Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630089N07Rik |
C |
T |
16: 97,867,651 (GRCm39) |
A104T |
probably damaging |
Het |
Abhd18 |
T |
A |
3: 40,884,627 (GRCm39) |
L222Q |
probably damaging |
Het |
Adam30 |
C |
T |
3: 98,070,348 (GRCm39) |
T727M |
possibly damaging |
Het |
Adh6b |
A |
T |
3: 138,058,729 (GRCm39) |
Q137L |
probably damaging |
Het |
Alpl |
C |
T |
4: 137,475,127 (GRCm39) |
V269I |
probably benign |
Het |
Ang2 |
C |
T |
14: 51,432,996 (GRCm39) |
G129S |
probably benign |
Het |
Atp6v0a1 |
A |
T |
11: 100,920,015 (GRCm39) |
H216L |
possibly damaging |
Het |
BC030500 |
C |
T |
8: 59,366,049 (GRCm39) |
T61I |
unknown |
Het |
Brpf1 |
T |
G |
6: 113,293,491 (GRCm39) |
L520R |
probably damaging |
Het |
Btbd10 |
A |
G |
7: 112,927,626 (GRCm39) |
I243T |
possibly damaging |
Het |
Bub1 |
C |
A |
2: 127,646,139 (GRCm39) |
C947F |
probably damaging |
Het |
C4b |
T |
C |
17: 34,953,459 (GRCm39) |
E1008G |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,155,323 (GRCm39) |
T1188A |
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,875,485 (GRCm39) |
T1770A |
unknown |
Het |
Cnn1 |
G |
T |
9: 22,010,557 (GRCm39) |
|
probably benign |
Het |
Colgalt2 |
T |
C |
1: 152,360,662 (GRCm39) |
M233T |
probably damaging |
Het |
Cox15 |
A |
T |
19: 43,735,181 (GRCm39) |
C195* |
probably null |
Het |
Cped1 |
A |
T |
6: 22,059,941 (GRCm39) |
R202S |
possibly damaging |
Het |
Dact2 |
A |
T |
17: 14,417,146 (GRCm39) |
C351* |
probably null |
Het |
Dbnl |
A |
G |
11: 5,738,582 (GRCm39) |
N8S |
probably benign |
Het |
Depdc1a |
T |
A |
3: 159,228,356 (GRCm39) |
N369K |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,415,005 (GRCm39) |
L243Q |
probably damaging |
Het |
Dscaml1 |
T |
A |
9: 45,341,759 (GRCm39) |
Y57N |
probably benign |
Het |
Eif2b3 |
A |
G |
4: 116,927,944 (GRCm39) |
T388A |
probably benign |
Het |
Eif4h |
A |
C |
5: 134,654,393 (GRCm39) |
|
probably null |
Het |
Elf1 |
C |
T |
14: 79,810,667 (GRCm39) |
Q288* |
probably null |
Het |
Fgl2 |
C |
T |
5: 21,580,677 (GRCm39) |
R340* |
probably null |
Het |
Fut4 |
T |
C |
9: 14,662,082 (GRCm39) |
D404G |
probably damaging |
Het |
Glmn |
G |
A |
5: 107,718,152 (GRCm39) |
P255L |
probably benign |
Het |
Gm14322 |
C |
T |
2: 177,411,481 (GRCm39) |
T97I |
probably benign |
Het |
Gm44511 |
C |
A |
6: 128,797,997 (GRCm39) |
C32F |
probably damaging |
Het |
Gm5478 |
A |
G |
15: 101,553,871 (GRCm39) |
F247S |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,739,563 (GRCm39) |
M2675K |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,849,000 (GRCm39) |
D368G |
possibly damaging |
Het |
Hnrnpul2 |
A |
G |
19: 8,798,064 (GRCm39) |
N140S |
probably benign |
Het |
Htr4 |
A |
T |
18: 62,561,209 (GRCm39) |
I157L |
probably damaging |
Het |
Kcnma1 |
T |
G |
14: 23,436,332 (GRCm39) |
M790L |
probably benign |
Het |
Kcnv1 |
G |
A |
15: 44,977,999 (GRCm39) |
S13L |
unknown |
Het |
Kctd20 |
C |
T |
17: 29,184,025 (GRCm39) |
R312* |
probably null |
Het |
Kdm3b |
T |
A |
18: 34,960,435 (GRCm39) |
I1340N |
probably damaging |
Het |
Kdm6b |
A |
G |
11: 69,292,919 (GRCm39) |
F1286L |
unknown |
Het |
Knl1 |
T |
A |
2: 118,899,524 (GRCm39) |
F408L |
probably benign |
Het |
Lypd5 |
G |
T |
7: 24,053,101 (GRCm39) |
G253W |
probably damaging |
Het |
Mea1 |
A |
G |
