Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg3 |
C |
T |
17: 57,183,316 (GRCm39) |
T19I |
probably damaging |
Het |
Alg1 |
T |
A |
16: 5,060,425 (GRCm39) |
M382K |
probably damaging |
Het |
Arhgap17 |
A |
G |
7: 122,879,286 (GRCm39) |
S822P |
unknown |
Het |
Bend7 |
A |
C |
2: 4,749,302 (GRCm39) |
T140P |
probably benign |
Het |
C1rb |
T |
G |
6: 124,557,865 (GRCm39) |
D667E |
probably benign |
Het |
Carmil1 |
A |
G |
13: 24,253,750 (GRCm39) |
C794R |
probably damaging |
Het |
Cd36 |
T |
C |
5: 18,000,608 (GRCm39) |
D365G |
probably null |
Het |
Cep164 |
T |
C |
9: 45,685,282 (GRCm39) |
N825S |
probably benign |
Het |
Cp |
T |
C |
3: 20,018,566 (GRCm39) |
L90P |
|
Het |
Cpeb2 |
C |
T |
5: 43,390,769 (GRCm39) |
|
probably benign |
Het |
Cramp1 |
A |
G |
17: 25,222,281 (GRCm39) |
S146P |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,617,130 (GRCm39) |
D1019E |
|
Het |
Dcaf17 |
G |
C |
2: 70,917,695 (GRCm39) |
V406L |
possibly damaging |
Het |
Ehmt1 |
A |
G |
2: 24,728,791 (GRCm39) |
V703A |
probably benign |
Het |
Ermp1 |
A |
C |
19: 29,609,916 (GRCm39) |
V293G |
probably benign |
Het |
Fancd2os |
C |
A |
6: 113,574,569 (GRCm39) |
V146F |
probably benign |
Het |
Galnt12 |
C |
T |
4: 47,117,983 (GRCm39) |
T426I |
probably damaging |
Het |
Gm11011 |
T |
A |
2: 169,429,289 (GRCm39) |
T44S |
unknown |
Het |
Gm2832 |
C |
T |
14: 41,000,843 (GRCm39) |
T27I |
|
Het |
Klhl32 |
A |
G |
4: 24,649,866 (GRCm39) |
V310A |
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,941,378 (GRCm39) |
C1728* |
probably null |
Het |
Lama2 |
T |
A |
10: 27,298,475 (GRCm39) |
N207I |
probably damaging |
Het |
Lpar5 |
A |
G |
6: 125,058,234 (GRCm39) |
|
probably benign |
Het |
Map3k8 |
T |
C |
18: 4,349,277 (GRCm39) |
I14V |
probably benign |
Het |
Marf1 |
A |
T |
16: 13,947,526 (GRCm39) |
V1151E |
probably damaging |
Het |
Me1 |
G |
A |
9: 86,495,685 (GRCm39) |
A274V |
probably damaging |
Het |
Mybpc1 |
A |
T |
10: 88,372,197 (GRCm39) |
I797N |
probably damaging |
Het |
Myo15a |
T |
A |
11: 60,372,566 (GRCm39) |
|
probably null |
Het |
N4bp2 |
A |
T |
5: 65,963,886 (GRCm39) |
D645V |
probably benign |
Het |
Nlrp4f |
G |
T |
13: 65,342,006 (GRCm39) |
D546E |
possibly damaging |
Het |
Npc1 |
T |
C |
18: 12,346,398 (GRCm39) |
D266G |
possibly damaging |
Het |
Or4a81 |
G |
A |
2: 89,618,778 (GRCm39) |
S306L |
probably benign |
Het |
Or8k16 |
A |
G |
2: 85,520,359 (GRCm39) |
I195M |
probably benign |
Het |
Pcdha12 |
C |
T |
18: 37,153,574 (GRCm39) |
R98W |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pigr |
T |
C |
1: 130,772,403 (GRCm39) |
I207T |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,700,895 (GRCm39) |
E596D |
probably benign |
Het |
Polr1e |
C |
T |
4: 45,018,691 (GRCm39) |
P7L |
probably benign |
Het |
Ppp5c |
G |
T |
7: 16,741,137 (GRCm39) |
Y313* |
probably null |
Het |
Sacs |
C |
A |
14: 61,441,611 (GRCm39) |
T1219K |
probably benign |
Het |
Scn3a |
A |
G |
2: 65,300,535 (GRCm39) |
V1277A |
probably damaging |
Het |
Serinc5 |
G |
T |
13: 92,844,607 (GRCm39) |
A450S |
possibly damaging |
Het |
Serinc5 |
T |
C |
13: 92,844,619 (GRCm39) |
C454R |
probably benign |
Het |
Slc12a6 |
G |
A |
2: 112,183,280 (GRCm39) |
V771I |
probably benign |
Het |
Slc4a1ap |
T |
C |
5: 31,685,463 (GRCm39) |
I247T |
probably benign |
Het |
Snx10 |
T |
A |
6: 51,565,888 (GRCm39) |
S184R |
probably damaging |
Het |
Tgm2 |
A |
T |
2: 157,971,241 (GRCm39) |
|
probably null |
Het |
Thap1 |
CAGCATCTGCTCGGAGCA |
CAGCA |
8: 26,650,884 (GRCm39) |
|
probably null |
Het |
Thsd7b |
T |
C |
1: 130,090,674 (GRCm39) |
|
probably null |
Het |
Tiam2 |
G |
A |
17: 3,487,585 (GRCm39) |
G702E |
probably damaging |
Het |
Tmco4 |
T |
A |
4: 138,747,387 (GRCm39) |
V212D |
probably damaging |
Het |
Usp48 |
G |
A |
4: 137,340,996 (GRCm39) |
G332E |
probably benign |
Het |
Vipas39 |
A |
G |
12: 87,288,021 (GRCm39) |
L482P |
probably damaging |
Het |
Vmn1r5 |
T |
A |
