Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot13 |
A |
T |
13: 25,002,154 (GRCm39) |
I96K |
probably benign |
Het |
Adam6a |
A |
G |
12: 113,509,291 (GRCm39) |
T555A |
probably benign |
Het |
Alms1 |
C |
T |
6: 85,598,351 (GRCm39) |
P1059L |
probably benign |
Het |
Apol7c |
T |
C |
15: 77,409,843 (GRCm39) |
T368A |
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,475,015 (GRCm39) |
L1557Q |
probably damaging |
Het |
Baz2a |
C |
T |
10: 127,960,326 (GRCm39) |
R1514W |
probably damaging |
Het |
Bmp3 |
T |
A |
5: 99,020,622 (GRCm39) |
D348E |
probably damaging |
Het |
Bves |
A |
G |
10: 45,230,913 (GRCm39) |
S295G |
probably damaging |
Het |
Carmil1 |
A |
G |
13: 24,204,052 (GRCm39) |
C1328R |
probably benign |
Het |
Ccnk |
T |
A |
12: 108,153,517 (GRCm39) |
Y93N |
probably damaging |
Het |
Ccr1 |
A |
T |
9: 123,764,089 (GRCm39) |
V147D |
probably damaging |
Het |
Cd24a |
G |
A |
10: 43,458,636 (GRCm39) |
G36S |
probably benign |
Het |
Cep104 |
A |
G |
4: 154,077,324 (GRCm39) |
Y569C |
probably damaging |
Het |
Chd2 |
A |
T |
7: 73,125,168 (GRCm39) |
I884N |
probably damaging |
Het |
Cnst |
A |
T |
1: 179,406,947 (GRCm39) |
|
probably benign |
Het |
Col22a1 |
A |
G |
15: 71,805,262 (GRCm39) |
L146P |
unknown |
Het |
Col25a1 |
G |
T |
3: 130,323,768 (GRCm39) |
R321L |
probably damaging |
Het |
Ctnnd2 |
T |
C |
15: 30,683,510 (GRCm39) |
Y504H |
possibly damaging |
Het |
D3Ertd751e |
C |
A |
3: 41,703,143 (GRCm39) |
Q73K |
probably damaging |
Het |
Dsc2 |
C |
T |
18: 20,168,332 (GRCm39) |
|
probably null |
Het |
Eya1 |
A |
T |
1: 14,373,076 (GRCm39) |
S14R |
probably damaging |
Het |
Fam131c |
A |
T |
4: 141,110,328 (GRCm39) |
|
probably null |
Het |
Flvcr2 |
T |
C |
12: 85,793,965 (GRCm39) |
F114L |
possibly damaging |
Het |
Fyn |
A |
G |
10: 39,408,120 (GRCm39) |
D321G |
possibly damaging |
Het |
Galnt5 |
A |
C |
2: 57,888,621 (GRCm39) |
M74L |
probably benign |
Het |
Garin4 |
G |
A |
1: 190,896,218 (GRCm39) |
R142C |
probably damaging |
Het |
Gas2l2 |
G |
A |
11: 83,313,288 (GRCm39) |
P675S |
probably benign |
Het |
Gm9508 |
G |
T |
10: 77,532,470 (GRCm39) |
Q200K |
unknown |
Het |
Greb1l |
G |
A |
18: 10,544,576 (GRCm39) |
S1390N |
probably benign |
Het |
Hdac5 |
G |
T |
11: 102,095,385 (GRCm39) |
T430K |
possibly damaging |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Khnyn |
C |
T |
14: 56,131,811 (GRCm39) |
P578S |
probably damaging |
Het |
Lepr |
A |
T |
4: 101,602,856 (GRCm39) |
T215S |
probably benign |
Het |
Lrfn5 |
G |
A |
12: 61,890,768 (GRCm39) |
V686I |
probably benign |
Het |
Mapkap1 |
T |
A |
2: 34,408,712 (GRCm39) |
H233Q |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,885,081 (GRCm39) |
I201T |
probably damaging |
Het |
Metrnl |
G |
A |
11: 121,606,734 (GRCm39) |
R263Q |
probably damaging |
Het |
Mettl22 |
A |
G |
16: 8,295,924 (GRCm39) |
