Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Adamts2 |
T |
A |
11: 50,694,639 (GRCm39) |
L1142* |
probably null |
Het |
Arl13b |
C |
A |
16: 62,622,150 (GRCm39) |
G381V |
probably damaging |
Het |
Ash1l |
G |
T |
3: 88,892,641 (GRCm39) |
V1507F |
probably damaging |
Het |
Babam2 |
T |
A |
5: 31,859,408 (GRCm39) |
F38I |
probably benign |
Het |
Bend4 |
T |
C |
5: 67,557,619 (GRCm39) |
Y399C |
probably damaging |
Het |
Btn1a1 |
A |
T |
13: 23,644,794 (GRCm39) |
|
probably null |
Het |
Cacna1g |
A |
T |
11: 94,319,973 (GRCm39) |
L1401Q |
probably damaging |
Het |
Cep192 |
T |
C |
18: 67,968,195 (GRCm39) |
V893A |
probably benign |
Het |
Cnot10 |
A |
T |
9: 114,447,012 (GRCm39) |
Y355N |
probably damaging |
Het |
Col6a5 |
G |
C |
9: 105,811,163 (GRCm39) |
S785R |
unknown |
Het |
Cpa3 |
A |
G |
3: 20,276,303 (GRCm39) |
L310P |
probably damaging |
Het |
Cux2 |
A |
G |
5: 122,015,152 (GRCm39) |
I247T |
probably benign |
Het |
Dab1 |
A |
G |
4: 104,561,449 (GRCm39) |
T245A |
probably benign |
Het |
Dmrta1 |
A |
T |
4: 89,579,985 (GRCm39) |
D315V |
probably damaging |
Het |
Dnah12 |
T |
A |
14: 26,583,762 (GRCm39) |
L599* |
probably null |
Het |
Dync1h1 |
T |
C |
12: 110,629,289 (GRCm39) |
I4231T |
possibly damaging |
Het |
Fat1 |
T |
C |
8: 45,476,000 (GRCm39) |
V1659A |
probably damaging |
Het |
Flot2 |
G |
A |
11: 77,949,888 (GRCm39) |
V406M |
probably damaging |
Het |
Galnt2 |
A |
G |
8: 125,032,362 (GRCm39) |
D75G |
probably damaging |
Het |
Gcnt3 |
A |
T |
9: 69,942,464 (GRCm39) |
C35S |
probably damaging |
Het |
Gp2 |
A |
G |
7: 119,052,118 (GRCm39) |
F199L |
probably benign |
Het |
Gramd2b |
C |
T |
18: 56,618,523 (GRCm39) |
P244S |
probably damaging |
Het |
Hhipl1 |
T |
C |
12: 108,278,203 (GRCm39) |
L177P |
probably damaging |
Het |
Homez |
T |
C |
14: 55,095,264 (GRCm39) |
E148G |
possibly damaging |
Het |
Kcnab3 |
G |
A |
11: 69,217,572 (GRCm39) |
C22Y |
possibly damaging |
Het |
Kcnh8 |
C |
A |
17: 53,185,009 (GRCm39) |
S430R |
probably damaging |
Het |
Kcnn2 |
T |
C |
18: 45,692,798 (GRCm39) |
C125R |
probably benign |
Het |
Klhl7 |
G |
A |
5: 24,346,185 (GRCm39) |
R277Q |
possibly damaging |
Het |
Krt78 |
A |
G |
15: 101,855,334 (GRCm39) |
S826P |
probably benign |
Het |
Krtap14 |
T |
C |
16: 88,622,919 (GRCm39) |
Y20C |
possibly damaging |
Het |
Lrcol1 |
A |
G |
5: 110,502,163 (GRCm39) |
|
probably null |
Het |
Lrrc10b |
G |
A |
19: 10,434,226 (GRCm39) |
P152S |
probably damaging |
Het |
Lrrn3 |
C |
G |
12: 41,503,124 (GRCm39) |
D398H |
probably damaging |
Het |
Map3k19 |
T |
C |
1: 127,749,932 (GRCm39) |
I1140V |
probably benign |
Het |
Mos |
G |
A |
4: 3,871,093 (GRCm39) |
T241M |
probably damaging |
Het |
Nol8 |
A |
G |
13: 49,807,901 (GRCm39) |
E39G |
possibly damaging |
Het |
Olfm1 |
T |
G |
2: 28,104,798 (GRCm39) |
S212A |
probably benign |
Het |
Or2ak6 |
T |
A |
11: 58,592,633 (GRCm39) |
F35L |
probably damaging |
Het |
Pip4p2 |
G |
T |
4: 14,912,458 (GRCm39) |
R189L |
probably damaging |
Het |
Plec |
G |
T |
15: 76,061,162 (GRCm39) |
T2947K |
probably damaging |
Het |
Pramel27 |
A |
T |
4: 143,578,187 (GRCm39) |
Q149L |
probably damaging |
Het |
Rasgrp3 |
A |
G |
17: 75,823,350 (GRCm39) |
M474V |
probably benign |
Het |
Ryr1 |
T |
C |
7: 28,719,408 (GRCm39) |
Y4333C |
unknown |
Het |
Scrn2 |
G |
C |
11: 96,924,326 (GRCm39) |
|
probably null |
Het |
Slc22a12 |
C |
A |
19: 6,587,791 (GRCm39) |
