Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AC163020.1 |
A |
G |
7: 46,959,305 (GRCm39) |
S229P |
possibly damaging |
Het |
Arap1 |
G |
A |
7: 101,047,643 (GRCm39) |
|
probably null |
Het |
Asb8 |
G |
A |
15: 98,039,248 (GRCm39) |
H51Y |
possibly damaging |
Het |
Capn10 |
T |
G |
1: 92,872,744 (GRCm39) |
V490G |
probably benign |
Het |
Ccdc138 |
T |
A |
10: 58,380,939 (GRCm39) |
|
probably benign |
Het |
Ccdc146 |
G |
A |
5: 21,604,730 (GRCm39) |
S36L |
probably benign |
Het |
Celsr1 |
C |
T |
15: 85,789,635 (GRCm39) |
|
probably null |
Het |
Clvs2 |
C |
A |
10: 33,389,256 (GRCm39) |
*328L |
probably null |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
D6Wsu163e |
G |
A |
6: 126,951,446 (GRCm39) |
|
probably benign |
Het |
Dstn |
A |
G |
2: 143,780,356 (GRCm39) |
K19E |
probably damaging |
Het |
Ehmt2 |
T |
A |
17: 35,125,553 (GRCm39) |
H134Q |
probably benign |
Het |
Faah |
G |
A |
4: 115,858,345 (GRCm39) |
P411S |
probably damaging |
Het |
Fn1 |
A |
G |
1: 71,681,237 (GRCm39) |
F364L |
probably damaging |
Het |
Gm5828 |
T |
C |
1: 16,839,768 (GRCm39) |
|
noncoding transcript |
Het |
Gmnc |
A |
T |
16: 26,779,196 (GRCm39) |
N270K |
possibly damaging |
Het |
Grip2 |
A |
T |
6: 91,765,133 (GRCm39) |
|
probably null |
Het |
Hmg20a |
A |
T |
9: 56,384,587 (GRCm39) |
Q119L |
possibly damaging |
Het |
Ipo7 |
T |
C |
7: 109,629,048 (GRCm39) |
I106T |
probably benign |
Het |
Ipo7 |
C |
T |
7: 109,638,456 (GRCm39) |
P241L |
probably damaging |
Het |
Katnb1 |
T |
C |
8: 95,824,801 (GRCm39) |
Y574H |
probably damaging |
Het |
Larp6 |
A |
C |
9: 60,644,849 (GRCm39) |
M330L |
probably benign |
Het |
Lrrc8e |
T |
C |
8: 4,281,754 (GRCm39) |
Y30H |
probably damaging |
Het |
Nav3 |
A |
T |
10: 109,606,194 (GRCm39) |
|
probably benign |
Het |
Nop56 |
T |
C |
2: 130,119,868 (GRCm39) |
V420A |
probably benign |
Het |
Nrg1 |
T |
C |
8: 32,407,855 (GRCm39) |
D126G |
probably benign |
Het |
Prdm1 |
T |
A |
10: 44,315,961 (GRCm39) |
N725I |
probably damaging |
Het |
Prl3a1 |
A |
G |
13: 27,459,051 (GRCm39) |
|
probably null |
Het |
Psmd2 |
T |
C |
16: 20,471,034 (GRCm39) |
L59P |
possibly damaging |
Het |
Ptgdr2 |
T |
C |
19: 10,918,395 (GRCm39) |
V304A |
probably benign |
Het |
Ptp4a2 |
T |
A |
4: 129,738,851 (GRCm39) |
|
probably benign |
Het |
Rasa3 |
A |
G |
8: 13,638,027 (GRCm39) |
V339A |
possibly damaging |
Het |
Sec24c |
G |
A |
14: 20,742,593 (GRCm39) |
|
probably null |
Het |
Serpinb9e |
A |
G |
13: 33,444,009 (GRCm39) |
D343G |
probably benign |
Het |
Sptbn5 |
A |
T |
2: 119,881,097 (GRCm39) |
|
noncoding transcript |
Het |
Stab1 |
A |
C |
14: 30,870,958 (GRCm39) |
V1297G |
probably benign |
Het |
Stk4 |
C |
T |
2: 163,942,448 (GRCm39) |
T360M |
probably benign |
Het |
Tafa5 |
C |
T |
15: 87,565,678 (GRCm39) |
|
probably benign |
Het |
Tmprss2 |
G |
A |
16: 97,398,005 (GRCm39) |
T57I |
probably benign |
Het |
Tnrc6a |
A |
G |
7: 122,770,301 (GRCm39) |
D697G |
probably damaging |
Het |
Vwa5b2 |
T |
A |
16: 20,423,066 (GRCm39) |
D1021E |
probably benign |
Het |
Wdr46 |
C |
A |
17: 34,168,057 (GRCm39) |
P543Q |
probably damaging |
Het |
Zfp1005 |
T |
A |
2: 150,109,620 (GRCm39) |
Y103* |
probably null |
Het |
Zfp287 |
T |
A |
11: 62,619,137 (GRCm39) |
D119V |
probably damaging |
Het |
Zxdc |
A |
G |
6: 90,361,225 (GRCm39) |
S737G |
possibly damaging |
Het |
|
Other mutations in Abca1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Abca1
|
APN |
4 |
53,059,255 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00778:Abca1
|
APN |
4 |
53,086,132 (GRCm39) |
missense |
probably benign |
|
IGL01013:Abca1
|
APN |
4 |
53,038,185 (GRCm39) |
nonsense |
