Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930488N24Rik |
T |
C |
17: 14,326,408 (GRCm39) |
|
noncoding transcript |
Het |
Adamdec1 |
T |
C |
14: 68,809,215 (GRCm39) |
N249S |
probably damaging |
Het |
Asxl1 |
T |
A |
2: 153,241,751 (GRCm39) |
V767E |
probably benign |
Het |
Atp6v1f |
T |
C |
6: 29,470,271 (GRCm39) |
|
probably benign |
Het |
Brix1 |
T |
C |
15: 10,483,378 (GRCm39) |
|
probably null |
Het |
Cap2 |
T |
C |
13: 46,684,501 (GRCm39) |
V2A |
probably damaging |
Het |
Chrnb2 |
A |
G |
3: 89,668,248 (GRCm39) |
C356R |
probably damaging |
Het |
Chtf8 |
C |
T |
8: 107,612,424 (GRCm39) |
G172R |
probably damaging |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Dact2 |
T |
A |
17: 14,416,991 (GRCm39) |
K403M |
possibly damaging |
Het |
Dhx40 |
A |
C |
11: 86,662,036 (GRCm39) |
L674V |
possibly damaging |
Het |
Dlc1 |
A |
G |
8: 37,044,285 (GRCm39) |
V1230A |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,329,935 (GRCm39) |
S3260T |
probably benign |
Het |
Eef1a2 |
T |
A |
2: 180,789,881 (GRCm39) |
D428V |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,344,273 (GRCm39) |
F178L |
possibly damaging |
Het |
Eif4a3l1 |
T |
G |
6: 136,306,262 (GRCm39) |
V241G |
probably benign |
Het |
F2 |
A |
T |
2: 91,465,316 (GRCm39) |
|
probably benign |
Het |
Fam186a |
T |
C |
15: 99,844,723 (GRCm39) |
D507G |
unknown |
Het |
Fbxo11 |
G |
A |
17: 88,372,702 (GRCm39) |
|
probably benign |
Het |
Fry |
A |
T |
5: 150,419,168 (GRCm39) |
M2871L |
probably benign |
Het |
Gabrr2 |
A |
G |
4: 33,095,512 (GRCm39) |
D442G |
probably damaging |
Het |
Gemin5 |
A |
G |
11: 58,055,103 (GRCm39) |
I214T |
probably benign |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Jhy |
C |
T |
9: 40,808,821 (GRCm39) |
|
probably benign |
Het |
Krtap5-5 |
A |
T |
7: 141,783,156 (GRCm39) |
C165S |
unknown |
Het |
Lce1k |
T |
A |
3: 92,714,134 (GRCm39) |
T17S |
unknown |
Het |
Map3k1 |
C |
T |
13: 111,909,146 (GRCm39) |
R268Q |
probably damaging |
Het |
Med13l |
T |
A |
5: 118,883,195 (GRCm39) |
H1351Q |
probably damaging |
Het |
Met |
T |
C |
6: 17,546,995 (GRCm39) |
V876A |
probably damaging |
Het |
Mical2 |
T |
C |
7: 111,936,107 (GRCm39) |
S903P |
probably benign |
Het |
Mkks |
A |
G |
2: 136,718,094 (GRCm39) |
V396A |
probably benign |
Het |
Mvk |
T |
C |
5: 114,594,060 (GRCm39) |
V305A |
probably benign |
Het |
Myo5a |
A |
G |
9: 75,081,360 (GRCm39) |
T982A |
probably benign |
Het |
N4bp1 |
A |
G |
8: 87,588,311 (GRCm39) |
V209A |
probably benign |
Het |
Nfkbib |
G |
T |
7: 28,461,173 (GRCm39) |
S158* |
probably null |
Het |
Nkx3-1 |
G |
A |
14: 69,428,367 (GRCm39) |
G72S |
probably benign |
Het |
Ogfr |
A |
G |
2: 180,235,518 (GRCm39) |
|
probably benign |
Het |
Or10a3 |
G |
A |
7: 108,480,624 (GRCm39) |
T63I |
probably benign |
Het |
Or2t43 |
G |
A |
11: 58,457,451 (GRCm39) |
S240F |
possibly damaging |
Het |
Or8s8 |
T |
C |
15: 98,354,796 (GRCm39) |
S202P |
probably damaging |
Het |
Pcdhga8 |
T |
A |
18: 37,948,978 (GRCm39) |
D131E |
probably damaging |
Het |
Plch1 |
A |
G |
3: 63,648,264 (GRCm39) |
|
probably benign |
Het |
Polrmt |
A |
G |
10: 79,582,385 (GRCm39) |
M1T |
probably null |
Het |
Ppp1r12a |
T |
C |
10: 108,066,451 (GRCm39) |
V214A |
probably damaging |
Het |
Prr5l |
A |
G |
2: 101,628,027 (GRCm39) |
|
probably benign |
Het |
Prss35 |
A |
G |
9: 86,638,175 (GRCm39) |
Q315R |
probably damaging |
Het |
Psg29 |
G |
T |
7: 16,945,837 (GRCm39) |
*469L |
probably null |
Het |
Psmd4 |
A |
G |
3: 94,943,170 (GRCm39) |
V78A |
probably damaging |
Het |
Rad9a |
C |
A |
19: 4,251,552 (GRCm39) |
|
probably benign |
Het |
Rfx7 |
G |
T |
9: 72,524,573 (GRCm39) |
V588F |
probably benign |
Het |
Rnase13 |
A |
C |
14: 52,160,052 (GRCm39) |
