Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
G |
5: 77,030,528 (GRCm39) |
S691P |
probably benign |
Het |
Adgrb3 |
T |
C |
1: 25,265,912 (GRCm39) |
|
probably null |
Het |
Ankar |
A |
G |
1: 72,718,714 (GRCm39) |
|
probably benign |
Het |
Aplf |
A |
T |
6: 87,623,015 (GRCm39) |
Y355N |
probably damaging |
Het |
Bms1 |
A |
G |
6: 118,366,350 (GRCm39) |
|
probably benign |
Het |
Catsperb |
T |
C |
12: 101,429,373 (GRCm39) |
I182T |
probably damaging |
Het |
Cd300ld2 |
T |
C |
11: 114,904,603 (GRCm39) |
D88G |
probably benign |
Het |
Cebpz |
T |
C |
17: 79,242,181 (GRCm39) |
N491S |
probably damaging |
Het |
Crybg2 |
T |
C |
4: 133,808,770 (GRCm39) |
S1415P |
probably damaging |
Het |
Ddc |
A |
G |
11: 11,779,131 (GRCm39) |
V331A |
probably benign |
Het |
Dhrs11 |
A |
G |
11: 84,713,943 (GRCm39) |
M136T |
probably damaging |
Het |
Eapp |
G |
A |
12: 54,732,733 (GRCm39) |
Q126* |
probably null |
Het |
Fam111a |
T |
A |
19: 12,565,142 (GRCm39) |
V297D |
probably damaging |
Het |
Fbxo10 |
A |
C |
4: 45,062,118 (GRCm39) |
L136R |
probably damaging |
Het |
Fbxo30 |
T |
A |
10: 11,167,118 (GRCm39) |
H613Q |
possibly damaging |
Het |
Frk |
A |
T |
10: 34,467,806 (GRCm39) |
|
probably null |
Het |
Gm10392 |
T |
A |
11: 77,408,307 (GRCm39) |
D104V |
probably benign |
Het |
Gpn1 |
A |
G |
5: 31,654,682 (GRCm39) |
E78G |
possibly damaging |
Het |
Hhip |
T |
C |
8: 80,716,905 (GRCm39) |
Y506C |
probably damaging |
Het |
Hid1 |
G |
A |
11: 115,247,576 (GRCm39) |
S274L |
possibly damaging |
Het |
Immp2l |
G |
T |
12: 41,750,548 (GRCm39) |
|
probably benign |
Het |
Klhl21 |
T |
C |
4: 152,094,081 (GRCm39) |
F228L |
possibly damaging |
Het |
Lamc1 |
T |
A |
1: 153,119,224 (GRCm39) |
|
probably null |
Het |
Lars1 |
G |
A |
18: 42,343,115 (GRCm39) |
R1101C |
probably damaging |
Het |
Lratd1 |
G |
A |
12: 14,200,409 (GRCm39) |
A106V |
probably benign |
Het |
Magi2 |
T |
C |
5: 19,432,330 (GRCm39) |
V15A |
probably benign |
Het |
Map2k7 |
T |
C |
8: 4,293,621 (GRCm39) |
|
probably null |
Het |
Mga |
T |
A |
2: 119,794,441 (GRCm39) |
H2590Q |
possibly damaging |
Het |
Mlxip |
T |
C |
5: 123,588,286 (GRCm39) |
I238T |
possibly damaging |
Het |
Mylk |
T |
A |
16: 34,695,956 (GRCm39) |
D230E |
probably benign |
Het |
Nacad |
T |
A |
11: 6,551,185 (GRCm39) |
T669S |
probably benign |
Het |
Nin |
C |
T |
12: 70,078,512 (GRCm39) |
M1691I |
probably benign |
Het |
Nlrp4d |
C |
T |
7: 10,116,164 (GRCm39) |
A203T |
probably damaging |
Het |
Or10aa1 |
T |
C |
1: 173,870,046 (GRCm39) |
F177L |
probably benign |
Het |
Or10q12 |
A |
T |
19: 13,745,874 (GRCm39) |
H56L |
probably benign |
Het |
Or4c106 |
T |
G |
2: 88,682,606 (GRCm39) |
F104C |
probably damaging |
Het |
Or4k5 |
C |
A |
14: 50,386,231 (GRCm39) |
M33I |
probably benign |
Het |
Or4k51 |
A |
T |
2: 111,584,770 (GRCm39) |
M59L |
probably damaging |
Het |
Or5ac19 |
A |
G |
16: 59,089,394 (GRCm39) |
V212A |
probably benign |
Het |
Osbp |
C |
A |
19: 11,955,193 (GRCm39) |
Q282K |
probably benign |
Het |
Osbpl2 |
A |
G |
2: 179,790,256 (GRCm39) |
S177G |
probably damaging |
Het |
Pax1 |
A |
G |
2: 147,208,175 (GRCm39) |
H261R |
possibly damaging |
Het |
Pcif1 |
A |
T |
