Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
T |
A |
5: 77,024,203 (GRCm39) |
I991L |
probably benign |
Het |
Abtb3 |
C |
A |
10: 85,223,520 (GRCm39) |
R110S |
unknown |
Het |
Actg2 |
C |
A |
6: 83,497,745 (GRCm39) |
G96V |
probably damaging |
Het |
Adh5 |
T |
A |
3: 138,156,812 (GRCm39) |
L166* |
probably null |
Het |
Akap13 |
A |
G |
7: 75,260,010 (GRCm39) |
D75G |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,739,947 (GRCm39) |
|
probably benign |
Het |
Arfgap1 |
T |
A |
2: 180,615,913 (GRCm39) |
D197E |
probably benign |
Het |
Aste1 |
T |
C |
9: 105,273,906 (GRCm39) |
|
probably null |
Het |
Atp8b2 |
T |
A |
3: 89,861,878 (GRCm39) |
N78I |
probably damaging |
Het |
Cacna2d3 |
T |
A |
14: 28,691,260 (GRCm39) |
|
probably benign |
Het |
Chrd |
T |
A |
16: 20,558,183 (GRCm39) |
W809R |
probably damaging |
Het |
Col2a1 |
C |
T |
15: 97,896,469 (GRCm39) |
G60D |
unknown |
Het |
Coro7 |
T |
A |
16: 4,497,475 (GRCm39) |
M1L |
probably damaging |
Het |
Cracdl |
A |
T |
1: 37,670,982 (GRCm39) |
F97Y |
probably damaging |
Het |
Dhx40 |
T |
C |
11: 86,688,569 (GRCm39) |
I285V |
probably benign |
Het |
Dop1a |
T |
C |
9: 86,432,222 (GRCm39) |
|
probably null |
Het |
Enox1 |
A |
T |
14: 77,848,764 (GRCm39) |
R358S |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,815,990 (GRCm39) |
V2724A |
probably damaging |
Het |
Fam221a |
A |
C |
6: 49,355,432 (GRCm39) |
Q178P |
probably damaging |
Het |
Fcho1 |
A |
C |
8: 72,163,141 (GRCm39) |
|
probably null |
Het |
Fndc1 |
A |
T |
17: 7,988,567 (GRCm39) |
V1165D |
unknown |
Het |
Gal3st2b |
A |
T |
1: 93,868,341 (GRCm39) |
N189Y |
possibly damaging |
Het |
Ghr |
T |
A |
15: 3,349,966 (GRCm39) |
D404V |
probably damaging |
Het |
Glis3 |
A |
T |
19: 28,508,919 (GRCm39) |
V355D |
probably damaging |
Het |
Gpr12 |
A |
C |
5: 146,520,349 (GRCm39) |
V32G |
possibly damaging |
Het |
Gspt1 |
T |
A |
16: 11,040,525 (GRCm39) |
L593F |
probably damaging |
Het |
H2-Q7 |
A |
T |
17: 35,659,007 (GRCm39) |
T153S |
probably damaging |
Het |
Hars2 |
A |
G |
18: 36,921,009 (GRCm39) |
I194V |
probably damaging |
Het |
Hdac9 |
T |
A |
12: 34,479,548 (GRCm39) |
T202S |
possibly damaging |
Het |
Hoxd13 |
T |
C |
2: 74,499,368 (GRCm39) |
Y239H |
probably damaging |
Het |
Insm2 |
C |
T |
12: 55,646,621 (GRCm39) |
Q122* |
probably null |
Het |
Insyn2b |
T |
A |
11: 34,352,677 (GRCm39) |
C240S |
possibly damaging |
Het |
Ip6k1 |
T |
A |
9: 107,922,651 (GRCm39) |
|
probably null |
Het |
Ippk |
T |
C |
13: 49,615,219 (GRCm39) |
V534A |
probably damaging |
Het |
Itch |
T |
G |
2: 155,051,914 (GRCm39) |
F611C |
probably damaging |
Het |
Itga1 |
A |
T |
13: 115,104,776 (GRCm39) |
N1083K |
probably damaging |
Het |
Itgae |
A |
C |
11: 73,006,969 (GRCm39) |
D405A |
probably damaging |
Het |
Kif18a |
T |
C |
2: 109,125,347 (GRCm39) |
S255P |
probably damaging |
Het |
Klhl24 |
C |
G |
16: 19,926,231 (GRCm39) |
T253R |
probably benign |
Het |
Krt81 |
T |
A |
15: 101,358,609 (GRCm39) |
T307S |
possibly damaging |
Het |
Lbr |
A |
T |
1: 181,656,354 (GRCm39) |
W265R |
probably damaging |
Het |
Lgals3bp |
T |
C |
11: 118,283,999 (GRCm39) |
T527A |
probably benign |
Het |
Lzts1 |
A |
C |
8: 69,593,397 (GRCm39) |
V70G |
probably damaging |
Het |
Map3k6 |
C |
T |