I29S |
probably benign |
Het |
Steap2 |
T |
C |
5: 5,725,866 (GRCm39) |
N386S |
possibly damaging |
Het |
Ston1 |
A |
G |
17: 88,952,680 (GRCm39) |
E719G |
probably damaging |
Het |
Stx4a |
A |
G |
7: 127,441,934 (GRCm39) |
|
probably null |
Het |
Tekt2 |
A |
G |
4: 126,217,263 (GRCm39) |
S212P |
possibly damaging |
Het |
Tex19.2 |
A |
T |
11: 121,007,782 (GRCm39) |
L222Q |
probably damaging |
Het |
Tmem50a |
A |
G |
4: 134,637,017 (GRCm39) |
I38T |
probably damaging |
Het |
Ubr2 |
A |
G |
17: 47,296,922 (GRCm39) |
V286A |
possibly damaging |
Het |
Ugt2b35 |
T |
C |
5: 87,151,159 (GRCm39) |
M255T |
possibly damaging |
Het |
Vmn2r17 |
T |
A |
5: 109,601,220 (GRCm39) |
F839L |
probably benign |
Het |
Wdr36 |
T |
C |
18: 32,992,314 (GRCm39) |
V617A |
possibly damaging |
Het |
Wtip |
A |
T |
7: 33,818,437 (GRCm39) |
|
probably null |
Het |
Yeats2 |
G |
A |
16: 20,026,418 (GRCm39) |
G765S |
probably benign |
Het |
Zbtb3 |
T |
C |
19: 8,781,331 (GRCm39) |
S315P |
probably benign |
Het |
Zdhhc8 |
T |
C |
16: 18,045,030 (GRCm39) |
M259V |
probably benign |
Het |
Zfp120 |
A |
G |
2: 149,961,440 (GRCm39) |
|
probably benign |
Het |
Zfp236 |
A |
T |
18: 82,627,543 (GRCm39) |
I1552N |
possibly damaging |
Het |
|
Other mutations in Gfra2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00424:Gfra2
|
APN |
14 |
71,205,679 (GRCm39) |
splice site |
probably benign |
|
IGL01303:Gfra2
|
APN |
14 |
71,133,292 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01380:Gfra2
|
APN |
14 |
71,204,586 (GRCm39) |
splice site |
probably benign |
|
IGL01528:Gfra2
|
APN |
14 |
71,203,738 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02203:Gfra2
|
APN |
14 |
71,204,524 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02270:Gfra2
|
APN |
14 |
71,163,347 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03104:Gfra2
|
APN |
14 |
71,205,725 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03270:Gfra2
|
APN |
14 |
71,163,344 (GRCm39) |
missense |
possibly damaging |
0.80 |
H8562:Gfra2
|
UTSW |
14 |
71,215,818 (GRCm39) |
missense |
possibly damaging |
0.94 |
H8786:Gfra2
|
UTSW |
14 |
71,215,818 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0423:Gfra2
|
UTSW |
14 |
71,133,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Gfra2
|
UTSW |
14 |
71,203,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4172:Gfra2
|
UTSW |
14 |
71,133,521 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4712:Gfra2
|
UTSW |
14 |
71,163,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Gfra2
|
UTSW |
14 |
71,163,361 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5424:Gfra2
|
UTSW |
14 |
71,133,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R6711:Gfra2
|
UTSW |
14 |
71,203,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R7290:Gfra2
|
UTSW |
14 |
71,163,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Gfra2
|
UTSW |
14 |
71,205,831 (GRCm39) |
missense |
probably benign |
0.00 |
R7814:Gfra2
|
UTSW |
14 |
71,133,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8159:Gfra2
|
UTSW |
14 |
71,133,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R8557:Gfra2
|
UTSW |
14 |
71,214,737 (GRCm39) |
missense |
probably benign |
0.05 |
R8831:Gfra2
|
UTSW |
14 |
71,204,503 (GRCm39) |
missense |
probably benign |
0.02 |
R8833:Gfra2
|
UTSW |
14 |
71,163,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Gfra2
|
UTSW |
14 |
71,138,935 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9073:Gfra2
|
UTSW |
14 |
71,138,935 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9444:Gfra2
|
UTSW |
14 |
71,203,751 (GRCm39) |
missense |
possibly damaging |
0.55 |
Z1177:Gfra2
|
UTSW |
14 |
71,215,932 (GRCm39) |
missense |
not run |
|
|