Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
T |
A |
4: 62,461,978 (GRCm39) |
|
probably null |
Het |
Ackr4 |
A |
G |
9: 103,976,660 (GRCm39) |
F96L |
possibly damaging |
Het |
Aco1 |
T |
C |
4: 40,186,376 (GRCm39) |
I596T |
possibly damaging |
Het |
Aff3 |
G |
A |
1: 38,244,135 (GRCm39) |
R879W |
probably benign |
Het |
Apob |
A |
G |
12: 8,061,135 (GRCm39) |
R3206G |
probably damaging |
Het |
Atg7 |
T |
A |
6: 114,663,057 (GRCm39) |
D224E |
possibly damaging |
Het |
Capn12 |
T |
C |
7: 28,582,626 (GRCm39) |
F167S |
probably damaging |
Het |
Ccdc3 |
T |
G |
2: 5,233,848 (GRCm39) |
V224G |
probably damaging |
Het |
Ces4a |
G |
A |
8: 105,874,714 (GRCm39) |
V452I |
probably damaging |
Het |
Cherp |
G |
A |
8: 73,215,852 (GRCm39) |
R834C |
|
Het |
Clptm1l |
T |
A |
13: 73,760,547 (GRCm39) |
I310N |
probably damaging |
Het |
Cog3 |
A |
T |
14: 75,978,003 (GRCm39) |
D230E |
probably damaging |
Het |
Crb1 |
T |
A |
1: 139,165,005 (GRCm39) |
I1101F |
probably damaging |
Het |
Cts6 |
A |
T |
13: 61,343,282 (GRCm39) |
M313K |
probably damaging |
Het |
Cyp2c66 |
T |
A |
19: 39,174,906 (GRCm39) |
C435* |
probably null |
Het |
Defb13 |
A |
G |
8: 22,438,562 (GRCm39) |
E40G |
probably benign |
Het |
Dis3l |
T |
C |
9: 64,219,112 (GRCm39) |
D606G |
possibly damaging |
Het |
Dop1b |
T |
C |
16: 93,568,675 (GRCm39) |
L1579P |
probably damaging |
Het |
Foxa3 |
A |
G |
7: 18,748,109 (GRCm39) |
V339A |
probably benign |
Het |
Gcn1 |
G |
A |
5: 115,747,921 (GRCm39) |
G1776E |
probably damaging |
Het |
Gls2 |
A |
G |
10: 128,037,154 (GRCm39) |
T232A |
probably benign |
Het |
Gprc6a |
A |
T |
10: 51,503,355 (GRCm39) |
Y169* |
probably null |
Het |
Guca2b |
T |
C |
4: 119,516,001 (GRCm39) |
S18G |
unknown |
Het |
Hars2 |
A |
G |
18: 36,922,288 (GRCm39) |
D301G |
possibly damaging |
Het |
Haus5 |
T |
A |
7: 30,358,984 (GRCm39) |
Q226L |
possibly damaging |
Het |
Hc |
G |
A |
2: 34,902,910 (GRCm39) |
|
probably null |
Het |
Hivep2 |
T |
C |
10: 14,004,011 (GRCm39) |
V203A |
probably damaging |
Het |
Hoxc8 |
A |
G |
15: 102,899,543 (GRCm39) |
Y111C |
probably damaging |
Het |
Hoxd13 |
G |
T |
2: 74,498,661 (GRCm39) |
R3L |
probably benign |
Het |
Hspa8 |
T |
G |
9: 40,713,897 (GRCm39) |
I130S |
probably damaging |
Het |
Ier5l |
C |
A |
2: 30,362,861 (GRCm39) |
C388F |
possibly damaging |
Het |
Ldc1 |
C |
T |
4: 130,109,156 (GRCm39) |
V295M |
possibly damaging |
Het |
Lmx1a |
A |
G |
1: 167,517,372 (GRCm39) |
N10S |
probably benign |
Het |
Map2 |
T |
C |
1: 66,454,272 (GRCm39) |
I1054T |
probably benign |
Het |
Me1 |
C |
T |
9: 86,501,790 (GRCm39) |
D268N |
probably damaging |
Het |
Muc6 |
G |
A |
7: 141,226,525 (GRCm39) |
P1501S |
unknown |
Het |
Myo1d |
T |
C |
11: 80,528,900 (GRCm39) |
M641V |
probably benign |
Het |
Nuggc |
G |
A |
14: 65,878,731 (GRCm39) |
R667K |