2: 164,728,647 (GRCm39) |
L274F |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,188,049 (GRCm39) |
S3420P |
probably benign |
Het |
Prss3 |
A |
C |
6: 41,354,561 (GRCm39) |
|
probably benign |
Het |
Ptk2b |
T |
C |
14: 66,400,563 (GRCm39) |
T751A |
possibly damaging |
Het |
Pus10 |
T |
C |
11: 23,623,239 (GRCm39) |
V126A |
probably damaging |
Het |
Rai14 |
A |
C |
15: 10,588,002 (GRCm39) |
D258E |
probably damaging |
Het |
Rbp3 |
T |
C |
14: 33,676,481 (GRCm39) |
V143A |
possibly damaging |
Het |
Sarm1 |
G |
A |
11: 78,374,153 (GRCm39) |
Q625* |
probably null |
Het |
Scgb1b21 |
T |
G |
7: 33,227,092 (GRCm39) |
|
noncoding transcript |
Het |
Scrn1 |
A |
T |
6: 54,497,754 (GRCm39) |
V279E |
probably damaging |
Het |
Sipa1l2 |
T |
C |
8: 126,148,634 (GRCm39) |
T1670A |
probably damaging |
Het |
Slc9a4 |
A |
T |
1: 40,640,122 (GRCm39) |
I305F |
probably benign |
Het |
Smarcc1 |
A |
G |
9: 110,042,685 (GRCm39) |
T918A |
probably damaging |
Het |
Tas2r109 |
A |
T |
6: 132,957,389 (GRCm39) |
H180Q |
probably benign |
Het |
Tas2r121 |
G |
A |
6: 132,677,193 (GRCm39) |
R260* |
probably null |
Het |
Tenm3 |
T |
C |
8: 48,732,109 (GRCm39) |
D1249G |
probably benign |
Het |
Tgtp1 |
C |
G |
11: 48,878,357 (GRCm39) |
G116A |
probably damaging |
Het |
Tial1 |
A |
G |
7: 128,045,634 (GRCm39) |
Y317H |
probably damaging |
Het |
Top6bl |
T |
A |
19: 4,702,199 (GRCm39) |
K282N |
probably damaging |
Het |
Trim66 |
A |
T |
7: 109,054,287 (GRCm39) |
W1308R |
probably damaging |
Het |
Ulk2 |
T |
G |
11: 61,674,371 (GRCm39) |
K878N |
possibly damaging |
Het |
Zfp41 |
T |
A |
15: 75,490,140 (GRCm39) |
S31T |
possibly damaging |
Het |
|
Other mutations in Decr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01657:Decr2
|
APN |
17 |
26,301,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Decr2
|
APN |
17 |
26,306,354 (GRCm39) |
missense |
probably benign |
0.01 |
R0003:Decr2
|
UTSW |
17 |
26,302,027 (GRCm39) |
missense |
probably benign |
0.00 |
R0003:Decr2
|
UTSW |
17 |
26,302,027 (GRCm39) |
missense |
probably benign |
0.00 |
R1588:Decr2
|
UTSW |
17 |
26,302,002 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1903:Decr2
|
UTSW |
17 |
26,306,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R1968:Decr2
|
UTSW |
17 |
26,302,053 (GRCm39) |
missense |
probably benign |
0.00 |
R2269:Decr2
|
UTSW |
17 |
26,302,858 (GRCm39) |
missense |
probably benign |
0.03 |
R4758:Decr2
|
UTSW |
17 |
26,307,914 (GRCm39) |
missense |
probably damaging |
0.96 |
R5021:Decr2
|
UTSW |
17 |
26,301,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Decr2
|
UTSW |
17 |
26,306,443 (GRCm39) |
splice site |
probably null |
|
R6608:Decr2
|
UTSW |
17 |
26,302,858 (GRCm39) |
missense |
probably benign |
0.30 |
R6661:Decr2
|
UTSW |
17 |
26,302,561 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8036:Decr2
|
UTSW |
17 |
26,301,962 (GRCm39) |
missense |
probably damaging |
0.97 |
R8799:Decr2
|
UTSW |
17 |
26,307,911 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8969:Decr2
|
UTSW |
17 |
26,306,355 (GRCm39) |
missense |
probably benign |
|
R9706:Decr2
|
UTSW |
17 |
26,302,869 (GRCm39) |
missense |
probably benign |
0.01 |
|