Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actmap |
T |
A |
7: 26,900,468 (GRCm39) |
M149K |
probably damaging |
Het |
Adamts12 |
A |
T |
15: 11,270,748 (GRCm39) |
S668C |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,626,711 (GRCm39) |
V709A |
possibly damaging |
Het |
Aim2 |
T |
A |
1: 173,291,442 (GRCm39) |
D282E |
possibly damaging |
Het |
Akap9 |
T |
A |
5: 4,012,266 (GRCm39) |
S990T |
possibly damaging |
Het |
Aloxe3 |
A |
T |
11: 69,019,480 (GRCm39) |
D131V |
probably null |
Het |
Ankrd28 |
A |
C |
14: 31,477,698 (GRCm39) |
C115G |
probably benign |
Het |
Anxa2 |
A |
T |
9: 69,393,812 (GRCm39) |
M217L |
probably benign |
Het |
Asah2 |
T |
C |
19: 31,972,758 (GRCm39) |
N659S |
probably benign |
Het |
Btaf1 |
A |
G |
19: 36,958,478 (GRCm39) |
D665G |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,361,221 (GRCm39) |
V282E |
probably damaging |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,577,530 (GRCm39) |
L92H |
probably damaging |
Het |
Cep104 |
T |
A |
4: 154,072,883 (GRCm39) |
D380E |
probably damaging |
Het |
Cfap74 |
T |
A |
4: 155,548,059 (GRCm39) |
|
probably benign |
Het |
Chd1 |
A |
T |
17: 17,598,079 (GRCm39) |
E55D |
probably benign |
Het |
Cldnd2 |
T |
A |
7: 43,091,613 (GRCm39) |
C65S |
possibly damaging |
Het |
Clec9a |
G |
T |
6: 129,393,299 (GRCm39) |
A108S |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,563,467 (GRCm39) |
D215G |
probably benign |
Het |
Col9a3 |
G |
A |
2: 180,252,474 (GRCm39) |
E373K |
probably damaging |
Het |
Deptor |
C |
A |
15: 55,044,406 (GRCm39) |
H191N |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,684 (GRCm39) |
I699N |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,809,333 (GRCm39) |
N3550K |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,994,035 (GRCm39) |
K3384R |
probably null |
Het |
Dnajc13 |
CT |
C |
9: 104,064,004 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
C |
A |
7: 105,323,056 (GRCm39) |
N521K |
probably benign |
Het |
Efhb |
G |
A |
17: 53,733,272 (GRCm39) |
T533I |
probably damaging |
Het |
Ercc4 |
A |
T |
16: 12,965,471 (GRCm39) |
H701L |
probably damaging |
Het |
Ern1 |
A |
T |
11: 106,325,676 (GRCm39) |
|
probably benign |
Het |
Etfb |
T |
C |
7: 43,093,624 (GRCm39) |
V17A |
probably damaging |
Het |
Evc |
T |
A |
5: 37,481,141 (GRCm39) |
M235L |
probably benign |
Het |
Fbxw22 |
T |
C |
9: 109,207,937 (GRCm39) |
I445V |
probably benign |
Het |
Fmnl2 |
A |
G |
2: 53,007,081 (GRCm39) |
T764A |
possibly damaging |
Het |
Fto |
T |
A |
8: 92,136,342 (GRCm39) |
D205E |
probably damaging |
Het |
Galntl6 |
G |
A |
8: 58,880,847 (GRCm39) |
P147L |
probably damaging |
Het |
Gm6871 |
T |
C |
7: 41,196,173 (GRCm39) |
I39V |
probably benign |
Het |
Gpr83 |
A |
G |
9: 14,777,470 (GRCm39) |
|
probably benign |
Het |
Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm39) |
H410L |
probably benign |
Het |
Helb |
T |
C |
10: 119,930,193 (GRCm39) |
|
probably null |
Het |
Ifi214 |
T |
C |
1: 173,354,157 (GRCm39) |
Q171R |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,721 (GRCm39) |
