Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arl6ip6 |
T |
A |
2: 53,092,936 (GRCm39) |
W154R |
probably damaging |
Het |
Ccnc |
T |
A |
4: 21,742,642 (GRCm39) |
Y156* |
probably null |
Het |
Clca3a1 |
A |
C |
3: 144,730,357 (GRCm39) |
W163G |
probably damaging |
Het |
Cntnap5b |
C |
T |
1: 100,311,310 (GRCm39) |
T972I |
probably damaging |
Het |
Cpn2 |
C |
T |
16: 30,079,338 (GRCm39) |
S121N |
probably benign |
Het |
Dcc |
T |
C |
18: 71,943,871 (GRCm39) |
E260G |
probably damaging |
Het |
Dnah6 |
A |
T |
6: 73,133,333 (GRCm39) |
N1091K |
possibly damaging |
Het |
Dpp9 |
G |
T |
17: 56,512,240 (GRCm39) |
F249L |
probably damaging |
Het |
Dscaml1 |
A |
G |
9: 45,662,551 (GRCm39) |
D1839G |
probably damaging |
Het |
Esr1 |
C |
T |
10: 4,997,890 (GRCm38) |
R481L |
probably benign |
Het |
Frem2 |
G |
T |
3: 53,493,016 (GRCm39) |
D1833E |
probably damaging |
Het |
Ftdc2 |
A |
T |
16: 58,458,059 (GRCm39) |
Y81N |
probably benign |
Het |
Ica1 |
T |
C |
6: 8,653,514 (GRCm39) |
D343G |
probably benign |
Het |
Il27 |
T |
C |
7: 126,188,555 (GRCm39) |
H206R |
probably benign |
Het |
Med14 |
A |
G |
X: 12,547,039 (GRCm39) |
V723A |
probably damaging |
Het |
Msh3 |
C |
A |
13: 92,481,472 (GRCm39) |
G347C |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,258,103 (GRCm39) |
M485L |
probably benign |
Het |
Or4c111 |
A |
G |
2: 88,843,953 (GRCm39) |
F152L |
probably benign |
Het |
Or4f60 |
A |
G |
2: 111,902,100 (GRCm39) |
V276A |
probably damaging |
Het |
Pcdhb5 |
T |
G |
18: 37,454,036 (GRCm39) |
L139V |
probably benign |
Het |
Rbfox1 |
A |
T |
16: 7,187,698 (GRCm39) |
K43N |
probably benign |
Het |
Scn5a |
G |
T |
9: 119,342,170 (GRCm39) |
|
probably null |
Het |
Senp7 |
G |
T |
16: 55,902,740 (GRCm39) |
R21L |
probably damaging |
Het |
Ssb |
G |
A |
2: 69,696,606 (GRCm39) |
V47I |
probably benign |
Het |
Ttll8 |
T |
A |
15: 88,817,731 (GRCm39) |
S221C |
probably damaging |
Het |
|
Other mutations in Nfasc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01088:Nfasc
|
APN |
1 |
132,570,514 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01958:Nfasc
|
APN |
1 |
132,536,176 (GRCm39) |
nonsense |
probably null |
|
IGL01999:Nfasc
|
APN |
1 |
132,532,985 (GRCm39) |
splice site |
probably benign |
|
IGL02170:Nfasc
|
APN |
1 |
132,538,104 (GRCm39) |
nonsense |
probably null |
|
IGL02187:Nfasc
|
APN |
1 |
132,498,219 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02192:Nfasc
|
APN |
1 |
132,498,219 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02452:Nfasc
|
APN |
1 |
132,548,662 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02698:Nfasc
|
APN |
1 |
132,562,475 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02797:Nfasc
|
APN |
1 |
132,538,186 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Nfasc
|
APN |
1 |
132,549,247 (GRCm39) |
splice site |
probably benign |
|
IGL03027:Nfasc
|
APN |
1 |
132,538,207 (GRCm39) |
missense |
probably damaging |
1.00 |
Fascist
|
UTSW |
1 |
132,539,343 (GRCm39) |
missense |
probably damaging |
1.00 |
jiggle
|
UTSW |
1 |
132,529,759 (GRCm39) |
missense |
probably damaging |
1.00 |
Partisan
|
UTSW |
1 |
132,533,287 (GRCm39) |
missense |
probably damaging |
1.00 |
Tremble
|
UTSW |
1 |
132,539,333 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4377001:Nfasc
|
UTSW |
1 |
132,510,804 (GRCm39) |
missense |
unknown |
|
R0240:Nfasc
|
UTSW |
1 |
132,529,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Nfasc
|
UTSW |
1 |
132,529,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Nfasc
|
UTSW |
1 |
132,564,731 (GRCm39) |
missense |
probably benign |
0.02 |
R0241:Nfasc
|
UTSW |
1 |
132,564,731 (GRCm39) |
missense |
probably benign |
0.02 |
R0418:Nfasc
|
UTSW |
1 |
132,539,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Nfasc
|
UTSW |
1 |
132,531,584 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0639:Nfasc
|
UTSW |
1 |
