Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr2 |
A |
G |
9: 121,738,588 (GRCm39) |
Y321C |
probably benign |
Het |
Angptl3 |
T |
C |
4: 98,919,728 (GRCm39) |
S163P |
probably damaging |
Het |
Ankle2 |
T |
C |
5: 110,382,234 (GRCm39) |
M70T |
probably benign |
Het |
Ankrd1 |
T |
A |
19: 36,095,273 (GRCm39) |
K138N |
probably damaging |
Het |
Ano8 |
A |
T |
8: 71,935,281 (GRCm39) |
I339N |
probably damaging |
Het |
Bltp3a |
A |
G |
17: 28,103,061 (GRCm39) |
Y365C |
probably damaging |
Het |
Cxcl2 |
A |
T |
5: 91,051,881 (GRCm39) |
|
probably null |
Het |
Exosc3 |
T |
C |
4: 45,320,619 (GRCm39) |
|
probably benign |
Het |
Fads2b |
C |
A |
2: 85,348,853 (GRCm39) |
K86N |
probably damaging |
Het |
Fat1 |
G |
A |
8: 45,489,824 (GRCm39) |
A3579T |
probably benign |
Het |
Fat4 |
G |
A |
3: 38,996,958 (GRCm39) |
V1726I |
possibly damaging |
Het |
Grm7 |
A |
G |
6: 111,230,981 (GRCm39) |
N468S |
probably damaging |
Het |
Hmgcll1 |
A |
T |
9: 75,982,198 (GRCm39) |
|
probably benign |
Het |
Igkv3-12 |
T |
A |
6: 70,495,542 (GRCm39) |
V23E |
probably benign |
Het |
Irx6 |
T |
C |
8: 93,402,919 (GRCm39) |
C95R |
possibly damaging |
Het |
Kif16b |
G |
A |
2: 142,549,324 (GRCm39) |
H1064Y |
probably benign |
Het |
Lrrc45 |
A |
T |
11: 120,609,272 (GRCm39) |
D377V |
possibly damaging |
Het |
Oasl1 |
A |
G |
5: 115,075,073 (GRCm39) |
K378E |
possibly damaging |
Het |
Pds5a |
T |
C |
5: 65,821,839 (GRCm39) |
T120A |
possibly damaging |
Het |
Phf8-ps |
G |
A |
17: 33,285,023 (GRCm39) |
T593I |
probably benign |
Het |
Plec |
T |
C |
15: 76,063,851 (GRCm39) |
E2141G |
possibly damaging |
Het |
Pou6f1 |
A |
G |
15: 100,478,724 (GRCm39) |
S395P |
probably damaging |
Het |
Prss12 |
A |
T |
3: 123,279,176 (GRCm39) |
K418* |
probably null |
Het |
Rtn3 |
G |
A |
19: 7,460,444 (GRCm39) |
A2V |
probably benign |
Het |
Rubcnl |
A |
G |
14: 75,281,898 (GRCm39) |
T452A |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 142,100,154 (GRCm39) |
I1395V |
probably benign |
Het |
Senp7 |
C |
A |
16: 55,973,832 (GRCm39) |
P351Q |
possibly damaging |
Het |
Slco1a7 |
T |
C |
6: 141,654,322 (GRCm39) |
K647E |
probably benign |
Het |
Spred3 |
A |
G |
7: 28,861,210 (GRCm39) |
L323P |
probably damaging |
Het |
Srprb |
A |
G |
9: 103,078,529 (GRCm39) |
F67S |
possibly damaging |
Het |
Tk2 |
T |
C |
8: 104,965,465 (GRCm39) |
S101G |
probably benign |
Het |
Tnxb |
A |
G |
17: 34,930,491 (GRCm39) |
T2059A |
probably damaging |
Het |
Trpm7 |
A |
G |
2: 126,658,751 (GRCm39) |
L1135P |
probably damaging |
Het |
Ush2a |
G |
A |
1: 188,460,907 (GRCm39) |
V2723M |
probably damaging |
Het |
Usp38 |
C |
T |
8: 81,719,967 (GRCm39) |
A421T |
probably damaging |
Het |
Vcan |
G |
T |
13: 89,833,277 (GRCm39) |
N3058K |
probably damaging |
Het |
Vmn1r221 |
G |
A |
13: 23,402,176 (GRCm39) |
|
noncoding transcript |
Het |
Vps11 |
C |
G |
9: 44,267,017 (GRCm39) |
G406A |
probably damaging |
Het |
Wnk2 |
C |
T |
13: 49,244,313 (GRCm39) |
D508N |
probably damaging |
Het |
|
Other mutations in Zbtb10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02174:Zbtb10
|
APN |
3 |
9,316,872 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02207:Zbtb10
|
APN |
3 |
9,345,525 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02499:Zbtb10
|
APN |
3 |
9,316,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02506:Zbtb10
|
APN |
3 |
9,330,297 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03294:Zbtb10
|
APN |
3 |
9,346,047 (GRCm39) |
missense |
probably benign |
0.18 |
R0510:Zbtb10
|
UTSW |
3 |
9,329,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Zbtb10
|
UTSW |
3 |
9,345,446 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2342:Zbtb10
|
UTSW |
3 |
9,330,255 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3407:Zbtb10
|
UTSW |
3 |
9,329,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R4301:Zbtb10
|
UTSW |
3 |
9,330,220 (GRCm39) |
missense |
probably damaging |
0.96 |
R4698:Zbtb10
|
UTSW |
3 |
9,329,610 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5184:Zbtb10
|
UTSW |
3 |
9,329,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R5443:Zbtb10
|
UTSW |
3 |
9,345,108 (GRCm39) |
missense |
probably benign |
|
R5665:Zbtb10
|
UTSW |
3 |
9,330,252 (GRCm39) |
missense |
probably damaging |
0.99 |
R5744:Zbtb10
|
UTSW |
3 |
9,329,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R5862:Zbtb10
|
UTSW |
3 |
9,330,276 (GRCm39) |
missense |
probably damaging |
0.98 |
R5909:Zbtb10
|
UTSW |
3 |
9,345,109 (GRCm39) |
missense |
probably benign |
0.14 |
R6547:Zbtb10
|
UTSW |
3 |
9,316,763 (GRCm39) |
missense |
probably benign |
0.38 |
R6612:Zbtb10
|
UTSW |
3 |
9,317,125 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7457:Zbtb10
|
UTSW |
3 |
9,316,538 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8985:Zbtb10
|
UTSW |
3 |
9,345,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R9191:Zbtb10
|
UTSW |
3 |
9,330,295 (GRCm39) |
missense |
probably damaging |
0.98 |
R9472:Zbtb10
|
UTSW |
3 |
9,343,355 (GRCm39) |
missense |
probably benign |
0.25 |
R9616:Zbtb10
|
UTSW |
3 |
9,316,473 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Zbtb10
|
UTSW |
3 |
9,343,391 (GRCm39) |
missense |
probably benign |
|
|