Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamdec1 |
A |
G |
14: 68,819,406 (GRCm39) |
|
probably null |
Het |
Adamts16 |
T |
A |
13: 70,927,763 (GRCm39) |
Q492L |
possibly damaging |
Het |
Aplnr |
A |
G |
2: 84,967,521 (GRCm39) |
D182G |
probably damaging |
Het |
Arnt2 |
G |
T |
7: 84,010,867 (GRCm39) |
S3* |
probably null |
Het |
Asxl3 |
T |
C |
18: 22,656,211 (GRCm39) |
V1407A |
probably benign |
Het |
Atg13 |
A |
T |
2: 91,515,107 (GRCm39) |
|
probably null |
Het |
Atm |
A |
T |
9: 53,365,579 (GRCm39) |
|
probably benign |
Het |
Birc6 |
T |
G |
17: 74,916,322 (GRCm39) |
V1746G |
possibly damaging |
Het |
Cbln1 |
G |
T |
8: 88,198,741 (GRCm39) |
T43K |
probably benign |
Het |
Cbx5 |
T |
C |
15: 103,108,127 (GRCm39) |
T173A |
probably damaging |
Het |
Cc2d2a |
A |
G |
5: 43,894,854 (GRCm39) |
Y1437C |
probably damaging |
Het |
Ccdc78 |
C |
A |
17: 26,008,210 (GRCm39) |
|
probably benign |
Het |
Cd2bp2 |
A |
G |
7: 126,793,000 (GRCm39) |
Y341H |
probably damaging |
Het |
Cdhr5 |
T |
A |
7: 140,856,291 (GRCm39) |
D88V |
probably damaging |
Het |
Ces1f |
T |
A |
8: 93,993,957 (GRCm39) |
T275S |
probably null |
Het |
Cimip4 |
T |
A |
15: 78,263,028 (GRCm39) |
M209L |
probably damaging |
Het |
Clca4a |
T |
C |
3: 144,666,478 (GRCm39) |
N458S |
probably benign |
Het |
Cog5 |
A |
G |
12: 31,889,840 (GRCm39) |
K521R |
probably damaging |
Het |
Csf2ra |
T |
A |
19: 61,214,006 (GRCm39) |
T305S |
probably benign |
Het |
Csmd3 |
T |
A |
15: 47,483,125 (GRCm39) |
|
probably benign |
Het |
Cts6 |
T |
A |
13: 61,349,313 (GRCm39) |
R132* |
probably null |
Het |
D5Ertd579e |
G |
T |
5: 36,773,809 (GRCm39) |
N195K |
probably damaging |
Het |
Ddx1 |
A |
G |
12: 13,273,809 (GRCm39) |
V606A |
probably damaging |
Het |
Dip2b |
G |
A |
15: 100,084,028 (GRCm39) |
D884N |
probably damaging |
Het |
Ehhadh |
A |
G |
16: 21,592,243 (GRCm39) |
|
probably null |
Het |
Enpp1 |
T |
A |
10: 24,529,815 (GRCm39) |
T608S |
probably benign |
Het |
Fancm |
T |
C |
12: 65,148,406 (GRCm39) |
Y674H |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,945,745 (GRCm39) |
V1546D |
probably damaging |
Het |
Fsd1 |
G |
A |
17: 56,297,522 (GRCm39) |
A158T |
probably benign |
Het |
Fzd2 |
T |
A |
11: 102,496,948 (GRCm39) |
M464K |
probably damaging |
Het |
Gjc2 |
A |
G |
11: 59,068,416 (GRCm39) |
F22S |
possibly damaging |
Het |
Gria2 |
T |
C |
3: 80,615,145 (GRCm39) |
Y445C |
probably damaging |
Het |
Hsdl1 |
T |
A |
8: 120,292,995 (GRCm39) |
I147F |
possibly damaging |
Het |
Ifi44 |
T |
C |
3: 151,451,273 (GRCm39) |
Y226C |
probably damaging |
Het |
Il16 |
A |
G |
7: 83,371,516 (GRCm39) |
C97R |
probably damaging |
Het |
Impg1 |
A |
T |
9: 80,252,843 (GRCm39) |
S369T |
probably damaging |
Het |
Jmjd1c |
A |
G |
10: 67,054,888 (GRCm39) |
T390A |
unknown |
Het |
Lgi1 |
A |
G |
19: 38,289,741 (GRCm39) |
E269G |
possibly damaging |
