Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
A |
11: 119,901,817 (GRCm39) |
S803C |
probably benign |
Het |
Abcc9 |
C |
T |
6: 142,625,034 (GRCm39) |
A454T |
probably damaging |
Het |
Abr |
T |
C |
11: 76,343,158 (GRCm39) |
E565G |
probably damaging |
Het |
Adam33 |
C |
A |
2: 130,893,266 (GRCm39) |
R753L |
probably benign |
Het |
Adgre1 |
A |
G |
17: 57,708,955 (GRCm39) |
T49A |
possibly damaging |
Het |
Ankra2 |
A |
T |
13: 98,404,950 (GRCm39) |
H153L |
probably damaging |
Het |
Ankrd26 |
T |
G |
6: 118,488,599 (GRCm39) |
E1353D |
probably benign |
Het |
Ankrd52 |
T |
G |
10: 128,215,200 (GRCm39) |
|
probably null |
Het |
Arhgef10l |
T |
A |
4: 140,270,068 (GRCm39) |
T619S |
possibly damaging |
Het |
Armh4 |
A |
G |
14: 50,010,789 (GRCm39) |
V306A |
possibly damaging |
Het |
Asgr1 |
T |
C |
11: 69,947,720 (GRCm39) |
V130A |
possibly damaging |
Het |
Atg10 |
C |
A |
13: 91,085,466 (GRCm39) |
C161F |
probably damaging |
Het |
Atm |
A |
T |
9: 53,401,554 (GRCm39) |
N1438K |
probably damaging |
Het |
BC107364 |
T |
A |
3: 96,343,322 (GRCm39) |
|
probably null |
Het |
Bcar3 |
G |
T |
3: 122,220,225 (GRCm39) |
A41S |
probably benign |
Het |
Btbd6 |
A |
G |
12: 112,940,932 (GRCm39) |
|
probably benign |
Het |
Cchcr1 |
A |
G |
17: 35,835,600 (GRCm39) |
T318A |
possibly damaging |
Het |
Celsr1 |
A |
T |
15: 85,809,719 (GRCm39) |
I2221N |
probably damaging |
Het |
Cept1 |
C |
T |
3: 106,440,761 (GRCm39) |
W48* |
probably null |
Het |
Cfap161 |
T |
A |
7: 83,442,484 (GRCm39) |
I85L |
probably benign |
Het |
Clasp1 |
A |
T |
1: 118,439,910 (GRCm39) |
R640* |
probably null |
Het |
Col5a1 |
T |
A |
2: 27,842,448 (GRCm39) |
I441N |
unknown |
Het |
Col9a1 |
C |
A |
1: 24,224,486 (GRCm39) |
L223I |
unknown |
Het |
Dnah2 |
T |
C |
11: 69,406,836 (GRCm39) |
D223G |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dpy19l1 |
A |
T |
9: 24,361,992 (GRCm39) |
M129K |
possibly damaging |
Het |
Ecpas |
A |
T |
4: 58,810,785 (GRCm39) |
I1524N |
probably damaging |
Het |
Fcgbpl1 |
C |
G |
7: 27,854,798 (GRCm39) |
P1808R |
probably damaging |
Het |
Fcrl1 |
C |
A |
3: 87,296,946 (GRCm39) |
H318Q |
probably benign |
Het |
Fkbp4 |
C |
T |
6: 128,410,194 (GRCm39) |
E256K |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,820,430 (GRCm39) |
T5388A |
possibly damaging |
Het |
Glrx |
G |
A |
13: 75,995,418 (GRCm39) |
|
probably null |
Het |
Gm7356 |
A |
T |
17: 14,221,726 (GRCm39) |
M101K |
probably damaging |
Het |
Gstp2 |
A |
T |
19: 4,090,499 (GRCm39) |
I162N |
probably benign |
Het |
Hectd3 |
A |
C |
4: 116,856,783 (GRCm39) |
K443N |
probably damaging |
Het |
Hmcn1 |
T |
A |
1: 150,540,535 (GRCm39) |
R2925W |
probably damaging |
Het |
Hspa1a |
G |
T |
17: 35,189,282 (GRCm39) |
N540K |
probably damaging |
Het |
Ints6 |
A |
T |
14: 62,938,235 (GRCm39) |
M649K |
probably benign |
Het |
Katnb1 |
T |
C |
8: 95,822,084 (GRCm39) |
V270A |
possibly damaging |
Het |
Kctd3 |
A |
G |
1: 188,704,561 (GRCm39) |
S737P |