E71G |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,553,304 (GRCm39) |
T4330A |
probably benign |
Het |
Mug1 |
A |
G |
6: 121,834,379 (GRCm39) |
T387A |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,135,550 (GRCm39) |
D379G |
probably benign |
Het |
Nbas |
A |
G |
12: 13,455,398 (GRCm39) |
D1204G |
possibly damaging |
Het |
Or14a256 |
A |
T |
7: 86,265,574 (GRCm39) |
L93Q |
possibly damaging |
Het |
Or51d1 |
A |
G |
7: 102,347,477 (GRCm39) |
T11A |
probably benign |
Het |
Or5k1 |
T |
A |
16: 58,617,250 (GRCm39) |
I320F |
probably benign |
Het |
Osbpl7 |
G |
A |
11: 96,941,662 (GRCm39) |
V62I |
probably benign |
Het |
Pak1ip1 |
A |
G |
13: 41,163,018 (GRCm39) |
N246S |
probably damaging |
Het |
Prim1 |
A |
G |
10: 127,851,845 (GRCm39) |
Y39C |
probably damaging |
Het |
Prl3b1 |
G |
T |
13: 27,427,827 (GRCm39) |
V46L |
probably benign |
Het |
Prss54 |
A |
T |
8: 96,292,199 (GRCm39) |
S127T |
probably benign |
Het |
Rasal3 |
G |
A |
17: 32,611,391 (GRCm39) |
T912M |
probably damaging |
Het |
Rrp12 |
T |
A |
19: 41,872,217 (GRCm39) |
T420S |
probably benign |
Het |
Rspo1 |
A |
G |
4: 124,898,831 (GRCm39) |
N51D |
probably damaging |
Het |
Rufy4 |
A |
G |
1: 74,172,035 (GRCm39) |
R253G |
probably benign |
Het |
Scaf1 |
G |
A |
7: 44,657,167 (GRCm39) |
R571C |
unknown |
Het |
Scn2a |
A |
T |
2: 65,532,323 (GRCm39) |
H645L |
probably damaging |
Het |
Sec24b |
A |
G |
3: 129,782,595 (GRCm39) |
S1132P |
probably damaging |
Het |
Slc1a2 |
A |
G |
2: 102,586,290 (GRCm39) |
K298R |
probably damaging |
Het |
Slc25a54 |
T |
A |
3: 109,014,573 (GRCm39) |
N230K |
probably benign |
Het |
Slc27a4 |
T |
G |
2: 29,705,664 (GRCm39) |
Y617* |
probably null |
Het |
Slc2a10 |
T |
C |
2: 165,357,269 (GRCm39) |
S310P |
probably damaging |
Het |
Snx33 |
C |
T |
9: 56,833,151 (GRCm39) |
R306H |
probably damaging |
Het |
Spag9 |
A |
T |
11: 93,980,258 (GRCm39) |
|
probably null |
Het |
Spg11 |
A |
T |
2: 121,932,270 (GRCm39) |
|
probably null |
Het |
Sycp2l |
A |
G |
13: 41,283,258 (GRCm39) |
T165A |
probably damaging |
Het |
Syt14 |
A |
G |
1: 192,615,571 (GRCm39) |
C189R |
probably damaging |
Het |
Taar9 |
A |
T |
10: 23,984,882 (GRCm39) |
L184Q |
probably damaging |
Het |
Tkt |
C |
T |
14: 30,281,815 (GRCm39) |
P111L |
probably damaging |
Het |
Trpc1 |
A |
T |
9: 95,603,197 (GRCm39) |
L445Q |
possibly damaging |
Het |
Usp53 |
A |
G |
3: 122,743,359 (GRCm39) |
S526P |
probably benign |
Het |
Vps54 |
T |
G |
11: 21,248,791 (GRCm39) |
W447G |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,340,177 (GRCm39) |
H806L |
probably benign |
Het |
Zfp451 |
A |
T |
1: 33,841,651 (GRCm39) |
H410Q |
unknown |
Het |
Zfp688 |
A |
G |
7: 127,018,484 (GRCm39) |
C214R |
probably damaging |
Het |
Zic4 |
A |
G |
9: 91,261,174 (GRCm39) |
D143G |
possibly damaging |
Het |
|
Other mutations in Ncor2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Ncor2
