Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 137,773,986 (GRCm39) |
D1058E |
probably damaging |
Het |
4933405L10Rik |
A |
T |
8: 106,435,563 (GRCm39) |
|
probably null |
Het |
Adamtsl3 |
T |
A |
7: 82,114,907 (GRCm39) |
|
probably benign |
Het |
Afdn |
C |
T |
17: 14,072,698 (GRCm39) |
P874S |
probably damaging |
Het |
Ankrd6 |
G |
A |
4: 32,815,326 (GRCm39) |
A391V |
probably damaging |
Het |
Arhgef28 |
T |
G |
13: 98,067,762 (GRCm39) |
T1388P |
probably damaging |
Het |
Asxl3 |
G |
T |
18: 22,657,508 (GRCm39) |
M1839I |
probably benign |
Het |
BC005537 |
T |
C |
13: 24,989,923 (GRCm39) |
F129L |
probably damaging |
Het |
Celf2 |
A |
G |
2: 6,726,226 (GRCm39) |
|
probably null |
Het |
Chid1 |
C |
T |
7: 141,076,590 (GRCm39) |
V325I |
probably benign |
Het |
Cnn3 |
T |
A |
3: 121,243,633 (GRCm39) |
D31E |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,559,317 (GRCm39) |
P1857L |
probably damaging |
Het |
Cpeb1 |
T |
A |
7: 81,001,618 (GRCm39) |
R430W |
probably benign |
Het |
Daw1 |
T |
C |
1: 83,169,059 (GRCm39) |
|
probably benign |
Het |
Dcaf13 |
A |
G |
15: 39,001,484 (GRCm39) |
Y264C |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,064,585 (GRCm39) |
I2666V |
probably damaging |
Het |
Dnai2 |
A |
C |
11: 114,645,158 (GRCm39) |
D531A |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,501,692 (GRCm39) |
F1833I |
probably damaging |
Het |
Efhd2 |
C |
T |
4: 141,587,183 (GRCm39) |
A200T |
probably damaging |
Het |
Epb41l5 |
T |
A |
1: 119,551,641 (GRCm39) |
|
probably benign |
Het |
Ermp1 |
A |
G |
19: 29,608,788 (GRCm39) |
Y164H |
possibly damaging |
Het |
Gkn2 |
T |
C |
6: 87,350,401 (GRCm39) |
|
probably benign |
Het |
Golgb1 |
A |
T |
16: 36,739,152 (GRCm39) |
Q2497L |
probably damaging |
Het |
Gzme |
A |
T |
14: 56,355,196 (GRCm39) |
M245K |
probably damaging |
Het |
Iars2 |
A |
T |
1: 185,054,585 (GRCm39) |
|
probably benign |
Het |
Icosl |
T |
A |
10: 77,909,775 (GRCm39) |
V240D |
probably damaging |
Het |
Igsf3 |
T |
C |
3: 101,334,709 (GRCm39) |
M262T |
probably benign |
Het |
Ing3 |
G |
T |
6: 21,971,236 (GRCm39) |
E336* |
probably null |
Het |
Kat2a |
A |
T |
11: 100,597,297 (GRCm39) |
V625E |
probably damaging |
Het |
Ksr1 |
A |
G |
11: 78,929,073 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,277,583 (GRCm39) |
M122L |
probably benign |
Het |
Mdfi |
A |
T |
17: 48,143,855 (GRCm39) |
|
probably benign |
Het |
Med13 |
A |
G |
11: 86,192,179 (GRCm39) |
|
probably benign |
Het |
Msh6 |
C |
T |
17: 88,294,112 (GRCm39) |
R956C |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,774,664 (GRCm39) |
E670G |
probably damaging |
Het |
Myo1d |
A |
G |
11: 80,375,158 (GRCm39) |
L972P |
probably damaging |
Het |
Or4s2b |
A |
G |
2: 88,509,018 (GRCm39) |
D266G |
probably damaging |
Het |
Or51ai2 |
G |
A |
7: 103,587,024 (GRCm39) |
A146T |
probably benign |
Het |
Or7g12 |
T |
A |
9: 18,899,447 (GRCm39) |
N54K |
probably benign |
Het |
Pde8b |
C |
G |
13: 95,244,325 (GRCm39) |
S143T |
possibly damaging |
Het |
Pias4 |
G |
T |
10: 80,993,364 (GRCm39) |
|
probably benign |
Het |
Prkca |
A |
G |
11: 107,872,480 (GRCm39) |
Y427H |
probably benign |
Het |
Psg25 |
G |
A |
7: 18,263,485 (GRCm39) |
Q113* |
probably null |
Het |
Rab3gap2 |
T |
A |
1: 184,982,123 (GRCm39) |
S392T |
probably damaging |
Het |
Scrib |
A |
G |
15: 75,938,756 (GRCm39) |
|
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,793,970 (GRCm39) |
|
probably benign |
Het |
Serpinb1c |
T |
A |
13: 33,070,266 (GRCm39) |
|
probably benign |
Het |
Serpinb9f |
T |
A |
13: 33,511,904 (GRCm39) |
W136R |
probably damaging |
Het |
Skic3 |
C |
T |
13: 76,331,010 (GRCm39) |
P1480L |
probably damaging |
Het |
Skint10 |
C |
A |
4: 112,573,102 (GRCm39) |
|
probably benign |
Het |
Slc25a13 |
T |
C |
6: 6,117,128 (GRCm39) |
T196A |
probably damaging |
Het |
Slc26a5 |
T |
C |
5: 22,052,230 (GRCm39) |
H33R |
probably damaging |
Het |
Slc27a6 |
T |
C |
18: 58,731,829 (GRCm39) |
|
