Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
A |
11: 110,069,655 (GRCm39) |
K1554* |
probably null |
Het |
Acads |
T |
C |
5: 115,255,757 (GRCm39) |
H26R |
probably benign |
Het |
Acer1 |
G |
A |
17: 57,265,406 (GRCm39) |
T141I |
probably damaging |
Het |
Adam15 |
C |
G |
3: 89,254,764 (GRCm39) |
V99L |
probably benign |
Het |
Ankrd13b |
A |
G |
11: 77,368,331 (GRCm39) |
V97A |
possibly damaging |
Het |
Anpep |
T |
C |
7: 79,491,720 (GRCm39) |
T94A |
probably benign |
Het |
Atp1a3 |
T |
C |
7: 24,694,119 (GRCm39) |
N345S |
probably damaging |
Het |
Btn1a1 |
T |
A |
13: 23,645,721 (GRCm39) |
N216I |
possibly damaging |
Het |
Cacna1s |
G |
A |
1: 136,002,831 (GRCm39) |
W62* |
probably null |
Het |
Ccdc141 |
C |
T |
2: 76,869,830 (GRCm39) |
V892I |
probably benign |
Het |
Ccdc180 |
T |
A |
4: 45,900,470 (GRCm39) |
I278K |
possibly damaging |
Het |
Cdc7 |
T |
G |
5: 107,122,564 (GRCm39) |
|
probably null |
Het |
Cpb1 |
C |
T |
3: 20,319,521 (GRCm39) |
V188M |
probably damaging |
Het |
Dock5 |
A |
G |
14: 68,095,371 (GRCm39) |
I101T |
possibly damaging |
Het |
Dqx1 |
T |
C |
6: 83,035,953 (GRCm39) |
V95A |
probably damaging |
Het |
Dvl1 |
T |
A |
4: 155,938,123 (GRCm39) |
D90E |
probably damaging |
Het |
Fam135b |
T |
C |
15: 71,335,879 (GRCm39) |
I438M |
probably benign |
Het |
Fpr1 |
A |
T |
17: 18,096,897 (GRCm39) |
M364K |
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Gpx7 |
C |
A |
4: 108,260,470 (GRCm39) |
V109F |
probably damaging |
Het |
Grhl2 |
T |
C |
15: 37,336,591 (GRCm39) |
|
probably null |
Het |
Grn |
A |
G |
11: 102,324,069 (GRCm39) |
T53A |
probably benign |
Het |
H1f4 |
T |
C |
13: 23,805,829 (GRCm39) |
|
probably benign |
Het |
H2-T9 |
T |
C |
17: 36,440,038 (GRCm39) |
Y32C |
probably damaging |
Het |
Hmgxb3 |
T |
C |
18: 61,280,454 (GRCm39) |
N683S |
probably damaging |
Het |
Iigp1 |
T |
C |
18: 60,523,983 (GRCm39) |
I367T |
probably benign |
Het |
Itfg2 |
T |
C |
6: 128,388,632 (GRCm39) |
E285G |
probably damaging |
Het |
Itgav |
T |
A |
2: 83,622,915 (GRCm39) |
C662* |
probably null |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Lipe |
T |
C |
7: 25,097,848 (GRCm39) |
T32A |
probably benign |
Het |
Lrrk2 |
A |
G |
15: 91,698,898 (GRCm39) |
Y2475C |
probably benign |
Het |
Mcc |
T |
C |
18: 44,582,330 (GRCm39) |
D607G |
probably damaging |
Het |
Mip |
T |
A |
10: 128,061,875 (GRCm39) |
L42* |
probably null |
Het |
Mlc1 |
A |
T |
15: 88,850,199 (GRCm39) |
D192E |
probably benign |
Het |
Mybl1 |
T |
C |
1: 9,752,095 (GRCm39) |
D260G |
probably damaging |
Het |
Ncln |
C |
T |
10: 81,323,519 (GRCm39) |
V51I |
probably benign |
Het |
Nlrp9a |
T |
C |
7: 26,257,297 (GRCm39) |
V305A |
probably benign |
Het |
Nodal |
G |
A |
10: 61,260,276 (GRCm39) |
R309Q |
possibly damaging |
Het |
Olr1 |
T |
C |
6: 129,476,881 (GRCm39) |
N128S |
possibly damaging |
Het |
Or10ak14 |
