Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
T |
C |
5: 114,333,315 (GRCm39) |
F480L |
probably damaging |
Het |
Actr6 |
A |
T |
10: 89,553,057 (GRCm39) |
I267N |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,737,380 (GRCm39) |
S2835P |
unknown |
Het |
Arfgef3 |
C |
T |
10: 18,511,453 (GRCm39) |
R753Q |
probably benign |
Het |
Arid3a |
A |
G |
10: 79,784,765 (GRCm39) |
T285A |
probably benign |
Het |
Atad5 |
T |
C |
11: 79,986,473 (GRCm39) |
V520A |
probably benign |
Het |
Atoh1 |
T |
G |
6: 64,707,241 (GRCm39) |
L312R |
probably damaging |
Het |
Brd10 |
T |
C |
19: 29,696,841 (GRCm39) |
K884R |
possibly damaging |
Het |
Cpt1a |
T |
C |
19: 3,408,258 (GRCm39) |
V179A |
|
Het |
Crocc2 |
C |
A |
1: 93,129,144 (GRCm39) |
N816K |
possibly damaging |
Het |
Csf2ra |
A |
T |
19: 61,214,721 (GRCm39) |
V201D |
probably damaging |
Het |
Dok1 |
C |
T |
6: 83,008,324 (GRCm39) |
V453I |
probably benign |
Het |
Erh |
G |
T |
12: 80,684,282 (GRCm39) |
A65E |
probably benign |
Het |
Etl4 |
G |
A |
2: 20,748,733 (GRCm39) |
S357N |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,811,246 (GRCm39) |
T1478A |
probably benign |
Het |
Gabra1 |
A |
G |
11: 42,026,320 (GRCm39) |
F324S |
probably damaging |
Het |
Gm11437 |
T |
C |
11: 84,043,530 (GRCm39) |
T254A |
probably benign |
Het |
Gria2 |
T |
C |
3: 80,599,706 (GRCm39) |
E726G |
probably damaging |
Het |
Gstm2 |
A |
T |
3: 107,892,382 (GRCm39) |
C115S |
possibly damaging |
Het |
Ighv1-12 |
T |
C |
12: 114,579,553 (GRCm39) |
T90A |
probably damaging |
Het |
Inf2 |
A |
G |
12: 112,572,703 (GRCm39) |
I690V |
unknown |
Het |
Kdm3b |
A |
G |
18: 34,970,650 (GRCm39) |
N1739S |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,615,893 (GRCm39) |
N3614K |
|
Het |
Mapk8ip3 |
A |
G |
17: 25,131,727 (GRCm39) |
L404P |
probably damaging |
Het |
Mcl1 |
T |
C |
3: 95,567,192 (GRCm39) |
F251S |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,744,579 (GRCm39) |
L4038* |
probably null |
Het |
Mmp8 |
T |
C |
9: 7,561,485 (GRCm39) |
V163A |
probably benign |
Het |
Myo18b |
C |
T |
5: 113,022,873 (GRCm39) |
|
probably benign |
Het |
Ndst1 |
C |
T |
18: 60,825,083 (GRCm39) |
R745H |
probably benign |
Het |
Or4d2b |
A |
G |
11: 87,780,284 (GRCm39) |
V146A |
probably benign |
Het |
Or8c18 |
T |
C |
9: 38,203,385 (GRCm39) |
F48S |
probably benign |
Het |
Pard3 |
C |
T |
8: 128,098,011 (GRCm39) |
R351C |
probably benign |
Het |
Pcdhgb4 |
A |
G |
18: 37,855,648 (GRCm39) |
D681G |
probably damaging |
Het |
Pde10a |
G |
A |
17: 9,160,063 (GRCm39) |
A163T |
possibly damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pelp1 |
A |
G |
11: 70,296,505 (GRCm39) |
L123S |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,906,621 (GRCm39) |
D1152G |
possibly damaging |
Het |
Rag1 |
T |
C |
2: 101,472,098 (GRCm39) |
T1015A |
probably benign |
Het |
Rock2 |
C |
T |
12: 16,990,422 (GRCm39) |
Q115* |
probably null |
Het |
Rorb |
T |
A |
19: 18,915,356 (GRCm39) |
H434L |
probably damaging |
Het |
Safb2 |
A |
T |
17: 56,882,975 (GRCm39) |
C219* |
probably null |
Het |
Sema3a |
A |
G |
5: 13,573,099 (GRCm39) |
H209R |
probably damaging |
Het |
Serpinb9g |
T |
G |
13: 33,679,131 (GRCm39) |
S334A |
probably benign |
Het |
Slc5a9 |
T |
A |
4: 111,741,147 (GRCm39) |
M500L |
probably benign |
Het |
Snap91 |
A |
G |
9: 86,651,611 (GRCm39) |
S810P |
unknown |
Het |
Spink5 |
G |
T |
18: 44,100,087 (GRCm39) |
A35S |
probably damaging |
