Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy4 |
A |
T |
14: 56,016,510 (GRCm39) |
C314S |
probably damaging |
Het |
Agr2 |
T |
A |
12: 36,048,634 (GRCm39) |
I128N |
probably damaging |
Het |
Akr1c6 |
T |
C |
13: 4,496,412 (GRCm39) |
I91T |
possibly damaging |
Het |
Ankrd45 |
A |
G |
1: 160,990,909 (GRCm39) |
I221V |
probably benign |
Het |
Armc3 |
A |
T |
2: 19,293,761 (GRCm39) |
L517F |
probably damaging |
Het |
Atp13a3 |
A |
T |
16: 30,141,766 (GRCm39) |
M1129K |
probably benign |
Het |
Atp6v0a4 |
T |
A |
6: 38,031,491 (GRCm39) |
Q670L |
probably benign |
Het |
Bank1 |
T |
C |
3: 135,806,185 (GRCm39) |
Y483C |
probably damaging |
Het |
Bcan |
A |
T |
3: 87,900,357 (GRCm39) |
|
probably benign |
Het |
Bcl11a |
G |
A |
11: 24,108,333 (GRCm39) |
E104K |
probably benign |
Het |
Clasp2 |
C |
T |
9: 113,673,208 (GRCm39) |
Q368* |
probably null |
Het |
Clcn1 |
T |
A |
6: 42,267,037 (GRCm39) |
Y71N |
probably benign |
Het |
Cul2 |
C |
T |
18: 3,429,634 (GRCm39) |
T498I |
possibly damaging |
Het |
Fat4 |
A |
G |
3: 39,035,390 (GRCm39) |
D3014G |
probably damaging |
Het |
Flnc |
T |
C |
6: 29,445,636 (GRCm39) |
|
probably benign |
Het |
Il36g |
C |
A |
2: 24,077,272 (GRCm39) |
S28* |
probably null |
Het |
Itgb3bp |
A |
G |
4: 99,677,923 (GRCm39) |
|
probably benign |
Het |
Itm2b |
G |
A |
14: 73,603,229 (GRCm39) |
P120L |
probably damaging |
Het |
Klk1b26 |
T |
C |
7: 43,662,151 (GRCm39) |
F3S |
possibly damaging |
Het |
Lin52 |
T |
C |
12: 84,504,732 (GRCm39) |
V39A |
probably damaging |
Het |
Magt1 |
A |
C |
X: 105,032,622 (GRCm39) |
N242K |
probably benign |
Het |
Nos3 |
A |
G |
5: 24,588,627 (GRCm39) |
M1118V |
probably damaging |
Het |
Or1j13 |
A |
T |
2: 36,369,734 (GRCm39) |
M136K |
probably damaging |
Het |
Or6k2 |
T |
C |
1: 173,987,110 (GRCm39) |
V257A |
probably damaging |
Het |
Pcdhb16 |
T |
C |
18: 37,612,396 (GRCm39) |
F452S |
probably damaging |
Het |
Prdm5 |
T |
A |
6: 65,833,116 (GRCm39) |
|
probably benign |
Het |
Rps6ka5 |
A |
G |
12: 100,524,907 (GRCm39) |
|
probably benign |
Het |
Slc22a5 |
A |
G |
11: 53,765,840 (GRCm39) |
F249L |
probably benign |
Het |
Spata31f1a |
C |
A |
4: 42,848,362 (GRCm39) |
G1265C |
probably benign |
Het |
Ttll2 |
T |
C |
17: 7,618,779 (GRCm39) |
K383E |
probably benign |
Het |
Ube2o |
G |
A |
11: 116,435,954 (GRCm39) |
P353L |
probably damaging |
Het |
Vmn1r63 |
T |
C |
7: 5,806,110 (GRCm39) |
D174G |
probably benign |
Het |
Vmn2r82 |
A |
G |
10: 79,192,643 (GRCm39) |
|
probably null |
Het |
Xpnpep2 |
T |
A |
X: 47,207,205 (GRCm39) |
|
probably benign |
Het |
Zfp352 |
T |
A |
4: 90,111,994 (GRCm39) |
S45T |
possibly damaging |
Het |
Zfp811 |
A |
G |
17: 33,017,855 (GRCm39) |
|
probably benign |
Het |
Zfyve19 |
G |
A |
2: 119,046,717 (GRCm39) |
A304T |
probably damaging |
Het |
|
Other mutations in Paqr5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02893:Paqr5
|
APN |
9 |
61,876,150 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4480001:Paqr5
|
UTSW |
9 |
61,863,438 (GRCm39) |
missense |
probably benign |
0.09 |
R0528:Paqr5
|
UTSW |
9 |
61,863,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R0686:Paqr5
|
UTSW |
9 |
61,880,076 (GRCm39) |
missense |
probably benign |
0.00 |
R0688:Paqr5
|
UTSW |
9 |
61,880,076 (GRCm39) |
missense |
probably benign |
0.00 |
R1323:Paqr5
|
UTSW |
9 |
61,868,810 (GRCm39) |
critical splice donor site |
probably null |
|
R1323:Paqr5
|
UTSW |
9 |
61,868,810 (GRCm39) |
critical splice donor site |
probably null |
|
R2872:Paqr5
|
UTSW |
9 |
61,876,061 (GRCm39) |
critical splice donor site |
probably null |
|
R2872:Paqr5
|
UTSW |
9 |
61,876,061 (GRCm39) |
critical splice donor site |
probably null |
|
R5663:Paqr5
|
UTSW |
9 |
61,876,144 (GRCm39) |
missense |
probably benign |
0.03 |
R6726:Paqr5
|
UTSW |
9 |
61,871,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6728:Paqr5
|
UTSW |
9 |
61,871,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Paqr5
|
UTSW |
9 |
61,871,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Paqr5
|
UTSW |
9 |
61,871,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Paqr5
|
UTSW |
9 |
61,876,064 (GRCm39) |
missense |
probably null |
1.00 |
R6857:Paqr5
|
UTSW |
9 |
61,883,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Paqr5
|
UTSW |
9 |
61,880,113 (GRCm39) |
nonsense |
probably null |
|
R7456:Paqr5
|
UTSW |
9 |
61,880,072 (GRCm39) |
missense |
probably benign |
0.13 |
R8362:Paqr5
|
UTSW |
9 |
61,879,945 (GRCm39) |
nonsense |
probably null |
|
R9204:Paqr5
|
UTSW |
9 |
61,868,826 (GRCm39) |
missense |
probably benign |
0.02 |
R9475:Paqr5
|
UTSW |
9 |
61,863,507 (GRCm39) |
missense |
probably damaging |
0.98 |
R9508:Paqr5
|
UTSW |
9 |
61,880,079 (GRCm39) |
missense |
probably benign |
0.00 |
R9549:Paqr5
|
UTSW |
9 |
61,863,543 (GRCm39) |
missense |
possibly damaging |
0.96 |
|