17: 46,992,614 (GRCm39) |
T21A |
probably benign |
Het |
Metrnl |
A |
G |
11: 121,606,842 (GRCm39) |
E299G |
possibly damaging |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Nxpe2 |
A |
T |
9: 48,238,073 (GRCm39) |
F61I |
probably benign |
Het |
Or6c1b |
T |
C |
10: 129,273,334 (GRCm39) |
Y218H |
probably benign |
Het |
Or6c70 |
T |
A |
10: 129,710,092 (GRCm39) |
D178V |
probably damaging |
Het |
Pgr |
C |
A |
9: 8,901,544 (GRCm39) |
P359Q |
probably damaging |
Het |
Pi4k2b |
G |
A |
5: 52,908,031 (GRCm39) |
V157I |
probably benign |
Het |
Plekhm1 |
A |
C |
11: 103,258,444 (GRCm39) |
F1031L |
probably damaging |
Het |
Pltp |
A |
G |
2: 164,696,301 (GRCm39) |
S124P |
probably damaging |
Het |
Polr3gl |
T |
A |
3: 96,487,154 (GRCm39) |
E177V |
probably benign |
Het |
Pstk |
G |
T |
7: 130,973,024 (GRCm39) |
R41L |
possibly damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,119,158 (GRCm39) |
E493G |
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,434,726 (GRCm39) |
L422P |
probably benign |
Het |
Rusc2 |
C |
T |
4: 43,401,351 (GRCm39) |
|
probably benign |
Het |
Sbno2 |
A |
G |
10: 79,911,090 (GRCm39) |
F6S |
probably benign |
Het |
Sh2d4a |
A |
G |
8: 68,798,695 (GRCm39) |
Y348C |
probably damaging |
Het |
Sh3rf3 |
A |
G |
10: 58,939,992 (GRCm39) |
|
probably null |
Het |
Sipa1l2 |
T |
C |
8: 126,177,125 (GRCm39) |
E1163G |
probably benign |
Het |
Strip1 |
G |
C |
3: 107,521,964 (GRCm39) |
A738G |
probably damaging |
Het |
Tdrkh |
C |
T |
3: 94,333,299 (GRCm39) |
R255C |
probably benign |
Het |
Tln1 |
A |
T |
4: 43,555,911 (GRCm39) |
M101K |
possibly damaging |
Het |
Trav6-2 |
A |
C |
14: 52,905,028 (GRCm39) |
|
probably benign |
Het |
Tspan11 |
A |
T |
6: 127,900,674 (GRCm39) |
I82F |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,779,320 (GRCm39) |
K1233E |
unknown |
Het |
Usp29 |
A |
T |
7: 6,965,917 (GRCm39) |
S587C |
probably damaging |
Het |
Vmn1r235 |
A |
T |
17: 21,482,056 (GRCm39) |
Q127L |
probably damaging |
Het |
Vmn1r65 |
C |
A |
7: 6,011,503 (GRCm39) |
A244S |
probably damaging |
Het |
Vmn2r18 |
A |
G |
5: 151,508,462 (GRCm39) |
S221P |
probably damaging |
Het |
Zfp229 |
T |
C |
17: 21,964,828 (GRCm39) |
S353P |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,930,150 (GRCm39) |
K52E |
probably benign |
Het |
|
Other mutations in Nbn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00833:Nbn
|
APN |
4 |
15,964,320 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00921:Nbn
|
APN |
4 |
15,963,833 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01621:Nbn
|
APN |
4 |
15,965,221 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02372:Nbn
|
APN |
4 |
15,986,613 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03392:Nbn
|
APN |
4 |
15,962,362 (GRCm39) |
missense |
probably damaging |
1.00 |
nebish
|
UTSW |
4 |
15,965,132 (GRCm39) |
critical splice acceptor site |
probably null |
|
zenobia
|
UTSW |
4 |
15,969,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Nbn
|
UTSW |
4 |
15,986,672 (GRCm39) |
splice site |
probably benign |
|
R0244:Nbn
|
UTSW |
4 |
15,979,353 (GRCm39) |
missense |
probably benign |
0.00 |
R0432:Nbn
|
UTSW |
4 |
15,983,951 (GRCm39) |
unclassified |
probably benign |
|
R0946:Nbn
|
UTSW |
4 |
15,970,719 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1076:Nbn
