Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb1 |
A |
C |
6: 88,815,261 (GRCm39) |
F290V |
probably damaging |
Het |
Adam26b |
G |
A |
8: 43,973,601 (GRCm39) |
S467L |
probably damaging |
Het |
Adgrv1 |
T |
A |
13: 81,647,244 (GRCm39) |
I3099F |
probably damaging |
Het |
Akap6 |
A |
G |
12: 53,188,997 (GRCm39) |
D2137G |
possibly damaging |
Het |
Arhgdig |
T |
C |
17: 26,419,275 (GRCm39) |
Y48C |
probably damaging |
Het |
Astn1 |
A |
G |
1: 158,337,460 (GRCm39) |
I389V |
possibly damaging |
Het |
Atp8a1 |
T |
C |
5: 67,817,226 (GRCm39) |
D920G |
probably benign |
Het |
BC016579 |
T |
A |
16: 45,449,818 (GRCm39) |
N200I |
probably damaging |
Het |
Casc3 |
T |
C |
11: 98,722,144 (GRCm39) |
Y661H |
probably damaging |
Het |
Cep120 |
A |
C |
18: 53,854,809 (GRCm39) |
V442G |
probably benign |
Het |
Cfap65 |
A |
G |
1: 74,943,841 (GRCm39) |
Y1557H |
probably damaging |
Het |
Chd2 |
G |
T |
7: 73,097,022 (GRCm39) |
Q1485K |
possibly damaging |
Het |
Cntrl |
T |
C |
2: 35,061,078 (GRCm39) |
F1967L |
probably benign |
Het |
Csmd1 |
G |
A |
8: 17,077,300 (GRCm39) |
T119M |
possibly damaging |
Het |
Dnah9 |
T |
C |
11: 66,046,356 (GRCm39) |
H64R |
probably benign |
Het |
Ep400 |
T |
C |
5: 110,813,703 (GRCm39) |
R2899G |
probably damaging |
Het |
Foxl2 |
A |
C |
9: 98,838,086 (GRCm39) |
T125P |
probably damaging |
Het |
Foxred1 |
A |
T |
9: 35,118,769 (GRCm39) |
|
probably null |
Het |
H2-Eb1 |
T |
A |
17: 34,533,133 (GRCm39) |
|
probably benign |
Het |
Heatr3 |
T |
C |
8: 88,884,869 (GRCm39) |
S378P |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,445,096 (GRCm39) |
|
probably benign |
Het |
Hps3 |
T |
G |
3: 20,057,443 (GRCm39) |
R780S |
probably damaging |
Het |
Ifi44 |
G |
A |
3: 151,455,135 (GRCm39) |
A30V |
probably damaging |
Het |
Il12rb1 |
G |
A |
8: 71,265,934 (GRCm39) |
|
probably benign |
Het |
Invs |
G |
A |
4: 48,392,628 (GRCm39) |
G281R |
possibly damaging |
Het |
Itgax |
C |
A |
7: 127,747,112 (GRCm39) |
|
probably benign |
Het |
Jade1 |
G |
T |
3: 41,568,218 (GRCm39) |
C762F |
possibly damaging |
Het |
Lama1 |
C |
T |
17: 68,079,813 (GRCm39) |
P1229S |
probably damaging |
Het |
Mmp15 |
C |
A |
8: 96,094,856 (GRCm39) |
D243E |
probably benign |
Het |
Mug2 |
A |
G |
6: 122,052,253 (GRCm39) |
T1004A |
probably benign |
Het |
Myh14 |
A |
T |
7: 44,314,791 (GRCm39) |
V44E |
probably damaging |
Het |
N4bp2l1 |
C |
A |
5: 150,517,869 (GRCm39) |
R11S |
possibly damaging |
Het |
Notch4 |
T |
A |
17: 34,784,306 (GRCm39) |
C36* |
probably null |
Het |
Nwd1 |
A |
G |
8: 73,397,672 (GRCm39) |
D637G |
probably damaging |
Het |
Ogfod1 |
T |
C |
8: 94,782,264 (GRCm39) |
I238T |
probably benign |
Het |
Pakap |
G |
A |
4: 57,688,441 (GRCm39) |
E95K |
probably damaging |
Het |
Papln |
A |
G |
12: 83,838,639 (GRCm39) |
D1256G |
possibly damaging |
Het |
Ppp1r26 |
T |
C |
2: 28,340,379 (GRCm39) |
L3P |
probably damaging |
Het |
Rbm10 |
C |
T |
X: 20,503,903 (GRCm39) |
|
probably benign |
Het |
Slc17a5 |
A |
T |
9: 78,460,372 (GRCm39) |
