Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110040M04Rik |
T |
A |
1: 151,080,480 (GRCm39) |
D189E |
probably benign |
Het |
Abca13 |
A |
T |
11: 9,240,501 (GRCm39) |
H788L |
probably benign |
Het |
Abcb1b |
A |
G |
5: 8,862,779 (GRCm39) |
I154V |
probably benign |
Het |
Acsm4 |
A |
G |
7: 119,293,872 (GRCm39) |
N81S |
probably benign |
Het |
Adamts5 |
G |
A |
16: 85,659,674 (GRCm39) |
H873Y |
probably benign |
Het |
Aox4 |
C |
T |
1: 58,268,020 (GRCm39) |
T200I |
possibly damaging |
Het |
Arhgap33 |
A |
G |
7: 30,229,367 (GRCm39) |
V336A |
probably damaging |
Het |
Brca1 |
C |
T |
11: 101,416,683 (GRCm39) |
E484K |
probably damaging |
Het |
Capn13 |
T |
A |
17: 73,672,964 (GRCm39) |
D113V |
probably benign |
Het |
Catsper2 |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
2: 121,228,053 (GRCm39) |
|
probably benign |
Het |
Ceacam3 |
G |
A |
7: 16,892,078 (GRCm39) |
E274K |
|
Het |
Cfh |
A |
T |
1: 140,030,254 (GRCm39) |
I891K |
probably damaging |
Het |
Cgn |
A |
G |
3: 94,670,332 (GRCm39) |
S1041P |
probably damaging |
Het |
Cldn18 |
T |
C |
9: 99,580,915 (GRCm39) |
D111G |
probably benign |
Het |
Cnp |
G |
A |
11: 100,467,261 (GRCm39) |
R68Q |
probably benign |
Het |
Cntn4 |
T |
A |
6: 106,674,525 (GRCm39) |
C1008* |
probably null |
Het |
Cntnap5a |
T |
C |
1: 116,029,323 (GRCm39) |
I259T |
probably benign |
Het |
Cubn |
A |
G |
2: 13,319,529 (GRCm39) |
I2897T |
probably benign |
Het |
Cyp2c39 |
T |
A |
19: 39,501,648 (GRCm39) |
L67Q |
probably damaging |
Het |
Dclk1 |
G |
A |
3: 55,387,854 (GRCm39) |
C100Y |
probably damaging |
Het |
Ddc |
C |
T |
11: 11,772,288 (GRCm39) |
W349* |
probably null |
Het |
Dennd3 |
A |
G |
15: 73,440,563 (GRCm39) |
E1198G |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,026,400 (GRCm39) |
D826G |
probably null |
Het |
Dpp4 |
T |
C |
2: 62,217,429 (GRCm39) |
Y56C |
probably damaging |
Het |
Etv6 |
A |
G |
6: 134,243,295 (GRCm39) |
D350G |
possibly damaging |
Het |
Fat1 |
C |
A |
8: 45,406,075 (GRCm39) |
P942Q |
probably damaging |
Het |
Fbxl5 |
A |
G |
5: 43,916,159 (GRCm39) |
F418L |
probably benign |
Het |
Fbxo11 |
T |
A |
17: 88,316,098 (GRCm39) |
H368L |
|
Het |
Fhl2 |
G |
T |
1: 43,167,546 (GRCm39) |
H182Q |
probably damaging |
Het |
Gabpa |
T |
A |
16: 84,649,461 (GRCm39) |
C223S |
probably damaging |
Het |
Greb1 |
A |
T |
12: 16,790,038 (GRCm39) |
N3K |
probably damaging |
Het |
Hmcn1 |
T |
G |
1: 150,684,473 (GRCm39) |
S366R |
probably benign |
Het |
Il17b |
A |
G |
18: 61,825,363 (GRCm39) |
Q133R |
probably benign |
Het |
Inha |
T |
A |
1: 75,486,211 (GRCm39) |
S169T |
probably benign |
Het |
Itsn1 |
G |
A |
16: 91,650,055 (GRCm39) |
R243H |
probably benign |
Het |
Kcnu1 |
G |
GA |
8: 26,403,675 (GRCm39) |
|
probably null |
Het |
Kdm1b |
A |
G |
13: 47,234,030 (GRCm39) |
E788G |
probably damaging |
Het |
Kdm2a |
A |
T |
19: 4,370,308 (GRCm39) |
I1059N |
probably damaging |
Het |
Klk1b9 |
G |
T |
7: 43,628,795 (GRCm39) |
G100C |
probably benign |
Het |
Knl1 |
T |
C |
2: 118,899,994 (GRCm39) |
V565A |
probably benign |