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,251 (GRCm39) |
Y819N |
probably damaging |
Het |
Spata46 |
C |
T |
1: 170,139,603 (GRCm39) |
Q201* |
probably null |
Het |
Taf6l |
A |
G |
19: 8,755,881 (GRCm39) |
F256L |
probably benign |
Het |
Tmco3 |
T |
A |
8: 13,342,039 (GRCm39) |
N104K |
probably damaging |
Het |
Tmem200c |
A |
G |
17: 69,149,249 (GRCm39) |
T611A |
probably damaging |
Het |
Tmem202 |
T |
G |
9: 59,432,655 (GRCm39) |
Y24S |
probably damaging |
Het |
Tpp1 |
A |
G |
7: 105,398,626 (GRCm39) |
L230P |
probably damaging |
Het |
Trim56 |
C |
T |
5: 137,141,846 (GRCm39) |
E557K |
probably benign |
Het |
Trrap |
C |
T |
5: 144,790,309 (GRCm39) |
L3590F |
probably damaging |
Het |
Tulp4 |
A |
G |
17: 6,189,387 (GRCm39) |
T70A |
possibly damaging |
Het |
Vcp |
G |
C |
4: 42,986,201 (GRCm39) |
A297G |
probably benign |
Het |
Vwf |
T |
A |
6: 125,603,234 (GRCm39) |
H861Q |
probably benign |
Het |
Wdr64 |
T |
C |
1: 175,599,751 (GRCm39) |
I536T |
probably benign |
Het |
Zfp850 |
T |
C |
7: 27,689,698 (GRCm39) |
N170S |
probably benign |
Het |
Zfp87 |
G |
A |
13: 74,524,544 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Sptbn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00227:Sptbn1
|
APN |
11 |
30,060,818 (GRCm39) |
nonsense |
probably null |
|
IGL01098:Sptbn1
|
APN |
11 |
30,109,385 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01843:Sptbn1
|
APN |
11 |
30,054,623 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02070:Sptbn1
|
APN |
11 |
30,095,979 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02075:Sptbn1
|
APN |
11 |
30,088,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02094:Sptbn1
|
APN |
11 |
30,050,659 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02102:Sptbn1
|
APN |
11 |
30,087,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02189:Sptbn1
|
APN |
11 |
30,067,871 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02256:Sptbn1
|
APN |
11 |
30,070,990 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02301:Sptbn1
|
APN |
11 |
30,092,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02354:Sptbn1
|
APN |
11 |
30,060,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02361:Sptbn1
|
APN |
11 |
30,060,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Sptbn1
|
APN |
11 |
30,069,491 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02504:Sptbn1
|
APN |
11 |
30,092,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02672:Sptbn1
|
APN |
11 |
30,087,239 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02733:Sptbn1
|
APN |
11 |
30,147,747 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02755:Sptbn1
|
APN |
11 |
30,092,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Sptbn1
|
UTSW |
11 |
30,073,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Sptbn1
|
UTSW |
11 |
30,073,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0139:Sptbn1
|
UTSW |
11 |
30,092,289 (GRCm39) |
missense |
probably benign |
0.00 |
R0370:Sptbn1
|
UTSW |
11 |
30,071,545 (GRCm39) |
missense |
probably benign |
|
R0389:Sptbn1
|
UTSW |
11 |
30,089,250 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0415:Sptbn1
|
UTSW |
11 |
30,099,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Sptbn1
|
UTSW |
11 |
30,095,985 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0601:Sptbn1
|
UTSW |
11 |
30,100,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Sptbn1
|
UTSW |
11 |
30,088,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Sptbn1
|
UTSW |
11 |
30,067,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0708:Sptbn1
|
UTSW |
11 |
30,064,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Sptbn1
|
UTSW |
11 |
30,060,902 (GRCm39) |
missense |
probably damaging |
0.96 |
R0755:Sptbn1
|
UTSW |
11 |
30,089,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0892:Sptbn1
|
UTSW |
11 |
30,092,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Sptbn1
|
UTSW |
11 |
30,071,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Sptbn1
