Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931414P19Rik |
G |
T |
14: 54,821,966 (GRCm39) |
H466Q |
probably damaging |
Het |
4933411K16Rik |
A |
T |
19: 42,041,322 (GRCm39) |
H151L |
probably damaging |
Het |
A330008L17Rik |
A |
G |
8: 100,148,389 (GRCm39) |
|
noncoding transcript |
Het |
Abcc5 |
C |
A |
16: 20,184,615 (GRCm39) |
V1015L |
probably benign |
Het |
Bach2 |
T |
A |
4: 32,563,150 (GRCm39) |
L539H |
probably damaging |
Het |
Birc6 |
A |
G |
17: 74,962,173 (GRCm39) |
K3929R |
probably damaging |
Het |
C1qtnf2 |
A |
G |
11: 43,382,148 (GRCm39) |
D320G |
probably benign |
Het |
Cbr2 |
A |
T |
11: 120,621,278 (GRCm39) |
H140Q |
probably benign |
Het |
Cbs |
T |
C |
17: 31,836,355 (GRCm39) |
|
probably benign |
Het |
Cdc42bpg |
T |
C |
19: 6,367,675 (GRCm39) |
V1015A |
probably damaging |
Het |
Cep104 |
T |
G |
4: 154,069,400 (GRCm39) |
M207R |
probably damaging |
Het |
Chil6 |
A |
T |
3: 106,313,274 (GRCm39) |
M25K |
probably benign |
Het |
Cln5 |
A |
G |
14: 103,310,795 (GRCm39) |
D154G |
probably damaging |
Het |
Col4a1 |
C |
A |
8: 11,259,650 (GRCm39) |
G1341V |
probably damaging |
Het |
Cplane2 |
C |
T |
4: 140,945,900 (GRCm39) |
R148C |
probably damaging |
Het |
Cx3cl1 |
A |
T |
8: 95,503,934 (GRCm39) |
|
probably benign |
Het |
Cyct |
T |
C |
2: 76,184,512 (GRCm39) |
K80E |
probably damaging |
Het |
Dhx37 |
T |
C |
5: 125,508,677 (GRCm39) |
K86R |
probably benign |
Het |
Dnah17 |
G |
A |
11: 117,931,984 (GRCm39) |
|
probably benign |
Het |
Etl4 |
T |
C |
2: 20,790,232 (GRCm39) |
V628A |
probably benign |
Het |
Fam234a |
T |
C |
17: 26,437,163 (GRCm39) |
E172G |
probably benign |
Het |
Foxp2 |
C |
T |
6: 15,379,830 (GRCm39) |
|
probably benign |
Het |
Frem1 |
A |
T |
4: 82,917,167 (GRCm39) |
F592Y |
probably damaging |
Het |
Gm10259 |
T |
G |
3: 25,266,693 (GRCm39) |
|
noncoding transcript |
Het |
Gm17521 |
C |
A |
X: 121,938,922 (GRCm39) |
G149C |
unknown |
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 |
Hap1 |
G |
T |
11: 100,246,847 (GRCm39) |
D19E |
probably damaging |
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 |
Mrpl50 |
T |
C |
4: 49,514,539 (GRCm39) |
E44G |
probably damaging |
Het |
Myg1 |
G |
C |
15: 102,246,171 (GRCm39) |
G349R |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,096,423 (GRCm39) |
I301V |
probably benign |
Het |
Ncapg2 |
A |
T |
12: 116,370,938 (GRCm39) |
|
probably benign |
Het |
Ncor2 |
T |
C |
5: 125,195,756 (GRCm39) |
|
probably benign |
Het |
Neo1 |
A |
G |
9: 58,820,452 (GRCm39) |
Y824H |
possibly damaging |
Het |
Or1o4 |
T |
A |
17: 37,591,140 (GRCm39) |
Y57F |
probably damaging |
Het |
Orc1 |
T |
A |
4: 108,462,828 (GRCm39) |
M635K |
probably damaging |
Het |
Phip |
A |
G |
9: 82,753,698 (GRCm39) |
I1682T |
probably benign |
Het |
