Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg2 |
A |
G |
6: 58,646,210 (GRCm39) |
H242R |
possibly damaging |
Het |
Adam1b |
G |
T |
5: 121,639,504 (GRCm39) |
R514S |
probably benign |
Het |
Adprs |
A |
G |
4: 126,210,368 (GRCm39) |
*371Q |
probably null |
Het |
Arid4a |
T |
C |
12: 71,106,849 (GRCm39) |
L307P |
probably benign |
Het |
Armc12 |
C |
T |
17: 28,757,675 (GRCm39) |
A269V |
probably benign |
Het |
Asb1 |
T |
A |
1: 91,480,078 (GRCm39) |
V259E |
probably damaging |
Het |
Atm |
T |
C |
9: 53,435,797 (GRCm39) |
Y171C |
probably damaging |
Het |
Atp8a2 |
A |
T |
14: 60,011,431 (GRCm39) |
F959L |
probably benign |
Het |
B4galt3 |
G |
T |
1: 171,101,917 (GRCm39) |
E34D |
possibly damaging |
Het |
Cacna1i |
A |
G |
15: 80,204,598 (GRCm39) |
N90S |
possibly damaging |
Het |
Cdc42ep2 |
T |
A |
19: 5,968,060 (GRCm39) |
*215L |
probably null |
Het |
Cep162 |
C |
T |
9: 87,126,361 (GRCm39) |
E184K |
probably benign |
Het |
Cnga3 |
C |
T |
1: 37,284,060 (GRCm39) |
P121L |
probably benign |
Het |
Cpt1b |
G |
A |
15: 89,306,524 (GRCm39) |
R285C |
probably damaging |
Het |
Defb18 |
T |
C |
1: 18,306,791 (GRCm39) |
Y55C |
probably damaging |
Het |
Depdc1b |
C |
T |
13: 108,493,959 (GRCm39) |
P116S |
probably damaging |
Het |
Dhx16 |
C |
T |
17: 36,192,183 (GRCm39) |
A74V |
possibly damaging |
Het |
Dse |
T |
C |
10: 34,028,316 (GRCm39) |
R925G |
possibly damaging |
Het |
Dsp |
C |
T |
13: 38,369,117 (GRCm39) |
L738F |
probably damaging |
Het |
Erv3 |
T |
C |
2: 131,698,261 (GRCm39) |
K33E |
possibly damaging |
Het |
Gas2l2 |
T |
A |
11: 83,312,907 (GRCm39) |
T802S |
probably benign |
Het |
Gdf9 |
T |
C |
11: 53,324,378 (GRCm39) |
L49S |
possibly damaging |
Het |
Gigyf1 |
G |
T |
5: 137,521,401 (GRCm39) |
|
probably benign |
Het |
Gm4792 |
T |
A |
10: 94,131,061 (GRCm39) |
I83L |
unknown |
Het |
Ighv9-3 |
A |
G |
12: 114,104,349 (GRCm39) |
L105P |
probably damaging |
Het |
Krtap5-1 |
C |
A |
7: 141,850,160 (GRCm39) |
W189L |
probably null |
Het |
Krtap5-3 |
T |
A |
7: 141,756,089 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,298,993 (GRCm39) |
E108D |
probably benign |
Het |
Lrrc66 |
G |
A |
5: 73,768,228 (GRCm39) |
P238S |
probably benign |
Het |
Ms4a4c |
C |
T |
19: 11,392,196 (GRCm39) |
Q6* |
probably null |
Het |
Or5b97 |
A |
G |
19: 12,879,096 (GRCm39) |
L16P |
probably damaging |
Het |
Or6d14 |
G |
T |
6: 116,534,289 (GRCm39) |
R301L |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pinx1 |
A |
G |
14: 64,156,972 (GRCm39) |
R300G |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,810,443 (GRCm39) |
H92Q |
probably damaging |
Het |
Rad54l2 |
T |
A |
9: 106,570,777 (GRCm39) |
Q1181L |
possibly damaging |
Het |
Rbl1 |
A |
T |
2: 157,038,174 (GRCm39) |
V131E |
probably damaging |
Het |
Rbp3 |
A |
G |
14: 33,677,621 (GRCm39) |
E523G |
probably benign |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Slc22a20 |
C |
A |
19: 6,035,698 (GRCm39) |
C130F |
probably damaging |
Het |
Smcr8 |
T |
C |
11: 60,670,979 (GRCm39) |
L709S |
probably damaging |
Het |
Spef2 |
A |
G |
15: 9,600,765 (GRCm39) |
|
probably benign |
Het |
Teddm1b |
T |
A |
1: 153,750,194 (GRCm39) |
M1K |
probably null |
Het |
Tes |
A |
G |
6: 17,097,327 (GRCm39) |
Y60C |
probably damaging |
Het |
Tmem104 |
T |
C |
11: 115,088,144 (GRCm39) |
L43P |
probably damaging |
Het |
Tnfaip3 |
T |
C |
10: 18,880,213 (GRCm39) |
E618G |
probably damaging |
Het |
Tnfaip3 |
T |
C |
10: 18,880,414 (GRCm39) |
D551G |
probably damaging |
Het |
Tnrc6a |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
7: 122,761,669 (GRCm39) |
|
probably benign |
Het |
Trim30b |
T |
A |
7: 104,015,236 (GRCm39) |
T51S |
