Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
A |
G |
8: 41,208,438 (GRCm39) |
D568G |
probably benign |
Het |
Angpt1 |
T |
C |
15: 42,386,965 (GRCm39) |
I130V |
probably benign |
Het |
Ankrd11 |
G |
T |
8: 123,622,194 (GRCm39) |
Q553K |
probably benign |
Het |
Ankrd42 |
A |
T |
7: 92,280,752 (GRCm39) |
H59Q |
possibly damaging |
Het |
Ankrd52 |
C |
T |
10: 128,218,249 (GRCm39) |
R318C |
probably damaging |
Het |
Arrdc5 |
G |
A |
17: 56,601,522 (GRCm39) |
T201M |
probably damaging |
Het |
Atxn1l |
A |
G |
8: 110,459,132 (GRCm39) |
S377P |
probably benign |
Het |
Baz2a |
T |
C |
10: 127,957,056 (GRCm39) |
F936S |
possibly damaging |
Het |
Bicc1 |
T |
C |
10: 70,766,483 (GRCm39) |
D913G |
probably damaging |
Het |
Blnk |
T |
A |
19: 40,961,082 (GRCm39) |
M21L |
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,587,401 (GRCm39) |
H132R |
probably benign |
Het |
Ccdc154 |
A |
G |
17: 25,382,442 (GRCm39) |
H88R |
probably benign |
Het |
Cfap20dc |
G |
T |
14: 8,511,171 (GRCm38) |
S414R |
possibly damaging |
Het |
Clic5 |
G |
T |
17: 44,586,179 (GRCm39) |
A223S |
probably benign |
Het |
Col28a1 |
T |
A |
6: 8,014,795 (GRCm39) |
Y870F |
possibly damaging |
Het |
Dnah11 |
T |
C |
12: 118,031,880 (GRCm39) |
T1763A |
probably benign |
Het |
Dnajc13 |
T |
C |
9: 104,042,221 (GRCm39) |
R2005G |
possibly damaging |
Het |
Dop1a |
G |
A |
9: 86,389,722 (GRCm39) |
G541S |
probably benign |
Het |
Drosha |
C |
T |
15: 12,865,153 (GRCm39) |
T627M |
probably damaging |
Het |
Ephb3 |
C |
T |
16: 21,037,268 (GRCm39) |
H455Y |
possibly damaging |
Het |
Eri1 |
A |
C |
8: 35,949,777 (GRCm39) |
C127G |
probably damaging |
Het |
Faf1 |
A |
T |
4: 109,783,153 (GRCm39) |
E548D |
probably benign |
Het |
Gm3285 |
C |
A |
10: 77,698,194 (GRCm39) |
C114* |
probably null |
Het |
Gm9736 |
C |
T |
10: 77,587,167 (GRCm39) |
V8I |
unknown |
Het |
Gnptab |
A |
T |
10: 88,276,174 (GRCm39) |
M1154L |
probably benign |
Het |
Grin1 |
G |
A |
2: 25,186,647 (GRCm39) |
T770M |
probably damaging |
Het |
Haus1 |
A |
G |
18: 77,854,570 (GRCm39) |
S67P |
possibly damaging |
Het |
Homer1 |
C |
A |
13: 93,492,562 (GRCm39) |
Q184K |
probably benign |
Het |
Hook2 |
A |
G |
8: 85,723,680 (GRCm39) |
T401A |
probably benign |
Het |
Il6st |
G |
A |
13: 112,631,907 (GRCm39) |
|
probably null |
Het |
Kcnh8 |
A |
T |
17: 53,212,038 (GRCm39) |
D612V |
probably damaging |
Het |
Ltbr |
C |
G |
6: 125,289,763 (GRCm39) |
E144Q |
probably benign |
Het |
Mcf2l |
G |
T |
8: 13,063,579 (GRCm39) |
R961L |
possibly damaging |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
Myo1b |
G |
T |
1: 51,797,160 (GRCm39) |
Q961K |
probably benign |
Het |
Myo1h |
C |
A |
5: 114,480,258 (GRCm39) |
T531N |
|
Het |
Ngly1 |
G |
A |
14: 16,283,445 (GRCm38) |
