Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921517D22Rik |
A |
T |
13: 59,838,486 (GRCm39) |
D115E |
probably benign |
Het |
Abcc1 |
T |
A |
16: 14,214,315 (GRCm39) |
L197Q |
probably damaging |
Het |
Adamts14 |
T |
G |
10: 61,057,706 (GRCm39) |
N547T |
probably benign |
Het |
Ampd3 |
T |
A |
7: 110,394,982 (GRCm39) |
S301R |
probably benign |
Het |
Atg9a |
G |
A |
1: 75,162,342 (GRCm39) |
Q523* |
probably null |
Het |
Atl1 |
A |
T |
12: 70,002,093 (GRCm39) |
T351S |
probably damaging |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Cacna1c |
T |
C |
6: 118,614,735 (GRCm39) |
I1315V |
|
Het |
Col12a1 |
C |
T |
9: 79,555,979 (GRCm39) |
G2013R |
probably damaging |
Het |
Cpne2 |
A |
G |
8: 95,280,040 (GRCm39) |
D153G |
probably benign |
Het |
Cryzl1 |
T |
C |
16: 91,489,251 (GRCm39) |
S205G |
probably benign |
Het |
Cux1 |
C |
T |
5: 136,594,251 (GRCm39) |
A5T |
probably benign |
Het |
Ddx60 |
T |
C |
8: 62,395,669 (GRCm39) |
|
probably null |
Het |
Dnajc13 |
G |
A |
9: 104,067,590 (GRCm39) |
P1190S |
probably benign |
Het |
Fbxw7 |
T |
A |
3: 84,881,859 (GRCm39) |
V526E |
|
Het |
Fig4 |
C |
A |
10: 41,139,097 (GRCm39) |
G369C |
probably damaging |
Het |
Gabra1 |
C |
T |
11: 42,026,315 (GRCm39) |
A326T |
probably damaging |
Het |
Gbe1 |
G |
A |
16: 70,284,964 (GRCm39) |
G429S |
probably benign |
Het |
Gtf3c5 |
A |
T |
2: 28,460,506 (GRCm39) |
H364Q |
probably benign |
Het |
Hcfc2 |
T |
A |
10: 82,574,201 (GRCm39) |
I125N |
probably damaging |
Het |
Hnrnpul1 |
A |
T |
7: 25,453,902 (GRCm39) |
D53E |
probably benign |
Het |
Ift56 |
T |
A |
6: 38,382,880 (GRCm39) |
H338Q |
probably damaging |
Het |
Il18 |
A |
T |
9: 50,492,818 (GRCm39) |
D128V |
possibly damaging |
Het |
Intu |
T |
A |
3: 40,608,202 (GRCm39) |
S71R |
probably damaging |
Het |
Klhl6 |
T |
C |
16: 19,775,940 (GRCm39) |
E206G |
possibly damaging |
Het |
Lcor |
T |
A |
19: 41,571,343 (GRCm39) |
S179T |
probably damaging |
Het |
Mcub |
A |
G |
3: 129,727,328 (GRCm39) |
F93L |
probably damaging |
Het |
Mdga2 |
T |
C |
12: 67,267,803 (GRCm39) |
Y5C |
unknown |
Het |
Naip1 |
C |
A |
13: 100,565,721 (GRCm39) |
V354L |
probably benign |
Het |
Naip5 |
A |
G |
13: 100,358,167 (GRCm39) |
V1023A |
probably benign |
Het |
Ndufaf1 |
A |
G |
2: 119,490,568 (GRCm39) |
L166P |
probably damaging |
Het |
Ninl |
A |
T |
2: 150,801,827 (GRCm39) |
L147H |
probably damaging |
Het |
Or4c12 |
A |
G |
2: 89,774,024 (GRCm39) |
V145A |
possibly damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,636 (GRCm39) |
I102T |
probably damaging |
Het |
Otogl |
C |
T |
10: 107,689,127 (GRCm39) |
|
probably null |
Het |
Otulin |
AT |
ATT |
15: 27,606,404 (GRCm39) |
|
probably null |
Het |
Prdm13 |
G |
T |
4: 21,679,327 (GRCm39) |
H388N |
unknown |
Het |
Pwwp2b |
T |
C |
