Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430550D23Rik |
A |
G |
2: 155,845,731 (GRCm39) |
F9S |
unknown |
Het |
Abhd10 |
A |
G |
16: 45,557,997 (GRCm39) |
F101L |
probably damaging |
Het |
Acp2 |
A |
G |
2: 91,034,651 (GRCm39) |
T93A |
probably benign |
Het |
Adamts9 |
C |
T |
6: 92,837,048 (GRCm39) |
|
probably benign |
Het |
Aknad1 |
T |
A |
3: 108,682,615 (GRCm39) |
|
probably benign |
Het |
Ank3 |
A |
T |
10: 69,822,785 (GRCm39) |
T485S |
probably benign |
Het |
Caly |
G |
A |
7: 139,652,503 (GRCm39) |
R82C |
probably damaging |
Het |
Cfhr2 |
A |
G |
1: 139,786,343 (GRCm39) |
L8P |
probably damaging |
Het |
Cpeb2 |
T |
A |
5: 43,438,775 (GRCm39) |
L869* |
probably null |
Het |
Cxxc1 |
A |
G |
18: 74,350,331 (GRCm39) |
K33E |
possibly damaging |
Het |
Cyp17a1 |
T |
C |
19: 46,659,533 (GRCm39) |
|
probably null |
Het |
Cyp4a30b |
G |
A |
4: 115,309,976 (GRCm39) |
W59* |
probably null |
Het |
Dennd4b |
T |
C |
3: 90,185,172 (GRCm39) |
V1204A |
probably damaging |
Het |
Dpyd |
T |
A |
3: 118,935,565 (GRCm39) |
D663E |
possibly damaging |
Het |
Esrrg |
A |
T |
1: 187,933,205 (GRCm39) |
|
probably benign |
Het |
Exoc2 |
A |
C |
13: 31,090,822 (GRCm39) |
L261V |
probably damaging |
Het |
Exosc9 |
T |
C |
3: 36,609,662 (GRCm39) |
L185S |
probably damaging |
Het |
Gcnt3 |
T |
C |
9: 69,941,728 (GRCm39) |
K280R |
probably benign |
Het |
Ighv1-64 |
A |
T |
12: 115,471,217 (GRCm39) |
M100K |
probably benign |
Het |
Impdh2 |
G |
A |
9: 108,441,978 (GRCm39) |
|
probably null |
Het |
Itsn2 |
T |
A |
12: 4,721,474 (GRCm39) |
I1068K |
probably damaging |
Het |
Kif5c |
T |
C |
2: 49,584,783 (GRCm39) |
C169R |
probably damaging |
Het |
Kndc1 |
A |
G |
7: 139,490,130 (GRCm39) |
S211G |
probably benign |
Het |
Lama2 |
T |
A |
10: 27,066,530 (GRCm39) |
E1117V |
probably damaging |
Het |
Lgals4 |
C |
T |
7: 28,540,921 (GRCm39) |
R282C |
probably damaging |
Het |
Lsg1 |
T |
A |
16: 30,399,865 (GRCm39) |
|
probably null |
Het |
Mab21l4 |
C |
T |
1: 93,082,208 (GRCm39) |
|
probably null |
Het |
Msh3 |
A |
G |
13: 92,411,374 (GRCm39) |
S608P |
possibly damaging |
Het |
Mslnl |
T |
A |
17: 25,964,062 (GRCm39) |
F464I |
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,460,586 (GRCm39) |
K1493N |
probably damaging |
Het |
Myo15a |
A |
T |
11: 60,401,679 (GRCm39) |
|
probably null |
Het |
Myo1b |
A |
T |
1: 51,794,896 (GRCm39) |
F1065I |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,345,136 (GRCm39) |
|
probably benign |
Het |
Or4f4-ps1 |
T |
A |
2: 111,330,497 (GRCm39) |
I300K |
probably damaging |
Het |
Or5b97 |
A |
G |
19: 12,878,274 (GRCm39) |
V290A |
possibly damaging |
Het |
Osbpl7 |
A |
G |
11: 96,943,194 (GRCm39) |
T149A |
probably benign |
Het |
Parp1 |
A |
G |
1: 180,396,690 (GRCm39) |
D31G |
probably benign |
Het |
Pcdha6 |
T |
A |
18: 37,101,203 (GRCm39) |
V132E |
possibly damaging |
