Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Anxa2 |
T |
C |
9: 69,398,764 (GRCm39) |
Y333H |
probably benign |
Het |
Arid1a |
A |
T |
4: 133,408,679 (GRCm39) |
F1558I |
unknown |
Het |
Aste1 |
A |
G |
9: 105,274,678 (GRCm39) |
D306G |
probably damaging |
Het |
Atp2a2 |
A |
G |
5: 122,596,590 (GRCm39) |
V843A |
possibly damaging |
Het |
Atrip |
T |
A |
9: 108,894,574 (GRCm39) |
H451L |
probably benign |
Het |
Cdc42bpb |
T |
C |
12: 111,295,664 (GRCm39) |
D200G |
probably damaging |
Het |
Ceacam19 |
A |
C |
7: 19,620,520 (GRCm39) |
M37R |
probably benign |
Het |
Cemip |
G |
A |
7: 83,606,872 (GRCm39) |
R782* |
probably null |
Het |
Cpe |
A |
T |
8: 65,070,654 (GRCm39) |
I197N |
probably benign |
Het |
Csmd2 |
C |
A |
4: 128,445,850 (GRCm39) |
P3307T |
|
Het |
Cyp4a12b |
C |
A |
4: 115,268,937 (GRCm39) |
Q20K |
possibly damaging |
Het |
Dcaf1 |
T |
C |
9: 106,715,878 (GRCm39) |
Y332H |
probably damaging |
Het |
Dclk3 |
A |
G |
9: 111,298,163 (GRCm39) |
H569R |
probably damaging |
Het |
Dcp1b |
A |
G |
6: 119,192,244 (GRCm39) |
S387G |
probably benign |
Het |
Ddx24 |
A |
G |
12: 103,383,819 (GRCm39) |
M590T |
possibly damaging |
Het |
Dixdc1 |
T |
G |
9: 50,613,268 (GRCm39) |
Q229P |
probably damaging |
Het |
Dnase1l3 |
T |
C |
14: 7,977,144 (GRCm38) |
R181G |
probably benign |
Het |
Dzip1l |
A |
T |
9: 99,549,735 (GRCm39) |
D735V |
probably damaging |
Het |
Edem3 |
T |
C |
1: 151,694,336 (GRCm39) |
S890P |
probably benign |
Het |
Fuom |
A |
G |
7: 139,679,455 (GRCm39) |
L155P |
unknown |
Het |
Gm6408 |
C |
A |
5: 146,421,160 (GRCm39) |
S263* |
probably null |
Het |
Helz |
C |
G |
11: 107,576,248 (GRCm39) |
S1814R |
unknown |
Het |
Hrc |
T |
C |
7: 44,986,100 (GRCm39) |
L417P |
probably benign |
Het |
Igdcc4 |
A |
C |
9: 65,039,035 (GRCm39) |
H894P |
probably damaging |
Het |
Lgr6 |
C |
A |
1: 134,930,981 (GRCm39) |
V296L |
probably damaging |
Het |
Map3k4 |
T |
A |
17: 12,482,998 (GRCm39) |
Y573F |
probably damaging |
Het |
Mest |
T |
C |
6: 30,746,299 (GRCm39) |
Y296H |
unknown |
Het |
Mettl21a |
C |
T |
1: 64,647,288 (GRCm39) |
V90M |
probably damaging |
Het |
Mfsd4b1 |
A |
T |
10: 39,883,374 (GRCm39) |
N25K |
probably damaging |
Het |
Mmd |
T |
A |
11: 90,167,579 (GRCm39) |
F203I |
probably damaging |
Het |
Myo15a |
G |
A |
11: 60,401,108 (GRCm39) |
V3028M |
probably benign |
Het |
Nlrp1a |
T |
A |
11: 70,998,826 (GRCm39) |
N859I |
unknown |
Het |
Nrcam |
T |
C |
12: 44,584,034 (GRCm39) |
L36P |
possibly damaging |
Het |
Nup107 |
C |
A |
10: 117,593,917 (GRCm39) |
E759* |
probably null |
Het |
Or14a259 |
A |
G |
7: 86,013,476 (GRCm39) |
I23T |
not run |
Het |
Pcdh7 |
T |
G |
5: 57,876,976 (GRCm39) |
I177S |
probably damaging |
Het |
Pde6a |
T |
C |
18: 61,365,938 (GRCm39) |
I221T |
probably benign |
Het |
Ptpn13 |
A |
T |
5: 103,709,828 (GRCm39) |
N1497I |
probably damaging |
Het |
Rmc1 |
T |
A |
18: 12,322,320 (GRCm39) |
I591N |
possibly damaging |
Het |
Rpl4 |
T |
A |
9: 64,084,661 (GRCm39) |
H245Q |
probably benign |
Het |
Rsf1 |
C |
CCACGGCGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Scara5 |
A |
G |
14: 65,968,600 (GRCm39) |
D291G |
possibly damaging |
Het |
Serpina1e |
T |
C |
12: 103,917,151 (GRCm39) |
K173E |
probably benign |
Het |
Slc5a1 |
C |
T |
5: 33,318,279 (GRCm39) |
T644I |
probably benign |
Het |
Slc6a13 |
A |
T |
6: 121,314,334 (GRCm39) |
T590S |
probably benign |
