Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam30 |
G |
T |
3: 98,068,307 (GRCm39) |
V47L |
probably benign |
Het |
Atm |
T |
C |
9: 53,370,134 (GRCm39) |
K2323R |
probably benign |
Het |
Bbx |
A |
G |
16: 50,020,813 (GRCm39) |
L865P |
probably damaging |
Het |
C2cd3 |
T |
A |
7: 100,081,430 (GRCm39) |
I1024N |
|
Het |
Cacna1e |
A |
T |
1: 154,343,510 (GRCm39) |
C1161S |
probably benign |
Het |
Caskin2 |
A |
T |
11: 115,702,730 (GRCm39) |
V26E |
possibly damaging |
Het |
Ccnb3 |
T |
G |
X: 6,874,413 (GRCm39) |
D722A |
probably damaging |
Het |
Cep135 |
C |
A |
5: 76,781,550 (GRCm39) |
Q846K |
probably benign |
Het |
Cfap44 |
A |
T |
16: 44,295,619 (GRCm39) |
D1639V |
possibly damaging |
Het |
Cfh |
G |
T |
1: 140,014,111 (GRCm39) |
R1238S |
probably damaging |
Het |
Dctn1 |
A |
T |
6: 83,169,835 (GRCm39) |
D712V |
probably damaging |
Het |
Ddx21 |
T |
C |
10: 62,424,479 (GRCm39) |
D574G |
probably damaging |
Het |
Dele1 |
A |
G |
18: 38,384,210 (GRCm39) |
T35A |
probably benign |
Het |
Dipk1b |
A |
G |
2: 26,525,989 (GRCm39) |
T308A |
probably benign |
Het |
Dlgap5 |
A |
G |
14: 47,638,989 (GRCm39) |
I443T |
probably damaging |
Het |
Dusp7 |
G |
A |
9: 106,250,966 (GRCm39) |
V364I |
|
Het |
Entpd1 |
G |
T |
19: 40,714,608 (GRCm39) |
R268L |
possibly damaging |
Het |
Frat2 |
T |
C |
19: 41,836,106 (GRCm39) |
D82G |
probably damaging |
Het |
Git1 |
T |
A |
11: 77,390,380 (GRCm39) |
I75N |
probably damaging |
Het |
Gpr171 |
T |
A |
3: 59,005,488 (GRCm39) |
I96F |
probably damaging |
Het |
Gzmb |
G |
T |
14: 56,497,845 (GRCm39) |
R132S |
probably benign |
Het |
Hecw1 |
C |
T |
13: 14,546,608 (GRCm39) |
R132H |
probably damaging |
Het |
Hey1 |
T |
G |
3: 8,729,651 (GRCm39) |
S269R |
probably benign |
Het |
Hgf |
T |
A |
5: 16,765,979 (GRCm39) |
N38K |
possibly damaging |
Het |
Lag3 |
T |
C |
6: 124,881,809 (GRCm39) |
R467G |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,583,527 (GRCm39) |
H705L |
probably damaging |
Het |
Lce3f |
T |
G |
3: 92,900,327 (GRCm39) |
S49R |
unknown |
Het |
Lrrc49 |
T |
C |
9: 60,578,594 (GRCm39) |
D250G |
probably damaging |
Het |
Lzts3 |
T |
C |
2: 130,477,248 (GRCm39) |
K400R |
possibly damaging |
Het |
Macc1 |
T |
C |
12: 119,409,711 (GRCm39) |
S160P |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,276,193 (GRCm39) |
T6155A |
possibly damaging |
Het |
Mboat4 |
C |
T |
8: 34,582,348 (GRCm39) |
T34I |
probably benign |
Het |
Nav3 |
T |
A |
10: 109,541,524 (GRCm39) |
Q1913L |
probably benign |
Het |
Notch4 |
T |
C |
17: 34,800,080 (GRCm39) |
S1014P |
probably benign |
Het |
Or1o4 |
T |
C |
17: 37,590,745 (GRCm39) |
T189A |
probably benign |
Het |
Or2h1b |
T |
C |
17: 37,462,123 (GRCm39) |
T247A |
possibly damaging |
Het |
Or52z1 |
T |
G |
7: 103,437,002 (GRCm39) |
I161L |
probably benign |
Het |
Orc2 |
A |
C |
1: 58,515,628 (GRCm39) |