Het |
Pcdhb8 |
T |
A |
18: 37,489,975 (GRCm39) |
L551Q |
possibly damaging |
Het |
Pcsk9 |
T |
A |
4: 106,311,808 (GRCm39) |
T190S |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,197,049 (GRCm39) |
T162S |
probably benign |
Het |
Pi4ka |
C |
T |
16: 17,136,234 (GRCm39) |
R908Q |
|
Het |
Pnpla8 |
A |
G |
12: 44,330,222 (GRCm39) |
E258G |
probably benign |
Het |
Prrc2c |
A |
T |
1: 162,537,127 (GRCm39) |
S643T |
unknown |
Het |
Rnf20 |
T |
G |
4: 49,655,964 (GRCm39) |
I970S |
possibly damaging |
Het |
Robo2 |
A |
T |
16: 73,755,247 (GRCm39) |
V758D |
probably damaging |
Het |
Robo4 |
G |
A |
9: 37,319,577 (GRCm39) |
S609N |
possibly damaging |
Het |
Rrbp1 |
G |
A |
2: 143,830,920 (GRCm39) |
Q416* |
probably null |
Het |
Rsf1 |
GCG |
GCGACGGCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
C |
A |
13: 11,701,833 (GRCm39) |
E2941D |
probably damaging |
Het |
Scd2 |
G |
T |
19: 44,289,743 (GRCm39) |
C246F |
probably benign |
Het |
Sh3rf1 |
G |
A |
8: 61,825,687 (GRCm39) |
V561I |
probably benign |
Het |
Slc4a4 |
T |
A |
5: 89,280,301 (GRCm39) |
D366E |
probably damaging |
Het |
Slfn14 |
T |
G |
11: 83,174,715 (GRCm39) |
Q92P |
probably damaging |
Het |
Slfn4 |
A |
T |
11: 83,077,770 (GRCm39) |
Y186F |
probably damaging |
Het |
Smpd4 |
T |
C |
16: 17,453,410 (GRCm39) |
L309P |
possibly damaging |
Het |
Smyd3 |
G |
T |
1: 178,920,482 (GRCm39) |
N217K |
probably benign |
Het |
Spen |
T |
C |
4: 141,197,129 (GRCm39) |
T3547A |
probably benign |
Het |
Suclg1 |
A |
T |
6: 73,253,729 (GRCm39) |
I126F |
unknown |
Het |
Tenm4 |
C |
T |
7: 96,555,148 (GRCm39) |
P2618S |
probably benign |
Het |
Tmprss15 |
A |
T |
16: 78,798,702 (GRCm39) |
I660N |
possibly damaging |
Het |
Trf |
A |
T |
9: 103,087,723 (GRCm39) |
V677D |
probably damaging |
Het |
Trim36 |
T |
C |
18: 46,302,452 (GRCm39) |
N532S |
probably benign |
Het |
Trim37 |
T |
C |
11: 87,037,885 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,570,454 (GRCm39) |
N26813S |
probably benign |
Het |
Vmn1r199 |
T |
A |
13: 22,567,537 (GRCm39) |
V277D |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 102,077,951 (GRCm39) |
D873G |
probably benign |
Het |
Wdr27 |
T |
C |
17: 15,103,929 (GRCm39) |
T726A |
probably damaging |
Het |
Wdr97 |
T |
C |
15: 76,240,775 (GRCm39) |
Y488H |
|
Het |
Wdtc1 |
A |
T |
4: 133,031,511 (GRCm39) |
C236* |
probably null |
Het |
Wnk4 |
A |
C |
11: 101,167,092 (GRCm39) |
S1083R |
unknown |
Het |
Wwc1 |
A |
T |
11: 35,774,234 (GRCm39) |
I342N |
probably damaging |
Het |
Zbtb40 |
A |
G |
4: 136,725,957 (GRCm39) |
L534P |
probably damaging |
Het |
Zfp62 |
T |
C |
11: 49,108,227 (GRCm39) |
C773R |
probably damaging |
Het |
Zfp709 |
T |
A |
8: 72,643,027 (GRCm39) |
I152N |
probably benign |
Het |
Zfp738 |
T |
C |
13: 67,819,550 (GRCm39) |
Y147C |
probably damaging |
Het |
Zscan18 |
A |
C |
