Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actbl2 |
G |
T |
13: 111,391,915 (GRCm39) |
M83I |
probably damaging |
Het |
Adgra2 |
T |
A |
8: 27,604,190 (GRCm39) |
M460K |
probably benign |
Het |
Aldh16a1 |
G |
A |
7: 44,799,189 (GRCm39) |
A31V |
probably damaging |
Het |
Ank2 |
T |
C |
3: 126,740,587 (GRCm39) |
|
probably benign |
Het |
Arrdc4 |
C |
A |
7: 68,398,793 (GRCm39) |
D8Y |
probably benign |
Het |
Auts2 |
A |
G |
5: 131,494,953 (GRCm39) |
Y110H |
probably damaging |
Het |
Blnk |
A |
T |
19: 40,922,903 (GRCm39) |
Y405N |
probably damaging |
Het |
Capsl |
T |
C |
15: 9,461,855 (GRCm39) |
F84L |
probably damaging |
Het |
Cdcp3 |
T |
C |
7: 130,858,735 (GRCm39) |
|
probably null |
Het |
Cenpl |
T |
C |
1: 160,902,465 (GRCm39) |
S46P |
probably benign |
Het |
Chd1l |
G |
A |
3: 97,494,483 (GRCm39) |
A399V |
probably damaging |
Het |
Chrnd |
C |
T |
1: 87,119,951 (GRCm39) |
R90C |
probably damaging |
Het |
Cyfip2 |
A |
T |
11: 46,182,347 (GRCm39) |
M37K |
probably benign |
Het |
Dnah11 |
T |
C |
12: 118,106,027 (GRCm39) |
E625G |
possibly damaging |
Het |
Dnah5 |
T |
G |
15: 28,372,557 (GRCm39) |
V2936G |
probably damaging |
Het |
Dock9 |
A |
G |
14: 121,783,433 (GRCm39) |
M2055T |
probably damaging |
Het |
Epb41l2 |
A |
T |
10: 25,344,026 (GRCm39) |
R274S |
probably damaging |
Het |
Erich3 |
A |
T |
3: 154,433,139 (GRCm39) |
H371L |
probably damaging |
Het |
Evi5l |
C |
A |
8: 4,253,080 (GRCm39) |
P454T |
probably benign |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Golgb1 |
T |
A |
16: 36,738,559 (GRCm39) |
C2299* |
probably null |
Het |
Heca |
G |
C |
10: 17,790,991 (GRCm39) |
|
probably null |
Het |
Hecw1 |
C |
T |
13: 14,697,414 (GRCm39) |
A9T |
probably benign |
Het |
Hs3st6 |
T |
A |
17: 24,977,542 (GRCm39) |
W341R |
probably damaging |
Het |
Kidins220 |
C |
T |
12: 25,107,533 (GRCm39) |
S1571L |
probably benign |
Het |
Klk1b9 |
A |
G |
7: 43,443,732 (GRCm39) |
E82G |
probably damaging |
Het |
Ltbp3 |
C |
A |
19: 5,795,685 (GRCm39) |
H180Q |
probably benign |
Het |
Mecom |
A |
G |
3: 30,034,741 (GRCm39) |
Y502H |
probably damaging |
Het |
Mfsd2a |
A |
G |
4: 122,843,165 (GRCm39) |
V372A |
probably benign |
Het |
Mrgprd |
A |
G |
7: 144,875,879 (GRCm39) |
D250G |
probably benign |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Naip6 |
C |
A |
13: 100,436,909 (GRCm39) |
S538I |
probably benign |
Het |
Or4f59 |
A |
G |
2: 111,873,113 (GRCm39) |
V88A |
probably benign |
Het |
Or52w1 |
A |
G |
7: 105,018,109 (GRCm39) |
Y192C |
probably damaging |
Het |
Pnpla6 |
T |
C |
8: 3,594,015 (GRCm39) |
V1342A |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,115,151 (GRCm39) |
E789G |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,532,783 (GRCm39) |
T1471A |
probably benign |
Het |
Scarb1 |
T |
A |
5: 125,381,395 (GRCm39) |
S50C |
probably damaging |
Het |
Slc4a8 |
C |
T |
15: 100,687,045 (GRCm39) |
T283M |
probably damaging |
Het |
Smc2 |
C |
A |
4: 52,462,814 (GRCm39) |
D601E |
probably benign |
Het |
Snx6 |
C |
A |
12: 54,798,798 (GRCm39) |
V221F |
probably damaging |
Het |
Spag17 |
A |
C |
3: 99,995,743 (GRCm39) |
K1794T |
probably benign |
Het |
Tpo |
A |
G |
12: 30,153,107 (GRCm39) |
W416R |
probably damaging |
