Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
A |
G |
9: 44,192,395 (GRCm39) |
F224L |
probably benign |
Het |
Adam39 |
A |
G |
8: 41,278,707 (GRCm39) |
D366G |
probably damaging |
Het |
Adamts14 |
T |
A |
10: 61,038,795 (GRCm39) |
E902V |
probably damaging |
Het |
Adamts6 |
T |
C |
13: 104,512,247 (GRCm39) |
C490R |
probably damaging |
Het |
Btbd3 |
T |
C |
2: 138,126,055 (GRCm39) |
V413A |
possibly damaging |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cdadc1 |
G |
T |
14: 59,813,197 (GRCm39) |
N403K |
probably damaging |
Het |
Cdc27 |
C |
T |
11: 104,399,211 (GRCm39) |
V734I |
possibly damaging |
Het |
Celf3 |
A |
G |
3: 94,392,667 (GRCm39) |
D122G |
probably benign |
Het |
Chgb |
T |
C |
2: 132,634,498 (GRCm39) |
S147P |
probably benign |
Het |
Col9a1 |
G |
A |
1: 24,278,396 (GRCm39) |
G808D |
probably damaging |
Het |
Cpne7 |
A |
G |
8: 123,861,177 (GRCm39) |
|
probably null |
Het |
Crhr1 |
T |
C |
11: 104,064,480 (GRCm39) |
F330S |
possibly damaging |
Het |
Csmd1 |
A |
C |
8: 15,971,056 (GRCm39) |
N3086K |
probably benign |
Het |
Ctnnb1 |
A |
G |
9: 120,786,650 (GRCm39) |
D624G |
probably damaging |
Het |
Dcaf8 |
G |
A |
1: 172,022,124 (GRCm39) |
R554H |
probably benign |
Het |
Dmbt1 |
T |
C |
7: 130,639,611 (GRCm39) |
Y50H |
possibly damaging |
Het |
Dmxl1 |
T |
C |
18: 50,055,679 (GRCm39) |
L2573P |
probably benign |
Het |
Ebf2 |
G |
A |
14: 67,661,548 (GRCm39) |
G559S |
probably benign |
Het |
Fancd2 |
A |
G |
6: 113,562,507 (GRCm39) |
|
probably benign |
Het |
Fkbp10 |
A |
T |
11: 100,313,936 (GRCm39) |
I427F |
probably benign |
Het |
Gipc1 |
T |
C |
8: 84,389,046 (GRCm39) |
|
probably null |
Het |
Gm1110 |
A |
T |
9: 26,807,095 (GRCm39) |
|
probably benign |
Het |
Gsdmc3 |
A |
G |
15: 63,731,455 (GRCm39) |
L359P |
probably damaging |
Het |
Hspg2 |
A |
G |
4: 137,291,341 (GRCm39) |
D3897G |
probably benign |
Het |
Ift122 |
T |
A |
6: 115,902,769 (GRCm39) |
M1117K |
possibly damaging |
Het |
Itgbl1 |
A |
T |
14: 124,209,617 (GRCm39) |
D456V |
probably damaging |
Het |
Itprid2 |
T |
A |
2: 79,491,257 (GRCm39) |
L1014Q |
probably damaging |
Het |
Kctd1 |
G |
T |
18: 15,119,491 (GRCm39) |
L675I |
|
Het |
Kyat3 |
C |
T |
3: 142,443,596 (GRCm39) |
T403M |
probably benign |
Het |
Ltbp2 |
T |
C |
12: 84,834,164 (GRCm39) |
T1442A |
probably benign |
Het |
Mier2 |
A |
C |
10: 79,376,790 (GRCm39) |
S45R |
unknown |
Het |
Mon2 |
T |
A |
10: 122,871,469 (GRCm39) |
K383* |
probably null |
Het |
Mroh4 |
G |
T |
15: 74,499,473 (GRCm39) |
T136K |
probably benign |
Het |
Mtif3 |
A |
T |
5: 146,895,846 (GRCm39) |
S80R |
probably benign |
Het |
Myh2 |
A |
C |
11: 67,068,188 (GRCm39) |
E272A |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,080,323 (GRCm39) |
Q1179R |
probably damaging |
Het |
Nfatc3 |
G |
A |
8: 106,835,402 (GRCm39) |
C916Y |
probably benign |
Het |
Or13a17 |
A |
T |
7: 140,271,642 (GRCm39) |
T275S |
probably benign |
Het |
Or2w2 |
T |
A |
13: 21,758,279 (GRCm39) |
T116S |
probably benign |
Het |
Or7g21 |
T |
A |
9: 19,032,582 (GRCm39) |
C107* |
probably null |
Het |
Orc2 |
T |
C |
1: 58,511,499 (GRCm39) |
D370G |