4: 132,979,023 (GRCm39) |
P1154S |
probably benign |
Het |
Masp1 |
T |
C |
16: 23,271,205 (GRCm39) |
D681G |
probably benign |
Het |
Mdga2 |
T |
C |
12: 66,533,526 (GRCm39) |
N948D |
probably benign |
Het |
Mettl4 |
A |
T |
17: 95,041,061 (GRCm39) |
F364L |
probably damaging |
Het |
Mosmo |
T |
C |
7: 120,277,055 (GRCm39) |
I23T |
probably benign |
Het |
Mtg1 |
G |
A |
7: 139,723,657 (GRCm39) |
V96I |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,036,803 (GRCm39) |
R966S |
possibly damaging |
Het |
Nid1 |
G |
A |
13: 13,683,353 (GRCm39) |
V1144I |
probably benign |
Het |
Or4a77 |
T |
C |
2: 89,486,910 (GRCm39) |
I292V |
probably benign |
Het |
Or52a33 |
A |
T |
7: 103,289,167 (GRCm39) |
M60K |
probably damaging |
Het |
Or55b4 |
C |
A |
7: 102,133,979 (GRCm39) |
C116F |
possibly damaging |
Het |
Oscar |
T |
G |
7: 3,614,238 (GRCm39) |
Y167S |
probably damaging |
Het |
Pa2g4 |
T |
C |
10: 128,396,559 (GRCm39) |
T200A |
probably benign |
Het |
Pcdh7 |
A |
G |
5: 57,877,126 (GRCm39) |
D227G |
probably benign |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Plce1 |
G |
A |
19: 38,747,384 (GRCm39) |
G1702R |
probably damaging |
Het |
Plxna2 |
C |
A |
1: 194,476,212 (GRCm39) |
T1144K |
possibly damaging |
Het |
Prl8a8 |
G |
A |
13: 27,695,450 (GRCm39) |
T99I |
probably benign |
Het |
Prr29 |
C |
A |
11: 106,267,085 (GRCm39) |
H83Q |
probably damaging |
Het |
Raly |
T |
A |
2: 154,701,664 (GRCm39) |
I108N |
possibly damaging |
Het |
Ranbp9 |
A |
T |
13: 43,573,098 (GRCm39) |
S475R |
probably benign |
Het |
Rogdi |
C |
A |
16: 4,831,362 (GRCm39) |
|
probably benign |
Het |
Rorc |
C |
T |
3: 94,280,214 (GRCm39) |
Q6* |
probably null |
Het |
Sacs |
T |
C |
14: 61,449,945 (GRCm39) |
L3997S |
probably damaging |
Het |
Scn2a |
A |
T |
2: 65,594,950 (GRCm39) |
Y1933F |
probably benign |
Het |
Sik3 |
T |
C |
9: 46,122,041 (GRCm39) |
L898P |
probably damaging |
Het |
Sipa1l1 |
A |
G |
12: 82,388,180 (GRCm39) |
I135M |
probably damaging |
Het |
Slc26a3 |
C |
A |
12: 31,500,934 (GRCm39) |
Q224K |
probably damaging |
Het |
Sobp |
G |
T |
10: 42,897,436 (GRCm39) |
N716K |
probably benign |
Het |
Spata16 |
A |
G |
3: 26,981,483 (GRCm39) |
D513G |
probably damaging |
Het |
Spata31h1 |
G |
A |
10: 82,125,777 (GRCm39) |
T2411I |
probably damaging |
Het |
Speer4a3 |
A |
T |
5: 26,154,842 (GRCm39) |
S253T |
possibly damaging |
Het |
Stac |
T |
C |
9: 111,401,394 (GRCm39) |
R351G |
possibly damaging |
Het |
Tecta |
T |
A |
9: 42,306,237 (GRCm39) |
T64S |
probably benign |
Het |
Tert |
G |
A |
13: 73,776,529 (GRCm39) |
V427M |
probably damaging |
Het |
Tex15 |
G |
A |
8: 34,060,748 (GRCm39) |
M333I |
probably benign |
Het |
Tmbim4 |
A |
T |
10: 120,056,664 (GRCm39) |
Q72L |
probably benign |
Het |
Trav9n-4 |
T |
C |
14: 53,532,256 (GRCm39) |
S37P |
probably benign |
Het |
Trpv5 |
A |
T |
6: 41,652,894 (GRCm39) |
M93K |
possibly damaging |
Het |
Ulk4 |
T |
C |
9: 121,087,876 (GRCm39) |
E272G |
probably benign |
Het |
Ulk4 |
T |
C |
9: 121,095,583 (GRCm39) |
T79A |
probably benign |
Het |
Upb1 |
A |
G |
10: 75,248,602 (GRCm39) |
N41D |
probably benign |
Het |
Wls |
A |
T |
3: 159,639,965 (GRCm39) |
Y532F |
probably damaging |
Het |
Zdhhc5 |
G |
A |
2: 84,545,355 (GRCm39) |
|
probably benign |
Het |
Zfp109 |
T |
