Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
T |
11: 109,999,479 (GRCm39) |
W1459R |
probably damaging |
Het |
Abca9 |
A |
T |
11: 110,032,488 (GRCm39) |
|
probably benign |
Het |
Adam25 |
T |
A |
8: 41,208,467 (GRCm39) |
C578S |
probably damaging |
Het |
Adam32 |
T |
A |
8: 25,412,353 (GRCm39) |
|
probably null |
Het |
Add1 |
T |
C |
5: 34,773,992 (GRCm39) |
V67A |
probably benign |
Het |
Aggf1 |
A |
T |
13: 95,492,988 (GRCm39) |
|
probably benign |
Het |
Ahcyl2 |
A |
T |
6: 29,891,242 (GRCm39) |
I449F |
probably benign |
Het |
Ak6 |
A |
G |
13: 100,791,650 (GRCm39) |
Y31C |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,188,037 (GRCm39) |
V1817A |
probably benign |
Het |
Arhgef17 |
G |
T |
7: 100,578,057 (GRCm39) |
P964T |
probably damaging |
Het |
Atxn7l3b |
A |
T |
10: 112,764,485 (GRCm39) |
L48Q |
possibly damaging |
Het |
Bbs10 |
T |
G |
10: 111,136,926 (GRCm39) |
S680A |
probably damaging |
Het |
Bcl7c |
G |
A |
7: 127,304,936 (GRCm39) |
T164I |
probably damaging |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
Ccdc83 |
T |
A |
7: 89,875,891 (GRCm39) |
T327S |
possibly damaging |
Het |
Coro1b |
T |
C |
19: 4,203,250 (GRCm39) |
Y364H |
probably damaging |
Het |
Cstf3 |
A |
G |
2: 104,482,791 (GRCm39) |
D313G |
probably damaging |
Het |
Dlgap5 |
T |
A |
14: 47,650,432 (GRCm39) |
|
probably null |
Het |
Dusp3 |
A |
T |
11: 101,872,547 (GRCm39) |
I83N |
probably damaging |
Het |
Eea1 |
A |
T |
10: 95,831,444 (GRCm39) |
K178N |
possibly damaging |
Het |
Efr3b |
T |
A |
12: 4,032,925 (GRCm39) |
D144V |
probably damaging |
Het |
Gfus |
C |
A |
15: 75,798,827 (GRCm39) |
D127Y |
probably damaging |
Het |
Gm1110 |
T |
A |
9: 26,794,514 (GRCm39) |
E504V |
probably null |
Het |
Got2 |
T |
C |
8: 96,614,881 (GRCm39) |
H18R |
probably benign |
Het |
Gprc5b |
T |
C |
7: 118,582,856 (GRCm39) |
M338V |
probably benign |
Het |
Has2 |
A |
T |
15: 56,531,831 (GRCm39) |
F295I |
probably damaging |
Het |
Hcn3 |
T |
C |
3: 89,056,107 (GRCm39) |
D519G |
probably damaging |
Het |
Ino80 |
T |
A |
2: 119,210,160 (GRCm39) |
D1377V |
probably benign |
Het |
Iqsec3 |
A |
T |
6: 121,390,521 (GRCm39) |
|
probably benign |
Het |
Kif3c |
T |
A |
12: 3,415,989 (GRCm39) |
S3R |
probably benign |
Het |
Krt17 |
A |
G |
11: 100,151,445 (GRCm39) |
I116T |
possibly damaging |
Het |
Lrba |
T |
C |
3: 86,275,816 (GRCm39) |
V1728A |
probably damaging |
Het |
Map3k6 |
G |
T |
4: 132,974,252 (GRCm39) |
V550L |
possibly damaging |
Het |
Mcph1 |
T |
C |
8: 18,838,487 (GRCm39) |
V803A |
probably damaging |
Het |
Med13 |
A |
G |
11: 86,210,702 (GRCm39) |
V480A |
probably benign |
Het |
Ms4a20 |
A |
G |
19: 11,074,311 (GRCm39) |
V207A |
possibly damaging |
Het |
Msh5 |
T |
C |
17: 35,248,630 (GRCm39) |
E772G |
probably null |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Ndfip2 |
T |
C |
14: 105,542,174 (GRCm39) |
L308P |
probably damaging |
Het |
Ndufb10 |
T |
C |
17: 24,943,209 (GRCm39) |
T34A |
probably benign |
Het |
Nipal3 |
A |
T |
4: 135,195,829 (GRCm39) |
I258N |
