Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
T |
A |
8: 41,207,671 (GRCm39) |
F312L |
probably benign |
Het |
Adprm |
A |
G |
11: 66,932,856 (GRCm39) |
F18L |
possibly damaging |
Het |
Ampd1 |
T |
G |
3: 103,006,981 (GRCm39) |
N735K |
possibly damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,081,649 (GRCm39) |
M168V |
probably damaging |
Het |
Bcl6 |
G |
A |
16: 23,793,600 (GRCm39) |
H116Y |
probably damaging |
Het |
Bmpr2 |
T |
A |
1: 59,890,383 (GRCm39) |
N338K |
probably damaging |
Het |
Bms1 |
A |
T |
6: 118,381,224 (GRCm39) |
Y697* |
probably null |
Het |
Ccdc33 |
A |
C |
9: 58,025,918 (GRCm39) |
F37C |
probably damaging |
Het |
Ccdc60 |
T |
A |
5: 116,426,507 (GRCm39) |
Q30L |
probably benign |
Het |
Cndp1 |
C |
A |
18: 84,650,036 (GRCm39) |
R219L |
probably damaging |
Het |
Cstdc4 |
T |
C |
16: 36,006,837 (GRCm39) |
|
probably null |
Het |
Daam2 |
C |
A |
17: 49,783,550 (GRCm39) |
D627Y |
probably damaging |
Het |
Dffb |
T |
C |
4: 154,057,416 (GRCm39) |
D87G |
possibly damaging |
Het |
Dnah2 |
T |
G |
11: 69,388,708 (GRCm39) |
T892P |
possibly damaging |
Het |
Dqx1 |
A |
G |
6: 83,043,092 (GRCm39) |
T610A |
probably benign |
Het |
Dspp |
A |
T |
5: 104,324,926 (GRCm39) |
I430L |
possibly damaging |
Het |
Dytn |
T |
A |
1: 63,672,854 (GRCm39) |
K516N |
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fmnl2 |
T |
A |
2: 52,993,773 (GRCm39) |
N389K |
possibly damaging |
Het |
Fn1 |
G |
A |
1: 71,665,336 (GRCm39) |
T927I |
probably damaging |
Het |
Foxn1 |
T |
C |
11: 78,261,989 (GRCm39) |
K127E |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,402,608 (GRCm39) |
F251S |
probably damaging |
Het |
Frrs1 |
A |
G |
3: 116,672,088 (GRCm39) |
D62G |
probably damaging |
Het |
Fut10 |
T |
A |
8: 31,726,148 (GRCm39) |
V301D |
probably damaging |
Het |
Gk5 |
A |
G |
9: 96,059,470 (GRCm39) |
|
probably null |
Het |
Glipr1l1 |
T |
A |
10: 111,914,279 (GRCm39) |
N213K |
probably benign |
Het |
Gm1110 |
A |
G |
9: 26,793,162 (GRCm39) |
F538S |
probably benign |
Het |
Gm7347 |
T |
A |
5: 26,262,366 (GRCm39) |
T52S |
probably benign |
Het |
Gsap |
T |
C |
5: 21,427,406 (GRCm39) |
I178T |
probably damaging |
Het |
H1f9 |
C |
A |
11: 94,858,928 (GRCm39) |
N74K |
probably damaging |
Het |
Hcn1 |
A |
T |
13: 117,739,556 (GRCm39) |
Q106L |
unknown |
Het |
Isg20l2 |
G |
T |
3: 87,839,288 (GRCm39) |
L166F |
possibly damaging |
Het |
Kcnq3 |
T |
A |
15: 65,876,612 (GRCm39) |
E510D |
probably damaging |
Het |
Kif26b |
G |
T |
1: 178,755,895 (GRCm39) |
R2003L |
probably damaging |
Het |
Kiss1r |
T |
C |
10: 79,754,641 (GRCm39) |
V45A |
probably damaging |
Het |
Krt14 |
G |
A |
11: 100,098,032 (GRCm39) |
R84* |
probably null |
Het |
Mbd5 |
T |
C |
2: 49,148,208 (GRCm39) |
M806T |
possibly damaging |
Het |
Mdga1 |
A |
T |
17: 30,058,847 (GRCm39) |
I13N |
possibly damaging |
Het |
Mfsd4b5 |
T |
C |
10: 39,850,758 (GRCm39) |
K73E |
probably benign |
Het |
Mterf2 |
C |
T |
10: 84,955,596 (GRCm39) |
G343R |
probably benign |
Het |
Mto1 |
T |
A |
9: 78,368,903 (GRCm39) |
F522I |
probably benign |
Het |
Myo18b |
T |
C |
5: 112,937,923 (GRCm39) |
E1734G |
probably damaging |
Het |
Myoz1 |
T |
C |
14: 20,703,787 (GRCm39) |
T53A |
probably benign |
Het |
Naxd |
T |
C |
8: 11,563,032 (GRCm39) |
L324P |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,005,334 (GRCm39) |
V18D |
probably damaging |
Het |
Nova1 |
T |
C |
12: 46,863,738 (GRCm39) |
T71A |
unknown |
Het |
Or10v5 |
T |
C |
19: 11,805,482 (GRCm39) |
R303G |
probably benign |
Het |
Or10z1 |
A |
G |
1: 174,078,448 (GRCm39) |
L15S |
possibly damaging |
Het |
Or1e29 |
C |
G |
