Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410137M14Rik |
G |
A |
17: 37,288,986 (GRCm39) |
|
probably benign |
Het |
Abhd15 |
A |
G |
11: 77,409,164 (GRCm39) |
T293A |
probably benign |
Het |
Aldh1l1 |
C |
T |
6: 90,539,647 (GRCm39) |
P192L |
probably benign |
Het |
Aldoart1 |
T |
G |
4: 72,770,779 (GRCm39) |
I10L |
probably benign |
Het |
Ankhd1 |
G |
A |
18: 36,778,166 (GRCm39) |
G1653D |
probably benign |
Het |
Ankk1 |
A |
C |
9: 49,330,664 (GRCm39) |
|
probably null |
Het |
Astn1 |
A |
G |
1: 158,428,072 (GRCm39) |
T748A |
possibly damaging |
Het |
Bmp7 |
C |
A |
2: 172,781,708 (GRCm39) |
R52L |
possibly damaging |
Het |
Ccdc33 |
G |
A |
9: 57,938,395 (GRCm39) |
P859S |
possibly damaging |
Het |
Ccny |
A |
G |
18: 9,449,644 (GRCm39) |
S10P |
probably damaging |
Het |
Cdc6 |
C |
A |
11: 98,801,287 (GRCm39) |
F179L |
probably benign |
Het |
Cdc7 |
T |
A |
5: 107,130,998 (GRCm39) |
V491E |
probably benign |
Het |
Cdh23 |
G |
T |
10: 60,432,509 (GRCm39) |
S138R |
possibly damaging |
Het |
Cenpc1 |
T |
C |
5: 86,185,614 (GRCm39) |
H299R |
probably benign |
Het |
Ciart |
A |
T |
3: 95,786,013 (GRCm39) |
M354K |
probably benign |
Het |
Clasrp |
G |
T |
7: 19,320,640 (GRCm39) |
|
probably benign |
Het |
Col4a3 |
G |
A |
1: 82,674,040 (GRCm39) |
G1132E |
unknown |
Het |
Crebbp |
G |
A |
16: 3,902,687 (GRCm39) |
T2184I |
probably benign |
Het |
Cyp2r1 |
A |
C |
7: 114,149,640 (GRCm39) |
M458R |
probably damaging |
Het |
Cyp7a1 |
C |
A |
4: 6,275,492 (GRCm39) |
R27M |
probably null |
Het |
Ddhd2 |
A |
G |
8: 26,242,192 (GRCm39) |
F116L |
probably damaging |
Het |
Dgkd |
G |
A |
1: 87,855,413 (GRCm39) |
R685K |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,415,066 (GRCm39) |
S223P |
probably benign |
Het |
Exph5 |
A |
T |
9: 53,283,979 (GRCm39) |
R353S |
possibly damaging |
Het |
F11 |
C |
A |
8: 45,705,155 (GRCm39) |
V129F |
probably benign |
Het |
F830045P16Rik |
A |
T |
2: 129,301,317 (GRCm39) |
S454T |
possibly damaging |
Het |
Fam124a |
T |
C |
14: 62,824,656 (GRCm39) |
I50T |
probably damaging |
Het |
Fam20c |
T |
C |
5: 138,741,982 (GRCm39) |
|
probably null |
Het |
Fam234b |
A |
G |
6: 135,203,912 (GRCm39) |
T405A |
probably benign |
Het |
Flywch1 |
G |
A |
17: 23,981,287 (GRCm39) |
Q132* |
probably null |
Het |
Foxo6 |
T |
C |
4: 120,144,166 (GRCm39) |
D95G |
probably benign |
Het |
Ggt5 |
T |
C |
10: 75,439,921 (GRCm39) |
F174S |
probably damaging |
Het |
Gm7104 |
G |
A |
12: 88,252,551 (GRCm39) |
|
noncoding transcript |
Het |
Gpr155 |
A |
G |
2: 73,203,977 (GRCm39) |
L279P |
probably damaging |
Het |
H2-T23 |
A |
G |
17: 36,343,083 (GRCm39) |
L98P |
probably damaging |
Het |
H4c16 |
G |
C |
6: 136,781,101 (GRCm39) |
R93G |
possibly damaging |
Het |
Heatr5a |
A |
G |
12: 52,002,186 (GRCm39) |
V250A |
probably benign |
Het |
Heyl |
A |
T |
4: 123,135,156 (GRCm39) |
I50F |
probably damaging |
Het |
Ifitm10 |
A |
T |
7: 141,909,771 (GRCm39) |
S179R |
probably damaging |
Het |
Isg15 |
A |
T |
4: 156,284,249 (GRCm39) |
I93N |
probably benign |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Itga10 |
G |
A |
3: 96,565,006 (GRCm39) |
V985I |
probably benign |
Het |
Kcnt2 |
T |
C |
1: 140,302,892 (GRCm39) |
I144T |
probably benign |
Het |
Klk1 |
A |
C |
7: 43,878,458 (GRCm39) |
K104T |
possibly damaging |
Het |
Lemd3 |
C |
A |
10: 120,769,347 (GRCm39) |
R654L |
probably damaging |
Het |
Lmod1 |
A |
T |
1: 135,292,125 (GRCm39) |
M327L |
probably benign |
Het |
Lonrf2 |
T |
C |
1: 38,846,131 (GRCm39) |
E347G |
probably benign |
Het |
Ltbp1 |
A |
G |
