Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadvl |
T |
C |
11: 69,902,388 (GRCm39) |
I415V |
probably benign |
Het |
Akap8l |
A |
G |
17: 32,564,370 (GRCm39) |
F6L |
possibly damaging |
Het |
Ano3 |
T |
A |
2: 110,527,400 (GRCm39) |
N603Y |
probably damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,634,813 (GRCm39) |
S116P |
probably damaging |
Het |
Ccdc110 |
A |
T |
8: 46,395,825 (GRCm39) |
Q572L |
probably benign |
Het |
Chit1 |
T |
C |
1: 134,070,980 (GRCm39) |
S20P |
probably damaging |
Het |
Col22a1 |
G |
A |
15: 71,762,338 (GRCm39) |
P107L |
possibly damaging |
Het |
Dpys |
T |
C |
15: 39,705,369 (GRCm39) |
H248R |
probably damaging |
Het |
Dsg2 |
A |
T |
18: 20,734,371 (GRCm39) |
K783I |
possibly damaging |
Het |
Efnb2 |
A |
T |
8: 8,670,637 (GRCm39) |
V321E |
probably damaging |
Het |
Eif1ad13 |
A |
G |
12: 87,762,565 (GRCm39) |
Y95C |
probably damaging |
Het |
Fbxo11 |
A |
T |
17: 88,320,086 (GRCm39) |
Y209N |
probably benign |
Het |
Gm35315 |
A |
T |
5: 110,225,955 (GRCm39) |
C495S |
possibly damaging |
Het |
Hrh1 |
A |
G |
6: 114,457,724 (GRCm39) |
Q335R |
possibly damaging |
Het |
Il12rb2 |
A |
G |
6: 67,333,670 (GRCm39) |
L203P |
probably damaging |
Het |
Itgav |
T |
C |
2: 83,624,614 (GRCm39) |
S735P |
probably damaging |
Het |
Klrg1 |
G |
T |
6: 122,248,412 (GRCm39) |
C162* |
probably null |
Het |
Mcc |
T |
C |
18: 44,578,931 (GRCm39) |
S651G |
possibly damaging |
Het |
Nkx2-2 |
T |
A |
2: 147,027,896 (GRCm39) |
I15F |
probably damaging |
Het |
Nppa |
G |
A |
4: 148,085,328 (GRCm39) |
V13I |
probably benign |
Het |
Obi1 |
A |
T |
14: 104,717,253 (GRCm39) |
C373* |
probably null |
Het |
Or8i2 |
G |
C |
2: 86,852,869 (GRCm39) |
F6L |
probably benign |
Het |
Pde2a |
A |
G |
7: 101,150,244 (GRCm39) |
N228D |
probably benign |
Het |
Pgpep1l |
C |
T |
7: 67,888,815 (GRCm39) |
|
probably null |
Het |
Plekhg3 |
A |
G |
12: 76,622,778 (GRCm39) |
N673D |
probably benign |
Het |
Plxna4 |
A |
G |
6: 32,493,672 (GRCm39) |
S315P |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,388,664 (GRCm39) |
|
probably null |
Het |
Rnf111 |
T |
C |
9: 70,336,889 (GRCm39) |
T925A |
probably damaging |
Het |
Spag9 |
T |
C |
11: 93,984,328 (GRCm39) |
F734L |
possibly damaging |
Het |
Tarbp1 |
A |
G |
8: 127,177,434 (GRCm39) |
V746A |
probably benign |
Het |
Tmtc1 |
A |
G |
6: 148,314,243 (GRCm39) |
F119L |
probably benign |
Het |
Ttc21b |
A |
G |
2: 66,057,244 (GRCm39) |
M576T |
probably benign |
Het |
Usp48 |
T |
A |
4: 137,362,232 (GRCm39) |
V765E |
probably damaging |
Het |
Vmn1r20 |
A |
G |
6: 57,409,093 (GRCm39) |
S140G |
probably benign |
Het |
Vwde |
A |
G |
6: 13,205,843 (GRCm39) |
S235P |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,414,649 (GRCm39) |
S504G |
probably benign |
Het |
Wnt5b |
A |
T |
6: 119,410,573 (GRCm39) |
L289Q |
possibly damaging |
Het |
Zfp142 |
G |
A |
1: 74,609,376 (GRCm39) |
|
probably null |
Het |
Zfp948 |
A |
G |
17: 21,807,813 (GRCm39) |
H335R |
probably benign |
Het |
|
Other mutations in Zfp385b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Zfp385b
|
APN |
2 |
77,307,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01684:Zfp385b
|
APN |
2 |
77,550,019 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02354:Zfp385b
|
APN |
2 |
77,280,647 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02361:Zfp385b
|
APN |
2 |
77,280,647 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Zfp385b
|
APN |
2 |
77,242,403 (GRCm39) |
missense |
probably benign |
0.00 |
R0008:Zfp385b
|
UTSW |
2 |
77,246,291 (GRCm39) |
missense |
probably benign |
0.27 |
R0008:Zfp385b
|
UTSW |
2 |
77,246,291 (GRCm39) |
missense |
probably benign |
0.27 |
R0243:Zfp385b
|
UTSW |
2 |
77,246,072 (GRCm39) |
critical splice donor site |
probably null |
|
R0403:Zfp385b
|
UTSW |
2 |
77,307,189 (GRCm39) |
missense |
probably damaging |
0.97 |
R1566:Zfp385b
|
UTSW |
2 |
77,246,257 (GRCm39) |
missense |
probably benign |
0.05 |
R1799:Zfp385b
|
UTSW |
2 |
77,246,316 (GRCm39) |
missense |
probably benign |
0.13 |
R3618:Zfp385b
|
UTSW |
2 |
77,246,233 (GRCm39) |
missense |
probably benign |
|
R3619:Zfp385b
|
UTSW |
2 |
77,246,233 (GRCm39) |
missense |
probably benign |
|
R4007:Zfp385b
|
UTSW |
2 |
77,549,836 (GRCm39) |
missense |
probably benign |
0.00 |
R6290:Zfp385b
|
UTSW |
2 |
77,280,612 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6298:Zfp385b
|
UTSW |
2 |
77,244,323 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6383:Zfp385b
|
UTSW |
2 |
77,246,185 (GRCm39) |
missense |
probably benign |
0.01 |
R6484:Zfp385b
|
UTSW |
2 |
77,549,992 (GRCm39) |
small insertion |
probably benign |
|
R6856:Zfp385b
|
UTSW |
2 |
77,246,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R7276:Zfp385b
|
UTSW |
2 |
77,280,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R8692:Zfp385b
|
UTSW |
2 |
77,549,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8982:Zfp385b
|
UTSW |
2 |
77,242,300 (GRCm39) |
missense |
probably damaging |
0.96 |
R9299:Zfp385b
|
UTSW |
2 |
77,246,115 (GRCm39) |
missense |
probably damaging |
1.00 |
|