Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930571K23Rik |
C |
A |
7: 124,968,311 (GRCm39) |
|
noncoding transcript |
Het |
Adra1d |
C |
A |
2: 131,404,055 (GRCm39) |
E12* |
probably null |
Het |
Ago4 |
A |
T |
4: 126,410,864 (GRCm39) |
D208E |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,250,881 (GRCm39) |
|
probably null |
Het |
Atxn2 |
C |
T |
5: 121,919,456 (GRCm39) |
S388L |
probably damaging |
Het |
Bbox1 |
A |
T |
2: 110,135,976 (GRCm39) |
M1K |
probably null |
Het |
Btaf1 |
G |
A |
19: 36,979,845 (GRCm39) |
R1538H |
probably benign |
Het |
Car11 |
G |
A |
7: 45,350,783 (GRCm39) |
G93E |
probably damaging |
Het |
Col18a1 |
A |
G |
10: 76,932,102 (GRCm39) |
L329P |
unknown |
Het |
Copb2 |
T |
A |
9: 98,453,701 (GRCm39) |
|
probably benign |
Het |
Cracdl |
T |
C |
1: 37,664,381 (GRCm39) |
M506V |
probably benign |
Het |
Dnah2 |
G |
T |
11: 69,415,032 (GRCm39) |
S234* |
probably null |
Het |
Dnah9 |
T |
C |
11: 65,895,995 (GRCm39) |
Y2460C |
probably damaging |
Het |
Dnai2 |
G |
C |
11: 114,647,993 (GRCm39) |
|
probably benign |
Het |
Dst |
C |
A |
1: 34,251,367 (GRCm39) |
T1814K |
probably benign |
Het |
F11 |
A |
G |
8: 45,701,675 (GRCm39) |
S353P |
probably damaging |
Het |
Fancm |
A |
T |
12: 65,160,544 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
T |
C |
2: 82,816,782 (GRCm39) |
S4172P |
probably benign |
Het |
G530012D18Rik |
T |
G |
1: 85,504,925 (GRCm39) |
|
probably benign |
Het |
Gca |
T |
G |
2: 62,520,318 (GRCm39) |
S159R |
probably damaging |
Het |
Gja8 |
T |
G |
3: 96,827,033 (GRCm39) |
T210P |
probably damaging |
Het |
Gm5117 |
T |
A |
8: 32,228,383 (GRCm39) |
|
noncoding transcript |
Het |
Gm5900 |
T |
A |
7: 104,599,571 (GRCm39) |
|
noncoding transcript |
Het |
Gpi1 |
A |
G |
7: 33,905,348 (GRCm39) |
S359P |
probably damaging |
Het |
Grm5 |
A |
G |
7: 87,685,299 (GRCm39) |
E472G |
probably benign |
Het |
Gsta5 |
T |
A |
9: 78,202,089 (GRCm39) |
M1K |
probably null |
Het |
Hoxd12 |
G |
A |
2: 74,505,815 (GRCm39) |
A129T |
possibly damaging |
Het |
Ifnlr1 |
G |
T |
4: 135,432,559 (GRCm39) |
D332Y |
probably damaging |
Het |
Ift140 |
T |
C |
17: 25,255,282 (GRCm39) |
I466T |
probably benign |
Het |
Kansl2 |
A |
G |
15: 98,426,742 (GRCm39) |
|
probably null |
Het |
Kat2a |
T |
C |
11: 100,602,968 (GRCm39) |
Q88R |
probably benign |
Het |
Kcnh7 |
T |
C |
2: 62,552,261 (GRCm39) |
D910G |
probably benign |
Het |
Klk1b1 |
T |
C |
7: 43,618,803 (GRCm39) |
V60A |
probably damaging |
Het |
Krt7 |
A |
C |
15: 101,310,538 (GRCm39) |
I62L |
probably benign |
Het |
Llgl1 |
A |
G |
11: 60,600,862 (GRCm39) |
K653E |
probably damaging |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Maco1 |
A |
G |
4: 134,531,699 (GRCm39) |
S657P |
probably damaging |
Het |
Mafb |
T |
G |
2: 160,208,496 (GRCm39) |
E34A |
probably damaging |
Het |
Meiob |
T |