probably benign |
Het |
Oprl1 |
T |
A |
2: 181,360,717 (GRCm39) |
C231S |
probably damaging |
Het |
Or11g26 |
T |
C |
14: 50,753,015 (GRCm39) |
F118S |
probably damaging |
Het |
Or13p10 |
A |
C |
4: 118,523,604 (GRCm39) |
N297H |
probably damaging |
Het |
Pard3b |
C |
A |
1: 62,676,957 (GRCm39) |
Q1163K |
probably benign |
Het |
Pik3c2a |
T |
C |
7: 116,017,283 (GRCm39) |
Y158C |
probably damaging |
Het |
Prune2 |
T |
G |
19: 17,098,629 (GRCm39) |
S1378A |
probably benign |
Het |
Ralgps2 |
G |
T |
1: 156,712,110 (GRCm39) |
T158K |
probably damaging |
Het |
Rbm42 |
T |
A |
7: 30,344,582 (GRCm39) |
E227V |
unknown |
Het |
Ripor3 |
T |
C |
2: 167,825,119 (GRCm39) |
R797G |
possibly damaging |
Het |
Ryr3 |
T |
A |
2: 112,492,855 (GRCm39) |
H3764L |
possibly damaging |
Het |
Sbno2 |
T |
C |
10: 79,900,221 (GRCm39) |
Y541C |
probably damaging |
Het |
Scn5a |
A |
G |
9: 119,365,030 (GRCm39) |
V396A |
probably damaging |
Het |
Slc36a3 |
A |
G |
11: 55,039,409 (GRCm39) |
L73P |
probably damaging |
Het |
Spag16 |
T |
C |
1: 69,934,407 (GRCm39) |
I278T |
probably benign |
Het |
Stx18 |
T |
A |
5: 38,285,450 (GRCm39) |
L274* |
probably null |
Het |
Terb1 |
A |
T |
8: 105,211,003 (GRCm39) |
N341K |
probably damaging |
Het |
Timm29 |
A |
G |
9: 21,505,001 (GRCm39) |
Y223C |
probably damaging |
Het |
Tmprss2 |
T |
A |
16: 97,369,665 (GRCm39) |
M370L |
probably benign |
Het |
Tmtc3 |
T |
A |
10: 100,283,296 (GRCm39) |
N753I |
probably damaging |
Het |
Tnpo3 |
A |
T |
6: 29,558,832 (GRCm39) |
C699* |
probably null |
Het |
Trav5d-4 |
G |
A |
14: 53,239,208 (GRCm39) |
W13* |
probably null |
Het |
Trdn |
A |
G |
10: 33,320,074 (GRCm39) |
|
probably null |
Het |
Tsg101 |
A |
T |
7: 46,558,808 (GRCm39) |
Y68N |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,664,062 (GRCm39) |
V11649A |
unknown |
Het |
Wnk2 |
A |
T |
13: 49,248,914 (GRCm39) |
V379D |
probably damaging |
Het |
Xpnpep1 |
A |
G |
19: 52,990,903 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Yme1l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Yme1l1
|
APN |
2 |
23,082,512 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01764:Yme1l1
|
APN |
2 |
23,052,556 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03289:Yme1l1
|
APN |
2 |
23,050,280 (GRCm39) |
missense |
probably benign |
|
R0043:Yme1l1
|
UTSW |
2 |
23,077,815 (GRCm39) |
missense |
probably damaging |
0.97 |
R0540:Yme1l1
|
UTSW |
2 |
23,082,527 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0583:Yme1l1
|
UTSW |
2 |
23,076,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0661:Yme1l1
|
UTSW |
2 |
23,081,054 (GRCm39) |
missense |
probably damaging |
0.96 |
R0673:Yme1l1
|
UTSW |
2 |
23,058,300 (GRCm39) |
missense |
probably benign |
0.03 |
R2154:Yme1l1
|
UTSW |
2 |
23,052,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R2241:Yme1l1