Het |
Knl1 |
A |
T |
2: 118,907,425 (GRCm39) |
N1650Y |
probably damaging |
Het |
Lpp |
T |
C |
16: 24,580,719 (GRCm39) |
V270A |
probably benign |
Het |
Lrrc15 |
A |
G |
16: 30,092,517 (GRCm39) |
L274P |
probably damaging |
Het |
Mertk |
C |
T |
2: 128,643,255 (GRCm39) |
L885F |
probably benign |
Het |
Mpst |
T |
A |
15: 78,294,361 (GRCm39) |
L31* |
probably null |
Het |
Ms4a10 |
T |
C |
19: 10,944,440 (GRCm39) |
T115A |
possibly damaging |
Het |
Myof |
A |
G |
19: 37,923,263 (GRCm39) |
I1330T |
possibly damaging |
Het |
Ncam2 |
T |
C |
16: 81,240,142 (GRCm39) |
I201T |
probably damaging |
Het |
Nefh |
T |
A |
11: 4,889,443 (GRCm39) |
K1059* |
probably null |
Het |
Nek1 |
T |
C |
8: 61,473,107 (GRCm39) |
Y168H |
probably damaging |
Het |
Nek11 |
T |
A |
9: 105,082,011 (GRCm39) |
T531S |
probably damaging |
Het |
Nelfa |
G |
A |
5: 34,059,127 (GRCm39) |
P243S |
possibly damaging |
Het |
Niban1 |
T |
C |
1: 151,512,193 (GRCm39) |
Y32H |
probably damaging |
Het |
Notum |
G |
T |
11: 120,550,974 (GRCm39) |
T64K |
|
Het |
Or13c7d |
T |
A |
4: 43,770,193 (GRCm39) |
K273* |
probably null |
Het |
Or52b2 |
A |
C |
7: 104,986,520 (GRCm39) |
Y134* |
probably null |
Het |
Or9i16 |
A |
G |
19: 13,864,861 (GRCm39) |
S238P |
probably damaging |
Het |
Otof |
A |
G |
5: 30,539,708 (GRCm39) |
I1035T |
possibly damaging |
Het |
Otud3 |
A |
G |
4: 138,624,925 (GRCm39) |
Y259H |
probably benign |
Het |
Per1 |
G |
T |
11: 68,993,554 (GRCm39) |
C368F |
probably damaging |
Het |
Pitrm1 |
G |
T |
13: 6,605,602 (GRCm39) |
R183L |
probably damaging |
Het |
Prl3a1 |
C |
T |
13: 27,459,118 (GRCm39) |
A119V |
|
Het |
Pycard |
C |
T |
7: 127,592,776 (GRCm39) |
G17E |
probably benign |
Het |
Rnf13 |
A |
G |
3: 57,740,430 (GRCm39) |
D249G |
possibly damaging |
Het |
Sdhaf2 |
T |
C |
19: 10,494,689 (GRCm39) |
Y33C |
probably damaging |
Het |
Sdk2 |
A |
G |
11: 113,691,061 (GRCm39) |
V1838A |
probably benign |
Het |
Sgo2b |
C |
T |
8: 64,380,274 (GRCm39) |
V853I |
probably benign |
Het |
Slc1a4 |
T |
C |
11: 20,282,403 (GRCm39) |
T24A |
probably benign |
Het |
Slc8a1 |
T |
C |
17: 81,955,407 (GRCm39) |
T544A |
probably benign |
Het |
Sntg2 |
T |
C |
12: 30,326,732 (GRCm39) |
N143S |
probably benign |
Het |
Sphkap |
T |
C |
1: 83,254,989 (GRCm39) |
E920G |
probably damaging |
Het |
Srgap2 |
T |
A |
1: 131,252,828 (GRCm39) |
H132L |
|
Het |
Srgap3 |
A |
T |
6: 112,748,524 (GRCm39) |
V376D |
probably damaging |
Het |
Stxbp5l |
T |
C |
16: 37,036,314 (GRCm39) |
K434E |
probably damaging |
Het |
Tab2 |
A |
T |
10: 7,795,005 (GRCm39) |
N492K |
possibly damaging |
Het |
Tbc1d32 |
T |
C |
10: 56,037,246 (GRCm39) |
Q666R |
possibly damaging |
Het |
Tekt4 |
T |
C |
17: 25,692,782 (GRCm39) |
|
probably null |
Het |
Tnni3k |
G |
A |
3: 154,667,724 (GRCm39) |
Q230* |
probably null |
Het |
Trp53bp1 |
A |
C |
2: 121,066,657 (GRCm39) |
S690A |
probably benign |
Het |
Trpa1 |
C |
A |
1: 14,989,077 (GRCm39) |
|
probably benign |
Het |
Trpm1 |
T |
G |
7: 63,858,132 (GRCm39) |
V324G |
probably damaging |
Het |
Usp29 |
A |
G |