6: 56,962,829 (GRCm39) |
M168K |
|
Het |
Vps13c |
T |
C |
9: 67,837,904 (GRCm39) |
L1818S |
possibly damaging |
Het |
Vwa2 |
A |
G |
19: 56,886,388 (GRCm39) |
I152V |
probably benign |
Het |
Zfp180 |
G |
A |
7: 23,804,399 (GRCm39) |
G273R |
probably damaging |
Het |
Zpld2 |
G |
A |
4: 133,929,312 (GRCm39) |
P331L |
probably benign |
Het |
|
Other mutations in Cyp2d10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00490:Cyp2d10
|
APN |
15 |
82,287,515 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL00840:Cyp2d10
|
APN |
15 |
82,288,691 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01293:Cyp2d10
|
APN |
15 |
82,287,210 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01339:Cyp2d10
|
APN |
15 |
82,288,042 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01871:Cyp2d10
|
APN |
15 |
82,288,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02132:Cyp2d10
|
APN |
15 |
82,288,808 (GRCm39) |
intron |
probably benign |
|
IGL02713:Cyp2d10
|
APN |
15 |
82,290,283 (GRCm39) |
unclassified |
probably benign |
|
IGL02869:Cyp2d10
|
APN |
15 |
82,288,069 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0102:Cyp2d10
|
UTSW |
15 |
82,288,794 (GRCm39) |
missense |
probably benign |
0.01 |
R0102:Cyp2d10
|
UTSW |
15 |
82,288,794 (GRCm39) |
missense |
probably benign |
0.01 |
R0279:Cyp2d10
|
UTSW |
15 |
82,289,540 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0331:Cyp2d10
|
UTSW |
15 |
82,291,227 (GRCm39) |
missense |
probably benign |
0.12 |
R1344:Cyp2d10
|
UTSW |
15 |
82,290,106 (GRCm39) |
critical splice donor site |
probably null |
|
R1418:Cyp2d10
|
UTSW |
15 |
82,290,106 (GRCm39) |
critical splice donor site |
probably null |
|
R1465:Cyp2d10
|
UTSW |
15 |
82,288,129 (GRCm39) |
splice site |
probably null |
|
R1465:Cyp2d10
|
UTSW |
15 |
82,288,129 (GRCm39) |
splice site |
probably null |
|
R1706:Cyp2d10
|
UTSW |
15 |
82,289,783 (GRCm39) |
missense |
probably damaging |
0.96 |
R1712:Cyp2d10
|
UTSW |
15 |
82,287,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Cyp2d10
|
UTSW |
15 |
82,289,495 (GRCm39) |
missense |
probably benign |
0.13 |
R1983:Cyp2d10
|
UTSW |
15 |
82,290,200 (GRCm39) |
missense |
probably benign |
0.15 |
R2056:Cyp2d10
|
UTSW |
15 |
82,288,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R2058:Cyp2d10
|
UTSW |
15 |
82,288,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R3707:Cyp2d10
|
UTSW |
15 |
82,287,217 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3708:Cyp2d10
|
UTSW |
15 |
82,287,217 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4042:Cyp2d10
|
UTSW |
15 |
82,290,269 (GRCm39) |
missense |
probably benign |
0.33 |
R4531:Cyp2d10
|
UTSW |
15 |
82,289,462 (GRCm39) |
missense |
probably benign |
0.31 |
R4694:Cyp2d10
|
UTSW |
15 |
82,288,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:Cyp2d10
|
UTSW |
15 |
82,287,967 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Cyp2d10
|
UTSW |
15 |
82,287,954 (GRCm39) |
missense |
probably benign |
0.07 |
R5072:Cyp2d10
|
UTSW |
15 |
82,287,954 (GRCm39) |
missense |
probably benign |
0.07 |
R5073:Cyp2d10
|
UTSW |
15 |
82,287,954 (GRCm39) |
missense |
probably benign |
0.07 |
R5074:Cyp2d10
|
UTSW |
15 |
82,287,954 (GRCm39) |
missense |
probably benign |
0.07 |
R5746:Cyp2d10
|
UTSW |
15 |
82,289,472 (GRCm39) |
missense |
probably benign |
0.38 |
R7096:Cyp2d10
|
UTSW |
15 |
82,289,462 (GRCm39) |
missense |
probably benign |
|
R7212:Cyp2d10
|
UTSW |
15 |
82,288,447 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7324:Cyp2d10
|
UTSW |
15 |
82,287,961 (GRCm39) |
missense |
probably damaging |
0.97 |
R7487:Cyp2d10
|
UTSW |
15 |
82,288,793 (GRCm39) |
missense |
probably benign |
0.00 |
R7915:Cyp2d10
|
UTSW |
15 |
82,288,628 (GRCm39) |
critical splice donor site |
probably null |
|
R9071:Cyp2d10
|
UTSW |
15 |
82,288,361 (GRCm39) |
missense |
probably damaging |
0.99 |
X0063:Cyp2d10
|
UTSW |
15 |
82,290,201 (GRCm39) |
missense |
probably benign |
0.01 |
|