Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
A |
G |
5: 144,982,156 (GRCm39) |
D247G |
possibly damaging |
Het |
1700123K08Rik |
A |
G |
5: 138,562,403 (GRCm39) |
|
probably null |
Het |
Abca8b |
C |
A |
11: 109,868,639 (GRCm39) |
G175V |
probably damaging |
Het |
Adad2 |
C |
T |
8: 120,341,500 (GRCm39) |
R171C |
probably benign |
Het |
Adgrv1 |
A |
C |
13: 81,669,236 (GRCm39) |
L2440R |
probably damaging |
Het |
Antxr1 |
A |
G |
6: 87,232,845 (GRCm39) |
V239A |
probably damaging |
Het |
Aoc1l2 |
G |
A |
6: 48,907,953 (GRCm39) |
V318I |
probably benign |
Het |
Arhgap28 |
G |
A |
17: 68,203,235 (GRCm39) |
Q73* |
probably null |
Het |
Arrdc5 |
C |
T |
17: 56,604,846 (GRCm39) |
R147H |
probably benign |
Het |
Ash1l |
T |
C |
3: 88,930,492 (GRCm39) |
Y1990H |
probably damaging |
Het |
Bank1 |
T |
C |
3: 135,772,148 (GRCm39) |
E494G |
probably damaging |
Het |
Bicral |
A |
T |
17: 47,119,418 (GRCm39) |
I701N |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,979,217 (GRCm39) |
Y699C |
probably damaging |
Het |
C3ar1 |
T |
G |
6: 122,827,537 (GRCm39) |
T227P |
probably benign |
Het |
Ccr3 |
C |
A |
9: 123,829,518 (GRCm39) |
D284E |
probably damaging |
Het |
Cdh13 |
T |
C |
8: 119,578,462 (GRCm39) |
V163A |
possibly damaging |
Het |
CK137956 |
C |
T |
4: 127,840,440 (GRCm39) |
|
probably null |
Het |
Cltc |
T |
C |
11: 86,612,472 (GRCm39) |
S529G |
probably benign |
Het |
Cplane2 |
C |
T |
4: 140,947,177 (GRCm39) |
P186L |
probably benign |
Het |
Ddx11 |
A |
G |
17: 66,457,021 (GRCm39) |
K783E |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,538,288 (GRCm39) |
|
probably null |
Het |
Eef2k |
A |
G |
7: 120,486,005 (GRCm39) |
H408R |
probably benign |
Het |
Esr1 |
A |
G |
10: 4,951,221 (GRCm39) |
K533R |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,406,109 (GRCm39) |
Y953* |
probably null |
Het |
Fosl1 |
T |
A |
19: 5,505,133 (GRCm39) |
|
probably null |
Het |
Frmd4b |
A |
G |
6: 97,283,752 (GRCm39) |
M373T |
probably benign |
Het |
Gm1968 |
A |
G |
16: 29,777,557 (GRCm39) |
|
noncoding transcript |
Het |
Gpr26 |
T |
C |
7: 131,568,694 (GRCm39) |
V13A |
possibly damaging |
Het |
Gtf3c1 |
T |
C |
7: 125,303,117 (GRCm39) |
N106S |
possibly damaging |
Het |
Itgb8 |
T |
G |
12: 119,134,429 (GRCm39) |
E546A |
probably damaging |
Het |
Itpr3 |
C |
T |
17: 27,337,540 (GRCm39) |
T2450M |
probably benign |
Het |
Kif1a |
A |
T |
1: 92,953,450 (GRCm39) |
Y1245N |
probably damaging |
Het |
Klrb1f |
G |
A |
6: 129,031,335 (GRCm39) |
|
probably null |
Het |
Lars1 |
A |
G |
18: 42,390,156 (GRCm39) |
L37P |
probably benign |
Het |
Lnpk |
T |
C |
2: 74,378,369 (GRCm39) |
T131A |
probably benign |
Het |
Mob3c |
C |
T |
4: 115,690,878 (GRCm39) |
T156I |
probably benign |
Het |
Nadk |
T |
A |
4: 155,668,628 (GRCm39) |
W100R |
probably damaging |
Het |
Npy6r |
A |
T |
18: 44,409,061 (GRCm39) |
I161F |
probably benign |
Het |
Or4c107 |
A |
C |
2: 88,789,170 (GRCm39) |
D120A |
probably damaging |
Het |
Or6c204 |
G |
A |
10: 129,022,426 (GRCm39) |
T288I |
probably damaging |
Het |
Pcdhga3 |
A |
G |
18: 37,808,276 (GRCm39) |
E243G |
possibly damaging |
Het |
Pdss2 |
A |
G |
10: 43,315,828 (GRCm39) |
T361A |
probably benign |
Het |
Pkd1l2 |
G |
T |
8: 117,769,059 (GRCm39) |
Q1198K |
probably benign |
Het |
Prdx1 |
T |
A |
4: 116,550,124 (GRCm39) |
I102N |
probably damaging |
Het |
Prss1 |
G |
A |
6: 41,438,147 (GRCm39) |
V25I |
probably benign |
Het |
Pspc1 |
A |
G |
14: 57,015,388 (GRCm39) |
Y77H |
probably damaging |
Het |
Rnf5 |
T |
C |
17: 34,820,712 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
C |
A |
7: 28,811,399 (GRCm39) |
M235I |
probably benign |
Het |
Sec24c |
A |
G |
14: 20,741,893 (GRCm39) |
Y776C |
probably damaging |
Het |
Sharpin |
A |
G |
15: 76,234,253 (GRCm39) |
|
probably null |
Het |
Slc12a4 |
C |
A |
8: 106,676,845 (GRCm39) |
V482L |
possibly damaging |
Het |
Slc38a1 |
C |
T |
15: 96,514,022 (GRCm39) |
|
probably null |
Het |
Smtn |
G |
T |
