Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam4 |
T |
C |
12: 81,466,723 (GRCm39) |
T633A |
possibly damaging |
Het |
Adgrv1 |
A |
T |
13: 81,714,471 (GRCm39) |
F937L |
probably benign |
Het |
Adipor2 |
A |
T |
6: 119,336,486 (GRCm39) |
F159Y |
probably damaging |
Het |
Ahcyl1 |
A |
G |
3: 107,575,645 (GRCm39) |
V380A |
probably damaging |
Het |
Akp3 |
A |
G |
1: 87,053,517 (GRCm39) |
K157E |
probably benign |
Het |
Arpc1a |
T |
A |
5: 145,045,203 (GRCm39) |
I364N |
possibly damaging |
Het |
Bach1 |
C |
G |
16: 87,516,603 (GRCm39) |
S381R |
probably benign |
Het |
Brms1l |
G |
A |
12: 55,912,863 (GRCm39) |
|
probably null |
Het |
Camk1d |
A |
G |
2: 5,680,777 (GRCm39) |
S6P |
unknown |
Het |
Ccdc112 |
C |
A |
18: 46,424,040 (GRCm39) |
V233L |
probably benign |
Het |
Ccdc113 |
A |
T |
8: 96,272,613 (GRCm39) |
N240I |
possibly damaging |
Het |
Ccdc168 |
A |
T |
1: 44,095,668 (GRCm39) |
V1810E |
possibly damaging |
Het |
Ccdc6 |
T |
C |
10: 70,004,951 (GRCm39) |
V232A |
possibly damaging |
Het |
Cct5 |
A |
G |
15: 31,592,883 (GRCm39) |
I409T |
possibly damaging |
Het |
Cd96 |
A |
G |
16: 45,856,298 (GRCm39) |
Y583H |
probably damaging |
Het |
Cdh22 |
C |
T |
2: 164,954,329 (GRCm39) |
V731M |
probably benign |
Het |
Clcn1 |
C |
T |
6: 42,282,494 (GRCm39) |
P521S |
probably damaging |
Het |
Clec18a |
C |
T |
8: 111,808,322 (GRCm39) |
A27T |
probably benign |
Het |
Cnnm2 |
C |
T |
19: 46,750,807 (GRCm39) |
A199V |
probably benign |
Het |
Copg1 |
G |
A |
6: 87,880,478 (GRCm39) |
A494T |
possibly damaging |
Het |
Cyp2j5 |
T |
A |
4: 96,552,244 (GRCm39) |
I2F |
probably benign |
Het |
Dgkg |
T |
A |
16: 22,384,065 (GRCm39) |
N463Y |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 117,976,007 (GRCm39) |
D2804G |
probably damaging |
Het |
Efcab12 |
T |
C |
6: 115,792,995 (GRCm39) |
N488D |
probably benign |
Het |
Etv5 |
G |
A |
16: 22,254,668 (GRCm39) |
P64L |
probably damaging |
Het |
Fbrs |
A |
G |
7: 127,084,272 (GRCm39) |
E468G |
probably benign |
Het |
Fcho1 |
A |
T |
8: 72,169,468 (GRCm39) |
M146K |
probably benign |
Het |
Gad1 |
A |
T |
2: 70,423,807 (GRCm39) |
M405L |
|
Het |
Gcc2 |
T |
A |
10: 58,106,592 (GRCm39) |
H609Q |
probably benign |
Het |
Gm11983 |
A |
T |
11: 6,786,902 (GRCm39) |
M75K |
unknown |
Het |
Gm4353 |
T |
A |
7: 115,682,871 (GRCm39) |
I237F |
probably damaging |
Het |
H1f0 |
C |
T |
15: 78,912,947 (GRCm39) |
P9L |
probably damaging |
Het |
Hcn4 |
A |
G |
9: 58,731,222 (GRCm39) |
D143G |
unknown |
Het |
Id1 |
T |
A |
2: 152,578,430 (GRCm39) |
V57D |
probably damaging |
Het |
Ifna13 |
T |
C |
4: 88,562,540 (GRCm39) |
Q28R |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Lonrf2 |
G |
A |
1: 38,875,538 (GRCm39) |
|
probably benign |
Het |
Magi3 |
C |
T |
3: 103,922,473 (GRCm39) |
A1415T |
probably benign |
Het |
Mia2 |
A |
G |
12: 59,148,371 (GRCm39) |
E77G |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,483,937 (GRCm39) |
Q6945L |
probably benign |
Het |
Nos2 |
G |
A |
11: 78,850,490 (GRCm39) |
R1116H |
probably damaging |
Het |
Or2w4 |
C |
T |
13: 21,795,224 (GRCm39) |
C305Y |
probably benign |
Het |
Parpbp |
A |
C |
10: 87,975,858 (GRCm39) |
V85G |
probably benign |
Het |
Pcmtd2 |
