Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
C |
2: 68,571,800 (GRCm39) |
S559P |
probably benign |
Het |
A430005L14Rik |
T |
A |
4: 154,044,314 (GRCm39) |
C42S |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,223,967 (GRCm39) |
T449S |
probably benign |
Het |
Acvr1c |
T |
A |
2: 58,205,987 (GRCm39) |
Q41L |
probably benign |
Het |
Adamts13 |
C |
T |
2: 26,864,002 (GRCm39) |
P60L |
probably benign |
Het |
Adamts20 |
T |
C |
15: 94,245,599 (GRCm39) |
T568A |
possibly damaging |
Het |
Ago1 |
T |
C |
4: 126,348,187 (GRCm39) |
I44V |
probably null |
Het |
Ankrd28 |
A |
T |
14: 31,467,293 (GRCm39) |
V39E |
possibly damaging |
Het |
Apaf1 |
A |
G |
10: 90,897,676 (GRCm39) |
V269A |
possibly damaging |
Het |
Astn1 |
A |
G |
1: 158,348,091 (GRCm39) |
N506D |
probably damaging |
Het |
BC051019 |
G |
A |
7: 109,319,758 (GRCm39) |
Q102* |
probably null |
Het |
Bpifb5 |
A |
G |
2: 154,075,199 (GRCm39) |
T376A |
possibly damaging |
Het |
Ccdc121rt1 |
G |
T |
1: 181,338,551 (GRCm39) |
Q134K |
probably benign |
Het |
Ccl20 |
ATT |
ATTT |
1: 83,095,576 (GRCm39) |
|
probably null |
Het |
Ccl6 |
G |
T |
11: 83,480,163 (GRCm39) |
P68T |
possibly damaging |
Het |
Cd300ld |
A |
T |
11: 114,878,156 (GRCm39) |
F119I |
probably benign |
Het |
Cdk2ap2 |
A |
G |
19: 4,147,903 (GRCm39) |
M57V |
possibly damaging |
Het |
Cemip2 |
A |
G |
19: 21,779,351 (GRCm39) |
D387G |
probably benign |
Het |
Chkb |
C |
T |
15: 89,312,969 (GRCm39) |
G36E |
probably damaging |
Het |
Col11a1 |
A |
G |
3: 113,958,942 (GRCm39) |
|
probably null |
Het |
Ctla2b |
T |
C |
13: 61,043,881 (GRCm39) |
Y120C |
probably damaging |
Het |
Ctnnd1 |
T |
C |
2: 84,450,704 (GRCm39) |
N172S |
probably benign |
Het |
Cyp2a22 |
G |
A |
7: 26,634,197 (GRCm39) |
P319L |
probably damaging |
Het |
Dcaf12 |
A |
C |
4: 41,302,804 (GRCm39) |
V117G |
probably damaging |
Het |
Ddx6 |
A |
G |
9: 44,518,831 (GRCm39) |
T48A |
probably benign |
Het |
Dgki |
T |
C |
6: 36,842,736 (GRCm39) |
D923G |
possibly damaging |
Het |
Dhx37 |
G |
T |
5: 125,504,528 (GRCm39) |
T345K |
probably damaging |
Het |
Dhx9 |
A |
T |
1: 153,331,857 (GRCm39) |
Y1370* |
probably null |
Het |
Dnah7b |
T |
C |
1: 46,181,247 (GRCm39) |
S1045P |
possibly damaging |
Het |
Dnmbp |
G |
C |
19: 43,838,612 (GRCm39) |
T1071S |
possibly damaging |
Het |
Dspp |
T |
A |
5: 104,326,425 (GRCm39) |
S929R |
unknown |
Het |
Dst |
A |
T |
1: 34,223,144 (GRCm39) |
E1625D |
probably damaging |
Het |
Egflam |
T |
A |
15: 7,272,048 (GRCm39) |
H630L |
probably benign |
Het |
Elane |
T |
C |
10: 79,723,593 (GRCm39) |
V186A |
possibly damaging |
Het |
Fam209 |
C |
A |
2: 172,314,689 (GRCm39) |
N59K |
probably benign |
Het |
Gbe1 |
A |
G |
16: 70,325,814 (GRCm39) |
E617G |
probably damaging |
Het |
Get3 |
T |
C |
8: 85,751,789 (GRCm39) |
S36G |
probably damaging |
Het |
Gfra1 |
A |
G |
19: 58,288,707 (GRCm39) |
L246P |
probably damaging |
Het |
Gria2 |
T |
C |
3: 80,618,112 (GRCm39) |
T308A |
probably benign |
Het |
Grip2 |
A |
T |
6: 91,756,831 (GRCm39) |
V540D |
probably benign |
Het |
Hhipl1 |
A |
T |
12: 108,288,118 (GRCm39) |
I575F |
possibly damaging |
Het |
Hmcn1 |
T |
A |
1: 150,614,364 (GRCm39) |
E1347D |
possibly damaging |
Het |
Itga2b |
C |
A |
11: 102,358,165 (GRCm39) |
A187S |
probably benign |
Het |
Kalrn |
C |
A |
16: 33,848,415 (GRCm39) |
R469M |
probably damaging |
Het |
Kif23 |
