Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004B18Rik |
C |
T |
3: 145,643,976 (GRCm39) |
P55S |
probably damaging |
Het |
Adgre4 |
T |
C |
17: 56,098,497 (GRCm39) |
S136P |
probably benign |
Het |
Aoc1l1 |
C |
T |
6: 48,952,687 (GRCm39) |
T204I |
probably damaging |
Het |
Arap1 |
C |
A |
7: 101,022,222 (GRCm39) |
A8E |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,480,401 (GRCm39) |
H174Q |
possibly damaging |
Het |
Btbd2 |
A |
G |
10: 80,480,539 (GRCm39) |
I358T |
probably benign |
Het |
Camkk2 |
G |
A |
5: 122,875,575 (GRCm39) |
R492* |
probably null |
Het |
Capn3 |
T |
C |
2: 120,294,421 (GRCm39) |
V23A |
probably benign |
Het |
Carm1 |
T |
G |
9: 21,491,606 (GRCm39) |
V225G |
probably benign |
Het |
Ccdc113 |
T |
A |
8: 96,267,459 (GRCm39) |
N141K |
probably benign |
Het |
Ccdc60 |
C |
A |
5: 116,284,243 (GRCm39) |
M298I |
probably benign |
Het |
Celsr3 |
C |
T |
9: 108,723,016 (GRCm39) |
P2801L |
probably benign |
Het |
Clec4n |
T |
A |
6: 123,207,505 (GRCm39) |
V23E |
probably damaging |
Het |
Cmtr2 |
T |
G |
8: 110,948,382 (GRCm39) |
L231V |
probably damaging |
Het |
Csrnp3 |
T |
G |
2: 65,853,363 (GRCm39) |
V585G |
probably null |
Het |
Ctnnd2 |
T |
C |
15: 30,647,257 (GRCm39) |
S318P |
probably damaging |
Het |
Cubn |
A |
T |
2: 13,344,828 (GRCm39) |
|
probably null |
Het |
Dgkd |
C |
A |
1: 87,857,549 (GRCm39) |
P754T |
possibly damaging |
Het |
Dnah7a |
A |
G |
1: 53,724,142 (GRCm39) |
S108P |
probably benign |
Het |
Dnajc24 |
A |
G |
2: 105,832,268 (GRCm39) |
|
probably benign |
Het |
Dner |
A |
T |
1: 84,423,177 (GRCm39) |
S475R |
probably damaging |
Het |
Dtnb |
T |
C |
12: 3,831,190 (GRCm39) |
L630P |
probably benign |
Het |
Dysf |
T |
C |
6: 84,050,885 (GRCm39) |
F411L |
probably benign |
Het |
Fbh1 |
G |
A |
2: 11,762,339 (GRCm39) |
A566V |
probably damaging |
Het |
Fbxw19 |
G |
T |
9: 109,315,004 (GRCm39) |
T186K |
probably benign |
Het |
Flacc1 |
A |
T |
1: 58,698,437 (GRCm39) |
V327D |
possibly damaging |
Het |
Gm4825 |
A |
G |
15: 85,395,245 (GRCm39) |
|
noncoding transcript |
Het |
Hmcn1 |
T |
C |
1: 150,551,742 (GRCm39) |
I2621V |
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,553,127 (GRCm39) |
E2521V |
possibly damaging |
Het |
Kcng1 |
A |
G |
2: 168,104,904 (GRCm39) |
V314A |
probably benign |
Het |
Kif13a |
G |
A |
13: 47,018,314 (GRCm39) |
|
probably benign |
Het |
Kif21a |
G |
A |
15: 90,855,051 (GRCm39) |
A703V |
probably damaging |
Het |
Kifc1 |
A |
G |
17: 34,103,561 (GRCm39) |
|
probably null |
Het |
Klk13 |
T |
A |
7: 43,370,431 (GRCm39) |
N31K |
possibly damaging |
Het |
Klri1 |
T |
A |
6: 129,674,347 (GRCm39) |
H221L |
probably benign |
Het |
Ltbp4 |
G |
A |
7: 27,028,443 (GRCm39) |
P273L |
unknown |
Het |
Med16 |
T |
C |
10: 79,742,929 (GRCm39) |
H14R |
possibly damaging |
Het |
Mpeg1 |
G |
A |
19: 12,440,275 (GRCm39) |
V578M |
probably damaging |
Het |
Mrgpra2a |
T |
A |
7: 47,076,983 (GRCm39) |
I92F |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,416,374 (GRCm39) |
C3107R |
possibly damaging |
Het |
Myo5a |
T |
A |
9: 75,055,139 (GRCm39) |
F441I |
probably damaging |
Het |
Ndst4 |
T |
A |
3: 125,232,331 (GRCm39) |
L300* |
probably null |
Het |
Nlgn2 |
G |
T |
11: 69,718,136 (GRCm39) |
D356E |