C |
T |
2: 181,496,837 (GRCm39) |
H273Y |
possibly damaging |
Het |
Pcp4l1 |
C |
T |
1: 171,001,998 (GRCm39) |
G54D |
probably damaging |
Het |
Pkdrej |
T |
C |
15: 85,704,070 (GRCm39) |
H622R |
probably benign |
Het |
Plxnd1 |
G |
T |
6: 115,945,754 (GRCm39) |
D906E |
probably benign |
Het |
Pnpla8 |
T |
C |
12: 44,330,305 (GRCm39) |
S286P |
probably damaging |
Het |
Prss36 |
C |
T |
7: 127,533,339 (GRCm39) |
V631I |
probably benign |
Het |
Ptpn9 |
A |
T |
9: 56,964,010 (GRCm39) |
N381I |
possibly damaging |
Het |
Ranbp9 |
A |
T |
13: 43,576,041 (GRCm39) |
I222N |
probably damaging |
Het |
Rev1 |
T |
C |
1: 38,092,173 (GRCm39) |
T1249A |
probably damaging |
Het |
Ripply2 |
G |
T |
9: 86,901,715 (GRCm39) |
W80C |
probably damaging |
Het |
Rnaseh2b |
C |
A |
14: 62,602,722 (GRCm39) |
P235Q |
probably benign |
Het |
Sacs |
T |
A |
14: 61,443,997 (GRCm39) |
F2014L |
probably damaging |
Het |
Serpinb9f |
A |
G |
13: 33,518,238 (GRCm39) |
N246S |
probably benign |
Het |
Sh3pxd2a |
A |
T |
19: 47,255,539 (GRCm39) |
S1088T |
probably damaging |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Skint3 |
A |
G |
4: 112,137,432 (GRCm39) |
I367V |
probably benign |
Het |
Slc20a2 |
G |
T |
8: 23,051,211 (GRCm39) |
E415* |
probably null |
Het |
Slc5a1 |
T |
A |
5: 33,310,025 (GRCm39) |
S418T |
probably benign |
Het |
Spats2 |
G |
T |
15: 99,076,446 (GRCm39) |
G175* |
probably null |
Het |
Srebf1 |
A |
T |
11: 60,095,015 (GRCm39) |
F485L |
possibly damaging |
Het |
St8sia4 |
A |
G |
1: 95,555,364 (GRCm39) |
V222A |
|
Het |
Stab1 |
C |
T |
14: 30,865,531 (GRCm39) |
E1786K |
probably benign |
Het |
Stat2 |
A |
G |
10: 128,112,657 (GRCm39) |
M58V |
probably benign |
Het |
Stat5a |
A |
G |
11: 100,765,870 (GRCm39) |
T319A |
probably benign |
Het |
Sufu |
A |
G |
19: 46,385,532 (GRCm39) |
|
probably benign |
Het |
Tle6 |
T |
A |
10: 81,426,880 (GRCm39) |
I579F |
probably damaging |
Het |
Tmem131l |
A |
T |
3: 83,845,459 (GRCm39) |
D390E |
probably benign |
Het |
Trim33 |
T |
A |
3: 103,228,979 (GRCm39) |
|
probably null |
Het |
Usp54 |
A |
G |
14: 20,611,678 (GRCm39) |
V1046A |
probably benign |
Het |
Vit |
G |
A |
17: 78,932,413 (GRCm39) |
G507R |
probably damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,695,590 (GRCm39) |
I274T |
probably damaging |
Het |
Vmn2r67 |
T |
A |
7: 84,804,917 (GRCm39) |
K65M |
possibly damaging |
Het |
Vmn2r86 |
C |
T |
10: 130,282,567 (GRCm39) |
G683E |
possibly damaging |
Het |
Vwa8 |
T |
C |
14: 79,335,871 (GRCm39) |
|
probably null |
Het |
Zdhhc14 |
A |
G |
17: 5,781,779 (GRCm39) |
D333G |
probably benign |
Het |
Zup1 |
G |
A |
10: 33,795,355 (GRCm39) |
S568L |
probably damaging |
Het |
|
Other mutations in Cpsf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00737:Cpsf2
|
APN |
12 |
101,949,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01114:Cpsf2
|
APN |
12 |
101,956,098 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01121:Cpsf2
|
APN |
12 |
101,954,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01377:Cpsf2
|
APN |
12 |
101,953,640 (GRCm39) |
splice site |
probably null |
|
IGL01465:Cpsf2
|
APN |
12 |
101,963,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02861:Cpsf2
