Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Chl1 |
T |
C |
6: 103,645,815 (GRCm39) |
|
probably benign |
Het |
Crtc3 |
T |
C |
7: 80,239,628 (GRCm39) |
M575V |
probably benign |
Het |
Cux1 |
T |
A |
5: 136,514,671 (GRCm39) |
N22I |
probably damaging |
Het |
Dcun1d2 |
G |
A |
8: 13,307,935 (GRCm39) |
R248W |
probably damaging |
Het |
Dlc1 |
G |
T |
8: 37,199,860 (GRCm39) |
H7Q |
probably benign |
Het |
Drd2 |
A |
G |
9: 49,307,004 (GRCm39) |
D30G |
probably benign |
Het |
Duxf3 |
GCCC |
GCC |
10: 58,066,944 (GRCm39) |
|
probably null |
Het |
E2f7 |
T |
C |
10: 110,616,874 (GRCm39) |
S705P |
probably benign |
Het |
Ephb3 |
G |
A |
16: 21,041,214 (GRCm39) |
S977N |
probably benign |
Het |
F13a1 |
T |
G |
13: 37,089,993 (GRCm39) |
D448A |
probably benign |
Het |
Fam216b |
T |
C |
14: 78,322,537 (GRCm39) |
T56A |
possibly damaging |
Het |
Fcho2 |
T |
C |
13: 98,886,391 (GRCm39) |
T408A |
probably benign |
Het |
Flvcr1 |
A |
T |
1: 190,740,364 (GRCm39) |
V552E |
|
Het |
Gab3 |
CTT |
CTTGTT |
X: 74,043,612 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,602 (GRCm39) |
|
probably benign |
Het |
Galnt15 |
A |
G |
14: 31,780,196 (GRCm39) |
K622E |
probably benign |
Het |
Gjb3 |
GCCAGATGCGCCCA |
GCCAGATGCGCCCAGATGCGCCCA |
4: 127,220,458 (GRCm39) |
|
probably null |
Het |
Gjb3 |
A |
AGATGCGCCCG |
4: 127,220,471 (GRCm39) |
|
probably null |
Het |
Gm5414 |
T |
G |
15: 101,536,345 (GRCm39) |
R93S |
probably benign |
Het |
Gtf2i |
A |
G |
5: 134,318,241 (GRCm39) |
*87Q |
probably null |
Het |
Il7r |
T |
A |
15: 9,510,270 (GRCm39) |
H261L |
probably benign |
Het |
Itsn1 |
T |
A |
16: 91,609,002 (GRCm39) |
M250K |
possibly damaging |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Liat1 |
A |
G |
11: 75,893,887 (GRCm39) |
D88G |
possibly damaging |
Het |
Lrrc47 |
C |
A |
4: 154,096,421 (GRCm39) |
T72K |
possibly damaging |
Het |
Map2k4 |
C |
A |
11: 65,581,599 (GRCm39) |
R371L |
probably benign |
Het |
Mmrn2 |
T |
C |
14: 34,118,587 (GRCm39) |
F158L |
probably benign |
Het |
Mtus1 |
A |
T |
8: 41,455,475 (GRCm39) |
L242Q |
probably damaging |
Het |
Myo5a |
T |
C |
9: 75,054,414 (GRCm39) |
|
probably null |
Het |
Or4p8 |
T |
C |
2: 88,727,321 (GRCm39) |
T207A |
probably damaging |
Het |
Pag1 |
T |
C |
3: 9,764,848 (GRCm39) |
T102A |
probably benign |
Het |
Pam |
A |
G |
1: 97,791,976 (GRCm39) |
S482P |
probably benign |
Het |
Pax1 |
T |
G |
2: 147,204,287 (GRCm39) |
W23G |
unknown |
Het |
Pcdhgb1 |
T |
A |
18: 37,813,989 (GRCm39) |
V160D |
possibly damaging |
Het |
Pdzph1 |
T |
C |
17: 59,280,125 (GRCm39) |
D719G |
probably damaging |
Het |
Phlda1 |
T |
C |
10: 111,342,474 (GRCm39) |
L70S |
possibly damaging |
Het |
Pikfyve |
G |
A |
1: 65,283,559 (GRCm39) |
R732K |
probably damaging |
Het |
Pkd1 |
G |
T |
17: 24,788,347 (GRCm39) |
V702F |
possibly damaging |
Het |
Pkhd1 |
A |
G |
1: 20,632,586 (GRCm39) |
Y610H |
probably benign |
Het |
Pofut1 |
T |
G |
2: 153,101,508 (GRCm39) |
H87Q |
probably benign |
Het |
Runx2 |
C |
A |
17: 45,046,443 (GRCm39) |
D109Y |
probably damaging |
Het |
Serpina1b |
T |
A |
12: 103,696,540 (GRCm39) |
I290F |
probably benign |
Het |
Sez6 |
G |
A |
11: 77,865,121 (GRCm39) |
E623K |
possibly damaging |
Het |
Sh3tc1 |
T |
C |
5: 35,874,321 (GRCm39) |
N198S |
probably benign |
Het |
Slc27a6 |
C |
A |
18: 58,742,330 (GRCm39) |
R515S |
probably benign |
Het |
Sorbs3 |
C |
T |