I245M |
probably benign |
Het |
Igdcc3 |
A |
G |
9: 65,089,279 (GRCm39) |
T492A |
probably damaging |
Het |
Ighv13-1 |
T |
C |
12: 114,231,252 (GRCm39) |
|
probably benign |
Het |
Igkv4-50 |
T |
C |
6: 69,677,984 (GRCm39) |
K40R |
probably benign |
Het |
Igkv8-18 |
T |
A |
6: 70,333,280 (GRCm39) |
I74N |
probably damaging |
Het |
Iho1 |
A |
G |
9: 108,282,584 (GRCm39) |
V368A |
probably benign |
Het |
Kbtbd7 |
T |
C |
14: 79,666,240 (GRCm39) |
*691Q |
probably null |
Het |
Khnyn |
T |
A |
14: 56,123,946 (GRCm39) |
|
probably null |
Het |
Kif26a |
G |
A |
12: 112,142,007 (GRCm39) |
A754T |
probably benign |
Het |
Llgl1 |
T |
A |
11: 60,597,051 (GRCm39) |
L194* |
probably null |
Het |
Map3k12 |
G |
T |
15: 102,409,717 (GRCm39) |
T686N |
probably benign |
Het |
Myo18a |
C |
A |
11: 77,720,585 (GRCm39) |
P741Q |
probably benign |
Het |
Ncaph2 |
G |
A |
15: 89,240,030 (GRCm39) |
|
probably benign |
Het |
Nfkb2 |
A |
G |
19: 46,297,403 (GRCm39) |
Q406R |
possibly damaging |
Het |
Or10g9b |
A |
T |
9: 39,917,564 (GRCm39) |
I227N |
probably damaging |
Het |
Or11g2 |
T |
A |
14: 50,856,026 (GRCm39) |
C116S |
probably benign |
Het |
Or1ad6 |
G |
A |
11: 50,860,093 (GRCm39) |
V83M |
possibly damaging |
Het |
Or2i1 |
T |
C |
17: 37,507,915 (GRCm39) |
T315A |
probably damaging |
Het |
Or2n1e |
T |
A |
17: 38,586,438 (GRCm39) |
Y259N |
probably damaging |
Het |
Or8b12 |
A |
T |
9: 37,657,831 (GRCm39) |
T134S |
probably benign |
Het |
Ostm1 |
C |
T |
10: 42,554,975 (GRCm39) |
|
probably benign |
Het |
Pabpc1 |
A |
T |
15: 36,599,528 (GRCm39) |
V389E |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,035,633 (GRCm39) |
|
probably null |
Het |
Phc2 |
C |
T |
4: 128,601,764 (GRCm39) |
T73M |
probably damaging |
Het |
Pkp4 |
G |
A |
2: 59,165,276 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
T |
A |
10: 3,907,506 (GRCm39) |
S808T |
probably benign |
Het |
Plk5 |
A |
T |
10: 80,194,631 (GRCm39) |
H118L |
probably damaging |
Het |
Pnlip |
T |
C |
19: 58,664,919 (GRCm39) |
I249T |
probably benign |
Het |
Ptov1 |
T |
C |
7: 44,516,533 (GRCm39) |
D134G |
probably benign |
Het |
Ptprb |
T |
C |
10: 116,155,238 (GRCm39) |
V664A |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,002,609 (GRCm39) |
S1566R |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,445,504 (GRCm39) |
S158P |
probably benign |
Het |
Rae1 |
G |
T |
2: 172,857,185 (GRCm39) |
|
probably benign |
Het |
Ros1 |
A |
C |
10: 52,018,325 (GRCm39) |
W778G |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,592,795 (GRCm39) |
M4653K |
possibly damaging |
Het |
Sacm1l |
G |
A |
9: 123,419,895 (GRCm39) |
V553I |
probably benign |
Het |
Samd4b |
G |
A |
7: 28,106,088 (GRCm39) |
R377W |
probably benign |
Het |
Selenoo |
A |
G |
15: 88,983,531 (GRCm39) |
Q524R |
probably benign |
Het |
Slc30a3 |
T |
C |
5: 31,250,638 (GRCm39) |
S22G |
probably benign |
Het |
Slc35g2 |
A |
C |
9: 100,434,555 (GRCm39) |
V372G |
probably benign |
Het |
Slc5a8 |
T |
C |
10: 88,761,649 (GRCm39) |
|
probably null |
Het |
Slc7a7 |
T |
C |