11: 3,479,582 (GRCm39) |
T495N |
probably damaging |
Het |
Sncaip |
A |
G |
18: 53,001,991 (GRCm39) |
T171A |
probably benign |
Het |
Sprr2e |
T |
C |
3: 92,260,399 (GRCm39) |
*77R |
probably null |
Het |
Syngap1 |
T |
A |
17: 27,178,754 (GRCm39) |
D443E |
possibly damaging |
Het |
Taldo1 |
T |
C |
7: 140,972,205 (GRCm39) |
V24A |
probably damaging |
Het |
Tfap2c |
T |
A |
2: 172,391,778 (GRCm39) |
N8K |
probably benign |
Het |
Tmem229a |
T |
C |
6: 24,955,580 (GRCm39) |
Y58C |
probably damaging |
Het |
Tubgcp3 |
T |
C |
8: 12,689,577 (GRCm39) |
Y563C |
probably damaging |
Het |
Ubr1 |
T |
A |
2: 120,722,593 (GRCm39) |
D1342V |
probably benign |
Het |
Usp7 |
C |
T |
16: 8,534,374 (GRCm39) |
|
probably null |
Het |
Wbp1 |
C |
T |
6: 83,097,216 (GRCm39) |
G75D |
probably damaging |
Het |
Zfp180 |
G |
T |
7: 23,804,315 (GRCm39) |
V245F |
probably benign |
Het |
Zfp414 |
C |
T |
17: 33,849,012 (GRCm39) |
T33I |
probably damaging |
Het |
Zfp646 |
T |
A |
7: 127,478,530 (GRCm39) |
C236S |
probably damaging |
Het |
|
Other mutations in Accsl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02336:Accsl
|
APN |
2 |
93,696,253 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02511:Accsl
|
APN |
2 |
93,692,111 (GRCm39) |
unclassified |
probably benign |
|
IGL03248:Accsl
|
APN |
2 |
93,693,129 (GRCm39) |
unclassified |
probably benign |
|
IGL03338:Accsl
|
APN |
2 |
93,686,092 (GRCm39) |
missense |
probably benign |
0.34 |
R0323:Accsl
|
UTSW |
2 |
93,691,425 (GRCm39) |
missense |
probably benign |
0.27 |
R0449:Accsl
|
UTSW |
2 |
93,696,419 (GRCm39) |
missense |
probably benign |
0.00 |
R1172:Accsl
|
UTSW |
2 |
93,696,589 (GRCm39) |
splice site |
probably benign |
|
R1173:Accsl
|
UTSW |
2 |
93,696,589 (GRCm39) |
splice site |
probably benign |
|
R1175:Accsl
|
UTSW |
2 |
93,696,589 (GRCm39) |
splice site |
probably benign |
|
R1752:Accsl
|
UTSW |
2 |
93,688,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R1952:Accsl
|
UTSW |
2 |
93,689,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:Accsl
|
UTSW |
2 |
93,689,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R2878:Accsl
|
UTSW |
2 |
93,689,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R4472:Accsl
|
UTSW |
2 |
93,694,337 (GRCm39) |
splice site |
probably null |
|
R4472:Accsl
|
UTSW |
2 |
93,694,336 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5400:Accsl
|
UTSW |
2 |
93,689,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R5502:Accsl
|
UTSW |
2 |
93,687,289 (GRCm39) |
critical splice donor site |
probably null |
|
R5636:Accsl
|
UTSW |
2 |
93,699,370 (GRCm39) |
missense |
probably benign |
0.41 |
R5799:Accsl
|
UTSW |
2 |
93,694,748 (GRCm39) |
splice site |
probably null |
|
R6376:Accsl
|
UTSW |
2 |
93,687,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Accsl
|
UTSW |
2 |
93,696,488 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7311:Accsl
|
UTSW |
2 |
93,696,160 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7564:Accsl
|
UTSW |
2 |
93,688,501 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7731:Accsl
|
UTSW |
2 |
93,691,363 (GRCm39) |
missense |
probably benign |
0.01 |
R7835:Accsl
|
UTSW |
2 |
93,696,329 (GRCm39) |
nonsense |
probably null |
|
R8184:Accsl
|
UTSW |
2 |
93,686,086 (GRCm39) |
missense |
probably benign |
0.19 |
R8305:Accsl
|
UTSW |
2 |
93,696,423 (GRCm39) |
missense |
probably benign |
0.00 |
R8824:Accsl
|
UTSW |
2 |
93,693,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R8868:Accsl
|
UTSW |
2 |
93,696,490 (GRCm39) |
missense |
probably benign |
0.00 |
R8954:Accsl
|
UTSW |
2 |
93,688,299 (GRCm39) |
missense |
probably benign |
0.06 |
R9172:Accsl
|
UTSW |
2 |
93,691,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9473:Accsl
|
UTSW |
2 |
93,686,092 (GRCm39) |
missense |
probably benign |
0.03 |
R9513:Accsl
|
UTSW |
2 |
93,699,498 (GRCm39) |
unclassified |
probably benign |
|
Z1088:Accsl
|
UTSW |
2 |
93,696,293 (GRCm39) |
missense |
probably benign |
0.00 |
|