Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,018,248 (GRCm39) |
I1124T |
probably damaging |
Het |
Acacb |
A |
G |
5: 114,367,975 (GRCm39) |
T1658A |
possibly damaging |
Het |
Acvrl1 |
C |
A |
15: 101,033,654 (GRCm39) |
P112Q |
probably damaging |
Het |
Ankar |
A |
T |
1: 72,738,170 (GRCm39) |
I4K |
possibly damaging |
Het |
Ankfn1 |
G |
C |
11: 89,332,252 (GRCm39) |
D431E |
possibly damaging |
Het |
Apobec4 |
T |
C |
1: 152,632,425 (GRCm39) |
V151A |
possibly damaging |
Het |
Atp10b |
A |
G |
11: 43,093,949 (GRCm39) |
S498G |
probably benign |
Het |
Azin1 |
A |
G |
15: 38,493,744 (GRCm39) |
V293A |
probably benign |
Het |
Ccdc88b |
T |
C |
19: 6,835,083 (GRCm39) |
E46G |
probably damaging |
Het |
Ccdc96 |
T |
C |
5: 36,642,219 (GRCm39) |
|
probably benign |
Het |
Ccnyl1 |
A |
G |
1: 64,752,290 (GRCm39) |
D169G |
probably benign |
Het |
Cdca3 |
T |
A |
6: 124,809,127 (GRCm39) |
V89E |
probably damaging |
Het |
Cdh19 |
A |
T |
1: 110,823,111 (GRCm39) |
|
probably null |
Het |
Chka |
G |
A |
19: 3,936,375 (GRCm39) |
V238I |
probably damaging |
Het |
Cntn3 |
T |
C |
6: 102,218,983 (GRCm39) |
K546E |
possibly damaging |
Het |
Crybg3 |
A |
G |
16: 59,360,180 (GRCm39) |
V787A |
probably damaging |
Het |
Dlgap3 |
T |
C |
4: 127,089,508 (GRCm39) |
|
probably null |
Het |
Dnah8 |
C |
T |
17: 30,902,608 (GRCm39) |
L889F |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,967,184 (GRCm39) |
E1658G |
probably damaging |
Het |
Dnajc11 |
A |
G |
4: 152,052,996 (GRCm39) |
D102G |
probably damaging |
Het |
Dync1i2 |
T |
G |
2: 71,064,018 (GRCm39) |
S121A |
probably damaging |
Het |
Ece1 |
G |
A |
4: 137,684,486 (GRCm39) |
E591K |
probably damaging |
Het |
Enthd1 |
G |
A |
15: 80,444,510 (GRCm39) |
S15L |
probably damaging |
Het |
Epb41l2 |
T |
A |
10: 25,347,524 (GRCm39) |
H372Q |
probably damaging |
Het |
Errfi1 |
T |
A |
4: 150,951,204 (GRCm39) |
Y211N |
probably damaging |
Het |
Fam193b |
G |
A |
13: 55,691,250 (GRCm39) |
T208M |
probably benign |
Het |
Flacc1 |
T |
C |
1: 58,717,507 (GRCm39) |
I135V |
possibly damaging |
Het |
Fmnl2 |
C |
T |
2: 52,997,552 (GRCm39) |
T501M |
possibly damaging |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gm4841 |
G |
T |
18: 60,403,135 (GRCm39) |
D319E |
probably benign |
Het |
Gucd1 |
A |
G |
10: 75,345,494 (GRCm39) |
F187S |
probably damaging |
Het |
Hcar2 |
GCGGATGCGCAC |
GC |
5: 124,002,752 (GRCm39) |
|
probably null |
Het |
Helz2 |
T |
C |
2: 180,880,210 (GRCm39) |
D502G |
probably damaging |
Het |
Hspa2 |
A |
G |
12: 76,451,639 (GRCm39) |
E111G |
possibly damaging |
Het |
Ift80 |
A |
G |
3: 68,869,623 (GRCm39) |
Y223H |
possibly damaging |
Het |
Il1rl1 |
A |
G |
1: 40,485,838 (GRCm39) |
K330E |
probably benign |
Het |
Il23r |
A |
T |
6: 67,400,645 (GRCm39) |
F562I |
probably damaging |
Het |
Isx |
T |
C |
8: 75,600,487 (GRCm39) |
|
probably null |
Het |
Jcad |
G |
A |
18: 4,674,055 (GRCm39) |
V606I |
probably benign |
Het |
Kcnn2 |
A |
T |
18: 45,816,187 (GRCm39) |
T333S |
possibly damaging |
Het |
Kcnq5 |
C |
T |
1: 21,473,274 (GRCm39) |
A630T |
probably damaging |
Het |
Kif2c |
T |
C |
4: 117,028,946 (GRCm39) |
M188V |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,903,086 (GRCm39) |
V321A |
possibly damaging |
Het |
Krtap4-8 |
A |
T |
11: 99,671,271 (GRCm39) |
|
probably benign |
Het |
Lcor |
G |
C |