A |
T |
9: 61,834,666 (GRCm39) |
C426* |
probably null |
Het |
Lck |
T |
C |
4: 129,442,730 (GRCm39) |
N475S |
probably benign |
Het |
Leng8 |
A |
G |
7: 4,148,073 (GRCm39) |
N642S |
probably damaging |
Het |
Lingo4 |
T |
A |
3: 94,310,382 (GRCm39) |
I440N |
probably damaging |
Het |
Lrrc4 |
A |
G |
6: 28,830,904 (GRCm39) |
F237S |
probably damaging |
Het |
Magel2 |
G |
A |
7: 62,028,844 (GRCm39) |
V583I |
unknown |
Het |
Naip2 |
A |
T |
13: 100,281,096 (GRCm39) |
I1316N |
probably damaging |
Het |
Naip6 |
C |
T |
13: 100,437,237 (GRCm39) |
G429S |
probably benign |
Het |
Noct |
C |
T |
3: 51,155,465 (GRCm39) |
R78C |
probably damaging |
Het |
Npbwr1 |
A |
G |
1: 5,987,394 (GRCm39) |
V40A |
possibly damaging |
Het |
Nsd2 |
A |
G |
5: 34,000,746 (GRCm39) |
N88D |
probably damaging |
Het |
Or1e29 |
T |
A |
11: 73,667,539 (GRCm39) |
I205F |
probably benign |
Het |
Or5ap2 |
T |
A |
2: 85,680,744 (GRCm39) |
V316E |
probably benign |
Het |
Or6c210 |
T |
A |
10: 129,496,290 (GRCm39) |
I205N |
probably benign |
Het |
Or8k28 |
T |
C |
2: 86,285,817 (GRCm39) |
H266R |
probably benign |
Het |
Pak5 |
T |
A |
2: 135,958,557 (GRCm39) |
H177L |
probably benign |
Het |
Pard3 |
C |
T |
8: 127,791,097 (GRCm39) |
|
probably null |
Het |
Pde4c |
A |
G |
8: 71,200,007 (GRCm39) |
|
probably null |
Het |
Pde6h |
T |
A |
6: 136,940,203 (GRCm39) |
I63N |
probably damaging |
Het |
Phldb2 |
T |
C |
16: 45,594,558 (GRCm39) |
K916E |
possibly damaging |
Het |
Ppig |
T |
C |
2: 69,571,988 (GRCm39) |
S236P |
unknown |
Het |
Ptprd |
T |
C |
4: 75,872,359 (GRCm39) |
Y1370C |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,493,083 (GRCm39) |
T352A |
probably benign |
Het |
Rab3gap1 |
A |
G |
1: 127,831,456 (GRCm39) |
Y177C |
possibly damaging |
Het |
Rasgef1a |
G |
A |
6: 118,066,157 (GRCm39) |
V457M |
probably benign |
Het |
Scel |
A |
T |
14: 103,848,226 (GRCm39) |
T616S |
possibly damaging |
Het |
Sel1l |
A |
T |
12: 91,793,324 (GRCm39) |
Y228* |
probably null |
Het |
Sgms1 |
A |
G |
19: 32,137,083 (GRCm39) |
V161A |
possibly damaging |
Het |
Slfnl1 |
T |
C |
4: 120,390,424 (GRCm39) |
L25P |
probably benign |
Het |
Smad5 |
A |
G |
13: 56,885,187 (GRCm39) |
T432A |
probably damaging |
Het |
Sohlh2 |
T |
C |
3: 55,099,762 (GRCm39) |
|
probably null |
Het |
Sphkap |
A |
T |
1: 83,254,383 (GRCm39) |
M835K |
probably damaging |
Het |
Sqor |
A |
C |
2: 122,640,018 (GRCm39) |
T174P |
probably damaging |
Het |
Stkld1 |
T |
C |
2: 26,842,759 (GRCm39) |
V577A |
probably damaging |
Het |
Sulf2 |
T |
A |
2: 165,922,773 (GRCm39) |
E652D |
probably benign |
Het |
Sycp2 |
T |
A |
2: 178,019,848 (GRCm39) |
Q556L |
probably benign |
Het |
Syk |
A |
G |
13: 52,765,274 (GRCm39) |
T134A |
probably benign |
Het |
Tas2r122 |
T |
A |
6: 132,688,585 (GRCm39) |
I103F |
possibly damaging |
Het |
Tex10 |
A |
G |
4: 48,451,940 (GRCm39) |
W729R |
probably damaging |
Het |
Tex261 |
G |
T |
6: 83,750,713 (GRCm39) |
P95T |
probably damaging |
Het |
Tm2d2 |
T |
C |
8: 25,507,523 (GRCm39) |
S47P |
probably benign |
Het |
Tmem95 |
A |
G |
11: 69,767,817 (GRCm39) |
S128P |
probably damaging |
Het |
Tnxb |
G |
A |
17: 34,911,553 (GRCm39) |
A1619T |
possibly damaging |
Het |
Trappc9 |
A |
G |
15: 72,929,885 (GRCm39) |
I157T |
probably damaging |
Het |
Unc13c |
T |
A |
9: 73,390,897 (GRCm39) |
|
probably null |
Het |
Upb1 |
A |
T |
10: 75,265,803 (GRCm39) |
