Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34 |
T |
G |
8: 44,104,208 (GRCm39) |
N479T |
probably damaging |
Het |
Add3 |
C |
G |
19: 53,227,892 (GRCm39) |
L526V |
probably damaging |
Het |
Alas1 |
T |
C |
9: 106,124,150 (GRCm39) |
T3A |
probably benign |
Het |
Arap3 |
C |
T |
18: 38,122,520 (GRCm39) |
D579N |
probably damaging |
Het |
Armc6 |
C |
A |
8: 70,675,248 (GRCm39) |
D326Y |
probably damaging |
Het |
Atp6v1e2 |
G |
A |
17: 87,251,813 (GRCm39) |
T195I |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,690,504 (GRCm39) |
E904G |
probably damaging |
Het |
Bhlhe40 |
T |
A |
6: 108,639,559 (GRCm39) |
D112E |
probably benign |
Het |
Brf1 |
T |
G |
12: 112,927,865 (GRCm39) |
K438T |
probably benign |
Het |
Cabs1 |
A |
T |
5: 88,128,145 (GRCm39) |
E265D |
probably damaging |
Het |
Ccdc162 |
T |
A |
10: 41,429,071 (GRCm39) |
M1937L |
probably benign |
Het |
Cd55b |
A |
T |
1: 130,339,230 (GRCm39) |
S299R |
possibly damaging |
Het |
Chordc1 |
A |
G |
9: 18,213,510 (GRCm39) |
*120W |
probably null |
Het |
Col17a1 |
C |
A |
19: 47,643,629 (GRCm39) |
|
probably null |
Het |
Cpne8 |
A |
T |
15: 90,385,621 (GRCm39) |
I469K |
possibly damaging |
Het |
Crtac1 |
G |
T |
19: 42,290,690 (GRCm39) |
S337* |
probably null |
Het |
Cx3cl1 |
T |
C |
8: 95,506,867 (GRCm39) |
S291P |
probably damaging |
Het |
Dhx36 |
G |
T |
3: 62,396,389 (GRCm39) |
Q423K |
probably benign |
Het |
Eif3h |
G |
T |
15: 51,650,219 (GRCm39) |
Q322K |
possibly damaging |
Het |
Exph5 |
G |
A |
9: 53,284,475 (GRCm39) |
V519I |
possibly damaging |
Het |
Fam184a |
C |
A |
10: 53,509,802 (GRCm39) |
E126* |
probably null |
Het |
Fam222b |
A |
G |
11: 78,044,577 (GRCm39) |
D46G |
probably damaging |
Het |
Fbxl6 |
C |
A |
15: 76,420,086 (GRCm39) |
R509L |
probably damaging |
Het |
Fgf14 |
T |
C |
14: 124,373,656 (GRCm39) |
Y86C |
probably damaging |
Het |
Fras1 |
A |
T |
5: 96,860,310 (GRCm39) |
I2119F |
probably benign |
Het |
Gpr37 |
G |
A |
6: 25,669,116 (GRCm39) |
T576I |
possibly damaging |
Het |
Hnrnpul2 |
G |
T |
19: 8,808,644 (GRCm39) |
R702L |
possibly damaging |
Het |
Iqgap1 |
T |
C |
7: 80,407,204 (GRCm39) |
N342S |
probably benign |
Het |
Kcnh6 |
T |
C |
11: 105,908,401 (GRCm39) |
V339A |
probably benign |
Het |
Klk1b9 |
A |
T |
7: 43,627,840 (GRCm39) |
N46I |
possibly damaging |
Het |
Kndc1 |
C |
A |
7: 139,519,751 (GRCm39) |
S1703R |
possibly damaging |
Het |
Lyn |
C |
A |
4: 3,756,428 (GRCm39) |
Y306* |
probably null |
Het |
Manba |
C |
T |
3: 135,223,770 (GRCm39) |
T219M |
probably benign |
Het |
Mastl |
T |
C |
2: 23,030,807 (GRCm39) |
|
probably null |
Het |
Med15 |
T |
G |
16: 17,473,038 (GRCm39) |
M550L |
possibly damaging |
Het |
Men1 |
G |
A |
19: 6,387,312 (GRCm39) |
|
probably null |
Het |
Msh4 |
C |
T |
3: 153,571,957 (GRCm39) |
|
probably null |
Het |
Myh6 |
G |
T |
14: 55,202,822 (GRCm39) |
D32E |
probably damaging |
Het |
Ntmt2 |
A |
G |
1: 163,530,753 (GRCm39) |
C229R |
probably benign |
Het |
Ntn4 |
A |
G |
10: 93,569,544 (GRCm39) |
D419G |
possibly damaging |
Het |
Nup155 |
C |
T |
15: 8,151,623 (GRCm39) |
P393S |
probably damaging |
Het |
Or2y1d |
T |
A |
11: 49,321,727 (GRCm39) |
C141* |
probably null |
Het |
Or6b2b |
A |
T |
1: 92,419,029 (GRCm39) |
F149L |
probably benign |
Het |
Pakap |
C |
T |
4: 57,709,876 (GRCm39) |
P274S |
probably damaging |
Het |
Papss2 |
A |
T |
19: 32,611,403 (GRCm39) |
|
probably null |
Het |
Pcdhgc3 |
T |
C |
18: 37,939,932 (GRCm39) |
V111A |
possibly damaging |
Het |
Pcnx2 |
C |
T |
8: 126,577,069 (GRCm39) |
V988I |
probably benign |
Het |
Pom121 |
C |
T |
5: 135,407,002 (GRCm39) |
G1178S |