|
UTSW |
11 |
30,070,785 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1460:Sptbn1
|
UTSW |
11 |
30,088,637 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1479:Sptbn1
|
UTSW |
11 |
30,063,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Sptbn1
|
UTSW |
11 |
30,071,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Sptbn1
|
UTSW |
11 |
30,087,301 (GRCm39) |
missense |
probably damaging |
0.97 |
R1663:Sptbn1
|
UTSW |
11 |
30,070,783 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1671:Sptbn1
|
UTSW |
11 |
30,092,245 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1680:Sptbn1
|
UTSW |
11 |
30,109,371 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1695:Sptbn1
|
UTSW |
11 |
30,086,124 (GRCm39) |
missense |
probably benign |
0.13 |
R1868:Sptbn1
|
UTSW |
11 |
30,064,781 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1918:Sptbn1
|
UTSW |
11 |
30,092,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Sptbn1
|
UTSW |
11 |
30,054,469 (GRCm39) |
missense |
probably damaging |
0.98 |
R2026:Sptbn1
|
UTSW |
11 |
30,054,559 (GRCm39) |
missense |
probably benign |
0.02 |
R2038:Sptbn1
|
UTSW |
11 |
30,109,293 (GRCm39) |
critical splice donor site |
probably null |
|
R2047:Sptbn1
|
UTSW |
11 |
30,088,360 (GRCm39) |
splice site |
probably benign |
|
R2312:Sptbn1
|
UTSW |
11 |
30,104,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Sptbn1
|
UTSW |
11 |
30,169,686 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3624:Sptbn1
|
UTSW |
11 |
30,090,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R3723:Sptbn1
|
UTSW |
11 |
30,087,335 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3862:Sptbn1
|
UTSW |
11 |
30,092,329 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4446:Sptbn1
|
UTSW |
11 |
30,089,114 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4582:Sptbn1
|
UTSW |
11 |
30,169,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R4705:Sptbn1
|
UTSW |
11 |
30,050,660 (GRCm39) |
missense |
probably benign |
|
R4707:Sptbn1
|
UTSW |
11 |
30,087,197 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4718:Sptbn1
|
UTSW |
11 |
30,104,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Sptbn1
|
UTSW |
11 |
30,067,759 (GRCm39) |
missense |
probably benign |
|
R4824:Sptbn1
|
UTSW |
11 |
30,068,295 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4855:Sptbn1
|
UTSW |
11 |
30,092,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Sptbn1
|
UTSW |
11 |
30,074,016 (GRCm39) |
missense |
probably benign |
0.05 |
R5071:Sptbn1
|
UTSW |
11 |
30,063,854 (GRCm39) |
critical splice donor site |
probably null |
|
R5153:Sptbn1
|
UTSW |
11 |
30,071,510 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5334:Sptbn1
|
UTSW |
11 |
30,087,364 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5462:Sptbn1
|
UTSW |
11 |
30,050,520 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5523:Sptbn1
|
UTSW |
11 |
30,087,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Sptbn1
|
UTSW |
11 |
30,093,174 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5724:Sptbn1
|
UTSW |
11 |
30,094,113 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5738:Sptbn1
|
UTSW |
11 |
30,095,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Sptbn1
|
UTSW |
11 |
30,095,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R5895:Sptbn1
|
UTSW |
11 |
30,073,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R5932:Sptbn1
|
UTSW |
11 |
30,086,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5966:Sptbn1
|
UTSW |
11 |
30,074,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Sptbn1
|
UTSW |
11 |
30,068,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Sptbn1
|
UTSW |
11 |
30,087,403 (GRCm39) |
missense |
probably damaging |
0.99 |
R6163:Sptbn1
|
UTSW |
11 |
30,109,443 (GRCm39) |
nonsense |
probably null |
|
R6226:Sptbn1
|
UTSW |
11 |
30,086,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6271:Sptbn1
|
UTSW |
