Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
G |
A |
16: 20,218,687 (GRCm39) |
R232C |
probably damaging |
Het |
Adam9 |
A |
G |
8: 25,454,926 (GRCm39) |
S732P |
probably damaging |
Het |
Add2 |
G |
A |
6: 86,069,901 (GRCm39) |
V140I |
probably benign |
Het |
Ahi1 |
G |
A |
10: 20,847,974 (GRCm39) |
G461S |
probably damaging |
Het |
Aoc1l2 |
A |
T |
6: 48,909,991 (GRCm39) |
S643C |
probably damaging |
Het |
Arhgef7 |
A |
G |
8: 11,869,659 (GRCm39) |
T432A |
possibly damaging |
Het |
Arsi |
T |
C |
18: 61,050,374 (GRCm39) |
I419T |
probably damaging |
Het |
Brca1 |
G |
A |
11: 101,399,047 (GRCm39) |
P1515L |
possibly damaging |
Het |
Brcc3 |
T |
A |
X: 74,493,647 (GRCm39) |
L222* |
probably null |
Het |
Brpf3 |
A |
T |
17: 29,025,010 (GRCm39) |
T28S |
probably benign |
Het |
Cdc20b |
T |
A |
13: 113,215,191 (GRCm39) |
V253E |
probably damaging |
Het |
Cnot6l |
T |
A |
5: 96,227,905 (GRCm39) |
S443C |
probably benign |
Het |
Copg1 |
G |
A |
6: 87,881,908 (GRCm39) |
A587T |
probably benign |
Het |
Crebrf |
A |
G |
17: 26,962,076 (GRCm39) |
D391G |
probably benign |
Het |
Crocc |
A |
T |
4: 140,769,502 (GRCm39) |
D283E |
probably damaging |
Het |
Cryga |
T |
C |
1: 65,142,318 (GRCm39) |
N25S |
probably benign |
Het |
Csnk1g1 |
T |
C |
9: 65,888,230 (GRCm39) |
F90L |
possibly damaging |
Het |
Cyp2j6 |
A |
G |
4: 96,433,965 (GRCm39) |
V115A |
probably benign |
Het |
Cyp3a11 |
T |
C |
5: 145,799,204 (GRCm39) |
I328V |
probably benign |
Het |
Dchs1 |
C |
A |
7: 105,415,134 (GRCm39) |
E683D |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,809,539 (GRCm39) |
|
probably benign |
Het |
Dqx1 |
T |
C |
6: 83,037,326 (GRCm39) |
S330P |
probably damaging |
Het |
Epg5 |
A |
G |
18: 78,066,580 (GRCm39) |
Y2160C |
probably damaging |
Het |
Ercc5 |
T |
C |
1: 44,213,100 (GRCm39) |
L742P |
probably damaging |
Het |
Fcgbpl1 |
T |
C |
7: 27,839,660 (GRCm39) |
I491T |
probably benign |
Het |
Flt1 |
C |
T |
5: 147,503,204 (GRCm39) |
|
probably benign |
Het |
Grip2 |
A |
G |
6: 91,756,194 (GRCm39) |
S498P |
probably damaging |
Het |
H2-T22 |
A |
G |
17: 36,353,278 (GRCm39) |
L14P |
possibly damaging |
Het |
Hephl1 |
C |
T |
9: 14,988,222 (GRCm39) |
G629S |
probably damaging |
Het |
Hsdl2 |
T |
A |
4: 59,606,523 (GRCm39) |
M162K |
unknown |
Het |
Kcnh8 |
C |
A |
17: 53,284,648 (GRCm39) |
|
probably null |
Het |
Krt76 |
T |
C |
15: 101,799,082 (GRCm39) |
Q201R |
probably damaging |
Het |
Lrpprc |
A |
T |
17: 85,078,322 (GRCm39) |
Y319N |
probably benign |
Het |
Lrrk2 |
T |
G |
15: 91,593,508 (GRCm39) |
I489R |
probably damaging |
Het |
Mboat1 |
G |
T |
13: 30,386,393 (GRCm39) |
D136Y |
probably damaging |
Het |
Msx2 |
C |
A |
13: 53,622,431 (GRCm39) |
R193L |
probably damaging |
Het |
Nfatc4 |
T |
G |
14: 56,069,111 (GRCm39) |
D625E |
possibly damaging |
Het |
Nup153 |
T |
C |
13: 46,870,657 (GRCm39) |
E86G |
probably benign |
Het |
Or2g7 |
G |
T |
17: 38,378,563 (GRCm39) |
R167L |
probably benign |
Het |
Or4k45 |
T |
A |
2: 111,395,559 (GRCm39) |
I77F |
probably benign |
Het |
Pard3b |
T |
C |
1: 62,205,628 (GRCm39) |
L474P |
probably damaging |
Het |
Pate11 |
T |
A |
9: 36,388,412 (GRCm39) |
M79K |
probably benign |
Het |
Pggt1b |
A |
T |
18: 46,396,039 (GRCm39) |
|
probably benign |
Het |
Pik3r2 |
A |
G |
8: 71,224,688 (GRCm39) |
|
probably benign |
Het |
Prr14 |
A |
G |
7: 127,073,898 (GRCm39) |
|
probably benign |
Het |
Rcbtb2 |
T |
C |
14: 73,415,869 (GRCm39) |
|
probably benign |
Het |
Rufy2 |
G |
A |
10: 62,840,515 (GRCm39) |
D429N |
probably benign |
Het |
S1pr5 |
T |
A |
9: 21,155,503 (GRCm39) |
T308S |
probably damaging |
Het |
Sephs1 |
A |
G |
2: 4,904,371 (GRCm39) |
T250A |
probably benign |
Het |
Serpina12 |
A |
G |
12: 104,004,354 (GRCm39) |
S93P |
probably benign |
Het |
Serpinb1b |
T |
G |
13: 33,273,675 (GRCm39) |
H123Q |
probably benign |
Het |
Sftpc |
C |
T |
14: 70,760,120 (GRCm39) |
V46I |
probably benign |
Het |
Skint8 |
T |
A |
4: 111,794,087 (GRCm39) |
