Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
T |
A |
5: 125,580,287 (GRCm39) |
I204N |
possibly damaging |
Het |
Acaca |
A |
G |
11: 84,263,453 (GRCm39) |
T2025A |
probably damaging |
Het |
B4galt3 |
C |
T |
1: 171,103,938 (GRCm39) |
R170C |
probably benign |
Het |
BC028528 |
T |
C |
3: 95,799,271 (GRCm39) |
|
probably null |
Het |
Ccdc73 |
A |
T |
2: 104,737,955 (GRCm39) |
Q17L |
possibly damaging |
Het |
Ccdc73 |
A |
G |
2: 104,745,012 (GRCm39) |
T50A |
possibly damaging |
Het |
Ccdc83 |
T |
C |
7: 89,908,677 (GRCm39) |
D19G |
probably damaging |
Het |
Ccn6 |
G |
A |
10: 39,029,239 (GRCm39) |
R230W |
probably damaging |
Het |
Cct8l1 |
T |
C |
5: 25,722,767 (GRCm39) |
V494A |
probably benign |
Het |
Chd1 |
T |
C |
17: 15,959,769 (GRCm39) |
F663L |
probably damaging |
Het |
Chn2 |
A |
T |
6: 54,270,065 (GRCm39) |
E319V |
probably damaging |
Het |
Cnnm1 |
T |
C |
19: 43,460,295 (GRCm39) |
V679A |
probably damaging |
Het |
Cntn6 |
C |
T |
6: 104,753,389 (GRCm39) |
T447I |
probably benign |
Het |
Cyp3a11 |
G |
T |
5: 145,795,581 (GRCm39) |
L457I |
probably benign |
Het |
Dera |
T |
A |
6: 137,807,193 (GRCm39) |
S214T |
possibly damaging |
Het |
Dmtf1 |
A |
G |
5: 9,171,404 (GRCm39) |
V501A |
possibly damaging |
Het |
Dnpep |
A |
G |
1: 75,292,671 (GRCm39) |
V114A |
probably damaging |
Het |
Dscam |
C |
T |
16: 96,592,110 (GRCm39) |
V722M |
probably benign |
Het |
Dsp |
A |
G |
13: 38,365,114 (GRCm39) |
N499S |
probably damaging |
Het |
Ecd |
A |
T |
14: 20,396,725 (GRCm39) |
Y53* |
probably null |
Het |
Esyt3 |
T |
C |
9: 99,200,119 (GRCm39) |
T692A |
probably benign |
Het |
Fat1 |
T |
A |
8: 45,478,659 (GRCm39) |
N2545K |
probably damaging |
Het |
Fndc3a |
A |
G |
14: 72,795,072 (GRCm39) |
|
probably null |
Het |
Fscn3 |
A |
G |
6: 28,430,567 (GRCm39) |
M246V |
probably benign |
Het |
Gde1 |
G |
T |
7: 118,291,007 (GRCm39) |
T106K |
probably benign |
Het |
Hacd4 |
A |
T |
4: 88,341,260 (GRCm39) |
M168K |
probably damaging |
Het |
Hmx3 |
A |
G |
7: 131,145,826 (GRCm39) |
E178G |
probably damaging |
Het |
Htt |
A |
G |
5: 34,961,171 (GRCm39) |
Y266C |
probably damaging |
Het |
Jkampl |
A |
T |
6: 73,446,039 (GRCm39) |
L170Q |
probably damaging |
Het |
Kif27 |
G |
T |
13: 58,451,359 (GRCm39) |
R990S |
probably damaging |
Het |
Krtap22-2 |
A |
T |
16: 88,807,534 (GRCm39) |
Y21* |
probably null |
Het |
Lrrc41 |
T |
A |
4: 115,952,405 (GRCm39) |
L661* |
probably null |
Het |
Lrrc63 |
T |
C |
14: 75,363,424 (GRCm39) |
T236A |
probably benign |
Het |
Mmp13 |
T |
C |
9: 7,272,892 (GRCm39) |
L84P |
probably damaging |
Het |
Myh8 |
T |
C |
11: 67,183,551 (GRCm39) |
I754T |
probably benign |
Het |
Neb |
A |
C |
2: 52,065,619 (GRCm39) |
D5961E |
probably benign |
Het |
Nlrx1 |
T |
C |
9: 44,175,374 (GRCm39) |
H134R |
probably benign |
Het |
Npepps |
A |
T |
11: 97,117,673 (GRCm39) |
M542K |
probably benign |
Het |
Nup160 |
C |
T |
2: 90,509,743 (GRCm39) |
|
probably benign |
Het |
Or3a1c |
T |
A |
11: 74,045,963 (GRCm39) |
|
probably null |
Het |
Or8g33 |
T |
A |
9: 39,337,888 (GRCm39) |
T160S |
possibly damaging |
Het |
Pikfyve |
T |
C |
1: 65,302,136 (GRCm39) |
|
probably null |
Het |
Ppp6r1 |
A |
T |
7: 4,643,377 (GRCm39) |
|
probably null |
Het |
Prss33 |
A |
G |
17: 24,054,072 (GRCm39) |
W45R |
probably damaging |
Het |
Ptprf |
A |
T |
4: 118,069,302 (GRCm39) |
Y980* |
probably null |
Het |
Qrich1 |
T |
C |
9: 108,436,531 (GRCm39) |
V743A |
probably benign |
Het |
Rev3l |
G |
A |
10: 39,659,329 (GRCm39) |
|
probably null |
Het |
Samd9l |
A |
T |
6: 3,376,369 (GRCm39) |
N297K |
probably benign |
Het |
Sap130 |
A |
G |
18: 31,813,527 (GRCm39) |
H528R |
possibly damaging |
Het |
Slc9b2 |
