Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c14 |
T |
C |
13: 4,113,620 (GRCm39) |
S51P |
probably damaging |
Het |
Arhgef38 |
T |
G |
3: 132,866,529 (GRCm39) |
K203Q |
|
Het |
Cacna1d |
G |
A |
14: 29,796,925 (GRCm39) |
R1517W |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,915,949 (GRCm39) |
M235K |
probably damaging |
Het |
Cdc42bpg |
T |
C |
19: 6,372,149 (GRCm39) |
S1414P |
probably damaging |
Het |
Dab2ip |
A |
G |
2: 35,602,891 (GRCm39) |
D395G |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,358,945 (GRCm39) |
E255G |
probably benign |
Het |
Dnaja1 |
T |
A |
4: 40,724,133 (GRCm39) |
M98K |
probably benign |
Het |
Dnajb7 |
G |
A |
15: 81,292,266 (GRCm39) |
R24C |
probably benign |
Het |
Dscc1 |
C |
A |
15: 54,947,505 (GRCm39) |
W225L |
probably damaging |
Het |
Epcam |
A |
G |
17: 87,947,960 (GRCm39) |
|
probably benign |
Het |
Fbn2 |
T |
C |
18: 58,257,344 (GRCm39) |
Y341C |
probably damaging |
Het |
Fry |
T |
G |
5: 150,322,728 (GRCm39) |
L1040R |
probably damaging |
Het |
Gm9639 |
C |
T |
10: 77,630,828 (GRCm39) |
C28Y |
unknown |
Het |
Hsd17b7 |
A |
G |
1: 169,794,833 (GRCm39) |
S69P |
probably damaging |
Het |
Igsf1 |
A |
G |
X: 48,884,191 (GRCm39) |
M2T |
possibly damaging |
Het |
Katnip |
T |
A |
7: 125,469,867 (GRCm39) |
D1445E |
probably damaging |
Het |
Kmt2d |
TGCTGCTGCTGCTGCTGCTGG |
TG |
15: 98,747,499 (GRCm39) |
|
probably null |
Het |
Lrp5 |
T |
C |
19: 3,654,190 (GRCm39) |
Y1079C |
probably damaging |
Het |
Lrp6 |
T |
C |
6: 134,457,467 (GRCm39) |
D779G |
probably damaging |
Het |
Nbea |
AC |
A |
3: 55,998,393 (GRCm39) |
|
probably null |
Het |
Pacsin1 |
A |
G |
17: 27,923,924 (GRCm39) |
D106G |
probably damaging |
Het |
Pcm1 |
T |
A |
8: 41,732,790 (GRCm39) |
D682E |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,023,231 (GRCm39) |
D269G |
probably benign |
Het |
Rcor1 |
T |
A |
12: 111,078,327 (GRCm39) |
V474E |
|
Het |
Rdh16 |
A |
G |
10: 127,649,306 (GRCm39) |
D254G |
probably benign |
Het |
Rp1 |
A |
T |
1: 4,418,675 (GRCm39) |
D812E |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,419,160 (GRCm39) |
S651P |
probably benign |
Het |
Sec16b |
G |
A |
1: 157,359,748 (GRCm39) |
|
probably benign |
Het |
Sephs2 |
C |
T |
7: 126,872,122 (GRCm39) |
G324S |
probably damaging |
Het |
Sirpb1a |
T |
C |
3: 15,481,992 (GRCm39) |
D112G |
probably damaging |
Het |
Slc25a47 |
C |
G |
12: 108,820,215 (GRCm39) |
T73S |
probably benign |
Het |
Slco4c1 |
A |
T |
1: 96,799,509 (GRCm39) |
L109H |
probably damaging |
Het |
Smc2 |
A |
G |
4: 52,470,848 (GRCm39) |
E845G |
possibly damaging |
Het |
Sstr3 |
G |
T |
15: 78,423,792 (GRCm39) |
N318K |
probably damaging |
Het |
Suz12 |
A |
G |
11: 79,904,087 (GRCm39) |
|
probably benign |
Het |
Sycp2 |
A |
G |
2: 178,035,931 (GRCm39) |
I252T |
probably damaging |
Het |
Syne3 |
T |
C |
12: 104,934,415 (GRCm39) |
Y118C |
probably damaging |
Het |
Tbx18 |
C |
A |
9: 87,611,521 (GRCm39) |
A170S |
probably damaging |
Het |
Trak2 |
T |
C |
1: 58,985,481 (GRCm39) |
N6D |
probably benign |
Het |
Ttn |
G |
A |
2: 76,720,868 (GRCm39) |
T6852I |
unknown |
Het |
Tufm |
A |
G |
7: 126,088,100 (GRCm39) |
E201G |
probably damaging |
Het |
Vwa3b |
C |
A |
1: 37,099,493 (GRCm39) |
P236Q |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,345,289 (GRCm39) |
Y2510C |
possibly damaging |
Het |
|
Other mutations in Dsg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Dsg2
|
APN |
18 |
20,734,826 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00979:Dsg2
|
APN |
18 |
20,715,824 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01081:Dsg2
