Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933434E20Rik |
A |
G |
3: 89,971,766 (GRCm39) |
T42A |
probably benign |
Het |
Actr3b |
T |
A |
5: 26,036,730 (GRCm39) |
I181K |
probably damaging |
Het |
Avl9 |
G |
T |
6: 56,713,468 (GRCm39) |
R242L |
probably benign |
Het |
B3galt4 |
T |
C |
17: 34,169,992 (GRCm39) |
E82G |
probably benign |
Het |
Bag1 |
G |
A |
4: 40,936,609 (GRCm39) |
T349I |
probably benign |
Het |
Brip1 |
A |
T |
11: 86,048,427 (GRCm39) |
L305Q |
probably damaging |
Het |
Cdipt |
A |
G |
7: 126,577,436 (GRCm39) |
T61A |
probably damaging |
Het |
Cmya5 |
T |
A |
13: 93,230,164 (GRCm39) |
R1641S |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,536,295 (GRCm39) |
D515G |
probably benign |
Het |
Cpsf4 |
T |
A |
5: 145,114,054 (GRCm39) |
L171Q |
probably damaging |
Het |
Cuzd1 |
A |
T |
7: 130,918,009 (GRCm39) |
|
probably null |
Het |
Dapk1 |
T |
A |
13: 60,873,101 (GRCm39) |
|
probably null |
Het |
Diaph1 |
A |
G |
18: 37,986,643 (GRCm39) |
V1114A |
possibly damaging |
Het |
Emx2 |
A |
T |
19: 59,452,348 (GRCm39) |
K211* |
probably null |
Het |
Fam170a |
T |
A |
18: 50,413,699 (GRCm39) |
C55S |
possibly damaging |
Het |
Fbxw26 |
A |
G |
9: 109,572,788 (GRCm39) |
S119P |
probably benign |
Het |
Fhip2a |
G |
A |
19: 57,369,839 (GRCm39) |
D461N |
probably benign |
Het |
Fryl |
G |
A |
5: 73,254,760 (GRCm39) |
T894M |
possibly damaging |
Het |
Gad1-ps |
C |
A |
10: 99,281,383 (GRCm39) |
|
noncoding transcript |
Het |
Gss |
T |
C |
2: 155,409,665 (GRCm39) |
E257G |
probably benign |
Het |
Klhdc1 |
A |
C |
12: 69,330,082 (GRCm39) |
S404R |
probably benign |
Het |
Kmt2e |
T |
A |
5: 23,702,532 (GRCm39) |
|
probably null |
Het |
Krt20 |
G |
A |
11: 99,328,602 (GRCm39) |
Q108* |
probably null |
Het |
Lmnb1 |
T |
A |
18: 56,876,331 (GRCm39) |
S480T |
probably benign |
Het |
Lyst |
T |
A |
13: 13,812,633 (GRCm39) |
M1015K |
probably benign |
Het |
Mdm1 |
T |
G |
10: 117,987,961 (GRCm39) |
S290A |
probably benign |
Het |
Mkln1 |
T |
A |
6: 31,426,439 (GRCm39) |
F238I |
probably damaging |
Het |
Mrgprb3 |
A |
G |
7: 48,292,984 (GRCm39) |
V189A |
probably benign |
Het |
Myrf |
G |
C |
19: 10,195,526 (GRCm39) |
T428S |
probably benign |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Neurod6 |
C |
T |
6: 55,656,614 (GRCm39) |
E8K |
probably benign |
Het |
Nlrp12 |
T |
C |
7: 3,282,659 (GRCm39) |
I747V |
probably benign |
Het |
Notch4 |
C |
T |
17: 34,784,337 (GRCm39) |
R43W |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,886,238 (GRCm39) |
|
probably benign |
Het |
Or10d3 |
A |
T |
9: 39,461,747 (GRCm39) |
I140N |
probably damaging |
Het |
Or5p57 |
A |
T |
7: 107,665,932 (GRCm39) |
Y24* |
probably null |
Het |
Or5w20 |
T |
C |
2: 87,727,199 (GRCm39) |
Y219H |
possibly damaging |
Het |
Or6ae1 |
A |
T |
7: 139,742,384 (GRCm39) |
S160T |
probably damaging |
Het |
Or6z5 |
T |
C |
7: 6,478,024 (GRCm39) |
V305A |
probably benign |
Het |
Or8b53 |
G |
T |
9: 38,667,114 (GRCm39) |
L43F |
probably damaging |
Het |
Orc5 |
C |
T |
5: 22,751,455 (GRCm39) |
V85I |
probably benign |
Het |
Pccb |
T |
C |
9: 100,864,850 (GRCm39) |
D468G |
probably damaging |
Het |
Pdzd2 |
A |
T |
15: 12,375,110 (GRCm39) |
V1675E |
probably benign |
Het |
Pkd1l3 |
C |
G |
8: 110,350,281 (GRCm39) |
D375E |
possibly damaging |
Het |
Pltp |
A |
T |
2: 164,696,320 (GRCm39) |
N97K |
probably damaging |
Het |
Polr1a |
T |
C |
6: 71,927,648 (GRCm39) |
|
probably null |
Het |
Prss42 |
G |
A |
9: 110,628,341 (GRCm39) |
V162I |
possibly damaging |
Het |
Rbfox2 |
A |
T |
15: 76,983,455 (GRCm39) |
Y269N |
probably damaging |
Het |
Rftn2 |
A |
T |
1: 55,253,354 (GRCm39) |
I83K |
probably damaging |
Het |
S1pr4 |
A |
T |
10: 81,334,823 (GRCm39) |
I217N |
probably damaging |
Het |
Slc23a2 |
T |
C |
2: 131,920,353 (GRCm39) |
K184R |
probably benign |
Het |
Slc6a19 |
T |
C |
13: 73,839,814 (GRCm39) |
N156S |
probably benign |
Het |
Svep1 |
C |
T |
4: 58,088,280 (GRCm39) |
G1723D |
probably damaging |
Het |
Tbc1d32 |
T |
A |
10: 56,068,994 (GRCm39) |
H358L |
possibly damaging |
Het |
Tex55 |
G |
A |
16: 38,649,064 (GRCm39) |
T15I |
probably benign |
Het |
Tigit |
G |
T |
16: 43,482,634 (GRCm39) |
N33K |
probably damaging |
Het |
Tmem25 |
T |
C |
9: 44,707,878 (GRCm39) |
Y139C |
probably damaging |
Het |
Trmt13 |
G |
A |
3: 116,376,275 (GRCm39) |
T372M |
probably damaging |
Het |
Ubr2 |
A |
T |
17: 47,294,224 (GRCm39) |
M303K |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,417,207 (GRCm39) |
E2952G |
probably damaging |
Het |
Zan |
T |
A |
5: 137,389,920 (GRCm39) |
I4851F |
unknown |
Het |
Zfand4 |
C |
T |
6: 116,265,015 (GRCm39) |
T160I |
probably benign |
Het |
Zfp1005 |
A |
G |
2: 150,109,993 (GRCm39) |
T228A |
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 |
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 |
R6888:Cstpp1
|
UTSW |
2 |
91,252,239 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|