|
probably benign |
Het |
Slc25a17 |
A |
G |
15: 81,207,907 (GRCm39) |
|
probably benign |
Het |
Socs4 |
T |
C |
14: 47,528,112 (GRCm39) |
F349S |
probably damaging |
Het |
Spata31f1a |
A |
G |
4: 42,851,238 (GRCm39) |
V306A |
probably damaging |
Het |
Tchhl1 |
A |
C |
3: 93,378,878 (GRCm39) |
E527D |
probably benign |
Het |
Tm7sf3 |
A |
G |
6: 146,507,787 (GRCm39) |
L425S |
possibly damaging |
Het |
Tmem266 |
G |
T |
9: 55,322,239 (GRCm39) |
V112L |
probably damaging |
Het |
Tmem30c |
T |
A |
16: 57,090,539 (GRCm39) |
I223F |
possibly damaging |
Het |
Tomm70a |
G |
A |
16: 56,942,535 (GRCm39) |
G104D |
probably benign |
Het |
Ttc17 |
G |
T |
2: 94,163,148 (GRCm39) |
A834E |
probably benign |
Het |
Ttn |
C |
T |
2: 76,561,534 (GRCm39) |
V20664M |
probably damaging |
Het |
|
Other mutations in Zbed5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02225:Zbed5
|
APN |
5 |
129,930,974 (GRCm39) |
splice site |
probably null |
|
IGL03334:Zbed5
|
APN |
5 |
129,931,196 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0449:Zbed5
|
UTSW |
5 |
129,930,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Zbed5
|
UTSW |
5 |
129,931,113 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1967:Zbed5
|
UTSW |
5 |
129,930,510 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2246:Zbed5
|
UTSW |
5 |
129,931,592 (GRCm39) |
missense |
probably benign |
0.01 |
R2925:Zbed5
|
UTSW |
5 |
129,932,039 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3053:Zbed5
|
UTSW |
5 |
129,930,987 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3701:Zbed5
|
UTSW |
5 |
129,932,000 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3702:Zbed5
|
UTSW |
5 |
129,932,000 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3916:Zbed5
|
UTSW |
5 |
129,931,118 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3917:Zbed5
|
UTSW |
5 |
129,931,118 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4547:Zbed5
|
UTSW |
5 |
129,931,692 (GRCm39) |
nonsense |
probably null |
|
R4548:Zbed5
|
UTSW |
5 |
129,931,692 (GRCm39) |
nonsense |
probably null |
|
R5195:Zbed5
|
UTSW |
5 |
129,931,019 (GRCm39) |
missense |
probably benign |
0.01 |
R5500:Zbed5
|
UTSW |
5 |
129,930,823 (GRCm39) |
nonsense |
probably null |
|
R5813:Zbed5
|
UTSW |
5 |
129,931,059 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6377:Zbed5
|
UTSW |
5 |
129,932,210 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6620:Zbed5
|
UTSW |
5 |
129,932,130 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6862:Zbed5
|
UTSW |
5 |
129,932,026 (GRCm39) |
missense |
probably benign |
|
R6931:Zbed5
|
UTSW |
5 |
129,932,170 (GRCm39) |
nonsense |
probably null |
|
R7223:Zbed5
|
UTSW |
5 |
129,929,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Zbed5
|
UTSW |
5 |
129,930,798 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7918:Zbed5
|
UTSW |
5 |
129,930,504 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7982:Zbed5
|
UTSW |
5 |
129,929,321 (GRCm39) |
missense |
possibly damaging |
0.79 |
|