Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A230072I06Rik |
T |
A |
8: 12,329,824 (GRCm39) |
L93H |
unknown |
Het |
A2ml1 |
A |
G |
6: 128,549,045 (GRCm39) |
Y246H |
probably damaging |
Het |
Akap11 |
C |
A |
14: 78,750,413 (GRCm39) |
C658F |
|
Het |
Arid2 |
T |
G |
15: 96,266,592 (GRCm39) |
S547A |
possibly damaging |
Het |
Atf1 |
C |
A |
15: 100,143,170 (GRCm39) |
D46E |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,459,634 (GRCm39) |
F303Y |
possibly damaging |
Het |
Btbd18 |
T |
A |
2: 84,498,260 (GRCm39) |
S633T |
possibly damaging |
Het |
Btg4 |
T |
G |
9: 51,030,445 (GRCm39) |
F182V |
probably benign |
Het |
Cacna1e |
G |
A |
1: 154,437,516 (GRCm39) |
S340F |
probably damaging |
Het |
Camta2 |
A |
G |
11: 70,576,903 (GRCm39) |
W41R |
probably damaging |
Het |
Cbl |
A |
T |
9: 44,074,696 (GRCm39) |
D455E |
probably benign |
Het |
Ccdc162 |
A |
T |
10: 41,488,864 (GRCm39) |
D1208E |
probably benign |
Het |
Cd177 |
A |
T |
7: 24,443,842 (GRCm39) |
M752K |
probably damaging |
Het |
Cep290 |
A |
T |
10: 100,380,793 (GRCm39) |
H100L |
possibly damaging |
Het |
Chrnb2 |
T |
A |
3: 89,668,698 (GRCm39) |
I206F |
probably damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,791,009 (GRCm39) |
L274S |
probably benign |
Het |
Cyp2c40 |
T |
A |
19: 39,791,015 (GRCm39) |
Y272F |
probably benign |
Het |
Cyp2d22 |
C |
A |
15: 82,258,556 (GRCm39) |
A102S |
probably benign |
Het |
Cyp51 |
C |
T |
5: 4,136,490 (GRCm39) |
E435K |
probably benign |
Het |
Dchs2 |
T |
C |
3: 83,262,929 (GRCm39) |
F3066L |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,192 (GRCm39) |
R1076L |
probably damaging |
Het |
Dkk2 |
C |
T |
3: 131,791,801 (GRCm39) |
A3V |
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,165,964 (GRCm39) |
F543S |
probably benign |
Het |
Dpt |
A |
T |
1: 164,624,481 (GRCm39) |
S61C |
probably damaging |
Het |
Drg2 |
A |
T |
11: 60,353,096 (GRCm39) |
Y243F |
probably damaging |
Het |
Dsg2 |
A |
G |
18: 20,716,061 (GRCm39) |
|
probably benign |
Het |
Dst |
T |
G |
1: 34,228,040 (GRCm39) |
L1878V |
possibly damaging |
Het |
F5 |
A |
G |
1: 164,036,509 (GRCm39) |
Y1890C |
probably benign |
Het |
Fat1 |
T |
C |
8: 45,405,739 (GRCm39) |
V830A |
probably damaging |
Het |
Fat2 |
C |
T |
11: 55,186,965 (GRCm39) |
D1294N |
probably benign |
Het |
Fbxo15 |
A |
G |
18: 84,983,618 (GRCm39) |
Y322C |
probably benign |
Het |
Fcsk |
A |
G |
8: 111,622,604 (GRCm39) |
F108S |
probably damaging |
Het |
Fhit |
A |
T |
14: 10,751,666 (GRCm38) |
N7K |
unknown |
Het |
Gabrb2 |
A |
G |
11: 42,488,370 (GRCm39) |
I279V |
probably damaging |
Het |
Galk2 |
T |
C |
2: 125,773,189 (GRCm39) |
F207S |
probably damaging |
Het |
Gtpbp3 |
C |
T |
8: 71,941,480 (GRCm39) |
L17F |
possibly damaging |
Het |
Gucy2c |
T |
A |
6: 136,714,446 (GRCm39) |
D460V |
probably benign |
Het |
Herc1 |
G |
A |
9: 66,400,462 (GRCm39) |
V4329I |
probably damaging |
Het |
Iqcn |
T |
C |
8: 71,162,067 (GRCm39) |
V420A |
probably benign |
Het |
Macf1 |
C |
A |
4: 123,263,660 (GRCm39) |
V6956L |
probably damaging |
Het |
Mill1 |
