Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts16 |
T |
A |
13: 70,927,717 (GRCm39) |
|
probably null |
Het |
Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
Aknad1 |
A |
G |
3: 108,659,099 (GRCm39) |
T38A |
possibly damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Arhgap21 |
T |
C |
2: 20,865,910 (GRCm39) |
E902G |
probably damaging |
Het |
Atg2b |
A |
G |
12: 105,635,588 (GRCm39) |
S227P |
possibly damaging |
Het |
Atp2c2 |
C |
T |
8: 120,461,182 (GRCm39) |
|
probably benign |
Het |
Atxn10 |
T |
C |
15: 85,260,864 (GRCm39) |
V203A |
probably damaging |
Het |
Chd9 |
A |
C |
8: 91,737,326 (GRCm39) |
E1468D |
probably benign |
Het |
Cntn5 |
T |
A |
9: 9,831,577 (GRCm39) |
D601V |
probably damaging |
Het |
Col4a2 |
G |
A |
8: 11,496,020 (GRCm39) |
G1547D |
probably benign |
Het |
Cul1 |
A |
G |
6: 47,485,179 (GRCm39) |
E270G |
probably damaging |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dmgdh |
C |
A |
13: 93,888,933 (GRCm39) |
T857K |
probably benign |
Het |
Ednra |
T |
G |
8: 78,398,211 (GRCm39) |
T279P |
probably benign |
Het |
Erbin |
A |
G |
13: 103,987,339 (GRCm39) |
I407T |
probably damaging |
Het |
Fggy |
A |
G |
4: 95,814,965 (GRCm39) |
Y440C |
probably damaging |
Het |
Flrt2 |
A |
T |
12: 95,747,566 (GRCm39) |
N635Y |
possibly damaging |
Het |
Fnbp1l |
A |
G |
3: 122,350,140 (GRCm39) |
I357T |
probably benign |
Het |
Gulp1 |
A |
G |
1: 44,793,513 (GRCm39) |
H58R |
possibly damaging |
Het |
Hid1 |
A |
T |
11: 115,245,464 (GRCm39) |
V446E |
probably damaging |
Het |
Igfn1 |
A |
G |
1: 135,897,561 (GRCm39) |
S1002P |
possibly damaging |
Het |
Klri1 |
A |
G |
6: 129,675,118 (GRCm39) |
|
probably null |
Het |
Kmt2d |
A |
C |
15: 98,762,259 (GRCm39) |
L409R |
probably damaging |
Het |
Ltn1 |
A |
C |
16: 87,208,669 (GRCm39) |
S810A |
possibly damaging |
Het |
Mysm1 |
G |
A |
4: 94,836,648 (GRCm39) |
Q721* |
probably null |
Het |
Nae1 |
A |
G |
8: 105,254,017 (GRCm39) |
V105A |
possibly damaging |
Het |
Nagpa |
C |
T |
16: 5,021,503 (GRCm39) |
V83M |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,221,789 (GRCm39) |
M150V |
possibly damaging |
Het |
Or5p52 |
C |
A |
7: 107,502,093 (GRCm39) |
H56Q |
probably benign |
Het |
Or8g28 |
A |
G |
9: 39,169,498 (GRCm39) |
S157P |
probably damaging |
Het |
Papola |
T |
A |
12: 105,773,468 (GRCm39) |
D162E |
probably benign |
Het |
Plxnc1 |
T |
C |
10: 94,680,041 (GRCm39) |
|
probably null |
Het |
Ppp1r16b |
T |
A |
2: 158,588,585 (GRCm39) |
|
probably null |
Het |
Ptprq |
T |
A |
10: 107,474,691 (GRCm39) |
E1338V |
probably damaging |
Het |
Puf60 |
G |
A |
15: 75,942,633 (GRCm39) |
H437Y |
probably benign |
Het |
Qsox2 |
C |
T |
2: 26,110,650 (GRCm39) |
V189I |
probably benign |
Het |
Rad51ap2 |
A |
T |
12: 11,507,776 (GRCm39) |
D566V |
probably benign |
Het |
Rb1cc1 |
T |
A |
1: 6,333,237 (GRCm39) |
|
probably null |
Het |
Rfpl4b |
C |
T |
10: 38,697,049 (GRCm39) |
C184Y |
possibly damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rundc3a |
GAGCC |
GAGCCAGCC |
11: 102,291,739 (GRCm39) |
|
probably null |
Het |
Scara5 |
A |
C |
14: 65,968,539 (GRCm39) |
M271L |
probably benign |
Het |
Sel1l2 |
A |
G |
2: 140,127,157 (GRCm39) |
L118P |
probably damaging |
Het |
Sema6a |
T |
A |
18: 47,439,416 (GRCm39) |
|
probably benign |
Het |
Siglech |
T |
A |
7: 55,418,252 (GRCm39) |
H73Q |
probably benign |
Het |
Sim1 |
A |
G |
10: 50,860,205 (GRCm39) |
D689G |
probably benign |
Het |
Skp2 |
T |
C |
15: 9,139,530 (GRCm39) |
E55G |
possibly damaging |
Het |
Slc1a1 |
T |
A |
19: 28,871,869 (GRCm39) |