R408Q |
probably damaging |
Het |
Nup133 |
T |
C |
8: 124,632,966 (GRCm39) |
E1055G |
possibly damaging |
Het |
Nutm2 |
A |
G |
13: 50,626,934 (GRCm39) |
K363R |
probably benign |
Het |
Obox8 |
A |
T |
7: 14,066,752 (GRCm39) |
Y97* |
probably null |
Het |
Odc1 |
A |
G |
12: 17,597,319 (GRCm39) |
D7G |
probably benign |
Het |
Ogfod2 |
C |
T |
5: 124,252,558 (GRCm39) |
T182I |
unknown |
Het |
Or2t49 |
A |
G |
11: 58,393,379 (GRCm39) |
M7T |
probably benign |
Het |
Or4c111 |
A |
T |
2: 88,844,324 (GRCm39) |
V28E |
possibly damaging |
Het |
Or8b12b |
T |
C |
9: 37,684,287 (GRCm39) |
S111P |
probably damaging |
Het |
Or8b46 |
G |
A |
9: 38,450,966 (GRCm39) |
M258I |
probably benign |
Het |
Parp4 |
A |
G |
14: 56,827,430 (GRCm39) |
D188G |
probably benign |
Het |
Phactr2 |
T |
C |
10: 13,122,922 (GRCm39) |
E400G |
probably benign |
Het |
Phlpp1 |
G |
A |
1: 106,100,397 (GRCm39) |
V222M |
possibly damaging |
Het |
Ppp1r16b |
T |
C |
2: 158,603,683 (GRCm39) |
V536A |
probably damaging |
Het |
Prex2 |
T |
C |
1: 11,223,833 (GRCm39) |
V719A |
possibly damaging |
Het |
Prpf8 |
C |
T |
11: 75,381,226 (GRCm39) |
A242V |
possibly damaging |
Het |
Prr14l |
A |
G |
5: 32,986,771 (GRCm39) |
L908P |
probably damaging |
Het |
Prrc2b |
A |
G |
2: 32,117,005 (GRCm39) |
N2146D |
possibly damaging |
Het |
Rtkn |
T |
C |
6: 83,126,993 (GRCm39) |
V333A |
possibly damaging |
Het |
Samd8 |
T |
C |
14: 21,825,442 (GRCm39) |
Y196H |
probably benign |
Het |
Six5 |
A |
G |
7: 18,828,784 (GRCm39) |
T75A |
probably benign |
Het |
Slc35a4 |
T |
A |
18: 36,814,591 (GRCm39) |
L42H |
probably damaging |
Het |
Svs3a |
A |
T |
2: 164,131,933 (GRCm39) |
D168V |
probably damaging |
Het |
Themis |
T |
A |
10: 28,637,422 (GRCm39) |
Y175* |
probably null |
Het |
Tspan33 |
G |
T |
6: 29,716,783 (GRCm39) |
R180L |
probably benign |
Het |
Ttc28 |
C |
T |
5: 111,232,958 (GRCm39) |
S145F |
probably damaging |
Het |
Txn2 |
G |
A |
15: 77,810,878 (GRCm39) |
T102I |
unknown |
Het |
Usp34 |
T |
A |
11: 23,376,183 (GRCm39) |
V1908E |
|
Het |
Vmn2r101 |
A |
G |
17: 19,809,350 (GRCm39) |
I160V |
probably null |
Het |
Vmn2r104 |
A |
T |
17: 20,250,358 (GRCm39) |
C638S |
possibly damaging |
Het |
Wdfy4 |
C |
T |
14: 32,682,777 (GRCm39) |
R3136Q |
|
Het |
Zan |
C |
A |
5: 137,396,552 (GRCm39) |
A4335S |
unknown |
Het |
Zfp180 |
G |
T |
7: 23,803,958 (GRCm39) |
V126F |
probably benign |
Het |
Zfp429 |
T |
A |
13: 67,538,931 (GRCm39) |
D171V |
possibly damaging |
Het |
Zfp638 |
T |
C |
6: 83,931,708 (GRCm39) |
I798T |
probably benign |
Het |
|
Other mutations in Dhx37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Dhx37
|
APN |
5 |
125,496,152 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02010:Dhx37
|
APN |
5 |