probably null |
|
IGL01510:Abca1
|
APN |
4 |
53,143,979 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01608:Abca1
|
APN |
4 |
53,038,158 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01845:Abca1
|
APN |
4 |
53,090,297 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02048:Abca1
|
APN |
4 |
53,069,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02249:Abca1
|
APN |
4 |
53,068,739 (GRCm39) |
nonsense |
probably null |
|
IGL02569:Abca1
|
APN |
4 |
53,034,061 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02622:Abca1
|
APN |
4 |
53,034,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R6720_abca1_529
|
UTSW |
4 |
53,083,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R0042:Abca1
|
UTSW |
4 |
53,059,245 (GRCm39) |
splice site |
probably benign |
|
R0042:Abca1
|
UTSW |
4 |
53,059,245 (GRCm39) |
splice site |
probably benign |
|
R0050:Abca1
|
UTSW |
4 |
53,069,910 (GRCm39) |
splice site |
probably benign |
|
R0107:Abca1
|
UTSW |
4 |
53,080,834 (GRCm39) |
missense |
probably benign |
0.00 |
R0127:Abca1
|
UTSW |
4 |
53,067,155 (GRCm39) |
missense |
probably benign |
0.00 |
R0178:Abca1
|
UTSW |
4 |
53,081,953 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0207:Abca1
|
UTSW |
4 |
53,086,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R0267:Abca1
|
UTSW |
4 |
53,046,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:Abca1
|
UTSW |
4 |
53,044,228 (GRCm39) |
missense |
probably benign |
|
R0586:Abca1
|
UTSW |
4 |
53,092,860 (GRCm39) |
missense |
probably benign |
0.00 |
R0587:Abca1
|
UTSW |
4 |
53,107,035 (GRCm39) |
missense |
probably benign |
0.00 |
R1403:Abca1
|
UTSW |
4 |
53,059,253 (GRCm39) |
splice site |
probably benign |
|
R1404:Abca1
|
UTSW |
4 |
53,059,253 (GRCm39) |
splice site |
probably benign |
|
R1558:Abca1
|
UTSW |
4 |
53,092,887 (GRCm39) |
missense |
probably null |
0.00 |
R1655:Abca1
|
UTSW |
4 |
53,050,964 (GRCm39) |
missense |
probably benign |
|
R1662:Abca1
|
UTSW |
4 |
53,090,251 (GRCm39) |
splice site |
probably null |
|
R1769:Abca1
|
UTSW |
4 |
53,074,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R1898:Abca1
|
UTSW |
4 |
53,071,977 (GRCm39) |
missense |
probably benign |
0.08 |
R1945:Abca1
|
UTSW |
4 |
53,061,509 (GRCm39) |
frame shift |
probably null |
|
R1966:Abca1
|
UTSW |
4 |
53,050,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:Abca1
|
UTSW |
4 |
53,069,881 (GRCm39) |
missense |
probably benign |
|
R2185:Abca1
|
UTSW |
4 |
53,089,830 (GRCm39) |
missense |
probably benign |
0.12 |
R2202:Abca1
|
UTSW |
4 |
53,090,291 (GRCm39) |
missense |
probably damaging |
0.96 |
R2203:Abca1
|
UTSW |
4 |
53,090,291 (GRCm39) |
missense |
probably damaging |
0.96 |
R2204:Abca1
|
UTSW |
4 |
53,090,291 (GRCm39) |
missense |
probably damaging |
0.96 |
R3056:Abca1
|
UTSW |
4 |
53,127,626 (GRCm39) |
missense |
probably benign |
|
R3849:Abca1
|
UTSW |
4 |
53,061,481 (GRCm39) |
splice site |
probably benign |
|
R3850:Abca1
|
UTSW |
4 |
53,061,481 (GRCm39) |
splice site |
probably benign |
|
R3906:Abca1
|
UTSW |
4 |
53,067,151 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3908:Abca1
|
UTSW |
4 |
53,067,151 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4050:Abca1
|
UTSW |
4 |
53,044,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R4204:Abca1
|
UTSW |
4 |
53,090,369 (GRCm39) |
missense |
probably benign |
0.00 |
R4225:Abca1
|
UTSW |
4 |
53,085,106 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4577:Abca1
|
UTSW |
4 |
53,062,568 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4979:Abca1
|
UTSW |
4 |
53,085,092 (GRCm39) |
splice site |
probably null |
|
R5022:Abca1
|
UTSW |
4 |
