Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
G |
17: 46,633,216 (GRCm39) |
F498L |
probably damaging |
Het |
Adamts6 |
A |
T |
13: 104,433,763 (GRCm39) |
D64V |
possibly damaging |
Het |
Agbl2 |
T |
C |
2: 90,620,187 (GRCm39) |
|
probably benign |
Het |
Angptl3 |
A |
G |
4: 98,919,692 (GRCm39) |
S151G |
probably benign |
Het |
Arhgap39 |
C |
T |
15: 76,619,086 (GRCm39) |
D833N |
probably damaging |
Het |
C4b |
G |
T |
17: 34,954,389 (GRCm39) |
L927I |
probably damaging |
Het |
Ccl3 |
T |
C |
11: 83,539,162 (GRCm39) |
T66A |
probably damaging |
Het |
Cdh20 |
T |
C |
1: 110,036,674 (GRCm39) |
L618P |
probably damaging |
Het |
Cfap65 |
T |
C |
1: 74,957,603 (GRCm39) |
T989A |
probably benign |
Het |
Cfhr4 |
A |
T |
1: 139,667,226 (GRCm39) |
D377E |
probably damaging |
Het |
Cnpy4 |
T |
C |
5: 138,185,899 (GRCm39) |
F18S |
possibly damaging |
Het |
Col6a5 |
A |
G |
9: 105,781,778 (GRCm39) |
|
probably benign |
Het |
Dppa2 |
G |
A |
16: 48,139,034 (GRCm39) |
R289H |
probably benign |
Het |
Evx2 |
T |
C |
2: 74,489,478 (GRCm39) |
T96A |
probably benign |
Het |
Gcgr |
G |
A |
11: 120,427,387 (GRCm39) |
G166S |
probably benign |
Het |
Gm5316 |
T |
C |
6: 122,877,150 (GRCm39) |
|
noncoding transcript |
Het |
Gria1 |
G |
A |
11: 57,119,799 (GRCm39) |
R292Q |
probably damaging |
Het |
Hars2 |
T |
A |
18: 36,919,261 (GRCm39) |
|
probably null |
Het |
Hkdc1 |
T |
A |
10: 62,236,019 (GRCm39) |
T508S |
probably benign |
Het |
Kif2b |
A |
T |
11: 91,467,410 (GRCm39) |
I291N |
probably damaging |
Het |
Lmbrd1 |
A |
T |
1: 24,784,001 (GRCm39) |
T377S |
probably benign |
Het |
Lrrc28 |
A |
G |
7: 67,278,090 (GRCm39) |
|
probably benign |
Het |
Mmp3 |
A |
T |
9: 7,455,638 (GRCm39) |
N463I |
probably benign |
Het |
Myh6 |
A |
G |
14: 55,196,065 (GRCm39) |
F578S |
probably damaging |
Het |
Ncbp1 |
T |
A |
4: 46,168,476 (GRCm39) |
M608K |
possibly damaging |
Het |
Nf1 |
T |
C |
11: 79,359,597 (GRCm39) |
F1412L |
probably damaging |
Het |
Nlrp5 |
T |
A |
7: 23,141,227 (GRCm39) |
W1083R |
probably damaging |
Het |
Nrsn1 |
T |
C |
13: 25,446,241 (GRCm39) |
Y45C |
probably benign |
Het |
Or3a1b |
T |
G |
11: 74,012,301 (GRCm39) |
M62R |
probably damaging |
Het |
Osbpl7 |
G |
T |
11: 96,958,368 (GRCm39) |
R881L |
probably damaging |
Het |
Papss1 |
A |
G |
3: 131,324,974 (GRCm39) |
E456G |
possibly damaging |
Het |
Pbxip1 |
T |
A |
3: 89,350,899 (GRCm39) |
|
probably benign |
Het |
Pcca |
A |
G |
14: 122,875,789 (GRCm39) |
|
probably benign |
Het |
Pde1a |
T |
A |
2: 79,695,414 (GRCm39) |
N511I |
probably damaging |
Het |
Prpf39 |
A |
T |
12: 65,103,030 (GRCm39) |
I435F |
probably benign |
Het |
Rnf213 |
C |
T |
11: 119,355,908 (GRCm39) |
T4117M |
probably damaging |
Het |
Sel1l2 |
A |
T |
2: 140,107,802 (GRCm39) |
M216K |
probably damaging |
Het |
Sidt2 |
A |
G |
9: 45,864,417 (GRCm39) |
|
probably null |
Het |
Sirt3 |
A |
T |
7: 140,449,400 (GRCm39) |
|
probably null |
Het |
Smpd4 |
T |
C |
16: 17,457,176 (GRCm39) |
V378A |
probably benign |
Het |
Svil |
T |
A |
18: 5,064,566 (GRCm39) |
S642T |
possibly damaging |
Het |
Tcp10a |
A |
G |
17: 7,593,950 (GRCm39) |
K92E |
probably benign |
Het |
Tmem144 |
T |
C |
3: 79,730,051 (GRCm39) |
D233G |
probably damaging |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Tnik |
T |
C |
3: 28,625,069 (GRCm39) |
S335P |
possibly damaging |
Het |
Ush2a |
T |
C |
1: 188,679,150 (GRCm39) |
L4786P |
probably damaging |
Het |
Utp11 |
A |
T |
4: 124,579,872 (GRCm39) |
|
probably benign |
Het |
Vmn1r67 |
A |
G |
7: 10,181,641 (GRCm39) |
N241D |
probably damaging |
Het |
Vmn2r11 |
A |
T |
5: 109,199,963 (GRCm39) |
C497S |
possibly damaging |
Het |
|
