Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
T |
A |
3: 59,843,896 (GRCm39) |
S197T |
possibly damaging |
Het |
Actl6b |
T |
C |
5: 137,565,535 (GRCm39) |
L377P |
probably damaging |
Het |
Apc |
C |
A |
18: 34,412,388 (GRCm39) |
Q236K |
possibly damaging |
Het |
Atn1 |
G |
A |
6: 124,723,182 (GRCm39) |
|
probably benign |
Het |
Ccr3 |
A |
G |
9: 123,829,714 (GRCm39) |
T350A |
possibly damaging |
Het |
Cdc42bpg |
T |
C |
19: 6,367,675 (GRCm39) |
V1015A |
probably damaging |
Het |
Chd2 |
A |
G |
7: 73,141,163 (GRCm39) |
Y577H |
possibly damaging |
Het |
Col1a2 |
A |
G |
6: 4,516,960 (GRCm39) |
|
probably benign |
Het |
Col4a1 |
C |
A |
8: 11,259,650 (GRCm39) |
G1341V |
probably damaging |
Het |
Commd9 |
C |
A |
2: 101,727,486 (GRCm39) |
N93K |
probably benign |
Het |
Cplane2 |
C |
T |
4: 140,945,900 (GRCm39) |
R148C |
probably damaging |
Het |
Cx3cl1 |
A |
T |
8: 95,503,934 (GRCm39) |
|
probably benign |
Het |
Dhx37 |
T |
C |
5: 125,508,677 (GRCm39) |
K86R |
probably benign |
Het |
Dlec1 |
T |
C |
9: 118,972,129 (GRCm39) |
|
probably benign |
Het |
Dnah17 |
G |
A |
11: 117,931,984 (GRCm39) |
|
probably benign |
Het |
Ffar2 |
A |
T |
7: 30,519,510 (GRCm39) |
I10N |
possibly damaging |
Het |
Gas2 |
T |
C |
7: 51,586,367 (GRCm39) |
|
probably null |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Grpel1 |
T |
A |
5: 36,626,827 (GRCm39) |
N36K |
probably benign |
Het |
Hgfac |
C |
A |
5: 35,205,506 (GRCm39) |
D595E |
probably damaging |
Het |
Kcnj10 |
A |
T |
1: 172,197,616 (GRCm39) |
S377C |
probably damaging |
Het |
Kcnq2 |
C |
T |
2: 180,746,693 (GRCm39) |
V369I |
possibly damaging |
Het |
Kcnt1 |
T |
C |
2: 25,805,880 (GRCm39) |
|
probably null |
Het |
Lpcat1 |
T |
C |
13: 73,637,212 (GRCm39) |
I114T |
possibly damaging |
Het |
Mast4 |
G |
T |
13: 102,875,319 (GRCm39) |
H1350N |
probably damaging |
Het |
Mcts1 |
T |
C |
X: 37,691,445 (GRCm39) |
|
probably benign |
Het |
Muc21 |
A |
G |
17: 35,932,504 (GRCm39) |
|
probably benign |
Het |
Myg1 |
G |
C |
15: 102,246,171 (GRCm39) |
G349R |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,195,756 (GRCm39) |
|
probably benign |
Het |
Or1o4 |
T |
A |
17: 37,591,140 (GRCm39) |
Y57F |
probably damaging |
Het |
Or5t17 |
T |
A |
2: 86,832,388 (GRCm39) |
I25K |
probably damaging |
Het |
Or9g4b |
C |
T |
2: 85,616,559 (GRCm39) |
R235* |
probably null |
Het |
Panx2 |
A |
G |
15: 88,952,664 (GRCm39) |
D377G |
probably damaging |
Het |
Pcdhb10 |
C |
A |
18: 37,545,470 (GRCm39) |
T182N |
probably damaging |
Het |
Pdha2 |
G |
T |
3: 140,916,889 (GRCm39) |
F206L |
possibly damaging |
Het |
Pgd |
T |
C |
4: 149,250,461 (GRCm39) |
|
probably benign |
Het |
Pgs1 |
C |
T |
11: 117,910,584 (GRCm39) |
|
probably null |
Het |
Rere |
T |
C |
4: 150,554,785 (GRCm39) |
V161A |
probably benign |
Het |
Rgs12 |
G |
A |
5: 35,123,359 (GRCm39) |
V381M |
possibly damaging |
Het |
Rrm2 |
G |
T |
12: 24,758,598 (GRCm39) |
A47S |
probably benign |
Het |
Rsph6a |
T |
C |
7: 18,791,539 (GRCm39) |
L236P |
probably damaging |
Het |
Rtkn2 |
A |
T |
10: 67,833,456 (GRCm39) |
|
probably null |
Het |
Rubcnl |
C |
T |
14: 75,269,665 (GRCm39) |
L108F |
possibly damaging |
Het |
Sap18b |
T |
C |
8: 96,552,185 (GRCm39) |
F65S |
probably damaging |
Het |
Scap |
A |
G |
9: 110,210,365 (GRCm39) |
M925V |
probably benign |
Het |
Slc7a8 |
A |
G |
14: 54,975,029 (GRCm39) |
I200T |
probably damaging |
Het |
Srrm3 |
A |
G |