7: 6,966,179 (GRCm39) |
E674G |
possibly damaging |
Het |
Vmn2r59 |
T |
C |
7: 41,661,299 (GRCm39) |
R839G |
probably damaging |
Het |
Vmn2r6 |
A |
G |
3: 64,445,724 (GRCm39) |
L667P |
probably damaging |
Het |
Vmn2r91 |
T |
A |
17: 18,356,305 (GRCm39) |
F657L |
possibly damaging |
Het |
Vps13d |
A |
G |
4: 144,824,701 (GRCm39) |
V2923A |
|
Het |
Xylb |
T |
A |
9: 119,201,022 (GRCm39) |
L220Q |
probably damaging |
Het |
Zbtb10 |
C |
T |
3: 9,316,473 (GRCm39) |
T95M |
probably benign |
Het |
Zfp263 |
C |
T |
16: 3,567,482 (GRCm39) |
P599L |
probably damaging |
Het |
Zfp532 |
A |
G |
18: 65,789,639 (GRCm39) |
E1026G |
probably benign |
Het |
Zfp78 |
A |
G |
7: 6,382,078 (GRCm39) |
N376S |
probably benign |
Het |
|
Other mutations in Gigyf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00490:Gigyf2
|
APN |
1 |
87,364,572 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01828:Gigyf2
|
APN |
1 |
87,346,820 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02222:Gigyf2
|
APN |
1 |
87,338,585 (GRCm39) |
splice site |
probably null |
|
IGL02259:Gigyf2
|
APN |
1 |
87,339,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02562:Gigyf2
|
APN |
1 |
87,335,097 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02565:Gigyf2
|
APN |
1 |
87,369,858 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02695:Gigyf2
|
APN |
1 |
87,344,549 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03264:Gigyf2
|
APN |
1 |
87,376,790 (GRCm39) |
splice site |
probably benign |
|
Flop
|
UTSW |
1 |
87,292,988 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Gigyf2
|
UTSW |
1 |
87,356,307 (GRCm39) |
unclassified |
probably benign |
|
PIT4260001:Gigyf2
|
UTSW |
1 |
87,346,828 (GRCm39) |
missense |
unknown |
|
R0041:Gigyf2
|
UTSW |
1 |
87,306,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R0126:Gigyf2
|
UTSW |
1 |
87,339,597 (GRCm39) |
splice site |
probably benign |
|
R0190:Gigyf2
|
UTSW |
1 |
87,356,410 (GRCm39) |
unclassified |
probably benign |
|
R0244:Gigyf2
|
UTSW |
1 |
87,306,737 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0492:Gigyf2
|
UTSW |
1 |
87,368,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Gigyf2
|
UTSW |
1 |
87,349,215 (GRCm39) |
missense |
probably benign |
0.00 |
R0612:Gigyf2
|
UTSW |
1 |
87,376,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Gigyf2
|
UTSW |
1 |
87,335,449 (GRCm39) |
splice site |
probably benign |
|
R0783:Gigyf2
|
UTSW |
1 |
87,334,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R1445:Gigyf2
|
UTSW |
1 |
87,371,360 (GRCm39) |
splice site |
probably benign |
|
R1620:Gigyf2
|
UTSW |
1 |
87,376,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Gigyf2
|
UTSW |
1 |
87,344,705 (GRCm39) |
missense |
probably benign |
0.44 |
R2008:Gigyf2
|
UTSW |
1 |
87,301,835 (GRCm39) |
critical splice donor site |
probably null |
|
R2111:Gigyf2
|
UTSW |
1 |
87,368,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R2112:Gigyf2
|
UTSW |
1 |
87,368,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R2180:Gigyf2
|
UTSW |
1 |
