Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actg1 |
T |
C |
11: 120,238,141 (GRCm39) |
Y190C |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,656,788 (GRCm39) |
I2902T |
probably damaging |
Het |
AI429214 |
G |
A |
8: 37,460,987 (GRCm39) |
G45D |
possibly damaging |
Het |
Ambra1 |
A |
G |
2: 91,599,372 (GRCm39) |
D164G |
probably damaging |
Het |
Ap3b1 |
A |
T |
13: 94,545,299 (GRCm39) |
Q184L |
probably benign |
Het |
Arhgef17 |
T |
C |
7: 100,580,027 (GRCm39) |
D307G |
possibly damaging |
Het |
AY761185 |
A |
T |
8: 21,434,571 (GRCm39) |
Y52* |
probably null |
Het |
Bfsp1 |
A |
G |
2: 143,668,639 (GRCm39) |
S647P |
probably benign |
Het |
C130073F10Rik |
A |
G |
4: 101,747,453 (GRCm39) |
V192A |
probably benign |
Het |
Cacna1g |
T |
A |
11: 94,350,033 (GRCm39) |
D604V |
probably benign |
Het |
Ccdc170 |
T |
C |
10: 4,496,854 (GRCm39) |
V458A |
possibly damaging |
Het |
Ccdc187 |
G |
A |
2: 26,179,746 (GRCm39) |
R238W |
probably damaging |
Het |
Cdh1 |
A |
G |
8: 107,384,946 (GRCm39) |
S380G |
probably benign |
Het |
Cdk5rap3 |
T |
C |
11: 96,807,018 (GRCm39) |
H4R |
probably benign |
Het |
Cftr |
G |
A |
6: 18,313,729 (GRCm39) |
|
probably null |
Het |
Dnajc16 |
A |
G |
4: 141,504,303 (GRCm39) |
V219A |
probably benign |
Het |
Drd3 |
A |
T |
16: 43,637,502 (GRCm39) |
I266F |
probably benign |
Het |
Dut |
A |
G |
2: 125,099,044 (GRCm39) |
D177G |
probably benign |
Het |
Esr1 |
A |
G |
10: 4,807,076 (GRCm39) |
I331V |
probably benign |
Het |
Gm11110 |
A |
G |
17: 57,409,143 (GRCm39) |
|
probably benign |
Het |
Grm7 |
G |
T |
6: 111,335,314 (GRCm39) |
G575V |
possibly damaging |
Het |
Heatr3 |
A |
G |
8: 88,897,512 (GRCm39) |
Y531C |
probably damaging |
Het |
Igfn1 |
A |
G |
1: 135,910,218 (GRCm39) |
V122A |
probably benign |
Het |
Igsf21 |
T |
C |
4: 139,762,054 (GRCm39) |
D208G |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,949,373 (GRCm39) |
Y1915H |
probably damaging |
Het |
Lamc1 |
A |
T |
1: 153,138,238 (GRCm39) |
D205E |
probably damaging |
Het |
Limch1 |
C |
T |
5: 67,179,269 (GRCm39) |
T713I |
probably benign |
Het |
Lrp1b |
A |
G |
2: 41,361,138 (GRCm39) |
I555T |
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,354,485 (GRCm39) |
F448I |
probably damaging |
Het |
Marchf6 |
T |
C |
15: 31,459,379 (GRCm39) |
K896E |
probably benign |
Het |
Mroh4 |
T |
C |
15: 74,485,098 (GRCm39) |
Y469C |
possibly damaging |
Het |
Niban3 |
G |
T |
8: 72,056,383 (GRCm39) |
R361L |
probably benign |
Het |
Nos3 |
T |
C |
5: 24,588,333 (GRCm39) |
V1060A |
possibly damaging |
Het |
Nr1h4 |
A |
G |
10: 89,292,404 (GRCm39) |
I406T |
probably damaging |
Het |
Odf2l |
T |
C |
3: 144,854,379 (GRCm39) |
|
probably null |
Het |
Or2y15 |
A |
T |
11: 49,351,087 (GRCm39) |
T194S |
probably damaging |
Het |
Or5d14 |
A |
G |
2: 87,880,608 (GRCm39) |
M120T |
probably damaging |
Het |
Pals2 |
T |
G |
6: 50,157,257 (GRCm39) |
|
probably null |
Het |
Pbx2 |
A |
G |
17: 34,813,081 (GRCm39) |
Y119C |
possibly damaging |
Het |
Pdcd6ip |
C |
A |
9: 113,500,905 (GRCm39) |
A526S |
probably benign |
Het |
Prx |
G |
A |