|
UTSW |
2 |
23,086,912 (GRCm39) |
nonsense |
probably null |
|
R2270:Yme1l1
|
UTSW |
2 |
23,065,232 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2345:Yme1l1
|
UTSW |
2 |
23,084,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R3837:Yme1l1
|
UTSW |
2 |
23,081,092 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4344:Yme1l1
|
UTSW |
2 |
23,063,073 (GRCm39) |
missense |
probably benign |
0.02 |
R4368:Yme1l1
|
UTSW |
2 |
23,050,223 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4412:Yme1l1
|
UTSW |
2 |
23,065,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Yme1l1
|
UTSW |
2 |
23,076,344 (GRCm39) |
critical splice donor site |
probably null |
|
R4472:Yme1l1
|
UTSW |
2 |
23,076,344 (GRCm39) |
critical splice donor site |
probably null |
|
R4934:Yme1l1
|
UTSW |
2 |
23,058,333 (GRCm39) |
nonsense |
probably null |
|
R5033:Yme1l1
|
UTSW |
2 |
23,084,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5388:Yme1l1
|
UTSW |
2 |
23,052,569 (GRCm39) |
missense |
probably benign |
0.01 |
R5389:Yme1l1
|
UTSW |
2 |
23,083,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Yme1l1
|
UTSW |
2 |
23,058,342 (GRCm39) |
missense |
probably damaging |
0.96 |
R5947:Yme1l1
|
UTSW |
2 |
23,085,318 (GRCm39) |
intron |
probably benign |
|
R6243:Yme1l1
|
UTSW |
2 |
23,083,184 (GRCm39) |
missense |
probably benign |
0.00 |
R6724:Yme1l1
|
UTSW |
2 |
23,084,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R6891:Yme1l1
|
UTSW |
2 |
23,085,401 (GRCm39) |
missense |
probably damaging |
0.99 |
R7016:Yme1l1
|
UTSW |
2 |
23,076,367 (GRCm39) |
splice site |
probably null |
|
R7565:Yme1l1
|
UTSW |
2 |
23,050,232 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7589:Yme1l1
|
UTSW |
2 |
23,050,274 (GRCm39) |
missense |
probably benign |
0.01 |
R7751:Yme1l1
|
UTSW |
2 |
23,077,856 (GRCm39) |
critical splice donor site |
probably null |
|
R7871:Yme1l1
|
UTSW |
2 |
23,071,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R7909:Yme1l1
|
UTSW |
2 |
23,084,769 (GRCm39) |
missense |
probably benign |
0.00 |
R8203:Yme1l1
|
UTSW |
2 |
23,054,538 (GRCm39) |
missense |
probably benign |
0.00 |
R8474:Yme1l1
|
UTSW |
2 |
23,052,584 (GRCm39) |
missense |
probably benign |
|
R8746:Yme1l1
|
UTSW |
2 |
23,052,543 (GRCm39) |
missense |
probably benign |
0.05 |
R9154:Yme1l1
|
UTSW |
2 |
23,077,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R9159:Yme1l1
|
UTSW |
2 |
23,063,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R9361:Yme1l1
|
UTSW |
2 |
23,081,063 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Yme1l1
|
UTSW |
2 |
23,083,196 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Yme1l1
|
UTSW |
2 |
23,052,529 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Yme1l1
|
UTSW |
2 |
23,076,889 (GRCm39) |
missense |
probably benign |
0.03 |
|