Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110051M20Rik |
A |
G |
2: 91,421,894 (GRCm38) |
Y41H |
probably damaging |
Het |
Actg1 |
T |
C |
11: 120,347,315 (GRCm38) |
Y190C |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,508,669 (GRCm38) |
I2902T |
probably damaging |
Het |
AI429214 |
G |
A |
8: 36,993,833 (GRCm38) |
G45D |
possibly damaging |
Het |
Ambra1 |
A |
G |
2: 91,769,027 (GRCm38) |
D164G |
probably damaging |
Het |
Ap3b1 |
A |
T |
13: 94,408,791 (GRCm38) |
Q184L |
probably benign |
Het |
Arhgef17 |
T |
C |
7: 100,930,820 (GRCm38) |
D307G |
possibly damaging |
Het |
AY761185 |
A |
T |
8: 20,944,555 (GRCm38) |
Y52* |
probably null |
Het |
Bfsp1 |
A |
G |
2: 143,826,719 (GRCm38) |
S647P |
probably benign |
Het |
C130073F10Rik |
A |
G |
4: 101,890,256 (GRCm38) |
V192A |
probably benign |
Het |
Cacna1g |
T |
A |
11: 94,459,207 (GRCm38) |
D604V |
probably benign |
Het |
Ccdc170 |
T |
C |
10: 4,546,854 (GRCm38) |
V458A |
possibly damaging |
Het |
Ccdc187 |
G |
A |
2: 26,289,734 (GRCm38) |
R238W |
probably damaging |
Het |
Cdh1 |
A |
G |
8: 106,658,314 (GRCm38) |
S380G |
probably benign |
Het |
Cdk5rap3 |
T |
C |
11: 96,916,192 (GRCm38) |
H4R |
probably benign |
Het |
Cftr |
G |
A |
6: 18,313,730 (GRCm38) |
|
probably null |
Het |
Dnajc16 |
A |
G |
4: 141,776,992 (GRCm38) |
V219A |
probably benign |
Het |
Drd3 |
A |
T |
16: 43,817,139 (GRCm38) |
I266F |
probably benign |
Het |
Dut |
A |
G |
2: 125,257,124 (GRCm38) |
D177G |
probably benign |
Het |
Esr1 |
A |
G |
10: 4,857,076 (GRCm38) |
I331V |
probably benign |
Het |
Fam129c |
G |
T |
8: 71,603,739 (GRCm38) |
R361L |
probably benign |
Het |
Gm11110 |
A |
G |
17: 57,102,143 (GRCm38) |
|
probably benign |
Het |
Grm7 |
G |
T |
6: 111,358,353 (GRCm38) |
G575V |
possibly damaging |
Het |
Heatr3 |
A |
G |
8: 88,170,884 (GRCm38) |
Y531C |
probably damaging |
Het |
Igfn1 |
A |
G |
1: 135,982,480 (GRCm38) |
V122A |
probably benign |
Het |
Igsf21 |
T |
C |
4: 140,034,743 (GRCm38) |
D208G |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,811,310 (GRCm38) |
Y1915H |
probably damaging |
Het |
Lamc1 |
A |
T |
1: 153,262,492 (GRCm38) |
D205E |
probably damaging |
Het |
Limch1 |
C |
T |
5: 67,021,926 (GRCm38) |
T713I |
probably benign |
Het |
Lrp1b |
A |
G |
2: 41,471,126 (GRCm38) |
I555T |
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,524,141 (GRCm38) |
F448I |
probably damaging |
Het |
March6 |
T |
C |
15: 31,459,233 (GRCm38) |
K896E |
probably benign |
Het |
Mpp6 |
T |
G |
6: 50,180,277 (GRCm38) |
|
probably null |
Het |
Mroh4 |
T |
C |
15: 74,613,249 (GRCm38) |
Y469C |
possibly damaging |
Het |
Nos3 |
T |
C |
5: 24,383,335 (GRCm38) |
V1060A |
possibly damaging |
Het |
Nr1h4 |
A |
G |
10: 89,456,542 (GRCm38) |
I406T |
probably damaging |
Het |
Odf2l |
T |
C |
3: 145,148,618 (GRCm38) |
|
probably null |
Het |
Olfr1162 |
A |
G |
2: 88,050,264 (GRCm38) |
M120T |
probably damaging |
Het |
Olfr1387 |
A |
T |
11: 49,460,260 (GRCm38) |
T194S |
probably damaging |
Het |
Pbx2 |
A |
G |
17: 34,594,107 (GRCm38) |
Y119C |
possibly damaging |
Het |
Pdcd6ip |
C |
A |
9: 113,671,837 (GRCm38) |
A526S |
probably benign |
Het |
Prx |
G |
A |
7: 27,519,634 (GRCm38) |
D1187N |
possibly damaging |
Het |
Ptpro |
G |
A |
6: 137,380,200 (GRCm38) |
V230I |
probably benign |
Het |
Rtn3 |
