Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
C |
17: 9,226,927 (GRCm39) |
V494A |
probably benign |
Het |
1700017B05Rik |
A |
T |
9: 57,166,041 (GRCm39) |
L111Q |
probably damaging |
Het |
Adgrf4 |
T |
G |
17: 42,977,424 (GRCm39) |
I640L |
possibly damaging |
Het |
Afdn |
T |
G |
17: 14,111,074 (GRCm39) |
|
probably null |
Het |
Ammecr1l |
A |
T |
18: 31,894,877 (GRCm39) |
|
probably benign |
Het |
Aox1 |
A |
T |
1: 58,375,808 (GRCm39) |
Y879F |
probably benign |
Het |
Arhgap45 |
G |
A |
10: 79,862,181 (GRCm39) |
|
probably null |
Het |
Arpp21 |
G |
T |
9: 111,955,514 (GRCm39) |
H542N |
probably benign |
Het |
Cdt1 |
G |
A |
8: 123,298,719 (GRCm39) |
R452Q |
probably damaging |
Het |
Clcn7 |
C |
T |
17: 25,372,667 (GRCm39) |
H149Y |
|
Het |
Clpp |
T |
G |
17: 57,297,421 (GRCm39) |
W32G |
probably benign |
Het |
Dnmt1 |
G |
T |
9: 20,819,785 (GRCm39) |
L1572M |
probably damaging |
Het |
Drd3 |
G |
T |
16: 43,627,741 (GRCm39) |
R128S |
probably damaging |
Het |
Elmo2 |
A |
T |
2: 165,146,849 (GRCm39) |
F243I |
possibly damaging |
Het |
Endou |
G |
A |
15: 97,618,126 (GRCm39) |
P128L |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,908,214 (GRCm39) |
M2596T |
probably benign |
Het |
Fbxl16 |
A |
G |
17: 26,035,703 (GRCm39) |
K100R |
probably benign |
Het |
Fbxo10 |
A |
G |
4: 45,062,230 (GRCm39) |
S99P |
possibly damaging |
Het |
Fez1 |
A |
T |
9: 36,778,999 (GRCm39) |
R225S |
probably benign |
Het |
Gm14326 |
A |
T |
2: 177,588,464 (GRCm39) |
H177Q |
probably damaging |
Het |
Gm32742 |
T |
A |
9: 51,054,546 (GRCm39) |
M1360L |
probably benign |
Het |
Hspg2 |
T |
C |
4: 137,271,677 (GRCm39) |
V2481A |
possibly damaging |
Het |
Ifnl3 |
A |
G |
7: 28,223,283 (GRCm39) |
K101E |
probably benign |
Het |
Il15 |
A |
T |
8: 83,064,204 (GRCm39) |
S77R |
probably damaging |
Het |
Ints13 |
T |
C |
6: 146,476,216 (GRCm39) |
D95G |
probably damaging |
Het |
Kcmf1 |
G |
A |
6: 72,819,929 (GRCm39) |
P357S |
probably benign |
Het |
Kcmf1 |
G |
T |
6: 72,825,289 (GRCm39) |
T268K |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,748,153 (GRCm39) |
I3057N |
unknown |
Het |
Lgi2 |
A |
G |
5: 52,695,832 (GRCm39) |
F376L |
probably damaging |
Het |
Lrig3 |
T |
G |
10: 125,832,993 (GRCm39) |
L289R |
probably damaging |
Het |
Mafk |
A |
G |
5: 139,785,876 (GRCm39) |
S25G |
probably benign |
Het |
Mpz |
T |
C |
1: 170,987,204 (GRCm39) |
|
probably null |
Het |
Nalcn |
A |
C |
14: 123,515,761 (GRCm39) |
I1680R |
probably benign |
Het |
Or13d1 |
C |
T |
4: 52,971,470 (GRCm39) |
P283L |
probably damaging |
Het |
Or5ak24 |
T |
A |
2: 85,260,902 (GRCm39) |
K90N |
probably benign |
Het |
Or5g26 |
C |
T |
2: 85,494,518 (GRCm39) |
V87M |
possibly damaging |
Het |
