Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
T |
A |
3: 59,654,693 (GRCm39) |
Y176N |
probably damaging |
Het |
Acsl5 |
G |
A |
19: 55,283,268 (GRCm39) |
V615I |
probably benign |
Het |
Ankk1 |
T |
C |
9: 49,338,153 (GRCm39) |
K47E |
probably benign |
Het |
Ankrd11 |
A |
T |
8: 123,620,544 (GRCm39) |
|
probably null |
Het |
Bcl9l |
T |
C |
9: 44,417,941 (GRCm39) |
V593A |
probably benign |
Het |
Cadps |
T |
C |
14: 12,376,685 (GRCm38) |
I1271V |
probably benign |
Het |
Ccdc125 |
T |
C |
13: 100,820,812 (GRCm39) |
W152R |
probably damaging |
Het |
Cep192 |
T |
C |
18: 67,984,808 (GRCm39) |
V1606A |
possibly damaging |
Het |
Csgalnact1 |
T |
C |
8: 68,854,036 (GRCm39) |
N255S |
probably benign |
Het |
Cxxc5 |
T |
A |
18: 35,992,109 (GRCm39) |
V170E |
probably damaging |
Het |
Defb6 |
C |
T |
8: 19,278,110 (GRCm39) |
R61C |
possibly damaging |
Het |
Dnah10 |
T |
A |
5: 124,824,810 (GRCm39) |
N655K |
probably benign |
Het |
Fry |
G |
A |
5: 150,323,136 (GRCm39) |
A1096T |
probably damaging |
Het |
Gli1 |
C |
T |
10: 127,173,284 (GRCm39) |
G125S |
probably damaging |
Het |
Igkv14-126 |
A |
T |
6: 67,873,424 (GRCm39) |
I51F |
possibly damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Jtb |
T |
C |
3: 90,141,284 (GRCm39) |
S87P |
probably benign |
Het |
Kdm6b |
A |
T |
11: 69,296,755 (GRCm39) |
I504N |
probably damaging |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Map2k4 |
A |
G |
11: 65,626,031 (GRCm39) |
I136T |
probably damaging |
Het |
Marchf4 |
T |
C |
1: 72,468,076 (GRCm39) |
T319A |
probably benign |
Het |
Nr2e3 |
TCCATCGGAGTGTTCCC |
TC |
9: 59,850,701 (GRCm39) |
|
probably benign |
Het |
Nt5e |
T |
C |
9: 88,251,108 (GRCm39) |
V459A |
probably damaging |
Het |
Ogdhl |
A |
G |
14: 32,054,822 (GRCm39) |
K257E |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or2g25 |
A |
G |
17: 37,970,630 (GRCm39) |
L198P |
probably damaging |
Het |
Osmr |
A |
T |
15: 6,866,540 (GRCm39) |
V378D |
probably damaging |
Het |
Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
Pdzd7 |
G |
T |
19: 45,025,310 (GRCm39) |
T395K |
probably damaging |
Het |
Rasgef1c |
A |
G |
11: 49,847,970 (GRCm39) |
D35G |
probably benign |
Het |
Rbm19 |
T |
C |
5: 120,279,642 (GRCm39) |
F770L |
probably damaging |
Het |
Rit2 |
C |
A |
18: 31,108,514 (GRCm39) |
C157F |
probably damaging |
Het |
Slc22a22 |
A |
G |
15: 57,119,869 (GRCm39) |
|
probably null |
Het |
Slc8b1 |
T |
C |
5: 120,651,403 (GRCm39) |
|
probably null |
Het |
Speer2 |
C |
A |
16: 69,655,783 (GRCm39) |
R14S |
possibly damaging |
Het |
Tas2r105 |
C |
A |
6: 131,663,836 (GRCm39) |
L197F |
possibly damaging |
Het |
Tmprss11b |
T |
A |
5: 86,812,957 (GRCm39) |
H113L |
possibly damaging |
Het |
Ttbk2 |
G |
A |
2: 120,653,040 (GRCm39) |
P64S |
probably damaging |
Het |
Urb1 |
A |
T |
16: 90,601,425 (GRCm39) |
H115Q |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,889,777 (GRCm39) |
|
probably benign |
Het |
Zbtb39 |
T |
A |
10: 127,577,429 (GRCm39) |
M1K |
probably null |
Het |
|
Other mutations in 4930579F01Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:4930579F01Rik
|
APN |
3 |
137,891,959 (GRCm39) |
intron |
probably benign |
|
IGL02121:4930579F01Rik
|
APN |
3 |
137,870,134 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02424:4930579F01Rik
|
APN |
3 |
137,880,466 (GRCm39) |
splice site |
probably benign |
|
R0008:4930579F01Rik
|
UTSW |
3 |
137,882,346 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0008:4930579F01Rik
|
UTSW |
3 |
137,882,346 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0373:4930579F01Rik
|
UTSW |
3 |
137,879,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R1082:4930579F01Rik
|
UTSW |
3 |
137,879,332 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1163:4930579F01Rik
|
UTSW |
3 |
137,882,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R1538:4930579F01Rik
|
UTSW |
3 |
137,889,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:4930579F01Rik
|
UTSW |
3 |
137,882,217 (GRCm39) |
critical splice donor site |
probably null |
|
R2364:4930579F01Rik
|
UTSW |
3 |
137,871,584 (GRCm39) |
missense |
probably benign |
0.00 |
R3978:4930579F01Rik
|
UTSW |
3 |
137,889,435 (GRCm39) |
missense |
probably benign |
0.01 |
R4108:4930579F01Rik
|
UTSW |
3 |
137,889,431 (GRCm39) |
missense |
probably benign |
0.14 |
R5960:4930579F01Rik
|
UTSW |
3 |
137,889,528 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6329:4930579F01Rik
|
UTSW |
3 |
137,879,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R6599:4930579F01Rik
|
UTSW |
3 |
137,882,250 (GRCm39) |
missense |
probably benign |
0.00 |
R6862:4930579F01Rik
|
UTSW |
3 |
137,891,949 (GRCm39) |
intron |
probably benign |
|
R6897:4930579F01Rik
|
UTSW |
3 |
137,889,534 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7092:4930579F01Rik
|
UTSW |
3 |
137,889,506 (GRCm39) |
missense |
probably benign |
0.08 |
R7919:4930579F01Rik
|
UTSW |
3 |
137,885,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R8381:4930579F01Rik
|
UTSW |
3 |
137,879,282 (GRCm39) |
critical splice donor site |
probably null |
|
R9024:4930579F01Rik
|
UTSW |
3 |
137,891,923 (GRCm39) |
missense |
unknown |
|
R9180:4930579F01Rik
|
UTSW |
3 |
137,889,470 (GRCm39) |
missense |
probably benign |
0.05 |
|