C |
7: 23,928,785 (GRCm39) |
D216G |
probably benign |
Het |
Zfp473 |
G |
A |
7: 44,381,798 (GRCm39) |
A845V |
probably damaging |
Het |
|
Other mutations in Ncapg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01410:Ncapg2
|
APN |
12 |
116,388,270 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01694:Ncapg2
|
APN |
12 |
116,370,850 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01724:Ncapg2
|
APN |
12 |
116,390,331 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01792:Ncapg2
|
APN |
12 |
116,389,438 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02098:Ncapg2
|
APN |
12 |
116,407,952 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02136:Ncapg2
|
APN |
12 |
116,424,203 (GRCm39) |
missense |
probably benign |
|
IGL02409:Ncapg2
|
APN |
12 |
116,384,337 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02580:Ncapg2
|
APN |
12 |
116,384,309 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02653:Ncapg2
|
APN |
12 |
116,389,526 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03073:Ncapg2
|
APN |
12 |
116,415,894 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03114:Ncapg2
|
APN |
12 |
116,415,993 (GRCm39) |
splice site |
probably benign |
|
IGL03199:Ncapg2
|
APN |
12 |
116,382,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Ncapg2
|
APN |
12 |
116,403,677 (GRCm39) |
missense |
possibly damaging |
0.90 |
P0033:Ncapg2
|
UTSW |
12 |
116,402,255 (GRCm39) |
missense |
probably benign |
0.03 |
R0008:Ncapg2
|
UTSW |
12 |
116,393,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Ncapg2
|
UTSW |
12 |
116,384,303 (GRCm39) |
splice site |
probably null |
|
R0379:Ncapg2
|
UTSW |
12 |
116,406,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R0568:Ncapg2
|
UTSW |
12 |
116,386,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R0771:Ncapg2
|
UTSW |
12 |
116,376,779 (GRCm39) |
nonsense |
probably null |
|
R1016:Ncapg2
|
UTSW |
12 |
116,402,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R1507:Ncapg2
|
UTSW |
12 |
116,424,186 (GRCm39) |
missense |
probably benign |
0.00 |
R1524:Ncapg2
|
UTSW |
12 |
116,398,198 (GRCm39) |
splice site |
probably benign |
|
R1596:Ncapg2
|
UTSW |
12 |
116,382,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Ncapg2
|
UTSW |
12 |
116,398,305 (GRCm39) |
frame shift |
probably null |
|
R1752:Ncapg2
|
UTSW |
12 |
116,390,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R2164:Ncapg2
|
UTSW |
12 |
116,414,095 (GRCm39) |
splice site |
probably null |
|
R2266:Ncapg2
|
UTSW |
12 |
116,393,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2366:Ncapg2
|
UTSW |
12 |
116,384,349 (GRCm39) |
nonsense |
probably null |
|
R2924:Ncapg2
|
UTSW |
12 |
116,402,349 (GRCm39) |
missense |
probably benign |
0.03 |
R2925:Ncapg2
|
UTSW |
12 |
116,402,349 (GRCm39) |
missense |
probably benign |
0.03 |
R3828:Ncapg2
|
UTSW |
12 |
116,370,938 (GRCm39) |
splice site |
probably benign |
|
R3829:Ncapg2
|
UTSW |
12 |
116,370,938 (GRCm39) |
splice site |
probably benign |
|
R4384:Ncapg2
|
UTSW |
12 |
116,403,497 (GRCm39) |
critical splice donor site |
probably null |
|
R4651:Ncapg2
|
UTSW |
12 |
116,389,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Ncapg2
|
UTSW |
12 |
116,404,238 (GRCm39) |
missense |
probably benign |
|
R4821:Ncapg2