possibly damaging |
Het |
Nup54 |
A |
G |
5: 92,570,423 (GRCm39) |
V328A |
probably damaging |
Het |
Oprm1 |
T |
C |
10: 6,739,071 (GRCm39) |
V66A |
possibly damaging |
Het |
Or10p21 |
T |
A |
10: 128,847,191 (GRCm39) |
F12L |
possibly damaging |
Het |
Or51ah3 |
G |
T |
7: 103,210,289 (GRCm39) |
V202F |
probably benign |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Or8b56 |
T |
A |
9: 38,739,111 (GRCm39) |
Y41* |
probably null |
Het |
Or9s14 |
T |
C |
1: 92,535,615 (GRCm39) |
F19L |
probably damaging |
Het |
Peg12 |
G |
A |
7: 62,113,296 (GRCm39) |
T267I |
unknown |
Het |
Phf20 |
A |
G |
2: 156,145,061 (GRCm39) |
S890G |
probably benign |
Het |
Plk2 |
C |
T |
13: 110,535,997 (GRCm39) |
T567M |
probably damaging |
Het |
Pola2 |
A |
T |
19: 5,992,370 (GRCm39) |
|
probably benign |
Het |
Ppp1r12b |
A |
G |
1: 134,793,514 (GRCm39) |
|
probably null |
Het |
Prickle1 |
A |
T |
15: 93,400,900 (GRCm39) |
L528* |
probably null |
Het |
Prpf6 |
T |
A |
2: 181,297,250 (GRCm39) |
N903K |
probably benign |
Het |
Ptprc |
G |
A |
1: 138,010,453 (GRCm39) |
A601V |
probably benign |
Het |
Ranbp1 |
A |
T |
16: 18,059,607 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
C |
T |
11: 54,582,075 (GRCm39) |
S1334L |
probably benign |
Het |
Rgs2 |
T |
C |
1: 143,878,022 (GRCm39) |
|
probably null |
Het |
Ripk2 |
A |
T |
4: 16,129,125 (GRCm39) |
|
probably null |
Het |
Rnf17 |
A |
G |
14: 56,719,650 (GRCm39) |
S967G |
probably null |
Het |
Rock2 |
T |
A |
12: 17,009,517 (GRCm39) |
|
probably benign |
Het |
Rpusd3 |
C |
T |
6: 113,392,514 (GRCm39) |
|
probably null |
Het |
Scgb1b20 |
G |
T |
7: 33,072,935 (GRCm39) |
V48L |
probably benign |
Het |
Sec16a |
T |
A |
2: 26,314,426 (GRCm39) |
|
probably null |
Het |
Serpina5 |
T |
A |
12: 104,069,589 (GRCm39) |
L267H |
probably damaging |
Het |
Slc12a3 |
C |
T |
8: 95,082,986 (GRCm39) |
H875Y |
probably benign |
Het |
Slc45a4 |
A |
G |
15: 73,453,763 (GRCm39) |
S745P |
probably benign |
Het |
Sucla2 |
T |
C |
14: 73,830,088 (GRCm39) |
V375A |
probably damaging |
Het |
Sun2 |
C |
A |
15: 79,621,277 (GRCm39) |
V213F |
probably damaging |
Het |
Taar2 |
G |
A |
10: 23,817,393 (GRCm39) |
R311H |
probably benign |
Het |
Tac1 |
C |
T |
6: 7,562,424 (GRCm39) |
R129C |
probably damaging |
Het |
Taf6 |
T |
C |
5: 138,180,975 (GRCm39) |
E202G |
probably benign |
Het |
Tex21 |
T |
A |
12: 76,286,307 (GRCm39) |
H64L |
probably benign |
Het |
Tgs1 |
A |
G |
4: 3,593,620 (GRCm39) |
S503G |
probably benign |
Het |
Tmem184c |
C |
T |
8: 78,324,441 (GRCm39) |
V350I |
possibly damaging |
Het |
Tnks1bp1 |
A |
G |
2: 84,901,273 (GRCm39) |
S960G |
possibly damaging |
Het |
Trbc2 |
T |
C |
6: 41,525,083 (GRCm39) |
|
probably benign |
Het |
Tubgcp2 |
A |
T |
7: 139,581,518 (GRCm39) |
|
probably benign |
Het |
Vmn1r39 |
T |
A |
6: 66,782,181 (GRCm39) |
T46S |
probably benign |
Het |
Vmn1r61 |
T |
C |
7: 5,613,699 (GRCm39) |
H205R |
probably benign |
Het |
Zdhhc14 |
T |
C |
17: 5,775,539 (GRCm39) |
S264P |
possibly damaging |
Het |
Zfp101 |
T |
A |
