Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
T |
2: 68,731,964 (GRCm38) |
M312L |
probably benign |
Het |
Adam7 |
C |
A |
14: 68,507,856 (GRCm38) |
D640Y |
possibly damaging |
Het |
Alcam |
T |
C |
16: 52,274,236 (GRCm38) |
Y384C |
probably damaging |
Het |
Apob |
A |
G |
12: 8,013,737 (GRCm38) |
E289G |
probably damaging |
Het |
Arhgap15 |
A |
T |
2: 44,063,857 (GRCm38) |
R198S |
probably benign |
Het |
Bbs2 |
G |
T |
8: 94,092,414 (GRCm38) |
S109* |
probably null |
Het |
Bfsp1 |
T |
C |
2: 143,826,971 (GRCm38) |
S569G |
probably benign |
Het |
Chst9 |
A |
T |
18: 15,453,239 (GRCm38) |
I89N |
probably benign |
Het |
Cntln |
A |
C |
4: 84,971,229 (GRCm38) |
E316D |
probably benign |
Het |
Csde1 |
T |
G |
3: 103,039,934 (GRCm38) |
D67E |
probably damaging |
Het |
Csf2rb |
T |
G |
15: 78,349,057 (GRCm38) |
S855A |
possibly damaging |
Het |
Cyp4a10 |
T |
A |
4: 115,532,615 (GRCm38) |
D472E |
probably damaging |
Het |
Cyp4f18 |
C |
A |
8: 72,009,096 (GRCm38) |
R49L |
probably benign |
Het |
Daam1 |
G |
T |
12: 71,944,274 (GRCm38) |
V221L |
unknown |
Het |
Dbr1 |
T |
G |
9: 99,583,891 (GRCm38) |
D507E |
probably benign |
Het |
Dhrs7c |
A |
G |
11: 67,815,801 (GRCm38) |
M188V |
probably benign |
Het |
Dicer1 |
A |
T |
12: 104,694,731 (GRCm38) |
L1688* |
probably null |
Het |
Dmpk |
C |
G |
7: 19,088,019 (GRCm38) |
L301V |
probably benign |
Het |
E2f3 |
G |
A |
13: 29,918,636 (GRCm38) |
T91I |
probably damaging |
Het |
Etaa1 |
A |
T |
11: 17,947,853 (GRCm38) |
V157E |
probably damaging |
Het |
Foxp2 |
A |
T |
6: 15,394,771 (GRCm38) |
T157S |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,551,346 (GRCm38) |
V2034A |
probably benign |
Het |
Fzd10 |
T |
C |
5: 128,602,116 (GRCm38) |
V300A |
possibly damaging |
Het |
Gbf1 |
A |
T |
19: 46,268,454 (GRCm38) |
M778L |
probably benign |
Het |
Gm17472 |
T |
A |
6: 42,981,134 (GRCm38) |
N112K |
probably benign |
Het |
Gria4 |
T |
C |
9: 4,424,330 (GRCm38) |
K845R |
probably benign |
Het |
Hspa4l |
T |
A |
3: 40,781,569 (GRCm38) |
S541T |
probably benign |
Het |
Igkv4-68 |
G |
A |
6: 69,304,942 (GRCm38) |
R82C |
probably damaging |
Het |
Itgb1 |
A |
T |
8: 128,720,010 (GRCm38) |
I383F |
probably damaging |
Het |
Kcnk12 |
T |
A |
17: 87,746,605 (GRCm38) |
K210* |
probably null |
Het |
Limch1 |
C |
G |
5: 66,993,173 (GRCm38) |
D163E |
probably damaging |
Het |
Mbd4 |
A |
T |
6: 115,849,402 (GRCm38) |
D188E |
probably damaging |
Het |
Myh9 |
C |
T |
15: 77,781,110 (GRCm38) |
|
probably null |
Het |
Nfatc4 |
A |
G |
14: 55,826,659 (GRCm38) |
E201G |
probably damaging |
Het |
Nrap |
G |
A |
19: 56,335,151 (GRCm38) |
H1330Y |
probably damaging |