14: 54,646,190 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,152,988 (GRCm39) |
Y135* |
probably null |
Het |
Slfn1 |
A |
T |
11: 83,012,661 (GRCm39) |
E259V |
probably damaging |
Het |
Slmap |
T |
C |
14: 26,189,690 (GRCm39) |
N156S |
probably damaging |
Het |
Smim29 |
A |
G |
17: 27,784,244 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,303,133 (GRCm39) |
R485S |
probably benign |
Het |
Sptbn2 |
T |
A |
19: 4,792,508 (GRCm39) |
F1388I |
probably damaging |
Het |
Stac2 |
C |
T |
11: 97,930,521 (GRCm39) |
G349E |
probably damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,400 (GRCm39) |
H422Q |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,043,256 (GRCm39) |
N538D |
possibly damaging |
Het |
Tmtc1 |
A |
C |
6: 148,186,478 (GRCm39) |
|
probably null |
Het |
Tns3 |
C |
T |
11: 8,400,986 (GRCm39) |
R1104H |
probably benign |
Het |
Tom1l2 |
C |
G |
11: 60,161,259 (GRCm39) |
R84P |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,219,478 (GRCm39) |
F2072L |
probably damaging |
Het |
Trim6 |
T |
C |
7: 103,881,855 (GRCm39) |
Y369H |
probably damaging |
Het |
Trpc7 |
A |
G |
13: 56,952,366 (GRCm39) |
S541P |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,814 (GRCm39) |
D732G |
possibly damaging |
Het |
Tsc2 |
C |
A |
17: 24,822,249 (GRCm39) |
V1141F |
possibly damaging |
Het |
Tspoap1 |
T |
A |
11: 87,656,473 (GRCm39) |
V257E |
probably benign |
Het |
Ttn |
A |
T |
2: 76,773,355 (GRCm39) |
M2395K |
unknown |
Het |
Ubd |
A |
C |
17: 37,506,593 (GRCm39) |
T160P |
probably benign |
Het |
Ubr7 |
A |
G |
12: 102,735,485 (GRCm39) |
T315A |
probably benign |
Het |
Ugt2b36 |
G |
T |
5: 87,229,397 (GRCm39) |
Y156* |
probably null |
Het |
Ulk4 |
G |
A |
9: 121,092,704 (GRCm39) |
R178* |
probably null |
Het |
Urod |
G |
A |
4: 116,848,870 (GRCm39) |
A92V |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,590,382 (GRCm39) |
D2364G |
possibly damaging |
Het |
Vmn1r87 |
A |
T |
7: 12,866,254 (GRCm39) |
M11K |
possibly damaging |
Het |
Vstm4 |
A |
G |
14: 32,639,859 (GRCm39) |
K96E |
possibly damaging |
Het |
Wwp1 |
T |
C |
4: 19,661,990 (GRCm39) |
D172G |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,682,716 (GRCm39) |
Q3385R |
unknown |
Het |
Zfp229 |
C |
T |
17: 21,964,267 (GRCm39) |
H166Y |
possibly damaging |
Het |
Zfp738 |
A |
T |
13: 67,818,033 (GRCm39) |
C653S |
probably damaging |
Het |
Zp2 |
C |
A |
7: 119,737,343 (GRCm39) |
V282L |
probably damaging |
Het |
|
Other mutations in Pank4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00822:Pank4
|
APN |
4 |
155,065,059 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01105:Pank4
|
APN |
4 |
155,056,922 (GRCm39) |
splice site |
probably benign |
|
IGL01291:Pank4
|
APN |
4 |
155,059,103 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01935:Pank4
|
APN |
4 |
155,063,987 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02366:Pank4
|
APN |
4 |
155,054,085 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02514:Pank4
|
APN |
4 |
155,054,922 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03028:Pank4
|
APN |
4 |
155,054,442 (GRCm39) |
unclassified |
