Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A230072I06Rik |
A |
T |
8: 12,329,688 (GRCm39) |
I48L |
unknown |
Het |
Abcc3 |
A |
C |
11: 94,241,787 (GRCm39) |
C1415G |
probably damaging |
Het |
Abcg5 |
G |
T |
17: 84,976,423 (GRCm39) |
H471Q |
probably damaging |
Het |
Actl6b |
G |
A |
5: 137,565,305 (GRCm39) |
R363Q |
probably damaging |
Het |
Adcy1 |
T |
A |
11: 7,111,362 (GRCm39) |
D884E |
probably benign |
Het |
Aldh3a1 |
A |
G |
11: 61,107,142 (GRCm39) |
Y282C |
probably damaging |
Het |
Amdhd2 |
A |
G |
17: 24,376,712 (GRCm39) |
|
probably null |
Het |
Arfgef3 |
A |
G |
10: 18,528,491 (GRCm39) |
S299P |
possibly damaging |
Het |
Asic2 |
A |
T |
11: 81,858,726 (GRCm39) |
N95K |
probably damaging |
Het |
Atp2c2 |
A |
G |
8: 120,476,033 (GRCm39) |
|
probably null |
Het |
Atrn |
T |
C |
2: 130,748,521 (GRCm39) |
L14P |
probably benign |
Het |
C8b |
A |
G |
4: 104,647,874 (GRCm39) |
Y355C |
probably damaging |
Het |
Carm1 |
A |
G |
9: 21,491,663 (GRCm39) |
E244G |
probably damaging |
Het |
Cd300c2 |
A |
T |
11: 114,891,844 (GRCm39) |
C39* |
probably null |
Het |
Cish |
T |
A |
9: 107,177,671 (GRCm39) |
F116I |
probably damaging |
Het |
Clstn1 |
G |
A |
4: 149,730,780 (GRCm39) |
R837Q |
probably benign |
Het |
Cox10 |
A |
G |
11: 63,855,306 (GRCm39) |
F325S |
probably damaging |
Het |
Cplane1 |
T |
C |
15: 8,211,620 (GRCm39) |
I320T |
probably benign |
Het |
Ctps1 |
A |
T |
4: 120,424,507 (GRCm39) |
S36T |
possibly damaging |
Het |
Dchs2 |
T |
C |
3: 83,192,670 (GRCm39) |
L1705P |
probably benign |
Het |
Defb25 |
C |
A |
2: 152,464,899 (GRCm39) |
V17L |
probably benign |
Het |
Dhx16 |
A |
G |
17: 36,199,000 (GRCm39) |
D782G |
probably damaging |
Het |
Dhx30 |
A |
G |
9: 109,917,319 (GRCm39) |
S399P |
probably benign |
Het |
Dhx58 |
T |
A |
11: 100,594,806 (GRCm39) |
K30M |
probably damaging |
Het |
Drc7 |
G |
A |
8: 95,788,845 (GRCm39) |
R301Q |
probably damaging |
Het |
Dsg1a |
T |
C |
18: 20,453,365 (GRCm39) |
V21A |
probably damaging |
Het |
Ercc6 |
T |
A |
14: 32,282,784 (GRCm39) |
|
probably null |
Het |
Fam193a |
A |
G |
5: 34,616,374 (GRCm39) |
T850A |
probably benign |
Het |
Fgf10 |
A |
G |
13: 118,925,671 (GRCm39) |
D150G |
probably damaging |
Het |
Flii |
A |
T |
11: 60,616,074 (GRCm39) |
N28K |
probably benign |
Het |
Gfi1 |
G |
A |
5: 107,868,138 (GRCm39) |
R377C |
probably damaging |
Het |
Gfra2 |
A |
T |
14: 71,204,503 (GRCm39) |
N324I |
probably benign |
Het |
Gm10308 |
A |
G |
17: 91,396,431 (GRCm39) |
R118G |
unknown |
Het |
Gm10801 |
T |
A |
2: 98,494,334 (GRCm39) |
V137E |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
Hsd3b9 |
A |
T |
3: 98,354,047 (GRCm39) |
W151R |
probably benign |
Het |
Ift80 |
G |
A |
3: 68,869,583 (GRCm39) |
A236V |
probably damaging |
Het |
Il1rn |
A |
T |
2: 24,239,505 (GRCm39) |
T134S |
possibly damaging |
Het |
Il6st |
G |
T |
13: 112,640,914 (GRCm39) |
D897Y |
probably damaging |
Het |
Imp4 |
T |
C |
1: 34,483,445 (GRCm39) |
M257T |
probably benign |
Het |
Impdh2 |
T |
C |
9: 108,441,957 (GRCm39) |
L377S |
probably damaging |
Het |
Kdm1b |
C |
A |
13: 47,217,617 (GRCm39) |
L359I |
possibly damaging |
Het |
Kidins220 |
A |
T |
12: 25,086,454 (GRCm39) |
