Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
C |
A |
1: 179,614,601 (GRCm39) |
K394N |
probably benign |
Het |
Banp |
A |
T |
8: 122,705,372 (GRCm39) |
T81S |
possibly damaging |
Het |
Btn2a2 |
T |
C |
13: 23,662,465 (GRCm39) |
E495G |
probably benign |
Het |
Cfap69 |
T |
C |
5: 5,690,190 (GRCm39) |
I158M |
possibly damaging |
Het |
Cgnl1 |
C |
A |
9: 71,628,873 (GRCm39) |
|
probably benign |
Het |
Clip1 |
T |
A |
5: 123,753,223 (GRCm39) |
Q186L |
probably damaging |
Het |
Clspn |
G |
A |
4: 126,471,243 (GRCm39) |
|
probably benign |
Het |
Ctdsp1 |
T |
C |
1: 74,433,884 (GRCm39) |
L155P |
probably damaging |
Het |
D5Ertd579e |
C |
T |
5: 36,773,682 (GRCm39) |
A238T |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,121,752 (GRCm39) |
Y1410C |
probably damaging |
Het |
Fam186a |
AGCCGCTGCCGCTGCCGCTGCCGC |
AGCCGCTGCCGCTGCCGC |
15: 99,844,107 (GRCm39) |
|
probably benign |
Het |
Farp2 |
T |
C |
1: 93,488,910 (GRCm39) |
|
probably null |
Het |
Galnt7 |
T |
G |
8: 57,985,729 (GRCm39) |
D547A |
probably damaging |
Het |
Gm1527 |
C |
A |
3: 28,956,440 (GRCm39) |
D135E |
probably damaging |
Het |
Grm5 |
T |
C |
7: 87,723,747 (GRCm39) |
I679T |
probably damaging |
Het |
Hectd4 |
C |
A |
5: 121,467,619 (GRCm39) |
R2523S |
possibly damaging |
Het |
Hps4 |
G |
A |
5: 112,525,905 (GRCm39) |
S642N |
possibly damaging |
Het |
Htr1f |
A |
T |
16: 64,746,637 (GRCm39) |
S218R |
probably damaging |
Het |
Lrit1 |
G |
A |
14: 36,776,891 (GRCm39) |
A4T |
unknown |
Het |
Ly6f |
G |
T |
15: 75,141,706 (GRCm39) |
D50Y |
probably damaging |
Het |
Mafg |
GGTTCTTCAGTGT |
GGT |
11: 120,520,415 (GRCm39) |
|
probably null |
Het |
Map2 |
T |
A |
1: 66,454,522 (GRCm39) |
Y1137* |
probably null |
Het |
Map4k3 |
C |
A |
17: 81,035,257 (GRCm39) |
R21L |
possibly damaging |
Het |
Mapk10 |
A |
T |
5: 103,186,442 (GRCm39) |
V90D |
probably damaging |
Het |
Mapkapk3 |
T |
A |
9: 107,136,067 (GRCm39) |
E219V |
probably damaging |
Het |
Mideas |
T |
C |
12: 84,199,327 (GRCm39) |
Y1040C |
probably damaging |
Het |
Mos |
T |
G |
4: 3,871,457 (GRCm39) |
I120L |
probably benign |
Het |
Mrgprb4 |
A |
G |
7: 47,848,679 (GRCm39) |
V83A |
probably benign |
Het |
Mrnip |
A |
G |
11: 50,065,768 (GRCm39) |
Q19R |
probably damaging |
Het |
Myrip |
T |
C |
9: 120,261,544 (GRCm39) |
S386P |
probably benign |
Het |
Mzt2 |
A |
G |
16: 15,666,568 (GRCm39) |
W141R |
probably benign |
Het |
Ncam1 |
A |
G |
9: 49,428,856 (GRCm39) |
Y710H |
probably damaging |
Het |
Nlrp9c |
G |
T |
7: 26,081,837 (GRCm39) |
L630I |
probably benign |
Het |
Odad2 |
A |
T |
18: 7,294,527 (GRCm39) |
S29T |
probably benign |
Het |
Oplah |
C |
A |
15: 76,189,876 (GRCm39) |
G150C |
probably benign |
Het |
Or4c11b |
A |
G |
2: 88,625,016 (GRCm39) |
T97A |
probably benign |
Het |
Or51q1 |
A |
T |
7: 103,628,581 (GRCm39) |
M61L |
probably damaging |
Het |
Or52a20 |
G |
A |
7: 103,366,737 (GRCm39) |
C312Y |
probably benign |
Het |
Or6k2 |
A |
G |
1: 173,986,369 (GRCm39) |
Q10R |
probably benign |
Het |
Patl1 |
A |
G |
19: 11,908,973 (GRCm39) |
K460R |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,179,100 (GRCm39) |
|
probably null |
Het |
Phldb2 |
T |
C |
16: 45,680,757 (GRCm39) |
I17V |
probably benign |
Het |
Ppp3r1 |
A |
G |
11: 17,144,789 (GRCm39) |
D134G |
probably damaging |
Het |
Ppp4r4 |
C |
T |
12: 103,570,315 (GRCm39) |
T763I |
probably benign |
Het |
Prmt9 |
A |
G |
8: 78,276,358 (GRCm39) |
D61G |
probably benign |
Het |
Ptk2 |
T |
C |
15: 73,131,457 (GRCm39) |
M589V |
possibly damaging |
Het |
Rabl6 |
A |
G |
2: 25,486,446 (GRCm39) |
W153R |
probably benign |
Het |
Rb1cc1 |
A |
G |
1: 6,319,109 (GRCm39) |
I843V |
|
Het |
Resf1 |
T |
C |
6: 149,230,368 (GRCm39) |
V1138A |
possibly damaging |
Het |
Rnf19b |
A |
G |
4: 128,977,940 (GRCm39) |
E719G |
|
Het |
Sart3 |
T |
C |
5: 113,892,410 (GRCm39) |
D363G |
possibly damaging |
Het |
Sgo2a |
C |
A |
1: 58,037,283 (GRCm39) |
D9E |
possibly damaging |
Het |