87,344,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R3438:Gigyf2
|
UTSW |
1 |
87,368,302 (GRCm39) |
missense |
probably damaging |
0.96 |
R3690:Gigyf2
|
UTSW |
1 |
87,349,238 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4089:Gigyf2
|
UTSW |
1 |
87,371,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R4411:Gigyf2
|
UTSW |
1 |
87,364,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R4412:Gigyf2
|
UTSW |
1 |
87,364,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R4489:Gigyf2
|
UTSW |
1 |
87,368,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R4743:Gigyf2
|
UTSW |
1 |
87,292,970 (GRCm39) |
nonsense |
probably null |
|
R4769:Gigyf2
|
UTSW |
1 |
87,368,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:Gigyf2
|
UTSW |
1 |
87,282,135 (GRCm39) |
unclassified |
probably benign |
|
R5215:Gigyf2
|
UTSW |
1 |
87,292,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R5326:Gigyf2
|
UTSW |
1 |
87,352,860 (GRCm39) |
unclassified |
probably benign |
|
R5771:Gigyf2
|
UTSW |
1 |
87,374,050 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5813:Gigyf2
|
UTSW |
1 |
87,368,485 (GRCm39) |
missense |
probably damaging |
0.99 |
R5964:Gigyf2
|
UTSW |
1 |
87,334,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R6026:Gigyf2
|
UTSW |
1 |
87,368,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R6035:Gigyf2
|
UTSW |
1 |
87,338,450 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6035:Gigyf2
|
UTSW |
1 |
87,338,450 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6784:Gigyf2
|
UTSW |
1 |
87,371,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R6800:Gigyf2
|
UTSW |
1 |
87,346,898 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6991:Gigyf2
|
UTSW |
1 |
87,334,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R7224:Gigyf2
|
UTSW |
1 |
87,331,447 (GRCm39) |
missense |
unknown |
|
R7464:Gigyf2
|
UTSW |
1 |
87,356,326 (GRCm39) |
missense |
unknown |
|
R7554:Gigyf2
|
UTSW |
1 |
87,335,292 (GRCm39) |
missense |
unknown |
|
R7658:Gigyf2
|
UTSW |
1 |
87,346,860 (GRCm39) |
missense |
unknown |
|
R7976:Gigyf2
|
UTSW |
1 |
87,331,458 (GRCm39) |
missense |
unknown |
|
R8032:Gigyf2
|
UTSW |
1 |
87,334,735 (GRCm39) |
missense |
unknown |
|
R8070:Gigyf2
|
UTSW |
1 |
87,368,629 (GRCm39) |
missense |
probably benign |
0.03 |
R8071:Gigyf2
|
UTSW |
1 |
87,374,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R8519:Gigyf2
|
UTSW |
1 |
87,338,431 (GRCm39) |
missense |
probably benign |
0.01 |
R8675:Gigyf2
|
UTSW |
1 |
87,331,438 (GRCm39) |
missense |
unknown |
|
R8849:Gigyf2
|
UTSW |
1 |
87,361,592 (GRCm39) |
missense |
unknown |
|
R8872:Gigyf2
|
UTSW |
1 |
87,307,725 (GRCm39) |
missense |
unknown |
|
R9184:Gigyf2
|
UTSW |
1 |
87,368,311 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9465:Gigyf2
|
UTSW |
1 |
87,334,775 (GRCm39) |
missense |
unknown |
|
R9502:Gigyf2
|
UTSW |
1 |
87,331,446 (GRCm39) |
missense |
unknown |
|
R9665:Gigyf2
|
UTSW |
1 |
87,331,457 (GRCm39) |
missense |
unknown |
|
X0065:Gigyf2
|
UTSW |
1 |
87,339,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|