Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ate1 |
A |
G |
7: 130,106,495 (GRCm39) |
S282P |
probably damaging |
Het |
Cacna1d |
T |
A |
14: 29,788,040 (GRCm39) |
Q1610L |
probably damaging |
Het |
Carmil2 |
C |
A |
8: 106,422,039 (GRCm39) |
R1103S |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,460,994 (GRCm39) |
Y219F |
probably benign |
Het |
Creb3l3 |
A |
G |
10: 80,925,172 (GRCm39) |
V224A |
probably benign |
Het |
Crnkl1 |
T |
A |
2: 145,774,247 (GRCm39) |
D72V |
possibly damaging |
Het |
Dhcr24 |
T |
C |
4: 106,431,075 (GRCm39) |
F255L |
probably benign |
Het |
Eef2kmt |
A |
T |
16: 5,063,135 (GRCm39) |
V335D |
probably damaging |
Het |
Elp2 |
T |
A |
18: 24,767,405 (GRCm39) |
W696R |
probably damaging |
Het |
Glb1l3 |
A |
C |
9: 26,740,343 (GRCm39) |
M329R |
probably damaging |
Het |
Gm4787 |
A |
T |
12: 81,425,132 (GRCm39) |
F342Y |
probably damaging |
Het |
Gpr137c |
C |
A |
14: 45,457,687 (GRCm39) |
L80I |
probably damaging |
Het |
Gpr83 |
A |
G |
9: 14,772,073 (GRCm39) |
I82V |
possibly damaging |
Het |
Greb1l |
C |
T |
18: 10,515,209 (GRCm39) |
T558I |
possibly damaging |
Het |
Hnrnpul2 |
T |
A |
19: 8,800,591 (GRCm39) |
|
probably benign |
Het |
Hspa2 |
T |
C |
12: 76,452,542 (GRCm39) |
V412A |
probably damaging |
Het |
Iqcd |
T |
C |
5: 120,740,587 (GRCm39) |
V306A |
probably damaging |
Het |
Lmod3 |
T |
C |
6: 97,225,275 (GRCm39) |
N182S |
probably benign |
Het |
Metrn |
T |
C |
17: 26,013,984 (GRCm39) |
T281A |
probably benign |
Het |
Mid1-ps1 |
G |
A |
Y: 90,773,563 (GRCm39) |
|
noncoding transcript |
Het |
Mmachc |
T |
A |
4: 116,563,215 (GRCm39) |
T47S |
probably damaging |
Het |
Nfia |
C |
A |
4: 97,909,074 (GRCm39) |
R277S |
probably damaging |
Het |
Or9m2 |
T |
A |
2: 87,821,262 (GRCm39) |
I269N |
possibly damaging |
Het |
Pcdha8 |
T |
C |
18: 37,125,914 (GRCm39) |
M132T |
probably benign |
Het |
Prkaa2 |
T |
C |
4: 104,908,444 (GRCm39) |
N144D |
probably damaging |
Het |
Ptprf |
C |
T |
4: 118,114,805 (GRCm39) |
R150H |
probably damaging |
Het |
Sfmbt1 |
T |
G |
14: 30,509,449 (GRCm39) |
D309E |
probably damaging |
Het |
Skint5 |
G |
T |
4: 113,743,011 (GRCm39) |
T352K |
unknown |
Het |
Slc16a10 |
G |
C |
10: 39,932,620 (GRCm39) |
H314D |
possibly damaging |
Het |
Slc28a2 |
C |
A |
2: 122,284,996 (GRCm39) |
A328E |
probably benign |
Het |
Ssc4d |
C |
A |
5: 135,999,170 (GRCm39) |
W11L |
possibly damaging |
Het |
Sycp2 |
C |
A |
2: 178,022,720 (GRCm39) |
M470I |
possibly damaging |
Het |
Tfap2c |
A |
T |
2: 172,398,110 (GRCm39) |
S413C |
probably damaging |
Het |
Unc13c |
A |
G |
9: 73,441,188 (GRCm39) |
|
probably null |
Het |
Vmn1r218 |
T |
C |
13: 23,320,971 (GRCm39) |
V26A |
possibly damaging |
Het |
Wipf3 |
G |
A |
6: 54,458,813 (GRCm39) |
G56D |
probably damaging |
Het |
Wiz |
T |
C |
17: 32,578,198 (GRCm39) |
E429G |
probably damaging |
Het |
Zer1 |
T |
C |
2: 29,997,535 (GRCm39) |
N457S |
probably damaging |
Het |
|
Other mutations in Zfp931 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02980:Zfp931
|
APN |
2 |
177,711,409 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1391:Zfp931
|
UTSW |
2 |
177,709,984 (GRCm39) |
missense |
probably benign |
0.01 |
R1907:Zfp931
|
UTSW |
2 |
177,711,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Zfp931
|
UTSW |
2 |
177,711,651 (GRCm39) |
missense |
probably null |
1.00 |
R2283:Zfp931
|
UTSW |
2 |
177,711,714 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4039:Zfp931
|
UTSW |
2 |
177,709,777 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4867:Zfp931
|
UTSW |
2 |
177,709,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Zfp931
|
UTSW |
2 |
177,709,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R5593:Zfp931
|
UTSW |
2 |
177,709,595 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7295:Zfp931
|
UTSW |
2 |
177,709,824 (GRCm39) |
nonsense |
probably null |
|
R8050:Zfp931
|
UTSW |
2 |
177,709,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Zfp931
|
UTSW |
2 |
177,709,709 (GRCm39) |
missense |
probably benign |
0.00 |
R8432:Zfp931
|
UTSW |
2 |
177,711,346 (GRCm39) |
makesense |
probably null |
|
R8806:Zfp931
|
UTSW |
2 |
177,709,589 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8866:Zfp931
|
UTSW |
2 |
177,710,178 (GRCm39) |
nonsense |
probably null |
|
R8987:Zfp931
|
UTSW |
2 |
177,709,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Zfp931
|
UTSW |
2 |
177,709,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Zfp931
|
UTSW |
2 |
177,709,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R9538:Zfp931
|
UTSW |
2 |
177,709,605 (GRCm39) |
missense |
probably benign |
0.04 |
|