Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
A |
T |
18: 6,620,232 (GRCm39) |
K54I |
probably damaging |
Het |
Ankrd34b |
T |
A |
13: 92,575,725 (GRCm39) |
I319K |
probably benign |
Het |
Art2b |
G |
A |
7: 101,229,590 (GRCm39) |
A103V |
probably damaging |
Het |
Atmin |
T |
G |
8: 117,679,665 (GRCm39) |
F126C |
probably damaging |
Het |
Cc2d1b |
A |
T |
4: 108,482,143 (GRCm39) |
N139I |
probably benign |
Het |
Cep128 |
T |
C |
12: 91,200,987 (GRCm39) |
Y794C |
probably damaging |
Het |
Cnep1r1 |
G |
A |
8: 88,856,447 (GRCm39) |
R99Q |
unknown |
Het |
Cpq |
G |
C |
15: 33,213,353 (GRCm39) |
R124P |
probably damaging |
Het |
Crtc3 |
A |
T |
7: 80,327,191 (GRCm39) |
V45D |
probably damaging |
Het |
Dchs2 |
T |
G |
3: 83,036,143 (GRCm39) |
S297A |
probably benign |
Het |
Dnah9 |
A |
T |
11: 65,777,506 (GRCm39) |
S3681T |
probably damaging |
Het |
Dock8 |
T |
C |
19: 25,165,731 (GRCm39) |
Y1872H |
possibly damaging |
Het |
Fbn2 |
T |
A |
18: 58,239,395 (GRCm39) |
Q558L |
probably damaging |
Het |
Fn1 |
A |
G |
1: 71,676,491 (GRCm39) |
V580A |
probably benign |
Het |
Fscn3 |
C |
T |
6: 28,434,472 (GRCm39) |
T349I |
probably benign |
Het |
Fsip2 |
T |
C |
2: 82,815,370 (GRCm39) |
V3701A |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,496,347 (GRCm39) |
V3913A |
probably benign |
Het |
Htt |
G |
A |
5: 35,063,062 (GRCm39) |
G2898D |
probably damaging |
Het |
Ighv3-4 |
T |
G |
12: 114,217,266 (GRCm39) |
E108D |
probably benign |
Het |
Irx5 |
G |
T |
8: 93,087,135 (GRCm39) |
E356* |
probably null |
Het |
Kcnh6 |
A |
G |
11: 105,909,971 (GRCm39) |
I499V |
possibly damaging |
Het |
Kcnj10 |
T |
A |
1: 172,196,963 (GRCm39) |
I159N |
probably damaging |
Het |
Kcnmb4 |
T |
A |
10: 116,282,238 (GRCm39) |
H153L |
probably benign |
Het |
Klhl8 |
T |
C |
5: 104,018,404 (GRCm39) |
N409S |
probably benign |
Het |
Ksr1 |
A |
G |
11: 78,936,014 (GRCm39) |
S117P |
probably benign |
Het |
Lrfn3 |
A |
T |
7: 30,059,244 (GRCm39) |
V327E |
probably damaging |
Het |
Mrc2 |
C |
A |
11: 105,229,740 (GRCm39) |
H724Q |
probably benign |
Het |
Mtf2 |
T |
A |
5: 108,248,805 (GRCm39) |
F372L |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,320,997 (GRCm39) |
D2703E |
probably damaging |
Het |
Nova1 |
T |
C |
12: 46,863,800 (GRCm39) |
Y50C |
unknown |
Het |
Ofcc1 |
T |
A |
13: 40,296,277 (GRCm39) |
Y519F |
probably benign |
Het |
Or2aj5 |
T |
A |
16: 19,424,511 (GRCm39) |
K301N |
probably damaging |
Het |
Or4f54 |
T |
C |
2: 111,123,348 (GRCm39) |
I245T |
probably damaging |
Het |
Or4f61 |
A |
T |
2: 111,922,682 (GRCm39) |
D121E |
probably damaging |
Het |
Or4p19 |
A |
C |
2: 88,242,723 (GRCm39) |
M93R |
probably damaging |
Het |
Pclo |
C |
T |
5: 14,719,325 (GRCm39) |
A1154V |
unknown |
Het |
Phrf1 |
A |
G |
7: 140,823,671 (GRCm39) |
D4G |
unknown |
Het |
Ppp4r3b |
A |
T |
11: 29,123,306 (GRCm39) |
M1L |
probably damaging |
Het |
Prmt7 |
A |
G |
8: 106,943,874 (GRCm39) |
|
probably null |
Het |
Retnlg |
A |
G |
16: 48,694,038 (GRCm39) |
T65A |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 109,911,896 (GRCm39) |
N1763D |
probably benign |
Het |
Scn7a |
A |
G |
2: 66,514,588 (GRCm39) |
F1062S |
possibly damaging |
Het |
Scube3 |
A |
C |
17: 28,383,027 (GRCm39) |
K402Q |
probably damaging |
Het |
Skic2 |
T |
A |
17: 35,059,166 (GRCm39) |
D1067V |
probably damaging |
Het |
Slc25a22 |
C |
A |
7: 141,013,871 (GRCm39) |
D30Y |
probably damaging |
Het |
Smim17 |
A |
T |
7: 6,427,720 (GRCm39) |
Q2L |
possibly damaging |
Het |
Son |
G |
T |
16: 91,453,366 (GRCm39) |
M704I |
probably benign |
Het |
Son |
C |
T |
16: 91,453,608 (GRCm39) |
S785F |
possibly damaging |
Het |
Tnfrsf21 |
G |
A |
17: 43,396,299 (GRCm39) |
V528M |
probably benign |
Het |
Tnks1bp1 |
T |
C |
2: 84,894,290 (GRCm39) |
S1406P |
probably benign |
Het |
Trim21 |
A |
T |
7: 102,212,908 (GRCm39) |
V130E |
probably benign |
Het |
Try5 |
T |
A |
6: 41,289,295 (GRCm39) |
I94F |
probably benign |
Het |
Tubb4a |
C |
T |
17: 57,388,169 (GRCm39) |
V286I |
probably benign |
Het |
Vmn1r180 |
T |
A |
7: 23,652,076 (GRCm39) |
S80T |
