Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahdc1 |
ACCACC |
ACCACCACC |
4: 132,790,062 (GRCm39) |
|
probably benign |
Het |
Ankhd1 |
GGCGGC |
GGCGGCCGCGGC |
18: 36,693,962 (GRCm39) |
|
probably benign |
Het |
Anks1b |
G |
A |
10: 89,869,087 (GRCm39) |
G49D |
probably damaging |
Het |
AY358078 |
T |
TAGGATAATGA |
14: 52,043,050 (GRCm39) |
|
probably null |
Het |
Ccdc170 |
CCA |
CCAGCA |
10: 4,511,024 (GRCm39) |
|
probably benign |
Het |
Cfap251 |
AAGAGGAGGAAGAGGAGGGGGAGAAGGAG |
AAGAGGAGGAAGAGGAGGGGGAGAAGGAGGAAAAGGAGAAAGAGGAGGAAGAGGAGGGGGAGAAGGAG |
5: 123,391,953 (GRCm39) |
|
probably benign |
Het |
Cntrl |
C |
A |
2: 35,065,201 (GRCm39) |
D2168E |
probably damaging |
Het |
Dab1 |
C |
A |
4: 104,570,849 (GRCm39) |
R195S |
probably benign |
Het |
Dnmt1 |
AGCACAGTTCCTACCTCGTT |
AGCACAGTTCCTACCTCGTTTTGGGGGCGGCGCACAGTTCCTACCTCGTT |
9: 20,821,422 (GRCm39) |
|
probably null |
Het |
Elp6 |
A |
T |
9: 110,148,777 (GRCm39) |
H222L |
probably damaging |
Het |
Entpd2 |
CTT |
CTTT |
2: 25,290,907 (GRCm39) |
|
probably null |
Het |
Fgf22 |
A |
G |
10: 79,592,680 (GRCm39) |
H125R |
probably benign |
Het |
Galnt18 |
G |
A |
7: 111,198,221 (GRCm39) |
R180C |
probably damaging |
Het |
Garin5a |
GTCTGAGGGAGGA |
GTCTGAGGGAGGAAGGCTGGATCCTGGATACCTGGATCTGAGGGAGGA |
7: 44,149,949 (GRCm39) |
|
probably null |
Het |
Garin5a |
GGGAGGA |
GGGAGGAAGGCTGGATCCTGGATACCTGGGTCTGATGGAGGA |
7: 44,149,955 (GRCm39) |
|
probably null |
Het |
Gm8369 |
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
19: 11,489,106 (GRCm39) |
|
probably null |
Het |
Gpsm1 |
C |
A |
2: 26,214,884 (GRCm39) |
H288Q |
probably damaging |
Het |
Ipo7 |
A |
G |
7: 109,648,001 (GRCm39) |
I628V |
probably benign |
Het |
Irag2 |
GCACATTG |
GCACATTGATCACATTG |
6: 145,119,510 (GRCm39) |
|
probably benign |
Het |
Itpkb |
C |
T |
1: 180,160,887 (GRCm39) |
R338W |
probably damaging |
Het |
Krtap28-10 |
CACAGC |
CACAGCAACAGC |
1: 83,019,859 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CCACCACAGCCACAG |
CCACCACAGCCACAGTCACCACAGCCACAG |
1: 83,019,987 (GRCm39) |
|
probably benign |
Het |
Krtap4-2 |
CAGCAGGGGCGGCA |
C |
11: 99,525,543 (GRCm39) |
|
probably null |
Het |
Krtap4-9 |
TGCTGTGTGTCCAGCTGCTGCAG |
TGCTGTGTGTCCAGCTGCTGCAGGCCCAGCGGCTGTGTGTCCAGCTGCTGCAG |
11: 99,676,225 (GRCm39) |
|
probably benign |
Het |
Larp4b |
G |
T |
13: 9,173,946 (GRCm39) |
G30V |
probably benign |
Het |
Map1a |
CTCCAGCTCCA |
CTCCAGCTCCAGCTCCAGCTCCAGCTCCAGGTCCAGCTCCA |
2: 121,136,789 (GRCm39) |
|
probably benign |
Het |
Mccc2 |
A |
C |
13: 100,136,796 (GRCm39) |
V53G |
probably damaging |
Het |
Meiosin |
T |
C |
7: 18,836,354 (GRCm39) |
N291S |
unknown |
Het |
Mug1 |
T |
A |
6: 121,861,533 (GRCm39) |
Y1332N |
probably damaging |
Het |
Nalf2 |
GCCGCC |
GCCGCCACCGCC |
X: 98,864,971 (GRCm39) |
|
probably benign |
Het |
Ndnf |
A |
G |
6: 65,681,313 (GRCm39) |
T531A |
probably damaging |
Het |
Ntsr2 |
T |
G |
12: 16,709,766 (GRCm39) |
V349G |
probably damaging |
Het |
Or2g25 |
A |
T |
17: 37,970,672 (GRCm39) |
I184N |
probably damaging |
Het |
P2ry14 |
A |
T |
3: 59,022,467 (GRCm39) |
I331N |
probably benign |
Het |
Pcdha11 |
T |
C |
18: 37,138,577 (GRCm39) |
S69P |
possibly damaging |
Het |
Ptp4a2 |
