Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
T |
C |
4: 103,092,689 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
G |
A |
13: 81,545,345 (GRCm39) |
R5647* |
probably null |
Het |
Agbl2 |
C |
T |
2: 90,627,827 (GRCm39) |
R211* |
probably null |
Het |
Akap9 |
A |
G |
5: 4,011,714 (GRCm39) |
K806E |
probably benign |
Het |
Atcay |
T |
C |
10: 81,060,294 (GRCm39) |
D14G |
possibly damaging |
Het |
Atp8b4 |
C |
T |
2: 126,220,626 (GRCm39) |
|
probably benign |
Het |
Bmp8b |
T |
C |
4: 123,018,308 (GRCm39) |
V393A |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,465,322 (GRCm39) |
D1695E |
probably damaging |
Het |
Cdh15 |
A |
G |
8: 123,587,705 (GRCm39) |
I210V |
probably damaging |
Het |
Cep250 |
T |
C |
2: 155,813,924 (GRCm39) |
L564P |
possibly damaging |
Het |
Cmpk1 |
T |
C |
4: 114,822,220 (GRCm39) |
T110A |
probably benign |
Het |
Cpsf3 |
T |
G |
12: 21,350,085 (GRCm39) |
I268S |
probably damaging |
Het |
Csmd2 |
C |
T |
4: 128,414,023 (GRCm39) |
A2621V |
probably benign |
Het |
Cyp2c40 |
T |
C |
19: 39,795,607 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
T |
A |
2: 103,998,292 (GRCm39) |
Y1837F |
probably damaging |
Het |
Degs2 |
A |
G |
12: 108,668,469 (GRCm39) |
F10S |
probably damaging |
Het |
Dytn |
T |
A |
1: 63,717,933 (GRCm39) |
|
probably benign |
Het |
Elfn2 |
G |
C |
15: 78,557,795 (GRCm39) |
P251A |
probably benign |
Het |
Epg5 |
T |
C |
18: 78,066,486 (GRCm39) |
|
probably benign |
Het |
Evc2 |
A |
G |
5: 37,574,811 (GRCm39) |
D1022G |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,856,304 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,151,675 (GRCm39) |
|
probably null |
Het |
Gm15217 |
T |
C |
14: 46,620,676 (GRCm39) |
|
probably null |
Het |
Gm17611 |
A |
T |
13: 50,130,435 (GRCm39) |
|
noncoding transcript |
Het |
Gpld1 |
G |
A |
13: 25,146,303 (GRCm39) |
W182* |
probably null |
Het |
Gsc |
T |
C |
12: 104,439,353 (GRCm39) |
I8V |
probably damaging |
Het |
Hck |
A |
G |
2: 152,976,052 (GRCm39) |
K197R |
probably benign |
Het |
Kat6b |
T |
C |
14: 21,720,301 (GRCm39) |
L1551P |
probably damaging |
Het |
Lrch1 |
C |
T |
14: 75,184,985 (GRCm39) |
G39D |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,259,148 (GRCm39) |
|
probably null |
Het |
Mroh9 |
A |
T |
1: 162,888,331 (GRCm39) |
V248E |
probably damaging |
Het |
Mrps15 |
C |
A |
4: 125,945,210 (GRCm39) |
|
probably benign |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Ndufa5 |
T |
C |
6: 24,522,750 (GRCm39) |
T31A |
probably benign |
Het |
Nfyb |
A |
G |
10: 82,586,594 (GRCm39) |
V190A |
possibly damaging |
Het |
Nos2 |
A |
G |
11: 78,819,409 (GRCm39) |
I40M |
probably benign |
Het |
Or2f2 |
T |
C |
6: 42,767,108 (GRCm39) |
I45T |
probably damaging |
Het |
Or5ar1 |
A |
T |
2: 85,671,859 (GRCm39) |
I92N |
probably damaging |
Het |
Or8k37 |
A |
T |
2: 86,469,674 (GRCm39) |
I126K |
probably damaging |
Het |
Otog |
T |
C |
7: 45,955,301 (GRCm39) |
S564P |
probably damaging |
Het |
Pak5 |
C |
T |
2: 135,958,549 (GRCm39) |
A180T |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,590,628 (GRCm39) |
|
probably benign |
Het |
Pkd1l3 |
C |
G |
8: 110,350,281 (GRCm39) |
D375E |
possibly damaging |
Het |
Plxnc1 |
T |
A |
10: 94,632,344 (GRCm39) |
N1431I |
probably damaging |
Het |
Prph |
A |
T |
15: 98,955,319 (GRCm39) |
I429L |
probably damaging |
Het |
Prrc2a |
A |
G |
17: 35,368,664 (GRCm39) |
|
probably benign |
Het |
Pwwp3a |
A |
T |
10: 80,064,859 (GRCm39) |
N30Y |
probably damaging |
Het |
Rad54b |
A |
T |
4: 11,563,394 (GRCm39) |
T18S |
probably benign |
Het |
Ranbp2 |
A |
G |
10: 58,321,590 (GRCm39) |
E2629G |
probably benign |
Het |
Rec114 |
G |
A |
9: 58,565,053 (GRCm39) |
T201I |
probably benign |
Het |
Rspo1 |
G |
A |
4: 124,885,190 (GRCm39) |
R22Q |
probably benign |
Het |
Sec23b |
A |
G |
2: 144,423,917 (GRCm39) |
E522G |
probably damaging |
Het |
Sgsm3 |
G |
A |
15: 80,893,971 (GRCm39) |
R502H |
possibly damaging |
Het |
Sh3pxd2b |
C |
A |
11: 32,373,023 (GRCm39) |
A730D |
possibly damaging |
Het |
Spag4 |
A |
G |
2: 155,909,899 (GRCm39) |
D187G |
probably damaging |
Het |
Srgap2 |
G |
A |
1: 131,264,175 (GRCm39) |
T465I |
probably damaging |
Het |
St3gal6 |
G |
T |
16: 58,293,818 (GRCm39) |
A237E |
probably damaging |
Het |
St3gal6 |
C |
A |
16: 58,293,816 (GRCm39) |
A238S |
probably damaging |
Het |
Tecpr1 |
C |
A |
5: 144,132,759 (GRCm39) |
R1159L |
probably benign |
Het |
Tmem63b |
A |
T |
17: 45,977,241 (GRCm39) |
