Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb1 |
A |
G |
6: 88,813,566 (GRCm39) |
F391L |
probably damaging |
Het |
AC140205.10 |
C |
A |
8: 21,323,181 (GRCm39) |
T192K |
probably benign |
Het |
Arid4b |
T |
A |
13: 14,329,557 (GRCm39) |
|
probably null |
Het |
Bahd1 |
G |
A |
2: 118,753,004 (GRCm39) |
R757H |
probably damaging |
Het |
Brip1 |
A |
T |
11: 85,965,124 (GRCm39) |
N855K |
possibly damaging |
Het |
Ces2f |
A |
G |
8: 105,677,586 (GRCm39) |
N197S |
probably damaging |
Het |
Chd4 |
A |
G |
6: 125,098,581 (GRCm39) |
T1520A |
probably damaging |
Het |
Cltc |
A |
C |
11: 86,624,456 (GRCm39) |
N159K |
probably damaging |
Het |
Cntn1 |
C |
T |
15: 92,189,645 (GRCm39) |
T656I |
probably damaging |
Het |
Crybg3 |
A |
G |
16: 59,380,458 (GRCm39) |
|
probably benign |
Het |
Dzip1l |
T |
A |
9: 99,521,907 (GRCm39) |
L181H |
probably damaging |
Het |
Fam3b |
C |
A |
16: 97,282,986 (GRCm39) |
|
probably null |
Het |
Fat1 |
T |
A |
8: 45,405,383 (GRCm39) |
N711K |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,834,088 (GRCm39) |
I4168T |
probably benign |
Het |
Fbxw20 |
T |
C |
9: 109,061,398 (GRCm39) |
D117G |
probably benign |
Het |
Gm8122 |
A |
G |
14: 43,091,525 (GRCm39) |
L81P |
unknown |
Het |
Hal |
T |
C |
10: 93,332,421 (GRCm39) |
|
probably benign |
Het |
Hgf |
T |
A |
5: 16,823,949 (GRCm39) |
Y715* |
probably null |
Het |
Hid1 |
T |
A |
11: 115,258,468 (GRCm39) |
|
probably benign |
Het |
Hyou1 |
T |
A |
9: 44,293,169 (GRCm39) |
V125E |
probably damaging |
Het |
Jrkl |
G |
A |
9: 13,245,146 (GRCm39) |
Q172* |
probably null |
Het |
Lamc3 |
A |
G |
2: 31,821,964 (GRCm39) |
E1304G |
probably benign |
Het |
Lman2l |
A |
C |
1: 36,478,804 (GRCm39) |
C103G |
probably damaging |
Het |
Lrfn5 |
T |
C |
12: 61,890,276 (GRCm39) |
S522P |
probably damaging |
Het |
Mark3 |
A |
T |
12: 111,570,957 (GRCm39) |
I86L |
possibly damaging |
Het |
Mfsd13a |
C |
T |
19: 46,360,431 (GRCm39) |
R328C |
probably damaging |
Het |
Mgst2 |
G |
A |
3: 51,571,949 (GRCm39) |
V26I |
probably damaging |
Het |
Neb |
A |
T |
2: 52,077,525 (GRCm39) |
Y158* |
probably null |
Het |
Nipbl |
T |
C |
15: 8,391,345 (GRCm39) |
I210V |
probably benign |
Het |
Or7g18 |
A |
T |
9: 18,786,907 (GRCm39) |
I95L |
probably damaging |
Het |
Or8j3b |
C |
T |
2: 86,205,523 (GRCm39) |
A78T |
possibly damaging |
Het |
Pcdhb8 |
C |
T |
18: 37,489,935 (GRCm39) |
P538S |
probably damaging |
Het |
Postn |
A |
G |
3: 54,278,376 (GRCm39) |
D295G |
probably damaging |
Het |
Prss38 |
T |
C |
11: 59,263,854 (GRCm39) |
Y286C |
probably damaging |
Het |
Psen2 |
A |
T |
1: 180,068,347 (GRCm39) |
V102E |
probably damaging |
Het |
Ptpn9 |
A |
T |
9: 56,943,847 (GRCm39) |
K126N |
possibly damaging |
Het |
Ptprd |
A |
G |
4: 76,046,922 (GRCm39) |
I435T |
probably damaging |
Het |
Rab39 |
T |
C |
9: 53,597,950 (GRCm39) |
K105R |
probably benign |
Het |
Robo2 |
C |
A |
16: 73,745,267 (GRCm39) |
R840L |
probably benign |
Het |
Rps6ka5 |
T |
A |
