Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
A |
G |
2: 19,528,929 (GRCm39) |
Y151H |
possibly damaging |
Het |
Aasdh |
A |
G |
5: 77,034,105 (GRCm39) |
I482T |
possibly damaging |
Het |
Abca3 |
G |
A |
17: 24,616,526 (GRCm39) |
M989I |
probably benign |
Het |
Acvr2b |
C |
T |
9: 119,257,627 (GRCm39) |
P220L |
probably damaging |
Het |
Aqr |
T |
C |
2: 113,986,758 (GRCm39) |
D204G |
possibly damaging |
Het |
Arpp19 |
G |
T |
9: 74,964,016 (GRCm39) |
D123Y |
probably damaging |
Het |
Bod1l |
A |
G |
5: 41,983,881 (GRCm39) |
I554T |
probably damaging |
Het |
Bpifa5 |
A |
G |
2: 154,005,420 (GRCm39) |
M1V |
probably null |
Het |
Cdh3 |
T |
A |
8: 107,263,695 (GRCm39) |
|
probably null |
Het |
Cep170 |
A |
T |
1: 176,607,960 (GRCm39) |
D165E |
possibly damaging |
Het |
Cfap46 |
CCTTCTTCT |
CCTTCT |
7: 139,218,816 (GRCm39) |
|
probably benign |
Het |
Cog3 |
A |
G |
14: 75,957,152 (GRCm39) |
L627P |
probably damaging |
Het |
Col23a1 |
C |
T |
11: 51,464,995 (GRCm39) |
L453F |
probably damaging |
Het |
Cyp2a22 |
T |
A |
7: 26,633,657 (GRCm39) |
Q351L |
probably benign |
Het |
Ddx4 |
T |
G |
13: 112,772,557 (GRCm39) |
K77N |
probably benign |
Het |
Ddx4 |
C |
A |
13: 112,772,556 (GRCm39) |
E78* |
probably null |
Het |
Decr1 |
A |
T |
4: 15,931,179 (GRCm39) |
N92K |
probably benign |
Het |
Dnm2 |
T |
C |
9: 21,411,571 (GRCm39) |
L600P |
probably damaging |
Het |
Ece2 |
A |
C |
16: 20,457,932 (GRCm39) |
N356H |
probably damaging |
Het |
Ern1 |
A |
T |
11: 106,317,734 (GRCm39) |
I130N |
possibly damaging |
Het |
Fat2 |
G |
A |
11: 55,187,097 (GRCm39) |
R1250C |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,005,505 (GRCm39) |
V1968D |
probably damaging |
Het |
Frmd6 |
A |
G |
12: 70,923,987 (GRCm39) |
K82E |
probably damaging |
Het |
Gm5431 |
A |
G |
11: 48,785,826 (GRCm39) |
V183A |
probably benign |
Het |
Golgb1 |
T |
C |
16: 36,735,984 (GRCm39) |
S1744P |
possibly damaging |
Het |
Hnrnpa3 |
C |
G |
2: 75,492,914 (GRCm39) |
Q213E |
possibly damaging |
Het |
Hspa1a |
A |
G |
17: 35,189,526 (GRCm39) |
F459S |
probably damaging |
Het |
Ice1 |
A |
G |
13: 70,751,283 (GRCm39) |
L1601P |
probably damaging |
Het |
Igkv19-93 |
T |
A |
6: 68,713,323 (GRCm39) |
D102V |
probably damaging |
Het |
Kansl1 |
G |
A |
11: 104,248,352 (GRCm39) |
T534I |
probably benign |
Het |
Lpin2 |
T |
A |
17: 71,538,264 (GRCm39) |
S303R |
probably damaging |
Het |
Lrpprc |
T |
A |
17: 85,048,065 (GRCm39) |
I845F |
probably benign |
Het |
Mdn1 |
A |
G |
4: 32,749,593 (GRCm39) |
T4259A |
probably benign |
Het |
Mtcl2 |
T |
C |
2: 156,863,339 (GRCm39) |
S1197G |
probably benign |
Het |
Mtss1 |
A |
G |
15: 58,815,568 (GRCm39) |
I664T |
probably benign |
Het |
Myh8 |
A |
G |
11: 67,192,793 (GRCm39) |
E1528G |
probably benign |
Het |
Myo5c |
A |
T |
9: 75,152,319 (GRCm39) |
E69V |
probably damaging |
Het |
Myom3 |
A |
T |
4: 135,513,203 (GRCm39) |
D627V |
probably benign |
Het |
Myom3 |
A |
G |
4: 135,528,314 (GRCm39) |
N1053S |
probably benign |
Het |
Or10a4 |
G |
A |
7: 106,697,464 (GRCm39) |
R264H |
possibly damaging |
Het |
Or2d2b |
A |
T |
7: 106,705,145 (GRCm39) |
S308T |
probably benign |
Het |
Or6z3 |
T |
C |
7: 6,463,547 (GRCm39) |
V13A |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,248,247 (GRCm39) |
S399T |
probably benign |
Het |
Plch2 |
T |
A |
4: 155,091,558 (GRCm39) |