|
APN |
5 |
125,119,807 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00519:Ncor2
|
APN |
5 |
125,161,988 (GRCm39) |
missense |
unknown |
|
IGL00900:Ncor2
|
APN |
5 |
125,102,848 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00950:Ncor2
|
APN |
5 |
125,163,954 (GRCm39) |
missense |
unknown |
|
IGL01320:Ncor2
|
APN |
5 |
125,186,991 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01382:Ncor2
|
APN |
5 |
125,132,837 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01573:Ncor2
|
APN |
5 |
125,162,090 (GRCm39) |
missense |
unknown |
|
IGL01721:Ncor2
|
APN |
5 |
125,128,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01875:Ncor2
|
APN |
5 |
125,142,934 (GRCm39) |
missense |
unknown |
|
IGL02090:Ncor2
|
APN |
5 |
125,111,467 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02192:Ncor2
|
APN |
5 |
125,101,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02396:Ncor2
|
APN |
5 |
125,114,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02934:Ncor2
|
APN |
5 |
125,102,621 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02997:Ncor2
|
APN |
5 |
125,196,634 (GRCm39) |
intron |
probably benign |
|
R0019:Ncor2
|
UTSW |
5 |
125,196,545 (GRCm39) |
critical splice donor site |
probably null |
|
R0331:Ncor2
|
UTSW |
5 |
125,161,981 (GRCm39) |
missense |
unknown |
|
R0333:Ncor2
|
UTSW |
5 |
125,111,408 (GRCm39) |
splice site |
probably benign |
|
R0403:Ncor2
|
UTSW |
5 |
125,110,401 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0557:Ncor2
|
UTSW |
5 |
125,183,369 (GRCm39) |
nonsense |
probably null |
|
R0562:Ncor2
|
UTSW |
5 |
125,162,093 (GRCm39) |
missense |
unknown |
|
R0671:Ncor2
|
UTSW |
5 |
125,126,451 (GRCm39) |
missense |
probably benign |
0.13 |
R0699:Ncor2
|
UTSW |
5 |
125,106,176 (GRCm39) |
unclassified |
probably benign |
|
R0865:Ncor2
|
UTSW |
5 |
125,116,046 (GRCm39) |
missense |
probably benign |
0.17 |
R1183:Ncor2
|
UTSW |
5 |
125,100,585 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1325:Ncor2
|
UTSW |
5 |
125,195,844 (GRCm39) |
intron |
probably benign |
|
R1344:Ncor2
|
UTSW |
5 |
125,102,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1433:Ncor2
|
UTSW |
5 |
125,187,039 (GRCm39) |
intron |
probably benign |
|
R1481:Ncor2
|
UTSW |
5 |
125,104,202 (GRCm39) |
nonsense |
probably null |
|
R1539:Ncor2
|
UTSW |
5 |
125,187,003 (GRCm39) |
missense |
probably benign |
0.07 |
R1558:Ncor2
|
UTSW |
5 |
125,110,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Ncor2
|
UTSW |
5 |
125,162,062 (GRCm39) |
missense |
unknown |
|
R1611:Ncor2
|
UTSW |
5 |
125,187,084 (GRCm39) |
intron |
probably benign |
|
R1764:Ncor2
|
UTSW |
5 |
125,105,679 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1789:Ncor2
|
UTSW |
5 |
125,096,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Ncor2
|
UTSW |
5 |
125,195,857 (GRCm39) |
intron |
probably benign |
