Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
C |
5: 124,228,176 (GRCm39) |
T22A |
possibly damaging |
Het |
Acsf2 |
C |
T |
11: 94,464,044 (GRCm39) |
V47M |
probably benign |
Het |
Ahcyl1 |
A |
T |
3: 107,579,388 (GRCm39) |
C215* |
probably null |
Het |
Ambn |
G |
T |
5: 88,613,050 (GRCm39) |
|
probably null |
Het |
Apol9b |
G |
T |
15: 77,619,656 (GRCm39) |
V151L |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,369,007 (GRCm39) |
Y1070C |
probably damaging |
Het |
Arnt |
T |
C |
3: 95,391,092 (GRCm39) |
L322P |
possibly damaging |
Het |
Bdnf |
A |
G |
2: 109,553,935 (GRCm39) |
D103G |
possibly damaging |
Het |
Ccdc9 |
A |
T |
7: 16,016,761 (GRCm39) |
D42E |
probably damaging |
Het |
Cdh13 |
A |
G |
8: 119,963,676 (GRCm39) |
T419A |
|
Het |
Chst13 |
G |
A |
6: 90,286,506 (GRCm39) |
P152L |
probably damaging |
Het |
Clasp2 |
A |
T |
9: 113,670,669 (GRCm39) |
R329W |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,470,459 (GRCm39) |
C2495R |
|
Het |
Cyba |
A |
T |
8: 123,154,394 (GRCm39) |
I43N |
possibly damaging |
Het |
Cyp2a5 |
A |
C |
7: 26,540,511 (GRCm39) |
T375P |
possibly damaging |
Het |
Cyp2r1 |
A |
G |
7: 114,152,369 (GRCm39) |
F196S |
probably damaging |
Het |
Efcab2 |
T |
C |
1: 178,308,887 (GRCm39) |
F130S |
probably damaging |
Het |
Eml6 |
T |
G |
11: 29,788,641 (GRCm39) |
|
probably null |
Het |
Fbln5 |
A |
T |
12: 101,734,728 (GRCm39) |
C181* |
probably null |
Het |
Gpc6 |
A |
G |
14: 117,163,432 (GRCm39) |
S29G |
probably benign |
Het |
Hadhb |
T |
G |
5: 30,368,711 (GRCm39) |
S13A |
probably benign |
Het |
Hook1 |
C |
T |
4: 95,901,505 (GRCm39) |
R488C |
probably damaging |
Het |
Icam5 |
A |
G |
9: 20,948,877 (GRCm39) |
Y743C |
probably damaging |
Het |
Il15ra |
T |
C |
2: 11,724,854 (GRCm39) |
V108A |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,152,753 (GRCm39) |
N223S |
probably benign |
Het |
Kat6b |
AGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGA |
14: 21,712,417 (GRCm39) |
|
probably benign |
Het |
Kcnk1 |
T |
C |
8: 126,756,281 (GRCm39) |
C268R |
probably damaging |
Het |
Kctd19 |
A |
T |
8: 106,120,249 (GRCm39) |
L264M |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,497,907 (GRCm39) |
D3949E |
probably damaging |
Het |
Kmt2c |
A |
T |
5: 25,554,860 (GRCm39) |
I1258K |
probably benign |
Het |
Lyst |
G |
A |
13: 13,857,653 (GRCm39) |
E2481K |
possibly damaging |
Het |
Megf10 |
T |
A |
18: 57,395,090 (GRCm39) |
I484N |
probably benign |
Het |
Mettl21e |
T |
C |
1: 44,245,857 (GRCm39) |
I130V |
probably benign |
Het |
Nmnat2 |
C |
A |
1: 152,962,181 (GRCm39) |
N140K |
possibly damaging |
Het |
Nsmaf |
T |
C |
4: 6,414,976 (GRCm39) |
K630R |
probably benign |
Het |
Or2t1 |
C |
T |
14: 14,328,756 (GRCm38) |
S215L |
probably benign |
Het |
Or5w15 |
A |
T |
2: 87,568,576 (GRCm39) |
F31I |
probably benign |
Het |