|
probably null |
Het |
Tmtc1 |
T |
A |
6: 148,317,256 (GRCm39) |
D78V |
probably damaging |
Het |
Tpp2 |
A |
G |
1: 44,029,722 (GRCm39) |
N68D |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,770,269 (GRCm39) |
A2641S |
probably benign |
Het |
Uimc1 |
T |
C |
13: 55,241,032 (GRCm39) |
K19E |
probably damaging |
Het |
Utrn |
T |
A |
10: 12,564,038 (GRCm39) |
E1274V |
probably null |
Het |
Vmn2r102 |
A |
T |
17: 19,914,630 (GRCm39) |
I732F |
probably damaging |
Het |
Wrn |
A |
T |
8: 33,758,778 (GRCm39) |
M792K |
probably benign |
Het |
Zfp451 |
A |
G |
1: 33,816,126 (GRCm39) |
I608T |
probably damaging |
Het |
|
Other mutations in Ampd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00839:Ampd1
|
APN |
3 |
103,007,010 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL00909:Ampd1
|
APN |
3 |
102,995,744 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01543:Ampd1
|
APN |
3 |
103,003,029 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Ampd1
|
APN |
3 |
103,002,201 (GRCm39) |
splice site |
probably benign |
|
IGL02390:Ampd1
|
APN |
3 |
102,986,357 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02637:Ampd1
|
APN |
3 |
103,002,199 (GRCm39) |
splice site |
probably benign |
|
IGL02735:Ampd1
|
APN |
3 |
102,992,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03151:Ampd1
|
APN |
3 |
102,999,786 (GRCm39) |
splice site |
probably null |
|
twinkle_toes
|
UTSW |
3 |
103,002,962 (GRCm39) |
nonsense |
probably null |
|
R0158:Ampd1
|
UTSW |
3 |
102,999,046 (GRCm39) |
nonsense |
probably null |
|
R0646:Ampd1
|
UTSW |
3 |
103,006,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Ampd1
|
UTSW |
3 |
103,006,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Ampd1
|
UTSW |
3 |
102,998,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Ampd1
|
UTSW |
3 |
103,006,442 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2131:Ampd1
|
UTSW |
3 |
103,002,194 (GRCm39) |
critical splice donor site |
probably null |
|
R3706:Ampd1
|
UTSW |
3 |
102,995,627 (GRCm39) |
splice site |
probably benign |
|
R4007:Ampd1
|
UTSW |
3 |
102,999,776 (GRCm39) |
missense |
probably damaging |
0.99 |
R4169:Ampd1
|
UTSW |
3 |
103,002,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R4525:Ampd1
|
UTSW |
3 |
103,002,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Ampd1
|
UTSW |
3 |
102,988,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Ampd1
|
UTSW |
3 |
103,006,981 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5514:Ampd1
|
UTSW |
3 |
102,986,488 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5839:Ampd1
|
UTSW |
3 |
102,992,744 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5872:Ampd1
|
UTSW |
3 |
102,986,446 (GRCm39) |
missense |
probably benign |
0.00 |
R5890:Ampd1
|
UTSW |
3 |
102,997,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R5986:Ampd1
|
UTSW |
3 |
102,992,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6272:Ampd1
|
UTSW |
3 |
102,992,699 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6473:Ampd1
|
UTSW |
3 |
103,002,962 (GRCm39) |
nonsense |
probably null |
|
R6504:Ampd1
|
UTSW |
3 |
103,006,911 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7051:Ampd1
|
UTSW |
3 |
102,997,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R7323:Ampd1
|
UTSW |
3 |
102,992,696 (GRCm39) |
missense |
probably benign |
|
R7424:Ampd1
|
UTSW |
3 |
102,995,758 (GRCm39) |
missense |
probably benign |
0.05 |
R7436:Ampd1
|
UTSW |
3 |
102,981,435 (GRCm39) |
critical splice donor site |
probably null |
|
R7546:Ampd1
|
UTSW |
3 |
103,003,028 (GRCm39) |
missense |
probably benign |
|
R8344:Ampd1
|
UTSW |
3 |
103,003,002 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8366:Ampd1
|
UTSW |
3 |
102,995,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R8423:Ampd1
|
UTSW |
3 |
102,988,305 (GRCm39) |
missense |
probably benign |
|
R8543:Ampd1
|
UTSW |
3 |
102,986,486 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8730:Ampd1
|
UTSW |
3 |
102,992,676 (GRCm39) |
nonsense |
probably null |
|
R8904:Ampd1
|
UTSW |
3 |
102,988,374 (GRCm39) |
missense |
probably benign |
0.12 |
R9017:Ampd1
|
UTSW |
3 |
102,995,786 (GRCm39) |
missense |
probably benign |
0.01 |
R9121:Ampd1
|
UTSW |
3 |
103,005,998 (GRCm39) |
nonsense |
probably null |
|
R9150:Ampd1
|
UTSW |
3 |
102,988,359 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9242:Ampd1
|
UTSW |
3 |
102,998,936 (GRCm39) |
missense |
probably damaging |
1.00 |
|