Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
G |
A |
4: 129,916,111 (GRCm39) |
D1468N |
probably damaging |
Het |
Aldh16a1 |
A |
G |
7: 44,794,951 (GRCm39) |
F506S |
probably damaging |
Het |
Ankfn1 |
A |
T |
11: 89,417,444 (GRCm39) |
M56K |
probably benign |
Het |
Atxn7l2 |
T |
C |
3: 108,114,756 (GRCm39) |
S97G |
probably benign |
Het |
Cacna1g |
C |
T |
11: 94,306,663 (GRCm39) |
G1905D |
probably benign |
Het |
Ccdc192 |
A |
T |
18: 57,800,376 (GRCm39) |
I176F |
possibly damaging |
Het |
Ccne1 |
A |
T |
7: 37,806,085 (GRCm39) |
M13K |
probably benign |
Het |
Chil3 |
A |
T |
3: 106,057,031 (GRCm39) |
Y304* |
probably null |
Het |
Chst15 |
A |
G |
7: 131,872,246 (GRCm39) |
F12L |
probably benign |
Het |
Cldn23 |
T |
A |
8: 36,292,826 (GRCm39) |
I221F |
probably damaging |
Het |
Col16a1 |
T |
C |
4: 129,946,652 (GRCm39) |
F92L |
unknown |
Het |
Col6a3 |
A |
T |
1: 90,710,057 (GRCm39) |
|
probably benign |
Het |
Cyp2w1 |
T |
A |
5: 139,340,314 (GRCm39) |
V199E |
possibly damaging |
Het |
Dmxl1 |
A |
G |
18: 49,997,240 (GRCm39) |
Y512C |
probably damaging |
Het |
Dop1a |
A |
T |
9: 86,397,396 (GRCm39) |
H900L |
probably damaging |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Eif3l |
T |
G |
15: 78,973,725 (GRCm39) |
M380R |
possibly damaging |
Het |
Fer1l5 |
A |
T |
1: 36,441,601 (GRCm39) |
K605N |
probably damaging |
Het |
Fgfbp1 |
T |
G |
5: 44,136,627 (GRCm39) |
N222H |
probably benign |
Het |
Flcn |
A |
G |
11: 59,690,233 (GRCm39) |
L273P |
possibly damaging |
Het |
Fzd10 |
C |
G |
5: 128,679,369 (GRCm39) |
P363R |
probably damaging |
Het |
Gabpa |
A |
G |
16: 84,638,209 (GRCm39) |
|
probably benign |
Het |
Garin4 |
A |
C |
1: 190,895,258 (GRCm39) |
S462A |
probably benign |
Het |
Gfi1 |
A |
G |
5: 107,873,425 (GRCm39) |
|
probably null |
Het |
Ift57 |
A |
G |
16: 49,579,777 (GRCm39) |
Q316R |
probably benign |
Het |
Itga11 |
T |
C |
9: 62,662,909 (GRCm39) |
F542L |
probably benign |
Het |
Kif28 |
G |
C |
1: 179,529,984 (GRCm39) |
L726V |
possibly damaging |
Het |
Krt90 |
A |
G |
15: 101,471,235 (GRCm39) |
I9T |
probably benign |
Het |
Lefty1 |
A |
T |
1: 180,765,241 (GRCm39) |
M270L |
probably benign |
Het |
Mipol1 |
A |
T |
12: 57,503,865 (GRCm39) |
E344D |
probably benign |
Het |
Mon2 |
A |
T |
10: 122,862,213 (GRCm39) |
M737K |
possibly damaging |
Het |
Mrpl14 |
A |
G |
17: 46,009,330 (GRCm39) |
N143S |
probably benign |
Het |
Nelfcd |
T |
A |
2: 174,268,717 (GRCm39) |
H589Q |
probably benign |
Het |
Npepps |
T |
C |
11: 97,131,757 (GRCm39) |
M366V |
probably damaging |
Het |
Or5b12 |
A |
T |
19: 12,897,479 (GRCm39) |
S65T |
probably damaging |
Het |
Platr25 |
T |
A |
13: 62,848,280 (GRCm39) |
H194L |
probably damaging |
Het |
Plekhg4 |
T |
C |
8: 106,102,284 (GRCm39) |
I127T |
probably benign |
Het |
Ralgapa1 |
A |
T |
12: 55,652,314 (GRCm39) |
|
probably benign |
Het |
Rarb |
A |
G |
14: 16,435,140 (GRCm38) |
V302A |
probably damaging |
Het |
Rc3h1 |
A |
C |
1: 160,792,673 (GRCm39) |
T1037P |
probably damaging |
Het |
Rnaset2a |
G |
A |
17: 8,356,760 (GRCm39) |
P102S |
probably damaging |
Het |
Scn10a |
A |
C |
9: 119,459,160 (GRCm39) |
S1166R |
probably damaging |
Het |
Scn3a |
A |
G |
2: 65,352,170 (GRCm39) |
M380T |
possibly damaging |
Het |
Serpinb13 |
A |
G |
1: 106,923,519 (GRCm39) |
I75V |
probably benign |
Het |
Slc35f5 |
G |
A |
1: 125,490,050 (GRCm39) |
A27T |
probably benign |
Het |
Slc45a3 |
G |
A |
1: 131,905,714 (GRCm39) |
V246I |
probably benign |
Het |
Slc7a14 |
G |
A |
3: 31,278,345 (GRCm39) |
T420I |
probably damaging |
Het |
Slc9a9 |
A |
G |
9: 94,818,493 (GRCm39) |