Het |
Smarca4 |
C |
T |
9: 21,578,658 (GRCm39) |
T938I |
possibly damaging |
Het |
Stxbp1 |
A |
T |
2: 32,691,832 (GRCm39) |
D453E |
probably benign |
Het |
Tcf12 |
C |
A |
9: 71,829,943 (GRCm39) |
V173L |
probably benign |
Het |
Tenm3 |
A |
G |
8: 49,099,368 (GRCm39) |
C146R |
probably damaging |
Het |
Trim11 |
T |
C |
11: 58,869,180 (GRCm39) |
C39R |
probably damaging |
Het |
Trim37 |
A |
G |
11: 87,068,821 (GRCm39) |
Y389C |
probably damaging |
Het |
Ttll8 |
C |
T |
15: 88,798,368 (GRCm39) |
G789D |
probably damaging |
Het |
Tubb2a |
C |
T |
13: 34,258,776 (GRCm39) |
S338N |
probably benign |
Het |
Ulk2 |
G |
A |
11: 61,744,127 (GRCm39) |
Q50* |
probably null |
Het |
Urgcp |
T |
C |
11: 5,666,406 (GRCm39) |
D687G |
probably benign |
Het |
Usp13 |
C |
T |
3: 32,892,054 (GRCm39) |
H78Y |
probably benign |
Het |
Vmn2r100 |
T |
A |
17: 19,742,296 (GRCm39) |
D223E |
probably benign |
Het |
Vwc2 |
G |
A |
11: 11,065,929 (GRCm39) |
A6T |
possibly damaging |
Het |
|
Other mutations in Septin14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00228:Septin14
|
APN |
5 |
129,760,715 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01622:Septin14
|
APN |
5 |
129,763,019 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01623:Septin14
|
APN |
5 |
129,763,019 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03088:Septin14
|
APN |
5 |
129,774,797 (GRCm39) |
splice site |
probably benign |
|
R0658:Septin14
|
UTSW |
5 |
129,774,972 (GRCm39) |
missense |
probably benign |
0.30 |
R1485:Septin14
|
UTSW |
5 |
129,770,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Septin14
|
UTSW |
5 |
129,774,819 (GRCm39) |
missense |
probably benign |
0.19 |
R2518:Septin14
|
UTSW |
5 |
129,776,099 (GRCm39) |
missense |
probably benign |
|
R2973:Septin14
|
UTSW |
5 |
129,776,086 (GRCm39) |
missense |
probably benign |
0.42 |
R4679:Septin14
|
UTSW |
5 |
129,770,090 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4906:Septin14
|
UTSW |
5 |
129,770,030 (GRCm39) |
missense |
probably benign |
0.39 |
R5004:Septin14
|
UTSW |
5 |
129,770,040 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5303:Septin14
|
UTSW |
5 |
129,766,712 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5329:Septin14
|
UTSW |
5 |
129,762,978 (GRCm39) |
critical splice donor site |
probably null |
|
R5393:Septin14
|
UTSW |
5 |
129,760,650 (GRCm39) |
missense |
probably benign |
0.01 |
R5542:Septin14
|
UTSW |
5 |
129,774,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R5725:Septin14
|
UTSW |
5 |
129,766,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Septin14
|
UTSW |
5 |
129,773,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Septin14
|
UTSW |
5 |
129,774,822 (GRCm39) |
missense |
probably benign |
0.05 |
R6815:Septin14
|
UTSW |
5 |
129,770,051 (GRCm39) |
missense |
probably benign |
|
R7064:Septin14
|
UTSW |
5 |
129,774,870 (GRCm39) |
missense |
probably benign |
0.00 |
R7703:Septin14
|
UTSW |
5 |
129,763,092 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8316:Septin14
|
UTSW |
5 |
129,773,194 (GRCm39) |
missense |
probably damaging |
0.99 |
R8898:Septin14
|
UTSW |
5 |
129,760,642 (GRCm39) |
missense |
possibly damaging |
0.64 |
X0066:Septin14
|
UTSW |
5 |
129,766,602 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Septin14
|
UTSW |
5 |
129,766,628 (GRCm39) |
missense |
probably benign |
0.35 |
|