A |
G |
4: 129,733,237 (GRCm39) |
|
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,741,446 (GRCm39) |
D2353G |
probably benign |
Het |
Rasa2 |
GCC |
GCCCCC |
9: 96,513,521 (GRCm39) |
|
probably benign |
Het |
Raver2 |
A |
T |
4: 100,960,195 (GRCm39) |
D225V |
probably damaging |
Het |
Rph3a |
A |
T |
5: 121,100,562 (GRCm39) |
|
probably null |
Het |
Sin3a |
T |
A |
9: 57,034,610 (GRCm39) |
V1261E |
possibly damaging |
Het |
Slc12a9 |
T |
A |
5: 137,323,812 (GRCm39) |
I368F |
probably damaging |
Het |
Spaca1 |
CTCGC |
CTCGCTGTCGC |
4: 34,049,853 (GRCm39) |
|
probably benign |
Het |
Strn |
C |
CCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCAGTG |
17: 78,984,717 (GRCm39) |
|
probably null |
Het |
Ush2a |
A |
C |
1: 187,995,666 (GRCm39) |
T146P |
probably damaging |
Het |
Usp37 |
A |
G |
1: 74,509,849 (GRCm39) |
L440P |
probably damaging |
Het |
Xpnpep1 |
T |
A |
19: 53,020,491 (GRCm39) |
I24L |
probably benign |
Het |
|
Other mutations in Spata31h1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Spata31h1
|
APN |
10 |
82,119,586 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01457:Spata31h1
|
APN |
10 |
82,120,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01540:Spata31h1
|
APN |
10 |
82,120,016 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02693:Spata31h1
|
APN |
10 |
82,121,092 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02867:Spata31h1
|
APN |
10 |
82,119,654 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02889:Spata31h1
|
APN |
10 |
82,119,654 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03080:Spata31h1
|
APN |
10 |
82,119,816 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03120:Spata31h1
|
APN |
10 |
82,120,869 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03351:Spata31h1
|
APN |
10 |
82,119,401 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4449:Spata31h1
|
UTSW |
10 |
82,121,303 (GRCm39) |
frame shift |
probably null |
|
FR4548:Spata31h1
|
UTSW |
10 |
82,126,830 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Spata31h1
|
UTSW |
10 |
82,121,303 (GRCm39) |
small deletion |
probably benign |
|
PIT4480001:Spata31h1
|
UTSW |
10 |
82,119,586 (GRCm39) |
missense |
probably benign |
0.06 |
R0102:Spata31h1
|
UTSW |
10 |
82,119,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Spata31h1
|
UTSW |
10 |
82,120,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R1303:Spata31h1
|
UTSW |
10 |
82,120,390 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2039:Spata31h1
|
UTSW |
10 |
82,120,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Spata31h1
|
UTSW |
10 |
82,119,789 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4740:Spata31h1
|
UTSW |
10 |
82,119,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4857:Spata31h1
|
UTSW |
10 |
82,119,682 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5017:Spata31h1
|
UTSW |
10 |
82,132,510 (GRCm39) |
missense |
unknown |
|
R5095:Spata31h1
|
UTSW |
10 |
82,119,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Spata31h1
|
UTSW |
10 |
82,119,652 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5388:Spata31h1
|
UTSW |
10 |
82,119,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R5642:Spata31h1