17: 75,583,427 (GRCm39) |
Y409C |
probably damaging |
Het |
Mecom |
A |
T |
3: 30,034,741 (GRCm39) |
Y312N |
probably damaging |
Het |
Mmut |
A |
G |
17: 41,252,342 (GRCm39) |
T295A |
probably benign |
Het |
Mrgprb3 |
C |
T |
7: 48,293,482 (GRCm39) |
C23Y |
possibly damaging |
Het |
Nadk |
C |
A |
4: 155,669,898 (GRCm39) |
L194I |
probably damaging |
Het |
Naxd |
A |
G |
8: 11,559,510 (GRCm39) |
I182V |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,358,846 (GRCm39) |
I1176K |
probably damaging |
Het |
Nol4l |
C |
A |
2: 153,371,441 (GRCm39) |
R81L |
possibly damaging |
Het |
Odad3 |
T |
G |
9: 21,903,154 (GRCm39) |
T419P |
possibly damaging |
Het |
Or4k47 |
T |
A |
2: 111,452,159 (GRCm39) |
R87W |
probably benign |
Het |
Or8g36 |
A |
T |
9: 39,422,674 (GRCm39) |
M114K |
probably damaging |
Het |
Or9s15 |
G |
T |
1: 92,524,691 (GRCm39) |
R150L |
probably benign |
Het |
Pcdh18 |
A |
G |
3: 49,709,389 (GRCm39) |
V642A |
probably benign |
Het |
Pdzk1 |
G |
A |
3: 96,763,164 (GRCm39) |
|
probably benign |
Het |
Per3 |
C |
T |
4: 151,118,395 (GRCm39) |
V233I |
probably benign |
Het |
Pisd |
G |
A |
5: 32,922,140 (GRCm39) |
P267S |
possibly damaging |
Het |
Prm1 |
T |
A |
16: 10,614,357 (GRCm39) |
|
probably benign |
Het |
Ptprj |
A |
G |
2: 90,293,439 (GRCm39) |
V548A |
probably damaging |
Het |
Ranbp3 |
G |
A |
17: 56,980,367 (GRCm39) |
|
probably benign |
Het |
Raver2 |
T |
A |
4: 100,960,009 (GRCm39) |
V163D |
probably damaging |
Het |
Rbm14 |
A |
T |
19: 4,853,905 (GRCm39) |
I159N |
possibly damaging |
Het |
Rfx6 |
G |
A |
10: 51,594,222 (GRCm39) |
V381I |
probably benign |
Het |
Rhobtb1 |
T |
C |
10: 69,108,693 (GRCm39) |
|
probably benign |
Het |
Rpl28-ps4 |
T |
A |
6: 117,190,856 (GRCm39) |
|
noncoding transcript |
Het |
Rsph10b |
A |
G |
5: 143,904,068 (GRCm39) |
|
probably null |
Het |
Rspo4 |
A |
G |
2: 151,715,013 (GRCm39) |
K217E |
unknown |
Het |
Scgb2b27 |
G |
A |
7: 33,712,710 (GRCm39) |
A44V |
possibly damaging |
Het |
Sec14l2 |
G |
A |
11: 4,061,435 (GRCm39) |
|
probably benign |
Het |
Sec31b |
T |
C |
19: 44,524,595 (GRCm39) |
N101D |
probably benign |
Het |
Sema6a |
A |
T |
18: 47,439,496 (GRCm39) |
C9* |
probably null |
Het |
Septin5 |
A |
C |
16: 18,441,762 (GRCm39) |
L331R |
probably benign |
Het |
Slc16a11 |
C |
A |
11: 70,106,477 (GRCm39) |
Y238* |
probably null |
Het |
Slc25a12 |
T |
C |
2: 71,142,892 (GRCm39) |
T210A |
probably benign |
Het |
Slc35f1 |
A |
T |
10: 52,965,443 (GRCm39) |
Y286F |
probably damaging |
Het |
Szt2 |
A |
T |
4: 118,233,645 (GRCm39) |
L2225* |
probably null |
Het |
Thap12 |
T |
C |
7: 98,365,827 (GRCm39) |
L665P |
probably damaging |
Het |
Tpsb2 |
T |
A |
17: 25,586,698 (GRCm39) |
W237R |
probably damaging |
Het |
Tyk2 |
T |
C |
9: 21,031,637 (GRCm39) |
D451G |
probably damaging |
Het |
Ube2j1 |
T |
A |
4: 33,049,696 (GRCm39) |
N231K |
probably benign |
Het |
Vmn1r225 |
A |
T |
17: 20,722,852 (GRCm39) |
T98S |
possibly damaging |
Het |
Vmn1r87 |
A |
T |
7: 12,865,748 (GRCm39) |
S180T |
probably benign |
Het |
Vmn2r6 |
A |
G |
3: 64,445,262 (GRCm39) |
V821A |
probably damaging |
Het |
Zfp689 |
C |
A |
7: 127,043,998 (GRCm39) |
G211C |
probably damaging |
Het |
Zfp827 |
A |
G |
8: 79,802,865 (GRCm39) |
D479G |
probably benign |
Het |
Zfp995 |
A |
C |
17: 22,099,575 (GRCm39) |
F220V |
probably damaging |
Het |
|
Other mutations in Fbh1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01615:Fbh1
|
APN |
2 |
11,762,334 (GRCm39) |
nonsense |
probably null |
|
IGL02081:Fbh1
|
APN |
2 |
11,768,938 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02082:Fbh1