T |
C |
3: 135,031,863 (GRCm39) |
V241A |
probably benign |
Het |
Snx14 |
A |
T |
9: 88,276,581 (GRCm39) |
V577E |
probably benign |
Het |
Srrm2 |
T |
C |
17: 24,034,876 (GRCm39) |
S507P |
probably benign |
Het |
Stat2 |
A |
G |
10: 128,117,969 (GRCm39) |
|
probably null |
Het |
Susd5 |
T |
C |
9: 113,925,752 (GRCm39) |
F545S |
probably benign |
Het |
Tafa2 |
T |
A |
10: 123,429,401 (GRCm39) |
M5K |
possibly damaging |
Het |
Tnnt2 |
A |
G |
1: 135,775,764 (GRCm39) |
T107A |
probably benign |
Het |
Trappc6b |
T |
A |
12: 59,094,953 (GRCm39) |
I41F |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,682,417 (GRCm39) |
|
probably benign |
Het |
Vmn1r88 |
A |
C |
7: 12,911,878 (GRCm39) |
D78A |
probably damaging |
Het |
Xpc |
C |
T |
6: 91,485,510 (GRCm39) |
D122N |
possibly damaging |
Het |
Xpo1 |
C |
T |
11: 23,241,623 (GRCm39) |
A890V |
probably damaging |
Het |
Zfp493 |
A |
G |
13: 67,934,680 (GRCm39) |
H211R |
probably damaging |
Het |
Zfp958 |
A |
T |
8: 4,679,190 (GRCm39) |
H405L |
probably damaging |
Het |
|
Other mutations in Gjc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01667:Gjc2
|
APN |
11 |
59,068,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02191:Gjc2
|
APN |
11 |
59,068,386 (GRCm39) |
missense |
probably damaging |
0.99 |
FR4342:Gjc2
|
UTSW |
11 |
59,073,569 (GRCm39) |
unclassified |
probably benign |
|
R0086:Gjc2
|
UTSW |
11 |
59,067,672 (GRCm39) |
missense |
probably benign |
0.39 |
R0201:Gjc2
|
UTSW |
11 |
59,068,416 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5211:Gjc2
|
UTSW |
11 |
59,068,284 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5395:Gjc2
|
UTSW |
11 |
59,068,315 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5560:Gjc2
|
UTSW |
11 |
59,068,185 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5906:Gjc2
|
UTSW |
11 |
59,067,667 (GRCm39) |
missense |
probably benign |
0.39 |
R6909:Gjc2
|
UTSW |
11 |
59,067,918 (GRCm39) |
missense |
unknown |
|
R7055:Gjc2
|
UTSW |
11 |
59,067,856 (GRCm39) |
missense |
unknown |
|
R7241:Gjc2
|
UTSW |
11 |
59,067,960 (GRCm39) |
missense |
unknown |
|
R8353:Gjc2
|
UTSW |
11 |
59,067,840 (GRCm39) |
missense |
unknown |
|
R8416:Gjc2
|
UTSW |
11 |
59,068,334 (GRCm39) |
missense |
probably damaging |
0.99 |
R8546:Gjc2
|
UTSW |
11 |
59,067,182 (GRCm39) |
missense |
unknown |
|
R9276:Gjc2
|
UTSW |
11 |
59,068,453 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Gjc2
|
UTSW |
11 |
59,068,443 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Gjc2
|
UTSW |
11 |
59,073,561 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1186:Gjc2
|
UTSW |
11 |
59,067,318 (GRCm39) |
missense |
unknown |
|
Z1187:Gjc2
|
UTSW |
11 |
59,073,561 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1187:Gjc2
|
UTSW |
11 |
59,067,259 (GRCm39) |
missense |
unknown |
|
Z1188:Gjc2
|
UTSW |
11 |
59,073,561 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1188:Gjc2
|
UTSW |
11 |
59,067,318 (GRCm39) |
missense |
unknown |
|
Z1188:Gjc2
|
UTSW |
11 |
59,067,259 (GRCm39) |
missense |
unknown |
|
Z1189:Gjc2
|
UTSW |
11 |
59,073,561 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1189:Gjc2
|
UTSW |
11 |
59,067,318 (GRCm39) |
missense |
unknown |
|
Z1190:Gjc2
|
UTSW |
11 |
59,073,561 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1191:Gjc2
|
UTSW |
11 |
59,073,561 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1191:Gjc2
|
UTSW |
11 |
59,067,318 (GRCm39) |
missense |
unknown |
|
Z1191:Gjc2
|
UTSW |
11 |
59,067,259 (GRCm39) |
missense |
unknown |
|
Z1192:Gjc2
|
UTSW |
11 |
59,073,561 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1192:Gjc2
|
UTSW |
11 |
59,067,318 (GRCm39) |
missense |
unknown |
|
|