Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
G |
A |
9: 55,914,587 (GRCm39) |
P52S |
unknown |
Het |
Adarb2 |
A |
G |
13: 8,620,420 (GRCm39) |
E302G |
probably damaging |
Het |
Adgrf5 |
T |
A |
17: 43,762,070 (GRCm39) |
L1255H |
probably damaging |
Het |
Adra1a |
T |
A |
14: 66,875,733 (GRCm39) |
I236N |
probably benign |
Het |
As3mt |
T |
C |
19: 46,708,891 (GRCm39) |
F295S |
probably damaging |
Het |
Bmp5 |
G |
A |
9: 75,780,642 (GRCm39) |
R313Q |
probably damaging |
Het |
Ccnj |
T |
A |
19: 40,833,394 (GRCm39) |
S191T |
probably benign |
Het |
Clk2 |
T |
A |
3: 89,080,852 (GRCm39) |
|
probably null |
Het |
Cpz |
T |
C |
5: 35,675,000 (GRCm39) |
E83G |
probably damaging |
Het |
Cts3 |
A |
G |
13: 61,715,434 (GRCm39) |
I133T |
probably benign |
Het |
Dars2 |
C |
T |
1: 160,874,342 (GRCm39) |
|
probably null |
Het |
Dsel |
A |
T |
1: 111,788,798 (GRCm39) |
V579D |
probably damaging |
Het |
Dync1h1 |
C |
A |
12: 110,602,076 (GRCm39) |
A2038E |
probably damaging |
Het |
Eaf1 |
A |
G |
14: 31,216,777 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
A |
C |
2: 82,828,524 (GRCm39) |
I6774L |
probably benign |
Het |
Glis2 |
T |
C |
16: 4,431,432 (GRCm39) |
F320L |
possibly damaging |
Het |
Hcar1 |
A |
G |
5: 124,017,693 (GRCm39) |
|
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,797,104 (GRCm39) |
H2211Q |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,559,496 (GRCm39) |
I2385T |
probably damaging |
Het |
Ifi44 |
T |
A |
3: 151,438,094 (GRCm39) |
M398L |
probably benign |
Het |
Il16 |
C |
T |
7: 83,293,249 (GRCm39) |
E1273K |
probably damaging |
Het |
Inpp5j |
G |
A |
11: 3,451,065 (GRCm39) |
T528I |
probably damaging |
Het |
Kbtbd6 |
C |
T |
14: 79,690,627 (GRCm39) |
P441S |
probably damaging |
Het |
Kcnt1 |
C |
T |
2: 25,753,855 (GRCm39) |
|
probably benign |
Het |
Kif26b |
T |
C |
1: 178,358,306 (GRCm39) |
L139P |
probably damaging |
Het |
Klb |
C |
T |
5: 65,505,974 (GRCm39) |
Q74* |
probably null |
Het |
L3mbtl1 |
G |
A |
2: 162,808,926 (GRCm39) |
V600I |
probably benign |
Het |
Lcp1 |
C |
T |
14: 75,447,946 (GRCm39) |
A317V |
possibly damaging |
Het |
Lipc |
C |
T |
9: 70,720,029 (GRCm39) |
G326D |
probably damaging |
Het |
Mbnl2 |
T |
A |
14: 120,616,694 (GRCm39) |
F103I |
probably benign |
Het |
Med16 |
A |
G |
10: 79,744,650 (GRCm39) |
|
probably null |
Het |
Mga |
T |
C |
2: 119,766,008 (GRCm39) |
V1424A |
possibly damaging |
Het |
Mocs2 |
G |
T |
13: 114,964,710 (GRCm39) |
|
probably null |
Het |
Morc1 |
C |
T |
16: 48,451,263 (GRCm39) |
|
probably null |
Het |
Mpc2 |
T |
A |
1: 165,307,080 (GRCm39) |
W94R |
probably damaging |
Het |
Mrm3 |
G |
A |
11: 76,141,002 (GRCm39) |
V337I |
possibly damaging |
Het |
N4bp3 |
T |
C |
11: 51,536,433 (GRCm39) |
H133R |
probably benign |
Het |
Ncam2 |
G |
T |
16: 81,420,256 (GRCm39) |
G810V |
probably damaging |
Het |
Nipbl |
T |
C |
15: 8,373,090 (GRCm39) |
E1052G |
possibly damaging |
Het |
Nlrp12 |
C |
T |
7: 3,297,887 (GRCm39) |
V95M |
probably damaging |
Het |
Nrip1 |
T |
C |
16: 76,090,244 (GRCm39) |
N438D |
possibly damaging |
Het |
Nsun4 |
C |
A |
4: 115,909,035 (GRCm39) |
M508I |
probably benign |
Het |
Pla2g2c |
T |
C |
4: 138,461,650 (GRCm39) |
S40P |
probably damaging |
Het |
Plec |
A |
G |
15: 76,082,178 (GRCm39) |
|
probably null |
Het |
Ppfia2 |
G |
T |
10: 106,693,356 (GRCm39) |
M620I |
possibly damaging |
Het |
Ppp6c |
A |
G |
2: 39,116,229 (GRCm39) |
Y9H |
probably damaging |
Het |
Prkd1 |
A |
T |
12: 50,695,617 (GRCm39) |
I47N |
possibly damaging |
Het |
Prr14l |
T |
C |
5: 32,988,028 (GRCm39) |
D489G |
probably benign |
Het |
Ptch2 |
T |
A |
4: 116,971,849 (GRCm39) |
Y1124N |
probably benign |
Het |
Ptpra |
T |
G |
2: 130,395,320 (GRCm39) |
Y808D |
probably damaging |
Het |
Rint1 |
T |
A |
5: 24,020,651 (GRCm39) |
F558Y |
possibly damaging |
Het |
Rnf215 |
T |
A |
11: 4,089,792 (GRCm39) |
C268* |
probably null |
Het |
Slc25a13 |
T |
C |
6: 6,181,100 (GRCm39) |
E28G |
possibly damaging |
Het |
Slc38a8 |
G |
T |
8: 120,226,554 (GRCm39) |
Y78* |
probably null |
Het |
Slc4a7 |
T |
C |
14: 14,775,000 (GRCm38) |
M810T |
probably damaging |
Het |
Slitrk1 |
A |
G |
