Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aipl1 |
T |
C |
11: 71,920,126 (GRCm39) |
D314G |
probably benign |
Het |
Ankrd12 |
T |
G |
17: 66,290,939 (GRCm39) |
E1498A |
probably benign |
Het |
Appl1 |
A |
T |
14: 26,647,372 (GRCm39) |
|
probably null |
Het |
Auh |
A |
G |
13: 53,063,349 (GRCm39) |
*116R |
probably null |
Het |
Ccdc7a |
T |
A |
8: 129,691,417 (GRCm39) |
H402L |
probably benign |
Het |
Ccr4 |
T |
C |
9: 114,321,235 (GRCm39) |
T277A |
probably benign |
Het |
Col18a1 |
C |
T |
10: 76,889,072 (GRCm39) |
V1302I |
probably benign |
Het |
Csnk1a1 |
T |
C |
18: 61,688,925 (GRCm39) |
I35T |
probably benign |
Het |
Csnk1e |
T |
C |
15: 79,304,882 (GRCm39) |
R374G |
possibly damaging |
Het |
Ddx11 |
A |
G |
17: 66,437,020 (GRCm39) |
R105G |
probably benign |
Het |
Denr |
C |
A |
5: 124,065,124 (GRCm39) |
T159K |
possibly damaging |
Het |
Dmp1 |
C |
A |
5: 104,359,571 (GRCm39) |
Y82* |
probably null |
Het |
Dok3 |
A |
G |
13: 55,671,833 (GRCm39) |
V246A |
probably benign |
Het |
Endov |
A |
C |
11: 119,382,723 (GRCm39) |
K57Q |
possibly damaging |
Het |
Fam83a |
A |
G |
15: 57,873,196 (GRCm39) |
T342A |
probably benign |
Het |
Fbln1 |
G |
A |
15: 85,116,773 (GRCm39) |
C275Y |
probably damaging |
Het |
Fhip1b |
T |
C |
7: 105,034,342 (GRCm39) |
N430D |
possibly damaging |
Het |
Foxi1 |
A |
G |
11: 34,157,530 (GRCm39) |
I165T |
possibly damaging |
Het |
Gm14496 |
A |
T |
2: 181,642,275 (GRCm39) |
I649F |
probably damaging |
Het |
Grin2b |
A |
G |
6: 135,899,967 (GRCm39) |
S305P |
probably damaging |
Het |
Grm1 |
G |
A |
10: 10,564,879 (GRCm39) |
T1143M |
possibly damaging |
Het |
Ifi202b |
C |
A |
1: 173,802,298 (GRCm39) |
|
probably null |
Het |
Klhl32 |
A |
T |
4: 24,629,194 (GRCm39) |
D491E |
probably damaging |
Het |
Klk1b1 |
C |
T |
7: 43,619,767 (GRCm39) |
R109C |
possibly damaging |
Het |
Krt13 |
A |
G |
11: 100,009,706 (GRCm39) |
L358P |
probably damaging |
Het |
Limk2 |
G |
A |
11: 3,321,162 (GRCm39) |
|
probably benign |
Het |
Mdn1 |
A |
G |
4: 32,756,453 (GRCm39) |
D4720G |
probably null |
Het |
Mkln1 |
T |
A |
6: 31,435,900 (GRCm39) |
Y286* |
probably null |
Het |
Muc6 |
C |
A |
7: 141,230,579 (GRCm39) |
E1143* |
probably null |
Het |
Myh15 |
A |
G |
16: 48,901,551 (GRCm39) |
I242M |
probably benign |
Het |
Nup88 |
C |
A |
11: 70,860,607 (GRCm39) |
L57F |
possibly damaging |
Het |
Obsl1 |
G |
T |
1: 75,480,501 (GRCm39) |
F374L |
possibly damaging |
Het |
Or51aa2 |
A |
G |
7: 103,188,183 (GRCm39) |
I86T |
possibly damaging |
Het |
Orm1 |
A |
T |
4: 63,264,355 (GRCm39) |
D137V |
probably damaging |
Het |
Osbpl2 |
T |
A |
2: 179,778,895 (GRCm39) |
D9E |
probably damaging |
Het |
P4ha3 |
G |
T |
7: 99,942,986 (GRCm39) |
D124Y |
probably damaging |
Het |
Poteg |
T |
C |
8: 27,943,354 (GRCm39) |
V208A |
probably benign |
Het |
Ppfibp1 |
A |
G |
6: 146,931,843 (GRCm39) |
D963G |
probably damaging |
Het |
Prdx6 |
G |
T |
1: 161,078,660 (GRCm39) |
D9E |
probably benign |
Het |
Prrc2b |
C |
A |
2: 32,104,666 (GRCm39) |
N1381K |
probably damaging |
Het |
Ptpn14 |
T |
A |
1: 189,565,598 (GRCm39) |
V222E |
possibly damaging |
Het |
Rasal1 |
C |
T |
5: 120,804,420 (GRCm39) |