C |
T |
7: 17,989,835 (GRCm39) |
A39V |
probably benign |
Het |
Mkln1 |
T |
A |
6: 31,469,588 (GRCm39) |
Y599* |
probably null |
Het |
Mrpl14 |
T |
A |
17: 46,009,039 (GRCm39) |
L46Q |
possibly damaging |
Het |
Myom2 |
G |
T |
8: 15,119,418 (GRCm39) |
R103L |
possibly damaging |
Het |
Naip2 |
A |
C |
13: 100,298,290 (GRCm39) |
I582S |
probably benign |
Het |
Ndst2 |
A |
T |
14: 20,778,232 (GRCm39) |
V449D |
probably damaging |
Het |
Nell1 |
T |
A |
7: 49,770,335 (GRCm39) |
H131Q |
probably benign |
Het |
Nos3 |
G |
C |
5: 24,572,218 (GRCm39) |
R97P |
probably benign |
Het |
Npc1 |
A |
T |
18: 12,327,297 (GRCm39) |
F1099L |
probably benign |
Het |
Nxpe5 |
T |
A |
5: 138,249,802 (GRCm39) |
W531R |
probably damaging |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or1j1 |
A |
T |
2: 36,702,330 (GRCm39) |
L258H |
probably damaging |
Het |
Or4c110 |
T |
C |
2: 88,832,712 (GRCm39) |
|
probably benign |
Het |
Or5b98 |
A |
T |
19: 12,931,366 (GRCm39) |
T138S |
probably benign |
Het |
Or6c210 |
A |
G |
10: 129,495,933 (GRCm39) |
D86G |
probably damaging |
Het |
Osmr |
T |
C |
15: 6,845,102 (GRCm39) |
N889S |
possibly damaging |
Het |
Oxct2b |
A |
G |
4: 123,010,301 (GRCm39) |
I74V |
possibly damaging |
Het |
Pakap |
A |
G |
4: 57,886,319 (GRCm39) |
T859A |
possibly damaging |
Het |
Phldb3 |
C |
A |
7: 24,326,134 (GRCm39) |
A572D |
probably damaging |
Het |
Pigr |
A |
G |
1: 130,774,247 (GRCm39) |
E409G |
probably damaging |
Het |
Ptprs |
T |
C |
17: 56,735,947 (GRCm39) |
E674G |
probably benign |
Het |
Ptpru |
G |
A |
4: 131,520,903 (GRCm39) |
T801I |
possibly damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,829,631 (GRCm39) |
D200V |
probably damaging |
Het |
Rb1cc1 |
A |
T |
1: 6,333,448 (GRCm39) |
R1429* |
probably null |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rnpep |
A |
T |
1: 135,211,514 (GRCm39) |
L78Q |
probably damaging |
Het |
Rtn2 |
A |
T |
7: 19,027,791 (GRCm39) |
I394F |
probably damaging |
Het |
Satb2 |
A |
T |
1: 56,870,623 (GRCm39) |
V572D |
possibly damaging |
Het |
Sds |
T |
C |
5: 120,617,001 (GRCm39) |
|
probably benign |
Het |
Serpina10 |
TTCCTCCTCCTCCTCCTCCTCCTCC |
TTCCTCCTCCTCCTCCTCCTCC |
12: 103,595,032 (GRCm39) |
|
probably benign |
Het |
Sgo2a |
T |
C |
1: 58,056,300 (GRCm39) |
I828T |
possibly damaging |
Het |
Slc25a33 |
T |
A |
4: 149,840,609 (GRCm39) |
K79N |
probably benign |
Het |
Slc25a51 |
A |
C |
4: 45,399,783 (GRCm39) |
F136V |
probably benign |
Het |
Slfn14 |
T |
A |
11: 83,174,119 (GRCm39) |
K291* |
probably null |
Het |
Sp100 |
A |
G |
1: 85,624,819 (GRCm39) |
K403E |
possibly damaging |
Het |
Spaca1 |
C |
T |
4: 34,049,837 (GRCm39) |
E54K |
possibly damaging |
Het |
Sympk |
T |
G |
7: 18,787,373 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
T |
10: 5,067,031 (GRCm39) |
V7078D |
probably damaging |
Het |
Tas2r121 |
T |
A |
6: 132,677,772 (GRCm39) |
I67L |
probably benign |
Het |
Tha1 |
T |
C |
11: 117,759,323 (GRCm39) |
K389E |
probably benign |
Het |
Thbs2 |
T |
A |
17: 14,900,584 (GRCm39) |
Q541L |