|
UTSW |
10 |
82,120,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Spata31h1
|
UTSW |
10 |
82,119,610 (GRCm39) |
missense |
probably damaging |
0.99 |
R6188:Spata31h1
|
UTSW |
10 |
82,121,091 (GRCm39) |
missense |
probably damaging |
0.96 |
R6215:Spata31h1
|
UTSW |
10 |
82,126,946 (GRCm39) |
missense |
probably benign |
0.07 |
R6252:Spata31h1
|
UTSW |
10 |
82,119,588 (GRCm39) |
missense |
probably benign |
0.30 |
R6275:Spata31h1
|
UTSW |
10 |
82,121,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R6303:Spata31h1
|
UTSW |
10 |
82,126,202 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6304:Spata31h1
|
UTSW |
10 |
82,126,202 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6313:Spata31h1
|
UTSW |
10 |
82,129,470 (GRCm39) |
missense |
probably benign |
0.00 |
R6323:Spata31h1
|
UTSW |
10 |
82,118,916 (GRCm39) |
missense |
probably benign |
0.27 |
R6374:Spata31h1
|
UTSW |
10 |
82,124,731 (GRCm39) |
unclassified |
probably benign |
|
R6407:Spata31h1
|
UTSW |
10 |
82,129,645 (GRCm39) |
missense |
probably benign |
0.16 |
R6468:Spata31h1
|
UTSW |
10 |
82,131,150 (GRCm39) |
missense |
probably benign |
0.01 |
R6490:Spata31h1
|
UTSW |
10 |
82,125,138 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6605:Spata31h1
|
UTSW |
10 |
82,131,871 (GRCm39) |
missense |
probably benign |
0.27 |
R6614:Spata31h1
|
UTSW |
10 |
82,127,482 (GRCm39) |
missense |
probably benign |
0.31 |
R6626:Spata31h1
|
UTSW |
10 |
82,128,667 (GRCm39) |
missense |
probably benign |
0.03 |
R6630:Spata31h1
|
UTSW |
10 |
82,122,906 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6646:Spata31h1
|
UTSW |
10 |
82,132,664 (GRCm39) |
missense |
unknown |
|
R6723:Spata31h1
|
UTSW |
10 |
82,125,657 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6751:Spata31h1
|
UTSW |
10 |
82,119,331 (GRCm39) |
missense |
probably benign |
0.06 |
R6850:Spata31h1
|
UTSW |
10 |
82,128,888 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6944:Spata31h1
|
UTSW |
10 |
82,132,056 (GRCm39) |
missense |
probably benign |
0.03 |
R6957:Spata31h1
|
UTSW |
10 |
82,129,620 (GRCm39) |
missense |
probably benign |
0.03 |
R6988:Spata31h1
|
UTSW |
10 |
82,127,733 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7069:Spata31h1
|
UTSW |
10 |
82,125,777 (GRCm39) |
missense |
probably damaging |
0.99 |
R7164:Spata31h1
|
UTSW |
10 |
82,122,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Spata31h1
|
UTSW |
10 |
82,122,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Spata31h1
|
UTSW |
10 |
82,127,461 (GRCm39) |
missense |
probably benign |
0.03 |
R7203:Spata31h1
|
UTSW |
10 |
82,129,248 (GRCm39) |
missense |
probably benign |
0.00 |
R7205:Spata31h1
|
UTSW |
10 |
82,125,161 (GRCm39) |
missense |
probably benign |
0.35 |
R7241:Spata31h1
|
UTSW |
10 |
82,122,876 (GRCm39) |
missense |
probably benign |
0.01 |
R7283:Spata31h1
|
UTSW |
10 |
82,127,131 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7305:Spata31h1
|
UTSW |
10 |
82,120,953 (GRCm39) |
missense |
probably benign |
0.06 |
R7358:Spata31h1
|
UTSW |
10 |
82,127,847 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7360:Spata31h1
|
UTSW |
10 |
82,132,341 (GRCm39) |
missense |