5: 135,886,068 (GRCm39) |
D336G |
probably damaging |
Het |
Stk11 |
T |
C |
10: 79,963,782 (GRCm39) |
|
probably null |
Het |
Tiam2 |
C |
G |
17: 3,557,976 (GRCm39) |
|
probably benign |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Trio |
T |
A |
15: 27,833,156 (GRCm39) |
K75N |
probably damaging |
Het |
Tspan18 |
T |
C |
2: 93,050,453 (GRCm39) |
I57V |
probably benign |
Het |
Ube3b |
C |
A |
5: 114,538,012 (GRCm39) |
Q368K |
probably damaging |
Het |
Zfhx4 |
A |
T |
3: 5,466,269 (GRCm39) |
K2142N |
probably damaging |
Het |
Zfp37 |
T |
C |
4: 62,110,800 (GRCm39) |
N88S |
probably benign |
Het |
Zswim8 |
C |
T |
14: 20,761,157 (GRCm39) |
R142* |
probably null |
Het |
|
Other mutations in Fam234a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00907:Fam234a
|
APN |
17 |
26,432,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02635:Fam234a
|
APN |
17 |
26,433,427 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0269:Fam234a
|
UTSW |
17 |
26,435,591 (GRCm39) |
missense |
probably benign |
|
R0617:Fam234a
|
UTSW |
17 |
26,435,591 (GRCm39) |
missense |
probably benign |
|
R1687:Fam234a
|
UTSW |
17 |
26,434,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Fam234a
|
UTSW |
17 |
26,435,629 (GRCm39) |
splice site |
probably null |
|
R2016:Fam234a
|
UTSW |
17 |
26,437,290 (GRCm39) |
missense |
probably benign |
0.07 |
R3827:Fam234a
|
UTSW |
17 |
26,437,163 (GRCm39) |
missense |
probably benign |
|
R3829:Fam234a
|
UTSW |
17 |
26,437,163 (GRCm39) |
missense |
probably benign |
|
R4133:Fam234a
|
UTSW |
17 |
26,432,532 (GRCm39) |
missense |
probably damaging |
0.99 |
R4190:Fam234a
|
UTSW |
17 |
26,432,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R4193:Fam234a
|
UTSW |
17 |
26,432,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R4858:Fam234a
|
UTSW |
17 |
26,435,591 (GRCm39) |
missense |
probably benign |
|
R4885:Fam234a
|
UTSW |
17 |
26,432,559 (GRCm39) |
missense |
probably benign |
0.00 |
R5117:Fam234a
|
UTSW |
17 |
26,432,512 (GRCm39) |
missense |
probably benign |
0.18 |
R5719:Fam234a
|
UTSW |
17 |
26,433,627 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5735:Fam234a
|
UTSW |
17 |
26,432,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R6271:Fam234a
|
UTSW |
17 |
26,437,211 (GRCm39) |
missense |
probably benign |
0.19 |
R6341:Fam234a
|
UTSW |
17 |
26,432,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R6365:Fam234a
|
UTSW |
17 |
26,439,429 (GRCm39) |
nonsense |
probably null |
|
R6621:Fam234a
|
UTSW |
17 |
26,432,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R7393:Fam234a
|
UTSW |
17 |
26,435,598 (GRCm39) |
missense |
probably benign |
0.01 |
R7801:Fam234a
|
UTSW |
17 |
26,437,172 (GRCm39) |
missense |
probably benign |
0.00 |
R7956:Fam234a
|
UTSW |
17 |
26,435,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Fam234a
|
UTSW |
17 |
26,437,672 (GRCm39) |
missense |
probably benign |
0.11 |
R8393:Fam234a
|
UTSW |
17 |
26,437,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Fam234a
|
UTSW |
17 |
26,435,531 (GRCm39) |
critical splice donor site |
probably benign |
|
R9417:Fam234a
|
UTSW |
17 |
26,435,225 (GRCm39) |
missense |
probably benign |
|
R9740:Fam234a
|
UTSW |
17 |
26,432,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R9758:Fam234a
|
UTSW |
17 |
26,432,627 (GRCm39) |
missense |
probably benign |
0.00 |
RF020:Fam234a
|
UTSW |
17 |
26,437,725 (GRCm39) |
missense |
probably benign |
0.42 |
|