probably benign |
Het |
Klra10 |
T |
C |
6: 130,249,507 (GRCm39) |
|
probably null |
Het |
Lmtk3 |
A |
G |
7: 45,448,013 (GRCm39) |
D1353G |
unknown |
Het |
Lrrk1 |
A |
G |
7: 65,912,481 (GRCm39) |
V1693A |
probably damaging |
Het |
Mpnd |
A |
T |
17: 56,316,575 (GRCm39) |
I85F |
probably damaging |
Het |
Myo3b |
A |
G |
2: 70,179,304 (GRCm39) |
T1173A |
probably benign |
Het |
Myof |
G |
A |
19: 37,892,279 (GRCm39) |
P1158L |
probably damaging |
Het |
Naip2 |
A |
C |
13: 100,298,549 (GRCm39) |
S496A |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,187,069 (GRCm39) |
|
probably benign |
Het |
Npepps |
C |
T |
11: 97,149,099 (GRCm39) |
|
probably null |
Het |
Opn5 |
T |
A |
17: 42,891,640 (GRCm39) |
I266F |
probably benign |
Het |
Or4a74 |
T |
G |
2: 89,439,790 (GRCm39) |
I219L |
probably damaging |
Het |
P2rx4 |
A |
G |
5: 122,845,763 (GRCm39) |
D16G |
probably damaging |
Het |
Padi2 |
G |
T |
4: 140,644,948 (GRCm39) |
V61L |
probably benign |
Het |
Pkd1l1 |
G |
A |
11: 8,813,911 (GRCm39) |
T1480I |
probably benign |
Het |
Plcb1 |
T |
C |
2: 135,177,371 (GRCm39) |
S568P |
probably damaging |
Het |
Rassf10 |
A |
G |
7: 112,554,914 (GRCm39) |
E505G |
probably damaging |
Het |
Rcan2 |
A |
G |
17: 44,147,225 (GRCm39) |
E21G |
probably benign |
Het |
Rhob |
G |
T |
12: 8,549,585 (GRCm39) |
C16* |
probably null |
Het |
Ryr3 |
T |
C |
2: 112,490,413 (GRCm39) |
N3807S |
probably damaging |
Het |
Sass6 |
T |
A |
3: 116,415,046 (GRCm39) |
N519K |
probably benign |
Het |
Slco1a8 |
A |
T |
6: 141,939,368 (GRCm39) |
N208K |
possibly damaging |
Het |
Smad9 |
A |
T |
3: 54,689,864 (GRCm39) |
D28V |
probably damaging |
Het |
Spmip8 |
A |
T |
8: 96,047,894 (GRCm39) |
|
probably null |
Het |
Tex14 |
G |
T |
11: 87,405,199 (GRCm39) |
G704C |
probably benign |
Het |
Tmc3 |
A |
G |
7: 83,271,524 (GRCm39) |
N892S |
probably benign |
Het |
Tnfaip2 |
T |
A |
12: 111,412,097 (GRCm39) |
L166Q |
probably damaging |
Het |
Triml2 |
A |
G |
8: 43,638,165 (GRCm39) |
|
probably null |
Het |
Trio |
A |
G |
15: 27,856,193 (GRCm39) |
V666A |
probably benign |
Het |
Tshz2 |
G |
T |
2: 169,726,584 (GRCm39) |
L393F |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,672,115 (GRCm39) |
|
probably benign |
Het |
Tubb5 |
A |
G |
17: 36,146,734 (GRCm39) |
Y159H |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,178,129 (GRCm39) |
Y35C |
probably damaging |
Het |
Utp4 |
T |
C |
8: 107,631,078 (GRCm39) |
|
probably null |
Het |
Vmn1r60 |
A |
T |
7: 5,547,864 (GRCm39) |
C79S |
probably damaging |
Het |
Wnt5b |
T |
C |
6: 119,410,751 (GRCm39) |
T230A |
probably damaging |
Het |
Zfp618 |
A |
T |
4: 63,050,943 (GRCm39) |
I575F |
probably damaging |
Het |
Zmym6 |
G |
T |
4: 127,017,176 (GRCm39) |
V894L |
possibly damaging |
Het |
Zpbp |
T |
C |
11: 11,412,318 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Fer1l5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4151001:Fer1l5
|
UTSW |
1 |
36,450,728 (GRCm39) |
missense |
