Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
T |
A |
9: 57,164,468 (GRCm39) |
K635N |
probably damaging |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,992,705 (GRCm39) |
M4663K |
possibly damaging |
Het |
C4b |
T |
A |
17: 34,960,212 (GRCm39) |
T280S |
probably benign |
Het |
Ccdc166 |
A |
G |
15: 75,852,869 (GRCm39) |
V366A |
probably benign |
Het |
Cdh23 |
A |
G |
10: 60,493,044 (GRCm39) |
|
probably null |
Het |
Col7a1 |
A |
G |
9: 108,792,292 (GRCm39) |
T1281A |
unknown |
Het |
Cul9 |
TTCCTCCTCCTCCTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCCTC |
17: 46,811,775 (GRCm39) |
|
probably benign |
Het |
Dbndd1 |
T |
A |
8: 124,233,484 (GRCm39) |
D127V |
probably damaging |
Het |
Ddx20 |
T |
A |
3: 105,590,825 (GRCm39) |
E197V |
probably damaging |
Het |
Dennd10 |
A |
G |
19: 60,814,324 (GRCm39) |
M96V |
probably benign |
Het |
Dnm3 |
A |
G |
1: 161,838,471 (GRCm39) |
S826P |
probably damaging |
Het |
Dnmt3a |
T |
C |
12: 3,945,643 (GRCm39) |
V24A |
probably benign |
Het |
Dop1b |
C |
A |
16: 93,567,392 (GRCm39) |
A1273E |
probably damaging |
Het |
Dsg1c |
T |
C |
18: 20,416,703 (GRCm39) |
V868A |
possibly damaging |
Het |
Dtx4 |
A |
G |
19: 12,462,626 (GRCm39) |
|
probably null |
Het |
Fbxo40 |
T |
A |
16: 36,789,914 (GRCm39) |
T399S |
possibly damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Gm14399 |
T |
C |
2: 174,973,371 (GRCm39) |
E96G |
probably damaging |
Het |
Gm14496 |
T |
G |
2: 181,642,147 (GRCm39) |
V606G |
probably benign |
Het |
Gpr156 |
A |
G |
16: 37,826,087 (GRCm39) |
E768G |
probably damaging |
Het |
Grm5 |
A |
T |
7: 87,723,704 (GRCm39) |
T665S |
probably damaging |
Het |
Hsdl2 |
A |
G |
4: 59,592,301 (GRCm39) |
|
probably benign |
Het |
Htt |
T |
C |
5: 35,064,928 (GRCm39) |
V3047A |
possibly damaging |
Het |
Igkv3-2 |
A |
T |
6: 70,676,011 (GRCm39) |
T107S |
probably benign |
Het |
Insyn2b |
G |
A |
11: 34,352,788 (GRCm39) |
E277K |
probably damaging |
Het |
Itih2 |
T |
A |
2: 10,101,272 (GRCm39) |
T899S |
probably benign |
Het |
Lhcgr |
T |
A |
17: 89,050,281 (GRCm39) |
Y415F |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Med4 |
C |
A |
14: 73,747,553 (GRCm39) |
S18* |
probably null |
Het |
Nefl |
T |
C |
14: 68,322,088 (GRCm39) |
V226A |
probably damaging |
Het |
Nploc4 |
T |
A |
11: 120,275,389 (GRCm39) |
N516Y |
probably damaging |
Het |
Or1o4 |
A |
G |
17: 37,590,501 (GRCm39) |
V270A |
probably benign |
Het |
Or6c66 |
A |
T |
10: 129,461,601 (GRCm39) |
F110I |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pcdha3 |
T |
G |
18: 37,079,752 (GRCm39) |
L165V |
possibly damaging |
Het |
Pcdhb12 |
T |
A |
18: 37,570,099 (GRCm39) |
V415D |
probably damaging |
Het |
Pcdhga10 |
T |
C |
18: 37,880,503 (GRCm39) |
I88T |
probably damaging |
Het |
Pigyl |
T |
A |
9: 22,069,292 (GRCm39) |
M1K |
probably null |
Het |
Prr27 |
T |
C |
5: 87,991,203 (GRCm39) |
S272P |
probably damaging |
Het |
Prss3 |
C |
T |
6: 41,350,780 (GRCm39) |
D237N |
probably benign |
Het |
Pstpip2 |
A |
G |
18: 77,958,078 (GRCm39) |
D150G |
probably damaging |
Het |
Robo4 |
T |
A |
9: 37,324,674 (GRCm39) |
D909E |
probably benign |
Het |
Serpinb3c |
A |
T |
1: 107,204,661 (GRCm39) |
Y28* |
probably null |
Het |
Slc26a3 |
T |
C |
12: 31,500,980 (GRCm39) |
|