H293Q |
probably benign |
Het |
Otoa |
A |
G |
7: 120,693,845 (GRCm39) |
Y75C |
probably damaging |
Het |
Pate2 |
T |
A |
9: 35,581,908 (GRCm39) |
|
probably null |
Het |
Phldb3 |
G |
A |
7: 24,326,726 (GRCm39) |
V585I |
probably damaging |
Het |
Plk3 |
ACACTCAC |
ACAC |
4: 116,989,090 (GRCm39) |
|
probably benign |
Het |
Pou2f1 |
A |
T |
1: 165,722,603 (GRCm39) |
N443K |
unknown |
Het |
Prkci |
T |
A |
3: 31,072,793 (GRCm39) |
F66I |
probably damaging |
Het |
Ptprz1 |
C |
T |
6: 23,002,334 (GRCm39) |
Q1475* |
probably null |
Het |
Qars1 |
C |
T |
9: 108,386,399 (GRCm39) |
R143C |
probably damaging |
Het |
Reln |
T |
C |
5: 22,160,194 (GRCm39) |
D2125G |
probably damaging |
Het |
Rp1 |
A |
T |
1: 4,417,136 (GRCm39) |
D1325E |
probably damaging |
Het |
Rpl36a-ps1 |
A |
T |
14: 99,231,694 (GRCm39) |
C15S |
probably damaging |
Het |
Rsf1 |
CG |
CGACGGCGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Scn9a |
A |
G |
2: 66,314,744 (GRCm39) |
I1658T |
probably damaging |
Het |
Serinc1 |
C |
T |
10: 57,395,577 (GRCm39) |
G370S |
probably benign |
Het |
Spef1 |
G |
T |
2: 131,013,829 (GRCm39) |
T197K |
probably damaging |
Het |
Spmap2l |
A |
G |
5: 77,164,453 (GRCm39) |
Y152C |
probably damaging |
Het |
Sptan1 |
G |
A |
2: 29,920,597 (GRCm39) |
V2363I |
probably damaging |
Het |
Ssh2 |
T |
A |
11: 77,346,102 (GRCm39) |
C1362* |
probably null |
Het |
Star |
T |
C |
8: 26,302,832 (GRCm39) |
V258A |
probably benign |
Het |
Sympk |
T |
C |
7: 18,778,873 (GRCm39) |
I588T |
possibly damaging |
Het |
Tas2r136 |
T |
C |
6: 132,754,584 (GRCm39) |
N181S |
probably damaging |
Het |
Tbc1d4 |
A |
T |
14: 101,724,952 (GRCm39) |
V555E |
probably benign |
Het |
Topaz1 |
G |
A |
9: 122,625,228 (GRCm39) |
V1438I |
probably benign |
Het |
Trmt112 |
T |
A |
19: 6,887,786 (GRCm39) |
M45K |
|
Het |
Tshr |
G |
A |
12: 91,503,992 (GRCm39) |
R310H |
probably damaging |
Het |
Ulk4 |
G |
T |
9: 121,090,988 (GRCm39) |
P238Q |
probably damaging |
Het |
Unc5a |
T |
C |
13: 55,145,774 (GRCm39) |
L312P |
possibly damaging |
Het |
Urb1 |
T |
C |
16: 90,566,290 (GRCm39) |
D1499G |
possibly damaging |
Het |
Ushbp1 |
A |
G |
8: 71,843,653 (GRCm39) |
S262P |
probably damaging |
Het |
Vmn1r173 |
G |
A |
7: 23,402,008 (GRCm39) |
R81K |
probably benign |
Het |
Vmn2r5 |
G |
A |
3: 64,399,159 (GRCm39) |
P607S |
probably benign |
Het |
Vtn |
G |
T |
11: 78,391,256 (GRCm39) |
G223V |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,394,589 (GRCm39) |
V1061A |
probably damaging |
Het |
Zfp169 |
T |
C |
13: 48,644,557 (GRCm39) |
E190G |
unknown |
Het |
Zfp616 |
T |
A |
11: 73,976,280 (GRCm39) |
C850S |
probably damaging |
Het |
|
Other mutations in Fermt3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01160:Fermt3
|
APN |
19 |
6,980,626 (GRCm39) |
splice site |
probably null |
|
IGL01724:Fermt3
|
APN |
