Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1a1 |
A |
G |
4: 116,498,260 (GRCm39) |
L95P |
probably damaging |
Het |
Amigo2 |
G |
T |
15: 97,143,389 (GRCm39) |
N344K |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,621,014 (GRCm39) |
D946G |
possibly damaging |
Het |
Ankrd12 |
T |
C |
17: 66,338,568 (GRCm39) |
|
probably null |
Het |
Atp8b5 |
A |
G |
4: 43,304,687 (GRCm39) |
N66S |
|
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Birc6 |
G |
A |
17: 74,835,533 (GRCm39) |
S24N |
probably null |
Het |
Bzw2 |
A |
T |
12: 36,173,982 (GRCm39) |
C97* |
probably null |
Het |
Capn12 |
T |
A |
7: 28,585,949 (GRCm39) |
|
probably benign |
Het |
Cdh1 |
T |
A |
8: 107,330,971 (GRCm39) |
F34Y |
probably damaging |
Het |
Cdh5 |
T |
C |
8: 104,852,092 (GRCm39) |
I69T |
possibly damaging |
Het |
Celsr2 |
G |
A |
3: 108,320,880 (GRCm39) |
T644I |
possibly damaging |
Het |
Cep85l |
A |
T |
10: 53,224,911 (GRCm39) |
L226Q |
possibly damaging |
Het |
Clasp2 |
T |
A |
9: 113,732,936 (GRCm39) |
M924K |
possibly damaging |
Het |
Col3a1 |
G |
A |
1: 45,379,139 (GRCm39) |
A850T |
unknown |
Het |
Cped1 |
C |
T |
6: 22,016,962 (GRCm39) |
P104S |
possibly damaging |
Het |
Cracd |
GCGCGAGGCCGAGAGGCAGGAGGAGGAAGCAAGACAACGCGAGGCCGAGAGGCAGG |
GCGCGAGGCCGAGAGGCAGG |
5: 77,004,801 (GRCm39) |
|
probably benign |
Het |
Cyp2c69 |
T |
C |
19: 39,869,910 (GRCm39) |
D104G |
possibly damaging |
Het |
Daw1 |
T |
A |
1: 83,187,011 (GRCm39) |
C274S |
probably damaging |
Het |
Dmtn |
T |
C |
14: 70,850,144 (GRCm39) |
T267A |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,055,112 (GRCm39) |
Y585H |
possibly damaging |
Het |
Dop1a |
A |
G |
9: 86,403,587 (GRCm39) |
I132V |
probably benign |
Het |
Dpysl5 |
C |
T |
5: 30,902,687 (GRCm39) |
R40C |
probably benign |
Het |
Dsg2 |
T |
G |
18: 20,723,126 (GRCm39) |
V384G |
probably damaging |
Het |
Elmo1 |
C |
T |
13: 20,748,630 (GRCm39) |
L492F |
probably damaging |
Het |
Epg5 |
C |
A |
18: 78,056,086 (GRCm39) |
D1753E |
possibly damaging |
Het |
Ext1 |
T |
C |
15: 52,955,723 (GRCm39) |
Y458C |
probably damaging |
Het |
Folr2 |
C |
T |
7: 101,489,408 (GRCm39) |
V244M |
unknown |
Het |
Galnt18 |
T |
C |
7: 111,378,709 (GRCm39) |
I16V |
possibly damaging |
Het |
Gm10036 |
C |
A |
18: 15,966,207 (GRCm39) |
Y119* |
probably null |
Het |
Gria4 |
A |
G |
9: 4,664,951 (GRCm39) |
S102P |
probably damaging |
Het |
Hc |
A |
T |
2: 34,890,861 (GRCm39) |
N1318K |
probably benign |
Het |
Htr2a |
C |
T |
14: 74,882,617 (GRCm39) |
T201I |
possibly damaging |
Het |
Ifitm1 |
T |
C |
7: 140,549,499 (GRCm39) |
L94P |
probably damaging |
Het |
Iqca1l |
T |
C |
5: 24,755,628 (GRCm39) |
D298G |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kank4 |
