Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
A |
T |
7: 45,678,482 (GRCm39) |
I56N |
possibly damaging |
Het |
Akr1c13 |
A |
T |
13: 4,255,372 (GRCm39) |
E321V |
possibly damaging |
Het |
Atp8b3 |
A |
T |
10: 80,357,662 (GRCm39) |
V1119D |
possibly damaging |
Het |
Cacna1e |
G |
T |
1: 154,319,646 (GRCm39) |
F1351L |
probably damaging |
Het |
Cadps2 |
A |
G |
6: 23,427,274 (GRCm39) |
W585R |
probably damaging |
Het |
Ccdc113 |
C |
T |
8: 96,263,086 (GRCm39) |
|
probably benign |
Het |
Ccer1 |
A |
T |
10: 97,529,912 (GRCm39) |
I192F |
unknown |
Het |
Chd8 |
T |
C |
14: 52,436,551 (GRCm39) |
N90S |
probably benign |
Het |
Clca3a1 |
A |
T |
3: 144,453,333 (GRCm39) |
C463* |
probably null |
Het |
Cplane1 |
T |
A |
15: 8,258,591 (GRCm39) |
V2279E |
possibly damaging |
Het |
Cyp2c65 |
T |
A |
19: 39,060,676 (GRCm39) |
C179S |
possibly damaging |
Het |
Dennd4b |
A |
G |
3: 90,182,874 (GRCm39) |
Q35R |
probably benign |
Het |
Enpep |
T |
C |
3: 129,063,983 (GRCm39) |
E928G |
possibly damaging |
Het |
Fem1c |
T |
C |
18: 46,638,629 (GRCm39) |
T458A |
probably benign |
Het |
Fezf2 |
A |
T |
14: 12,342,498 (GRCm38) |
*456R |
probably null |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Iqcm |
T |
G |
8: 76,615,188 (GRCm39) |
L423R |
probably damaging |
Het |
Kcnc4 |
C |
A |
3: 107,355,534 (GRCm39) |
V305L |
probably benign |
Het |
Kif1a |
G |
A |
1: 92,953,455 (GRCm39) |
T1337I |
possibly damaging |
Het |
Lpxn |
A |
G |
19: 12,810,450 (GRCm39) |
D298G |
probably damaging |
Het |
Lypd8 |
A |
G |
11: 58,281,046 (GRCm39) |
T203A |
possibly damaging |
Het |
Mrps28 |
C |
T |
3: 8,965,119 (GRCm39) |
V107M |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,774,324 (GRCm39) |
E586G |
possibly damaging |
Het |
Pdzk1 |
C |
T |
3: 96,776,417 (GRCm39) |
A459V |
possibly damaging |
Het |
Rbpj |
A |
G |
5: 53,808,728 (GRCm39) |
D285G |
probably damaging |
Het |
Rimbp3 |
T |
C |
16: 17,029,300 (GRCm39) |
L908P |
probably damaging |
Het |
Samd4b |
T |
C |
7: 28,101,334 (GRCm39) |
|
probably null |
Het |
Slc28a2b |
A |
C |
2: 122,355,572 (GRCm39) |
Y588S |
possibly damaging |
Het |
Stau2 |
C |
T |
1: 16,416,161 (GRCm39) |
G401S |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,957,867 (GRCm39) |
I697K |
possibly damaging |
Het |
Ttc17 |
A |
C |
2: 94,205,491 (GRCm39) |
V285G |
possibly damaging |
Het |
Unc5b |
A |
G |
10: 60,602,864 (GRCm39) |
F845S |
probably damaging |
Het |
Vmn1r19 |
A |
T |
6: 57,382,245 (GRCm39) |
Q266L |
probably benign |
Het |
Vmn2r106 |
T |
C |
17: 20,499,227 (GRCm39) |
N228S |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,882,836 (GRCm39) |
F919S |
possibly damaging |
Het |
Zbtb38 |
C |
T |
9: 96,570,461 (GRCm39) |
V208I |
probably benign |
Het |
Zfp990 |
A |
T |
4: 145,263,427 (GRCm39) |
T142S |
probably damaging |
Het |
Zfp990 |
C |
A |
4: 145,263,428 (GRCm39) |
T142N |
probably damaging |
Het |
|
Other mutations in Gm21738 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Gm21738
|
APN |
14 |
19,418,885 (GRCm38) |
missense |
probably benign |
|
IGL01010:Gm21738
|
APN |
14 |
19,417,361 (GRCm38) |
missense |
probably benign |
0.03 |
IGL01018:Gm21738
|
APN |
14 |
19,418,856 (GRCm38) |
missense |
probably benign |
0.39 |
IGL01865:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01869:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01873:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01877:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01878:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01879:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01880:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01882:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01883:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01884:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01885:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01886:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01888:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01891:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01892:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01893:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01894:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01896:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01898:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01899:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01900:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01901:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01902:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01903:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01904:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01905:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01906:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01908:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01909:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01910:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01911:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01912:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01913:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01914:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01915:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01916:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01917:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01918:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01919:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01922:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01923:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01924:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01925:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01926:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01932:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01940:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01949:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
PIT4131001:Gm21738
|
UTSW |
14 |
19,417,330 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4142001:Gm21738
|
UTSW |
14 |
19,417,330 (GRCm38) |
missense |
probably benign |
0.00 |
R0831:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R0831:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R0976:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1029:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1146:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1231:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1231:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1402:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1402:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1638:Gm21738
|
UTSW |
14 |
19,418,908 (GRCm38) |
missense |
probably benign |
|
R1874:Gm21738
|
UTSW |
14 |
19,418,824 (GRCm38) |
missense |
possibly damaging |
0.64 |
R4392:Gm21738
|
UTSW |
14 |
19,417,178 (GRCm38) |
missense |
probably benign |
|
R4393:Gm21738
|
UTSW |
14 |
19,417,178 (GRCm38) |
missense |
probably benign |
|
R5049:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R5257:Gm21738
|
UTSW |
14 |
19,415,942 (GRCm38) |
missense |
probably benign |
|
R6756:Gm21738
|
UTSW |
14 |
19,418,824 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6915:Gm21738
|
UTSW |
14 |
19,415,933 (GRCm38) |
missense |
probably benign |
|
V5622:Gm21738
|
UTSW |
14 |
19,417,180 (GRCm38) |
missense |
probably damaging |
1.00 |
|