Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm4 |
A |
G |
7: 119,302,646 (GRCm39) |
|
probably benign |
Het |
Asb18 |
A |
G |
1: 89,942,296 (GRCm39) |
S2P |
probably damaging |
Het |
Atp2b2 |
A |
G |
6: 113,770,715 (GRCm39) |
F398S |
probably damaging |
Het |
BC034090 |
T |
G |
1: 155,101,856 (GRCm39) |
D136A |
probably damaging |
Het |
Ces5a |
A |
C |
8: 94,246,260 (GRCm39) |
F310V |
probably damaging |
Het |
Chsy1 |
T |
C |
7: 65,820,779 (GRCm39) |
V338A |
probably benign |
Het |
Dbh |
A |
G |
2: 27,064,944 (GRCm39) |
E385G |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,591,543 (GRCm39) |
|
probably benign |
Het |
F2rl1 |
A |
G |
13: 95,650,097 (GRCm39) |
S262P |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,147,045 (GRCm39) |
N3984D |
probably benign |
Het |
Fbxo38 |
A |
T |
18: 62,659,234 (GRCm39) |
H354Q |
probably benign |
Het |
Fgf6 |
T |
A |
6: 127,001,095 (GRCm39) |
V201D |
probably damaging |
Het |
Gm16181 |
A |
T |
17: 35,442,933 (GRCm39) |
|
probably benign |
Het |
Gm6811 |
T |
C |
17: 21,314,311 (GRCm39) |
|
noncoding transcript |
Het |
Gna11 |
A |
G |
10: 81,366,771 (GRCm39) |
F313S |
probably damaging |
Het |
Gprc6a |
C |
T |
10: 51,491,968 (GRCm39) |
A523T |
probably damaging |
Het |
Il22 |
T |
C |
10: 118,041,785 (GRCm39) |
|
probably null |
Het |
Insr |
T |
C |
8: 3,308,574 (GRCm39) |
Y154C |
probably damaging |
Het |
Irak4 |
T |
A |
15: 94,449,780 (GRCm39) |
D86E |
probably benign |
Het |
Itk |
C |
A |
11: 46,225,764 (GRCm39) |
W529L |
probably damaging |
Het |
Klhl6 |
C |
A |
16: 19,765,887 (GRCm39) |
A572S |
probably benign |
Het |
Ldhc |
C |
T |
7: 46,519,112 (GRCm39) |
R112C |
probably damaging |
Het |
Lrrc56 |
T |
C |
7: 140,779,685 (GRCm39) |
|
probably benign |
Het |
Mdh2 |
A |
G |
5: 135,818,567 (GRCm39) |
E274G |
probably damaging |
Het |
N4bp1 |
G |
T |
8: 87,575,161 (GRCm39) |
D711E |
probably benign |
Het |
Ngly1 |
T |
A |
14: 16,281,866 (GRCm38) |
I248K |
probably damaging |
Het |
Or2ab1 |
A |
G |
11: 58,489,149 (GRCm39) |
N309S |
probably damaging |
Het |
Or7e176 |
T |
C |
9: 20,171,556 (GRCm39) |
I140T |
probably damaging |
Het |
Pbrm1 |
A |
G |
14: 30,829,241 (GRCm39) |
E1421G |
probably damaging |
Het |
Pcca |
G |
A |
14: 122,822,518 (GRCm39) |
R112H |
possibly damaging |
Het |
Pgrmc2 |
T |
C |
3: 41,023,061 (GRCm39) |
|
probably benign |
Het |
Podnl1 |
G |
A |
8: 84,858,818 (GRCm39) |
V548I |
probably benign |
Het |
Pogz |
A |
T |
3: 94,782,402 (GRCm39) |
|
probably benign |
Het |
Ppp1r3a |
A |
G |
6: 14,754,771 (GRCm39) |
Y159H |
probably damaging |
Het |
Rax |
T |
C |
18: 66,071,231 (GRCm39) |
K135E |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,420,264 (GRCm39) |
S283P |
probably damaging |
Het |
Rpusd4 |
T |
C |
9: 35,179,273 (GRCm39) |
S30P |
probably benign |
Het |
Samd13 |
T |
C |
3: 146,352,070 (GRCm39) |
T75A |
probably benign |
Het |
Sfxn4 |
A |
G |
19: 60,848,508 (GRCm39) |
W22R |
probably damaging |
Het |
Sh3pxd2a |
T |
A |
19: 47,412,955 (GRCm39) |
R43W |
probably damaging |
Het |
Smc5 |
A |
G |
19: 23,251,022 (GRCm39) |
V54A |
probably benign |
Het |
Snap47 |
A |
G |
11: 59,319,424 (GRCm39) |
I238T |
probably damaging |
Het |
Tecpr2 |
T |
G |
12: 110,934,267 (GRCm39) |
I1309S |
possibly damaging |
Het |
Trappc8 |
A |
G |
18: 20,953,992 (GRCm39) |
L1310P |
probably damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,915,408 (GRCm39) |
H118Q |
probably benign |
Het |
Zbtb17 |
C |
T |
4: 141,194,244 (GRCm39) |
T731I |
probably damaging |
Het |
Zfp287 |
A |
G |
11: 62,606,062 (GRCm39) |
F282L |
probably damaging |
Het |
|
Other mutations in Rbm7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01088:Rbm7
|
APN |
9 |
48,402,149 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Rbm7
|
APN |
9 |
48,405,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R1432:Rbm7
|
UTSW |
9 |
48,401,245 (GRCm39) |
missense |
probably benign |
0.07 |
R1480:Rbm7
|
UTSW |
9 |
48,401,016 (GRCm39) |
missense |
probably benign |
|
R1681:Rbm7
|
UTSW |
9 |
48,401,021 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1848:Rbm7
|
UTSW |
9 |
48,402,194 (GRCm39) |
missense |
probably benign |
0.08 |
R4790:Rbm7
|
UTSW |
9 |
48,406,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R8677:Rbm7
|
UTSW |
9 |
48,401,273 (GRCm39) |
nonsense |
probably null |
|
R9341:Rbm7
|
UTSW |
9 |
48,400,969 (GRCm39) |
missense |
probably damaging |
0.97 |
R9343:Rbm7
|
UTSW |
9 |
48,400,969 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Rbm7
|
UTSW |
9 |
48,401,195 (GRCm39) |
missense |
probably damaging |
0.97 |
|