Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810408A11Rik |
A |
G |
11: 69,789,207 (GRCm39) |
S331P |
possibly damaging |
Het |
4930433I11Rik |
A |
G |
7: 40,644,226 (GRCm39) |
M632V |
probably benign |
Het |
9930111J21Rik2 |
A |
C |
11: 48,910,507 (GRCm39) |
V642G |
probably damaging |
Het |
Abcd4 |
A |
T |
12: 84,651,171 (GRCm39) |
|
probably benign |
Het |
Acsbg1 |
T |
C |
9: 54,525,462 (GRCm39) |
E363G |
probably damaging |
Het |
Ank3 |
T |
A |
10: 69,823,084 (GRCm39) |
H584Q |
|
Het |
Ankrd11 |
A |
T |
8: 123,620,765 (GRCm39) |
L1029Q |
possibly damaging |
Het |
Anpep |
C |
T |
7: 79,490,641 (GRCm39) |
V292I |
probably benign |
Het |
Atmin |
G |
A |
8: 117,681,525 (GRCm39) |
D175N |
possibly damaging |
Het |
B4galt6 |
T |
C |
18: 20,821,450 (GRCm39) |
I359M |
possibly damaging |
Het |
Bicd2 |
A |
G |
13: 49,532,905 (GRCm39) |
D497G |
probably damaging |
Het |
Calcr |
C |
T |
6: 3,707,489 (GRCm39) |
|
probably benign |
Het |
Camkk2 |
G |
T |
5: 122,882,002 (GRCm39) |
D418E |
probably benign |
Het |
Cntn3 |
A |
T |
6: 102,146,014 (GRCm39) |
Y942* |
probably null |
Het |
Col8a1 |
C |
T |
16: 57,449,138 (GRCm39) |
R124H |
probably damaging |
Het |
Coro7 |
T |
C |
16: 4,486,619 (GRCm39) |
T185A |
possibly damaging |
Het |
Creb3 |
C |
T |
4: 43,566,747 (GRCm39) |
P364S |
probably benign |
Het |
Csf1r |
A |
T |
18: 61,250,728 (GRCm39) |
T480S |
probably benign |
Het |
Csnk1g1 |
T |
A |
9: 65,909,553 (GRCm39) |
H223Q |
probably damaging |
Het |
Ctns |
C |
T |
11: 73,078,613 (GRCm39) |
V171M |
probably benign |
Het |
Dhx15 |
A |
T |
5: 52,311,568 (GRCm39) |
N637K |
probably benign |
Het |
Eif4g1 |
T |
C |
16: 20,494,232 (GRCm39) |
Y103H |
probably damaging |
Het |
Eif4g2 |
C |
T |
7: 110,676,629 (GRCm39) |
R295H |
probably damaging |
Het |
Fat1 |
C |
T |
8: 45,477,206 (GRCm39) |
P2084L |
probably benign |
Het |
Fat4 |
A |
G |
3: 39,064,647 (GRCm39) |
R4868G |
probably damaging |
Het |
Fbxo31 |
A |
T |
8: 122,282,014 (GRCm39) |
Y295* |
probably null |
Het |
Fmn2 |
C |
A |
1: 174,437,404 (GRCm39) |
T1125N |
possibly damaging |
Het |
Foxi2 |
C |
A |
7: 135,012,133 (GRCm39) |
P7Q |
probably damaging |
Het |
Hmx1 |
C |
T |
5: 35,549,100 (GRCm39) |
P131L |
probably damaging |
Het |
Hrh2 |
T |
C |
13: 54,368,171 (GRCm39) |
L49P |
probably damaging |
Het |
Hycc2 |
T |
C |
1: 58,585,285 (GRCm39) |
T171A |
possibly damaging |
Het |
Igkv6-14 |
A |
G |
6: 70,412,125 (GRCm39) |
V53A |
possibly damaging |
Het |
Kcnb2 |
C |
A |
1: 15,780,876 (GRCm39) |
Q583K |
probably benign |
Het |
Kcns3 |
A |
G |
12: 11,141,692 (GRCm39) |
S336P |
probably damaging |
Het |
Kremen2 |
G |
T |
17: 23,961,720 (GRCm39) |
F262L |
probably damaging |
Het |
Krtap9-1 |
T |
A |
11: 99,764,577 (GRCm39) |
C104* |
probably null |
Het |
Ky |
A |
G |
9: 102,405,102 (GRCm39) |
Y199C |
probably damaging |
Het |
L1td1 |
T |
G |
4: 98,622,215 (GRCm39) |
L259R |
probably damaging |
Het |
Lrba |
A |
G |
3: 86,261,062 (GRCm39) |
T1473A |
probably benign |
Het |
Lrp6 |
A |
T |
6: 134,484,624 (GRCm39) |
L333* |
probably null |
Het |
Lrrc23 |
T |
C |
6: 124,753,043 (GRCm39) |
N201S |
probably benign |
Het |
Map4k4 |
C |
A |
1: 40,043,142 (GRCm39) |
P666T |
possibly damaging |
Het |
Matn1 |
T |
A |
4: 130,679,514 (GRCm39) |
D389E |
probably damaging |
Het |
Mdc1 |
G |
T |
17: 36,158,475 (GRCm39) |
G285V |
probably benign |
Het |
Mettl17 |
T |
C |
14: 52,128,187 (GRCm39) |
|
probably null |
Het |
Mknk1 |
A |
T |
4: 115,730,506 (GRCm39) |
|
probably benign |
Het |
Nfya |
T |
C |
17: 48,699,445 (GRCm39) |
T213A |
probably damaging |
Het |
Nmrk1 |
C |
T |
19: 18,616,902 (GRCm39) |
T17M |
probably damaging |
Het |
Ntrk1 |
A |
C |
3: 87,693,396 (GRCm39) |
D245E |
probably benign |
Het |
Nup160 |
C |
A |
2: 90,563,545 (GRCm39) |
H1370Q |
possibly damaging |
Het |
Or11h6 |
A |
C |
14: 50,880,703 (GRCm39) |
K316Q |
probably benign |
Het |
Or5w8 |
T |
C |
2: 87,688,161 (GRCm39) |