Het |
Ttc13 |
C |
A |
8: 125,409,930 (GRCm39) |
K427N |
probably damaging |
Het |
Upf3a |
A |
T |
8: 13,837,466 (GRCm39) |
N137I |
possibly damaging |
Het |
Ush2a |
C |
T |
1: 188,581,243 (GRCm39) |
Q3708* |
probably null |
Het |
Zbtb17 |
G |
A |
4: 141,190,694 (GRCm39) |
G171S |
probably benign |
Het |
Zfp451 |
A |
G |
1: 33,852,816 (GRCm39) |
F33L |
probably damaging |
Het |
Zfp454 |
A |
G |
11: 50,763,876 (GRCm39) |
F408L |
probably damaging |
Het |
Zfp639 |
T |
C |
3: 32,571,237 (GRCm39) |
Y40H |
probably damaging |
Het |
|
Other mutations in Muc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
Eeyore
|
APN |
7 |
141,693,356 (GRCm38) |
missense |
probably benign |
0.35 |
kenny
|
APN |
7 |
0 () |
nonsense |
|
|
Winnie
|
APN |
7 |
141,286,029 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Muc2
|
APN |
7 |
141,306,132 (GRCm39) |
missense |
probably benign |
|
IGL01482:Muc2
|
APN |
7 |
141,307,797 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01875:Muc2
|
APN |
7 |
141,306,477 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02088:Muc2
|
APN |
7 |
141,305,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02415:Muc2
|
APN |
7 |
141,305,609 (GRCm39) |
nonsense |
probably null |
|
IGL02548:Muc2
|
APN |
7 |
141,305,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02836:Muc2
|
APN |
7 |
141,300,450 (GRCm39) |
unclassified |
probably benign |
|
IGL03196:Muc2
|
APN |
7 |
141,301,367 (GRCm39) |
missense |
probably damaging |
0.97 |
Muskatenwein
|
UTSW |
7 |
141,307,176 (GRCm39) |
missense |
unknown |
|
nomoco
|
UTSW |
7 |
141,307,456 (GRCm39) |
missense |
probably damaging |
1.00 |
Schlendrian
|
UTSW |
7 |
141,281,925 (GRCm39) |
missense |
probably damaging |
1.00 |
Seco
|
UTSW |
7 |
141,284,976 (GRCm39) |
missense |
probably damaging |
1.00 |
BB001:Muc2
|
UTSW |
7 |
141,281,631 (GRCm39) |
missense |
probably damaging |
1.00 |
BB011:Muc2
|
UTSW |
7 |
141,281,631 (GRCm39) |
missense |
probably damaging |
1.00 |
E0370:Muc2
|
UTSW |
7 |
141,282,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R0127:Muc2
|
UTSW |
7 |
141,302,691 (GRCm39) |
missense |
probably benign |
0.00 |
R0179:Muc2
|
UTSW |
7 |
141,302,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R0201:Muc2
|
UTSW |
7 |
141,699,185 (GRCm38) |
frame shift |
probably null |
|
R0299:Muc2
|
UTSW |
7 |
141,306,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R0547:Muc2
|
UTSW |
7 |
141,699,185 (GRCm38) |
frame shift |
probably null |
|
R0699:Muc2
|
UTSW |
7 |
141,306,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R0900:Muc2
|
UTSW |
7 |
141,699,185 (GRCm38) |
frame shift |
probably null |
|
R1348:Muc2
|
UTSW |
7 |
141,699,185 (GRCm38) |
frame shift |
probably null |
|
R1466:Muc2
|
UTSW |
7 |
141,302,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Muc2
|
UTSW |
7 |
141,302,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R1625:Muc2
|
UTSW |
7 |
141,283,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Muc2
|
UTSW |
7 |
141,287,444 (GRCm39) |
missense |
probably damaging |
0.99 |
R2149:Muc2
|
UTSW |
7 |
141,699,185 (GRCm38) |
frame shift |
probably null |
|
R2163:Muc2
|
UTSW |
7 |
141,699,185 (GRCm38) |
frame shift |
probably null |