possibly damaging |
Het |
Pate7 |
A |
T |
9: 35,688,069 (GRCm39) |
|
probably benign |
Het |
Pcdhga6 |
T |
A |
18: 37,840,716 (GRCm39) |
N145K |
probably benign |
Het |
Pih1d2 |
A |
G |
9: 50,536,232 (GRCm39) |
M296V |
probably benign |
Het |
Prickle4 |
A |
T |
17: 47,999,772 (GRCm39) |
|
probably benign |
Het |
Rabl6 |
G |
A |
2: 25,477,541 (GRCm39) |
P303L |
probably damaging |
Het |
Rara |
T |
G |
11: 98,862,595 (GRCm39) |
I332S |
probably damaging |
Het |
Reln |
A |
G |
5: 22,090,512 (GRCm39) |
F3449L |
possibly damaging |
Het |
Rhoq |
T |
C |
17: 87,271,767 (GRCm39) |
L61P |
|
Het |
Rigi |
A |
G |
4: 40,239,650 (GRCm39) |
I16T |
probably damaging |
Het |
Slc6a15 |
G |
A |
10: 103,230,953 (GRCm39) |
W226* |
probably null |
Het |
Spef2 |
A |
T |
15: 9,725,263 (GRCm39) |
S165T |
possibly damaging |
Het |
Stab2 |
T |
C |
10: 86,785,782 (GRCm39) |
N620S |
possibly damaging |
Het |
Suds3 |
A |
G |
5: 117,232,973 (GRCm39) |
|
probably null |
Het |
Sult1b1 |
A |
G |
5: 87,682,900 (GRCm39) |
I15T |
possibly damaging |
Het |
Synm |
C |
A |
7: 67,384,672 (GRCm39) |
V997L |
probably damaging |
Het |
Tgfbi |
C |
A |
13: 56,778,391 (GRCm39) |
D387E |
probably benign |
Het |
Thrb |
T |
C |
14: 17,981,886 (GRCm38) |
C4R |
possibly damaging |
Het |
Tk2 |
A |
G |
8: 104,957,809 (GRCm39) |
V179A |
possibly damaging |
Het |
Trim25 |
T |
C |
11: 88,907,027 (GRCm39) |
V462A |
probably benign |
Het |
Tub |
T |
C |
7: 108,629,393 (GRCm39) |
Y483H |
probably damaging |
Het |
Vav1 |
A |
G |
17: 57,603,710 (GRCm39) |
T131A |
probably benign |
Het |
Vav1 |
A |
G |
17: 57,631,650 (GRCm39) |
T781A |
probably benign |
Het |
Zfp568 |
T |
A |
7: 29,716,683 (GRCm39) |
H194Q |
probably benign |
Het |
Zfp683 |
A |
T |
4: 133,781,239 (GRCm39) |
Q18L |
probably benign |
Het |
|
Other mutations in Zbtb34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02721:Zbtb34
|
APN |
2 |
33,301,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R0398:Zbtb34
|
UTSW |
2 |
33,301,060 (GRCm39) |
nonsense |
probably null |
|
R1767:Zbtb34
|
UTSW |
2 |
33,301,348 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4973:Zbtb34
|
UTSW |
2 |
33,301,626 (GRCm39) |
missense |
probably benign |
0.28 |
R5150:Zbtb34
|
UTSW |
2 |
33,301,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Zbtb34
|
UTSW |
2 |
33,301,842 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6489:Zbtb34
|
UTSW |
2 |
33,301,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Zbtb34
|
UTSW |
2 |
33,302,145 (GRCm39) |
missense |
probably damaging |
0.97 |
R7973:Zbtb34
|
UTSW |
2 |
33,301,531 (GRCm39) |
missense |
probably benign |
|
R8142:Zbtb34
|
UTSW |
2 |
33,302,493 (GRCm39) |
nonsense |
probably null |
|
R8909:Zbtb34
|
UTSW |
2 |
33,301,701 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9038:Zbtb34
|
UTSW |
2 |
33,301,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R9337:Zbtb34
|
UTSW |
2 |
33,301,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R9727:Zbtb34
|
UTSW |
2 |
33,301,533 (GRCm39) |
missense |
probably benign |
|
Z1088:Zbtb34
|
UTSW |
2 |
33,301,120 (GRCm39) |
missense |
probably damaging |
1.00 |
|