|
UTSW |
12 |
116,379,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R4845:Ncapg2
|
UTSW |
12 |
116,404,208 (GRCm39) |
missense |
probably damaging |
0.96 |
R5135:Ncapg2
|
UTSW |
12 |
116,391,406 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5294:Ncapg2
|
UTSW |
12 |
116,391,414 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5334:Ncapg2
|
UTSW |
12 |
116,390,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Ncapg2
|
UTSW |
12 |
116,376,697 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5888:Ncapg2
|
UTSW |
12 |
116,389,420 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5938:Ncapg2
|
UTSW |
12 |
116,393,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R5978:Ncapg2
|
UTSW |
12 |
116,388,291 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6016:Ncapg2
|
UTSW |
12 |
116,390,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6026:Ncapg2
|
UTSW |
12 |
116,406,641 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6155:Ncapg2
|
UTSW |
12 |
116,401,631 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6509:Ncapg2
|
UTSW |
12 |
116,391,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R6675:Ncapg2
|
UTSW |
12 |
116,398,281 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6912:Ncapg2
|
UTSW |
12 |
116,390,202 (GRCm39) |
missense |
probably benign |
|
R7339:Ncapg2
|
UTSW |
12 |
116,378,454 (GRCm39) |
missense |
probably damaging |
0.96 |
R7440:Ncapg2
|
UTSW |
12 |
116,414,033 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7445:Ncapg2
|
UTSW |
12 |
116,382,888 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7704:Ncapg2
|
UTSW |
12 |
116,382,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Ncapg2
|
UTSW |
12 |
116,390,197 (GRCm39) |
missense |
probably benign |
|
R8132:Ncapg2
|
UTSW |
12 |
116,407,967 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8166:Ncapg2
|
UTSW |
12 |
116,376,036 (GRCm39) |
missense |
probably benign |
0.00 |
R8351:Ncapg2
|
UTSW |
12 |
116,403,647 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8526:Ncapg2
|
UTSW |
12 |
116,403,679 (GRCm39) |
missense |
probably benign |
0.00 |
R8692:Ncapg2
|
UTSW |
12 |
116,414,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R8739:Ncapg2
|
UTSW |
12 |
116,379,098 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8766:Ncapg2
|
UTSW |
12 |
116,390,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R8929:Ncapg2
|
UTSW |
12 |
116,415,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R9046:Ncapg2
|
UTSW |
12 |
116,376,145 (GRCm39) |
missense |
probably benign |
0.01 |
R9187:Ncapg2
|
UTSW |
12 |
116,402,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R9344:Ncapg2
|
UTSW |
12 |
116,388,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R9444:Ncapg2
|
UTSW |
12 |
116,370,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R9580:Ncapg2
|
UTSW |
12 |
116,424,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R9634:Ncapg2
|
UTSW |
12 |
116,379,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R9749:Ncapg2
|
UTSW |
12 |
116,411,368 (GRCm39) |
nonsense |
probably null |
|
X0020:Ncapg2
|
UTSW |
12 |
116,388,327 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ncapg2
|
UTSW |
12 |
116,402,225 (GRCm39) |
missense |
probably damaging |
0.99 |
|