Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
C |
16: 4,682,143 (GRCm39) |
F991S |
probably benign |
Het |
4931406B18Rik |
A |
G |
7: 43,147,296 (GRCm39) |
I218T |
possibly damaging |
Het |
9930111J21Rik2 |
C |
T |
11: 48,910,538 (GRCm39) |
A632T |
possibly damaging |
Het |
Akt1 |
A |
T |
12: 112,625,050 (GRCm39) |
L166Q |
probably null |
Het |
Alpk2 |
A |
T |
18: 65,399,319 (GRCm39) |
D2086E |
probably damaging |
Het |
Ankrd11 |
A |
T |
8: 123,621,043 (GRCm39) |
C915* |
probably null |
Het |
Ankrd44 |
T |
C |
1: 54,801,506 (GRCm39) |
T274A |
probably damaging |
Het |
Ankrd44 |
A |
T |
1: 54,774,209 (GRCm39) |
I398K |
probably damaging |
Het |
Arhgef2 |
A |
G |
3: 88,550,283 (GRCm39) |
T663A |
probably benign |
Het |
Btbd16 |
G |
A |
7: 130,425,033 (GRCm39) |
M471I |
possibly damaging |
Het |
Btbd16 |
C |
A |
7: 130,425,034 (GRCm39) |
Q472K |
probably damaging |
Het |
Cdc37 |
G |
A |
9: 21,054,509 (GRCm39) |
R39C |
probably damaging |
Het |
Cop1 |
T |
A |
1: 159,077,643 (GRCm39) |
D159E |
probably benign |
Het |
Crtac1 |
C |
T |
19: 42,402,390 (GRCm39) |
V73I |
probably benign |
Het |
Cryz |
T |
A |
3: 154,312,155 (GRCm39) |
V84E |
probably damaging |
Het |
Ctnnd2 |
C |
T |
15: 30,669,689 (GRCm39) |
L433F |
probably benign |
Het |
Ctsq |
C |
A |
13: 61,184,874 (GRCm39) |
D271Y |
probably benign |
Het |
Cyp3a25 |
A |
C |
5: 145,931,673 (GRCm39) |
|
probably null |
Het |
Dmbt1 |
G |
C |
7: 130,655,797 (GRCm39) |
W412C |
probably benign |
Het |
Eif4e1b |
G |
A |
13: 54,934,529 (GRCm39) |
V131I |
possibly damaging |
Het |
Epha1 |
A |
G |
6: 42,341,568 (GRCm39) |
V494A |
possibly damaging |
Het |
Fbxl4 |
T |
C |
4: 22,433,641 (GRCm39) |
S593P |
probably damaging |
Het |
Fbxo41 |
G |
A |
6: 85,456,883 (GRCm39) |
P429S |
probably benign |
Het |
Fem1al |
T |
C |
11: 29,774,288 (GRCm39) |
N390D |
probably benign |
Het |
Fgfr3 |
G |
A |
5: 33,887,347 (GRCm39) |
C204Y |
probably damaging |
Het |
Gbf1 |
T |
C |
19: 46,272,861 (GRCm39) |
V1665A |
possibly damaging |
Het |
Htt |
T |
A |
5: 35,062,741 (GRCm39) |
V2825E |
probably damaging |
Het |
Irs1 |
A |
T |
1: 82,267,646 (GRCm39) |
V190E |
probably damaging |
Het |
Kics2 |
T |
C |
10: 121,576,052 (GRCm39) |
|
probably benign |
Het |
Klk1 |
T |
C |
7: 43,878,161 (GRCm39) |
|
probably null |
Het |
Kmt2d |
T |
C |
15: 98,747,905 (GRCm39) |
|
probably benign |
Het |
Meox1 |
T |
C |
11: 101,770,169 (GRCm39) |
E186G |
probably damaging |
Het |
Micu2 |
G |
A |
14: 58,209,201 (GRCm39) |
R86W |
probably damaging |
Het |
Mrgprb1 |
A |
T |
7: 48,097,432 (GRCm39) |
I160K |
probably damaging |
Het |
Nckap1l |
T |
A |
15: 103,384,085 (GRCm39) |
M561K |
possibly damaging |
Het |
Or4c104 |
A |
T |
2: 88,586,749 (GRCm39) |
I90N |
probably damaging |
Het |
Or52s6 |
A |
T |
7: 103,091,635 (GRCm39) |
S232T |
probably damaging |
Het |
Or56b35 |
A |
T |
7: 104,963,213 (GRCm39) |
M1L |
probably benign |
Het |
Otoa |
T |
A |
7: 120,721,200 (GRCm39) |
L405H |
probably damaging |
Het |
Phyhip |
A |
T |
14: 70,704,314 (GRCm39) |
M178L |
probably benign |
Het |
Pkd1l3 |
A |
T |
8: 110,382,152 (GRCm39) |
N1630I |
probably damaging |
Het |
Plek2 |
T |
A |
12: 78,940,883 (GRCm39) |
T247S |
probably benign |
Het |
Rhbdl3 |
T |
C |
11: 80,228,409 (GRCm39) |
V293A |
probably damaging |
Het |
Rock2 |
T |
A |
12: 16,992,810 (GRCm39) |
F193Y |
probably damaging |
Het |
Scn3a |
C |
T |
2: 65,291,057 (GRCm39) |
M1896I |
probably benign |
Het |
Snrnp200 |
T |
C |
2: 127,067,933 (GRCm39) |
V810A |
probably damaging |
Het |
Taar4 |
G |
A |
10: 23,836,639 (GRCm39) |
S83N |
probably damaging |
Het |
Tdpoz4 |
A |
T |
3: 93,704,806 (GRCm39) |
T368S |
probably benign |
Het |
Tec |
T |
A |
5: 72,926,087 (GRCm39) |
I322F |
