Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933412E24Rik |
G |
T |
15: 59,887,194 (GRCm39) |
C415* |
probably null |
Het |
Adamtsl2 |
A |
C |
2: 26,992,842 (GRCm39) |
I652L |
probably benign |
Het |
Adgrl4 |
T |
C |
3: 151,248,872 (GRCm39) |
I720T |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,261,284 (GRCm39) |
C604* |
probably null |
Het |
Amh |
AGCGCCTTGG |
AG |
10: 80,641,419 (GRCm39) |
|
probably null |
Het |
B3galt2 |
C |
A |
1: 143,522,207 (GRCm39) |
N114K |
probably benign |
Het |
Bud23 |
A |
T |
5: 135,084,897 (GRCm39) |
M59K |
probably benign |
Het |
C3 |
C |
T |
17: 57,531,401 (GRCm39) |
|
probably null |
Het |
C9orf72 |
A |
C |
4: 35,197,098 (GRCm39) |
H322Q |
probably damaging |
Het |
Cc2d2a |
A |
T |
5: 43,871,873 (GRCm39) |
D903V |
probably damaging |
Het |
Ccdc9b |
G |
A |
2: 118,591,128 (GRCm39) |
A135V |
probably benign |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cdan1 |
A |
C |
2: 120,551,230 (GRCm39) |
L1097V |
probably damaging |
Het |
Cdc26 |
T |
A |
4: 62,313,155 (GRCm39) |
N62I |
probably benign |
Het |
Cenpq |
A |
T |
17: 41,235,178 (GRCm39) |
|
probably null |
Het |
Cep295 |
T |
C |
9: 15,239,200 (GRCm39) |
S1858G |
probably damaging |
Het |
Clasp1 |
T |
C |
1: 118,433,261 (GRCm39) |
S247P |
probably damaging |
Het |
Cyp2w1 |
C |
T |
5: 139,339,623 (GRCm39) |
T71I |
probably damaging |
Het |
Dcaf1 |
T |
C |
9: 106,741,793 (GRCm39) |
F1336S |
probably damaging |
Het |
Dennd6b |
G |
A |
15: 89,074,506 (GRCm39) |
Q104* |
probably null |
Het |
Dglucy |
T |
A |
12: 100,816,361 (GRCm39) |
|
probably null |
Het |
Dnajc9 |
A |
G |
14: 20,438,158 (GRCm39) |
V148A |
possibly damaging |
Het |
Dnmbp |
T |
A |
19: 43,890,579 (GRCm39) |
D396V |
possibly damaging |
Het |
Dock10 |
T |
A |
1: 80,583,540 (GRCm39) |
I221F |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,486,579 (GRCm39) |
N1032S |
probably benign |
Het |
Dsg4 |
A |
C |
18: 20,589,888 (GRCm39) |
Y346S |
probably benign |
Het |
Dync1i2 |
A |
G |
2: 71,079,759 (GRCm39) |
H417R |
probably benign |
Het |
Dysf |
G |
A |
6: 84,167,884 (GRCm39) |
|
probably null |
Het |
Elovl1 |
A |
G |
4: 118,287,707 (GRCm39) |
M1V |
probably null |
Het |
Eva1c |
A |
G |
16: 90,701,135 (GRCm39) |
S257G |
probably benign |
Het |
Eya2 |
A |
T |
2: 165,566,723 (GRCm39) |
D258V |
probably damaging |
Het |
Fam193a |
A |
G |
5: 34,593,841 (GRCm39) |
T113A |
probably damaging |
Het |
Fbxw15 |
G |
A |
9: 109,387,314 (GRCm39) |
S227F |
probably damaging |
Het |
Fstl5 |
G |
T |
3: 76,500,783 (GRCm39) |
R404L |
possibly damaging |
Het |
Glud1 |
T |
C |
14: 34,047,541 (GRCm39) |
|
probably benign |
Het |
Gm10770 |
A |
C |
2: 150,021,258 (GRCm39) |
H86Q |
probably damaging |
Het |
Gzme |
C |
T |
14: 56,355,871 (GRCm39) |
G147D |
probably damaging |
Het |
Herc3 |
T |
C |
6: 58,865,645 (GRCm39) |
V746A |
probably damaging |
Het |
Hmga1 |
A |
G |
17: 27,778,592 (GRCm39) |
E17G |
probably damaging |
Het |
Kdelr2 |
A |
T |
5: 143,406,567 (GRCm39) |
K206* |
probably null |
Het |
Kng2 |
A |
G |
16: 22,806,993 (GRCm39) |
|
probably null |
Het |
Lrrc41 |
G |
A |
4: 115,946,248 (GRCm39) |
R321H |
possibly damaging |
Het |
Mapkapk2 |
A |
T |
1: 130,986,498 (GRCm39) |
M1K |
probably null |
Het |
Me2 |
A |
G |
18: 73,924,929 (GRCm39) |
F263L |
probably damaging |
Het |
Mkks |
A |
G |
2: 136,722,287 (GRCm39) |
L290P |
probably damaging |
Het |
Mmp12 |
T |
A |
9: 7,354,772 (GRCm39) |
I255N |
probably damaging |
Het |
Mogs |
A |
G |
6: 83,093,784 (GRCm39) |
D251G |
probably benign |
Het |
Morf4l1 |
T |
A |
9: 89,984,401 (GRCm39) |
Y65F |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,094,676 (GRCm39) |
D5169G |
probably damaging |
Het |
Nin |
A |
G |
12: 70,089,665 (GRCm39) |
L1250P |