14: 70,445,004 (GRCm39) |
V25I |
probably benign |
Het |
Speg |
A |
G |
1: 75,399,378 (GRCm39) |
E2275G |
probably benign |
Het |
Tmem161b |
C |
T |
13: 84,440,503 (GRCm39) |
T307I |
possibly damaging |
Het |
Tmem30a |
T |
C |
9: 79,678,581 (GRCm39) |
D361G |
probably damaging |
Het |
Tmprss11c |
T |
C |
5: 86,385,495 (GRCm39) |
T326A |
probably benign |
Het |
Tpbg |
T |
C |
9: 85,726,916 (GRCm39) |
V295A |
possibly damaging |
Het |
Ulk4 |
A |
T |
9: 120,903,003 (GRCm39) |
I1158N |
|
Het |
Utp20 |
C |
A |
10: 88,604,679 (GRCm39) |
A1739S |
probably benign |
Het |
Utp20 |
T |
C |
10: 88,611,180 (GRCm39) |
N1379S |
probably damaging |
Het |
Vmn1r66 |
T |
A |
7: 10,008,110 (GRCm39) |
I308F |
possibly damaging |
Het |
Vmn2r101 |
A |
T |
17: 19,809,807 (GRCm39) |
T198S |
probably benign |
Het |
Vps16 |
T |
C |
2: 130,281,593 (GRCm39) |
I318T |
probably damaging |
Het |
Wdr11 |
T |
A |
7: 129,226,451 (GRCm39) |
W750R |
probably damaging |
Het |
Zfp608 |
A |
G |
18: 55,031,648 (GRCm39) |
I764T |
probably benign |
Het |
Zfp708 |
C |
A |
13: 67,218,564 (GRCm39) |
D420Y |
probably damaging |
Het |
|
Other mutations in Noc3l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01399:Noc3l
|
APN |
19 |
38,804,099 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03237:Noc3l
|
APN |
19 |
38,803,125 (GRCm39) |
splice site |
probably null |
|
R0062:Noc3l
|
UTSW |
19 |
38,803,253 (GRCm39) |
missense |
probably benign |
0.01 |
R0306:Noc3l
|
UTSW |
19 |
38,796,094 (GRCm39) |
missense |
probably damaging |
0.96 |
R0409:Noc3l
|
UTSW |
19 |
38,806,371 (GRCm39) |
splice site |
probably benign |
|
R0427:Noc3l
|
UTSW |
19 |
38,778,095 (GRCm39) |
missense |
probably benign |
|
R0478:Noc3l
|
UTSW |
19 |
38,798,450 (GRCm39) |
critical splice donor site |
probably null |
|
R4714:Noc3l
|
UTSW |
19 |
38,804,157 (GRCm39) |
missense |
probably benign |
0.00 |
R4720:Noc3l
|
UTSW |
19 |
38,778,066 (GRCm39) |
missense |
probably benign |
0.00 |
R4857:Noc3l
|
UTSW |
19 |
38,781,244 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4864:Noc3l
|
UTSW |
19 |
38,778,081 (GRCm39) |
missense |
probably benign |
|
R5511:Noc3l
|
UTSW |
19 |
38,782,625 (GRCm39) |
missense |
probably benign |
0.32 |
R5586:Noc3l
|
UTSW |
19 |
38,803,139 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6144:Noc3l
|
UTSW |
19 |
38,787,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Noc3l
|
UTSW |
19 |
38,784,349 (GRCm39) |
splice site |
probably null |
|
R7095:Noc3l
|
UTSW |
19 |
38,800,789 (GRCm39) |
missense |
probably benign |
0.01 |
R7256:Noc3l
|
UTSW |
19 |
38,800,800 (GRCm39) |
missense |
probably benign |
0.03 |
R7343:Noc3l
|
UTSW |
19 |
38,783,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R7937:Noc3l
|
UTSW |
19 |
38,783,447 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8049:Noc3l
|
UTSW |
19 |
38,800,873 (GRCm39) |
missense |
probably benign |
|
R8313:Noc3l
|
UTSW |
19 |
38,784,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R8398:Noc3l
|
UTSW |
19 |
38,783,554 (GRCm39) |
missense |
probably benign |
0.22 |
R8422:Noc3l
|
UTSW |
19 |
38,795,547 (GRCm39) |
missense |
probably benign |
0.08 |
R8888:Noc3l
|
UTSW |
19 |
38,798,751 (GRCm39) |
missense |
probably damaging |
0.97 |
R8895:Noc3l
|
UTSW |
19 |
38,798,751 (GRCm39) |
missense |
probably damaging |
0.97 |
R9149:Noc3l
|
UTSW |
19 |
38,800,835 (GRCm39) |
nonsense |
probably null |
|
|