I963L |
possibly damaging |
Het |
Mdm4 |
T |
C |
1: 132,931,601 (GRCm39) |
R148G |
probably benign |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Ncor1 |
A |
T |
11: 62,260,234 (GRCm39) |
D505E |
probably benign |
Het |
Necab3 |
A |
T |
2: 154,396,607 (GRCm39) |
L107Q |
probably damaging |
Het |
Nkx2-4 |
G |
A |
2: 146,927,114 (GRCm39) |
P51L |
probably benign |
Het |
Nol11 |
T |
C |
11: 107,067,662 (GRCm39) |
T388A |
probably benign |
Het |
Npc1 |
T |
A |
18: 12,333,877 (GRCm39) |
M735L |
probably benign |
Het |
Nr1h3 |
C |
A |
2: 91,021,091 (GRCm39) |
R232L |
probably benign |
Het |
Nrcam |
T |
A |
12: 44,591,680 (GRCm39) |
|
probably null |
Het |
Or1j13 |
G |
A |
2: 36,369,794 (GRCm39) |
T116I |
possibly damaging |
Het |
Or52s1b |
T |
A |
7: 102,822,203 (GRCm39) |
I214L |
probably benign |
Het |
Pabpn1 |
T |
C |
14: 55,131,914 (GRCm39) |
V101A |
probably damaging |
Het |
Pcare |
A |
T |
17: 72,059,305 (GRCm39) |
V124E |
probably benign |
Het |
Pcbp2 |
A |
G |
15: 102,394,453 (GRCm39) |
D217G |
probably benign |
Het |
Pcdhb12 |
A |
G |
18: 37,570,386 (GRCm39) |
M511V |
probably benign |
Het |
Phf3 |
T |
A |
1: 30,860,347 (GRCm39) |
K828* |
probably null |
Het |
Plcg1 |
G |
C |
2: 160,589,732 (GRCm39) |
K85N |
probably benign |
Het |
Prag1 |
A |
T |
8: 36,613,891 (GRCm39) |
T1148S |
probably benign |
Het |
Prmt3 |
A |
G |
7: 49,478,729 (GRCm39) |
E430G |
probably null |
Het |
Prx |
G |
T |
7: 27,217,538 (GRCm39) |
V819F |
probably damaging |
Het |
Ptpn18 |
A |
T |
1: 34,511,271 (GRCm39) |
R338W |
probably null |
Het |
Rab6a |
T |
C |
7: 100,283,931 (GRCm39) |
Y128H |
probably benign |
Het |
Rgs2 |
T |
C |
1: 143,877,497 (GRCm39) |
Y186C |
probably damaging |
Het |
Rhbdl1 |
C |
T |
17: 26,053,857 (GRCm39) |
V342M |
probably damaging |
Het |
Rpn1 |
A |
G |
6: 88,061,775 (GRCm39) |
Q88R |
probably benign |
Het |
Slc19a2 |
C |
T |
1: 164,084,443 (GRCm39) |
T111M |
probably damaging |
Het |
Slc35e4 |
G |
A |
11: 3,863,087 (GRCm39) |
P34L |
possibly damaging |
Het |
Slc7a6os |
A |
T |
8: 106,937,189 (GRCm39) |
D90E |
probably benign |
Het |
Ssh3 |
A |
G |
19: 4,319,053 (GRCm39) |
V19A |
possibly damaging |
Het |
Susd1 |
C |
T |
4: 59,379,594 (GRCm39) |
|
probably benign |
Het |
Tcf19 |
A |
T |
17: 35,825,794 (GRCm39) |
M121K |
possibly damaging |
Het |
Tcp11 |
G |
A |
17: 28,299,193 (GRCm39) |
R21C |
probably damaging |
Het |
Tcp11l2 |
A |
G |
10: 84,449,522 (GRCm39) |
I496V |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 48,729,417 (GRCm39) |
A1530T |
|
Het |
Tmem127 |
T |
A |
2: 127,098,979 (GRCm39) |
V171D |
probably damaging |
Het |
Tyrp1 |
G |
A |
4: 80,753,399 (GRCm39) |
C30Y |
probably damaging |
Het |
Usp48 |
A |
T |
4: 137,341,080 (GRCm39) |
D360V |
probably damaging |
Het |
Vamp4 |
T |
A |
1: 162,401,952 (GRCm39) |
D11E |
possibly damaging |
Het |
Vmn1r14 |
T |
C |
6: 57,210,505 (GRCm39) |
F28L |
probably benign |
Het |
Vmn2r69 |
G |
T |
7: 85,059,018 (GRCm39) |
C514* |
probably null |
Het |
Vmn2r84 |
G |
A |
10: 130,226,968 (GRCm39) |
A290V |
probably benign |
Het |
Zfp1007 |
A |
T |
5: 109,824,174 (GRCm39) |
S425R |
probably benign |
Het |
Zhx3 |
T |
A |
2: 160,622,691 (GRCm39) |
