Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd3 |
A |
T |
3: 121,566,009 (GRCm39) |
D443E |
probably benign |
Het |
Arhgef5 |
A |
G |
6: 43,252,874 (GRCm39) |
D1037G |
probably benign |
Het |
B3glct |
T |
A |
5: 149,653,399 (GRCm39) |
L148* |
probably null |
Het |
Cacna1e |
G |
A |
1: 154,317,940 (GRCm39) |
P1481S |
probably damaging |
Het |
Cacna1h |
C |
A |
17: 25,596,641 (GRCm39) |
R117L |
probably damaging |
Het |
Cct6b |
A |
T |
11: 82,632,175 (GRCm39) |
V271E |
probably damaging |
Het |
Cenpf |
A |
G |
1: 189,389,483 (GRCm39) |
S1450P |
probably damaging |
Het |
Cul1 |
G |
A |
6: 47,500,722 (GRCm39) |
R707H |
probably damaging |
Het |
Dcakd |
A |
G |
11: 102,885,831 (GRCm39) |
L191P |
possibly damaging |
Het |
Dhx32 |
T |
C |
7: 133,322,957 (GRCm39) |
*612W |
probably null |
Het |
Disp1 |
T |
A |
1: 182,869,913 (GRCm39) |
T836S |
probably benign |
Het |
Dppa4 |
T |
A |
16: 48,111,393 (GRCm39) |
V126D |
probably damaging |
Het |
Fkbp4 |
A |
T |
6: 128,410,517 (GRCm39) |
V273E |
probably damaging |
Het |
Gpr31b |
A |
G |
17: 13,270,831 (GRCm39) |
Y113H |
probably damaging |
Het |
Gpr33 |
T |
C |
12: 52,070,377 (GRCm39) |
I221V |
probably damaging |
Het |
Klhl1 |
A |
G |
14: 96,755,729 (GRCm39) |
F9L |
probably benign |
Het |
Larp4b |
T |
A |
13: 9,208,695 (GRCm39) |
N449K |
probably damaging |
Het |
Loxhd1 |
T |
C |
18: 77,492,647 (GRCm39) |
S1363P |
probably damaging |
Het |
Lrrc8a |
T |
C |
2: 30,145,366 (GRCm39) |
V60A |
probably benign |
Het |
Matn3 |
A |
G |
12: 8,998,195 (GRCm39) |
H51R |
probably benign |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Mtrf1 |
T |
C |
14: 79,638,885 (GRCm39) |
C6R |
possibly damaging |
Het |
Myh6 |
T |
C |
14: 55,194,038 (GRCm39) |
S784G |
probably benign |
Het |
Nfkb2 |
G |
T |
19: 46,296,006 (GRCm39) |
E170D |
probably benign |
Het |
Nipal3 |
T |
C |
4: 135,179,715 (GRCm39) |
Y401C |
probably benign |
Het |
Pcdhb20 |
A |
G |
18: 37,637,585 (GRCm39) |
E37G |
probably damaging |
Het |
Pelp1 |
G |
A |
11: 70,285,688 (GRCm39) |
P727S |
possibly damaging |
Het |
Prkca |
T |
C |
11: 107,869,169 (GRCm39) |
D472G |
possibly damaging |
Het |
Ptprg |
A |
G |
14: 12,122,120 (GRCm38) |
H328R |
probably benign |
Het |
Rtl1 |
C |
T |
12: 109,559,173 (GRCm39) |
E889K |
unknown |
Het |
Rubcn |
T |
C |
16: 32,647,293 (GRCm39) |
D715G |
possibly damaging |
Het |
Snurf |
C |
T |
7: 59,649,133 (GRCm39) |
E15K |
possibly damaging |
Het |
Sptbn5 |
G |
A |
2: 119,876,965 (GRCm39) |
|
probably benign |
Het |
Srp72 |
T |
G |
5: 77,135,781 (GRCm39) |
L237R |
probably damaging |
Het |
Syne3 |
T |
C |
12: 104,921,937 (GRCm39) |
E406G |
probably damaging |
Het |
Tgm2 |
A |
G |
2: 157,970,640 (GRCm39) |
S340P |
probably damaging |
Het |
Trim41 |
GCCTAGGCGCCCA |
G |
11: 48,698,192 (GRCm39) |
|
probably benign |
Het |
Tsc22d1 |
T |
C |
14: 76,653,657 (GRCm39) |
|
probably benign |
Het |
Tsc22d2 |
G |
T |
3: 58,324,583 (GRCm39) |
|
probably benign |
Het |
Vmn1r42 |
T |
C |
6: 89,822,084 (GRCm39) |
I162V |
possibly damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,708,191 (GRCm39) |
|
probably null |
Het |
Wnt3 |
T |
C |
11: 103,703,596 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Fam98b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02642:Fam98b
|
APN |
2 |
117,090,793 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03175:Fam98b
|
APN |
2 |
117,089,719 (GRCm39) |
missense |
probably benign |
0.24 |
R0384:Fam98b
|
UTSW |
2 |
117,098,328 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1035:Fam98b
|
UTSW |
2 |
117,101,120 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2207:Fam98b
|
UTSW |
2 |
117,098,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R3121:Fam98b
|
UTSW |
2 |
117,098,408 (GRCm39) |
missense |
probably damaging |
0.98 |
R4273:Fam98b
|
UTSW |
2 |
117,090,712 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5276:Fam98b
|
UTSW |
2 |
117,089,779 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5325:Fam98b
|
UTSW |
2 |
117,101,132 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5460:Fam98b
|
UTSW |
2 |
117,089,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R5627:Fam98b
|
UTSW |
2 |
117,098,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R6787:Fam98b
|
UTSW |
2 |
117,093,402 (GRCm39) |
critical splice donor site |
probably null |
|
R7252:Fam98b
|
UTSW |
2 |
117,094,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7502:Fam98b
|
UTSW |
2 |
117,094,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R8182:Fam98b
|
UTSW |
2 |
117,080,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R8272:Fam98b
|
UTSW |
2 |
117,093,335 (GRCm39) |
missense |
probably benign |
0.00 |
R8439:Fam98b
|
UTSW |
2 |
117,101,381 (GRCm39) |
missense |
unknown |
|
R9454:Fam98b
|
UTSW |
2 |
117,080,250 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
|