|
R3008:Muc2
|
UTSW |
7 |
141,281,347 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3110:Muc2
|
UTSW |
7 |
141,299,225 (GRCm39) |
unclassified |
probably benign |
|
R3112:Muc2
|
UTSW |
7 |
141,299,225 (GRCm39) |
unclassified |
probably benign |
|
R3424:Muc2
|
UTSW |
7 |
141,279,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R3786:Muc2
|
UTSW |
7 |
141,283,590 (GRCm39) |
missense |
probably benign |
0.01 |
R3854:Muc2
|
UTSW |
7 |
141,308,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R3964:Muc2
|
UTSW |
7 |
141,286,233 (GRCm39) |
missense |
probably benign |
0.17 |
R3965:Muc2
|
UTSW |
7 |
141,286,233 (GRCm39) |
missense |
probably benign |
0.17 |
R3966:Muc2
|
UTSW |
7 |
141,286,233 (GRCm39) |
missense |
probably benign |
0.17 |
R3973:Muc2
|
UTSW |
7 |
141,300,541 (GRCm39) |
unclassified |
probably benign |
|
R3974:Muc2
|
UTSW |
7 |
141,300,541 (GRCm39) |
unclassified |
probably benign |
|
R3976:Muc2
|
UTSW |
7 |
141,300,541 (GRCm39) |
unclassified |
probably benign |
|
R4327:Muc2
|
UTSW |
7 |
141,281,577 (GRCm39) |
missense |
probably damaging |
0.96 |
R4694:Muc2
|
UTSW |
7 |
141,306,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:Muc2
|
UTSW |
7 |
141,299,345 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4769:Muc2
|
UTSW |
7 |
141,286,260 (GRCm39) |
critical splice donor site |
probably null |
|
R4798:Muc2
|
UTSW |
7 |
141,307,877 (GRCm39) |
missense |
probably benign |
0.01 |
R4900:Muc2
|
UTSW |
7 |
141,303,280 (GRCm39) |
missense |
probably benign |
0.32 |
R5383:Muc2
|
UTSW |
7 |
141,307,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Muc2
|
UTSW |
7 |
141,305,169 (GRCm39) |
missense |
probably benign |
0.00 |
R5615:Muc2
|
UTSW |
7 |
141,277,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R5856:Muc2
|
UTSW |
7 |
141,299,381 (GRCm39) |
unclassified |
probably benign |
|
R5919:Muc2
|
UTSW |
7 |
141,281,171 (GRCm39) |
missense |
probably damaging |
0.97 |
R5953:Muc2
|
UTSW |
7 |
141,287,951 (GRCm39) |
missense |
probably damaging |
0.96 |
R5979:Muc2
|
UTSW |
7 |
141,305,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5979:Muc2
|
UTSW |
7 |
141,283,493 (GRCm39) |
splice site |
probably null |
|
R6175:Muc2
|
UTSW |
7 |
141,282,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R6213:Muc2
|
UTSW |
7 |
141,305,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R6281:Muc2
|
UTSW |
7 |
141,306,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6390:Muc2
|
UTSW |
7 |
141,305,883 (GRCm39) |
missense |
probably damaging |
0.97 |
R6485:Muc2
|
UTSW |
7 |
141,300,473 (GRCm39) |
unclassified |
probably benign |
|
R6582:Muc2
|
UTSW |
7 |
141,282,941 (GRCm39) |
missense |
probably benign |
0.00 |
R6683:Muc2
|
UTSW |
7 |
141,305,214 (GRCm39) |
missense |
probably benign |
0.38 |
R6896:Muc2
|
UTSW |
7 |
141,306,432 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6906:Muc2
|
UTSW |
7 |
141,284,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6924:Muc2
|
UTSW |
7 |
141,284,077 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7040:Muc2
|
UTSW |
7 |
141,305,194 (GRCm39) |
missense |
unknown |
|
R7222:Muc2
|
UTSW |
7 |
141,290,758 (GRCm39) |
missense |
|
|
R7251:Muc2
|
UTSW |
7 |
