Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
A |
G |
11: 110,110,430 (GRCm39) |
V573A |
possibly damaging |
Het |
Abcc9 |
A |
G |
6: 142,571,836 (GRCm39) |
|
probably benign |
Het |
Actg1 |
A |
G |
11: 120,237,839 (GRCm39) |
S234P |
probably benign |
Het |
Acvr2a |
A |
G |
2: 48,780,311 (GRCm39) |
D177G |
probably damaging |
Het |
Adamts12 |
T |
C |
15: 11,300,054 (GRCm39) |
C914R |
probably damaging |
Het |
Adprhl1 |
A |
G |
8: 13,298,621 (GRCm39) |
I103T |
possibly damaging |
Het |
Als2cl |
C |
T |
9: 110,713,205 (GRCm39) |
L32F |
probably damaging |
Het |
Ank2 |
T |
C |
3: 126,739,570 (GRCm39) |
|
probably benign |
Het |
Ankrd52 |
T |
A |
10: 128,225,710 (GRCm39) |
S959R |
possibly damaging |
Het |
Bnc2 |
C |
A |
4: 84,449,872 (GRCm39) |
A122S |
probably benign |
Het |
Cert1 |
A |
T |
13: 96,739,663 (GRCm39) |
K226N |
probably benign |
Het |
Cfap54 |
C |
T |
10: 92,875,013 (GRCm39) |
V443M |
probably damaging |
Het |
Cilk1 |
C |
T |
9: 78,060,978 (GRCm39) |
T208I |
probably benign |
Het |
Clca4b |
T |
A |
3: 144,617,267 (GRCm39) |
R794S |
probably damaging |
Het |
Cyp2c65 |
T |
C |
19: 39,049,514 (GRCm39) |
L14P |
unknown |
Het |
Ggt5 |
T |
C |
10: 75,440,608 (GRCm39) |
M243T |
probably benign |
Het |
Gmds |
A |
G |
13: 32,124,482 (GRCm39) |
I292T |
probably benign |
Het |
Gpcpd1 |
A |
T |
2: 132,386,355 (GRCm39) |
V341E |
probably damaging |
Het |
Grm3 |
A |
G |
5: 9,620,167 (GRCm39) |
F359S |
probably damaging |
Het |
Hcn1 |
A |
T |
13: 118,010,441 (GRCm39) |
K340* |
probably null |
Het |
Heatr9 |
T |
C |
11: 83,403,258 (GRCm39) |
E427G |
probably benign |
Het |
Kif26b |
G |
A |
1: 178,358,195 (GRCm39) |
G102D |
unknown |
Het |
Mark3 |
T |
C |
12: 111,584,760 (GRCm39) |
F119L |
probably damaging |
Het |
Melk |
T |
C |
4: 44,350,959 (GRCm39) |
V500A |
probably benign |
Het |
Mrpl41 |
A |
G |
2: 24,864,295 (GRCm39) |
F126L |
probably damaging |
Het |
Or10c1 |
C |
A |
17: 37,522,307 (GRCm39) |
A146S |
probably benign |
Het |
Or6c3b |
C |
T |
10: 129,527,699 (GRCm39) |
M70I |
probably benign |
Het |
Pax7 |
A |
T |
4: 139,506,928 (GRCm39) |
S372T |
probably benign |
Het |
Pax7 |
A |
T |
4: 139,556,906 (GRCm39) |
I118N |
probably damaging |
Het |
Plcl1 |
G |
T |
1: 55,735,671 (GRCm39) |
M337I |
possibly damaging |
Het |
Poc1a |
G |
T |
9: 106,227,012 (GRCm39) |
|
probably benign |
Het |
Rabgef1 |
A |
G |
5: 130,240,844 (GRCm39) |
Y321C |
probably damaging |
Het |
Rhobtb3 |
A |
C |
13: 76,061,389 (GRCm39) |
L252R |
probably benign |
Het |
Rlf |
A |
G |
4: 121,004,063 (GRCm39) |
V1639A |
probably benign |
Het |
Tff1 |
A |
G |
17: 31,381,682 (GRCm39) |
V65A |
probably damaging |
Het |
Trpm4 |
G |
T |
7: 44,971,258 (GRCm39) |
D222E |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,643,741 (GRCm39) |
D13162E |
probably damaging |
Het |
Unc5d |
A |
T |
8: 29,209,723 (GRCm39) |
S466T |
probably benign |
Het |
Vmn1r73 |
A |
G |
7: 11,490,683 (GRCm39) |
Y167C |
probably damaging |
Het |
Vwde |
C |
T |
6: 13,208,323 (GRCm39) |
|
probably null |
Het |
Xpr1 |
T |
C |
1: 155,204,430 (GRCm39) |
|
probably null |
Het |
Zbtb40 |
A |
G |
4: 136,728,604 (GRCm39) |
V413A |
possibly damaging |
Het |
|
Other mutations in A530064D06Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01377:A530064D06Rik
|
APN |
17 |
48,460,108 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01761:A530064D06Rik
|
APN |
17 |
48,460,127 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02001:A530064D06Rik
|
APN |
17 |
48,473,842 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02995:A530064D06Rik
|
APN |
17 |
48,470,456 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03109:A530064D06Rik
|
APN |
17 |
48,473,628 (GRCm39) |
missense |
probably benign |
0.13 |
FR4340:A530064D06Rik
|
UTSW |
17 |
48,470,549 (GRCm39) |
small deletion |
probably benign |
|
FR4589:A530064D06Rik
|
UTSW |
17 |
48,470,549 (GRCm39) |
small deletion |
probably benign |
|
IGL02984:A530064D06Rik
|
UTSW |
17 |
48,470,448 (GRCm39) |
missense |
probably benign |
0.06 |
R0206:A530064D06Rik
|
UTSW |
17 |
48,470,486 (GRCm39) |
missense |
probably benign |
0.00 |
R0206:A530064D06Rik
|
UTSW |
17 |
48,470,486 (GRCm39) |
missense |
probably benign |
0.00 |
R0660:A530064D06Rik
|
UTSW |
17 |
48,473,759 (GRCm39) |
missense |
probably benign |
0.18 |
R0664:A530064D06Rik
|
UTSW |
17 |
48,473,759 (GRCm39) |
missense |
probably benign |
0.18 |
R0671:A530064D06Rik
|
UTSW |
17 |
48,473,824 (GRCm39) |
missense |
probably benign |
0.05 |
R1587:A530064D06Rik
|
UTSW |
17 |
48,473,585 (GRCm39) |
missense |
probably benign |
0.20 |
R4087:A530064D06Rik
|
UTSW |
17 |
48,473,678 (GRCm39) |
missense |
probably damaging |
0.96 |
R4089:A530064D06Rik
|
UTSW |
17 |
48,473,678 (GRCm39) |
missense |
probably damaging |
0.96 |
R4963:A530064D06Rik
|
UTSW |
17 |
48,470,582 (GRCm39) |
missense |
probably benign |
0.34 |
R5083:A530064D06Rik
|
UTSW |
17 |
48,473,558 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5219:A530064D06Rik
|
UTSW |
17 |
48,470,518 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6175:A530064D06Rik
|
UTSW |
17 |
48,460,016 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6189:A530064D06Rik
|
UTSW |
17 |
48,474,222 (GRCm39) |
start gained |
probably benign |
|
R6420:A530064D06Rik
|
UTSW |
17 |
48,473,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R6439:A530064D06Rik
|
UTSW |
17 |
48,473,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:A530064D06Rik
|
UTSW |
17 |
48,460,057 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:A530064D06Rik
|
UTSW |
17 |
48,473,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|