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 |
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 |
Zfp385b |
ATCTTCTTCTTCT |
ATCTTCTTCTTCTTCT |
2: 77,549,992 (GRCm39) |
|
probably benign |
Het |
Zfp948 |
A |
G |
17: 21,807,813 (GRCm39) |
H335R |
probably benign |
Het |
|
Other mutations in Tarbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00985:Tarbp1
|
APN |
8 |
127,185,900 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Tarbp1
|
APN |
8 |
127,154,894 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01475:Tarbp1
|
APN |
8 |
127,160,701 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01688:Tarbp1
|
APN |
8 |
127,174,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01772:Tarbp1
|
APN |
8 |
127,173,970 (GRCm39) |
splice site |
probably benign |
|
IGL02402:Tarbp1
|
APN |
8 |
127,177,567 (GRCm39) |
splice site |
probably benign |
|
IGL02899:Tarbp1
|
APN |
8 |
127,180,583 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03006:Tarbp1
|
APN |
8 |
127,170,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03273:Tarbp1
|
APN |
8 |
127,180,574 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Tarbp1
|
UTSW |
8 |
127,157,586 (GRCm39) |
missense |
probably damaging |
0.96 |
R0048:Tarbp1
|
UTSW |
8 |
127,174,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Tarbp1
|
UTSW |
8 |
127,165,667 (GRCm39) |
splice site |
probably benign |
|
R0383:Tarbp1
|
UTSW |
8 |
127,174,223 (GRCm39) |
missense |
probably benign |
0.00 |
R0455:Tarbp1
|
UTSW |
8 |
127,167,612 (GRCm39) |
missense |
probably benign |
0.00 |
R0738:Tarbp1
|
UTSW |
8 |
127,165,540 (GRCm39) |
critical splice donor site |
probably null |
|
R1345:Tarbp1
|
UTSW |
8 |
127,175,069 (GRCm39) |
missense |
probably benign |
0.03 |
R1370:Tarbp1
|
UTSW |
8 |
127,175,069 (GRCm39) |
missense |
probably benign |
0.03 |
R1617:Tarbp1
|
UTSW |
8 |
127,171,007 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1628:Tarbp1
|
UTSW |
8 |
127,157,599 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1702:Tarbp1
|
UTSW |
8 |
127,154,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R1873:Tarbp1
|
UTSW |
8 |
127,173,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Tarbp1
|
UTSW |
8 |
127,154,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Tarbp1
|
UTSW |
8 |
127,154,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Tarbp1
|
UTSW |
8 |
127,174,333 (GRCm39) |
splice site |
probably null |
|
R2877:Tarbp1
|
UTSW |
8 |
127,154,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R3008:Tarbp1
|
UTSW |
8 |
127,174,160 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3875:Tarbp1
|
UTSW |
8 |
127,165,538 (GRCm39) |
splice site |
probably benign |
|
R3905:Tarbp1
|
UTSW |
8 |
127,154,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Tarbp1
|
UTSW |
8 |
127,167,510 (GRCm39) |
missense |
probably benign |
0.00 |
R4420:Tarbp1
|
UTSW |
8 |
127,173,819 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4570:Tarbp1
|
UTSW |
8 |
127,178,972 (GRCm39) |
missense |
probably benign |
0.00 |
R4610:Tarbp1
|
UTSW |
8 |
127,201,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Tarbp1
|
UTSW |
8 |
127,173,934 (GRCm39) |
missense |
probably damaging |
0.96 |
R4802:Tarbp1
|
UTSW |
8 |
127,201,628 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4951:Tarbp1
|
UTSW |
8 |
127,174,184 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4953:Tarbp1
|
UTSW |
8 |
127,174,184 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5254:Tarbp1
|
UTSW |
8 |
127,193,895 (GRCm39) |
missense |
probably damaging |
0.96 |
R5255:Tarbp1
|
UTSW |
8 |
127,155,709 (GRCm39) |
missense |
probably benign |
0.16 |
R5638:Tarbp1
|
UTSW |
8 |
127,177,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Tarbp1
|
UTSW |
8 |
127,174,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R5707:Tarbp1
|
UTSW |
8 |
127,193,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R5896:Tarbp1
|
UTSW |
8 |
127,179,667 (GRCm39) |
missense |
probably benign |
0.05 |
R6087:Tarbp1
|
UTSW |
8 |
127,155,709 (GRCm39) |
missense |
probably benign |
0.00 |
R6117:Tarbp1
|
UTSW |
8 |
127,154,280 (GRCm39) |
missense |
probably benign |
0.00 |
R6132:Tarbp1
|
UTSW |
8 |
127,161,548 (GRCm39) |
missense |
probably benign |
0.17 |
R6168:Tarbp1
|
UTSW |
8 |
127,175,144 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6419:Tarbp1
|
UTSW |
8 |
127,185,783 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6766:Tarbp1
|
UTSW |
8 |
127,174,139 (GRCm39) |
missense |
probably benign |
0.41 |
R6775:Tarbp1
|
UTSW |
8 |
127,163,568 (GRCm39) |
missense |
probably benign |
0.16 |
R6960:Tarbp1
|
UTSW |
8 |
127,155,778 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7054:Tarbp1
|
UTSW |
8 |
127,201,234 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7068:Tarbp1
|
UTSW |
8 |
127,153,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Tarbp1
|
UTSW |
8 |
127,184,416 (GRCm39) |
missense |
probably benign |
0.19 |
R7519:Tarbp1
|
UTSW |
8 |
127,160,639 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7760:Tarbp1
|
UTSW |
8 |
127,179,546 (GRCm39) |
missense |
not run |
|
R7837:Tarbp1
|
UTSW |
8 |
127,201,300 (GRCm39) |
missense |
probably benign |
0.00 |
R7882:Tarbp1
|
UTSW |
8 |
127,183,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R7982:Tarbp1
|
UTSW |
8 |
127,171,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R8166:Tarbp1
|
UTSW |
8 |
127,153,867 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8517:Tarbp1
|
UTSW |
8 |
127,170,934 (GRCm39) |
missense |
probably benign |
0.29 |
R8838:Tarbp1
|
UTSW |
8 |
127,177,569 (GRCm39) |
splice site |
probably benign |
|
R8880:Tarbp1
|
UTSW |
8 |
127,198,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R9061:Tarbp1
|
UTSW |
8 |
127,173,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9123:Tarbp1
|
UTSW |
8 |
127,174,202 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9125:Tarbp1
|
UTSW |
8 |
127,174,202 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9364:Tarbp1
|
UTSW |
8 |
127,177,462 (GRCm39) |
missense |
probably benign |
0.01 |
R9474:Tarbp1
|
UTSW |
8 |
127,155,779 (GRCm39) |
missense |
probably benign |
0.44 |
R9670:Tarbp1
|
UTSW |
8 |
127,183,262 (GRCm39) |
missense |
probably null |
1.00 |
|