141,278,965 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7282:Muc2
|
UTSW |
7 |
141,306,481 (GRCm39) |
missense |
|
|
R7315:Muc2
|
UTSW |
7 |
141,276,645 (GRCm39) |
missense |
probably damaging |
0.99 |
R7421:Muc2
|
UTSW |
7 |
141,301,863 (GRCm39) |
missense |
|
|
R7556:Muc2
|
UTSW |
7 |
141,307,439 (GRCm39) |
missense |
|
|
R7651:Muc2
|
UTSW |
7 |
141,290,750 (GRCm39) |
missense |
|
|
R7710:Muc2
|
UTSW |
7 |
141,287,452 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7776:Muc2
|
UTSW |
7 |
141,290,942 (GRCm39) |
missense |
|
|
R7813:Muc2
|
UTSW |
7 |
141,282,543 (GRCm39) |
splice site |
probably null |
|
R7843:Muc2
|
UTSW |
7 |
141,281,662 (GRCm39) |
missense |
probably benign |
0.03 |
R7869:Muc2
|
UTSW |
7 |
141,303,471 (GRCm39) |
missense |
|
|
R7924:Muc2
|
UTSW |
7 |
141,281,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7993:Muc2
|
UTSW |
7 |
141,308,173 (GRCm39) |
missense |
|
|
R8053:Muc2
|
UTSW |
7 |
141,284,575 (GRCm39) |
missense |
probably benign |
0.01 |
R8068:Muc2
|
UTSW |
7 |
141,298,422 (GRCm39) |
missense |
|
|
R8099:Muc2
|
UTSW |
7 |
141,299,175 (GRCm39) |
splice site |
probably null |
|
R8192:Muc2
|
UTSW |
7 |
141,305,215 (GRCm39) |
missense |
|
|
R8194:Muc2
|
UTSW |
7 |
141,290,801 (GRCm39) |
missense |
|
|
R8545:Muc2
|
UTSW |
7 |
141,306,130 (GRCm39) |
missense |
unknown |
|
R8701:Muc2
|
UTSW |
7 |
141,281,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R8883:Muc2
|
UTSW |
7 |
141,287,469 (GRCm39) |
missense |
probably damaging |
0.98 |
R8894:Muc2
|
UTSW |
7 |
141,280,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Muc2
|
UTSW |
7 |
141,279,643 (GRCm39) |
missense |
probably benign |
0.00 |
R9024:Muc2
|
UTSW |
7 |
141,287,936 (GRCm39) |
missense |
probably damaging |
0.98 |
R9032:Muc2
|
UTSW |
7 |
141,287,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R9085:Muc2
|
UTSW |
7 |
141,287,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:Muc2
|
UTSW |
7 |
141,290,816 (GRCm39) |
missense |
|
|
R9104:Muc2
|
UTSW |
7 |
141,286,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R9114:Muc2
|
UTSW |
7 |
141,287,983 (GRCm39) |
nonsense |
probably null |
|
R9270:Muc2
|
UTSW |
7 |
141,290,816 (GRCm39) |
missense |
|
|
R9297:Muc2
|
UTSW |
7 |
141,302,759 (GRCm39) |
missense |
|
|
R9325:Muc2
|
UTSW |
7 |
141,298,559 (GRCm39) |
missense |
|
|
R9354:Muc2
|
UTSW |
7 |
141,307,157 (GRCm39) |
missense |
|
|
R9386:Muc2
|
UTSW |
7 |
141,279,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R9529:Muc2
|
UTSW |
7 |
141,287,453 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9550:Muc2
|
UTSW |
7 |
141,308,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Muc2
|
UTSW |
7 |
141,300,559 (GRCm39) |
missense |
|
|
R9607:Muc2
|
UTSW |
7 |
141,305,190 (GRCm39) |
missense |
|
|
R9646:Muc2
|
UTSW |
7 |
141,276,643 (GRCm39) |
missense |
probably benign |
|
R9651:Muc2
|
UTSW |
7 |
141,288,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R9774:Muc2
|
UTSW |
7 |
141,285,811 (GRCm39) |
missense |
probably benign |
|
R9784:Muc2
|
UTSW |
7 |
141,280,785 (GRCm39) |
nonsense |
probably null |
|
Z1176:Muc2
|
UTSW |
7 |
141,300,451 (GRCm39) |
missense |
|
|
Z1177:Muc2
|
UTSW |
7 |
141,298,531 (GRCm39) |
missense |
|
|
|