Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
C |
T |
6: 86,932,150 (GRCm39) |
Q374* |
probably null |
Het |
Adam19 |
A |
G |
11: 46,027,077 (GRCm39) |
D570G |
probably damaging |
Het |
Aqr |
G |
A |
2: 113,979,451 (GRCm39) |
T328M |
probably damaging |
Het |
Bltp3b |
T |
A |
10: 89,644,383 (GRCm39) |
M29K |
probably benign |
Het |
Boc |
G |
A |
16: 44,313,187 (GRCm39) |
T559I |
probably damaging |
Het |
Cadps |
A |
T |
14: 12,473,497 (GRCm38) |
I876N |
possibly damaging |
Het |
Cdh9 |
A |
G |
15: 16,855,930 (GRCm39) |
T657A |
probably damaging |
Het |
Cep104 |
T |
C |
4: 154,086,734 (GRCm39) |
S794P |
possibly damaging |
Het |
Cep72 |
T |
C |
13: 74,188,260 (GRCm39) |
Q211R |
probably benign |
Het |
Coq6 |
T |
A |
12: 84,415,413 (GRCm39) |
D145E |
probably benign |
Het |
Crym |
T |
C |
7: 119,801,116 (GRCm39) |
E11G |
probably benign |
Het |
Csmd3 |
A |
T |
15: 47,508,864 (GRCm39) |
M2907K |
possibly damaging |
Het |
Cspg4 |
A |
C |
9: 56,793,932 (GRCm39) |
I556L |
probably benign |
Het |
Cwf19l2 |
T |
A |
9: 3,456,831 (GRCm39) |
D721E |
probably damaging |
Het |
Defb36 |
T |
A |
2: 152,454,503 (GRCm39) |
V54E |
probably damaging |
Het |
Dlg5 |
C |
A |
14: 24,242,981 (GRCm39) |
E55* |
probably null |
Het |
Dna2 |
G |
T |
10: 62,802,452 (GRCm39) |
A857S |
possibly damaging |
Het |
E330034G19Rik |
A |
G |
14: 24,346,892 (GRCm39) |
K60E |
possibly damaging |
Het |
Eps8l2 |
G |
A |
7: 140,934,920 (GRCm39) |
R76Q |
possibly damaging |
Het |
Fbxl18 |
A |
G |
5: 142,881,022 (GRCm39) |
|
probably benign |
Het |
Flnc |
T |
A |
6: 29,444,044 (GRCm39) |
C619* |
probably null |
Het |
Ftcd |
A |
G |
10: 76,423,967 (GRCm39) |
K503E |
probably benign |
Het |
Gbp2b |
C |
T |
3: 142,317,126 (GRCm39) |
A494V |
possibly damaging |
Het |
Gfral |
C |
T |
9: 76,115,900 (GRCm39) |
A25T |
probably benign |
Het |
Gins2 |
T |
A |
8: 121,315,684 (GRCm39) |
D24V |
possibly damaging |
Het |
Gm10985 |
T |
C |
3: 53,752,683 (GRCm39) |
I22T |
probably damaging |
Het |
Golga4 |
T |
A |
9: 118,387,251 (GRCm39) |
S1458T |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 35,006,640 (GRCm39) |
K176R |
probably damaging |
Het |
Gsto1 |
T |
C |
19: 47,846,338 (GRCm39) |
W62R |
probably damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,722,360 (GRCm39) |
T121I |
probably benign |
Het |
Gxylt1 |
A |
G |
15: 93,152,180 (GRCm39) |
|
probably null |
Het |
Hs6st1 |
C |
T |
1: 36,142,719 (GRCm39) |
P218L |
probably benign |
Het |
Itpr3 |
C |
T |
17: 27,322,880 (GRCm39) |
T1119M |
possibly damaging |
Het |
Kif5c |
A |
G |
2: 49,620,211 (GRCm39) |
D226G |
possibly damaging |
Het |
Klk1b1 |
T |
A |
7: 43,620,593 (GRCm39) |
S228T |
probably damaging |
Het |
Krt1 |
A |
G |
15: 101,755,340 (GRCm39) |
F473S |
probably benign |
Het |
Large1 |
A |
G |
8: 73,564,081 (GRCm39) |
S562P |
possibly damaging |
Het |
Lpxn |
T |
A |
19: 12,810,023 (GRCm39) |
M265K |
possibly damaging |
Het |
Lrriq1 |
G |
