Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
G |
A |
4: 144,349,750 (GRCm39) |
V336I |
probably benign |
Het |
Aadacl4fm4 |
A |
T |
4: 144,397,216 (GRCm39) |
L172* |
probably null |
Het |
Abca7 |
G |
A |
10: 79,838,833 (GRCm39) |
V669I |
probably damaging |
Het |
Abcg3 |
T |
C |
5: 105,083,860 (GRCm39) |
T637A |
probably benign |
Het |
Afap1l1 |
A |
T |
18: 61,866,812 (GRCm39) |
V749E |
probably benign |
Het |
Arfgef3 |
A |
G |
10: 18,470,767 (GRCm39) |
L1666S |
probably damaging |
Het |
Atp2b1 |
A |
G |
10: 98,858,877 (GRCm39) |
N284D |
possibly damaging |
Het |
Ccdc196 |
T |
A |
12: 78,244,141 (GRCm39) |
D31E |
probably damaging |
Het |
Ccdc24 |
T |
C |
4: 117,727,123 (GRCm39) |
T196A |
probably benign |
Het |
Cdc20b |
G |
A |
13: 113,220,509 (GRCm39) |
G463S |
probably damaging |
Het |
Ceacam5 |
A |
T |
7: 17,486,212 (GRCm39) |
R570* |
probably null |
Het |
Cit |
G |
A |
5: 116,023,022 (GRCm39) |
C283Y |
probably damaging |
Het |
Cpa5 |
A |
T |
6: 30,614,053 (GRCm39) |
Q65L |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,797,624 (GRCm39) |
I1363V |
possibly damaging |
Het |
D2hgdh |
C |
A |
1: 93,763,025 (GRCm39) |
T270N |
possibly damaging |
Het |
Dnah8 |
G |
T |
17: 30,981,653 (GRCm39) |
L3058F |
probably damaging |
Het |
Dock4 |
T |
C |
12: 40,862,325 (GRCm39) |
|
probably null |
Het |
Ear6 |
A |
G |
14: 52,091,885 (GRCm39) |
Y144C |
probably damaging |
Het |
Fam53a |
T |
C |
5: 33,767,829 (GRCm39) |
Y27C |
probably benign |
Het |
Fgf2 |
A |
G |
3: 37,458,860 (GRCm39) |
K85E |
probably damaging |
Het |
Fubp1 |
A |
T |
3: 151,931,783 (GRCm39) |
Q37L |
probably benign |
Het |
Gabra2 |
G |
T |
5: 71,251,882 (GRCm39) |
P22T |
probably damaging |
Het |
Gm10401 |
T |
C |
5: 115,236,245 (GRCm39) |
|
probably benign |
Het |
Iglv3 |
A |
G |
16: 19,060,034 (GRCm39) |
I98T |
probably damaging |
Het |
Nlrp2 |
C |
T |
7: 5,311,709 (GRCm39) |
R922H |
probably benign |
Het |
Nr1h4 |
T |
C |
10: 89,290,607 (GRCm39) |
T474A |
probably damaging |
Het |
Pcdhb20 |
A |
C |
18: 37,639,218 (GRCm39) |
E581D |
probably benign |
Het |
Pidd1 |
G |
T |
7: 141,019,331 (GRCm39) |
T750K |
probably benign |
Het |
Pigq |
A |
T |
17: 26,150,630 (GRCm39) |
|
probably benign |
Het |
Rab44 |
A |
G |
17: 29,358,784 (GRCm39) |
E324G |
probably benign |
Het |
Slc24a3 |
C |
T |
2: 145,458,630 (GRCm39) |
Q537* |
probably null |
Het |
Slc34a1 |
T |
C |
13: 24,006,372 (GRCm39) |
I466T |
possibly damaging |
Het |
Slc7a10 |
T |
C |
7: 34,894,689 (GRCm39) |
V116A |
probably damaging |
Het |
Taf15 |
T |
A |
11: 83,389,915 (GRCm39) |
N228K |
probably damaging |
Het |
Tbx19 |
A |
T |
1: 164,975,202 (GRCm39) |
|
probably null |
Het |
Tgoln1 |
A |
G |
6: 72,592,538 (GRCm39) |
V314A |
possibly damaging |
Het |
Them4 |
A |
T |
3: 94,231,678 (GRCm39) |
I172F |
probably damaging |
Het |
Tmc7 |
T |
A |
7: 118,146,846 (GRCm39) |
Y477F |
probably benign |
Het |
Tmem132a |
A |
G |
19: 10,840,669 (GRCm39) |
L421P |
probably damaging |
Het |
Vamp5 |
G |
A |
6: 72,357,424 (GRCm39) |
|
probably benign |
Het |
Vmn2r11 |
T |
G |
5: 109,194,976 (GRCm39) |
R783S |
possibly damaging |
Het |
Zfp180 |
G |
T |
7: 23,805,306 (GRCm39) |
C575F |
probably damaging |
Het |
Zfp189 |
A |
T |
4: 49,529,026 (GRCm39) |
N43I |
probably damaging |
Het |
Zfp36l2 |
A |
G |
17: 84,493,521 (GRCm39) |
|
probably benign |
Het |
Zfp592 |
T |
C |
7: 80,673,576 (GRCm39) |
V180A |
probably benign |
Het |
Zfp605 |
C |
T |
5: 110,275,311 (GRCm39) |
P143L |
probably benign |
Het |
Zfp646 |
T |
C |
7: 127,482,505 (GRCm39) |
S1561P |
probably benign |
Het |
|
Other mutations in Dnajb8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00495:Dnajb8
|
APN |
6 |
88,199,836 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01671:Dnajb8
|
APN |
6 |
88,199,902 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01838:Dnajb8
|
APN |
6 |
88,200,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01976:Dnajb8
|
APN |
6 |
88,199,508 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03135:Dnajb8
|
APN |
6 |
88,200,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Dnajb8
|
UTSW |
6 |
88,199,467 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R0762:Dnajb8
|
UTSW |
6 |
88,200,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R2519:Dnajb8
|
UTSW |
6 |
88,199,857 (GRCm39) |
missense |
probably benign |
|
R5861:Dnajb8
|
UTSW |
6 |
88,200,088 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5946:Dnajb8
|
UTSW |
6 |
88,199,575 (GRCm39) |
missense |
probably benign |
0.37 |
R6575:Dnajb8
|
UTSW |
6 |
88,200,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R6767:Dnajb8
|
UTSW |
6 |
88,199,634 (GRCm39) |
missense |
probably damaging |
0.97 |
R6872:Dnajb8
|
UTSW |
6 |
88,200,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8189:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8190:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8191:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8192:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8193:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8210:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8219:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8221:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8224:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8225:Dnajb8
|
UTSW |
6 |
88,199,940 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9244:Dnajb8
|
UTSW |
6 |
88,199,884 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dnajb8
|
UTSW |
6 |
88,199,827 (GRCm39) |
missense |
probably benign |
|
Z1176:Dnajb8
|
UTSW |
6 |
88,199,892 (GRCm39) |
missense |
possibly damaging |
0.79 |
|