Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
T |
C |
4: 148,029,488 (GRCm39) |
I486T |
probably damaging |
Het |
4933427D14Rik |
T |
C |
11: 72,089,567 (GRCm39) |
R106G |
probably damaging |
Het |
Cfap54 |
A |
G |
10: 92,675,333 (GRCm39) |
S2863P |
possibly damaging |
Het |
Copa |
T |
A |
1: 171,948,812 (GRCm39) |
S1155T |
probably benign |
Het |
Crot |
T |
C |
5: 9,027,541 (GRCm39) |
T264A |
probably benign |
Het |
Ddx3y |
G |
A |
Y: 1,267,170 (GRCm39) |
A232V |
probably damaging |
Het |
Dst |
T |
G |
1: 34,050,979 (GRCm39) |
V25G |
probably benign |
Het |
Ehbp1 |
C |
T |
11: 22,087,867 (GRCm39) |
A406T |
probably benign |
Het |
Eml5 |
A |
T |
12: 98,768,724 (GRCm39) |
|
probably benign |
Het |
Eps8 |
A |
T |
6: 137,486,153 (GRCm39) |
M453K |
probably benign |
Het |
Galnt3 |
T |
C |
2: 65,937,374 (GRCm39) |
D112G |
possibly damaging |
Het |
Glra4 |
C |
T |
X: 135,663,542 (GRCm39) |
A336T |
probably damaging |
Het |
Gmppb |
A |
G |
9: 107,927,338 (GRCm39) |
D95G |
probably benign |
Het |
Gprc6a |
T |
C |
10: 51,504,544 (GRCm39) |
Y100C |
possibly damaging |
Het |
Gpx6 |
C |
A |
13: 21,501,828 (GRCm39) |
S150Y |
probably damaging |
Het |
Hsd17b3 |
A |
T |
13: 64,207,300 (GRCm39) |
V247D |
probably damaging |
Het |
Htr7 |
T |
C |
19: 36,034,160 (GRCm39) |
D165G |
probably damaging |
Het |
Igha |
T |
C |
12: 113,219,972 (GRCm39) |
|
probably benign |
Het |
Igsf10 |
A |
G |
3: 59,239,345 (GRCm39) |
C279R |
probably damaging |
Het |
Irak4 |
A |
G |
15: 94,452,621 (GRCm39) |
E182G |
possibly damaging |
Het |
Lipo3 |
A |
T |
19: 33,535,723 (GRCm39) |
V274E |
probably damaging |
Het |
Lrpprc |
A |
C |
17: 85,078,269 (GRCm39) |
|
probably null |
Het |
Mast1 |
T |
C |
8: 85,645,393 (GRCm39) |
Y684C |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,722,363 (GRCm39) |
F2382L |
probably benign |
Het |
Mepe |
C |
T |
5: 104,484,944 (GRCm39) |
P28L |
probably benign |
Het |
Mrgpra3 |
T |
A |
7: 47,239,414 (GRCm39) |
I171F |
probably benign |
Het |
Myh3 |
C |
T |
11: 66,987,262 (GRCm39) |
Q1371* |
probably null |
Het |
Nodal |
T |
A |
10: 61,258,833 (GRCm39) |
V90E |
probably benign |
Het |
Npas4 |
A |
T |
19: 5,036,579 (GRCm39) |
H528Q |
probably benign |
Het |
Nt5dc3 |
T |
C |
10: 86,660,100 (GRCm39) |
V382A |
probably damaging |
Het |
Pcdh18 |
G |
A |
3: 49,709,035 (GRCm39) |
T293I |
probably damaging |
Het |
Phf20l1 |
A |
G |
15: 66,513,665 (GRCm39) |
D947G |
probably damaging |
Het |
Phf8-ps |
A |
T |
17: 33,285,405 (GRCm39) |
S466T |
probably benign |
Het |
Pla2r1 |
A |
G |
2: 60,279,306 (GRCm39) |
V758A |
probably benign |
Het |
Plod2 |
G |
T |
9: 92,480,672 (GRCm39) |
G422* |
probably null |
Het |
Ppp1r12a |
T |
C |
10: 108,089,341 (GRCm39) |
V660A |
probably benign |
Het |
Prdm6 |
T |
C |
18: 53,673,278 (GRCm39) |
I186T |
possibly damaging |
Het |
Prkd3 |
G |
A |
17: 79,266,570 (GRCm39) |
|
probably benign |
Het |
Prrc2a |
A |
G |
17: 35,376,908 (GRCm39) |
L734P |
probably damaging |
Het |
Rnf128 |
C |
A |
X: 138,565,271 (GRCm39) |
L282I |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,359,879 (GRCm39) |
N4424S |
|
Het |
Scrn3 |
T |
C |
2: 73,166,121 (GRCm39) |
S385P |
possibly damaging |
Het |
Serpina1d |
A |
T |
12: 103,734,107 (GRCm39) |
S66T |
probably benign |
Het |
Setd3 |
T |
C |
12: 108,131,417 (GRCm39) |
K3R |
possibly damaging |
Het |
Slc2a7 |
A |
G |
4: 150,242,667 (GRCm39) |
|
probably null |
Het |
Smad4 |
G |
T |
18: 73,810,807 (GRCm39) |
T59K |
possibly damaging |
Het |
Spc25 |
A |
G |
2: 69,032,945 (GRCm39) |
L60P |
probably damaging |
Het |
Stam |
A |
C |
2: 14,143,772 (GRCm39) |
H354P |
probably damaging |
Het |
Tesk1 |
C |
T |
4: 43,445,786 (GRCm39) |
P280S |
possibly damaging |
Het |
Tmem120a |
C |
G |
5: 135,765,131 (GRCm39) |
R254P |
probably benign |
Het |
Traf5 |
T |
C |
1: 191,729,837 (GRCm39) |
T405A |
probably benign |
Het |
Trav7-4 |
A |
G |
14: 53,699,119 (GRCm39) |
S89G |
probably benign |
Het |
Tsc22d1 |
T |
C |
14: 76,656,049 (GRCm39) |
S761P |
probably damaging |
Het |
Ugt1a10 |
C |
A |
1: 88,143,862 (GRCm39) |
H361N |
probably damaging |
Het |
Ugt2b1 |
C |
A |
5: 87,065,534 (GRCm39) |
V502L |
probably benign |
Het |
Vip |
T |
A |
10: 5,592,590 (GRCm39) |
S77T |
possibly damaging |
Het |
Wdr72 |
A |
T |
9: 74,125,979 (GRCm39) |
M1025L |
probably benign |
Het |
Zfp541 |
A |
G |
7: 15,806,147 (GRCm39) |
D94G |
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 |
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 |
|
|
|