132,531,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Nfasc
|
UTSW |
1 |
132,536,176 (GRCm39) |
nonsense |
probably null |
|
R1103:Nfasc
|
UTSW |
1 |
132,534,795 (GRCm39) |
splice site |
probably benign |
|
R1269:Nfasc
|
UTSW |
1 |
132,538,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Nfasc
|
UTSW |
1 |
132,536,241 (GRCm39) |
missense |
probably damaging |
0.96 |
R1749:Nfasc
|
UTSW |
1 |
132,539,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R1773:Nfasc
|
UTSW |
1 |
132,538,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Nfasc
|
UTSW |
1 |
132,538,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Nfasc
|
UTSW |
1 |
132,538,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Nfasc
|
UTSW |
1 |
132,524,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Nfasc
|
UTSW |
1 |
132,510,760 (GRCm39) |
intron |
probably benign |
|
R2413:Nfasc
|
UTSW |
1 |
132,523,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R2428:Nfasc
|
UTSW |
1 |
132,523,392 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2472:Nfasc
|
UTSW |
1 |
132,515,959 (GRCm39) |
intron |
probably benign |
|
R2517:Nfasc
|
UTSW |
1 |
132,525,501 (GRCm39) |
splice site |
probably null |
|
R3850:Nfasc
|
UTSW |
1 |
132,559,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:Nfasc
|
UTSW |
1 |
132,538,043 (GRCm39) |
splice site |
probably benign |
|
R4061:Nfasc
|
UTSW |
1 |
132,525,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Nfasc
|
UTSW |
1 |
132,523,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Nfasc
|
UTSW |
1 |
132,559,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R4343:Nfasc
|
UTSW |
1 |
132,559,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R4345:Nfasc
|
UTSW |
1 |
132,559,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R4452:Nfasc
|
UTSW |
1 |
132,562,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R4818:Nfasc
|
UTSW |
1 |
132,531,568 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4851:Nfasc
|
UTSW |
1 |
132,529,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Nfasc
|
UTSW |
1 |
132,512,185 (GRCm39) |
intron |
probably benign |
|
R5768:Nfasc
|
UTSW |
1 |
132,532,883 (GRCm39) |
missense |
probably benign |
0.00 |
R6145:Nfasc
|
UTSW |
1 |
132,562,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6335:Nfasc
|
UTSW |
1 |
132,504,132 (GRCm39) |
missense |
probably damaging |
0.98 |
R6379:Nfasc
|
UTSW |
1 |
132,498,280 (GRCm39) |
nonsense |
probably null |
|
R6486:Nfasc
|
UTSW |
1 |
132,532,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Nfasc
|
UTSW |
1 |
132,548,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R7062:Nfasc
|
UTSW |
1 |
132,529,707 (GRCm39) |
critical splice donor site |
probably null |
|
R7084:Nfasc
|
UTSW |
1 |
132,498,247 (GRCm39) |
missense |
unknown |
|
R7275:Nfasc
|
UTSW |
1 |
132,562,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R7286:Nfasc
|
UTSW |
1 |
132,529,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Nfasc
|
UTSW |
1 |
132,501,511 (GRCm39) |
missense |
unknown |
|
R7838:Nfasc
|
UTSW |
1 |
132,533,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Nfasc
|
UTSW |
1 |
132,527,751 (GRCm39) |
missense |
not run |
|
R7938:Nfasc
|
UTSW |
1 |
132,533,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R8083:Nfasc
|
UTSW |
1 |
132,524,320 (GRCm39) |
missense |
probably benign |
0.00 |
R8482:Nfasc
|
UTSW |
1 |
132,532,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9027:Nfasc
|
UTSW |
1 |
132,539,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R9164:Nfasc
|
UTSW |
1 |
132,562,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Nfasc
|
UTSW |
1 |
132,527,866 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9651:Nfasc
|
UTSW |
1 |
132,527,791 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Nfasc
|
UTSW |
1 |
132,562,376 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Nfasc
|
UTSW |
1 |
132,559,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|