Het |
Lrp6 |
G |
T |
6: 134,427,860 (GRCm39) |
Y1577* |
probably null |
Het |
Lrrc74a |
G |
T |
12: 86,808,547 (GRCm39) |
|
probably benign |
Het |
Man1c1 |
A |
T |
4: 134,367,709 (GRCm39) |
|
probably null |
Het |
Map1lc3b |
A |
C |
8: 122,317,289 (GRCm39) |
Q9P |
possibly damaging |
Het |
Mboat1 |
G |
A |
13: 30,386,358 (GRCm39) |
R124H |
probably benign |
Het |
Mcu |
A |
G |
10: 59,292,499 (GRCm39) |
L60P |
probably damaging |
Het |
Mrs2 |
G |
T |
13: 25,202,517 (GRCm39) |
Q75K |
probably benign |
Het |
Muc2 |
CGTG |
CGTGTG |
7: 141,699,185 (GRCm38) |
|
probably null |
Het |
Neb |
G |
A |
2: 52,096,890 (GRCm39) |
|
probably benign |
Het |
Nlrp2 |
C |
T |
7: 5,331,328 (GRCm39) |
G356D |
probably benign |
Het |
Notch3 |
A |
G |
17: 32,375,122 (GRCm39) |
|
probably benign |
Het |
Npr2 |
A |
C |
4: 43,641,617 (GRCm39) |
S474R |
probably damaging |
Het |
Nup58 |
A |
G |
14: 60,482,065 (GRCm39) |
F100L |
probably benign |
Het |
Osbpl6 |
A |
C |
2: 76,376,386 (GRCm39) |
D87A |
possibly damaging |
Het |
Pabpc2 |
A |
T |
18: 39,908,360 (GRCm39) |
M542L |
probably benign |
Het |
Papln |
A |
G |
12: 83,829,801 (GRCm39) |
|
probably benign |
Het |
Parpbp |
T |
C |
10: 87,928,758 (GRCm39) |
I561V |
possibly damaging |
Het |
Pcdhb13 |
C |
T |
18: 37,575,634 (GRCm39) |
A4V |
probably benign |
Het |
Pelp1 |
T |
C |
11: 70,286,530 (GRCm39) |
T533A |
possibly damaging |
Het |
Poldip3 |
T |
A |
15: 83,019,497 (GRCm39) |
M182L |
probably benign |
Het |
Por |
T |
C |
5: 135,760,032 (GRCm39) |
S240P |
possibly damaging |
Het |
Pramel15 |
A |
T |
4: 144,103,843 (GRCm39) |
|
probably benign |
Het |
Pramel28 |
T |
C |
4: 143,691,460 (GRCm39) |
E421G |
probably damaging |
Het |
Prss37 |
A |
C |
6: 40,493,283 (GRCm39) |
L61R |
probably damaging |
Het |
Psmd1 |
C |
T |
1: 86,046,338 (GRCm39) |
T702M |
probably benign |
Het |
Pxdn |
G |
T |
12: 30,052,430 (GRCm39) |
G869V |
possibly damaging |
Het |
Rabgap1l |
A |
G |
1: 160,281,315 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
T |
C |
11: 54,510,767 (GRCm39) |
V228A |
probably damaging |
Het |
Rnf169 |
T |
C |
7: 99,575,210 (GRCm39) |
R462G |
possibly damaging |
Het |
Rnft2 |
A |
G |
5: 118,332,745 (GRCm39) |
|
probably benign |
Het |
Sgo2b |
T |
C |
8: 64,379,670 (GRCm39) |
D1054G |
probably benign |
Het |
Sh3bgr |
T |
C |
16: 96,029,717 (GRCm39) |
|
probably benign |
Het |
Slc12a4 |
A |
G |
8: 106,671,982 (GRCm39) |
V910A |
possibly damaging |
Het |
Slc6a12 |
A |
T |
6: 121,332,331 (GRCm39) |
I222F |
probably benign |
Het |
Spty2d1 |
G |
A |
7: 46,647,649 (GRCm39) |
R427* |
probably null |
Het |
Ssc5d |
A |
G |
7: 4,947,662 (GRCm39) |
T1339A |
probably benign |
Het |
Sspo |
A |
C |
6: 48,432,686 (GRCm39) |
E854A |
possibly damaging |
Het |
Stx7 |
A |
G |
10: 24,060,977 (GRCm39) |
|
probably benign |
Het |
Styk1 |
A |
T |
6: 131,278,693 (GRCm39) |
|