|
R1901:Ncor2
|
UTSW |
5 |
125,102,489 (GRCm39) |
missense |
probably benign |
0.39 |
R1946:Ncor2
|
UTSW |
5 |
125,111,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Ncor2
|
UTSW |
5 |
125,115,982 (GRCm39) |
missense |
probably damaging |
0.99 |
R2048:Ncor2
|
UTSW |
5 |
125,161,996 (GRCm39) |
missense |
unknown |
|
R2137:Ncor2
|
UTSW |
5 |
125,107,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R2270:Ncor2
|
UTSW |
5 |
125,115,019 (GRCm39) |
missense |
probably benign |
0.33 |
R2380:Ncor2
|
UTSW |
5 |
125,113,144 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2570:Ncor2
|
UTSW |
5 |
125,105,864 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2918:Ncor2
|
UTSW |
5 |
125,102,824 (GRCm39) |
missense |
probably damaging |
0.99 |
R2921:Ncor2
|
UTSW |
5 |
125,132,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2922:Ncor2
|
UTSW |
5 |
125,132,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2923:Ncor2
|
UTSW |
5 |
125,132,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R3116:Ncor2
|
UTSW |
5 |
125,101,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R3768:Ncor2
|
UTSW |
5 |
125,105,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Ncor2
|
UTSW |
5 |
125,195,756 (GRCm39) |
intron |
probably benign |
|
R3829:Ncor2
|
UTSW |
5 |
125,195,756 (GRCm39) |
intron |
probably benign |
|
R3830:Ncor2
|
UTSW |
5 |
125,195,756 (GRCm39) |
intron |
probably benign |
|
R3951:Ncor2
|
UTSW |
5 |
125,109,320 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4175:Ncor2
|
UTSW |
5 |
125,128,020 (GRCm39) |
missense |
probably damaging |
0.99 |
R4360:Ncor2
|
UTSW |
5 |
125,106,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Ncor2
|
UTSW |
5 |
125,179,705 (GRCm39) |
critical splice donor site |
probably null |
|
R4490:Ncor2
|
UTSW |
5 |
125,113,879 (GRCm39) |
splice site |
probably null |
|
R4573:Ncor2
|
UTSW |
5 |
125,132,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R4611:Ncor2
|
UTSW |
5 |
125,107,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Ncor2
|
UTSW |
5 |
125,114,124 (GRCm39) |
critical splice donor site |
probably null |
|
R4851:Ncor2
|
UTSW |
5 |
125,110,431 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4853:Ncor2
|
UTSW |
5 |
125,158,247 (GRCm39) |
missense |
unknown |
|
R4853:Ncor2
|
UTSW |
5 |
125,102,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R4896:Ncor2
|
UTSW |
5 |
125,126,404 (GRCm39) |
critical splice donor site |
probably null |
|
R4997:Ncor2
|
UTSW |
5 |
125,111,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R5057:Ncor2
|
UTSW |
5 |
125,125,130 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5253:Ncor2
|
UTSW |
5 |
125,103,994 (GRCm39) |
missense |
probably benign |
0.44 |
R5461:Ncor2
|
UTSW |
5 |
125,104,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Ncor2
|
UTSW |
5 |
125,144,975 (GRCm39) |
nonsense |
probably null |