C |
17: 25,035,571 (GRCm39) |
|
probably benign |
Het |
Mllt10 |
C |
A |
2: 18,069,935 (GRCm39) |
D30E |
possibly damaging |
Het |
Mprip |
T |
A |
11: 59,640,334 (GRCm39) |
|
probably benign |
Het |
Muc5b |
A |
T |
7: 141,412,798 (GRCm39) |
N1915Y |
unknown |
Het |
Mycbp2 |
C |
T |
14: 103,392,691 (GRCm39) |
R3290Q |
probably damaging |
Het |
Ntaq1 |
C |
A |
15: 58,017,020 (GRCm39) |
A145D |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,933,140 (GRCm39) |
|
probably benign |
Het |
Olfm3 |
T |
A |
3: 114,915,959 (GRCm39) |
V277D |
probably damaging |
Het |
Omp |
A |
T |
7: 97,794,552 (GRCm39) |
M25K |
possibly damaging |
Het |
Or10d4b |
T |
A |
9: 39,534,727 (GRCm39) |
F101I |
probably damaging |
Het |
Or4b12 |
C |
T |
2: 90,095,950 (GRCm39) |
V275I |
probably damaging |
Het |
Or4k40 |
G |
A |
2: 111,250,796 (GRCm39) |
P167S |
possibly damaging |
Het |
Or52n2c |
G |
A |
7: 104,574,894 (GRCm39) |
H26Y |
probably benign |
Het |
Otoa |
C |
T |
7: 120,759,695 (GRCm39) |
T1099I |
probably benign |
Het |
Pcdh15 |
T |
G |
10: 74,467,331 (GRCm39) |
S1715A |
probably benign |
Het |
Pcnx4 |
T |
C |
12: 72,613,746 (GRCm39) |
W564R |
probably damaging |
Het |
Pde12 |
T |
C |
14: 26,386,681 (GRCm39) |
*609W |
probably null |
Het |
Pitpnm2 |
T |
C |
5: 124,274,389 (GRCm39) |
E240G |
probably damaging |
Het |
Plppr4 |
G |
T |
3: 117,125,355 (GRCm39) |
N161K |
probably damaging |
Het |
Pramel27 |
G |
A |
4: 143,578,561 (GRCm39) |
V274I |
probably benign |
Het |
Ptprd |
C |
A |
4: 76,004,248 (GRCm39) |
|
probably null |
Het |
Rgs9 |
T |
C |
11: 109,159,798 (GRCm39) |
Y178C |
probably benign |
Het |
Rims2 |
T |
G |
15: 39,449,048 (GRCm39) |
S1217R |
probably damaging |
Het |
Rorc |
C |
T |
3: 94,296,427 (GRCm39) |
T208I |
probably benign |
Het |
Ryr3 |
C |
T |
2: 112,506,249 (GRCm39) |
E3458K |
probably benign |
Het |
Scn5a |
A |
T |
9: 119,362,751 (GRCm39) |
V623E |
probably benign |
Het |
Slc28a2 |
C |
T |
2: 122,281,497 (GRCm39) |
Q229* |
probably null |
Het |
Slc35f3 |
C |
T |
8: 127,025,445 (GRCm39) |
|
probably benign |
Het |
Spg11 |
T |
G |
2: 121,905,791 (GRCm39) |
I1285L |
probably benign |
Het |
Sstr2 |
A |
T |
11: 113,515,749 (GRCm39) |
I223F |
probably damaging |
Het |
Susd1 |
A |
T |
4: 59,349,855 (GRCm39) |
V527E |
possibly damaging |
Het |
Tas1r2 |
A |
G |
4: 139,387,162 (GRCm39) |
N207S |
probably damaging |
Het |
Trappc10 |
A |
G |
10: 78,047,357 (GRCm39) |
S380P |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,571,336 (GRCm39) |
D26519G |
probably damaging |
Het |
Vmn1r215 |
A |
G |
13: 23,260,343 (GRCm39) |
I128V |
probably benign |
Het |
Vmn1r37 |
T |
C |
6: 66,708,935 (GRCm39) |
L150P |
probably damaging |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r52 |
G |
T |
7: 9,904,795 (GRCm39) |
A348E |
probably benign |
Het |
Ypel5 |
T |
C |
17: 73,153,386 (GRCm39) |