7: 12,503,625 (GRCm39) |
S645A |
probably benign |
Het |
Zw10 |
A |
G |
9: 48,988,861 (GRCm39) |
Y709C |
probably damaging |
Het |
|
Other mutations in Nup153 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00657:Nup153
|
APN |
13 |
46,834,626 (GRCm39) |
unclassified |
probably benign |
|
IGL01312:Nup153
|
APN |
13 |
46,840,300 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01459:Nup153
|
APN |
13 |
46,866,402 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01646:Nup153
|
APN |
13 |
46,837,583 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03064:Nup153
|
APN |
13 |
46,847,315 (GRCm39) |
missense |
probably benign |
|
IGL03288:Nup153
|
APN |
13 |
46,858,681 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03369:Nup153
|
APN |
13 |
46,854,459 (GRCm39) |
splice site |
probably null |
|
IGL03371:Nup153
|
APN |
13 |
46,836,628 (GRCm39) |
missense |
probably benign |
0.34 |
R0193:Nup153
|
UTSW |
13 |
46,863,130 (GRCm39) |
missense |
probably benign |
0.01 |
R0244:Nup153
|
UTSW |
13 |
46,847,412 (GRCm39) |
missense |
probably benign |
0.03 |
R0448:Nup153
|
UTSW |
13 |
46,870,657 (GRCm39) |
missense |
probably benign |
0.00 |
R0943:Nup153
|
UTSW |
13 |
46,850,248 (GRCm39) |
splice site |
probably benign |
|
R1219:Nup153
|
UTSW |
13 |
46,840,695 (GRCm39) |
missense |
probably benign |
0.01 |
R1381:Nup153
|
UTSW |
13 |
46,842,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Nup153
|
UTSW |
13 |
46,847,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Nup153
|
UTSW |
13 |
46,847,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Nup153
|
UTSW |
13 |
46,835,113 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1824:Nup153
|
UTSW |
13 |
46,867,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Nup153
|
UTSW |
13 |
46,854,502 (GRCm39) |
missense |
probably damaging |
0.98 |
R2108:Nup153
|
UTSW |
13 |
46,846,986 (GRCm39) |
critical splice donor site |
probably null |
|
R2110:Nup153
|
UTSW |
13 |
46,837,404 (GRCm39) |
missense |
probably benign |
0.00 |
R2111:Nup153
|
UTSW |
13 |
46,837,404 (GRCm39) |
missense |
probably benign |
0.00 |
R2173:Nup153
|
UTSW |
13 |
46,855,076 (GRCm39) |
splice site |
probably benign |
|
R2231:Nup153
|
UTSW |
13 |
46,863,103 (GRCm39) |
critical splice donor site |
probably null |
|
R3879:Nup153
|
UTSW |
13 |
46,837,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4634:Nup153
|
UTSW |
13 |
46,840,706 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4662:Nup153
|
UTSW |
13 |
46,840,750 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4932:Nup153
|
UTSW |
13 |
46,866,213 (GRCm39) |
nonsense |
probably null |
|
R5011:Nup153
|
UTSW |
13 |
46,840,879 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5023:Nup153
|
UTSW |
13 |
46,834,585 (GRCm39) |
unclassified |
probably benign |
|
R5069:Nup153
|
UTSW |
13 |
46,863,268 (GRCm39) |