Y210F |
probably damaging |
Het |
Urb1 |
T |
C |
16: 90,559,232 (GRCm39) |
M1684V |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,232,158 (GRCm39) |
P727S |
possibly damaging |
Het |
Zfp1004 |
T |
A |
2: 150,034,867 (GRCm39) |
M396K |
probably benign |
Het |
Zfp551 |
A |
T |
7: 12,150,276 (GRCm39) |
S378T |
probably damaging |
Het |
Zfp598 |
T |
C |
17: 24,888,898 (GRCm39) |
V56A |
possibly damaging |
Het |
Zfp945 |
C |
T |
17: 23,076,223 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Agtpbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00544:Agtpbp1
|
APN |
13 |
59,597,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00808:Agtpbp1
|
APN |
13 |
59,609,908 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01298:Agtpbp1
|
APN |
13 |
59,652,040 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01628:Agtpbp1
|
APN |
13 |
59,655,877 (GRCm39) |
splice site |
probably benign |
|
IGL01921:Agtpbp1
|
APN |
13 |
59,660,297 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02189:Agtpbp1
|
APN |
13 |
59,648,275 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02325:Agtpbp1
|
APN |
13 |
59,648,303 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02700:Agtpbp1
|
APN |
13 |
59,676,233 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02821:Agtpbp1
|
APN |
13 |
59,630,415 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03130:Agtpbp1
|
APN |
13 |
59,622,403 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03167:Agtpbp1
|
APN |
13 |
59,679,894 (GRCm39) |
splice site |
probably benign |
|
IGL03218:Agtpbp1
|
APN |
13 |
59,648,021 (GRCm39) |
missense |
possibly damaging |
0.94 |
bobs
|
UTSW |
13 |
59,630,385 (GRCm39) |
missense |
possibly damaging |
0.53 |
drunk
|
UTSW |
13 |
59,660,136 (GRCm39) |
critical splice donor site |
probably benign |
|
gru
|
UTSW |
13 |
59,621,560 (GRCm39) |
missense |
probably damaging |
1.00 |
rio
|
UTSW |
13 |
59,673,055 (GRCm39) |
critical splice acceptor site |
probably benign |
|
shreds
|
UTSW |
13 |
59,609,902 (GRCm39) |
missense |
probably damaging |
1.00 |
Unfocused
|
UTSW |
13 |
59,609,884 (GRCm39) |
nonsense |
probably null |
|
wobble
|
UTSW |
13 |
59,622,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Agtpbp1
|
UTSW |
13 |
59,648,014 (GRCm39) |
missense |
probably benign |
0.00 |
R0025:Agtpbp1
|
UTSW |
13 |
59,648,014 (GRCm39) |
missense |
probably benign |
0.00 |
R0276:Agtpbp1
|
UTSW |
13 |
59,609,845 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0413:Agtpbp1
|
UTSW |
13 |
59,661,966 (GRCm39) |
missense |
probably damaging |
0.99 |
R0559:Agtpbp1
|
UTSW |
13 |
59,644,814 (GRCm39) |
missense |
probably benign |
0.32 |
R0848:Agtpbp1
|
UTSW |
13 |
59,681,753 (GRCm39) |
intron |
probably benign |
|
R0943:Agtpbp1
|
UTSW |
13 |
59,648,416 (GRCm39) |
missense |
probably benign |
|
R1196:Agtpbp1
|
UTSW |
13 |
59,598,132 (GRCm39) |
unclassified |
probably benign |
|
R1421:Agtpbp1
|
UTSW |
13 |
59,643,389 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1531:Agtpbp1
|
UTSW |
13 |
59,648,448 (GRCm39) |
splice site |
probably null |
|
R1833:Agtpbp1
|
UTSW |
13 |
59,613,797 (GRCm39) |
critical splice donor site |
probably null |
|
R1864:Agtpbp1
|
UTSW |
13 |
59,598,016 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1994:Agtpbp1
|
UTSW |
13 |
59,678,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1995:Agtpbp1