probably benign |
Het |
Vmn2r114 |
A |
C |
17: 23,529,286 (GRCm39) |
I272S |
probably damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,234,033 (GRCm39) |
Y726* |
probably null |
Het |
Zdhhc16 |
T |
C |
19: 41,926,465 (GRCm39) |
F83L |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,979,137 (GRCm39) |
L425F |
probably damaging |
Het |
|
Other mutations in Cic |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Cic
|
APN |
7 |
24,991,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01668:Cic
|
APN |
7 |
24,990,629 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02229:Cic
|
APN |
7 |
24,990,375 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02506:Cic
|
APN |
7 |
24,990,282 (GRCm39) |
missense |
probably benign |
|
IGL02794:Cic
|
APN |
7 |
24,985,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03065:Cic
|
APN |
7 |
24,985,246 (GRCm39) |
splice site |
probably benign |
|
IGL03304:Cic
|
APN |
7 |
24,984,274 (GRCm39) |
missense |
probably damaging |
1.00 |
Capuccino
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
Cassock
|
UTSW |
7 |
24,988,338 (GRCm39) |
nonsense |
probably null |
|
Monkey
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850_Cic_466
|
UTSW |
7 |
24,972,327 (GRCm39) |
missense |
probably damaging |
0.98 |
1mM(1):Cic
|
UTSW |
7 |
24,990,214 (GRCm39) |
splice site |
probably benign |
|
IGL03046:Cic
|
UTSW |
7 |
24,990,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0027:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0038:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0063:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0064:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0118:Cic
|
UTSW |
7 |
24,985,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0241:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0377:Cic
|
UTSW |
7 |
24,985,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R0462:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0462:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Cic
|
UTSW |
7 |
24,984,662 (GRCm39) |
missense |
probably benign |
|
R1253:Cic
|
UTSW |
7 |
24,990,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Cic
|
UTSW |
7 |
24,979,162 (GRCm39) |
intron |
probably benign |
|
R1462:Cic
|
UTSW |
7 |
24,971,032 (GRCm39) |
missense |
probably damaging |
0.98 |
R1462:Cic
|
UTSW |
7 |
24,971,032 (GRCm39) |
missense |
probably damaging |
0.98 |
R1519:Cic
|
UTSW |
7 |
24,993,235 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1586:Cic
|
UTSW |
7 |
24,985,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Cic
|
UTSW |
7 |
24,987,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Cic
|
UTSW |
7 |
24,986,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Cic
|
UTSW |
7 |
24,970,961 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2063:Cic
|
UTSW |
7 |
24,972,876 (GRCm39) |
missense |
probably damaging |
0.98 |
R2161:Cic
|
UTSW |
7 |
24,987,559 (GRCm39) |
splice site |
probably null |
|
R2495:Cic
|
UTSW |
7 |
24,991,201 (GRCm39) |
splice site |
probably benign |
|
R2865:Cic
|
UTSW |
7 |
24,972,646 (GRCm39) |
missense |
probably damaging |
0.96 |
R3692:Cic
|
UTSW |
7 |
24,988,338 (GRCm39) |
nonsense |
probably null |
|
R3709:Cic
|
UTSW |
7 |
24,986,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R3710:Cic
|
UTSW |
7 |
24,986,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R3872:Cic
|
UTSW |
7 |
24,971,124 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3946:Cic
|
UTSW |
7 |
24,971,771 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4199:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
frame shift |
probably null |
|
R4426:Cic
|
UTSW |
7 |
24,993,433 (GRCm39) |
utr 3 prime |
probably benign |
|
R4502:Cic
|
UTSW |
7 |
24,987,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Cic
|
UTSW |
7 |
24,972,203 (GRCm39) |
missense |
probably benign |
0.33 |
R4586:Cic
|
UTSW |
7 |
24,972,203 (GRCm39) |
missense |
probably benign |
0.33 |
R4614:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
frame shift |
probably null |
|
R4664:Cic
|