Other mutations in Frmd4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Frmd4a
|
APN |
2 |
4,599,525 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00508:Frmd4a
|
APN |
2 |
4,599,545 (GRCm39) |
nonsense |
probably null |
|
IGL01331:Frmd4a
|
APN |
2 |
4,607,036 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01774:Frmd4a
|
APN |
2 |
4,540,047 (GRCm39) |
splice site |
probably benign |
|
IGL01909:Frmd4a
|
APN |
2 |
4,608,844 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02170:Frmd4a
|
APN |
2 |
4,570,988 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02269:Frmd4a
|
APN |
2 |
4,609,045 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02377:Frmd4a
|
APN |
2 |
4,539,385 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03308:Frmd4a
|
APN |
2 |
4,502,837 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0066:Frmd4a
|
UTSW |
2 |
4,477,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Frmd4a
|
UTSW |
2 |
4,477,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Frmd4a
|
UTSW |
2 |
4,577,252 (GRCm39) |
critical splice donor site |
probably null |
|
R0128:Frmd4a
|
UTSW |
2 |
4,608,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R0130:Frmd4a
|
UTSW |
2 |
4,608,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R0376:Frmd4a
|
UTSW |
2 |
4,577,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R0529:Frmd4a
|
UTSW |
2 |
4,610,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R1593:Frmd4a
|
UTSW |
2 |
4,477,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Frmd4a
|
UTSW |
2 |
4,539,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Frmd4a
|
UTSW |
2 |
4,577,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R2100:Frmd4a
|
UTSW |
2 |
4,610,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R2310:Frmd4a
|
UTSW |
2 |
4,577,210 (GRCm39) |
frame shift |
probably null |
|
R2340:Frmd4a
|
UTSW |
2 |
4,591,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R2426:Frmd4a
|
UTSW |
2 |
4,534,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Frmd4a
|
UTSW |
2 |
4,539,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R3409:Frmd4a
|
UTSW |
2 |
4,157,839 (GRCm39) |
intron |
probably benign |
|
R3772:Frmd4a
|
UTSW |
2 |
4,595,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R3773:Frmd4a
|
UTSW |
2 |
4,595,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R3932:Frmd4a
|
UTSW |
2 |
4,542,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R4094:Frmd4a
|
UTSW |
2 |
4,615,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4226:Frmd4a
|
UTSW |
2 |
4,337,889 (GRCm39) |
missense |
probably benign |
0.00 |
R4299:Frmd4a
|
UTSW |
2 |
4,337,882 (GRCm39) |
missense |
probably benign |
0.02 |
R4304:Frmd4a
|
UTSW |
2 |
4,337,889 (GRCm39) |
missense |
probably benign |
0.00 |
R4306:Frmd4a
|
UTSW |
2 |
4,337,889 (GRCm39) |
missense |
probably benign |
0.00 |
R4307:Frmd4a
|
UTSW |
2 |
4,337,889 (GRCm39) |
missense |
probably benign |
0.00 |
R4346:Frmd4a
|
UTSW |
2 |
4,612,844 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4360:Frmd4a
|
UTSW |
2 |
4,606,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4384:Frmd4a
|
UTSW |
2 |
4,599,374 (GRCm39) |
nonsense |
probably null |
|
R4547:Frmd4a
|
UTSW |
2 |
4,477,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Frmd4a
|
UTSW |
2 |
4,608,490 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4577:Frmd4a
|
UTSW |
2 |
4,608,490 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4578:Frmd4a
|
UTSW |
2 |
4,608,490 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4688:Frmd4a
|
UTSW |
2 |
4,542,122 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4764:Frmd4a
|
UTSW |
2 |
4,608,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R4826:Frmd4a