probably damaging |
Het |
Prss33 |
A |
G |
17: 24,053,203 (GRCm39) |
C213R |
probably damaging |
Het |
Scap |
G |
A |
9: 110,207,435 (GRCm39) |
|
probably null |
Het |
Shfl |
T |
C |
9: 20,784,461 (GRCm39) |
Y182H |
possibly damaging |
Het |
Sirpb1c |
T |
A |
3: 15,902,550 (GRCm39) |
I10F |
possibly damaging |
Het |
Slc28a2b |
A |
G |
2: 122,317,214 (GRCm39) |
E25G |
probably damaging |
Het |
Spata31e2 |
C |
A |
1: 26,723,579 (GRCm39) |
A534S |
probably benign |
Het |
Spink5 |
T |
C |
18: 44,096,419 (GRCm39) |
L16P |
probably damaging |
Het |
Sting1 |
C |
T |
18: 35,868,318 (GRCm39) |
A261T |
probably damaging |
Het |
Stk4 |
T |
G |
2: 163,952,146 (GRCm39) |
M1R |
probably null |
Het |
Stub1 |
A |
T |
17: 26,050,106 (GRCm39) |
Y253* |
probably null |
Het |
Tasor |
C |
A |
14: 27,169,454 (GRCm39) |
N338K |
probably damaging |
Het |
Tbce |
A |
G |
13: 14,203,875 (GRCm39) |
V29A |
probably damaging |
Het |
Tchhl1 |
A |
G |
3: 93,379,065 (GRCm39) |
R590G |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,186,231 (GRCm39) |
P613L |
unknown |
Het |
Vmn2r3 |
G |
T |
3: 64,182,939 (GRCm39) |
C253* |
probably null |
Het |
Wfdc8 |
C |
A |
2: 164,441,906 (GRCm39) |
E215D |
possibly damaging |
Het |
Zfp874b |
T |
C |
13: 67,621,975 (GRCm39) |
D441G |
probably benign |
Het |
Zscan4d |
G |
T |
7: 10,899,169 (GRCm39) |
P36Q |
possibly damaging |
Het |
|
Other mutations in Ero1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01015:Ero1b
|
APN |
13 |
12,616,623 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02738:Ero1b
|
APN |
13 |
12,619,322 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03033:Ero1b
|
APN |
13 |
12,596,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Ero1b
|
UTSW |
13 |
12,589,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R0801:Ero1b
|
UTSW |
13 |
12,596,568 (GRCm39) |
missense |
probably benign |
0.10 |
R1665:Ero1b
|
UTSW |
13 |
12,594,142 (GRCm39) |
critical splice donor site |
probably null |
|
R1851:Ero1b
|
UTSW |
13 |
12,619,292 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1928:Ero1b
|
UTSW |
13 |
12,616,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:Ero1b
|
UTSW |
13 |
12,615,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R3719:Ero1b
|
UTSW |
13 |
12,598,493 (GRCm39) |
critical splice donor site |
probably null |
|
R4873:Ero1b
|
UTSW |
13 |
12,619,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R4875:Ero1b
|
UTSW |
13 |
12,619,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R5053:Ero1b
|
UTSW |
13 |
12,614,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R5338:Ero1b
|
UTSW |
13 |
12,589,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5415:Ero1b
|
UTSW |
13 |
12,616,656 (GRCm39) |
missense |
probably benign |
0.02 |
R5800:Ero1b
|
UTSW |
13 |
12,617,190 (GRCm39) |
splice site |
probably null |
|
R5907:Ero1b
|
UTSW |
13 |
12,615,207 (GRCm39) |
missense |
probably damaging |
0.98 |
R5909:Ero1b
|
UTSW |
13 |
12,594,139 (GRCm39) |
missense |
probably benign |
0.18 |
R6029:Ero1b
|
UTSW |
13 |
12,589,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R7234:Ero1b
|
UTSW |
13 |
12,615,203 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7331:Ero1b
|
UTSW |
13 |
12,615,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7577:Ero1b
|
UTSW |
13 |
12,617,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R8477:Ero1b
|
UTSW |
13 |
12,616,672 (GRCm39) |
missense |
probably benign |
0.02 |
R8528:Ero1b
|
UTSW |
13 |
12,614,757 (GRCm39) |
nonsense |
probably null |
|
R9371:Ero1b
|
UTSW |
13 |
12,589,728 (GRCm39) |
missense |
probably damaging |
1.00 |
|