Het |
Nudt14 |
A |
G |
12: 112,935,028 (GRCm38) |
S151P |
probably damaging |
Het |
Olfr297 |
C |
A |
7: 86,527,116 (GRCm38) |
R120S |
probably damaging |
Het |
Olfr58 |
T |
A |
9: 19,783,218 (GRCm38) |
F28L |
possibly damaging |
Het |
Olfr706 |
T |
A |
7: 106,886,596 (GRCm38) |
T74S |
possibly damaging |
Het |
Otx1 |
C |
A |
11: 21,997,037 (GRCm38) |
A91S |
probably damaging |
Het |
Paqr9 |
A |
G |
9: 95,560,110 (GRCm38) |
D51G |
probably damaging |
Het |
Pcgf5 |
T |
A |
19: 36,437,183 (GRCm38) |
F80I |
probably damaging |
Het |
Pkhd1 |
T |
G |
1: 20,547,341 (GRCm38) |
S1007R |
probably benign |
Het |
Rab30 |
T |
C |
7: 92,835,913 (GRCm38) |
Y196H |
probably benign |
Het |
Setd2 |
A |
T |
9: 110,551,230 (GRCm38) |
D1371V |
probably damaging |
Het |
Slc48a1 |
A |
T |
15: 97,790,700 (GRCm38) |
I140F |
possibly damaging |
Het |
Sorl1 |
A |
G |
9: 42,033,583 (GRCm38) |
V882A |
probably benign |
Het |
Sptbn2 |
G |
T |
19: 4,724,184 (GRCm38) |
G88W |
probably damaging |
Het |
Tdrd12 |
A |
G |
7: 35,490,030 (GRCm38) |
V427A |
possibly damaging |
Het |
Tekt2 |
T |
C |
4: 126,324,670 (GRCm38) |
D69G |
probably benign |
Het |
Tie1 |
C |
T |
4: 118,480,510 (GRCm38) |
V463I |
probably benign |
Het |
Tmem150c |
G |
T |
5: 100,079,954 (GRCm38) |
H217N |
probably damaging |
Het |
Tnks2 |
G |
A |
19: 36,888,852 (GRCm38) |
G1080R |
probably damaging |
Het |
Ttll4 |
G |
A |
1: 74,687,852 (GRCm38) |
|
probably null |
Het |
|
Other mutations in Nbeal2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Nbeal2
|
APN |
9 |
110,635,869 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00784:Nbeal2
|
APN |
9 |
110,629,763 (GRCm38) |
splice site |
probably benign |
|
IGL00826:Nbeal2
|
APN |
9 |
110,626,903 (GRCm38) |
missense |
probably benign |
|
IGL00885:Nbeal2
|
APN |
9 |
110,638,661 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01348:Nbeal2
|
APN |
9 |
110,629,146 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01511:Nbeal2
|
APN |
9 |
110,629,234 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01571:Nbeal2
|
APN |
9 |
110,632,758 (GRCm38) |
missense |
possibly damaging |
0.63 |
IGL01612:Nbeal2
|
APN |
9 |
110,644,678 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01924:Nbeal2
|
APN |
9 |
110,631,414 (GRCm38) |
missense |
probably benign |
0.23 |
IGL02056:Nbeal2
|
APN |
9 |
110,627,324 (GRCm38) |
missense |
probably benign |
0.17 |
IGL02481:Nbeal2
|
APN |
9 |
110,625,995 (GRCm38) |
nonsense |
probably null |
|
IGL02483:Nbeal2
|
APN |
9 |
110,625,995 (GRCm38) |
nonsense |
probably null |
|
IGL02502:Nbeal2
|
APN |
9 |
110,633,768 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02631:Nbeal2