probably damaging |
Het |
Nomo1 |
G |
T |
7: 45,715,717 (GRCm39) |
G721V |
possibly damaging |
Het |
Notch2 |
T |
G |
3: 98,029,242 (GRCm39) |
C1002G |
probably damaging |
Het |
Npat |
T |
C |
9: 53,481,522 (GRCm39) |
Y1077H |
probably benign |
Het |
Or1e1c |
T |
A |
11: 73,266,170 (GRCm39) |
N198K |
probably damaging |
Het |
Or4g17 |
G |
A |
2: 111,209,491 (GRCm39) |
V49I |
probably benign |
Het |
Or4p21 |
A |
T |
2: 88,276,367 (GRCm39) |
F305Y |
probably damaging |
Het |
Or5h25 |
A |
G |
16: 58,930,118 (GRCm39) |
L285P |
probably damaging |
Het |
Or8c16 |
T |
C |
9: 38,130,548 (GRCm39) |
I143T |
probably benign |
Het |
Otop2 |
A |
T |
11: 115,215,504 (GRCm39) |
I142F |
probably benign |
Het |
Pacsin3 |
A |
G |
2: 91,093,460 (GRCm39) |
E279G |
possibly damaging |
Het |
Pafah2 |
A |
G |
4: 134,140,758 (GRCm39) |
T243A |
probably benign |
Het |
Pcdhgc5 |
A |
G |
18: 37,954,913 (GRCm39) |
H729R |
probably benign |
Het |
Plcd1 |
T |
C |
9: 118,900,874 (GRCm39) |
D756G |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,102,962 (GRCm39) |
E2707G |
probably damaging |
Het |
Rit2 |
C |
T |
18: 31,449,951 (GRCm39) |
G16S |
probably damaging |
Het |
Sec24c |
A |
G |
14: 20,738,922 (GRCm39) |
|
probably benign |
Het |
Skint5 |
G |
T |
4: 113,434,858 (GRCm39) |
T1037K |
unknown |
Het |
Slc28a2 |
T |
A |
2: 122,290,876 (GRCm39) |
|
probably null |
Het |
Slc41a2 |
G |
A |
10: 83,137,130 (GRCm39) |
A259V |
probably damaging |
Het |
Slc6a17 |
T |
A |
3: 107,380,895 (GRCm39) |
I537F |
possibly damaging |
Het |
Slco1a7 |
T |
C |
6: 141,700,084 (GRCm39) |
|
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,707,196 (GRCm39) |
|
probably benign |
Het |
Smg1 |
T |
C |
7: 117,738,938 (GRCm39) |
I3489V |
probably benign |
Het |
Sytl3 |
T |
C |
17: 6,967,082 (GRCm39) |
L142P |
probably damaging |
Het |
Tektl1 |
A |
T |
10: 78,584,502 (GRCm39) |
M340K |
probably benign |
Het |
Tfr2 |
C |
T |
5: 137,581,707 (GRCm39) |
T598I |
probably damaging |
Het |
Tmc2 |
A |
G |
2: 130,102,145 (GRCm39) |
Q770R |
probably benign |
Het |
Tnc |
C |
T |
4: 63,932,231 (GRCm39) |
V728M |
probably damaging |
Het |
Trim68 |
A |
T |
7: 102,329,597 (GRCm39) |
M177K |
possibly damaging |
Het |
Trmt11 |
T |
C |
10: 30,435,184 (GRCm39) |
D325G |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,935,862 (GRCm39) |
T582I |
probably damaging |
Het |
Usp13 |
G |
A |
3: 32,969,919 (GRCm39) |
E682K |
probably benign |
Het |
Usp9y |
A |
G |
Y: 1,384,454 (GRCm39) |
V688A |
possibly damaging |
Het |
Uts2r |
A |
G |
11: 121,052,095 (GRCm39) |
T320A |
possibly damaging |
Het |
Vmn1r34 |
A |
T |
6: 66,614,480 (GRCm39) |
M86K |
probably damaging |
Het |
Vsig10 |
A |
G |
5: 117,456,880 (GRCm39) |
|
probably benign |
Het |
Zbtb41 |
T |
A |
1: 139,368,132 (GRCm39) |
C607S |
probably benign |
Het |
|
Other mutations in Cdc27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00505:Cdc27
|
APN |
11 |
104,412,258 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00673:Cdc27
|
APN |
11 |
104,419,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00949:Cdc27
|
APN |
11 |
104,420,229 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01529:Cdc27
|
APN |
11 |
104,398,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01894:Cdc27
|
APN |
11 |
104,417,747 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02096:Cdc27
|
APN |
11 |
104,419,394 (GRCm39) |
splice site |
probably benign |
|
IGL02124:Cdc27
|
APN |
11 |
104,413,557 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02444:Cdc27
|
APN |
11 |
104,413,542 (GRCm39) |
splice site |
probably benign |
|
IGL02589:Cdc27
|
APN |
11 |
104,396,470 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02851:Cdc27
|
APN |
11 |
104,417,807 (GRCm39) |