probably benign |
|
IGL03033:Pank4
|
APN |
4 |
155,059,172 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU05:Pank4
|
UTSW |
4 |
155,059,103 (GRCm39) |
missense |
probably damaging |
0.98 |
R0518:Pank4
|
UTSW |
4 |
155,061,082 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1196:Pank4
|
UTSW |
4 |
155,062,630 (GRCm39) |
missense |
probably damaging |
0.99 |
R1566:Pank4
|
UTSW |
4 |
155,064,978 (GRCm39) |
missense |
probably damaging |
0.98 |
R1581:Pank4
|
UTSW |
4 |
155,059,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Pank4
|
UTSW |
4 |
155,054,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Pank4
|
UTSW |
4 |
155,060,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Pank4
|
UTSW |
4 |
155,056,977 (GRCm39) |
missense |
probably benign |
|
R2943:Pank4
|
UTSW |
4 |
155,055,931 (GRCm39) |
missense |
probably benign |
0.01 |
R3911:Pank4
|
UTSW |
4 |
155,054,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R4162:Pank4
|
UTSW |
4 |
155,064,051 (GRCm39) |
critical splice donor site |
probably null |
|
R4404:Pank4
|
UTSW |
4 |
155,064,613 (GRCm39) |
missense |
probably benign |
0.00 |
R4619:Pank4
|
UTSW |
4 |
155,061,076 (GRCm39) |
missense |
probably benign |
0.07 |
R4732:Pank4
|
UTSW |
4 |
155,055,847 (GRCm39) |
missense |
probably benign |
0.01 |
R4733:Pank4
|
UTSW |
4 |
155,055,847 (GRCm39) |
missense |
probably benign |
0.01 |
R4747:Pank4
|
UTSW |
4 |
155,063,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Pank4
|
UTSW |
4 |
155,059,091 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5218:Pank4
|
UTSW |
4 |
155,064,185 (GRCm39) |
missense |
probably benign |
0.01 |
R5278:Pank4
|
UTSW |
4 |
155,056,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R5774:Pank4
|
UTSW |
4 |
155,065,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6004:Pank4
|
UTSW |
4 |
155,061,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Pank4
|
UTSW |
4 |
155,056,693 (GRCm39) |
splice site |
probably null |
|
R7105:Pank4
|
UTSW |
4 |
155,064,624 (GRCm39) |
missense |
probably benign |
0.07 |
R7253:Pank4
|
UTSW |
4 |
155,055,377 (GRCm39) |
missense |
probably benign |
0.02 |
R7481:Pank4
|
UTSW |
4 |
155,054,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R7565:Pank4
|
UTSW |
4 |
155,065,007 (GRCm39) |
missense |
probably benign |
0.08 |
R7718:Pank4
|
UTSW |
4 |
155,059,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R7736:Pank4
|
UTSW |
4 |
155,054,204 (GRCm39) |
missense |
probably benign |
0.03 |
R8144:Pank4
|
UTSW |
4 |
155,054,537 (GRCm39) |
missense |
probably benign |
0.01 |
R8967:Pank4
|
UTSW |
4 |
155,055,415 (GRCm39) |
missense |
probably benign |
0.09 |
R9012:Pank4
|
UTSW |
4 |
155,062,847 (GRCm39) |
unclassified |
probably benign |
|
R9040:Pank4
|
UTSW |
4 |
155,064,559 (GRCm39) |
missense |
probably benign |
0.00 |
R9478:Pank4
|
UTSW |
4 |
155,064,565 (GRCm39) |
missense |
probably benign |
|
Z1177:Pank4
|
UTSW |
4 |
155,059,241 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Pank4
|
UTSW |
4 |
155,059,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|