|
APN |
2 |
11,768,938 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02084:Fbh1
|
APN |
2 |
11,768,938 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02086:Fbh1
|
APN |
2 |
11,768,938 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02369:Fbh1
|
APN |
2 |
11,751,969 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02584:Fbh1
|
APN |
2 |
11,764,769 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03138:Fbh1
|
UTSW |
2 |
11,754,320 (GRCm39) |
intron |
probably benign |
|
R0384:Fbh1
|
UTSW |
2 |
11,754,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R0479:Fbh1
|
UTSW |
2 |
11,763,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0972:Fbh1
|
UTSW |
2 |
11,768,899 (GRCm39) |
splice site |
probably benign |
|
R1420:Fbh1
|
UTSW |
2 |
11,772,493 (GRCm39) |
missense |
probably benign |
0.01 |
R1827:Fbh1
|
UTSW |
2 |
11,768,699 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1832:Fbh1
|
UTSW |
2 |
11,772,211 (GRCm39) |
missense |
probably benign |
0.08 |
R1960:Fbh1
|
UTSW |
2 |
11,762,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R2040:Fbh1
|
UTSW |
2 |
11,774,706 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2102:Fbh1
|
UTSW |
2 |
11,763,100 (GRCm39) |
missense |
probably benign |
0.18 |
R3236:Fbh1
|
UTSW |
2 |
11,774,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R3975:Fbh1
|
UTSW |
2 |
11,772,021 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4504:Fbh1
|
UTSW |
2 |
11,753,828 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4505:Fbh1
|
UTSW |
2 |
11,753,828 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4507:Fbh1
|
UTSW |
2 |
11,753,828 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4799:Fbh1
|
UTSW |
2 |
11,760,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Fbh1
|
UTSW |
2 |
11,767,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R4994:Fbh1
|
UTSW |
2 |
11,769,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Fbh1
|
UTSW |
2 |
11,753,804 (GRCm39) |
missense |
probably damaging |
0.97 |
R5801:Fbh1
|
UTSW |
2 |
11,774,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R6255:Fbh1
|
UTSW |
2 |
11,753,257 (GRCm39) |
missense |
probably benign |
0.31 |
R7011:Fbh1
|
UTSW |
2 |
11,767,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7177:Fbh1
|
UTSW |
2 |
11,760,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R7243:Fbh1
|
UTSW |
2 |
11,756,336 (GRCm39) |
missense |
probably benign |
0.11 |
R7331:Fbh1
|
UTSW |
2 |
11,768,797 (GRCm39) |
missense |
probably benign |
|
R7361:Fbh1
|
UTSW |
2 |
11,751,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R7460:Fbh1
|
UTSW |
2 |
11,761,496 (GRCm39) |
missense |
probably benign |
0.38 |
R7541:Fbh1
|
UTSW |
2 |
11,754,348 (GRCm39) |
missense |
probably benign |
0.05 |
R8000:Fbh1
|
UTSW |
2 |
11,772,100 (GRCm39) |
missense |
probably benign |
0.21 |
R8010:Fbh1
|
UTSW |
2 |
11,772,443 (GRCm39) |
missense |
probably benign |
0.15 |
R8056:Fbh1
|
UTSW |
2 |
11,748,441 (GRCm39) |
missense |
probably benign |
0.01 |
R8517:Fbh1
|
UTSW |
2 |
11,782,241 (GRCm39) |
critical splice donor site |
probably null |
|
R8686:Fbh1
|
UTSW |
2 |
11,760,469 (GRCm39) |
missense |
probably benign |
0.00 |
R8883:Fbh1
|
UTSW |
2 |
11,753,922 (GRCm39) |
missense |
probably benign |
0.21 |
R9093:Fbh1
|
UTSW |
2 |
11,764,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R9306:Fbh1
|
UTSW |
2 |
11,772,387 (GRCm39) |
missense |
probably benign |
0.00 |
R9342:Fbh1
|
UTSW |
2 |
11,754,414 (GRCm39) |
missense |
probably benign |
0.01 |
|