L30P |
probably damaging |
Het |
Zfp985 |
A |
G |
4: 147,667,443 (GRCm39) |
T104A |
possibly damaging |
Het |
|
Other mutations in Ppp1r37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0313:Ppp1r37
|
UTSW |
7 |
19,267,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0718:Ppp1r37
|
UTSW |
7 |
19,266,179 (GRCm39) |
missense |
probably benign |
|
R0883:Ppp1r37
|
UTSW |
7 |
19,266,102 (GRCm39) |
missense |
probably benign |
0.01 |
R1606:Ppp1r37
|
UTSW |
7 |
19,268,924 (GRCm39) |
missense |
probably damaging |
0.97 |
R2220:Ppp1r37
|
UTSW |
7 |
19,266,371 (GRCm39) |
missense |
probably null |
0.43 |
R2256:Ppp1r37
|
UTSW |
7 |
19,295,943 (GRCm39) |
unclassified |
probably benign |
|
R2257:Ppp1r37
|
UTSW |
7 |
19,295,943 (GRCm39) |
unclassified |
probably benign |
|
R2325:Ppp1r37
|
UTSW |
7 |
19,266,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R3401:Ppp1r37
|
UTSW |
7 |
19,266,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R3402:Ppp1r37
|
UTSW |
7 |
19,266,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R4006:Ppp1r37
|
UTSW |
7 |
19,268,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Ppp1r37
|
UTSW |
7 |
19,265,445 (GRCm39) |
missense |
probably benign |
|
R4956:Ppp1r37
|
UTSW |
7 |
19,266,636 (GRCm39) |
nonsense |
probably null |
|
R5156:Ppp1r37
|
UTSW |
7 |
19,295,900 (GRCm39) |
unclassified |
probably benign |
|
R5582:Ppp1r37
|
UTSW |
7 |
19,266,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R5659:Ppp1r37
|
UTSW |
7 |
19,269,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R5918:Ppp1r37
|
UTSW |
7 |
19,266,036 (GRCm39) |
missense |
probably benign |
0.02 |
R6172:Ppp1r37
|
UTSW |
7 |
19,266,329 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6659:Ppp1r37
|
UTSW |
7 |
19,266,048 (GRCm39) |
missense |
probably benign |
0.00 |
R7626:Ppp1r37
|
UTSW |
7 |
19,295,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R7779:Ppp1r37
|
UTSW |
7 |
19,266,712 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7785:Ppp1r37
|
UTSW |
7 |
19,265,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Ppp1r37
|
UTSW |
7 |
19,267,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Ppp1r37
|
UTSW |
7 |
19,265,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R8185:Ppp1r37
|
UTSW |
7 |
19,266,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Ppp1r37
|
UTSW |
7 |
19,269,014 (GRCm39) |
missense |
probably benign |
0.12 |
R9224:Ppp1r37
|
UTSW |
7 |
19,265,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R9417:Ppp1r37
|
UTSW |
7 |
19,269,658 (GRCm39) |
missense |
probably damaging |
0.98 |
R9453:Ppp1r37
|
UTSW |
7 |
19,295,796 (GRCm39) |
missense |
probably damaging |
0.99 |
R9777:Ppp1r37
|
UTSW |
7 |
19,295,783 (GRCm39) |
missense |
probably benign |
0.23 |
Z1177:Ppp1r37
|
UTSW |
7 |
19,268,997 (GRCm39) |
nonsense |
probably null |
|
|