|
APN |
9 |
110,630,208 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02637:Nbeal2
|
APN |
9 |
110,625,977 (GRCm38) |
missense |
possibly damaging |
0.62 |
IGL02727:Nbeal2
|
APN |
9 |
110,639,285 (GRCm38) |
splice site |
probably benign |
|
IGL02887:Nbeal2
|
APN |
9 |
110,628,276 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02896:Nbeal2
|
APN |
9 |
110,639,292 (GRCm38) |
critical splice donor site |
probably null |
|
IGL03110:Nbeal2
|
APN |
9 |
110,631,433 (GRCm38) |
missense |
probably damaging |
1.00 |
Antonym
|
UTSW |
9 |
110,630,252 (GRCm38) |
missense |
probably damaging |
1.00 |
Beowulf
|
UTSW |
9 |
110,637,937 (GRCm38) |
missense |
possibly damaging |
0.65 |
Blackmail
|
UTSW |
9 |
110,629,639 (GRCm38) |
missense |
probably damaging |
1.00 |
dog
|
UTSW |
9 |
110,635,341 (GRCm38) |
missense |
possibly damaging |
0.89 |
extortion
|
UTSW |
9 |
110,630,243 (GRCm38) |
missense |
probably damaging |
1.00 |
legion
|
UTSW |
9 |
110,629,179 (GRCm38) |
missense |
probably damaging |
1.00 |
litigious
|
UTSW |
9 |
110,628,195 (GRCm38) |
missense |
probably damaging |
1.00 |
mall
|
UTSW |
9 |
110,632,886 (GRCm38) |
missense |
probably damaging |
1.00 |
Mollusca
|
UTSW |
9 |
110,645,438 (GRCm38) |
splice site |
probably null |
|
Schleuter
|
UTSW |
9 |
110,628,744 (GRCm38) |
missense |
possibly damaging |
0.69 |
shellfish
|
UTSW |
9 |
110,628,720 (GRCm38) |
missense |
probably damaging |
1.00 |
Sophomoric
|
UTSW |
9 |
110,633,047 (GRCm38) |
missense |
probably damaging |
1.00 |
F5770:Nbeal2
|
UTSW |
9 |
110,637,937 (GRCm38) |
missense |
possibly damaging |
0.65 |
R0032:Nbeal2
|
UTSW |
9 |
110,637,868 (GRCm38) |
splice site |
probably benign |
|
R0084:Nbeal2
|
UTSW |
9 |
110,643,710 (GRCm38) |
critical splice donor site |
probably null |
|
R0147:Nbeal2
|
UTSW |
9 |
110,642,143 (GRCm38) |
nonsense |
probably null |
|
R0294:Nbeal2
|
UTSW |
9 |
110,632,859 (GRCm38) |
missense |
probably damaging |
1.00 |
R0310:Nbeal2
|
UTSW |
9 |
110,638,163 (GRCm38) |
missense |
probably damaging |
1.00 |
R0494:Nbeal2
|
UTSW |
9 |
110,627,187 (GRCm38) |
missense |
probably damaging |
1.00 |
R0550:Nbeal2
|
UTSW |
9 |
110,642,158 (GRCm38) |
missense |
probably benign |
0.01 |
R0630:Nbeal2
|
UTSW |
9 |
110,636,034 (GRCm38) |
splice site |
probably benign |
|
R0762:Nbeal2
|
UTSW |
9 |
110,643,808 (GRCm38) |
splice site |
probably benign |
|
R0862:Nbeal2
|
UTSW |
9 |
110,628,195 (GRCm38) |
missense |
probably damaging |
1.00 |
R0864:Nbeal2
|
UTSW |
9 |
110,628,195 (GRCm38) |
missense |
probably damaging |
1.00 |
R1225:Nbeal2
|
UTSW |
9 |
110,632,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R1240:Nbeal2