Or5p62 |
A |
T |
7: 107,771,701 (GRCm39) |
N83K |
probably benign |
Het |
Otof |
A |
C |
5: 30,528,912 (GRCm39) |
I1827S |
possibly damaging |
Het |
Oxgr1 |
A |
G |
14: 120,259,614 (GRCm39) |
Y198H |
probably damaging |
Het |
P3h2 |
T |
A |
16: 25,784,559 (GRCm39) |
N645I |
probably damaging |
Het |
Pbld2 |
A |
G |
10: 62,889,691 (GRCm39) |
T158A |
probably benign |
Het |
Pdgfrb |
C |
T |
18: 61,206,315 (GRCm39) |
R608C |
probably damaging |
Het |
Pdia5 |
T |
C |
16: 35,228,049 (GRCm39) |
T408A |
probably benign |
Het |
Pik3cg |
A |
G |
12: 32,226,845 (GRCm39) |
V1014A |
probably benign |
Het |
Prpf8 |
A |
G |
11: 75,399,374 (GRCm39) |
T2180A |
probably damaging |
Het |
Rabgap1l |
A |
T |
1: 160,551,742 (GRCm39) |
Y245* |
probably null |
Het |
Rerg |
T |
C |
6: 137,044,033 (GRCm39) |
T28A |
possibly damaging |
Het |
Rhcg |
A |
G |
7: 79,249,216 (GRCm39) |
I335T |
probably damaging |
Het |
Rmnd1 |
C |
T |
10: 4,353,873 (GRCm39) |
V78I |
probably damaging |
Het |
Ryr2 |
A |
C |
13: 11,664,662 (GRCm39) |
V3547G |
probably benign |
Het |
Scnn1a |
C |
A |
6: 125,314,770 (GRCm39) |
Q324K |
probably benign |
Het |
Serpinb6e |
G |
A |
13: 34,016,698 (GRCm39) |
T345I |
probably damaging |
Het |
Smchd1 |
T |
C |
17: 71,668,955 (GRCm39) |
T1687A |
probably benign |
Het |
Smim45 |
A |
T |
15: 82,136,774 (GRCm39) |
|
probably benign |
Het |
Speer4f2 |
A |
C |
5: 17,581,661 (GRCm39) |
H201P |
|
Het |
Spef2 |
G |
A |
15: 9,725,257 (GRCm39) |
R167C |
probably damaging |
Het |
Srp68 |
A |
G |
11: 116,162,733 (GRCm39) |
|
probably null |
Het |
Tbc1d14 |
A |
T |
5: 36,669,884 (GRCm39) |
F455I |
probably benign |
Het |
Tet3 |
A |
G |
6: 83,432,006 (GRCm39) |
V10A |
possibly damaging |
Het |
Tlr3 |
A |
T |
8: 45,850,810 (GRCm39) |
S696T |
probably benign |
Het |
Tmem63b |
T |
C |
17: 45,978,709 (GRCm39) |
N300S |
probably benign |
Het |
Tmprss11g |
T |
C |
5: 86,637,150 (GRCm39) |
I328M |
probably damaging |
Het |
Tpm3 |
C |
T |
3: 89,980,029 (GRCm39) |
|
probably benign |
Het |
Trim28 |
T |
A |
7: 12,758,833 (GRCm39) |
L63Q |
probably damaging |
Het |
Unc5b |
G |
A |
10: 60,613,265 (GRCm39) |
R324C |
probably damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,507,204 (GRCm39) |
N107K |
possibly damaging |
Het |
Vmn2r88 |
A |
G |
14: 51,656,100 (GRCm39) |
T770A |
|
Het |
Zcchc2 |
C |
A |
1: 105,958,211 (GRCm39) |
P894Q |
probably damaging |
Het |
Zfhx2 |
A |
G |
14: 55,303,229 (GRCm39) |
V1585A |
probably benign |
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 |
R4927:Ccdc192
|
UTSW |
18 |
57,863,888 (GRCm39) |
nonsense |
probably null |
|
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 |
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 |
|