unknown |
|
R7362:Spata31h1
|
UTSW |
10 |
82,128,831 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7385:Spata31h1
|
UTSW |
10 |
82,123,729 (GRCm39) |
missense |
probably benign |
0.05 |
R7385:Spata31h1
|
UTSW |
10 |
82,123,571 (GRCm39) |
missense |
probably benign |
0.03 |
R7472:Spata31h1
|
UTSW |
10 |
82,119,421 (GRCm39) |
missense |
probably benign |
0.03 |
R7493:Spata31h1
|
UTSW |
10 |
82,152,264 (GRCm39) |
missense |
unknown |
|
R7493:Spata31h1
|
UTSW |
10 |
82,124,798 (GRCm39) |
nonsense |
probably null |
|
R7498:Spata31h1
|
UTSW |
10 |
82,127,113 (GRCm39) |
missense |
probably benign |
0.03 |
R7512:Spata31h1
|
UTSW |
10 |
82,128,469 (GRCm39) |
missense |
probably benign |
0.31 |
R7560:Spata31h1
|
UTSW |
10 |
82,120,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7591:Spata31h1
|
UTSW |
10 |
82,128,046 (GRCm39) |
missense |
probably benign |
0.16 |
R7636:Spata31h1
|
UTSW |
10 |
82,130,973 (GRCm39) |
missense |
probably benign |
0.01 |
R7640:Spata31h1
|
UTSW |
10 |
82,130,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R7709:Spata31h1
|
UTSW |
10 |
82,126,366 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7790:Spata31h1
|
UTSW |
10 |
82,123,329 (GRCm39) |
missense |
probably benign |
0.06 |
R7875:Spata31h1
|
UTSW |
10 |
82,123,456 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7878:Spata31h1
|
UTSW |
10 |
82,119,856 (GRCm39) |
missense |
probably benign |
0.04 |
R7899:Spata31h1
|
UTSW |
10 |
82,118,731 (GRCm39) |
missense |
unknown |
|
R7905:Spata31h1
|
UTSW |
10 |
82,131,936 (GRCm39) |
missense |
probably benign |
0.03 |
R7975:Spata31h1
|
UTSW |
10 |
82,119,823 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7988:Spata31h1
|
UTSW |
10 |
82,131,934 (GRCm39) |
missense |
probably benign |
0.03 |
R8076:Spata31h1
|
UTSW |
10 |
82,132,520 (GRCm39) |
nonsense |
probably null |
|
R8144:Spata31h1
|
UTSW |
10 |
82,130,433 (GRCm39) |
nonsense |
probably null |
|
R8429:Spata31h1
|
UTSW |
10 |
82,125,301 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8465:Spata31h1
|
UTSW |
10 |
82,152,298 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8470:Spata31h1
|
UTSW |
10 |
82,126,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R8509:Spata31h1
|
UTSW |
10 |
82,126,950 (GRCm39) |
missense |
probably benign |
0.01 |
R8515:Spata31h1
|
UTSW |
10 |
82,124,436 (GRCm39) |
missense |
probably benign |
0.00 |
R8672:Spata31h1
|
UTSW |
10 |
82,127,726 (GRCm39) |
missense |
probably benign |
0.01 |
R8700:Spata31h1
|
UTSW |
10 |
82,127,859 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8827:Spata31h1
|
UTSW |
10 |
82,129,617 (GRCm39) |
missense |
probably benign |
0.07 |
R8872:Spata31h1
|
UTSW |
10 |
82,128,619 (GRCm39) |
missense |
probably benign |
0.07 |
R8875:Spata31h1
|
UTSW |
10 |
82,123,476 (GRCm39) |
missense |
probably benign |
0.16 |
R8884:Spata31h1
|
UTSW |
10 |
82,119,486 (GRCm39) |
missense |
probably damaging |
0.96 |
R8906:Spata31h1
|
UTSW |
10 |
82,122,379 (GRCm39) |
missense |
probably benign |
0.02 |
R8924:Spata31h1
|
UTSW |
10 |
82,131,295 (GRCm39) |
missense |
probably benign |
0.03 |
R8949:Spata31h1
|
UTSW |
10 |
82,123,753 (GRCm39) |
missense |
probably benign |
0.00 |