|
R5638:Ncor2
|
UTSW |
5 |
125,125,364 (GRCm39) |
missense |
probably benign |
0.33 |
R5879:Ncor2
|
UTSW |
5 |
125,103,839 (GRCm39) |
unclassified |
probably benign |
|
R5967:Ncor2
|
UTSW |
5 |
125,146,048 (GRCm39) |
missense |
unknown |
|
R5999:Ncor2
|
UTSW |
5 |
125,110,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:Ncor2
|
UTSW |
5 |
125,097,075 (GRCm39) |
missense |
probably benign |
0.14 |
R6109:Ncor2
|
UTSW |
5 |
125,132,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R6423:Ncor2
|
UTSW |
5 |
125,164,966 (GRCm39) |
missense |
unknown |
|
R6462:Ncor2
|
UTSW |
5 |
125,101,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Ncor2
|
UTSW |
5 |
125,187,069 (GRCm39) |
intron |
probably benign |
|
R7074:Ncor2
|
UTSW |
5 |
125,126,430 (GRCm39) |
nonsense |
probably null |
|
R7261:Ncor2
|
UTSW |
5 |
125,187,143 (GRCm39) |
splice site |
probably null |
|
R7263:Ncor2
|
UTSW |
5 |
125,109,196 (GRCm39) |
missense |
|
|
R7273:Ncor2
|
UTSW |
5 |
125,100,687 (GRCm39) |
missense |
|
|
R7282:Ncor2
|
UTSW |
5 |
125,097,104 (GRCm39) |
missense |
|
|
R7570:Ncor2
|
UTSW |
5 |
125,107,153 (GRCm39) |
missense |
|
|
R7725:Ncor2
|
UTSW |
5 |
125,100,630 (GRCm39) |
missense |
|
|
R7747:Ncor2
|
UTSW |
5 |
125,104,102 (GRCm39) |
missense |
|
|
R7748:Ncor2
|
UTSW |
5 |
125,187,031 (GRCm39) |
missense |
unknown |
|
R7825:Ncor2
|
UTSW |
5 |
125,114,141 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8008:Ncor2
|
UTSW |
5 |
125,144,983 (GRCm39) |
missense |
unknown |
|
R8126:Ncor2
|
UTSW |
5 |
125,183,268 (GRCm39) |
missense |
unknown |
|
R8137:Ncor2
|
UTSW |
5 |
125,114,957 (GRCm39) |
missense |
|
|
R8706:Ncor2
|
UTSW |
5 |
125,145,010 (GRCm39) |
missense |
unknown |
|
R8751:Ncor2
|
UTSW |
5 |
125,115,964 (GRCm39) |
missense |
|
|
R8819:Ncor2
|
UTSW |
5 |
125,106,291 (GRCm39) |
missense |
|
|
R8820:Ncor2
|
UTSW |
5 |
125,106,291 (GRCm39) |
missense |
|
|
R8824:Ncor2
|
UTSW |
5 |
125,195,821 (GRCm39) |
missense |
|
|
R8867:Ncor2
|
UTSW |
5 |
125,179,739 (GRCm39) |
missense |
unknown |
|
R8919:Ncor2
|
UTSW |
5 |
125,106,253 (GRCm39) |
missense |
|
|
R8922:Ncor2
|
UTSW |
5 |
125,163,939 (GRCm39) |
missense |
unknown |
|
R9076:Ncor2
|
UTSW |
5 |
125,111,086 (GRCm39) |
missense |
|
|
R9249:Ncor2
|
UTSW |
5 |
125,186,988 (GRCm39) |
missense |
unknown |
|
R9276:Ncor2
|
UTSW |
5 |
125,113,150 (GRCm39) |
missense |
|
|
R9362:Ncor2
|
UTSW |
5 |
125,095,265 (GRCm39) |
missense |
|
|
R9667:Ncor2
|
UTSW |
5 |
125,125,545 (GRCm39) |
missense |
unknown |
|
R9684:Ncor2
|
UTSW |
5 |
125,102,139 (GRCm39) |
missense |
|
|
Z1088:Ncor2
|
UTSW |
5 |
125,163,904 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Ncor2
|
UTSW |
5 |
125,144,852 (GRCm39) |
missense |
unknown |
|
Z1177:Ncor2
|
UTSW |
5 |
125,113,913 (GRCm39) |
missense |
|
|
Z1177:Ncor2
|
UTSW |
5 |
125,125,058 (GRCm39) |
missense |
probably damaging |
0.98 |
|