V214A |
probably benign |
Het |
Or6x1 |
T |
A |
9: 40,098,663 (GRCm39) |
V84E |
probably damaging |
Het |
Parp4 |
G |
A |
14: 56,866,556 (GRCm39) |
R1040H |
probably benign |
Het |
Pdia4 |
C |
A |
6: 47,785,200 (GRCm39) |
E56* |
probably null |
Het |
Pdia5 |
A |
G |
16: 35,269,784 (GRCm39) |
F175S |
probably damaging |
Het |
Piezo2 |
C |
T |
18: 63,242,956 (GRCm39) |
S621N |
probably benign |
Het |
Pigw |
T |
C |
11: 84,768,643 (GRCm39) |
T229A |
possibly damaging |
Het |
Rasa3 |
T |
C |
8: 13,626,381 (GRCm39) |
Y734C |
probably benign |
Het |
Rfx7 |
T |
A |
9: 72,500,505 (GRCm39) |
|
probably benign |
Het |
Rims1 |
T |
C |
1: 22,633,181 (GRCm39) |
D178G |
possibly damaging |
Het |
Ros1 |
A |
G |
10: 51,954,769 (GRCm39) |
V1853A |
possibly damaging |
Het |
Rps7 |
A |
G |
12: 28,681,714 (GRCm39) |
I139T |
probably benign |
Het |
Sall3 |
T |
C |
18: 81,029,708 (GRCm39) |
D15G |
possibly damaging |
Het |
Scn1a |
A |
T |
2: 66,133,983 (GRCm39) |
V137D |
probably benign |
Het |
Slc23a3 |
G |
A |
1: 75,106,173 (GRCm39) |
P349S |
probably benign |
Het |
Slc35a5 |
C |
G |
16: 44,964,021 (GRCm39) |
R404P |
probably damaging |
Het |
Stard13 |
A |
T |
5: 150,986,607 (GRCm39) |
M301K |
probably benign |
Het |
Suclg2 |
A |
G |
6: 95,632,489 (GRCm39) |
F60S |
probably damaging |
Het |
Tecpr2 |
T |
A |
12: 110,904,668 (GRCm39) |
F887L |
possibly damaging |
Het |
Tekt4 |
G |
T |
17: 25,691,033 (GRCm39) |
W113L |
probably damaging |
Het |
Tep1 |
G |
A |
14: 51,085,080 (GRCm39) |
S901F |
probably damaging |
Het |
Tex11 |
C |
T |
X: 100,059,191 (GRCm39) |
V190I |
possibly damaging |
Het |
Thbs1 |
T |
A |
2: 117,949,957 (GRCm39) |
|
probably null |
Het |
Tm9sf4 |
T |
A |
2: 153,040,295 (GRCm39) |
V425D |
probably damaging |
Het |
Tpo |
A |
G |
12: 30,105,137 (GRCm39) |
L911P |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,729,301 (GRCm39) |
Q5332R |
unknown |
Het |
Wdr59 |
A |
T |
8: 112,223,466 (GRCm39) |
D169E |
|
Het |
Zfp799 |
C |
A |
17: 33,039,166 (GRCm39) |
G367C |
probably damaging |
Het |
|
Other mutations in Neurod1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01558:Neurod1
|
APN |
2 |
79,284,363 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01814:Neurod1
|
APN |
2 |
79,285,003 (GRCm39) |
missense |
probably damaging |
1.00 |
accelerando
|
UTSW |
2 |
79,284,370 (GRCm39) |
missense |
probably benign |
0.20 |
cruz
|
UTSW |
2 |
79,284,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R0427:Neurod1
|
UTSW |
2 |
79,284,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Neurod1
|
UTSW |
2 |
79,284,781 (GRCm39) |
missense |
probably benign |
0.10 |
R1795:Neurod1
|
UTSW |
2 |
79,284,673 (GRCm39) |
missense |
probably benign |
0.13 |
R3783:Neurod1
|
UTSW |
2 |
79,284,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3785:Neurod1
|
UTSW |
2 |
79,284,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3786:Neurod1
|
UTSW |
2 |
79,284,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Neurod1
|
UTSW |
2 |
79,284,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Neurod1
|
UTSW |
2 |
79,284,370 (GRCm39) |
missense |
probably benign |
0.20 |
R4978:Neurod1
|
UTSW |
2 |
79,284,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Neurod1
|
UTSW |
2 |
79,284,505 (GRCm39) |
missense |
probably benign |
0.00 |
R7098:Neurod1
|
UTSW |
2 |
79,285,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R7401:Neurod1
|
UTSW |
2 |
79,285,290 (GRCm39) |
missense |
probably benign |
0.14 |
R7576:Neurod1
|
UTSW |
2 |
79,284,689 (GRCm39) |
nonsense |
probably null |
|
R8465:Neurod1
|
UTSW |
2 |
79,284,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R9039:Neurod1
|
UTSW |
2 |
79,284,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R9068:Neurod1
|
UTSW |
2 |
79,285,218 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9225:Neurod1
|
UTSW |
2 |
79,284,731 (GRCm39) |
missense |
probably benign |
0.00 |
|