17: 33,601,213 (GRCm39) |
H181L |
possibly damaging |
Het |
|
Other mutations in Ccdc110 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01898:Ccdc110
|
APN |
8 |
46,395,161 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02175:Ccdc110
|
APN |
8 |
46,393,660 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02471:Ccdc110
|
APN |
8 |
46,394,793 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02524:Ccdc110
|
APN |
8 |
46,394,979 (GRCm39) |
missense |
probably benign |
|
IGL02887:Ccdc110
|
APN |
8 |
46,396,221 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03227:Ccdc110
|
APN |
8 |
46,394,586 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03238:Ccdc110
|
APN |
8 |
46,394,859 (GRCm39) |
missense |
probably benign |
0.00 |
droll
|
UTSW |
8 |
46,395,864 (GRCm39) |
missense |
probably benign |
0.10 |
humorless
|
UTSW |
8 |
46,396,487 (GRCm39) |
missense |
probably benign |
0.03 |
R0049:Ccdc110
|
UTSW |
8 |
46,395,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Ccdc110
|
UTSW |
8 |
46,395,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Ccdc110
|
UTSW |
8 |
46,388,194 (GRCm39) |
missense |
probably benign |
0.00 |
R0218:Ccdc110
|
UTSW |
8 |
46,387,761 (GRCm39) |
splice site |
probably benign |
|
R0280:Ccdc110
|
UTSW |
8 |
46,396,487 (GRCm39) |
missense |
probably benign |
0.03 |
R0332:Ccdc110
|
UTSW |
8 |
46,396,001 (GRCm39) |
nonsense |
probably null |
|
R0371:Ccdc110
|
UTSW |
8 |
46,395,843 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0469:Ccdc110
|
UTSW |
8 |
46,388,194 (GRCm39) |
missense |
probably benign |
0.00 |
R0502:Ccdc110
|
UTSW |
8 |
46,387,761 (GRCm39) |
splice site |
probably benign |
|
R0510:Ccdc110
|
UTSW |
8 |
46,388,194 (GRCm39) |
missense |
probably benign |
0.00 |
R0534:Ccdc110
|
UTSW |
8 |
46,388,175 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0647:Ccdc110
|
UTSW |
8 |
46,396,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R0714:Ccdc110
|
UTSW |
8 |
46,396,047 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0721:Ccdc110
|
UTSW |
8 |
46,395,026 (GRCm39) |
missense |
probably benign |
|
R1029:Ccdc110
|
UTSW |
8 |
46,394,817 (GRCm39) |
missense |
probably damaging |
0.98 |
R1147:Ccdc110
|
UTSW |
8 |
46,397,121 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1147:Ccdc110
|
UTSW |
8 |
46,397,121 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1170:Ccdc110
|
UTSW |
8 |
46,394,922 (GRCm39) |
missense |
probably benign |
0.22 |
R1340:Ccdc110
|
UTSW |
8 |
46,395,218 (GRCm39) |
missense |
probably benign |
0.02 |
R1540:Ccdc110
|
UTSW |
8 |
46,395,362 (GRCm39) |
nonsense |
probably null |
|
R1587:Ccdc110
|
UTSW |
8 |
46,394,783 (GRCm39) |
missense |
probably benign |
0.01 |
R1602:Ccdc110
|
UTSW |
8 |
46,391,955 (GRCm39) |
missense |
probably benign |
0.12 |
R1629:Ccdc110
|
UTSW |
8 |
46,395,164 (GRCm39) |
missense |
probably benign |
0.08 |
R1842:Ccdc110
|
UTSW |
8 |
46,393,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R1933:Ccdc110
|
UTSW |
8 |