probably benign |
0.27 |
R5580:Fer1l5
|
UTSW |
1 |
36,424,539 (GRCm39) |
nonsense |
probably null |
|
R5848:Fer1l5
|
UTSW |
1 |
36,428,016 (GRCm39) |
missense |
probably benign |
0.39 |
R5930:Fer1l5
|
UTSW |
1 |
36,424,254 (GRCm39) |
nonsense |
probably null |
|
R6193:Fer1l5
|
UTSW |
1 |
36,448,517 (GRCm39) |
missense |
probably benign |
0.20 |
R6195:Fer1l5
|
UTSW |
1 |
36,414,367 (GRCm39) |
splice site |
probably null |
|
R6207:Fer1l5
|
UTSW |
1 |
36,424,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R6233:Fer1l5
|
UTSW |
1 |
36,414,367 (GRCm39) |
splice site |
probably null |
|
R6349:Fer1l5
|
UTSW |
1 |
36,450,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R6514:Fer1l5
|
UTSW |
1 |
36,442,697 (GRCm39) |
missense |
probably benign |
0.01 |
R6611:Fer1l5
|
UTSW |
1 |
36,445,735 (GRCm39) |
missense |
probably benign |
0.01 |
R6634:Fer1l5
|
UTSW |
1 |
36,450,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R6733:Fer1l5
|
UTSW |
1 |
36,447,753 (GRCm39) |
critical splice donor site |
probably null |
|
R6816:Fer1l5
|
UTSW |
1 |
36,445,591 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7225:Fer1l5
|
UTSW |
1 |
36,460,033 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7316:Fer1l5
|
UTSW |
1 |
36,457,197 (GRCm39) |
missense |
probably benign |
0.41 |
R7455:Fer1l5
|
UTSW |
1 |
36,428,064 (GRCm39) |
missense |
probably benign |
0.00 |
R7473:Fer1l5
|
UTSW |
1 |
36,460,689 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7702:Fer1l5
|
UTSW |
1 |
36,459,775 (GRCm39) |
nonsense |
probably null |
|
R7714:Fer1l5
|
UTSW |
1 |
36,440,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R7872:Fer1l5
|
UTSW |
1 |
36,460,967 (GRCm39) |
missense |
probably benign |
0.00 |
R7881:Fer1l5
|
UTSW |
1 |
36,446,117 (GRCm39) |
missense |
not run |
|
R7984:Fer1l5
|
UTSW |
1 |
36,447,702 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8326:Fer1l5
|
UTSW |
1 |
36,415,841 (GRCm39) |
missense |
probably benign |
0.04 |
R8523:Fer1l5
|
UTSW |
1 |
36,426,271 (GRCm39) |
missense |
probably benign |
0.27 |
R8528:Fer1l5
|
UTSW |
1 |
36,456,855 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8975:Fer1l5
|
UTSW |
1 |
36,456,897 (GRCm39) |
missense |
probably benign |
0.13 |
R9011:Fer1l5
|
UTSW |
1 |
36,441,601 (GRCm39) |
missense |
probably damaging |
0.96 |
R9084:Fer1l5
|
UTSW |
1 |
36,429,619 (GRCm39) |
missense |
probably benign |
0.00 |
R9140:Fer1l5
|
UTSW |
1 |
36,460,047 (GRCm39) |
intron |
probably benign |
|
R9180:Fer1l5
|
UTSW |
1 |
36,449,999 (GRCm39) |
missense |
probably null |
1.00 |
R9312:Fer1l5
|
UTSW |
1 |
36,460,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Fer1l5
|
UTSW |
1 |
36,442,662 (GRCm39) |
missense |
probably damaging |
0.97 |
R9655:Fer1l5
|
UTSW |
1 |
36,460,696 (GRCm39) |
missense |
probably benign |
0.40 |
Z1176:Fer1l5
|
UTSW |
1 |
36,429,644 (GRCm39) |
nonsense |
probably null |
|
Z1177:Fer1l5
|
UTSW |
1 |
36,448,275 (GRCm39) |
missense |
probably benign |
0.03 |
|