probably null |
Het |
Slc6a1 |
A |
T |
6: 114,279,493 (GRCm39) |
I91F |
probably benign |
Het |
Smcr8 |
T |
G |
11: 60,669,118 (GRCm39) |
Y89D |
probably damaging |
Het |
Sspo |
T |
A |
6: 48,443,247 (GRCm39) |
M1898K |
probably benign |
Het |
Tbl1xr1 |
T |
A |
3: 22,246,233 (GRCm39) |
I251K |
probably damaging |
Het |
Thbs4 |
C |
T |
13: 92,913,501 (GRCm39) |
D140N |
probably benign |
Het |
Tmbim6 |
G |
A |
15: 99,303,633 (GRCm39) |
A108T |
probably benign |
Het |
Trim10 |
T |
G |
17: 37,186,328 (GRCm39) |
L301R |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,671,161 (GRCm39) |
I607N |
possibly damaging |
Het |
Vmn2r9 |
T |
A |
5: 108,995,929 (GRCm39) |
I240F |
probably damaging |
Het |
Xpot |
T |
A |
10: 121,436,765 (GRCm39) |
I873F |
possibly damaging |
Het |
Zfhx4 |
G |
A |
3: 5,464,267 (GRCm39) |
S1475N |
probably damaging |
Het |
Zfp712 |
A |
G |
13: 67,189,079 (GRCm39) |
S483P |
possibly damaging |
Het |
Zswim7 |
A |
T |
11: 62,158,373 (GRCm39) |
H122Q |
probably benign |
Het |
|
Other mutations in Elovl4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
hershey
|
UTSW |
9 |
83,688,091 (GRCm39) |
start codon destroyed |
probably null |
0.31 |
R0278:Elovl4
|
UTSW |
9 |
83,665,248 (GRCm39) |
missense |
probably benign |
0.00 |
R0563:Elovl4
|
UTSW |
9 |
83,667,087 (GRCm39) |
critical splice donor site |
probably null |
|
R0739:Elovl4
|
UTSW |
9 |
83,667,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R0771:Elovl4
|
UTSW |
9 |
83,667,168 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1970:Elovl4
|
UTSW |
9 |
83,662,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R2316:Elovl4
|
UTSW |
9 |
83,662,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R3777:Elovl4
|
UTSW |
9 |
83,667,201 (GRCm39) |
frame shift |
probably null |
|
R3779:Elovl4
|
UTSW |
9 |
83,667,201 (GRCm39) |
frame shift |
probably null |
|
R4823:Elovl4
|
UTSW |
9 |
83,662,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Elovl4
|
UTSW |
9 |
83,688,091 (GRCm39) |
start codon destroyed |
probably null |
0.31 |
R5264:Elovl4
|
UTSW |
9 |
83,662,817 (GRCm39) |
missense |
probably benign |
0.19 |
R5275:Elovl4
|
UTSW |
9 |
83,662,714 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5295:Elovl4
|
UTSW |
9 |
83,662,714 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5364:Elovl4
|
UTSW |
9 |
83,672,076 (GRCm39) |
missense |
probably benign |
0.21 |
R5897:Elovl4
|
UTSW |
9 |
83,672,157 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6433:Elovl4
|
UTSW |
9 |
83,667,231 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6668:Elovl4
|
UTSW |
9 |
83,688,039 (GRCm39) |
missense |
probably benign |
0.02 |
R6844:Elovl4
|
UTSW |
9 |
83,672,164 (GRCm39) |
missense |
probably benign |
0.09 |
R6897:Elovl4
|
UTSW |
9 |
83,665,278 (GRCm39) |
missense |
probably benign |
0.05 |
R6933:Elovl4
|
UTSW |
9 |
83,667,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7534:Elovl4
|
UTSW |
9 |
83,672,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R7544:Elovl4
|
UTSW |
9 |
83,665,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Elovl4
|
UTSW |
9 |
83,670,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R8303:Elovl4
|
UTSW |
9 |
83,670,320 (GRCm39) |
critical splice donor site |
probably null |
|
|