C |
T |
19: 7,457,249 (GRCm38) |
M440I |
probably benign |
Het |
Sar1b |
T |
C |
11: 51,788,192 (GRCm38) |
I96T |
probably damaging |
Het |
Sds |
T |
C |
5: 120,480,900 (GRCm38) |
|
probably null |
Het |
Secisbp2 |
A |
G |
13: 51,679,941 (GRCm38) |
T706A |
probably benign |
Het |
Sorcs3 |
A |
T |
19: 48,693,824 (GRCm38) |
M433L |
possibly damaging |
Het |
Sppl2a |
A |
G |
2: 126,904,992 (GRCm38) |
V472A |
probably damaging |
Het |
Tbc1d9 |
A |
G |
8: 83,271,588 (GRCm38) |
E1258G |
possibly damaging |
Het |
Tbxas1 |
C |
A |
6: 38,952,074 (GRCm38) |
|
probably benign |
Het |
Tg |
T |
C |
15: 66,696,246 (GRCm38) |
I1333T |
probably damaging |
Het |
Tmem108 |
C |
T |
9: 103,499,716 (GRCm38) |
G178D |
probably damaging |
Het |
Tmem174 |
A |
G |
13: 98,637,061 (GRCm38) |
L87P |
probably damaging |
Het |
Tmppe |
T |
A |
9: 114,404,701 (GRCm38) |
S23T |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,761,103 (GRCm38) |
T21074I |
probably benign |
Het |
Tub |
A |
G |
7: 109,029,298 (GRCm38) |
M338V |
probably null |
Het |
Vmn1r160 |
A |
T |
7: 22,872,106 (GRCm38) |
R295* |
probably null |
Het |
Vps52 |
T |
C |
17: 33,963,206 (GRCm38) |
V518A |
probably benign |
Het |
Wdr59 |
A |
G |
8: 111,451,043 (GRCm38) |
V909A |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,948,781 (GRCm38) |
T1241A |
probably benign |
Het |
Znfx1 |
A |
T |
2: 167,038,940 (GRCm38) |
I308N |
possibly damaging |
Het |
|
Other mutations in Zfp882 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00676:Zfp882
|
APN |
8 |
71,913,827 (GRCm38) |
missense |
probably benign |
|
R0244:Zfp882
|
UTSW |
8 |
71,913,523 (GRCm38) |
missense |
possibly damaging |
0.79 |
R0270:Zfp882
|
UTSW |
8 |
71,914,615 (GRCm38) |
missense |
probably benign |
0.05 |
R0636:Zfp882
|
UTSW |
8 |
71,914,337 (GRCm38) |
missense |
probably benign |
0.01 |
R0840:Zfp882
|
UTSW |
8 |
71,914,686 (GRCm38) |
nonsense |
probably null |
|
R1299:Zfp882
|
UTSW |
8 |
71,913,473 (GRCm38) |
missense |
probably damaging |
1.00 |
R4439:Zfp882
|
UTSW |
8 |
71,913,609 (GRCm38) |
missense |
probably damaging |
0.97 |
R4829:Zfp882
|
UTSW |
8 |
71,914,389 (GRCm38) |
missense |
probably damaging |
1.00 |
R5028:Zfp882
|
UTSW |
8 |
71,914,654 (GRCm38) |
missense |
possibly damaging |
0.70 |
R5296:Zfp882
|
UTSW |
8 |
71,914,360 (GRCm38) |
missense |
probably damaging |
1.00 |
R5882:Zfp882
|
UTSW |
8 |
71,913,459 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5974:Zfp882
|
UTSW |
8 |
71,913,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R6052:Zfp882
|
UTSW |
8 |
71,914,505 (GRCm38) |
missense |
probably benign |
0.01 |
R6383:Zfp882
|
UTSW |
8 |
71,914,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R6987:Zfp882
|
UTSW |
8 |
71,914,673 (GRCm38) |
missense |
probably benign |
0.01 |
R7045:Zfp882
|
UTSW |
8 |
71,913,249 (GRCm38) |
critical splice donor site |
probably null |
|
R7780:Zfp882
|
UTSW |
8 |
71,914,229 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7793:Zfp882
|
UTSW |
8 |
71,913,141 (GRCm38) |
missense |
probably damaging |
1.00 |
R8386:Zfp882
|
UTSW |
8 |
71,914,118 (GRCm38) |
missense |
probably benign |
0.00 |
R9452:Zfp882
|
UTSW |
8 |
71,914,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R9694:Zfp882
|
UTSW |
8 |
71,914,071 (GRCm38) |
missense |
probably benign |
0.01 |
|