UTSW |
7 |
24,990,099 (GRCm39) |
small deletion |
probably benign |
|
R4688:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
frame shift |
probably null |
|
R4695:Cic
|
UTSW |
7 |
24,973,013 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4696:Cic
|
UTSW |
7 |
24,987,908 (GRCm39) |
missense |
probably benign |
|
R4746:Cic
|
UTSW |
7 |
24,987,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Cic
|
UTSW |
7 |
24,991,636 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4767:Cic
|
UTSW |
7 |
24,971,025 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4776:Cic
|
UTSW |
7 |
24,982,308 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4820:Cic
|
UTSW |
7 |
24,971,157 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4850:Cic
|
UTSW |
7 |
24,972,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R4851:Cic
|
UTSW |
7 |
24,972,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R4922:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
small insertion |
probably benign |
|
R4989:Cic
|
UTSW |
7 |
24,986,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5131:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
small insertion |
probably benign |
|
R5718:Cic
|
UTSW |
7 |
24,972,203 (GRCm39) |
missense |
probably benign |
0.33 |
R5801:Cic
|
UTSW |
7 |
24,970,863 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5949:Cic
|
UTSW |
7 |
24,971,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Cic
|
UTSW |
7 |
24,971,423 (GRCm39) |
missense |
probably benign |
0.33 |
R6246:Cic
|
UTSW |
7 |
24,971,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R6283:Cic
|
UTSW |
7 |
24,985,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Cic
|
UTSW |
7 |
24,972,248 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6481:Cic
|
UTSW |
7 |
24,987,706 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6919:Cic
|
UTSW |
7 |
24,971,202 (GRCm39) |
missense |
probably benign |
0.04 |
R6920:Cic
|
UTSW |
7 |
24,990,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Cic
|
UTSW |
7 |
24,970,736 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7002:Cic
|
UTSW |
7 |
24,971,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R7113:Cic
|
UTSW |
7 |
24,972,869 (GRCm39) |
missense |
probably benign |
0.08 |
R7560:Cic
|
UTSW |
7 |
24,972,278 (GRCm39) |
missense |
probably damaging |
0.98 |
R7680:Cic
|
UTSW |
7 |
24,991,856 (GRCm39) |
missense |
probably damaging |
0.96 |
R7698:Cic
|
UTSW |
7 |
24,972,597 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7746:Cic
|
UTSW |
7 |
24,988,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7841:Cic
|
UTSW |
7 |
24,985,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Cic
|
UTSW |
7 |
24,984,551 (GRCm39) |
missense |
probably benign |
0.10 |
R7916:Cic
|
UTSW |
7 |
24,987,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R7920:Cic
|
UTSW |
7 |
24,971,384 (GRCm39) |
missense |
probably benign |
|
R8056:Cic
|
UTSW |
7 |
24,990,366 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8226:Cic
|
UTSW |
7 |
24,987,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8281:Cic
|
UTSW |
7 |
24,971,249 (GRCm39) |
missense |
probably benign |
|
R8847:Cic
|
UTSW |
7 |
24,970,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R9083:Cic
|
UTSW |
7 |
24,985,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R9140:Cic
|
UTSW |
7 |
24,985,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R9200:Cic
|
UTSW |
7 |
24,971,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R9208:Cic
|
UTSW |
7 |
24,987,502 (GRCm39) |
missense |
probably benign |
0.07 |
R9301:Cic
|
UTSW |
7 |
24,991,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Cic
|
UTSW |
7 |
24,971,414 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9569:Cic
|
UTSW |
7 |
24,972,120 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9752:Cic
|
UTSW |
7 |
24,971,403 (GRCm39) |
missense |
probably damaging |
0.96 |
V7732:Cic
|
UTSW |
7 |
24,991,670 (GRCm39) |
missense |
probably benign |
|
Z1176:Cic
|
UTSW |
7 |
24,970,444 (GRCm39) |
missense |
possibly damaging |
0.91 |
|