11 |
30,050,660 (GRCm39) |
missense |
probably benign |
0.00 |
R6443:Sptbn1
|
UTSW |
11 |
30,089,429 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6591:Sptbn1
|
UTSW |
11 |
30,063,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R6616:Sptbn1
|
UTSW |
11 |
30,074,030 (GRCm39) |
missense |
probably benign |
0.08 |
R6691:Sptbn1
|
UTSW |
11 |
30,063,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R6751:Sptbn1
|
UTSW |
11 |
30,067,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Sptbn1
|
UTSW |
11 |
30,064,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R6863:Sptbn1
|
UTSW |
11 |
30,096,777 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6885:Sptbn1
|
UTSW |
11 |
30,088,634 (GRCm39) |
missense |
probably benign |
0.26 |
R6892:Sptbn1
|
UTSW |
11 |
30,092,187 (GRCm39) |
missense |
probably benign |
0.27 |
R6998:Sptbn1
|
UTSW |
11 |
30,050,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R7043:Sptbn1
|
UTSW |
11 |
30,053,323 (GRCm39) |
missense |
probably benign |
0.02 |
R7092:Sptbn1
|
UTSW |
11 |
30,087,119 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7272:Sptbn1
|
UTSW |
11 |
30,064,859 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7301:Sptbn1
|
UTSW |
11 |
30,067,798 (GRCm39) |
nonsense |
probably null |
|
R7379:Sptbn1
|
UTSW |
11 |
30,089,292 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7774:Sptbn1
|
UTSW |
11 |
30,092,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R7813:Sptbn1
|
UTSW |
11 |
30,088,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Sptbn1
|
UTSW |
11 |
30,088,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Sptbn1
|
UTSW |
11 |
30,104,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Sptbn1
|
UTSW |
11 |
30,092,153 (GRCm39) |
missense |
probably damaging |
0.98 |
R7877:Sptbn1
|
UTSW |
11 |
30,079,601 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7902:Sptbn1
|
UTSW |
11 |
30,086,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R8060:Sptbn1
|
UTSW |
11 |
30,051,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R8116:Sptbn1
|
UTSW |
11 |
30,089,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8169:Sptbn1
|
UTSW |
11 |
30,147,783 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8208:Sptbn1
|
UTSW |
11 |
30,074,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Sptbn1
|
UTSW |
11 |
30,063,906 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8412:Sptbn1
|
UTSW |
11 |
30,088,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R8470:Sptbn1
|
UTSW |
11 |
30,070,758 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8544:Sptbn1
|
UTSW |
11 |
30,169,750 (GRCm39) |
start gained |
probably benign |
|
R8674:Sptbn1
|
UTSW |
11 |
30,089,352 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8846:Sptbn1
|
UTSW |
11 |
30,075,009 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8889:Sptbn1
|
UTSW |
11 |
30,067,800 (GRCm39) |
missense |
probably benign |
0.03 |
R8892:Sptbn1
|
UTSW |
11 |
30,067,800 (GRCm39) |
missense |
probably benign |
0.03 |
R8927:Sptbn1
|
UTSW |
11 |
30,088,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Sptbn1
|
UTSW |
11 |
30,088,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Sptbn1
|
UTSW |
11 |
30,073,869 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9115:Sptbn1
|
UTSW |
11 |
30,087,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Sptbn1
|
UTSW |
11 |
30,104,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Sptbn1
|
UTSW |
11 |
30,087,551 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9237:Sptbn1
|
UTSW |
11 |
30,096,803 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sptbn1
|
UTSW |
11 |
30,147,787 (GRCm39) |
missense |
probably benign |
0.13 |
Z1176:Sptbn1
|
UTSW |
11 |
30,087,439 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sptbn1
|
UTSW |
11 |
30,070,659 (GRCm39) |
missense |
probably benign |
0.27 |
Z1177:Sptbn1
|
UTSW |
11 |
30,064,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|