19 |
6,979,143 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01748:Fermt3
|
APN |
19 |
6,980,834 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02392:Fermt3
|
APN |
19 |
6,996,183 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02956:Fermt3
|
APN |
19 |
6,979,712 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03146:Fermt3
|
APN |
19 |
6,980,631 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03216:Fermt3
|
APN |
19 |
6,976,748 (GRCm39) |
missense |
probably benign |
0.00 |
Cholera
|
UTSW |
19 |
6,979,792 (GRCm39) |
missense |
possibly damaging |
0.74 |
Colombia
|
UTSW |
19 |
6,991,245 (GRCm39) |
missense |
possibly damaging |
0.63 |
P0026:Fermt3
|
UTSW |
19 |
6,991,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R0180:Fermt3
|
UTSW |
19 |
6,979,711 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0445:Fermt3
|
UTSW |
19 |
6,980,667 (GRCm39) |
missense |
probably benign |
0.29 |
R1202:Fermt3
|
UTSW |
19 |
6,980,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R1475:Fermt3
|
UTSW |
19 |
6,996,242 (GRCm39) |
splice site |
probably null |
|
R1668:Fermt3
|
UTSW |
19 |
6,996,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R2179:Fermt3
|
UTSW |
19 |
6,991,782 (GRCm39) |
missense |
probably benign |
0.14 |
R2311:Fermt3
|
UTSW |
19 |
6,991,530 (GRCm39) |
missense |
probably damaging |
0.97 |
R3976:Fermt3
|
UTSW |
19 |
6,979,792 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4087:Fermt3
|
UTSW |
19 |
6,980,945 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4667:Fermt3
|
UTSW |
19 |
6,980,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R6108:Fermt3
|
UTSW |
19 |
6,991,782 (GRCm39) |
missense |
probably benign |
0.14 |
R6452:Fermt3
|
UTSW |
19 |
6,992,105 (GRCm39) |
missense |
probably benign |
0.00 |
R6994:Fermt3
|
UTSW |
19 |
6,977,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7334:Fermt3
|
UTSW |
19 |
6,980,406 (GRCm39) |
missense |
probably benign |
0.03 |
R7357:Fermt3
|
UTSW |
19 |
6,980,211 (GRCm39) |
missense |
probably benign |
|
R8804:Fermt3
|
UTSW |
19 |
6,991,694 (GRCm39) |
critical splice donor site |
probably benign |
|
R8854:Fermt3
|
UTSW |
19 |
6,991,310 (GRCm39) |
missense |
probably damaging |
0.98 |
R8883:Fermt3
|
UTSW |
19 |
6,980,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R9160:Fermt3
|
UTSW |
19 |
6,991,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R9277:Fermt3
|
UTSW |
19 |
6,991,245 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9296:Fermt3
|
UTSW |
19 |
6,980,865 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9347:Fermt3
|
UTSW |
19 |
6,980,664 (GRCm39) |
missense |
probably damaging |
0.98 |
R9595:Fermt3
|
UTSW |
19 |
6,979,619 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fermt3
|
UTSW |
19 |
6,992,047 (GRCm39) |
missense |
probably benign |
0.29 |
|