|
UTSW |
9 |
110,627,108 (GRCm38) |
missense |
probably damaging |
0.98 |
R1450:Nbeal2
|
UTSW |
9 |
110,633,672 (GRCm38) |
splice site |
probably benign |
|
R1519:Nbeal2
|
UTSW |
9 |
110,636,305 (GRCm38) |
missense |
probably damaging |
1.00 |
R1655:Nbeal2
|
UTSW |
9 |
110,632,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R1668:Nbeal2
|
UTSW |
9 |
110,638,893 (GRCm38) |
missense |
probably damaging |
1.00 |
R1705:Nbeal2
|
UTSW |
9 |
110,625,196 (GRCm38) |
missense |
probably damaging |
1.00 |
R1784:Nbeal2
|
UTSW |
9 |
110,630,857 (GRCm38) |
nonsense |
probably null |
|
R1834:Nbeal2
|
UTSW |
9 |
110,627,129 (GRCm38) |
missense |
probably damaging |
1.00 |
R1997:Nbeal2
|
UTSW |
9 |
110,632,198 (GRCm38) |
missense |
probably damaging |
1.00 |
R2013:Nbeal2
|
UTSW |
9 |
110,634,071 (GRCm38) |
missense |
probably benign |
0.09 |
R2014:Nbeal2
|
UTSW |
9 |
110,634,071 (GRCm38) |
missense |
probably benign |
0.09 |
R2055:Nbeal2
|
UTSW |
9 |
110,635,307 (GRCm38) |
missense |
possibly damaging |
0.92 |
R2086:Nbeal2
|
UTSW |
9 |
110,634,071 (GRCm38) |
missense |
probably benign |
0.09 |
R2113:Nbeal2
|
UTSW |
9 |
110,625,406 (GRCm38) |
missense |
probably damaging |
1.00 |
R2167:Nbeal2
|
UTSW |
9 |
110,638,308 (GRCm38) |
missense |
probably damaging |
1.00 |
R2201:Nbeal2
|
UTSW |
9 |
110,630,250 (GRCm38) |
missense |
probably benign |
0.16 |
R2309:Nbeal2
|
UTSW |
9 |
110,626,570 (GRCm38) |
missense |
probably damaging |
1.00 |
R2378:Nbeal2
|
UTSW |
9 |
110,630,808 (GRCm38) |
missense |
probably damaging |
0.99 |
R2945:Nbeal2
|
UTSW |
9 |
110,628,068 (GRCm38) |
missense |
possibly damaging |
0.82 |
R3052:Nbeal2
|
UTSW |
9 |
110,633,085 (GRCm38) |
missense |
possibly damaging |
0.93 |
R3076:Nbeal2
|
UTSW |
9 |
110,631,700 (GRCm38) |
missense |
probably damaging |
1.00 |
R3176:Nbeal2
|
UTSW |
9 |
110,636,887 (GRCm38) |
splice site |
probably benign |
|
R3974:Nbeal2
|
UTSW |
9 |
110,633,846 (GRCm38) |
missense |
probably damaging |
1.00 |
R4183:Nbeal2
|
UTSW |
9 |
110,636,675 (GRCm38) |
missense |
probably benign |
|
R4342:Nbeal2
|
UTSW |
9 |
110,631,793 (GRCm38) |
intron |
probably benign |
|
R4654:Nbeal2
|
UTSW |
9 |
110,632,004 (GRCm38) |
missense |
probably damaging |
1.00 |
R4707:Nbeal2
|
UTSW |
9 |
110,632,055 (GRCm38) |
missense |
probably benign |
0.10 |
R4822:Nbeal2
|
UTSW |
9 |
110,636,315 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4854:Nbeal2
|
UTSW |
9 |
110,631,396 (GRCm38) |
missense |
probably damaging |
1.00 |
R4860:Nbeal2
|
UTSW |
9 |
110,635,194 (GRCm38) |
missense |
probably benign |
0.00 |
R4860:Nbeal2
|
UTSW |
9 |
110,635,194 (GRCm38) |
missense |