Slc27a5 |
A |
G |
7: 12,725,097 (GRCm39) |
V450A |
probably benign |
Het |
Slc8b1 |
T |
A |
5: 120,668,416 (GRCm39) |
Y483N |
probably damaging |
Het |
Slco1b2 |
A |
G |
6: 141,617,974 (GRCm39) |
T475A |
probably damaging |
Het |
Slfn3 |
T |
C |
11: 83,103,458 (GRCm39) |
F110L |
probably benign |
Het |
Spata31e5 |
T |
C |
1: 28,815,975 (GRCm39) |
I686V |
probably benign |
Het |
Ssr2 |
T |
A |
3: 88,495,269 (GRCm39) |
Y175N |
probably damaging |
Het |
Tagap |
A |
T |
17: 8,150,280 (GRCm39) |
N222Y |
probably damaging |
Het |
Tecta |
C |
T |
9: 42,278,479 (GRCm39) |
V1010M |
probably benign |
Het |
Trim36 |
A |
T |
18: 46,300,664 (GRCm39) |
I669N |
possibly damaging |
Het |
Ubp1 |
A |
G |
9: 113,799,319 (GRCm39) |
T425A |
probably benign |
Het |
Usp47 |
T |
C |
7: 111,681,713 (GRCm39) |
I508T |
probably damaging |
Het |
Vit |
G |
A |
17: 78,934,278 (GRCm39) |
D627N |
probably damaging |
Het |
Vmn2r59 |
A |
T |
7: 41,695,884 (GRCm39) |
I176N |
probably benign |
Het |
|
Other mutations in Cnst |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00917:Cnst
|
APN |
1 |
179,452,557 (GRCm39) |
splice site |
probably benign |
|
Doldrums
|
UTSW |
1 |
179,432,638 (GRCm39) |
splice site |
probably null |
|
ennui
|
UTSW |
1 |
179,434,100 (GRCm39) |
critical splice donor site |
probably null |
|
R0360:Cnst
|
UTSW |
1 |
179,407,100 (GRCm39) |
missense |
probably benign |
0.00 |
R1391:Cnst
|
UTSW |
1 |
179,407,051 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1743:Cnst
|
UTSW |
1 |
179,437,957 (GRCm39) |
missense |
probably benign |
0.18 |
R1909:Cnst
|
UTSW |
1 |
179,450,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R3856:Cnst
|
UTSW |
1 |
179,407,279 (GRCm39) |
missense |
probably benign |
0.02 |
R4565:Cnst
|
UTSW |
1 |
179,432,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5041:Cnst
|
UTSW |
1 |
179,432,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R5072:Cnst
|
UTSW |
1 |
179,450,451 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5087:Cnst
|
UTSW |
1 |
179,450,378 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5294:Cnst
|
UTSW |
1 |
179,438,005 (GRCm39) |
missense |
probably benign |
0.03 |
R5349:Cnst
|
UTSW |
1 |
179,450,462 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5394:Cnst
|
UTSW |
1 |
179,429,301 (GRCm39) |
splice site |
probably benign |
|
R6020:Cnst
|
UTSW |
1 |
179,437,440 (GRCm39) |
missense |
probably benign |
|
R6198:Cnst
|
UTSW |
1 |
179,420,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R6669:Cnst
|
UTSW |
1 |
179,432,638 (GRCm39) |
splice site |
probably null |
|
R6767:Cnst
|
UTSW |
1 |
179,437,519 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7007:Cnst
|
UTSW |
1 |
179,438,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Cnst
|
UTSW |
1 |
179,406,947 (GRCm39) |
start gained |
probably benign |
|
R7356:Cnst
|
UTSW |
1 |
179,434,095 (GRCm39) |
missense |
probably benign |
0.01 |
R7730:Cnst
|
UTSW |
1 |
179,452,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R7900:Cnst
|
UTSW |
1 |
179,450,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R8073:Cnst
|
UTSW |
1 |
179,434,002 (GRCm39) |
missense |
probably benign |
0.00 |
R8194:Cnst
|
UTSW |
1 |
179,437,759 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:Cnst
|
UTSW |
1 |
179,420,274 (GRCm39) |
missense |
probably benign |
0.00 |
R8857:Cnst
|
UTSW |
1 |
179,437,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Cnst
|
UTSW |
1 |
179,437,587 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9062:Cnst
|
UTSW |
1 |
179,434,100 (GRCm39) |
critical splice donor site |
probably null |
|
R9190:Cnst
|
UTSW |
1 |
179,407,039 (GRCm39) |
small deletion |
probably benign |
|
R9287:Cnst
|
UTSW |
1 |
179,407,108 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9429:Cnst
|
UTSW |
1 |
179,432,566 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Cnst
|
UTSW |
1 |
179,407,130 (GRCm39) |
missense |
probably damaging |
0.99 |
|