Ppp2r1b |
A |
G |
9: 50,773,794 (GRCm39) |
N223S |
probably benign |
Het |
Ralb |
A |
T |
1: 119,399,447 (GRCm39) |
C204S |
probably benign |
Het |
Rgs12 |
G |
A |
5: 35,123,359 (GRCm39) |
V381M |
possibly damaging |
Het |
Rtkn2 |
A |
T |
10: 67,833,456 (GRCm39) |
|
probably null |
Het |
Srrm3 |
A |
G |
5: 135,886,068 (GRCm39) |
D336G |
probably damaging |
Het |
Stk11 |
T |
C |
10: 79,963,782 (GRCm39) |
|
probably null |
Het |
Svep1 |
A |
G |
4: 58,096,177 (GRCm39) |
L1481P |
probably damaging |
Het |
Tiam2 |
C |
G |
17: 3,557,976 (GRCm39) |
|
probably benign |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Tmprss11b |
T |
C |
5: 86,809,449 (GRCm39) |
T348A |
probably damaging |
Het |
Ube3b |
C |
A |
5: 114,538,012 (GRCm39) |
Q368K |
probably damaging |
Het |
Veph1 |
T |
A |
3: 66,066,748 (GRCm39) |
E413D |
possibly damaging |
Het |
Vmn2r91 |
T |
G |
17: 18,325,759 (GRCm39) |
W126G |
probably damaging |
Het |
Yrdc |
T |
A |
4: 124,745,554 (GRCm39) |
M1K |
probably null |
Het |
Zfp445 |
T |
C |
9: 122,682,142 (GRCm39) |
M600V |
probably benign |
Het |
|
Other mutations in Commd9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00475:Commd9
|
APN |
2 |
101,725,501 (GRCm39) |
nonsense |
probably null |
|
IGL02232:Commd9
|
APN |
2 |
101,731,324 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03109:Commd9
|
APN |
2 |
101,727,515 (GRCm39) |
missense |
probably benign |
|
R1873:Commd9
|
UTSW |
2 |
101,727,502 (GRCm39) |
missense |
probably benign |
0.09 |
R1933:Commd9
|
UTSW |
2 |
101,731,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Commd9
|
UTSW |
2 |
101,727,486 (GRCm39) |
missense |
probably benign |
0.18 |
R3828:Commd9
|
UTSW |
2 |
101,727,486 (GRCm39) |
missense |
probably benign |
0.18 |
R3968:Commd9
|
UTSW |
2 |
101,727,486 (GRCm39) |
missense |
probably benign |
0.18 |
R3969:Commd9
|
UTSW |
2 |
101,727,486 (GRCm39) |
missense |
probably benign |
0.18 |
R3970:Commd9
|
UTSW |
2 |
101,727,486 (GRCm39) |
missense |
probably benign |
0.18 |
R4059:Commd9
|
UTSW |
2 |
101,725,499 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4795:Commd9
|
UTSW |
2 |
101,729,241 (GRCm39) |
missense |
probably benign |
0.00 |
R5289:Commd9
|
UTSW |
2 |
101,729,239 (GRCm39) |
missense |
probably benign |
0.00 |
R5426:Commd9
|
UTSW |
2 |
101,729,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Commd9
|
UTSW |
2 |
101,731,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7209:Commd9
|
UTSW |
2 |
101,725,483 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7425:Commd9
|
UTSW |
2 |
101,730,245 (GRCm39) |
nonsense |
probably null |
|
R7552:Commd9
|
UTSW |
2 |
101,731,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R9615:Commd9
|
UTSW |
2 |
101,727,436 (GRCm39) |
missense |
possibly damaging |
0.82 |
|