probably benign |
0.00 |
R4990:Nbeal2
|
UTSW |
9 |
110,634,803 (GRCm38) |
missense |
probably benign |
0.10 |
R4991:Nbeal2
|
UTSW |
9 |
110,638,767 (GRCm38) |
missense |
probably damaging |
1.00 |
R5021:Nbeal2
|
UTSW |
9 |
110,637,463 (GRCm38) |
missense |
probably damaging |
0.99 |
R5057:Nbeal2
|
UTSW |
9 |
110,631,005 (GRCm38) |
missense |
probably damaging |
1.00 |
R5092:Nbeal2
|
UTSW |
9 |
110,626,728 (GRCm38) |
splice site |
probably null |
|
R5161:Nbeal2
|
UTSW |
9 |
110,629,868 (GRCm38) |
missense |
probably benign |
|
R5217:Nbeal2
|
UTSW |
9 |
110,632,090 (GRCm38) |
missense |
possibly damaging |
0.56 |
R5408:Nbeal2
|
UTSW |
9 |
110,637,520 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5540:Nbeal2
|
UTSW |
9 |
110,631,733 (GRCm38) |
missense |
probably damaging |
1.00 |
R5866:Nbeal2
|
UTSW |
9 |
110,631,492 (GRCm38) |
missense |
probably damaging |
1.00 |
R5925:Nbeal2
|
UTSW |
9 |
110,629,880 (GRCm38) |
missense |
probably benign |
0.00 |
R6057:Nbeal2
|
UTSW |
9 |
110,641,877 (GRCm38) |
missense |
possibly damaging |
0.81 |
R6180:Nbeal2
|
UTSW |
9 |
110,625,147 (GRCm38) |
missense |
probably damaging |
1.00 |
R6191:Nbeal2
|
UTSW |
9 |
110,627,990 (GRCm38) |
critical splice donor site |
probably null |
|
R6232:Nbeal2
|
UTSW |
9 |
110,638,734 (GRCm38) |
missense |
probably damaging |
1.00 |
R6372:Nbeal2
|
UTSW |
9 |
110,628,744 (GRCm38) |
missense |
possibly damaging |
0.69 |
R6423:Nbeal2
|
UTSW |
9 |
110,625,994 (GRCm38) |
missense |
probably damaging |
1.00 |
R6543:Nbeal2
|
UTSW |
9 |
110,644,458 (GRCm38) |
missense |
probably benign |
|
R6648:Nbeal2
|
UTSW |
9 |
110,637,642 (GRCm38) |
missense |
probably damaging |
1.00 |
R6722:Nbeal2
|
UTSW |
9 |
110,632,992 (GRCm38) |
missense |
probably damaging |
1.00 |
R6738:Nbeal2
|
UTSW |
9 |
110,636,905 (GRCm38) |
missense |
possibly damaging |
0.93 |
R6916:Nbeal2
|
UTSW |
9 |
110,626,108 (GRCm38) |
missense |
probably damaging |
1.00 |
R6935:Nbeal2
|
UTSW |
9 |
110,639,391 (GRCm38) |
missense |
probably damaging |
1.00 |
R7022:Nbeal2
|
UTSW |
9 |
110,638,618 (GRCm38) |
missense |
probably damaging |
1.00 |
R7023:Nbeal2
|
UTSW |
9 |
110,638,618 (GRCm38) |
missense |
probably damaging |
1.00 |
R7050:Nbeal2
|
UTSW |
9 |
110,628,720 (GRCm38) |
missense |
probably damaging |
1.00 |
R7072:Nbeal2
|
UTSW |
9 |
110,626,051 (GRCm38) |
missense |
probably benign |
0.01 |
R7073:Nbeal2
|
UTSW |
9 |
110,626,109 (GRCm38) |
missense |
probably damaging |
0.99 |
R7099:Nbeal2
|
UTSW |
9 |
110,645,438 (GRCm38) |
splice site |
probably null |
|
R7354:Nbeal2
|
UTSW |
9 |
110,629,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R7394:Nbeal2