|
APN |
18 |
20,722,999 (GRCm39) |
unclassified |
probably benign |
|
IGL01358:Dsg2
|
APN |
18 |
20,734,850 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02002:Dsg2
|
APN |
18 |
20,712,233 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02263:Dsg2
|
APN |
18 |
20,723,077 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02410:Dsg2
|
APN |
18 |
20,735,189 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02553:Dsg2
|
APN |
18 |
20,725,467 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03036:Dsg2
|
APN |
18 |
20,712,134 (GRCm39) |
missense |
probably damaging |
0.99 |
dissolute
|
UTSW |
18 |
20,729,008 (GRCm39) |
splice site |
probably null |
|
Dysjunction
|
UTSW |
18 |
20,715,996 (GRCm39) |
nonsense |
probably null |
|
weg
|
UTSW |
18 |
20,713,708 (GRCm39) |
nonsense |
probably null |
|
R0094:Dsg2
|
UTSW |
18 |
20,724,910 (GRCm39) |
missense |
probably benign |
0.08 |
R0094:Dsg2
|
UTSW |
18 |
20,724,910 (GRCm39) |
missense |
probably benign |
0.08 |
R0105:Dsg2
|
UTSW |
18 |
20,735,111 (GRCm39) |
missense |
probably benign |
0.03 |
R0105:Dsg2
|
UTSW |
18 |
20,735,111 (GRCm39) |
missense |
probably benign |
0.03 |
R0112:Dsg2
|
UTSW |
18 |
20,716,099 (GRCm39) |
missense |
probably benign |
0.02 |
R0305:Dsg2
|
UTSW |
18 |
20,715,752 (GRCm39) |
splice site |
probably benign |
|
R0380:Dsg2
|
UTSW |
18 |
20,715,996 (GRCm39) |
nonsense |
probably null |
|
R0401:Dsg2
|
UTSW |
18 |
20,725,565 (GRCm39) |
splice site |
probably benign |
|
R0421:Dsg2
|
UTSW |
18 |
20,712,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R0578:Dsg2
|
UTSW |
18 |
20,727,291 (GRCm39) |
missense |
probably benign |
0.00 |
R0667:Dsg2
|
UTSW |
18 |
20,706,556 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1223:Dsg2
|
UTSW |
18 |
20,706,550 (GRCm39) |
missense |
probably benign |
0.23 |
R1433:Dsg2
|
UTSW |
18 |
20,715,780 (GRCm39) |
missense |
probably damaging |
0.98 |
R1543:Dsg2
|
UTSW |
18 |
20,727,268 (GRCm39) |
missense |
probably benign |
0.33 |
R1730:Dsg2
|
UTSW |
18 |
20,724,937 (GRCm39) |
missense |
probably benign |
0.01 |
R1783:Dsg2
|
UTSW |
18 |
20,724,937 (GRCm39) |
missense |
probably benign |
0.01 |
R1946:Dsg2
|
UTSW |
18 |
20,713,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Dsg2
|
UTSW |
18 |
20,734,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Dsg2
|
UTSW |
18 |
20,734,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R2027:Dsg2
|
UTSW |
18 |
20,716,061 (GRCm39) |
unclassified |
probably benign |
|
R2109:Dsg2
|
UTSW |
18 |
20,725,346 (GRCm39) |
missense |
probably benign |
0.00 |
R2143:Dsg2
|
UTSW |
18 |
20,712,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Dsg2
|
UTSW |
18 |
20,729,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R2343:Dsg2
|
UTSW |
18 |
20,735,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R2937:Dsg2
|
UTSW |
18 |
20,712,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R3710:Dsg2
|
UTSW |
18 |
20,735,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R3734:Dsg2
|
UTSW |
18 |
20,735,004 (GRCm39) |
missense |
probably benign |
0.41 |
R3773:Dsg2
|
UTSW |
18 |
20,724,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R4176:Dsg2
|
UTSW |
18 |
20,713,720 (GRCm39) |
missense |
probably benign |
0.25 |
R4213:Dsg2
|
UTSW |
18 |
20,731,571 (GRCm39) |
missense |
probably benign |
0.01 |
R4299:Dsg2
|
UTSW |
18 |
20,729,008 (GRCm39) |
splice site |
probably null |
|
R4515:Dsg2
|
UTSW |
18 |
20,734,444 (GRCm39) |
missense |
probably benign |
|
R4649:Dsg2
|
UTSW |
18 |
20,735,302 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4940:Dsg2