V114E |
probably benign |
Het |
Slc26a6 |
G |
A |
9: 108,738,916 (GRCm39) |
G614D |
probably benign |
Het |
Sptbn2 |
C |
T |
19: 4,795,992 (GRCm39) |
Q1724* |
probably null |
Het |
Tet3 |
T |
C |
6: 83,345,050 (GRCm39) |
T1796A |
probably damaging |
Het |
Tmem117 |
A |
C |
15: 94,829,714 (GRCm39) |
D183A |
possibly damaging |
Het |
Trmt44 |
A |
G |
5: 35,721,403 (GRCm39) |
S587P |
probably benign |
Het |
Ttn |
G |
T |
2: 76,619,166 (GRCm39) |
|
probably benign |
Het |
Tubgcp5 |
G |
A |
7: 55,458,285 (GRCm39) |
V399M |
probably benign |
Het |
Txndc2 |
T |
A |
17: 65,945,130 (GRCm39) |
D349V |
probably damaging |
Het |
Uggt2 |
T |
A |
14: 119,250,915 (GRCm39) |
N1194I |
probably benign |
Het |
Vmn1r178 |
A |
T |
7: 23,593,329 (GRCm39) |
I53L |
probably benign |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Nrg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Nrg2
|
APN |
18 |
36,154,271 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01396:Nrg2
|
APN |
18 |
36,178,905 (GRCm39) |
splice site |
probably benign |
|
R0179:Nrg2
|
UTSW |
18 |
36,155,468 (GRCm39) |
missense |
probably benign |
0.13 |
R0976:Nrg2
|
UTSW |
18 |
36,154,144 (GRCm39) |
missense |
probably benign |
0.21 |
R1387:Nrg2
|
UTSW |
18 |
36,329,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R1487:Nrg2
|
UTSW |
18 |
36,185,965 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1882:Nrg2
|
UTSW |
18 |
36,154,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Nrg2
|
UTSW |
18 |
36,329,897 (GRCm39) |
unclassified |
probably benign |
|
R2090:Nrg2
|
UTSW |
18 |
36,151,496 (GRCm39) |
missense |
probably benign |
0.00 |
R2183:Nrg2
|
UTSW |
18 |
36,329,804 (GRCm39) |
missense |
probably benign |
0.11 |
R4664:Nrg2
|
UTSW |
18 |
36,185,948 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4677:Nrg2
|
UTSW |
18 |
36,154,152 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4860:Nrg2
|
UTSW |
18 |
36,329,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Nrg2
|
UTSW |
18 |
36,329,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R5091:Nrg2
|
UTSW |
18 |
36,185,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Nrg2
|
UTSW |
18 |
36,329,642 (GRCm39) |
missense |
probably damaging |
0.98 |
R6968:Nrg2
|
UTSW |
18 |
36,329,499 (GRCm39) |
missense |
probably benign |
0.01 |
R7186:Nrg2
|
UTSW |
18 |
36,178,973 (GRCm39) |
missense |
probably benign |
0.17 |
R7304:Nrg2
|
UTSW |
18 |
36,178,994 (GRCm39) |
missense |
probably benign |
0.24 |
R7467:Nrg2
|
UTSW |
18 |
36,155,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7564:Nrg2
|
UTSW |
18 |
36,157,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7876:Nrg2
|
UTSW |
18 |
36,330,140 (GRCm39) |
missense |
unknown |
|
R8113:Nrg2
|
UTSW |
18 |
36,154,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R8133:Nrg2
|
UTSW |
18 |
36,165,430 (GRCm39) |
missense |
probably benign |
0.00 |
R8214:Nrg2
|
UTSW |
18 |
36,329,729 (GRCm39) |
missense |
probably benign |
0.02 |
R8261:Nrg2
|
UTSW |
18 |
36,165,428 (GRCm39) |
missense |
probably benign |
0.11 |
R9000:Nrg2
|
UTSW |
18 |
36,151,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R9131:Nrg2
|
UTSW |
18 |
36,157,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Nrg2
|
UTSW |
18 |
36,157,401 (GRCm39) |
missense |
probably null |
|
R9512:Nrg2
|
UTSW |
18 |
36,179,010 (GRCm39) |
missense |
probably benign |
0.11 |
R9667:Nrg2
|
UTSW |
18 |
36,165,430 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Nrg2
|
UTSW |
18 |
36,151,523 (GRCm39) |
missense |
probably damaging |
0.96 |
|