A |
10: 103,006,457 (GRCm39) |
P1223S |
possibly damaging |
Het |
Map3k9 |
A |
G |
12: 81,778,798 (GRCm39) |
L505P |
possibly damaging |
Het |
Morn2 |
A |
G |
17: 80,604,709 (GRCm39) |
D128G |
probably damaging |
Het |
Msl2 |
A |
G |
9: 100,978,936 (GRCm39) |
K437E |
possibly damaging |
Het |
Msr1 |
T |
C |
8: 40,064,760 (GRCm39) |
I305V |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,598,066 (GRCm39) |
E3237G |
possibly damaging |
Het |
Mxra8 |
T |
C |
4: 155,925,465 (GRCm39) |
M58T |
probably damaging |
Het |
Myo16 |
A |
G |
8: 10,372,676 (GRCm39) |
D125G |
probably damaging |
Het |
Myom2 |
A |
G |
8: 15,152,546 (GRCm39) |
Q631R |
probably benign |
Het |
Nlrp1b |
T |
A |
11: 71,072,229 (GRCm39) |
H538L |
probably benign |
Het |
Nme3 |
T |
A |
17: 25,115,823 (GRCm39) |
|
probably null |
Het |
Nop2 |
T |
C |
6: 125,110,726 (GRCm39) |
S68P |
probably benign |
Het |
Nploc4 |
C |
T |
11: 120,275,440 (GRCm39) |
V499M |
probably benign |
Het |
Nub1 |
A |
G |
5: 24,913,814 (GRCm39) |
E565G |
possibly damaging |
Het |
Or1e19 |
C |
T |
11: 73,316,272 (GRCm39) |
C179Y |
probably damaging |
Het |
Or6e1 |
A |
G |
14: 54,519,825 (GRCm39) |
F176L |
probably damaging |
Het |
Or7e168 |
A |
G |
9: 19,719,674 (GRCm39) |
D20G |
probably damaging |
Het |
Or9g3 |
G |
A |
2: 85,589,994 (GRCm39) |
S242F |
probably damaging |
Het |
Parl |
A |
G |
16: 20,101,762 (GRCm39) |
M90T |
probably damaging |
Het |
Pelo |
T |
C |
13: 115,226,152 (GRCm39) |
I102V |
probably benign |
Het |
Pigt |
T |
A |
2: 164,343,482 (GRCm39) |
Y319* |
probably null |
Het |
Plb1 |
A |
G |
5: 32,521,543 (GRCm39) |
T1465A |
unknown |
Het |
Plxna4 |
T |
C |
6: 32,134,915 (GRCm39) |
N1763D |
possibly damaging |
Het |
Pmpca |
A |
G |
2: 26,280,553 (GRCm39) |
E133G |
probably damaging |
Het |
Pus7l |
G |
A |
15: 94,425,746 (GRCm39) |
P552S |
probably benign |
Het |
Qsox2 |
A |
G |
2: 26,115,230 (GRCm39) |
M1T |
probably null |
Het |
Ralb |
C |
T |
1: 119,411,265 (GRCm39) |
V25I |
probably damaging |
Het |
Rbbp6 |
A |
G |
7: 122,601,057 (GRCm39) |
|
probably benign |
Het |
Rnf43 |
A |
G |
11: 87,618,271 (GRCm39) |
E187G |
probably damaging |
Het |
Rpl31 |
C |
T |
1: 39,409,108 (GRCm39) |
R41C |
probably benign |
Het |
Scap |
A |
G |
9: 110,206,712 (GRCm39) |
S386G |
probably damaging |
Het |
Skint10 |
T |
C |
4: 112,573,067 (GRCm39) |
Y243C |
probably damaging |
Het |
Stpg2 |
A |
G |
3: 139,125,547 (GRCm39) |
T447A |
probably benign |
Het |
Tas1r1 |
G |
A |
4: 152,122,782 (GRCm39) |
A21V |
probably damaging |
Het |
Tas2r122 |
C |
T |
6: 132,688,335 (GRCm39) |
G186E |
probably benign |
Het |
Tenm4 |
C |
A |
7: 96,545,416 (GRCm39) |
Y2477* |
probably null |
Het |
Them7 |
A |
G |
2: 105,209,153 (GRCm39) |
T158A |
probably benign |
Het |
Ttc41 |
T |
C |
10: 86,596,784 (GRCm39) |
|
probably null |
Het |
Ttk |
T |
A |
9: 83,744,588 (GRCm39) |
N593K |
possibly damaging |
Het |
Tulp1 |
A |
G |
17: 28,578,172 (GRCm39) |