V159D |
probably damaging |
Het |
Slc25a11 |
T |
C |
11: 70,536,405 (GRCm39) |
N134S |
probably benign |
Het |
Slc25a24 |
T |
C |
3: 109,064,332 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
C |
G |
9: 41,915,384 (GRCm39) |
V1282L |
probably damaging |
Het |
Sptan1 |
T |
A |
2: 29,916,822 (GRCm39) |
I2170N |
probably damaging |
Het |
Syne4 |
A |
G |
7: 30,014,345 (GRCm39) |
|
probably benign |
Het |
Tcam1 |
G |
A |
11: 106,174,904 (GRCm39) |
E120K |
probably benign |
Het |
Tg |
C |
A |
15: 66,636,291 (GRCm39) |
P626Q |
probably damaging |
Het |
Thoc6 |
T |
A |
17: 23,888,550 (GRCm39) |
D196V |
probably damaging |
Het |
Tpi1 |
A |
G |
6: 124,791,066 (GRCm39) |
F57S |
probably damaging |
Het |
Tril |
A |
G |
6: 53,794,793 (GRCm39) |
*810Q |
probably null |
Het |
Trrap |
T |
A |
5: 144,776,377 (GRCm39) |
V2972D |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,591,624 (GRCm39) |
V12688E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,551,283 (GRCm39) |
M31370V |
probably damaging |
Het |
Txndc11 |
A |
G |
16: 10,909,625 (GRCm39) |
F307S |
probably damaging |
Het |
Vmn1r40 |
C |
T |
6: 89,691,642 (GRCm39) |
S153L |
probably benign |
Het |
Vmn2r95 |
A |
G |
17: 18,672,005 (GRCm39) |
T581A |
possibly damaging |
Het |
Wdtc1 |
A |
G |
4: 133,024,811 (GRCm39) |
F462S |
probably damaging |
Het |
Zfp101 |
A |
G |
17: 33,601,295 (GRCm39) |
S154P |
possibly damaging |
Het |
Zmym6 |
A |
G |
4: 127,002,487 (GRCm39) |
N481D |
probably benign |
Het |
|
Other mutations in Mcmdc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02374:Mcmdc2
|
APN |
1 |
9,982,207 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03087:Mcmdc2
|
APN |
1 |
10,001,170 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03230:Mcmdc2
|
APN |
1 |
10,002,221 (GRCm39) |
unclassified |
probably benign |
|
R0313:Mcmdc2
|
UTSW |
1 |
10,002,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R0685:Mcmdc2
|
UTSW |
1 |
9,982,039 (GRCm39) |
critical splice donor site |
probably null |
|
R0926:Mcmdc2
|
UTSW |
1 |
9,990,801 (GRCm39) |
nonsense |
probably null |
|
R1590:Mcmdc2
|
UTSW |
1 |
9,986,780 (GRCm39) |
nonsense |
probably null |
|
R1867:Mcmdc2
|
UTSW |
1 |
10,001,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Mcmdc2
|
UTSW |
1 |
10,001,026 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5199:Mcmdc2
|
UTSW |
1 |
9,990,660 (GRCm39) |
missense |
probably benign |
0.37 |
R5341:Mcmdc2
|
UTSW |
1 |
10,011,142 (GRCm39) |
frame shift |
probably null |
|
R5459:Mcmdc2
|
UTSW |
1 |
10,007,309 (GRCm39) |
missense |
probably benign |
0.06 |
R5748:Mcmdc2
|
UTSW |
1 |
9,982,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R6808:Mcmdc2
|
UTSW |
1 |
10,004,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Mcmdc2
|
UTSW |
1 |
10,001,003 (GRCm39) |
splice site |
probably null |
|
R7123:Mcmdc2
|
UTSW |
1 |
10,010,643 (GRCm39) |
missense |
unknown |
|
R7233:Mcmdc2
|
UTSW |
1 |
10,002,408 (GRCm39) |
critical splice donor site |
probably null |
|
R7498:Mcmdc2
|
UTSW |
1 |
9,989,302 (GRCm39) |
missense |
probably benign |
|
R7646:Mcmdc2
|
UTSW |
1 |
9,982,360 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7834:Mcmdc2
|
UTSW |
1 |
9,982,399 (GRCm39) |
critical splice donor site |
probably null |
|
R8118:Mcmdc2
|
UTSW |
1 |
9,986,599 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8194:Mcmdc2
|
UTSW |
1 |
9,986,867 (GRCm39) |
missense |
probably benign |
|
R8283:Mcmdc2
|
UTSW |
1 |
10,004,263 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8434:Mcmdc2
|
UTSW |
1 |
9,990,806 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8523:Mcmdc2
|
UTSW |
1 |
9,981,946 (GRCm39) |
start codon destroyed |
probably null |
0.87 |
R9244:Mcmdc2
|
UTSW |
1 |
9,985,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R9281:Mcmdc2
|
UTSW |
1 |
9,994,425 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Mcmdc2
|
UTSW |
1 |
9,982,191 (GRCm39) |
missense |
possibly damaging |
0.93 |
|