19: 41,574,334 (GRCm39) |
A1030P |
probably benign |
Het |
Lgals3bp |
A |
C |
11: 118,289,295 (GRCm39) |
L52R |
probably damaging |
Het |
Lipk |
C |
A |
19: 33,999,099 (GRCm39) |
H126Q |
probably damaging |
Het |
Lpgat1 |
T |
C |
1: 191,495,779 (GRCm39) |
Y323H |
probably damaging |
Het |
Lrp2 |
T |
G |
2: 69,311,517 (GRCm39) |
N2654H |
probably damaging |
Het |
Lsm14b |
C |
T |
2: 179,669,774 (GRCm39) |
Q6* |
probably null |
Het |
Lysmd3 |
C |
T |
13: 81,817,584 (GRCm39) |
A187V |
possibly damaging |
Het |
Map2k5 |
A |
G |
9: 63,201,001 (GRCm39) |
S211P |
probably damaging |
Het |
Mlph |
A |
T |
1: 90,869,419 (GRCm39) |
I474F |
probably damaging |
Het |
Mpped2 |
T |
C |
2: 106,614,091 (GRCm39) |
S142P |
probably damaging |
Het |
Nemf |
A |
C |
12: 69,371,062 (GRCm39) |
M678R |
probably benign |
Het |
Nfe2l1 |
A |
T |
11: 96,718,515 (GRCm39) |
Y7N |
probably damaging |
Het |
Nfkbie |
T |
G |
17: 45,867,232 (GRCm39) |
D122E |
probably benign |
Het |
Noc3l |
C |
A |
19: 38,778,066 (GRCm39) |
A783S |
probably benign |
Het |
Nol8 |
T |
C |
13: 49,816,229 (GRCm39) |
V761A |
probably damaging |
Het |
Nvl |
A |
G |
1: 180,929,152 (GRCm39) |
L743P |
probably damaging |
Het |
Or1j1 |
T |
A |
2: 36,702,484 (GRCm39) |
I207F |
probably benign |
Het |
Plcb1 |
A |
G |
2: 135,093,667 (GRCm39) |
K160R |
possibly damaging |
Het |
Plekhg3 |
G |
T |
12: 76,625,096 (GRCm39) |
G1313C |
possibly damaging |
Het |
Plekhh1 |
GTCAAA |
G |
12: 79,122,194 (GRCm39) |
|
probably null |
Het |
Popdc3 |
G |
A |
10: 45,191,002 (GRCm39) |
V38I |
probably benign |
Het |
Prdx3 |
A |
T |
19: 60,858,551 (GRCm39) |
V114D |
possibly damaging |
Het |
Prkdc |
T |
A |
16: 15,485,579 (GRCm39) |
S469T |
probably benign |
Het |
Rbm22 |
G |
A |
18: 60,697,463 (GRCm39) |
R56H |
probably damaging |
Het |
Reln |
A |
T |
5: 22,491,894 (GRCm39) |
F113I |
possibly damaging |
Het |
Rims1 |
A |
G |
1: 22,497,731 (GRCm39) |
Y808H |
probably damaging |
Het |
Rsbn1 |
C |
A |
3: 103,836,336 (GRCm39) |
T458N |
possibly damaging |
Het |
Serpina3b |
A |
G |
12: 104,096,889 (GRCm39) |
S57G |
possibly damaging |
Het |
Skor2 |
G |
T |
18: 76,948,878 (GRCm39) |
|
probably null |
Het |
Slc22a4 |
A |
T |
11: 53,879,719 (GRCm39) |
Y447N |
probably damaging |
Het |
Slco1a7 |
C |
A |
6: 141,668,948 (GRCm39) |
A495S |
probably damaging |
Het |
Stx19 |
G |
T |
16: 62,642,682 (GRCm39) |
R166L |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,205,869 (GRCm39) |
T170A |
possibly damaging |
Het |
Sycp2 |
T |
G |
2: 178,016,225 (GRCm39) |
S746R |
probably benign |
Het |
Tchh |
G |
T |
3: 93,355,189 (GRCm39) |
R1543L |
unknown |
Het |
Tjp2 |
T |
C |
19: 24,078,169 (GRCm39) |
D908G |
probably damaging |
Het |
Ttc8 |
C |
A |
12: 98,946,068 (GRCm39) |
A452E |
possibly damaging |
Het |
Unc5a |
T |
A |
13: 55,151,696 (GRCm39) |
W709R |
probably null |
Het |
Unc80 |
T |
A |
1: 66,549,951 (GRCm39) |
S736R |
possibly damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,742,788 (GRCm39) |
H387Q |
probably benign |
Het |
Vmn2r39 |
C |
T |
7: 9,026,469 (GRCm39) |
|
probably null |
Het |
Vmn2r88 |
T |
A |
14: 51,650,702 (GRCm39) |
D138E |
probably benign |
Het |
Vwce |
T |
C |
19: 10,625,831 (GRCm39) |
F448L |
possibly damaging |
Het |
Wdr75 |
C |
T |
1: 45,861,645 (GRCm39) |
S695F |
probably benign |
Het |
Zfand4 |
T |
C |
6: 116,265,122 (GRCm39) |