Y84F |
probably damaging |
Het |
Ppp1r13b |
A |
G |
12: 111,802,160 (GRCm39) |
S278P |
probably benign |
Het |
Prol1 |
A |
G |
5: 88,475,736 (GRCm39) |
Y42C |
probably damaging |
Het |
Pum2 |
A |
G |
12: 8,798,205 (GRCm39) |
E906G |
probably damaging |
Het |
Pwwp3a |
T |
A |
10: 80,068,848 (GRCm39) |
C331S |
probably benign |
Het |
Rbp2 |
G |
T |
9: 98,372,700 (GRCm39) |
S13I |
probably benign |
Het |
Rbp4 |
G |
A |
19: 38,113,428 (GRCm39) |
T30M |
probably benign |
Het |
Selenbp1 |
T |
C |
3: 94,851,157 (GRCm39) |
L351P |
possibly damaging |
Het |
Serpinb6b |
T |
C |
13: 33,156,255 (GRCm39) |
F115S |
probably damaging |
Het |
Tigd3 |
A |
T |
19: 5,942,870 (GRCm39) |
Y87N |
probably damaging |
Het |
Tigd5 |
T |
A |
15: 75,782,871 (GRCm39) |
L411H |
probably damaging |
Het |
Ttc3 |
T |
C |
16: 94,258,272 (GRCm39) |
|
probably null |
Het |
Zfand4 |
T |
C |
6: 116,250,575 (GRCm39) |
F2L |
probably damaging |
Het |
Zfhx3 |
C |
T |
8: 109,682,020 (GRCm39) |
T3153M |
possibly damaging |
Het |
Zfp697 |
T |
G |
3: 98,334,855 (GRCm39) |
C207G |
possibly damaging |
Het |
Zfp935 |
T |
C |
13: 62,602,685 (GRCm39) |
T172A |
probably benign |
Het |
Znrf3 |
G |
T |
11: 5,230,865 (GRCm39) |
L883I |
probably benign |
Het |
|
Other mutations in Uhmk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01634:Uhmk1
|
APN |
1 |
170,034,682 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02451:Uhmk1
|
APN |
1 |
170,040,095 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0452:Uhmk1
|
UTSW |
1 |
170,039,971 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0507:Uhmk1
|
UTSW |
1 |
170,034,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Uhmk1
|
UTSW |
1 |
170,036,222 (GRCm39) |
critical splice donor site |
probably null |
|
R1466:Uhmk1
|
UTSW |
1 |
170,036,222 (GRCm39) |
critical splice donor site |
probably null |
|
R1584:Uhmk1
|
UTSW |
1 |
170,036,222 (GRCm39) |
critical splice donor site |
probably null |
|
R1676:Uhmk1
|
UTSW |
1 |
170,027,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R1806:Uhmk1
|
UTSW |
1 |
170,038,628 (GRCm39) |
missense |
probably damaging |
0.98 |
R2039:Uhmk1
|
UTSW |
1 |
170,039,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4567:Uhmk1
|
UTSW |
1 |
170,032,686 (GRCm39) |
nonsense |
probably null |
|
R4658:Uhmk1
|
UTSW |
1 |
170,034,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Uhmk1
|
UTSW |
1 |
170,027,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R5186:Uhmk1
|
UTSW |
1 |
170,038,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R5686:Uhmk1
|
UTSW |
1 |
170,038,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R6210:Uhmk1
|
UTSW |
1 |
170,039,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R6238:Uhmk1
|
UTSW |
1 |
170,027,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R6682:Uhmk1
|
UTSW |
1 |
170,039,804 (GRCm39) |
critical splice donor site |
probably null |
|
R7522:Uhmk1
|
UTSW |
1 |
170,042,809 (GRCm39) |
start codon destroyed |
probably benign |
0.00 |
R7582:Uhmk1
|
UTSW |
1 |
170,027,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R7916:Uhmk1
|
UTSW |
1 |
170,032,757 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9097:Uhmk1
|
UTSW |
1 |
170,042,879 (GRCm39) |
unclassified |
probably benign |
|
R9483:Uhmk1
|
UTSW |
1 |
170,034,913 (GRCm39) |
critical splice donor site |
probably null |
|
|