Y492F |
probably benign |
Het |
|
Other mutations in Abcf3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Abcf3
|
APN |
16 |
20,370,434 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01570:Abcf3
|
APN |
16 |
20,378,748 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02239:Abcf3
|
APN |
16 |
20,369,386 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0158:Abcf3
|
UTSW |
16 |
20,371,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Abcf3
|
UTSW |
16 |
20,378,918 (GRCm39) |
splice site |
probably null |
|
R0579:Abcf3
|
UTSW |
16 |
20,369,398 (GRCm39) |
missense |
probably benign |
|
R0671:Abcf3
|
UTSW |
16 |
20,369,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R0799:Abcf3
|
UTSW |
16 |
20,378,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Abcf3
|
UTSW |
16 |
20,378,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R1393:Abcf3
|
UTSW |
16 |
20,379,180 (GRCm39) |
missense |
probably benign |
0.01 |
R2356:Abcf3
|
UTSW |
16 |
20,379,249 (GRCm39) |
missense |
probably benign |
0.01 |
R2910:Abcf3
|
UTSW |
16 |
20,378,982 (GRCm39) |
missense |
probably damaging |
0.98 |
R2911:Abcf3
|
UTSW |
16 |
20,378,982 (GRCm39) |
missense |
probably damaging |
0.98 |
R3081:Abcf3
|
UTSW |
16 |
20,378,114 (GRCm39) |
missense |
probably benign |
0.09 |
R3852:Abcf3
|
UTSW |
16 |
20,379,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Abcf3
|
UTSW |
16 |
20,367,808 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4752:Abcf3
|
UTSW |
16 |
20,369,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Abcf3
|
UTSW |
16 |
20,370,425 (GRCm39) |
missense |
probably benign |
0.05 |
R5672:Abcf3
|
UTSW |
16 |
20,368,002 (GRCm39) |
missense |
probably benign |
0.00 |
R5817:Abcf3
|
UTSW |
16 |
20,367,833 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6013:Abcf3
|
UTSW |
16 |
20,369,311 (GRCm39) |
splice site |
probably null |
|
R6019:Abcf3
|
UTSW |
16 |
20,371,201 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6026:Abcf3
|
UTSW |
16 |
20,369,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R6952:Abcf3
|
UTSW |
16 |
20,368,484 (GRCm39) |
splice site |
probably null |
|
R7327:Abcf3
|
UTSW |
16 |
20,367,430 (GRCm39) |
missense |
probably benign |
0.03 |
R7431:Abcf3
|
UTSW |
16 |
20,377,539 (GRCm39) |
missense |
probably benign |
0.00 |
R7539:Abcf3
|
UTSW |
16 |
20,371,382 (GRCm39) |
critical splice donor site |
probably null |
|
R7764:Abcf3
|
UTSW |
16 |
20,368,040 (GRCm39) |
missense |
probably benign |
0.36 |
R8358:Abcf3
|
UTSW |
16 |
20,367,796 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8391:Abcf3
|
UTSW |
16 |
20,368,968 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8416:Abcf3
|
UTSW |
16 |
20,369,023 (GRCm39) |
missense |
probably benign |
0.02 |
R8821:Abcf3
|
UTSW |
16 |
20,369,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Abcf3
|
UTSW |
16 |
20,368,056 (GRCm39) |
missense |
probably benign |
|
R9160:Abcf3
|
UTSW |
16 |
20,379,246 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9501:Abcf3
|
UTSW |
16 |
20,379,125 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Abcf3
|
UTSW |
16 |
20,378,447 (GRCm39) |
missense |
probably benign |
0.11 |
|