125,495,777 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02412:Dhx37
|
APN |
5 |
125,508,692 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02484:Dhx37
|
APN |
5 |
125,496,401 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02986:Dhx37
|
APN |
5 |
125,496,379 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Dhx37
|
UTSW |
5 |
125,504,594 (GRCm39) |
unclassified |
probably benign |
|
R0010:Dhx37
|
UTSW |
5 |
125,508,680 (GRCm39) |
missense |
probably benign |
0.02 |
R0019:Dhx37
|
UTSW |
5 |
125,507,098 (GRCm39) |
missense |
probably benign |
0.36 |
R0485:Dhx37
|
UTSW |
5 |
125,499,295 (GRCm39) |
missense |
probably benign |
0.00 |
R0959:Dhx37
|
UTSW |
5 |
125,500,496 (GRCm39) |
missense |
probably benign |
|
R1101:Dhx37
|
UTSW |
5 |
125,492,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Dhx37
|
UTSW |
5 |
125,498,103 (GRCm39) |
missense |
probably damaging |
0.96 |
R1309:Dhx37
|
UTSW |
5 |
125,494,502 (GRCm39) |
nonsense |
probably null |
|
R1777:Dhx37
|
UTSW |
5 |
125,506,995 (GRCm39) |
missense |
probably benign |
|
R2001:Dhx37
|
UTSW |
5 |
125,504,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Dhx37
|
UTSW |
5 |
125,498,166 (GRCm39) |
missense |
probably damaging |
0.98 |
R3826:Dhx37
|
UTSW |
5 |
125,508,677 (GRCm39) |
missense |
probably benign |
0.04 |
R3829:Dhx37
|
UTSW |
5 |
125,508,677 (GRCm39) |
missense |
probably benign |
0.04 |
R3830:Dhx37
|
UTSW |
5 |
125,508,677 (GRCm39) |
missense |
probably benign |
0.04 |
R4007:Dhx37
|
UTSW |
5 |
125,501,995 (GRCm39) |
splice site |
probably benign |
|
R5058:Dhx37
|
UTSW |
5 |
125,499,295 (GRCm39) |
missense |
probably benign |
0.00 |
R5158:Dhx37
|
UTSW |
5 |
125,492,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Dhx37
|
UTSW |
5 |
125,506,867 (GRCm39) |
missense |
probably benign |
|
R5789:Dhx37
|
UTSW |
5 |
125,498,103 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5834:Dhx37
|
UTSW |
5 |
125,502,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R6066:Dhx37
|
UTSW |
5 |
125,501,730 (GRCm39) |
missense |
probably benign |
0.18 |
R6490:Dhx37
|
UTSW |
5 |
125,496,196 (GRCm39) |
missense |
probably benign |
0.00 |
R6967:Dhx37
|
UTSW |
5 |
125,499,231 (GRCm39) |
missense |
probably benign |
0.07 |
R8036:Dhx37
|
UTSW |
5 |
125,501,739 (GRCm39) |
missense |
probably benign |
|
R9177:Dhx37
|
UTSW |
5 |
125,507,958 (GRCm39) |
missense |
probably benign |
0.00 |
R9294:Dhx37
|
UTSW |
5 |
125,499,736 (GRCm39) |
missense |
probably benign |
|
Z1088:Dhx37
|
UTSW |
5 |
125,493,655 (GRCm39) |
missense |
possibly damaging |
0.72 |
Z1177:Dhx37
|
UTSW |
5 |
125,502,536 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Dhx37
|
UTSW |
5 |
125,502,044 (GRCm39) |
missense |
possibly damaging |
0.81 |
|