Or8b38 |
G |
T |
9: 37,972,707 (GRCm39) |
L30F |
probably benign |
Het |
Or8g26 |
T |
C |
9: 39,096,172 (GRCm39) |
S230P |
possibly damaging |
Het |
Pafah1b2 |
G |
A |
9: 45,884,284 (GRCm39) |
Q123* |
probably null |
Het |
Ptprb |
T |
A |
10: 116,155,353 (GRCm39) |
N415K |
probably benign |
Het |
Rev3l |
T |
A |
10: 39,701,033 (GRCm39) |
D1843E |
probably benign |
Het |
Rps6ka4 |
T |
A |
19: 6,809,372 (GRCm39) |
R427S |
possibly damaging |
Het |
Scgb2b24 |
A |
T |
7: 33,436,795 (GRCm39) |
L106I |
probably benign |
Het |
Skint9 |
A |
T |
4: 112,248,915 (GRCm39) |
M171K |
probably benign |
Het |
Spata17 |
A |
G |
1: 186,844,756 (GRCm39) |
V281A |
possibly damaging |
Het |
Spef1 |
A |
T |
2: 131,014,625 (GRCm39) |
V99E |
probably damaging |
Het |
Srpra |
C |
T |
9: 35,126,015 (GRCm39) |
T431I |
probably damaging |
Het |
Stk32c |
G |
A |
7: 138,768,173 (GRCm39) |
P36L |
unknown |
Het |
Taar7d |
T |
C |
10: 23,903,739 (GRCm39) |
I207T |
probably benign |
Het |
Tle1 |
G |
A |
4: 72,044,504 (GRCm39) |
T501I |
probably damaging |
Het |
Tmem88b |
A |
T |
4: 155,868,733 (GRCm39) |
W172R |
probably damaging |
Het |
Usp48 |
G |
A |
4: 137,340,996 (GRCm39) |
G332E |
probably benign |
Het |
Vcl |
G |
T |
14: 21,070,726 (GRCm39) |
V771L |
probably benign |
Het |
Vmn1r200 |
T |
A |
13: 22,579,911 (GRCm39) |
M238K |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,793,621 (GRCm39) |
|
probably benign |
Het |
Vsig10l |
G |
T |
7: 43,112,795 (GRCm39) |
E18* |
probably null |
Het |
Wdfy3 |
A |
G |
5: 102,000,478 (GRCm39) |
L2964P |
probably benign |
Het |
Zfp334 |
G |
A |
2: 165,222,271 (GRCm39) |
R591W |
probably damaging |
Het |
Zpld2 |
G |
A |
4: 133,929,312 (GRCm39) |
P331L |
probably benign |
Het |
|
Other mutations in Glyatl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2140:Glyatl3
|
UTSW |
17 |
41,221,975 (GRCm39) |
missense |
probably benign |
0.01 |
R2142:Glyatl3
|
UTSW |
17 |
41,221,975 (GRCm39) |
missense |
probably benign |
0.01 |
R4246:Glyatl3
|
UTSW |
17 |
41,220,989 (GRCm39) |
missense |
probably benign |
0.15 |
R4939:Glyatl3
|
UTSW |
17 |
41,220,914 (GRCm39) |
splice site |
probably null |
|
R5134:Glyatl3
|
UTSW |
17 |
41,215,921 (GRCm39) |
missense |
probably benign |
0.08 |
R6966:Glyatl3
|
UTSW |
17 |
41,215,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7897:Glyatl3
|
UTSW |
17 |
41,215,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R9005:Glyatl3
|
UTSW |
17 |
41,223,619 (GRCm39) |
nonsense |
probably null |
|
R9185:Glyatl3
|
UTSW |
17 |
41,225,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Glyatl3
|
UTSW |
17 |
41,221,016 (GRCm39) |
missense |
probably benign |
0.25 |
R9307:Glyatl3
|
UTSW |
17 |
41,223,553 (GRCm39) |
critical splice donor site |
probably null |
|
R9397:Glyatl3
|
UTSW |
17 |
41,223,565 (GRCm39) |
nonsense |
probably null |
|
|