R8957:Spata31h1
|
UTSW |
10 |
82,124,908 (GRCm39) |
missense |
probably benign |
0.07 |
R9042:Spata31h1
|
UTSW |
10 |
82,123,185 (GRCm39) |
missense |
probably benign |
0.08 |
R9056:Spata31h1
|
UTSW |
10 |
82,127,101 (GRCm39) |
missense |
probably benign |
0.01 |
R9062:Spata31h1
|
UTSW |
10 |
82,126,945 (GRCm39) |
missense |
probably benign |
0.03 |
R9074:Spata31h1
|
UTSW |
10 |
82,123,894 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9086:Spata31h1
|
UTSW |
10 |
82,124,577 (GRCm39) |
missense |
probably benign |
0.07 |
R9113:Spata31h1
|
UTSW |
10 |
82,131,352 (GRCm39) |
nonsense |
probably null |
|
R9119:Spata31h1
|
UTSW |
10 |
82,131,553 (GRCm39) |
missense |
probably benign |
0.03 |
R9132:Spata31h1
|
UTSW |
10 |
82,127,896 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9141:Spata31h1
|
UTSW |
10 |
82,126,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R9151:Spata31h1
|
UTSW |
10 |
82,120,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R9155:Spata31h1
|
UTSW |
10 |
82,120,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9159:Spata31h1
|
UTSW |
10 |
82,118,524 (GRCm39) |
nonsense |
probably null |
|
R9197:Spata31h1
|
UTSW |
10 |
82,120,401 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9212:Spata31h1
|
UTSW |
10 |
82,118,979 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9245:Spata31h1
|
UTSW |
10 |
82,123,554 (GRCm39) |
missense |
probably benign |
0.10 |
R9304:Spata31h1
|
UTSW |
10 |
82,131,930 (GRCm39) |
missense |
probably benign |
0.07 |
R9309:Spata31h1
|
UTSW |
10 |
82,130,986 (GRCm39) |
missense |
probably benign |
0.00 |
R9329:Spata31h1
|
UTSW |
10 |
82,121,439 (GRCm39) |
missense |
probably benign |
0.06 |
R9356:Spata31h1
|
UTSW |
10 |
82,125,157 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9423:Spata31h1
|
UTSW |
10 |
82,123,459 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9426:Spata31h1
|
UTSW |
10 |
82,126,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R9457:Spata31h1
|
UTSW |
10 |
82,122,573 (GRCm39) |
missense |
probably benign |
0.02 |
R9509:Spata31h1
|
UTSW |
10 |
82,132,229 (GRCm39) |
missense |
probably benign |
0.03 |
R9612:Spata31h1
|
UTSW |
10 |
82,125,453 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9674:Spata31h1
|
UTSW |
10 |
82,120,030 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9726:Spata31h1
|
UTSW |
10 |
82,118,605 (GRCm39) |
missense |
unknown |
|
RF055:Spata31h1
|
UTSW |
10 |
82,126,827 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Spata31h1
|
UTSW |
10 |
82,129,062 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Spata31h1
|
UTSW |
10 |
82,125,730 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Spata31h1
|
UTSW |
10 |
82,118,371 (GRCm39) |
missense |
unknown |
|
Z1177:Spata31h1
|
UTSW |
10 |
82,123,251 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Spata31h1
|
UTSW |
10 |
82,122,960 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Spata31h1
|
UTSW |
10 |
82,121,632 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1177:Spata31h1
|
UTSW |
10 |
82,125,520 (GRCm39) |
nonsense |
probably null |
|
Z1187:Spata31h1
|
UTSW |
10 |
82,124,390 (GRCm39) |
small deletion |
probably benign |
|
|