V289A |
possibly damaging |
Het |
Unc93a2 |
T |
C |
17: 7,631,202 (GRCm39) |
T456A |
probably benign |
Het |
Usp34 |
A |
C |
11: 23,438,336 (GRCm39) |
Q278P |
probably damaging |
Het |
Vmn2r78 |
T |
A |
7: 86,570,737 (GRCm39) |
D418E |
probably benign |
Het |
Vmn2r90 |
C |
T |
17: 17,932,336 (GRCm39) |
A81V |
probably damaging |
Het |
Xpc |
T |
A |
6: 91,475,117 (GRCm39) |
N636I |
probably damaging |
Het |
Zfp563 |
A |
T |
17: 33,308,431 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tmcc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00816:Tmcc2
|
APN |
1 |
132,308,436 (GRCm39) |
missense |
probably benign |
|
IGL01991:Tmcc2
|
APN |
1 |
132,288,830 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02259:Tmcc2
|
APN |
1 |
132,288,898 (GRCm39) |
missense |
probably benign |
|
IGL02310:Tmcc2
|
APN |
1 |
132,286,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02551:Tmcc2
|
APN |
1 |
132,285,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03301:Tmcc2
|
APN |
1 |
132,288,557 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03347:Tmcc2
|
APN |
1 |
132,285,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Tmcc2
|
UTSW |
1 |
132,308,444 (GRCm39) |
missense |
probably benign |
0.10 |
R0233:Tmcc2
|
UTSW |
1 |
132,288,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R0233:Tmcc2
|
UTSW |
1 |
132,288,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R1146:Tmcc2
|
UTSW |
1 |
132,285,493 (GRCm39) |
small deletion |
probably benign |
|
R1146:Tmcc2
|
UTSW |
1 |
132,285,493 (GRCm39) |
small deletion |
probably benign |
|
R1538:Tmcc2
|
UTSW |
1 |
132,308,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R2428:Tmcc2
|
UTSW |
1 |
132,288,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Tmcc2
|
UTSW |
1 |
132,288,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Tmcc2
|
UTSW |
1 |
132,308,517 (GRCm39) |
missense |
probably benign |
0.43 |
R5364:Tmcc2
|
UTSW |
1 |
132,285,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R5596:Tmcc2
|
UTSW |
1 |
132,288,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Tmcc2
|
UTSW |
1 |
132,285,429 (GRCm39) |
missense |
probably damaging |
0.98 |
R5931:Tmcc2
|
UTSW |
1 |
132,285,493 (GRCm39) |
small deletion |
probably benign |
|
R6278:Tmcc2
|
UTSW |
1 |
132,286,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R7404:Tmcc2
|
UTSW |
1 |
132,288,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R7806:Tmcc2
|
UTSW |
1 |
132,288,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:Tmcc2
|
UTSW |
1 |
132,288,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R7903:Tmcc2
|
UTSW |
1 |
132,288,199 (GRCm39) |
missense |
probably benign |
0.00 |
R9458:Tmcc2
|
UTSW |
1 |
132,286,747 (GRCm39) |
missense |
probably damaging |
1.00 |
RF012:Tmcc2
|
UTSW |
1 |
132,288,756 (GRCm39) |
missense |
probably damaging |
1.00 |
X0052:Tmcc2
|
UTSW |
1 |
132,288,071 (GRCm39) |
missense |
probably benign |
|
|