V388L |
probably benign |
Het |
Slc4a11 |
A |
G |
2: 130,526,866 (GRCm39) |
V754A |
probably damaging |
Het |
Slco2b1 |
A |
G |
7: 99,335,195 (GRCm39) |
F195S |
probably damaging |
Het |
Slfn9 |
A |
C |
11: 82,872,216 (GRCm39) |
M840R |
possibly damaging |
Het |
Speer4b |
T |
C |
5: 27,706,263 (GRCm39) |
N35D |
probably damaging |
Het |
Taf1d |
T |
A |
9: 15,221,250 (GRCm39) |
D185E |
probably damaging |
Het |
Taok2 |
A |
G |
7: 126,475,213 (GRCm39) |
L245P |
probably damaging |
Het |
Tent4a |
A |
T |
13: 69,651,019 (GRCm39) |
|
probably null |
Het |
Ticam2 |
T |
C |
18: 46,693,846 (GRCm39) |
I80M |
probably damaging |
Het |
Tmem268 |
G |
A |
4: 63,502,164 (GRCm39) |
V331I |
probably benign |
Het |
Tsga10 |
T |
C |
1: 37,840,931 (GRCm39) |
E425G |
probably damaging |
Het |
Ttc7 |
A |
G |
17: 87,654,133 (GRCm39) |
|
probably null |
Het |
Ttf1 |
C |
T |
2: 28,954,668 (GRCm39) |
H11Y |
possibly damaging |
Het |
Unc13a |
T |
C |
8: 72,107,489 (GRCm39) |
H601R |
probably damaging |
Het |
Vmn2r102 |
A |
T |
17: 19,880,661 (GRCm39) |
M1L |
probably benign |
Het |
Vmn2r120 |
G |
T |
17: 57,816,125 (GRCm39) |
N743K |
probably damaging |
Het |
Wnt6 |
C |
A |
1: 74,823,295 (GRCm39) |
|
probably null |
Het |
Wnt6 |
A |
C |
1: 74,823,296 (GRCm39) |
|
probably null |
Het |
Wnt8a |
T |
A |
18: 34,680,525 (GRCm39) |
C297S |
probably damaging |
Het |
Zfp786 |
T |
C |
6: 47,797,087 (GRCm39) |
Q617R |
probably benign |
Het |
Zfp91 |
A |
G |
19: 12,753,774 (GRCm39) |
|
probably null |
Het |
Zw10 |
T |
A |
9: 48,979,983 (GRCm39) |
F371L |
probably damaging |
Het |
|
Other mutations in Ccdc192 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00863:Ccdc192
|
APN |
18 |
57,727,158 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01646:Ccdc192
|
APN |
18 |
57,800,417 (GRCm39) |
nonsense |
probably null |
|
R0115:Ccdc192
|
UTSW |
18 |
57,727,214 (GRCm39) |
splice site |
probably benign |
|
R0285:Ccdc192
|
UTSW |
18 |
57,666,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R1087:Ccdc192
|
UTSW |
18 |
57,863,870 (GRCm39) |
missense |
probably damaging |
0.96 |
R1923:Ccdc192
|
UTSW |
18 |
57,666,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R5133:Ccdc192
|
UTSW |
18 |
57,697,041 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5508:Ccdc192
|
UTSW |
18 |
57,671,156 (GRCm39) |
splice site |
probably null |
|
R5509:Ccdc192
|
UTSW |
18 |
57,671,156 (GRCm39) |
splice site |
probably null |
|
R5510:Ccdc192
|
UTSW |
18 |
57,671,156 (GRCm39) |
splice site |
probably null |
|
R5511:Ccdc192
|
UTSW |
18 |
57,671,156 (GRCm39) |
splice site |
probably null |
|
R6629:Ccdc192
|
UTSW |
18 |
57,863,852 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7089:Ccdc192
|
UTSW |
18 |
57,725,059 (GRCm39) |
missense |
probably benign |
0.11 |
R7545:Ccdc192
|
UTSW |
18 |
57,863,895 (GRCm39) |
missense |
probably damaging |
0.98 |
R7700:Ccdc192
|
UTSW |
18 |
57,696,388 (GRCm39) |
splice site |
probably null |
|
R8045:Ccdc192
|
UTSW |
18 |
57,863,991 (GRCm39) |
missense |
probably damaging |
0.99 |
R8098:Ccdc192
|
UTSW |
18 |
57,800,403 (GRCm39) |
missense |
probably benign |
0.02 |
R8973:Ccdc192
|
UTSW |
18 |
57,725,139 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9011:Ccdc192
|
UTSW |
18 |
57,800,376 (GRCm39) |
missense |
possibly damaging |
0.61 |
X0021:Ccdc192
|
UTSW |
18 |
57,727,197 (GRCm39) |
missense |
probably damaging |
0.99 |
|