|
UTSW |
9 |
110,630,189 (GRCm38) |
critical splice donor site |
probably null |
|
R7397:Nbeal2
|
UTSW |
9 |
110,628,032 (GRCm38) |
missense |
possibly damaging |
0.78 |
R7552:Nbeal2
|
UTSW |
9 |
110,653,917 (GRCm38) |
missense |
probably benign |
0.16 |
R7619:Nbeal2
|
UTSW |
9 |
110,625,818 (GRCm38) |
missense |
probably benign |
0.19 |
R7821:Nbeal2
|
UTSW |
9 |
110,630,252 (GRCm38) |
missense |
probably damaging |
1.00 |
R7902:Nbeal2
|
UTSW |
9 |
110,637,547 (GRCm38) |
missense |
probably benign |
|
R7923:Nbeal2
|
UTSW |
9 |
110,631,446 (GRCm38) |
nonsense |
probably null |
|
R8018:Nbeal2
|
UTSW |
9 |
110,629,157 (GRCm38) |
unclassified |
probably benign |
|
R8190:Nbeal2
|
UTSW |
9 |
110,626,090 (GRCm38) |
missense |
probably benign |
0.04 |
R8297:Nbeal2
|
UTSW |
9 |
110,635,341 (GRCm38) |
missense |
possibly damaging |
0.89 |
R8404:Nbeal2
|
UTSW |
9 |
110,634,389 (GRCm38) |
missense |
possibly damaging |
0.48 |
R8502:Nbeal2
|
UTSW |
9 |
110,634,389 (GRCm38) |
missense |
possibly damaging |
0.48 |
R8737:Nbeal2
|
UTSW |
9 |
110,627,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R8782:Nbeal2
|
UTSW |
9 |
110,630,805 (GRCm38) |
missense |
probably benign |
0.04 |
R8807:Nbeal2
|
UTSW |
9 |
110,629,639 (GRCm38) |
missense |
probably damaging |
1.00 |
R8877:Nbeal2
|
UTSW |
9 |
110,630,243 (GRCm38) |
missense |
probably damaging |
1.00 |
R9057:Nbeal2
|
UTSW |
9 |
110,627,150 (GRCm38) |
missense |
probably benign |
|
R9267:Nbeal2
|
UTSW |
9 |
110,633,047 (GRCm38) |
missense |
probably damaging |
1.00 |
R9313:Nbeal2
|
UTSW |
9 |
110,634,368 (GRCm38) |
missense |
probably damaging |
1.00 |
R9352:Nbeal2
|
UTSW |
9 |
110,627,848 (GRCm38) |
missense |
probably benign |
0.03 |
R9482:Nbeal2
|
UTSW |
9 |
110,633,998 (GRCm38) |
missense |
probably benign |
0.25 |
R9533:Nbeal2
|
UTSW |
9 |
110,644,661 (GRCm38) |
missense |
probably benign |
0.01 |
R9566:Nbeal2
|
UTSW |
9 |
110,628,921 (GRCm38) |
missense |
probably benign |
0.00 |
R9769:Nbeal2
|
UTSW |
9 |
110,626,279 (GRCm38) |
missense |
probably benign |
0.01 |
V7583:Nbeal2
|
UTSW |
9 |
110,637,937 (GRCm38) |
missense |
possibly damaging |
0.65 |
X0017:Nbeal2
|
UTSW |
9 |
110,644,278 (GRCm38) |
missense |
probably benign |
0.02 |
X0065:Nbeal2
|
UTSW |
9 |
110,644,413 (GRCm38) |
splice site |
probably benign |
|
Z1088:Nbeal2
|
UTSW |
9 |
110,632,372 (GRCm38) |
missense |
possibly damaging |
0.51 |
Z1176:Nbeal2
|
UTSW |
9 |
110,638,835 (GRCm38) |
missense |
probably benign |
|
Z1176:Nbeal2
|
UTSW |
9 |
110,625,816 (GRCm38) |
missense |
probably benign |
0.01 |
Z1177:Nbeal2
|
UTSW |
9 |
110,629,854 (GRCm38) |
missense |
probably benign |
0.03 |
|