11: 73,668,007 (GRCm39) |
V49L |
probably benign |
Het |
Or2j6 |
T |
C |
7: 139,980,083 (GRCm39) |
D292G |
probably damaging |
Het |
Or52b1 |
A |
G |
7: 104,978,811 (GRCm39) |
V196A |
possibly damaging |
Het |
Otof |
T |
A |
5: 30,540,238 (GRCm39) |
Y981F |
probably damaging |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pex1 |
A |
G |
5: 3,670,597 (GRCm39) |
K7E |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,120,946 (GRCm39) |
S73P |
possibly damaging |
Het |
Plxnb1 |
T |
A |
9: 108,929,498 (GRCm39) |
I118N |
possibly damaging |
Het |
Prcc |
T |
C |
3: 87,779,560 (GRCm39) |
D158G |
probably damaging |
Het |
Ptpn7 |
C |
A |
1: 135,066,877 (GRCm39) |
R245S |
possibly damaging |
Het |
Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
Pwp2 |
A |
G |
10: 78,018,527 (GRCm39) |
C86R |
probably benign |
Het |
Rfng |
T |
G |
11: 120,673,876 (GRCm39) |
D178A |
probably damaging |
Het |
Rhpn1 |
T |
C |
15: 75,580,090 (GRCm39) |
I51T |
probably damaging |
Het |
Rnasel |
G |
T |
1: 153,629,843 (GRCm39) |
E120* |
probably null |
Het |
Sall2 |
T |
G |
14: 52,553,112 (GRCm39) |
S26R |
possibly damaging |
Het |
Scn10a |
A |
G |
9: 119,451,987 (GRCm39) |
V1312A |
possibly damaging |
Het |
Sdk2 |
C |
A |
11: 113,684,587 (GRCm39) |
R1958L |
probably damaging |
Het |
Slc52a2 |
T |
A |
15: 76,424,751 (GRCm39) |
C330S |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,668,788 (GRCm39) |
I987N |
possibly damaging |
Het |
Srrt |
A |
T |
5: 137,294,271 (GRCm39) |
Y486N |
probably damaging |
Het |
Stat5b |
A |
T |
11: 100,695,831 (GRCm39) |
N50K |
possibly damaging |
Het |
Strip2 |
T |
A |
6: 29,931,265 (GRCm39) |
D405E |
probably benign |
Het |
Tcstv6 |
T |
A |
13: 120,298,474 (GRCm39) |
|
probably null |
Het |
Tnc |
A |
T |
4: 63,924,739 (GRCm39) |
D986E |
probably damaging |
Het |
Tph2 |
T |
C |
10: 114,915,621 (GRCm39) |
N473S |
probably benign |
Het |
Tpp1 |
C |
T |
7: 105,401,232 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,689,076 (GRCm39) |
Y2H |
probably damaging |
Het |
Ttc21a |
A |
T |
9: 119,795,195 (GRCm39) |
E1072V |
probably damaging |
Het |
Zfat |
T |
C |
15: 68,050,762 (GRCm39) |
D753G |
probably damaging |
Het |
Zmym2 |
T |
A |
14: 57,159,051 (GRCm39) |
S609T |
probably damaging |
Het |
|
Other mutations in Septin4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00941:Septin4
|
APN |
11 |
87,480,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00963:Septin4
|
APN |
11 |
87,474,199 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01803:Septin4
|
APN |
11 |
87,459,075 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01993:Septin4
|
APN |
11 |
87,458,555 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02566:Septin4
|
APN |
11 |
87,458,468 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03087:Septin4
|
APN |
11 |
87,476,071 (GRCm39) |
splice site |
probably benign |
|
IGL03213:Septin4
|
APN |
11 |
87,458,184 (GRCm39) |
splice site |
probably null |
|
IGL03268:Septin4
|
APN |
11 |
87,480,529 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03388:Septin4
|
APN |
11 |
87,459,042 (GRCm39) |
nonsense |
probably null |
|
R0050:Septin4
|
UTSW |
11 |
87,458,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R0077:Septin4
|
UTSW |
11 |
87,472,022 (GRCm39) |
missense |
probably benign |
|
R1479:Septin4
|
UTSW |
11 |
87,458,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R1730:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R1739:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R1762:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R1783:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R1784:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R1785:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R1851:Septin4