14: 109,150,591 (GRCm39) |
V40A |
possibly damaging |
Het |
Sobp |
A |
T |
10: 42,898,831 (GRCm39) |
S251R |
probably damaging |
Het |
Spata31d1a |
G |
A |
13: 59,851,015 (GRCm39) |
S371L |
probably benign |
Het |
Tada2b |
T |
C |
5: 36,634,180 (GRCm39) |
T133A |
possibly damaging |
Het |
Tbc1d20 |
A |
G |
2: 152,146,881 (GRCm39) |
D90G |
probably benign |
Het |
Tek |
T |
A |
4: 94,715,533 (GRCm39) |
I408K |
probably benign |
Het |
Tgfb2 |
A |
G |
1: 186,382,077 (GRCm39) |
F150S |
probably benign |
Het |
Tmem63b |
T |
C |
17: 45,977,517 (GRCm39) |
T370A |
probably benign |
Het |
Tmem94 |
G |
T |
11: 115,677,082 (GRCm39) |
R118L |
possibly damaging |
Het |
Tspan17 |
C |
G |
13: 54,940,434 (GRCm39) |
L34V |
probably benign |
Het |
Vmn1r238 |
A |
T |
18: 3,123,151 (GRCm39) |
Y88N |
probably damaging |
Het |
Vmn1r85 |
A |
G |
7: 12,818,964 (GRCm39) |
I60T |
probably damaging |
Het |
Vmn2r96 |
T |
C |
17: 18,803,029 (GRCm39) |
M313T |
probably benign |
Het |
Zp3r |
G |
A |
1: 130,511,217 (GRCm39) |
S387F |
probably benign |
Het |
|
Other mutations in Mdm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00494:Mdm1
|
APN |
10 |
118,000,346 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01400:Mdm1
|
APN |
10 |
117,993,156 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01504:Mdm1
|
APN |
10 |
117,982,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02070:Mdm1
|
APN |
10 |
117,982,523 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02149:Mdm1
|
APN |
10 |
117,983,970 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02817:Mdm1
|
APN |
10 |
118,000,251 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03076:Mdm1
|
APN |
10 |
117,995,588 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4696001:Mdm1
|
UTSW |
10 |
117,994,445 (GRCm39) |
missense |
probably benign |
|
R0071:Mdm1
|
UTSW |
10 |
117,982,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0071:Mdm1
|
UTSW |
10 |
117,982,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0166:Mdm1
|
UTSW |
10 |
118,002,585 (GRCm39) |
missense |
probably damaging |
0.96 |
R0218:Mdm1
|
UTSW |
10 |
117,992,783 (GRCm39) |
splice site |
probably benign |
|
R0446:Mdm1
|
UTSW |
10 |
117,987,961 (GRCm39) |
missense |
probably benign |
0.01 |
R0605:Mdm1
|
UTSW |
10 |
117,982,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Mdm1
|
UTSW |
10 |
117,986,847 (GRCm39) |
missense |
probably benign |
0.02 |
R2870:Mdm1
|
UTSW |
10 |
117,986,847 (GRCm39) |
missense |
probably benign |
0.02 |
R2873:Mdm1
|
UTSW |
10 |
117,986,847 (GRCm39) |
missense |
probably benign |
0.02 |
R4816:Mdm1
|
UTSW |
10 |
117,982,782 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5571:Mdm1
|
UTSW |
10 |
117,995,588 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5623:Mdm1
|
UTSW |
10 |
117,986,694 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5806:Mdm1
|
UTSW |
10 |
118,002,563 (GRCm39) |
missense |
probably benign |
|
R6537:Mdm1
|
UTSW |
10 |
117,994,481 (GRCm39) |
missense |
probably benign |
0.00 |
R6539:Mdm1
|
UTSW |
10 |
117,986,863 (GRCm39) |
critical splice donor site |
probably null |
|
R6891:Mdm1
|
UTSW |
10 |
117,983,937 (GRCm39) |
missense |
probably benign |
0.04 |
R6952:Mdm1
|
UTSW |
10 |
118,003,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R7176:Mdm1
|
UTSW |
10 |
117,978,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7442:Mdm1
|
UTSW |
10 |
117,982,590 (GRCm39) |
missense |
probably benign |
0.16 |
R7464:Mdm1
|
UTSW |
10 |
117,988,171 (GRCm39) |
missense |
probably benign |
0.00 |
R8068:Mdm1
|
UTSW |
10 |
117,982,709 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8964:Mdm1
|
UTSW |
10 |
118,002,585 (GRCm39) |
missense |
probably damaging |
0.96 |
R9049:Mdm1
|
UTSW |
10 |
117,982,605 (GRCm39) |
missense |
probably benign |
0.01 |
R9347:Mdm1
|
UTSW |
10 |
117,982,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9509:Mdm1
|
UTSW |
10 |
117,982,730 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Mdm1
|
UTSW |
10 |
117,994,267 (GRCm39) |
missense |
possibly damaging |
0.67 |
Z1177:Mdm1
|
UTSW |
10 |
117,994,401 (GRCm39) |
missense |
possibly damaging |
0.93 |
|