possibly damaging |
Het |
Teddm2 |
T |
C |
1: 153,726,146 (GRCm39) |
I190V |
probably benign |
Het |
Tmem117 |
A |
G |
15: 94,992,765 (GRCm39) |
E475G |
probably damaging |
Het |
Trip10 |
T |
A |
17: 57,569,460 (GRCm39) |
Y495N |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,638,695 (GRCm39) |
V4035A |
possibly damaging |
Het |
Utrn |
C |
T |
10: 12,558,062 (GRCm39) |
V1466M |
possibly damaging |
Het |
Vasp |
A |
G |
7: 18,991,816 (GRCm39) |
|
probably benign |
Het |
Vmn1r89 |
A |
T |
7: 12,953,857 (GRCm39) |
M130L |
possibly damaging |
Het |
Vmn2r2 |
A |
T |
3: 64,034,036 (GRCm39) |
D495E |
possibly damaging |
Het |
Zfp213 |
A |
G |
17: 23,780,160 (GRCm39) |
V120A |
possibly damaging |
Het |
|
Other mutations in Cnnm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01615:Cnnm1
|
APN |
19 |
43,460,375 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02370:Cnnm1
|
APN |
19 |
43,460,389 (GRCm39) |
critical splice donor site |
probably null |
|
R0329:Cnnm1
|
UTSW |
19 |
43,430,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R0400:Cnnm1
|
UTSW |
19 |
43,456,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R1417:Cnnm1
|
UTSW |
19 |
43,458,162 (GRCm39) |
missense |
probably benign |
0.05 |
R1478:Cnnm1
|
UTSW |
19 |
43,460,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R1743:Cnnm1
|
UTSW |
19 |
43,460,352 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2290:Cnnm1
|
UTSW |
19 |
43,479,941 (GRCm39) |
missense |
probably benign |
|
R2509:Cnnm1
|
UTSW |
19 |
43,430,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:Cnnm1
|
UTSW |
19 |
43,458,086 (GRCm39) |
missense |
possibly damaging |
0.58 |
R3107:Cnnm1
|
UTSW |
19 |
43,430,000 (GRCm39) |
missense |
probably damaging |
0.97 |
R3109:Cnnm1
|
UTSW |
19 |
43,430,000 (GRCm39) |
missense |
probably damaging |
0.97 |
R3922:Cnnm1
|
UTSW |
19 |
43,428,884 (GRCm39) |
start codon destroyed |
probably null |
|
R3923:Cnnm1
|
UTSW |
19 |
43,428,884 (GRCm39) |
start codon destroyed |
probably null |
|
R4804:Cnnm1
|
UTSW |
19 |
43,480,014 (GRCm39) |
missense |
probably benign |
0.02 |
R5199:Cnnm1
|
UTSW |
19 |
43,483,425 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5347:Cnnm1
|
UTSW |
19 |
43,430,301 (GRCm39) |
missense |
probably benign |
0.42 |
R5964:Cnnm1
|
UTSW |
19 |
43,458,162 (GRCm39) |
missense |
probably benign |
0.42 |
R5969:Cnnm1
|
UTSW |
19 |
43,479,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Cnnm1
|
UTSW |
19 |
43,453,705 (GRCm39) |
critical splice donor site |
probably null |
|
R7072:Cnnm1
|
UTSW |
19 |
43,429,296 (GRCm39) |
missense |
probably benign |
|
R7092:Cnnm1
|
UTSW |
19 |
43,430,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Cnnm1
|
UTSW |
19 |
43,473,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R7432:Cnnm1
|
UTSW |
19 |
43,456,710 (GRCm39) |
missense |
probably benign |
0.09 |
R7445:Cnnm1
|
UTSW |
19 |
43,429,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8728:Cnnm1
|
UTSW |
19 |
43,473,365 (GRCm39) |
missense |
probably benign |
0.00 |
R9108:Cnnm1
|
UTSW |
19 |
43,464,649 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9114:Cnnm1
|
UTSW |
19 |
43,429,395 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9131:Cnnm1
|
UTSW |
19 |
43,429,839 (GRCm39) |
missense |
probably benign |
|
R9232:Cnnm1
|
UTSW |
19 |
43,480,325 (GRCm39) |
missense |
probably benign |
0.12 |
R9357:Cnnm1
|
UTSW |
19 |
43,429,827 (GRCm39) |
missense |
probably damaging |
0.96 |
R9690:Cnnm1
|
UTSW |
19 |
43,460,345 (GRCm39) |
missense |
probably benign |
0.07 |
R9711:Cnnm1
|
UTSW |
19 |
43,483,469 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9792:Cnnm1
|
UTSW |
19 |
43,482,252 (GRCm39) |
critical splice donor site |
probably null |
|
|