|
APN |
12 |
101,965,825 (GRCm39) |
missense |
probably benign |
0.00 |
R0469:Cpsf2
|
UTSW |
12 |
101,955,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Cpsf2
|
UTSW |
12 |
101,956,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Cpsf2
|
UTSW |
12 |
101,955,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Cpsf2
|
UTSW |
12 |
101,951,490 (GRCm39) |
missense |
probably benign |
0.09 |
R0697:Cpsf2
|
UTSW |
12 |
101,949,443 (GRCm39) |
missense |
probably benign |
0.34 |
R0837:Cpsf2
|
UTSW |
12 |
101,963,501 (GRCm39) |
splice site |
probably benign |
|
R1475:Cpsf2
|
UTSW |
12 |
101,951,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Cpsf2
|
UTSW |
12 |
101,965,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Cpsf2
|
UTSW |
12 |
101,956,306 (GRCm39) |
missense |
probably benign |
0.33 |
R1996:Cpsf2
|
UTSW |
12 |
101,964,867 (GRCm39) |
missense |
probably benign |
0.18 |
R2063:Cpsf2
|
UTSW |
12 |
101,949,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R2164:Cpsf2
|
UTSW |
12 |
101,951,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Cpsf2
|
UTSW |
12 |
101,956,088 (GRCm39) |
missense |
probably benign |
0.00 |
R3082:Cpsf2
|
UTSW |
12 |
101,955,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R3732:Cpsf2
|
UTSW |
12 |
101,953,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R3732:Cpsf2
|
UTSW |
12 |
101,953,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R3733:Cpsf2
|
UTSW |
12 |
101,953,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R4627:Cpsf2
|
UTSW |
12 |
101,956,154 (GRCm39) |
missense |
probably benign |
0.18 |
R4665:Cpsf2
|
UTSW |
12 |
101,949,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Cpsf2
|
UTSW |
12 |
101,949,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Cpsf2
|
UTSW |
12 |
101,963,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Cpsf2
|
UTSW |
12 |
101,963,091 (GRCm39) |
missense |
probably damaging |
0.99 |
R4847:Cpsf2
|
UTSW |
12 |
101,963,561 (GRCm39) |
missense |
probably benign |
0.18 |
R4923:Cpsf2
|
UTSW |
12 |
101,948,243 (GRCm39) |
missense |
probably benign |
|
R4975:Cpsf2
|
UTSW |
12 |
101,949,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Cpsf2
|
UTSW |
12 |
101,953,532 (GRCm39) |
nonsense |
probably null |
|
R5440:Cpsf2
|
UTSW |
12 |
101,963,138 (GRCm39) |
missense |
probably benign |
|
R5601:Cpsf2
|
UTSW |
12 |
101,951,614 (GRCm39) |
splice site |
probably null |
|
R5603:Cpsf2
|
UTSW |
12 |
101,964,890 (GRCm39) |
missense |
probably benign |
0.02 |
R5841:Cpsf2
|
UTSW |
12 |
101,951,497 (GRCm39) |
missense |
probably damaging |
0.99 |
R6153:Cpsf2
|
UTSW |
12 |
101,965,619 (GRCm39) |
splice site |
probably null |
|
R6663:Cpsf2
|
UTSW |
12 |
101,965,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Cpsf2
|
UTSW |
12 |
101,967,051 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8357:Cpsf2
|
UTSW |
12 |
101,968,929 (GRCm39) |
missense |
probably damaging |
0.99 |
R8457:Cpsf2
|
UTSW |
12 |
101,968,929 (GRCm39) |
missense |
probably damaging |
0.99 |
R9123:Cpsf2
|
UTSW |
12 |
101,963,555 (GRCm39) |
missense |
probably damaging |
0.96 |
V8831:Cpsf2
|
UTSW |
12 |
101,969,400 (GRCm39) |
missense |
probably damaging |
1.00 |
|