|
UTSW |
18 |
20,712,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R4949:Dsg2
|
UTSW |
18 |
20,723,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Dsg2
|
UTSW |
18 |
20,734,578 (GRCm39) |
missense |
probably benign |
0.26 |
R5078:Dsg2
|
UTSW |
18 |
20,729,140 (GRCm39) |
critical splice donor site |
probably null |
|
R5155:Dsg2
|
UTSW |
18 |
20,731,715 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5398:Dsg2
|
UTSW |
18 |
20,712,190 (GRCm39) |
missense |
probably benign |
0.45 |
R5503:Dsg2
|
UTSW |
18 |
20,713,708 (GRCm39) |
nonsense |
probably null |
|
R6133:Dsg2
|
UTSW |
18 |
20,723,146 (GRCm39) |
missense |
probably benign |
0.00 |
R6163:Dsg2
|
UTSW |
18 |
20,731,726 (GRCm39) |
critical splice donor site |
probably null |
|
R6226:Dsg2
|
UTSW |
18 |
20,712,506 (GRCm39) |
missense |
probably damaging |
0.98 |
R6228:Dsg2
|
UTSW |
18 |
20,727,350 (GRCm39) |
critical splice donor site |
probably null |
|
R6241:Dsg2
|
UTSW |
18 |
20,723,274 (GRCm39) |
splice site |
probably null |
|
R6482:Dsg2
|
UTSW |
18 |
20,734,371 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6524:Dsg2
|
UTSW |
18 |
20,716,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R6856:Dsg2
|
UTSW |
18 |
20,734,859 (GRCm39) |
missense |
probably damaging |
0.98 |
R7058:Dsg2
|
UTSW |
18 |
20,725,332 (GRCm39) |
missense |
probably benign |
0.00 |
R7108:Dsg2
|
UTSW |
18 |
20,734,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Dsg2
|
UTSW |
18 |
20,712,511 (GRCm39) |
missense |
probably damaging |
0.98 |
R7207:Dsg2
|
UTSW |
18 |
20,734,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R7256:Dsg2
|
UTSW |
18 |
20,724,988 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7315:Dsg2
|
UTSW |
18 |
20,712,217 (GRCm39) |
missense |
probably damaging |
0.97 |
R7471:Dsg2
|
UTSW |
18 |
20,713,675 (GRCm39) |
missense |
probably benign |
0.08 |
R7558:Dsg2
|
UTSW |
18 |
20,727,291 (GRCm39) |
missense |
probably benign |
0.00 |
R8094:Dsg2
|
UTSW |
18 |
20,716,061 (GRCm39) |
unclassified |
probably benign |
|
R8118:Dsg2
|
UTSW |
18 |
20,715,858 (GRCm39) |
missense |
probably benign |
0.11 |
R8157:Dsg2
|
UTSW |
18 |
20,713,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Dsg2
|
UTSW |
18 |
20,708,121 (GRCm39) |
missense |
probably benign |
0.19 |
R8308:Dsg2
|
UTSW |
18 |
20,708,121 (GRCm39) |
missense |
probably benign |
0.19 |
R8488:Dsg2
|
UTSW |
18 |
20,734,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8520:Dsg2
|
UTSW |
18 |
20,712,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Dsg2
|
UTSW |
18 |
20,723,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R8675:Dsg2
|
UTSW |
18 |
20,734,975 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8750:Dsg2
|
UTSW |
18 |
20,708,069 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8773:Dsg2
|
UTSW |
18 |
20,716,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R8888:Dsg2
|
UTSW |
18 |
20,723,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R8895:Dsg2
|
UTSW |
18 |
20,723,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R8912:Dsg2
|
UTSW |
18 |
20,715,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R8925:Dsg2
|
UTSW |
18 |
20,725,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R8927:Dsg2
|
UTSW |
18 |
20,725,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Dsg2
|
UTSW |
18 |
20,715,847 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1176:Dsg2
|
UTSW |
18 |
20,713,678 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dsg2
|
UTSW |
18 |
20,735,306 (GRCm39) |
nonsense |
probably null |
|
|