Het |
Stxbp5l |
G |
A |
16: 36,954,892 (GRCm39) |
T887I |
|
Het |
Tacc2 |
T |
C |
7: 130,227,823 (GRCm39) |
F1503L |
probably benign |
Het |
Tectb |
A |
G |
19: 55,180,000 (GRCm39) |
E272G |
probably damaging |
Het |
Trdn |
A |
T |
10: 33,015,117 (GRCm39) |
I24F |
probably benign |
Het |
Tshr |
G |
A |
12: 91,504,211 (GRCm39) |
S383N |
probably benign |
Het |
Tspan1 |
C |
A |
4: 116,020,970 (GRCm39) |
C149F |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,570,862 (GRCm39) |
L26677Q |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,270,017 (GRCm39) |
F1755I |
possibly damaging |
Het |
Vps13d |
T |
A |
4: 144,772,873 (GRCm39) |
I4047F |
|
Het |
Zfp1010 |
A |
C |
2: 176,958,551 (GRCm39) |
S29R |
probably benign |
Het |
Zfp369 |
T |
A |
13: 65,443,529 (GRCm39) |
L336* |
probably null |
Het |
Zfp518a |
A |
C |
19: 40,901,870 (GRCm39) |
K600Q |
possibly damaging |
Het |
Zfp984 |
T |
C |
4: 147,840,623 (GRCm39) |
H76R |
possibly damaging |
Het |
Zscan10 |
G |
A |
17: 23,826,116 (GRCm39) |
G138S |
probably benign |
Het |
|
Other mutations in Elp4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00648:Elp4
|
APN |
2 |
105,672,711 (GRCm39) |
splice site |
probably benign |
|
IGL01407:Elp4
|
APN |
2 |
105,622,653 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02173:Elp4
|
APN |
2 |
105,533,088 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02370:Elp4
|
APN |
2 |
105,624,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Elp4
|
UTSW |
2 |
105,622,559 (GRCm39) |
critical splice donor site |
probably null |
|
R0685:Elp4
|
UTSW |
2 |
105,622,622 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0893:Elp4
|
UTSW |
2 |
105,727,290 (GRCm39) |
splice site |
probably benign |
|
R1117:Elp4
|
UTSW |
2 |
105,672,656 (GRCm39) |
missense |
probably benign |
0.00 |
R1496:Elp4
|
UTSW |
2 |
105,662,506 (GRCm39) |
missense |
probably benign |
0.31 |
R1542:Elp4
|
UTSW |
2 |
105,624,954 (GRCm39) |
missense |
probably benign |
0.02 |
R1911:Elp4
|
UTSW |
2 |
105,533,088 (GRCm39) |
missense |
probably damaging |
0.96 |
R2311:Elp4
|
UTSW |
2 |
105,672,677 (GRCm39) |
missense |
probably benign |
0.00 |
R2997:Elp4
|
UTSW |
2 |
105,644,661 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3079:Elp4
|
UTSW |
2 |
105,639,790 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3683:Elp4
|
UTSW |
2 |
105,533,106 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4747:Elp4
|
UTSW |
2 |
105,624,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Elp4
|
UTSW |
2 |
105,639,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R5438:Elp4
|
UTSW |
2 |
105,734,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Elp4
|
UTSW |
2 |
105,644,609 (GRCm39) |
critical splice donor site |
probably null |
|
R6414:Elp4
|
UTSW |
2 |
105,734,788 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7228:Elp4
|
UTSW |
2 |
105,622,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Elp4
|
UTSW |
2 |
105,622,652 (GRCm39) |
missense |
not run |
|
R7560:Elp4
|
UTSW |
2 |
105,624,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7671:Elp4
|
UTSW |
2 |
105,734,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R8376:Elp4
|
UTSW |
2 |
105,672,653 (GRCm39) |
missense |
probably benign |
0.00 |
R9170:Elp4
|
UTSW |
2 |
105,624,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R9761:Elp4
|
UTSW |
2 |
105,624,904 (GRCm39) |
missense |
probably damaging |
0.99 |
|