7: 138,835,099 (GRCm39) |
V180A |
probably damaging |
Het |
Reep4 |
T |
A |
14: 70,783,951 (GRCm39) |
S23T |
probably damaging |
Het |
Rusc2 |
T |
A |
4: 43,425,378 (GRCm39) |
L1161Q |
probably damaging |
Het |
Scgb1b3 |
G |
A |
7: 31,075,404 (GRCm39) |
|
probably null |
Het |
Scn10a |
G |
T |
9: 119,499,455 (GRCm39) |
N279K |
probably benign |
Het |
Smurf2 |
A |
G |
11: 106,715,578 (GRCm39) |
L643S |
probably damaging |
Het |
Sox12 |
G |
A |
2: 152,239,192 (GRCm39) |
P143S |
unknown |
Het |
Specc1 |
C |
T |
11: 62,009,501 (GRCm39) |
T339I |
possibly damaging |
Het |
Tas2r139 |
T |
C |
6: 42,118,720 (GRCm39) |
V284A |
probably benign |
Het |
Thumpd3 |
T |
A |
6: 113,040,107 (GRCm39) |
C330* |
probably null |
Het |
Ttn |
A |
G |
2: 76,537,298 (GRCm39) |
S34877P |
possibly damaging |
Het |
Zfp568 |
T |
C |
7: 29,697,629 (GRCm39) |
S104P |
possibly damaging |
Het |
Zfp933 |
G |
A |
4: 147,912,910 (GRCm39) |
H50Y |
possibly damaging |
Het |
|
Other mutations in Phf11b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00560:Phf11b
|
APN |
14 |
59,562,324 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01116:Phf11b
|
APN |
14 |
59,560,631 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01446:Phf11b
|
APN |
14 |
59,578,740 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02224:Phf11b
|
APN |
14 |
59,563,515 (GRCm39) |
splice site |
probably benign |
|
IGL03062:Phf11b
|
APN |
14 |
59,562,373 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Phf11b
|
UTSW |
14 |
59,560,611 (GRCm39) |
splice site |
probably benign |
|
R1795:Phf11b
|
UTSW |
14 |
59,565,554 (GRCm39) |
missense |
probably benign |
0.00 |
R3774:Phf11b
|
UTSW |
14 |
59,563,506 (GRCm39) |
missense |
probably benign |
0.45 |
R4553:Phf11b
|
UTSW |
14 |
59,578,734 (GRCm39) |
missense |
probably benign |
0.10 |
R5460:Phf11b
|
UTSW |
14 |
59,568,713 (GRCm39) |
missense |
probably benign |
0.01 |
R5620:Phf11b
|
UTSW |
14 |
59,558,953 (GRCm39) |
missense |
probably benign |
0.01 |
R5985:Phf11b
|
UTSW |
14 |
59,559,027 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5990:Phf11b
|
UTSW |
14 |
59,562,375 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6775:Phf11b
|
UTSW |
14 |
59,576,094 (GRCm39) |
missense |
probably benign |
0.14 |
R6836:Phf11b
|
UTSW |
14 |
59,565,572 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7197:Phf11b
|
UTSW |
14 |
59,563,507 (GRCm39) |
missense |
probably benign |
0.06 |
R7953:Phf11b
|
UTSW |
14 |
59,568,722 (GRCm39) |
missense |
probably benign |
0.35 |
R8043:Phf11b
|
UTSW |
14 |
59,568,722 (GRCm39) |
missense |
probably benign |
0.35 |
R8229:Phf11b
|
UTSW |
14 |
59,568,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9585:Phf11b
|
UTSW |
14 |
59,568,704 (GRCm39) |
missense |
probably benign |
0.02 |
|