splice site |
probably benign |
|
IGL02861:Cdc27
|
APN |
11 |
104,413,657 (GRCm39) |
splice site |
probably benign |
|
IGL02952:Cdc27
|
APN |
11 |
104,408,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03103:Cdc27
|
APN |
11 |
104,403,806 (GRCm39) |
missense |
probably benign |
0.21 |
R0344:Cdc27
|
UTSW |
11 |
104,417,817 (GRCm39) |
splice site |
probably benign |
|
R0365:Cdc27
|
UTSW |
11 |
104,419,250 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0366:Cdc27
|
UTSW |
11 |
104,396,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R0426:Cdc27
|
UTSW |
11 |
104,403,853 (GRCm39) |
splice site |
probably null |
|
R0505:Cdc27
|
UTSW |
11 |
104,419,114 (GRCm39) |
missense |
probably benign |
|
R0639:Cdc27
|
UTSW |
11 |
104,422,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R0925:Cdc27
|
UTSW |
11 |
104,416,875 (GRCm39) |
critical splice donor site |
probably null |
|
R0927:Cdc27
|
UTSW |
11 |
104,396,467 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1414:Cdc27
|
UTSW |
11 |
104,412,251 (GRCm39) |
missense |
probably benign |
0.26 |
R1822:Cdc27
|
UTSW |
11 |
104,413,648 (GRCm39) |
missense |
probably benign |
0.16 |
R2449:Cdc27
|
UTSW |
11 |
104,396,464 (GRCm39) |
missense |
probably benign |
0.03 |
R3404:Cdc27
|
UTSW |
11 |
104,398,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R3405:Cdc27
|
UTSW |
11 |
104,398,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R3406:Cdc27
|
UTSW |
11 |
104,398,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R3776:Cdc27
|
UTSW |
11 |
104,406,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Cdc27
|
UTSW |
11 |
104,398,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Cdc27
|
UTSW |
11 |
104,425,640 (GRCm39) |
missense |
probably benign |
0.10 |
R4451:Cdc27
|
UTSW |
11 |
104,408,221 (GRCm39) |
missense |
probably benign |
0.05 |
R4452:Cdc27
|
UTSW |
11 |
104,408,221 (GRCm39) |
missense |
probably benign |
0.05 |
R4530:Cdc27
|
UTSW |
11 |
104,419,252 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4956:Cdc27
|
UTSW |
11 |
104,420,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R4988:Cdc27
|
UTSW |
11 |
104,416,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5098:Cdc27
|
UTSW |
11 |
104,398,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R5130:Cdc27
|
UTSW |
11 |
104,425,600 (GRCm39) |
missense |
probably benign |
0.07 |
R5384:Cdc27
|
UTSW |
11 |
104,397,966 (GRCm39) |
missense |
probably benign |
0.02 |
R5876:Cdc27
|
UTSW |
11 |
104,406,244 (GRCm39) |
missense |
probably benign |
0.30 |
R6238:Cdc27
|
UTSW |
11 |
104,419,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Cdc27
|
UTSW |
11 |
104,419,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Cdc27
|
UTSW |
11 |
104,425,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Cdc27
|
UTSW |
11 |
104,413,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R6485:Cdc27
|
UTSW |
11 |
104,396,474 (GRCm39) |
missense |
probably benign |
0.15 |
R7237:Cdc27
|
UTSW |
11 |
104,408,245 (GRCm39) |
missense |
probably benign |
|
R7315:Cdc27
|
UTSW |
11 |
104,406,270 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7534:Cdc27
|
UTSW |
11 |
104,399,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R7838:Cdc27
|
UTSW |
11 |
104,403,830 (GRCm39) |
missense |
probably damaging |
0.98 |
R8150:Cdc27
|
UTSW |
11 |
104,406,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Cdc27
|
UTSW |
11 |
104,408,317 (GRCm39) |
missense |
probably benign |
0.06 |
R8935:Cdc27
|
UTSW |
11 |
104,398,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Cdc27
|
UTSW |
11 |
104,399,211 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9336:Cdc27
|
UTSW |
11 |
104,396,496 (GRCm39) |
missense |
probably benign |
0.00 |
|