R431C |
probably benign |
Het |
Rexo5 |
A |
T |
7: 119,433,508 (GRCm39) |
M422L |
probably benign |
Het |
Rnf17 |
TG |
T |
14: 56,661,999 (GRCm39) |
132 |
probably null |
Het |
Robo2 |
A |
T |
16: 73,730,588 (GRCm39) |
I1008N |
probably damaging |
Het |
Sidt1 |
T |
A |
16: 44,106,755 (GRCm39) |
Y225F |
probably benign |
Het |
Slc6a15 |
A |
T |
10: 103,225,048 (GRCm39) |
E45D |
probably benign |
Het |
Spata31d1a |
T |
G |
13: 59,850,668 (GRCm39) |
M487L |
probably benign |
Het |
St6galnac1 |
C |
A |
11: 116,666,325 (GRCm39) |
|
probably benign |
Het |
Tcp11l2 |
A |
G |
10: 84,449,469 (GRCm39) |
Y478C |
probably damaging |
Het |
Tdrd12 |
G |
T |
7: 35,223,482 (GRCm39) |
C67* |
probably null |
Het |
Tead2 |
G |
A |
7: 44,867,505 (GRCm39) |
G78D |
probably damaging |
Het |
Tfpi2 |
A |
T |
6: 3,963,849 (GRCm39) |
N194K |
probably damaging |
Het |
Timd2 |
A |
G |
11: 46,568,027 (GRCm39) |
|
probably null |
Het |
Tmem270 |
T |
C |
5: 134,930,557 (GRCm39) |
T235A |
probably benign |
Het |
Tnrc18 |
T |
C |
5: 142,774,157 (GRCm39) |
D224G |
|
Het |
Tsga10 |
G |
T |
1: 37,840,959 (GRCm39) |
Q416K |
probably benign |
Het |
Ulk1 |
C |
A |
5: 110,935,531 (GRCm39) |
L911F |
probably damaging |
Het |
Usp8 |
T |
C |
2: 126,584,491 (GRCm39) |
S567P |
probably benign |
Het |
Vmn2r-ps158 |
C |
T |
7: 42,697,270 (GRCm39) |
P776S |
probably damaging |
Het |
Zdhhc3 |
A |
C |
9: 122,918,143 (GRCm39) |
C129G |
probably damaging |
Het |
|
Other mutations in Noc4l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01483:Noc4l
|
APN |
5 |
110,796,824 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02249:Noc4l
|
APN |
5 |
110,801,081 (GRCm39) |
unclassified |
probably benign |
|
wood
|
UTSW |
5 |
110,796,758 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4280001:Noc4l
|
UTSW |
5 |
110,799,305 (GRCm39) |
missense |
probably benign |
0.38 |
R0326:Noc4l
|
UTSW |
5 |
110,800,241 (GRCm39) |
nonsense |
probably null |
|
R0544:Noc4l
|
UTSW |
5 |
110,798,989 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1196:Noc4l
|
UTSW |
5 |
110,798,450 (GRCm39) |
missense |
probably damaging |
0.97 |
R1496:Noc4l
|
UTSW |
5 |
110,797,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1587:Noc4l
|
UTSW |
5 |
110,800,889 (GRCm39) |
missense |
probably benign |
|
R1699:Noc4l
|
UTSW |
5 |
110,797,713 (GRCm39) |
nonsense |
probably null |
|
R2113:Noc4l
|
UTSW |
5 |
110,798,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2874:Noc4l
|
UTSW |
5 |
110,796,969 (GRCm39) |
missense |
probably benign |
0.00 |
R4080:Noc4l
|
UTSW |
5 |
110,797,738 (GRCm39) |
missense |
probably benign |
0.01 |
R5097:Noc4l
|
UTSW |
5 |
110,799,212 (GRCm39) |
missense |
probably benign |
|
R5875:Noc4l
|
UTSW |
5 |
110,799,176 (GRCm39) |
critical splice donor site |
probably null |
|
R6903:Noc4l
|
UTSW |
5 |
110,797,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R7328:Noc4l
|
UTSW |
5 |
110,796,789 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7816:Noc4l
|
UTSW |
5 |
110,797,539 (GRCm39) |
missense |
probably benign |
0.44 |
R8770:Noc4l
|
UTSW |
5 |
110,796,758 (GRCm39) |
missense |
possibly damaging |
0.94 |
|