C |
T |
4: 98,653,747 (GRCm39) |
V894I |
possibly damaging |
Het |
Kcnip2 |
T |
A |
19: 45,785,100 (GRCm39) |
|
probably benign |
Het |
Klhl29 |
A |
T |
12: 5,187,542 (GRCm39) |
L274H |
possibly damaging |
Het |
Lamb1 |
A |
G |
12: 31,352,953 (GRCm39) |
T885A |
possibly damaging |
Het |
Ldc1 |
T |
C |
4: 130,105,223 (GRCm39) |
K316E |
probably benign |
Het |
Lipi |
A |
T |
16: 75,352,710 (GRCm39) |
L376I |
probably benign |
Het |
Lrrc37 |
T |
A |
11: 103,509,656 (GRCm39) |
T771S |
unknown |
Het |
Malrd1 |
A |
T |
2: 15,850,038 (GRCm39) |
N1219I |
unknown |
Het |
Mrc1 |
A |
C |
2: 14,312,760 (GRCm39) |
N894T |
probably damaging |
Het |
Mrpl35 |
C |
T |
6: 71,793,271 (GRCm39) |
A127T |
possibly damaging |
Het |
Naip2 |
T |
C |
13: 100,325,644 (GRCm39) |
H88R |
probably benign |
Het |
Nek5 |
C |
T |
8: 22,580,495 (GRCm39) |
|
probably null |
Het |
Nlrc5 |
G |
A |
8: 95,252,118 (GRCm39) |
V1880I |
probably benign |
Het |
Noc3l |
T |
A |
19: 38,798,751 (GRCm39) |
K282N |
probably damaging |
Het |
Nwd2 |
T |
C |
5: 63,963,241 (GRCm39) |
Y942H |
probably damaging |
Het |
Or10ag2 |
T |
C |
2: 87,248,659 (GRCm39) |
V87A |
probably benign |
Het |
Or4f62 |
G |
A |
2: 111,986,974 (GRCm39) |
R226H |
probably benign |
Het |
Or52d1 |
T |
A |
7: 103,756,302 (GRCm39) |
I272N |
probably damaging |
Het |
Osbpl9 |
C |
A |
4: 108,930,333 (GRCm39) |
A221S |
probably benign |
Het |
Paip1 |
T |
C |
13: 119,566,801 (GRCm39) |
L45S |
probably benign |
Het |
Pccb |
A |
T |
9: 100,905,305 (GRCm39) |
|
probably benign |
Het |
Pgap3 |
A |
G |
11: 98,281,602 (GRCm39) |
F199L |
possibly damaging |
Het |
Pik3c2g |
A |
T |
6: 139,676,092 (GRCm39) |
K79* |
probably null |
Het |
Pou3f1 |
C |
G |
4: 124,552,152 (GRCm39) |
A218G |
possibly damaging |
Het |
Ptk2b |
T |
A |
14: 66,412,242 (GRCm39) |
N383I |
probably benign |
Het |
Rad52 |
C |
T |
6: 119,890,041 (GRCm39) |
R56C |
probably damaging |
Het |
Rdh7 |
A |
T |
10: 127,724,430 (GRCm39) |
F18Y |
probably benign |
Het |
Scart2 |
C |
T |
7: 139,841,532 (GRCm39) |
P279S |
possibly damaging |
Het |
Septin5 |
A |
G |
16: 18,441,861 (GRCm39) |
M315T |
possibly damaging |
Het |
Slc27a6 |
A |
G |
18: 58,715,306 (GRCm39) |
Y303C |
probably damaging |
Het |
Slc7a7 |
T |
A |
14: 54,607,293 (GRCm39) |
M495L |
probably benign |
Het |
Sntg1 |
T |
A |
1: 8,748,074 (GRCm39) |
|
probably null |
Het |
Spdye4a |
T |
G |
5: 143,211,418 (GRCm39) |
S49R |
probably benign |
Het |
Spred2 |
T |
A |
11: 19,951,019 (GRCm39) |
I72N |
probably benign |
Het |
Stox1 |
A |
T |
10: 62,495,386 (GRCm39) |
H962Q |
probably benign |
Het |
Susd2 |
G |
T |
10: 75,475,452 (GRCm39) |
A484D |
possibly damaging |
Het |
Syt14 |
A |
G |