7: 27,219,059 (GRCm39) |
D1187N |
possibly damaging |
Het |
Ptpro |
G |
A |
6: 137,357,198 (GRCm39) |
V230I |
probably benign |
Het |
Rtn3 |
C |
T |
19: 7,434,614 (GRCm39) |
M440I |
probably benign |
Het |
Sar1b |
T |
C |
11: 51,679,019 (GRCm39) |
I96T |
probably damaging |
Het |
Sds |
T |
C |
5: 120,618,965 (GRCm39) |
|
probably null |
Het |
Secisbp2 |
A |
G |
13: 51,833,977 (GRCm39) |
T706A |
probably benign |
Het |
Sorcs3 |
A |
T |
19: 48,682,263 (GRCm39) |
M433L |
possibly damaging |
Het |
Sppl2a |
A |
G |
2: 126,746,912 (GRCm39) |
V472A |
probably damaging |
Het |
Tbc1d9 |
A |
G |
8: 83,998,217 (GRCm39) |
E1258G |
possibly damaging |
Het |
Tbxas1 |
C |
A |
6: 38,929,008 (GRCm39) |
|
probably benign |
Het |
Tg |
T |
C |
15: 66,568,095 (GRCm39) |
I1333T |
probably damaging |
Het |
Tmem108 |
C |
T |
9: 103,376,915 (GRCm39) |
G178D |
probably damaging |
Het |
Tmem174 |
A |
G |
13: 98,773,569 (GRCm39) |
L87P |
probably damaging |
Het |
Tmppe |
T |
A |
9: 114,233,769 (GRCm39) |
S23T |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,591,447 (GRCm39) |
T21074I |
probably benign |
Het |
Tub |
A |
G |
7: 108,628,505 (GRCm39) |
M338V |
probably null |
Het |
Vmn1r160 |
A |
T |
7: 22,571,531 (GRCm39) |
R295* |
probably null |
Het |
Vps52 |
T |
C |
17: 34,182,180 (GRCm39) |
V518A |
probably benign |
Het |
Wdr59 |
A |
G |
8: 112,177,675 (GRCm39) |
V909A |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,925,742 (GRCm39) |
T1241A |
probably benign |
Het |
Zfp882 |
G |
A |
8: 72,668,130 (GRCm39) |
C319Y |
probably benign |
Het |
Znfx1 |
A |
T |
2: 166,880,860 (GRCm39) |
I308N |
possibly damaging |
Het |
|
Other mutations in Cstpp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02737:Cstpp1
|
APN |
2 |
91,135,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R6768_1110051M20Rik_026
|
UTSW |
2 |
91,252,303 (GRCm39) |
missense |
probably damaging |
0.97 |
BB004:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
BB014:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Cstpp1
|
UTSW |
2 |
91,112,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Cstpp1
|
UTSW |
2 |
91,252,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R0446:Cstpp1
|
UTSW |
2 |
91,135,109 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0846:Cstpp1
|
UTSW |
2 |
91,214,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R6768:Cstpp1
|
UTSW |
2 |
91,252,303 (GRCm39) |
missense |
probably damaging |
0.97 |
R7751:Cstpp1
|
UTSW |
2 |
91,214,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R7754:Cstpp1
|
UTSW |
2 |
91,135,188 (GRCm39) |
splice site |
probably null |
|
R7808:Cstpp1
|
UTSW |
2 |
91,274,939 (GRCm39) |
start gained |
probably benign |
|
R7927:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Cstpp1
|
UTSW |
2 |
91,107,343 (GRCm39) |
missense |
probably benign |
0.39 |
R9610:Cstpp1
|
UTSW |
2 |
91,135,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Cstpp1
|
UTSW |
2 |
91,135,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9709:Cstpp1
|
UTSW |
2 |
91,112,099 (GRCm39) |
missense |
probably benign |
0.00 |
|