A |
T |
4: 118,611,421 (GRCm39) |
F105I |
probably damaging |
Het |
Or12j5 |
A |
G |
7: 140,083,832 (GRCm39) |
I180T |
probably damaging |
Het |
Or14a256 |
T |
C |
7: 86,264,884 (GRCm39) |
Y323C |
probably benign |
Het |
Orc1 |
T |
A |
4: 108,461,757 (GRCm39) |
C585S |
probably benign |
Het |
Pcmtd2 |
A |
T |
2: 181,496,922 (GRCm39) |
I300F |
probably damaging |
Het |
Pfkfb4 |
C |
T |
9: 108,854,110 (GRCm39) |
|
probably benign |
Het |
Phactr3 |
T |
A |
2: 177,920,810 (GRCm39) |
L180Q |
possibly damaging |
Het |
Pigo |
T |
C |
4: 43,021,083 (GRCm39) |
T612A |
probably benign |
Het |
Plch1 |
T |
A |
3: 63,616,952 (GRCm39) |
D766V |
probably damaging |
Het |
Plekhh3 |
T |
C |
11: 101,054,973 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
T |
G |
2: 111,058,399 (GRCm39) |
L131F |
probably damaging |
Het |
Ppp1r12b |
T |
A |
1: 134,800,570 (GRCm39) |
T547S |
probably damaging |
Het |
Prkcb |
T |
A |
7: 122,116,079 (GRCm39) |
M186K |
probably damaging |
Het |
Prpf3 |
A |
T |
3: 95,757,112 (GRCm39) |
|
probably benign |
Het |
Psg23 |
T |
C |
7: 18,344,369 (GRCm39) |
D362G |
possibly damaging |
Het |
Reg3a |
T |
C |
6: 78,358,114 (GRCm39) |
L15P |
probably damaging |
Het |
Scrib |
A |
T |
15: 75,941,223 (GRCm39) |
I5N |
probably damaging |
Het |
Speg |
C |
T |
1: 75,399,326 (GRCm39) |
Q2005* |
probably null |
Het |
Sppl3 |
A |
T |
5: 115,212,923 (GRCm39) |
S51C |
possibly damaging |
Het |
Sspo |
A |
G |
6: 48,434,534 (GRCm39) |
T1009A |
probably damaging |
Het |
Syce1l |
A |
G |
8: 114,381,579 (GRCm39) |
Q164R |
probably benign |
Het |
Sympk |
T |
C |
7: 18,768,409 (GRCm39) |
V126A |
possibly damaging |
Het |
Tas2r110 |
T |
A |
6: 132,844,987 (GRCm39) |
I6K |
unknown |
Het |
Tas2r120 |
A |
T |
6: 132,634,731 (GRCm39) |
H271L |
probably damaging |
Het |
Tlcd3a |
A |
G |
11: 76,093,057 (GRCm39) |
D33G |
probably benign |
Het |
Tnn |
T |
A |
1: 159,943,856 (GRCm39) |
T986S |
possibly damaging |
Het |
Trim5 |
T |
C |
7: 103,928,845 (GRCm39) |
H32R |
probably damaging |
Het |
Ttc13 |
A |
G |
8: 125,410,573 (GRCm39) |
I360T |
possibly damaging |
Het |
Uaca |
A |
G |
9: 60,778,781 (GRCm39) |
E1054G |
probably damaging |
Het |
Usp16 |
T |
A |
16: 87,268,736 (GRCm39) |
|
probably null |
Het |
Wee1 |
T |
A |
7: 109,730,043 (GRCm39) |
S382R |
probably damaging |
Het |
Wnt11 |
T |
C |
7: 98,495,771 (GRCm39) |
S92P |
probably damaging |
Het |
Zfp1004 |
C |
G |
2: 150,034,141 (GRCm39) |
P185R |
probably damaging |
Het |
Zfp786 |
A |
G |
6: 47,797,160 (GRCm39) |
C593R |
probably damaging |
Het |
Zfp879 |
T |
G |
11: 50,723,989 (GRCm39) |
I283L |
possibly 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 |
|
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 |
R6321:Muc2
|
UTSW |
7 |
141,287,397 (GRCm39) |
missense |
probably benign |
0.28 |
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 |
|
|
|