|
UTSW |
4 |
15,970,719 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1563:Nbn
|
UTSW |
4 |
15,981,668 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1579:Nbn
|
UTSW |
4 |
15,964,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R1660:Nbn
|
UTSW |
4 |
15,971,771 (GRCm39) |
missense |
probably benign |
0.06 |
R1663:Nbn
|
UTSW |
4 |
15,970,903 (GRCm39) |
missense |
probably benign |
0.13 |
R2005:Nbn
|
UTSW |
4 |
15,979,351 (GRCm39) |
missense |
probably benign |
0.01 |
R2010:Nbn
|
UTSW |
4 |
15,969,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Nbn
|
UTSW |
4 |
15,979,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Nbn
|
UTSW |
4 |
15,970,904 (GRCm39) |
missense |
probably benign |
0.01 |
R2229:Nbn
|
UTSW |
4 |
15,970,904 (GRCm39) |
missense |
probably benign |
0.01 |
R2356:Nbn
|
UTSW |
4 |
15,970,863 (GRCm39) |
missense |
probably damaging |
0.96 |
R2869:Nbn
|
UTSW |
4 |
15,963,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Nbn
|
UTSW |
4 |
15,963,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3508:Nbn
|
UTSW |
4 |
15,962,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R3745:Nbn
|
UTSW |
4 |
15,976,163 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3753:Nbn
|
UTSW |
4 |
15,964,269 (GRCm39) |
missense |
probably damaging |
0.98 |
R4756:Nbn
|
UTSW |
4 |
15,981,470 (GRCm39) |
missense |
probably benign |
0.00 |
R5042:Nbn
|
UTSW |
4 |
15,981,446 (GRCm39) |
missense |
probably benign |
0.10 |
R5177:Nbn
|
UTSW |
4 |
15,965,132 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5229:Nbn
|
UTSW |
4 |
15,963,893 (GRCm39) |
missense |
probably damaging |
0.98 |
R5368:Nbn
|
UTSW |
4 |
15,969,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R5431:Nbn
|
UTSW |
4 |
15,986,593 (GRCm39) |
missense |
probably benign |
|
R6025:Nbn
|
UTSW |
4 |
15,981,347 (GRCm39) |
missense |
probably damaging |
0.97 |
R6375:Nbn
|
UTSW |
4 |
15,979,327 (GRCm39) |
missense |
probably benign |
|
R6543:Nbn
|
UTSW |
4 |
15,986,605 (GRCm39) |
missense |
probably benign |
0.39 |
R6655:Nbn
|
UTSW |
4 |
15,981,696 (GRCm39) |
missense |
probably damaging |
0.98 |
R6965:Nbn
|
UTSW |
4 |
15,970,863 (GRCm39) |
missense |
probably benign |
0.25 |
R7090:Nbn
|
UTSW |
4 |
15,981,350 (GRCm39) |
missense |
probably benign |
0.06 |
R7159:Nbn
|
UTSW |
4 |
15,983,677 (GRCm39) |
splice site |
probably null |
|
R7241:Nbn
|
UTSW |
4 |
15,991,190 (GRCm39) |
missense |
probably benign |
0.00 |
R7267:Nbn
|
UTSW |
4 |
15,979,320 (GRCm39) |
missense |
probably benign |
0.00 |
R7597:Nbn
|
UTSW |
4 |
15,963,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R7937:Nbn
|
UTSW |
4 |
15,958,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R8110:Nbn
|
UTSW |
4 |
15,981,588 (GRCm39) |
missense |
probably benign |
0.02 |
R8317:Nbn
|
UTSW |
4 |
15,970,893 (GRCm39) |
missense |
probably damaging |
0.96 |
R8327:Nbn
|
UTSW |
4 |
15,981,470 (GRCm39) |
missense |
probably benign |
0.00 |
R8727:Nbn
|
UTSW |
4 |
15,963,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R8747:Nbn
|
UTSW |
4 |
15,981,555 (GRCm39) |
missense |
probably damaging |
0.96 |
R8909:Nbn
|
UTSW |
4 |
15,970,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R8973:Nbn
|
UTSW |
4 |
15,986,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|