|
UTSW |
2 |
4,606,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Frmd4a
|
UTSW |
2 |
4,534,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R5053:Frmd4a
|
UTSW |
2 |
4,608,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5392:Frmd4a
|
UTSW |
2 |
4,599,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R5733:Frmd4a
|
UTSW |
2 |
4,305,768 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5762:Frmd4a
|
UTSW |
2 |
4,488,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Frmd4a
|
UTSW |
2 |
4,337,927 (GRCm39) |
missense |
probably benign |
0.02 |
R5932:Frmd4a
|
UTSW |
2 |
4,534,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R6117:Frmd4a
|
UTSW |
2 |
4,607,060 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6328:Frmd4a
|
UTSW |
2 |
4,595,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R6622:Frmd4a
|
UTSW |
2 |
4,610,873 (GRCm39) |
missense |
probably benign |
0.00 |
R6903:Frmd4a
|
UTSW |
2 |
4,591,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Frmd4a
|
UTSW |
2 |
4,570,923 (GRCm39) |
|
|
|
R7098:Frmd4a
|
UTSW |
2 |
4,577,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R7258:Frmd4a
|
UTSW |
2 |
4,305,764 (GRCm39) |
missense |
probably benign |
|
R7336:Frmd4a
|
UTSW |
2 |
4,478,025 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7582:Frmd4a
|
UTSW |
2 |
4,599,408 (GRCm39) |
frame shift |
probably null |
|
R7607:Frmd4a
|
UTSW |
2 |
4,596,747 (GRCm39) |
nonsense |
probably null |
|
R7697:Frmd4a
|
UTSW |
2 |
4,488,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7750:Frmd4a
|
UTSW |
2 |
4,606,160 (GRCm39) |
missense |
probably benign |
0.14 |
R7795:Frmd4a
|
UTSW |
2 |
4,595,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:Frmd4a
|
UTSW |
2 |
4,596,728 (GRCm39) |
intron |
probably benign |
|
R7899:Frmd4a
|
UTSW |
2 |
4,608,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Frmd4a
|
UTSW |
2 |
4,608,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R8399:Frmd4a
|
UTSW |
2 |
4,577,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R8778:Frmd4a
|
UTSW |
2 |
4,478,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R8876:Frmd4a
|
UTSW |
2 |
4,606,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R9074:Frmd4a
|
UTSW |
2 |
4,608,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R9075:Frmd4a
|
UTSW |
2 |
4,608,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R9076:Frmd4a
|
UTSW |
2 |
4,608,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R9105:Frmd4a
|
UTSW |
2 |
4,539,994 (GRCm39) |
missense |
probably damaging |
0.96 |
R9213:Frmd4a
|
UTSW |
2 |
4,608,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Frmd4a
|
UTSW |
2 |
4,612,844 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9230:Frmd4a
|
UTSW |
2 |
4,612,844 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9235:Frmd4a
|
UTSW |
2 |
4,599,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R9266:Frmd4a
|
UTSW |
2 |
4,610,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R9301:Frmd4a
|
UTSW |
2 |
4,157,904 (GRCm39) |
missense |
probably benign |
0.27 |
R9307:Frmd4a
|
UTSW |
2 |
4,609,044 (GRCm39) |
missense |
probably benign |
|
R9365:Frmd4a
|
UTSW |
2 |
4,606,973 (GRCm39) |
missense |
probably benign |
0.01 |
R9476:Frmd4a
|
UTSW |
2 |
4,608,324 (GRCm39) |
missense |
probably benign |
0.32 |
R9484:Frmd4a
|
UTSW |
2 |
4,609,026 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9510:Frmd4a
|
UTSW |
2 |
4,608,324 (GRCm39) |
missense |
probably benign |
0.32 |
R9513:Frmd4a
|
UTSW |
2 |
4,608,711 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Frmd4a
|
UTSW |
2 |
4,502,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|