T296A |
probably benign |
Het |
Smyd2 |
G |
A |
1: 189,628,833 (GRCm39) |
H157Y |
probably damaging |
Het |
Spata32 |
T |
A |
11: 103,100,677 (GRCm39) |
H30L |
probably benign |
Het |
Srarp |
T |
C |
4: 141,160,344 (GRCm39) |
E163G |
possibly damaging |
Het |
Tcstv2a |
A |
G |
13: 120,725,746 (GRCm39) |
T137A |
probably damaging |
Het |
Tmed8 |
A |
G |
12: 87,220,938 (GRCm39) |
I216T |
probably damaging |
Het |
Tnni3k |
A |
T |
3: 154,562,186 (GRCm39) |
L697Q |
probably damaging |
Het |
Tra2b |
G |
A |
16: 22,065,940 (GRCm39) |
R286C |
unknown |
Het |
Trav7-6 |
A |
G |
14: 53,954,604 (GRCm39) |
K65E |
probably benign |
Het |
Ttn |
T |
C |
2: 76,540,506 (GRCm39) |
D34160G |
possibly damaging |
Het |
Umad1 |
T |
A |
6: 8,373,931 (GRCm39) |
C36* |
probably null |
Het |
Ush2a |
A |
T |
1: 188,638,676 (GRCm39) |
T4029S |
probably damaging |
Het |
Usp9y |
C |
T |
Y: 1,316,978 (GRCm39) |
S1857N |
probably benign |
Het |
Vwa3b |
A |
G |
1: 37,154,767 (GRCm39) |
N517S |
probably damaging |
Het |
Zfp583 |
G |
A |
7: 6,319,627 (GRCm39) |
P462S |
probably damaging |
Het |
|
Other mutations in Actr10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02084:Actr10
|
APN |
12 |
71,001,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Actr10
|
APN |
12 |
70,990,289 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02628:Actr10
|
APN |
12 |
71,001,430 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03202:Actr10
|
APN |
12 |
70,987,605 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03266:Actr10
|
APN |
12 |
71,003,440 (GRCm39) |
missense |
probably benign |
0.00 |
R0505:Actr10
|
UTSW |
12 |
71,006,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Actr10
|
UTSW |
12 |
71,008,770 (GRCm39) |
missense |
probably benign |
0.23 |
R1919:Actr10
|
UTSW |
12 |
70,989,104 (GRCm39) |
missense |
probably benign |
0.00 |
R2151:Actr10
|
UTSW |
12 |
70,987,575 (GRCm39) |
nonsense |
probably null |
|
R2201:Actr10
|
UTSW |
12 |
71,006,795 (GRCm39) |
missense |
probably damaging |
0.97 |
R4259:Actr10
|
UTSW |
12 |
70,999,759 (GRCm39) |
missense |
probably benign |
0.02 |
R4261:Actr10
|
UTSW |
12 |
70,999,759 (GRCm39) |
missense |
probably benign |
0.02 |
R5138:Actr10
|
UTSW |
12 |
71,008,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5326:Actr10
|
UTSW |
12 |
71,001,430 (GRCm39) |
unclassified |
probably benign |
|
R5542:Actr10
|
UTSW |
12 |
71,001,430 (GRCm39) |
unclassified |
probably benign |
|
R6248:Actr10
|
UTSW |
12 |
70,999,733 (GRCm39) |
missense |
probably benign |
0.00 |
R6882:Actr10
|
UTSW |
12 |
71,003,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7102:Actr10
|
UTSW |
12 |
70,999,805 (GRCm39) |
critical splice donor site |
probably null |
|
R7758:Actr10
|
UTSW |
12 |
70,989,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R7800:Actr10
|
UTSW |
12 |
70,990,283 (GRCm39) |
missense |
probably benign |
0.26 |
R8766:Actr10
|
UTSW |
12 |
71,001,430 (GRCm39) |
critical splice donor site |
probably null |
|
R8850:Actr10
|
UTSW |
12 |
70,989,032 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9068:Actr10
|
UTSW |
12 |
70,989,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Actr10
|
UTSW |
12 |
70,990,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Actr10
|
UTSW |
12 |
71,006,818 (GRCm39) |
critical splice donor site |
probably null |
|
X0012:Actr10
|
UTSW |
12 |
70,987,639 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Actr10
|
UTSW |
12 |
71,006,733 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Actr10
|
UTSW |
12 |
71,008,803 (GRCm39) |
missense |
probably damaging |
0.99 |
|