probably damaging |
Het |
Nlrp2 |
T |
C |
7: 5,330,737 (GRCm39) |
E553G |
probably damaging |
Het |
Oas1f |
G |
A |
5: 120,994,502 (GRCm39) |
C341Y |
possibly damaging |
Het |
Olfm5 |
A |
T |
7: 103,809,619 (GRCm39) |
C111S |
possibly damaging |
Het |
Oplah |
G |
A |
15: 76,181,664 (GRCm39) |
T1119I |
probably damaging |
Het |
Or2ag15 |
T |
C |
7: 106,340,601 (GRCm39) |
E180G |
probably damaging |
Het |
Or5d46 |
T |
C |
2: 88,170,545 (GRCm39) |
L212P |
probably damaging |
Het |
Or6c74 |
C |
T |
10: 129,870,187 (GRCm39) |
Q231* |
probably null |
Het |
Or6f2 |
A |
T |
7: 139,756,596 (GRCm39) |
I188L |
probably benign |
Het |
Or8b12c |
A |
G |
9: 37,715,242 (GRCm39) |
I12V |
probably benign |
Het |
Or8g51 |
T |
A |
9: 38,609,500 (GRCm39) |
H58L |
probably benign |
Het |
Pde10a |
T |
C |
17: 9,161,750 (GRCm39) |
I477T |
possibly damaging |
Het |
Pde4b |
A |
G |
4: 102,454,657 (GRCm39) |
E108G |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,198,855 (GRCm39) |
T338S |
probably benign |
Het |
Pgghg |
A |
G |
7: 140,523,260 (GRCm39) |
M180V |
probably benign |
Het |
Phactr4 |
G |
A |
4: 132,104,559 (GRCm39) |
T256I |
probably benign |
Het |
Pot1b |
A |
T |
17: 55,969,531 (GRCm39) |
Y546N |
probably damaging |
Het |
Rangap1 |
T |
C |
15: 81,590,704 (GRCm39) |
T463A |
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,756,317 (GRCm39) |
I13V |
probably null |
Het |
Rbak |
A |
T |
5: 143,160,437 (GRCm39) |
Y205* |
probably null |
Het |
Reg3b |
A |
T |
6: 78,348,797 (GRCm39) |
K31M |
probably damaging |
Het |
Rfpl4 |
A |
T |
7: 5,118,533 (GRCm39) |
Y12* |
probably null |
Het |
Rnase6 |
A |
G |
14: 51,367,889 (GRCm39) |
N94D |
possibly damaging |
Het |
Rtn4 |
T |
C |
11: 29,686,464 (GRCm39) |
L273P |
probably damaging |
Het |
Ryr3 |
A |
C |
2: 112,624,812 (GRCm39) |
F2203V |
probably damaging |
Het |
Sae1 |
A |
T |
7: 16,102,490 (GRCm39) |
D161E |
possibly damaging |
Het |
Sema5a |
T |
C |
15: 32,562,877 (GRCm39) |
F296S |
possibly damaging |
Het |
Sh3rf1 |
C |
A |
8: 61,837,897 (GRCm39) |
P814Q |
probably damaging |
Het |
Slc22a29 |
C |
A |
19: 8,146,557 (GRCm39) |
R415M |
probably benign |
Het |
Slc25a25 |
C |
T |
2: 32,310,663 (GRCm39) |
|
probably null |
Het |
Slco4c1 |
T |
A |
1: 96,795,654 (GRCm39) |
M135L |
probably benign |
Het |
Slfn1 |
A |
G |
11: 83,012,579 (GRCm39) |
I232V |
possibly damaging |
Het |
Slitrk1 |
T |
A |
14: 109,149,622 (GRCm39) |
N363I |
probably damaging |
Het |
Srr |
A |
G |
11: 74,799,542 (GRCm39) |
V311A |
probably damaging |
Het |
Tasor |
T |
C |
14: 27,160,621 (GRCm39) |
S128P |
probably damaging |
Het |
Tasor |
C |
T |
14: 27,201,746 (GRCm39) |
H1419Y |
possibly damaging |
Het |
Tenm1 |
T |
C |
X: 41,916,078 (GRCm39) |
D402G |
probably benign |
Het |
Topors |
T |
C |
4: 40,261,044 (GRCm39) |
R747G |
unknown |
Het |
Trank1 |
A |
T |
9: 111,220,696 (GRCm39) |
I2478F |
probably damaging |
Het |
Trim69 |
A |
G |
2: 121,998,165 (GRCm39) |
N46D |
probably benign |
Het |
Trpm1 |
T |
A |
7: 63,879,978 (GRCm39) |
L661Q |
probably damaging |
Het |
Ttbk1 |
A |
C |
17: 46,791,150 (GRCm39) |
F45V |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,644,649 (GRCm39) |
K4708R |
probably damaging |
Het |
Unkl |
A |
G |
17: 25,428,619 (GRCm39) |
