Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadm |
T |
C |
3: 153,644,720 (GRCm39) |
D68G |
probably damaging |
Het |
Amer3 |
A |
G |
1: 34,625,761 (GRCm39) |
|
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,617,390 (GRCm39) |
L2133P |
probably damaging |
Het |
Bcdin3d |
G |
T |
15: 99,368,673 (GRCm39) |
H175Q |
probably damaging |
Het |
Brd8 |
C |
A |
18: 34,741,117 (GRCm39) |
|
probably benign |
Het |
C1rl |
C |
A |
6: 124,470,806 (GRCm39) |
T38N |
possibly damaging |
Het |
Cd160 |
T |
C |
3: 96,707,927 (GRCm39) |
T140A |
probably benign |
Het |
Cdk16 |
T |
G |
X: 20,563,167 (GRCm39) |
D381E |
probably benign |
Het |
Cpq |
G |
A |
15: 33,381,546 (GRCm39) |
G303D |
probably damaging |
Het |
Dmp1 |
T |
C |
5: 104,359,536 (GRCm39) |
S71P |
probably damaging |
Het |
Enc1 |
A |
C |
13: 97,382,042 (GRCm39) |
D184A |
possibly damaging |
Het |
Enkur |
T |
C |
2: 21,199,198 (GRCm39) |
D112G |
probably benign |
Het |
Esrra |
A |
T |
19: 6,890,218 (GRCm39) |
V59E |
possibly damaging |
Het |
F830016B08Rik |
A |
G |
18: 60,433,058 (GRCm39) |
N47S |
probably benign |
Het |
Fads1 |
T |
A |
19: 10,163,785 (GRCm39) |
V189D |
probably damaging |
Het |
Fam167a |
T |
A |
14: 63,689,721 (GRCm39) |
I6N |
probably damaging |
Het |
Fhip2a |
A |
G |
19: 57,373,782 (GRCm39) |
N681D |
possibly damaging |
Het |
Fryl |
T |
A |
5: 73,252,809 (GRCm39) |
I953L |
probably benign |
Het |
Gm10610 |
T |
A |
7: 83,198,813 (GRCm39) |
|
noncoding transcript |
Het |
Grik5 |
G |
T |
7: 24,758,408 (GRCm39) |
N338K |
possibly damaging |
Het |
Gstt2 |
A |
G |
10: 75,668,652 (GRCm39) |
I72T |
probably benign |
Het |
Gusb |
T |
C |
5: 130,029,376 (GRCm39) |
|
probably null |
Het |
Hccs |
A |
G |
X: 168,098,588 (GRCm39) |
|
probably benign |
Het |
Hoxb4 |
A |
G |
11: 96,211,050 (GRCm39) |
K217E |
probably damaging |
Het |
Hpd |
C |
T |
5: 123,319,503 (GRCm39) |
V22I |
possibly damaging |
Het |
Ighv1-47 |
A |
G |
12: 114,954,844 (GRCm39) |
Y79H |
probably damaging |
Het |
Il7r |
C |
A |
15: 9,513,133 (GRCm39) |
|
probably benign |
Het |
Lama1 |
A |
T |
17: 68,119,361 (GRCm39) |
M2613L |
probably benign |
Het |
Lama2 |
G |
A |
10: 27,343,269 (GRCm39) |
H68Y |
probably damaging |
Het |
Lce1c |
C |
A |
3: 92,587,845 (GRCm39) |
|
probably benign |
Het |
Lmx1a |
G |
T |
1: 167,672,192 (GRCm39) |
|
probably benign |
Het |
Lrfn1 |
T |
C |
7: 28,158,113 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
T |
A |
10: 103,057,322 (GRCm39) |
|
probably null |
Het |
Mri1 |
A |
T |
8: 84,983,702 (GRCm39) |
L63Q |
probably damaging |
Het |
Mrps11 |
G |
T |
7: 78,438,522 (GRCm39) |
|
probably null |
Het |
Mtif2 |
C |
A |
11: 29,494,395 (GRCm39) |
Q666K |
probably benign |
Het |
Mtr |
A |
T |
13: 12,210,118 (GRCm39) |
|
probably benign |
Het |
Mug1 |
A |
G |
6: 121,859,544 (GRCm39) |
N1181S |
probably benign |
Het |
Myom1 |
A |
T |
17: 71,408,093 (GRCm39) |
E1209V |
possibly damaging |
Het |
Nhsl1 |
A |
G |
10: 18,284,138 (GRCm39) |
I26M |
possibly damaging |
Het |
Nlrp1a |
T |
A |
11: 71,014,358 (GRCm39) |
K297N |
probably benign |
Het |
Obox5 |
T |
C |
7: 15,491,972 (GRCm39) |
V129A |
probably benign |
Het |
Pex16 |
C |
T |
2: 92,206,981 (GRCm39) |
A53V |
probably damaging |
Het |
Pfpl |
T |
C |
19: 12,407,107 (GRCm39) |
F453L |
probably damaging |
Het |
Pip5k1b |
G |
T |
19: 24,323,731 (GRCm39) |
H406N |
probably benign |
Het |
Pip5k1c |
C |
A |
10: 81,153,155 (GRCm39) |
|
probably null |
Het |
Plcxd3 |
T |
C |
15: 4,546,122 (GRCm39) |
F42S |
possibly damaging |
Het |
Pnpla7 |
T |
C |
2: 24,940,288 (GRCm39) |
F1056L |
probably benign |
Het |
Rapgef1 |
T |
C |
2: 29,590,872 (GRCm39) |
|
probably benign |
Het |
Rdh11 |
G |
A |
12: 79,232,110 (GRCm39) |
|
probably benign |
Het |
Serac1 |
A |
G |
17: 6,096,021 (GRCm39) |
F576S |
possibly damaging |
Het |
Slc45a4 |
A |
T |
15: 73,458,664 (GRCm39) |
M295K |
probably benign |
Het |
Taf1c |
T |
C |
8: 120,325,796 (GRCm39) |
T689A |
probably benign |
Het |
Timm10b |
G |
T |
7: 105,317,645 (GRCm39) |
|
probably benign |
Het |
Tle5 |
A |
T |
10: 81,397,126 (GRCm39) |
Q34L |
possibly damaging |
Het |
Tnc |
A |
T |
4: 63,883,816 (GRCm39) |
|
probably benign |
Het |
Toporsl |
T |
C |
4: 52,611,114 (GRCm39) |
W336R |
probably benign |
Het |
Usp54 |
C |
A |
14: 20,615,140 (GRCm39) |
|
probably benign |
Het |
Vmn1r233 |
T |
C |
17: 21,214,291 (GRCm39) |
R220G |
probably damaging |
Het |
|
Other mutations in Fam98b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
R5616:Fam98b
|
UTSW |
2 |
117,098,267 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
|