probably benign |
Het |
Trmt44 |
G |
T |
5: 35,722,744 (GRCm39) |
H441Q |
probably benign |
Het |
Tshr |
C |
A |
12: 91,504,059 (GRCm39) |
D332E |
probably benign |
Het |
Usp10 |
C |
T |
8: 120,683,367 (GRCm39) |
T746M |
possibly damaging |
Het |
Vmn1r8 |
A |
T |
6: 57,013,138 (GRCm39) |
D63V |
possibly damaging |
Het |
Vps13a |
A |
C |
19: 16,731,684 (GRCm39) |
L143V |
probably damaging |
Het |
Wnt3a |
T |
A |
11: 59,166,043 (GRCm39) |
H79L |
probably damaging |
Het |
Zbtb7a |
C |
T |
10: 80,980,141 (GRCm39) |
R112W |
probably damaging |
Het |
|
Other mutations in Dnajc21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01321:Dnajc21
|
APN |
15 |
10,447,188 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02797:Dnajc21
|
APN |
15 |
10,461,441 (GRCm39) |
missense |
probably damaging |
0.96 |
R0032:Dnajc21
|
UTSW |
15 |
10,461,963 (GRCm39) |
missense |
probably benign |
0.32 |
R0032:Dnajc21
|
UTSW |
15 |
10,461,963 (GRCm39) |
missense |
probably benign |
0.32 |
R1480:Dnajc21
|
UTSW |
15 |
10,460,037 (GRCm39) |
splice site |
probably null |
|
R1694:Dnajc21
|
UTSW |
15 |
10,451,649 (GRCm39) |
missense |
probably benign |
0.00 |
R1777:Dnajc21
|
UTSW |
15 |
10,449,693 (GRCm39) |
missense |
probably benign |
0.00 |
R2420:Dnajc21
|
UTSW |
15 |
10,462,021 (GRCm39) |
missense |
probably benign |
0.00 |
R2421:Dnajc21
|
UTSW |
15 |
10,462,021 (GRCm39) |
missense |
probably benign |
0.00 |
R2422:Dnajc21
|
UTSW |
15 |
10,462,021 (GRCm39) |
missense |
probably benign |
0.00 |
R4065:Dnajc21
|
UTSW |
15 |
10,451,639 (GRCm39) |
critical splice donor site |
probably null |
|
R4182:Dnajc21
|
UTSW |
15 |
10,460,019 (GRCm39) |
splice site |
probably null |
|
R4546:Dnajc21
|
UTSW |
15 |
10,447,183 (GRCm39) |
missense |
probably benign |
0.01 |
R4644:Dnajc21
|
UTSW |
15 |
10,464,003 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4939:Dnajc21
|
UTSW |
15 |
10,449,683 (GRCm39) |
missense |
probably damaging |
0.96 |
R5075:Dnajc21
|
UTSW |
15 |
10,461,963 (GRCm39) |
missense |
probably benign |
0.32 |
R5187:Dnajc21
|
UTSW |
15 |
10,464,050 (GRCm39) |
missense |
probably benign |
0.21 |
R5273:Dnajc21
|
UTSW |
15 |
10,454,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R5590:Dnajc21
|
UTSW |
15 |
10,462,363 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5643:Dnajc21
|
UTSW |
15 |
10,462,001 (GRCm39) |
missense |
probably benign |
|
R5644:Dnajc21
|
UTSW |
15 |
10,462,001 (GRCm39) |
missense |
probably benign |
|
R5729:Dnajc21
|
UTSW |
15 |
10,449,682 (GRCm39) |
missense |
probably benign |
0.01 |
R6614:Dnajc21
|
UTSW |
15 |
10,470,349 (GRCm39) |
critical splice donor site |
probably null |
|
R6815:Dnajc21
|
UTSW |
15 |
10,447,777 (GRCm39) |
splice site |
probably null |
|
R7016:Dnajc21
|
UTSW |
15 |
10,461,493 (GRCm39) |
nonsense |
probably null |
|
R7076:Dnajc21
|
UTSW |
15 |
10,449,717 (GRCm39) |
missense |
probably benign |
|
R7584:Dnajc21
|
UTSW |
15 |
10,462,381 (GRCm39) |
nonsense |
probably null |
|
R7624:Dnajc21
|
UTSW |
15 |
10,461,320 (GRCm39) |
missense |
probably damaging |
0.98 |
R7624:Dnajc21
|
UTSW |
15 |
10,461,318 (GRCm39) |
missense |
probably benign |
0.07 |
R7676:Dnajc21
|
UTSW |
15 |
10,462,430 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7788:Dnajc21
|
UTSW |
15 |
10,460,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R7845:Dnajc21
|
UTSW |
15 |
10,447,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R9174:Dnajc21
|
UTSW |
15 |
10,462,076 (GRCm39) |
nonsense |
probably null |
|
R9416:Dnajc21
|
UTSW |
15 |
10,462,048 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9566:Dnajc21
|
UTSW |
15 |
10,464,019 (GRCm39) |
missense |
possibly damaging |
0.47 |
|