R |
probably damaging |
Het |
Dock8 |
A |
T |
19: 25,072,914 (GRCm39) |
Y398F |
possibly damaging |
Het |
Drosha |
T |
A |
15: 12,889,803 (GRCm39) |
C890* |
probably null |
Het |
Eed |
A |
G |
7: 89,626,149 (GRCm39) |
S75P |
probably benign |
Het |
Efcab3 |
T |
C |
11: 104,885,143 (GRCm39) |
L4134S |
possibly damaging |
Het |
Etaa1 |
A |
C |
11: 17,896,833 (GRCm39) |
I428S |
probably benign |
Het |
F5 |
A |
T |
1: 164,021,062 (GRCm39) |
D1179V |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,405,379 (GRCm39) |
V710A |
possibly damaging |
Het |
Fmo4 |
G |
A |
1: 162,621,538 (GRCm39) |
Q558* |
probably null |
Het |
Gm7361 |
A |
G |
5: 26,463,960 (GRCm39) |
I72V |
probably benign |
Het |
Grm4 |
A |
G |
17: 27,654,294 (GRCm39) |
V552A |
probably benign |
Het |
Krt13 |
T |
A |
11: 100,010,202 (GRCm39) |
I260F |
probably damaging |
Het |
Krtap3-3 |
T |
C |
11: 99,441,490 (GRCm39) |
D49G |
probably damaging |
Het |
Lpin1 |
T |
C |
12: 16,614,554 (GRCm39) |
E409G |
probably benign |
Het |
Ly9 |
A |
G |
1: 171,428,576 (GRCm39) |
V238A |
possibly damaging |
Het |
Map2k6 |
T |
C |
11: 110,381,703 (GRCm39) |
|
probably null |
Het |
Mylk2 |
T |
C |
2: 152,759,315 (GRCm39) |
L362P |
probably damaging |
Het |
Or4c120 |
T |
A |
2: 89,000,942 (GRCm39) |
I205F |
probably benign |
Het |
Or4c3 |
A |
G |
2: 89,851,975 (GRCm39) |
V145A |
probably benign |
Het |
Or51a6 |
T |
A |
7: 102,604,622 (GRCm39) |
Y69F |
possibly damaging |
Het |
Pcdha9 |
G |
A |
18: 37,130,972 (GRCm39) |
V14M |
probably benign |
Het |
Pdzrn4 |
A |
T |
15: 92,578,418 (GRCm39) |
E380D |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,239,364 (GRCm39) |
Y739H |
possibly damaging |
Het |
Pigk |
A |
G |
3: 152,446,486 (GRCm39) |
H195R |
probably benign |
Het |
Plin2 |
T |
C |
4: 86,580,236 (GRCm39) |
D175G |
probably null |
Het |
Plk4 |
T |
A |
3: 40,763,408 (GRCm39) |
H526Q |
probably benign |
Het |
Pom121l12 |
A |
T |
11: 14,549,489 (GRCm39) |
D65V |
probably damaging |
Het |
Sh3bp2 |
G |
A |
5: 34,718,947 (GRCm39) |
V495I |
probably damaging |
Het |
Slx4ip |
T |
A |
2: 136,888,669 (GRCm39) |
C117S |
probably damaging |
Het |
Tmtc2 |
A |
T |
10: 105,409,551 (GRCm39) |
S20R |
probably benign |
Het |
Unc79 |
A |
G |
12: 102,987,269 (GRCm39) |
Y186C |
probably damaging |
Het |
Vmn2r106 |
C |
T |
17: 20,488,725 (GRCm39) |
C558Y |
probably damaging |
Het |
Vmn2r26 |
T |
C |
6: 124,038,348 (GRCm39) |
L641P |
probably damaging |
Het |
Wdr17 |
A |
T |
8: 55,114,495 (GRCm39) |
S674T |
probably benign |
Het |
Zfp959 |
T |
C |
17: 56,202,854 (GRCm39) |
F10L |
probably damaging |
Het |
|
Other mutations in Prb1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00670:Prb1a
|
APN |
6 |
132,184,109 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01017:Prb1a
|
APN |
6 |
132,184,194 (GRCm39) |
missense |
unknown |
|
R0369:Prb1a
|
UTSW |
6 |
132,184,620 (GRCm39) |
nonsense |
probably null |
|
R1500:Prb1a
|
UTSW |
6 |
132,184,439 (GRCm39) |
missense |
unknown |
|
R1544:Prb1a
|
UTSW |
6 |
132,186,424 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1544:Prb1a
|
UTSW |
6 |
132,186,423 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1559:Prb1a
|
UTSW |
6 |
132,185,507 (GRCm39) |
missense |
unknown |
|
R2142:Prb1a
|
UTSW |
6 |
132,184,166 (GRCm39) |
missense |
unknown |
|
R2655:Prb1a
|
UTSW |
6 |
132,187,425 (GRCm39) |
missense |
unknown |
|
R4065:Prb1a
|
UTSW |
6 |
132,184,658 (GRCm39) |
missense |
unknown |
|
R4505:Prb1a
|
UTSW |
6 |
132,184,533 (GRCm39) |
nonsense |
probably null |
|
R5925:Prb1a
|
UTSW |
6 |
132,187,475 (GRCm39) |
missense |
unknown |
|
R6525:Prb1a
|
UTSW |
6 |
132,184,467 (GRCm39) |
missense |
unknown |
|
R6745:Prb1a
|
UTSW |
6 |
132,186,383 (GRCm39) |
splice site |
probably null |
|
R7192:Prb1a
|
UTSW |
6 |
132,184,335 (GRCm39) |
missense |
unknown |
|
R7536:Prb1a
|
UTSW |
6 |
132,184,184 (GRCm39) |
missense |
unknown |
|
R8483:Prb1a
|
UTSW |
6 |
132,185,398 (GRCm39) |
missense |
unknown |
|
R9139:Prb1a
|
UTSW |
6 |
132,185,306 (GRCm39) |
missense |
unknown |
|
R9365:Prb1a
|
UTSW |
6 |
132,184,201 (GRCm39) |
missense |
unknown |
|
R9559:Prb1a
|
UTSW |
6 |
132,184,388 (GRCm39) |
missense |
unknown |
|
|