|
UTSW |
11 |
87,459,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R1862:Septin4
|
UTSW |
11 |
87,458,061 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1913:Septin4
|
UTSW |
11 |
87,457,838 (GRCm39) |
missense |
probably benign |
|
R1957:Septin4
|
UTSW |
11 |
87,481,193 (GRCm39) |
missense |
probably benign |
0.02 |
R2131:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R2133:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R2140:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R2141:Septin4
|
UTSW |
11 |
87,474,262 (GRCm39) |
missense |
probably benign |
0.26 |
R2252:Septin4
|
UTSW |
11 |
87,480,637 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3149:Septin4
|
UTSW |
11 |
87,458,070 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3176:Septin4
|
UTSW |
11 |
87,458,070 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3276:Septin4
|
UTSW |
11 |
87,458,070 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3696:Septin4
|
UTSW |
11 |
87,476,060 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4018:Septin4
|
UTSW |
11 |
87,475,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4021:Septin4
|
UTSW |
11 |
87,458,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R4117:Septin4
|
UTSW |
11 |
87,459,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R4193:Septin4
|
UTSW |
11 |
87,474,142 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4196:Septin4
|
UTSW |
11 |
87,479,598 (GRCm39) |
missense |
probably damaging |
0.96 |
R4332:Septin4
|
UTSW |
11 |
87,458,730 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4515:Septin4
|
UTSW |
11 |
87,458,883 (GRCm39) |
missense |
probably benign |
|
R4663:Septin4
|
UTSW |
11 |
87,458,429 (GRCm39) |
missense |
probably damaging |
0.98 |
R4952:Septin4
|
UTSW |
11 |
87,458,598 (GRCm39) |
missense |
probably benign |
0.00 |
R5012:Septin4
|
UTSW |
11 |
87,475,230 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5149:Septin4
|
UTSW |
11 |
87,480,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R5176:Septin4
|
UTSW |
11 |
87,458,358 (GRCm39) |
missense |
probably benign |
0.02 |
R5711:Septin4
|
UTSW |
11 |
87,458,723 (GRCm39) |
missense |
probably benign |
0.07 |
R5891:Septin4
|
UTSW |
11 |
87,479,750 (GRCm39) |
unclassified |
probably benign |
|
R6090:Septin4
|
UTSW |
11 |
87,480,343 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6145:Septin4
|
UTSW |
11 |
87,476,072 (GRCm39) |
splice site |
probably null |
|
R6257:Septin4
|
UTSW |
11 |
87,481,175 (GRCm39) |
missense |
probably benign |
0.07 |
R6305:Septin4
|
UTSW |
11 |
87,458,145 (GRCm39) |
missense |
probably benign |
0.00 |
R6704:Septin4
|
UTSW |
11 |
87,479,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Septin4
|
UTSW |
11 |
87,481,193 (GRCm39) |
missense |
probably benign |
0.02 |
R7090:Septin4
|
UTSW |
11 |
87,475,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R7784:Septin4
|
UTSW |
11 |
87,469,834 (GRCm39) |
missense |
probably benign |
|
R7790:Septin4
|
UTSW |
11 |
87,480,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R8320:Septin4
|
UTSW |
11 |
87,480,560 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9289:Septin4
|
UTSW |
11 |
87,459,792 (GRCm39) |
nonsense |
probably null |
|
R9613:Septin4
|
UTSW |
11 |
87,469,823 (GRCm39) |
missense |
possibly damaging |
0.53 |
T0970:Septin4
|
UTSW |
11 |
87,458,558 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Septin4
|
UTSW |
11 |
87,458,748 (GRCm39) |
missense |
probably benign |
|
|