1: 192,579,866 (GRCm39) |
S473P |
probably damaging |
Het |
Tpx2 |
T |
C |
2: 152,724,255 (GRCm39) |
Y344H |
probably damaging |
Het |
Ttc17 |
T |
C |
2: 94,157,049 (GRCm39) |
N411S |
probably benign |
Het |
Ttf2 |
A |
T |
3: 100,870,028 (GRCm39) |
F348L |
probably benign |
Het |
Ttn |
A |
T |
2: 76,663,650 (GRCm39) |
V11675E |
unknown |
Het |
Usp2 |
G |
T |
9: 43,986,894 (GRCm39) |
R64L |
probably benign |
Het |
|
Other mutations in Frmd6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0629:Frmd6
|
UTSW |
12 |
70,930,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R0662:Frmd6
|
UTSW |
12 |
70,946,218 (GRCm39) |
nonsense |
probably null |
|
R0747:Frmd6
|
UTSW |
12 |
70,910,830 (GRCm39) |
missense |
probably benign |
|
R1144:Frmd6
|
UTSW |
12 |
70,923,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R1366:Frmd6
|
UTSW |
12 |
70,934,663 (GRCm39) |
splice site |
probably benign |
|
R1763:Frmd6
|
UTSW |
12 |
70,940,396 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2135:Frmd6
|
UTSW |
12 |
70,941,771 (GRCm39) |
missense |
probably benign |
0.00 |
R2342:Frmd6
|
UTSW |
12 |
70,930,592 (GRCm39) |
nonsense |
probably null |
|
R3963:Frmd6
|
UTSW |
12 |
70,940,638 (GRCm39) |
missense |
probably benign |
0.00 |
R3982:Frmd6
|
UTSW |
12 |
70,934,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R4010:Frmd6
|
UTSW |
12 |
70,946,327 (GRCm39) |
missense |
probably benign |
|
R4416:Frmd6
|
UTSW |
12 |
70,924,023 (GRCm39) |
missense |
probably benign |
0.04 |
R4823:Frmd6
|
UTSW |
12 |
70,919,349 (GRCm39) |
missense |
probably benign |
0.22 |
R4861:Frmd6
|
UTSW |
12 |
70,940,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R5368:Frmd6
|
UTSW |
12 |
70,910,874 (GRCm39) |
nonsense |
probably null |
|
R5806:Frmd6
|
UTSW |
12 |
70,936,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Frmd6
|
UTSW |
12 |
70,910,685 (GRCm39) |
start gained |
probably benign |
|
R6253:Frmd6
|
UTSW |
12 |
70,923,987 (GRCm39) |
missense |
probably damaging |
0.99 |
R6781:Frmd6
|
UTSW |
12 |
70,946,417 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7051:Frmd6
|
UTSW |
12 |
70,944,170 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7156:Frmd6
|
UTSW |
12 |
70,923,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Frmd6
|
UTSW |
12 |
70,933,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R9368:Frmd6
|
UTSW |
12 |
70,933,865 (GRCm39) |
critical splice donor site |
probably null |
|
U24488:Frmd6
|
UTSW |
12 |
70,940,653 (GRCm39) |
missense |
probably damaging |
0.97 |
X0022:Frmd6
|
UTSW |
12 |
70,910,882 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Frmd6
|
UTSW |
12 |
70,927,452 (GRCm39) |
missense |
probably benign |
0.03 |
|