|
UTSW |
13 |
59,678,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Agtpbp1
|
UTSW |
13 |
59,648,135 (GRCm39) |
missense |
probably benign |
0.00 |
R2397:Agtpbp1
|
UTSW |
13 |
59,622,383 (GRCm39) |
missense |
probably benign |
0.10 |
R2918:Agtpbp1
|
UTSW |
13 |
59,644,829 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3873:Agtpbp1
|
UTSW |
13 |
59,608,410 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3924:Agtpbp1
|
UTSW |
13 |
59,648,221 (GRCm39) |
missense |
probably benign |
0.01 |
R4649:Agtpbp1
|
UTSW |
13 |
59,676,213 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4913:Agtpbp1
|
UTSW |
13 |
59,647,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Agtpbp1
|
UTSW |
13 |
59,648,386 (GRCm39) |
missense |
probably benign |
|
R4969:Agtpbp1
|
UTSW |
13 |
59,648,392 (GRCm39) |
missense |
probably benign |
|
R5066:Agtpbp1
|
UTSW |
13 |
59,622,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R5139:Agtpbp1
|
UTSW |
13 |
59,648,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R5194:Agtpbp1
|
UTSW |
13 |
59,648,453 (GRCm39) |
missense |
probably benign |
0.19 |
R5269:Agtpbp1
|
UTSW |
13 |
59,621,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Agtpbp1
|
UTSW |
13 |
59,621,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5558:Agtpbp1
|
UTSW |
13 |
59,630,394 (GRCm39) |
missense |
probably benign |
0.05 |
R5687:Agtpbp1
|
UTSW |
13 |
59,648,329 (GRCm39) |
missense |
probably benign |
|
R5824:Agtpbp1
|
UTSW |
13 |
59,613,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Agtpbp1
|
UTSW |
13 |
59,681,860 (GRCm39) |
nonsense |
probably null |
|
R6109:Agtpbp1
|
UTSW |
13 |
59,621,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Agtpbp1
|
UTSW |
13 |
59,598,114 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6413:Agtpbp1
|
UTSW |
13 |
59,647,834 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6498:Agtpbp1
|
UTSW |
13 |
59,624,854 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6747:Agtpbp1
|
UTSW |
13 |
59,692,167 (GRCm39) |
splice site |
probably null |
|
R6950:Agtpbp1
|
UTSW |
13 |
59,598,080 (GRCm39) |
missense |
probably benign |
0.32 |
R7030:Agtpbp1
|
UTSW |
13 |
59,652,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Agtpbp1
|
UTSW |
13 |
59,613,852 (GRCm39) |
missense |
probably benign |
0.11 |
R7196:Agtpbp1
|
UTSW |
13 |
59,680,994 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7535:Agtpbp1
|
UTSW |
13 |
59,652,067 (GRCm39) |
missense |
probably benign |
|
R7683:Agtpbp1
|
UTSW |
13 |
59,660,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R7713:Agtpbp1
|
UTSW |
13 |
59,661,966 (GRCm39) |
missense |
probably damaging |
0.99 |
R8081:Agtpbp1
|
UTSW |
13 |
59,676,221 (GRCm39) |
nonsense |
probably null |
|
R8210:Agtpbp1
|
UTSW |
13 |
59,630,385 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8861:Agtpbp1
|
UTSW |
13 |
59,643,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R9163:Agtpbp1
|
UTSW |
13 |
59,609,884 (GRCm39) |
nonsense |
probably null |
|
R9199:Agtpbp1
|
UTSW |
13 |
59,613,808 (GRCm39) |
missense |
probably benign |
0.00 |
R9389:Agtpbp1
|
UTSW |
13 |
59,613,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9414:Agtpbp1
|
UTSW |
13 |
59,609,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R9435:Agtpbp1
|
UTSW |
13 |
59,622,429 (GRCm39) |
missense |
probably benign |
0.35 |
|