Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afmid |
A |
G |
11: 117,726,530 (GRCm39) |
D226G |
probably benign |
Het |
Ago2 |
T |
C |
15: 72,979,215 (GRCm39) |
|
probably null |
Het |
Aldh1a1 |
C |
A |
19: 20,608,034 (GRCm39) |
D285E |
probably benign |
Het |
Alms1 |
T |
C |
6: 85,599,820 (GRCm39) |
S1549P |
probably damaging |
Het |
Apmap |
T |
C |
2: 150,442,171 (GRCm39) |
S68G |
probably benign |
Het |
Atp8a1 |
A |
T |
5: 67,906,414 (GRCm39) |
I500N |
probably benign |
Het |
B3gnt7 |
A |
C |
1: 86,233,510 (GRCm39) |
D135A |
probably benign |
Het |
Bms1 |
A |
T |
6: 118,381,240 (GRCm39) |
L692H |
probably damaging |
Het |
Cdk17 |
T |
A |
10: 93,064,559 (GRCm39) |
V276E |
probably damaging |
Het |
Cep290 |
A |
T |
10: 100,393,970 (GRCm39) |
E2059V |
possibly damaging |
Het |
Cpxm2 |
C |
A |
7: 131,645,839 (GRCm39) |
G693V |
probably damaging |
Het |
Crocc |
A |
T |
4: 140,762,507 (GRCm39) |
V661E |
probably damaging |
Het |
D1Pas1 |
A |
T |
1: 186,700,206 (GRCm39) |
N45I |
probably damaging |
Het |
Ddx19a |
C |
T |
8: 111,705,781 (GRCm39) |
W223* |
probably null |
Het |
Ddx60 |
C |
A |
8: 62,416,756 (GRCm39) |
S567Y |
probably damaging |
Het |
Dhx36 |
A |
T |
3: 62,401,176 (GRCm39) |
N363K |
probably damaging |
Het |
Gm57859 |
C |
A |
11: 113,578,783 (GRCm39) |
|
probably null |
Het |
Gpr151 |
G |
A |
18: 42,712,450 (GRCm39) |
T76M |
probably benign |
Het |
Inhbc |
C |
T |
10: 127,193,318 (GRCm39) |
V233I |
probably benign |
Het |
Ippk |
C |
T |
13: 49,599,839 (GRCm39) |
L233F |
probably damaging |
Het |
Lama2 |
A |
G |
10: 26,862,847 (GRCm39) |
V2972A |
probably damaging |
Het |
Lrrc37a |
T |
C |
11: 103,394,612 (GRCm39) |
Q271R |
probably benign |
Het |
Mia2 |
A |
T |
12: 59,220,892 (GRCm39) |
K1083N |
possibly damaging |
Het |
Mphosph9 |
A |
C |
5: 124,453,481 (GRCm39) |
L277R |
probably damaging |
Het |
Myo7b |
A |
T |
18: 32,099,341 (GRCm39) |
F1694I |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,973,015 (GRCm39) |
|
probably null |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or2w6 |
T |
C |
13: 21,842,707 (GRCm39) |
Y262C |
probably damaging |
Het |
Pcdh10 |
A |
G |
3: 45,347,156 (GRCm39) |
T984A |
probably benign |
Het |
Pcdh20 |
T |
C |
14: 88,708,312 (GRCm39) |
S39G |
probably benign |
Het |
Pdia3 |
T |
A |
2: 121,266,892 (GRCm39) |
Y467* |
probably null |
Het |
Ptpn13 |
C |
A |
5: 103,745,556 (GRCm39) |
|
probably null |
Het |
Reln |
A |
G |
5: 22,152,431 (GRCm39) |
M2345T |
probably damaging |
Het |
Rnf126 |
A |
T |
10: 79,602,603 (GRCm39) |
I20N |
probably benign |
Het |
Satb1 |
A |
G |
17: 52,089,981 (GRCm39) |
S289P |
possibly damaging |
Het |
Scd4 |
A |
T |
19: 44,326,003 (GRCm39) |
H119L |
probably damaging |
Het |
Sco2 |
T |
C |
15: 89,256,574 (GRCm39) |
T27A |
probably benign |
Het |
Slc39a14 |
A |
T |
14: 70,544,194 (GRCm39) |
I464N |
probably damaging |
Het |
Slc4a8 |
T |
A |
15: 100,686,092 (GRCm39) |
V220E |
probably benign |
Het |
Tmf1 |
T |
A |
6: 97,150,364 (GRCm39) |
T448S |
probably benign |
Het |
Tspan33 |
G |
A |
6: 29,710,688 (GRCm39) |
R87Q |
probably damaging |
Het |
Vmn2r91 |
A |
T |
17: 18,326,464 (GRCm39) |
M250L |
probably benign |
Het |
Zc3h7a |
A |
T |
16: 10,974,050 (GRCm39) |
V245D |
probably damaging |
Het |
|
Other mutations in Themis3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01413:Themis3
|
APN |
17 |
66,863,092 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01893:Themis3
|
APN |
17 |
66,866,622 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02065:Themis3
|
APN |
17 |
66,862,900 (GRCm39) |
missense |
probably benign |
0.02 |
Nosedive
|
UTSW |
17 |
66,866,949 (GRCm39) |
missense |
probably benign |
0.18 |
Weightless
|
UTSW |
17 |
66,862,605 (GRCm39) |
missense |
probably benign |
|
R0345:Themis3
|
UTSW |
17 |
66,866,540 (GRCm39) |
critical splice donor site |
probably null |
|
R0538:Themis3
|
UTSW |
17 |
66,900,265 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0583:Themis3
|
UTSW |
17 |
66,866,748 (GRCm39) |
missense |
probably benign |
0.01 |
R1494:Themis3
|
UTSW |
17 |
66,866,949 (GRCm39) |
missense |
probably benign |
0.18 |
R1713:Themis3
|
UTSW |
17 |
66,862,848 (GRCm39) |
missense |
probably benign |
0.00 |
R2271:Themis3
|
UTSW |
17 |
66,862,699 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4214:Themis3
|
UTSW |
17 |
66,867,012 (GRCm39) |
missense |
probably benign |
0.09 |
R5575:Themis3
|
UTSW |
17 |
66,862,321 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6018:Themis3
|
UTSW |
17 |
66,900,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R7804:Themis3
|
UTSW |
17 |
66,862,605 (GRCm39) |
missense |
probably benign |
|
R8241:Themis3
|
UTSW |
17 |
66,866,962 (GRCm39) |
missense |
probably benign |
0.00 |
R8268:Themis3
|
UTSW |
17 |
66,862,786 (GRCm39) |
missense |
probably benign |
|
R8762:Themis3
|
UTSW |
17 |
66,866,676 (GRCm39) |
missense |
probably benign |
0.00 |
R8980:Themis3
|
UTSW |
17 |
66,862,536 (GRCm39) |
missense |
probably damaging |
0.97 |
R9051:Themis3
|
UTSW |
17 |
66,862,864 (GRCm39) |
missense |
probably benign |
0.07 |
R9429:Themis3
|
UTSW |
17 |
66,866,665 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Themis3
|
UTSW |
17 |
66,862,497 (GRCm39) |
missense |
possibly damaging |
0.64 |
|