missense |
probably benign |
0.05 |
R5137:Nup153
|
UTSW |
13 |
46,837,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R5323:Nup153
|
UTSW |
13 |
46,870,682 (GRCm39) |
missense |
probably benign |
0.19 |
R5345:Nup153
|
UTSW |
13 |
46,840,341 (GRCm39) |
nonsense |
probably null |
|
R5536:Nup153
|
UTSW |
13 |
46,836,485 (GRCm39) |
missense |
probably benign |
0.01 |
R5613:Nup153
|
UTSW |
13 |
46,840,747 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5620:Nup153
|
UTSW |
13 |
46,837,482 (GRCm39) |
nonsense |
probably null |
|
R5764:Nup153
|
UTSW |
13 |
46,840,803 (GRCm39) |
missense |
probably damaging |
0.97 |
R5849:Nup153
|
UTSW |
13 |
46,840,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R6454:Nup153
|
UTSW |
13 |
46,863,136 (GRCm39) |
splice site |
probably null |
|
R6701:Nup153
|
UTSW |
13 |
46,840,541 (GRCm39) |
missense |
probably benign |
0.00 |
R6721:Nup153
|
UTSW |
13 |
46,854,502 (GRCm39) |
missense |
probably damaging |
0.98 |
R6737:Nup153
|
UTSW |
13 |
46,842,682 (GRCm39) |
missense |
probably benign |
0.08 |
R6789:Nup153
|
UTSW |
13 |
46,870,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R6820:Nup153
|
UTSW |
13 |
46,863,459 (GRCm39) |
missense |
probably benign |
0.09 |
R6837:Nup153
|
UTSW |
13 |
46,847,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Nup153
|
UTSW |
13 |
46,853,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7052:Nup153
|
UTSW |
13 |
46,840,949 (GRCm39) |
missense |
probably benign |
0.09 |
R7091:Nup153
|
UTSW |
13 |
46,837,404 (GRCm39) |
missense |
probably benign |
|
R7357:Nup153
|
UTSW |
13 |
46,870,642 (GRCm39) |
missense |
probably benign |
0.32 |
R7389:Nup153
|
UTSW |
13 |
46,854,463 (GRCm39) |
critical splice donor site |
probably null |
|
R7423:Nup153
|
UTSW |
13 |
46,850,120 (GRCm39) |
critical splice donor site |
probably null |
|
R7453:Nup153
|
UTSW |
13 |
46,834,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R7611:Nup153
|
UTSW |
13 |
46,840,798 (GRCm39) |
missense |
probably benign |
0.01 |
R7876:Nup153
|
UTSW |
13 |
46,835,084 (GRCm39) |
missense |
probably benign |
|
R7909:Nup153
|
UTSW |
13 |
46,847,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R7938:Nup153
|
UTSW |
13 |
46,842,855 (GRCm39) |
splice site |
probably null |
|
R8804:Nup153
|
UTSW |
13 |
46,840,635 (GRCm39) |
missense |
probably benign |
0.04 |
R8916:Nup153
|
UTSW |
13 |
46,863,462 (GRCm39) |
nonsense |
probably null |
|
R9025:Nup153
|
UTSW |
13 |
46,837,709 (GRCm39) |
missense |
probably benign |
0.36 |
R9217:Nup153
|
UTSW |
13 |
46,835,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R9390:Nup153
|
UTSW |
13 |
46,840,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Nup153
|
UTSW |
13 |
46,840,211 (GRCm39) |
missense |
probably benign |
0.01 |
R9714:Nup153
|
UTSW |
13 |
46,866,435 (GRCm39) |
missense |
possibly damaging |
0.55 |
|