|
probably benign |
Het |
Uros |
A |
T |
7: 133,288,735 (GRCm39) |
N257K |
probably benign |
Het |
Usp25 |
A |
G |
16: 76,873,259 (GRCm39) |
Y439C |
probably damaging |
Het |
Vgf |
A |
G |
5: 137,061,029 (GRCm39) |
|
probably benign |
Het |
Vmn2r8 |
A |
T |
5: 108,947,152 (GRCm39) |
D533E |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,702,995 (GRCm39) |
Y653N |
probably damaging |
Het |
Zfp358 |
T |
C |
8: 3,545,742 (GRCm39) |
V135A |
possibly damaging |
Het |
|
Other mutations in Grhl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00766:Grhl2
|
APN |
15 |
37,336,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Grhl2
|
APN |
15 |
37,338,018 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02140:Grhl2
|
APN |
15 |
37,270,830 (GRCm39) |
splice site |
probably benign |
|
IGL02307:Grhl2
|
APN |
15 |
37,288,532 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02375:Grhl2
|
APN |
15 |
37,291,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02508:Grhl2
|
APN |
15 |
37,310,009 (GRCm39) |
splice site |
probably benign |
|
clayton
|
UTSW |
15 |
37,291,920 (GRCm39) |
splice site |
probably null |
|
R0462:Grhl2
|
UTSW |
15 |
37,344,919 (GRCm39) |
missense |
probably benign |
0.00 |
R1421:Grhl2
|
UTSW |
15 |
37,309,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1548:Grhl2
|
UTSW |
15 |
37,336,567 (GRCm39) |
missense |
probably benign |
0.32 |
R1912:Grhl2
|
UTSW |
15 |
37,358,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R3110:Grhl2
|
UTSW |
15 |
37,336,591 (GRCm39) |
critical splice donor site |
probably null |
|
R3112:Grhl2
|
UTSW |
15 |
37,336,591 (GRCm39) |
critical splice donor site |
probably null |
|
R4261:Grhl2
|
UTSW |
15 |
37,361,067 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4830:Grhl2
|
UTSW |
15 |
37,335,903 (GRCm39) |
splice site |
probably null |
|
R4910:Grhl2
|
UTSW |
15 |
37,291,920 (GRCm39) |
splice site |
probably null |
|
R4929:Grhl2
|
UTSW |
15 |
37,361,046 (GRCm39) |
missense |
probably benign |
|
R4952:Grhl2
|
UTSW |
15 |
37,287,493 (GRCm39) |
missense |
probably benign |
0.13 |
R5742:Grhl2
|
UTSW |
15 |
37,328,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7142:Grhl2
|
UTSW |
15 |
37,279,826 (GRCm39) |
missense |
probably benign |
0.05 |
R7208:Grhl2
|
UTSW |
15 |
37,335,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Grhl2
|
UTSW |
15 |
37,291,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7519:Grhl2
|
UTSW |
15 |
37,336,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7538:Grhl2
|
UTSW |
15 |
37,328,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Grhl2
|
UTSW |
15 |
37,328,574 (GRCm39) |
missense |
probably damaging |
0.96 |
R8027:Grhl2
|
UTSW |
15 |
37,279,727 (GRCm39) |
missense |
probably benign |
|
R8047:Grhl2
|
UTSW |
15 |
37,336,465 (GRCm39) |
missense |
probably benign |
0.00 |
R8555:Grhl2
|
UTSW |
15 |
37,233,507 (GRCm39) |
intron |
probably benign |
|
R8818:Grhl2
|
UTSW |
15 |
37,270,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Grhl2
|
UTSW |
15 |
37,270,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Grhl2
|
UTSW |
15 |
37,344,904 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Grhl2
|
UTSW |
15 |
37,333,531 (GRCm39) |
missense |
unknown |
|
|