|
probably null |
Het |
Zfp511 |
T |
A |
7: 139,617,424 (GRCm39) |
|
probably null |
Het |
Zfyve9 |
T |
C |
4: 108,501,565 (GRCm39) |
K584E |
possibly damaging |
Het |
|
Other mutations in Htr2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Htr2a
|
APN |
14 |
74,943,645 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00946:Htr2a
|
APN |
14 |
74,943,582 (GRCm39) |
nonsense |
probably null |
|
IGL01660:Htr2a
|
APN |
14 |
74,943,194 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02200:Htr2a
|
APN |
14 |
74,943,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02369:Htr2a
|
APN |
14 |
74,943,722 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02724:Htr2a
|
APN |
14 |
74,882,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02887:Htr2a
|
APN |
14 |
74,882,583 (GRCm39) |
missense |
probably benign |
0.05 |
R0038:Htr2a
|
UTSW |
14 |
74,943,687 (GRCm39) |
missense |
probably benign |
0.00 |
R0038:Htr2a
|
UTSW |
14 |
74,943,687 (GRCm39) |
missense |
probably benign |
0.00 |
R0117:Htr2a
|
UTSW |
14 |
74,882,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R0367:Htr2a
|
UTSW |
14 |
74,879,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Htr2a
|
UTSW |
14 |
74,943,764 (GRCm39) |
missense |
probably benign |
0.00 |
R0729:Htr2a
|
UTSW |
14 |
74,879,587 (GRCm39) |
missense |
probably benign |
|
R1507:Htr2a
|
UTSW |
14 |
74,943,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Htr2a
|
UTSW |
14 |
74,943,293 (GRCm39) |
nonsense |
probably null |
|
R1539:Htr2a
|
UTSW |
14 |
74,882,608 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1735:Htr2a
|
UTSW |
14 |
74,943,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R1747:Htr2a
|
UTSW |
14 |
74,943,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Htr2a
|
UTSW |
14 |
74,943,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Htr2a
|
UTSW |
14 |
74,882,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R2348:Htr2a
|
UTSW |
14 |
74,882,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Htr2a
|
UTSW |
14 |
74,943,262 (GRCm39) |
missense |
probably benign |
0.00 |
R3401:Htr2a
|
UTSW |
14 |
74,882,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R4006:Htr2a
|
UTSW |
14 |
74,879,581 (GRCm39) |
missense |
probably benign |
|
R4007:Htr2a
|
UTSW |
14 |
74,879,581 (GRCm39) |
missense |
probably benign |
|
R4093:Htr2a
|
UTSW |
14 |
74,943,789 (GRCm39) |
missense |
probably benign |
|
R4094:Htr2a
|
UTSW |
14 |
74,943,789 (GRCm39) |
missense |
probably benign |
|
R4095:Htr2a
|
UTSW |
14 |
74,943,789 (GRCm39) |
missense |
probably benign |
|
R4502:Htr2a
|
UTSW |
14 |
74,879,428 (GRCm39) |
missense |
probably benign |
0.02 |
R4932:Htr2a
|
UTSW |
14 |
74,879,462 (GRCm39) |
missense |
probably benign |
|
R5651:Htr2a
|
UTSW |
14 |
74,943,143 (GRCm39) |
missense |
probably damaging |
0.98 |
R5935:Htr2a
|
UTSW |
14 |
74,882,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Htr2a
|
UTSW |
14 |
74,882,474 (GRCm39) |
nonsense |
probably null |
|
R6937:Htr2a
|
UTSW |
14 |
74,882,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R7138:Htr2a
|
UTSW |
14 |
74,943,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R8888:Htr2a
|
UTSW |
14 |
74,882,617 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9423:Htr2a
|
UTSW |
14 |
74,943,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|