46,396,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R1934:Ccdc110
|
UTSW |
8 |
46,396,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Ccdc110
|
UTSW |
8 |
46,396,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R2043:Ccdc110
|
UTSW |
8 |
46,395,864 (GRCm39) |
missense |
probably benign |
0.10 |
R2093:Ccdc110
|
UTSW |
8 |
46,395,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Ccdc110
|
UTSW |
8 |
46,395,876 (GRCm39) |
missense |
probably benign |
0.00 |
R3613:Ccdc110
|
UTSW |
8 |
46,395,843 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3923:Ccdc110
|
UTSW |
8 |
46,395,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Ccdc110
|
UTSW |
8 |
46,395,705 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4773:Ccdc110
|
UTSW |
8 |
46,396,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Ccdc110
|
UTSW |
8 |
46,396,437 (GRCm39) |
missense |
probably benign |
0.35 |
R4911:Ccdc110
|
UTSW |
8 |
46,395,944 (GRCm39) |
missense |
probably benign |
0.00 |
R4923:Ccdc110
|
UTSW |
8 |
46,396,460 (GRCm39) |
missense |
probably benign |
0.29 |
R5104:Ccdc110
|
UTSW |
8 |
46,395,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R5561:Ccdc110
|
UTSW |
8 |
46,393,646 (GRCm39) |
missense |
probably benign |
0.02 |
R5966:Ccdc110
|
UTSW |
8 |
46,395,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Ccdc110
|
UTSW |
8 |
46,396,536 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6141:Ccdc110
|
UTSW |
8 |
46,394,807 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6326:Ccdc110
|
UTSW |
8 |
46,395,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R6366:Ccdc110
|
UTSW |
8 |
46,396,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R6405:Ccdc110
|
UTSW |
8 |
46,394,734 (GRCm39) |
nonsense |
probably null |
|
R6482:Ccdc110
|
UTSW |
8 |
46,395,825 (GRCm39) |
missense |
probably benign |
0.00 |
R6815:Ccdc110
|
UTSW |
8 |
46,395,024 (GRCm39) |
missense |
probably benign |
0.19 |
R7387:Ccdc110
|
UTSW |
8 |
46,395,233 (GRCm39) |
missense |
probably benign |
0.00 |
R7680:Ccdc110
|
UTSW |
8 |
46,394,688 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8099:Ccdc110
|
UTSW |
8 |
46,395,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R8114:Ccdc110
|
UTSW |
8 |
46,396,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Ccdc110
|
UTSW |
8 |
46,395,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R8295:Ccdc110
|
UTSW |
8 |
46,396,416 (GRCm39) |
missense |
probably damaging |
0.97 |
R8532:Ccdc110
|
UTSW |
8 |
46,396,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Ccdc110
|
UTSW |
8 |
46,395,875 (GRCm39) |
missense |
probably benign |
0.00 |
R9073:Ccdc110
|
UTSW |
8 |
46,395,875 (GRCm39) |
missense |
probably benign |
0.00 |
R9088:Ccdc110
|
UTSW |
8 |
46,394,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R9803:Ccdc110
|
UTSW |
8 |
46,395,626 (GRCm39) |
missense |
probably benign |
|
X0053:Ccdc110
|
UTSW |
8 |
46,395,998 (GRCm39) |
missense |
possibly damaging |
0.56 |
X0054:Ccdc110
|
UTSW |
8 |
46,394,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|