12: 100,547,578 (GRCm39) |
I311F |
probably damaging |
Het |
Ryr1 |
G |
T |
7: 28,793,667 (GRCm39) |
T1267K |
possibly damaging |
Het |
Sis |
G |
A |
3: 72,863,482 (GRCm39) |
T252I |
probably damaging |
Het |
Slc41a3 |
A |
T |
6: 90,612,312 (GRCm39) |
S201C |
probably damaging |
Het |
Slitrk1 |
A |
C |
14: 109,148,735 (GRCm39) |
S659A |
probably benign |
Het |
Snx25 |
A |
T |
8: 46,488,715 (GRCm39) |
M880K |
probably damaging |
Het |
Tbxas1 |
C |
T |
6: 39,004,713 (GRCm39) |
T320I |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tnxb |
C |
T |
17: 34,897,636 (GRCm39) |
Q804* |
probably null |
Het |
Tpst1 |
T |
A |
5: 130,131,343 (GRCm39) |
M271K |
probably benign |
Het |
Trank1 |
C |
T |
9: 111,194,265 (GRCm39) |
T763I |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,703,462 (GRCm39) |
H729Q |
probably damaging |
Het |
Tshz3 |
A |
T |
7: 36,469,030 (GRCm39) |
T340S |
probably damaging |
Het |
Ttc5 |
T |
C |
14: 51,018,962 (GRCm39) |
K52E |
probably benign |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,651,099 (GRCm39) |
H166R |
possibly damaging |
Het |
Wsb2 |
T |
G |
5: 117,501,643 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tex44 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02579:Tex44
|
APN |
1 |
86,354,169 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02683:Tex44
|
APN |
1 |
86,355,465 (GRCm39) |
missense |
probably benign |
0.01 |
R0589:Tex44
|
UTSW |
1 |
86,355,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1077:Tex44
|
UTSW |
1 |
86,354,777 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Tex44
|
UTSW |
1 |
86,354,834 (GRCm39) |
missense |
probably benign |
0.16 |
R1468:Tex44
|
UTSW |
1 |
86,354,834 (GRCm39) |
missense |
probably benign |
0.16 |
R1483:Tex44
|
UTSW |
1 |
86,354,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R1485:Tex44
|
UTSW |
1 |
86,355,640 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1527:Tex44
|
UTSW |
1 |
86,355,368 (GRCm39) |
missense |
probably benign |
0.01 |
R2058:Tex44
|
UTSW |
1 |
86,354,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Tex44
|
UTSW |
1 |
86,354,811 (GRCm39) |
missense |
probably benign |
0.04 |
R4524:Tex44
|
UTSW |
1 |
86,355,298 (GRCm39) |
missense |
probably benign |
0.03 |
R6191:Tex44
|
UTSW |
1 |
86,354,306 (GRCm39) |
unclassified |
probably benign |
|
R6658:Tex44
|
UTSW |
1 |
86,354,751 (GRCm39) |
missense |
probably benign |
0.01 |
R6731:Tex44
|
UTSW |
1 |
86,354,207 (GRCm39) |
missense |
probably benign |
0.04 |
R7526:Tex44
|
UTSW |
1 |
86,354,237 (GRCm39) |
missense |
probably benign |
0.33 |
R7625:Tex44
|
UTSW |
1 |
86,354,459 (GRCm39) |
nonsense |
probably null |
|
R8251:Tex44
|
UTSW |
1 |
86,354,936 (GRCm39) |
missense |
probably benign |
0.05 |
R8446:Tex44
|
UTSW |
1 |
86,354,696 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9369:Tex44
|
UTSW |
1 |
86,355,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R9625:Tex44
|
UTSW |
1 |
86,354,253 (GRCm39) |
missense |
unknown |
|
|