probably benign |
Het |
Tmem163 |
T |
G |
1: 127,596,374 (GRCm39) |
|
probably benign |
Het |
Tmppe |
C |
CT |
9: 114,233,707 (GRCm39) |
|
probably null |
Het |
Tmx2 |
A |
G |
2: 84,503,426 (GRCm39) |
V229A |
probably benign |
Het |
Top2b |
T |
C |
14: 16,383,174 (GRCm38) |
L54P |
probably damaging |
Het |
Trim62 |
A |
T |
4: 128,796,343 (GRCm39) |
Y280F |
probably benign |
Het |
Tssk4 |
A |
T |
14: 55,889,016 (GRCm39) |
K181* |
probably null |
Het |
Tssk4 |
A |
T |
14: 55,889,017 (GRCm39) |
K181M |
probably damaging |
Het |
Ubn1 |
A |
G |
16: 4,882,478 (GRCm39) |
D313G |
probably damaging |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Ugt1a10 |
C |
T |
1: 88,145,971 (GRCm39) |
P473L |
probably damaging |
Het |
|
Other mutations in Prss22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02112:Prss22
|
APN |
17 |
24,212,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02247:Prss22
|
APN |
17 |
24,215,363 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02952:Prss22
|
APN |
17 |
24,215,697 (GRCm39) |
missense |
probably damaging |
1.00 |
G1Funyon:Prss22
|
UTSW |
17 |
24,212,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Prss22
|
UTSW |
17 |
24,212,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Prss22
|
UTSW |
17 |
24,215,662 (GRCm39) |
missense |
probably benign |
0.05 |
R1767:Prss22
|
UTSW |
17 |
24,215,331 (GRCm39) |
missense |
probably benign |
0.34 |
R1851:Prss22
|
UTSW |
17 |
24,215,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Prss22
|
UTSW |
17 |
24,215,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R2144:Prss22
|
UTSW |
17 |
24,213,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Prss22
|
UTSW |
17 |
24,215,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R4108:Prss22
|
UTSW |
17 |
24,212,847 (GRCm39) |
missense |
probably benign |
|
R6299:Prss22
|
UTSW |
17 |
24,215,408 (GRCm39) |
missense |
probably damaging |
0.96 |
R7358:Prss22
|
UTSW |
17 |
24,215,419 (GRCm39) |
missense |
probably benign |
0.06 |
R7487:Prss22
|
UTSW |
17 |
24,216,971 (GRCm39) |
missense |
probably damaging |
0.98 |
R7765:Prss22
|
UTSW |
17 |
24,213,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R7857:Prss22
|
UTSW |
17 |
24,212,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8119:Prss22
|
UTSW |
17 |
24,213,701 (GRCm39) |
nonsense |
probably null |
|
R8301:Prss22
|
UTSW |
17 |
24,212,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R8466:Prss22
|
UTSW |
17 |
24,215,802 (GRCm39) |
missense |
probably benign |
0.22 |
R8815:Prss22
|
UTSW |
17 |
24,215,662 (GRCm39) |
missense |
probably benign |
0.05 |
R9183:Prss22
|
UTSW |
17 |
24,213,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R9447:Prss22
|
UTSW |
17 |
24,212,837 (GRCm39) |
missense |
probably benign |
|
R9483:Prss22
|
UTSW |
17 |
24,215,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|