53,041,570 (GRCm39) |
frame shift |
probably null |
|
R5168:Abca1
|
UTSW |
4 |
53,086,070 (GRCm39) |
missense |
probably benign |
|
R5363:Abca1
|
UTSW |
4 |
53,132,963 (GRCm39) |
missense |
probably benign |
0.00 |
R5439:Abca1
|
UTSW |
4 |
53,042,381 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5604:Abca1
|
UTSW |
4 |
53,067,168 (GRCm39) |
splice site |
probably null |
|
R5614:Abca1
|
UTSW |
4 |
53,046,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Abca1
|
UTSW |
4 |
53,079,631 (GRCm39) |
missense |
probably benign |
|
R6001:Abca1
|
UTSW |
4 |
53,075,555 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6151:Abca1
|
UTSW |
4 |
53,085,261 (GRCm39) |
missense |
probably benign |
|
R6185:Abca1
|
UTSW |
4 |
53,078,089 (GRCm39) |
missense |
probably benign |
0.31 |
R6262:Abca1
|
UTSW |
4 |
53,092,917 (GRCm39) |
missense |
probably benign |
0.01 |
R6455:Abca1
|
UTSW |
4 |
53,042,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R6472:Abca1
|
UTSW |
4 |
53,085,991 (GRCm39) |
critical splice donor site |
probably null |
|
R6564:Abca1
|
UTSW |
4 |
53,034,031 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6720:Abca1
|
UTSW |
4 |
53,083,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R6903:Abca1
|
UTSW |
4 |
53,143,952 (GRCm39) |
missense |
probably benign |
0.17 |
R6960:Abca1
|
UTSW |
4 |
53,072,924 (GRCm39) |
missense |
probably benign |
0.00 |
R7065:Abca1
|
UTSW |
4 |
53,074,233 (GRCm39) |
missense |
probably damaging |
0.98 |
R7142:Abca1
|
UTSW |
4 |
53,082,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Abca1
|
UTSW |
4 |
53,067,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R7520:Abca1
|
UTSW |
4 |
53,078,114 (GRCm39) |
missense |
probably benign |
|
R7547:Abca1
|
UTSW |
4 |
53,109,269 (GRCm39) |
missense |
probably benign |
0.02 |
R7793:Abca1
|
UTSW |
4 |
53,042,367 (GRCm39) |
missense |
not run |
|
R7863:Abca1
|
UTSW |
4 |
53,107,179 (GRCm39) |
missense |
probably benign |
|
R7877:Abca1
|
UTSW |
4 |
53,046,135 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8010:Abca1
|
UTSW |
4 |
53,127,600 (GRCm39) |
missense |
probably benign |
|
R8058:Abca1
|
UTSW |
4 |
53,081,954 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8181:Abca1
|
UTSW |
4 |
53,059,303 (GRCm39) |
missense |
probably benign |
0.21 |
R8471:Abca1
|
UTSW |
4 |
53,044,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Abca1
|
UTSW |
4 |
53,090,358 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8774-TAIL:Abca1
|
UTSW |
4 |
53,090,358 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8806:Abca1
|
UTSW |
4 |
53,084,520 (GRCm39) |
missense |
probably benign |
0.17 |
R8841:Abca1
|
UTSW |
4 |
53,143,925 (GRCm39) |
splice site |
probably benign |
|
R9081:Abca1
|
UTSW |
4 |
53,109,162 (GRCm39) |
critical splice donor site |
probably null |
|
R9483:Abca1
|
UTSW |
4 |
53,060,351 (GRCm39) |
missense |
probably benign |
0.11 |
R9532:Abca1
|
UTSW |
4 |
53,109,284 (GRCm39) |
missense |
probably benign |
|
R9621:Abca1
|
UTSW |
4 |
53,092,918 (GRCm39) |
missense |
probably benign |
0.00 |
R9638:Abca1
|
UTSW |
4 |
53,092,806 (GRCm39) |
missense |
probably damaging |
0.96 |
RF005:Abca1
|
UTSW |
4 |
53,049,125 (GRCm39) |
missense |
probably damaging |
0.97 |
RF024:Abca1
|
UTSW |
4 |
53,049,125 (GRCm39) |
missense |
probably damaging |
0.97 |
X0023:Abca1
|
UTSW |
4 |
53,049,038 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Abca1
|
UTSW |
4 |
53,086,133 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Abca1
|
UTSW |
4 |
53,080,799 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Abca1
|
UTSW |
4 |
53,079,584 (GRCm39) |
missense |
probably benign |
0.00 |
|