probably benign |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Tmem94 |
T |
C |
11: 115,679,218 (GRCm39) |
|
probably null |
Het |
Tnfsf13 |
A |
G |
11: 69,575,983 (GRCm39) |
C35R |
probably damaging |
Het |
Trcg1 |
C |
A |
9: 57,149,564 (GRCm39) |
Q379K |
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,168,007 (GRCm39) |
S1507P |
probably damaging |
Het |
Uckl1 |
A |
G |
2: 181,215,049 (GRCm39) |
I268T |
probably damaging |
Het |
Uvrag |
T |
C |
7: 98,641,174 (GRCm39) |
K289E |
possibly damaging |
Het |
Vmn2r104 |
C |
A |
17: 20,250,483 (GRCm39) |
C596F |
possibly damaging |
Het |
Vmn2r11 |
A |
T |
5: 109,201,626 (GRCm39) |
F293I |
probably damaging |
Het |
Vps13b |
T |
A |
15: 35,669,052 (GRCm39) |
|
probably null |
Het |
Wipf1 |
G |
A |
2: 73,267,879 (GRCm39) |
P173L |
possibly damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zscan4f |
T |
A |
7: 11,135,154 (GRCm39) |
C187S |
possibly damaging |
Het |
|
Other mutations in Kirrel3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00919:Kirrel3
|
APN |
9 |
34,926,549 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01369:Kirrel3
|
APN |
9 |
34,927,737 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01837:Kirrel3
|
APN |
9 |
34,946,224 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01950:Kirrel3
|
APN |
9 |
34,939,625 (GRCm39) |
splice site |
probably benign |
|
IGL01973:Kirrel3
|
APN |
9 |
34,927,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01994:Kirrel3
|
APN |
9 |
34,931,429 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03184:Kirrel3
|
APN |
9 |
34,919,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Kirrel3
|
UTSW |
9 |
34,912,259 (GRCm39) |
missense |
probably benign |
0.06 |
R0033:Kirrel3
|
UTSW |
9 |
34,912,259 (GRCm39) |
missense |
probably benign |
0.06 |
R0038:Kirrel3
|
UTSW |
9 |
34,823,066 (GRCm39) |
splice site |
probably null |
|
R0038:Kirrel3
|
UTSW |
9 |
34,823,066 (GRCm39) |
splice site |
probably null |
|
R0390:Kirrel3
|
UTSW |
9 |
34,931,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Kirrel3
|
UTSW |
9 |
34,946,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R0786:Kirrel3
|
UTSW |
9 |
34,946,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Kirrel3
|
UTSW |
9 |
34,939,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R0962:Kirrel3
|
UTSW |
9 |
34,912,293 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1716:Kirrel3
|
UTSW |
9 |
34,934,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Kirrel3
|
UTSW |
9 |
34,850,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R4289:Kirrel3
|
UTSW |
9 |
34,934,769 (GRCm39) |
missense |
probably benign |
0.44 |
R4888:Kirrel3
|
UTSW |
9 |
34,924,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Kirrel3
|
UTSW |
9 |
34,855,735 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5121:Kirrel3
|
UTSW |
9 |
34,924,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Kirrel3
|
UTSW |
9 |
34,919,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R5572:Kirrel3
|
UTSW |
9 |
34,912,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Kirrel3
|
UTSW |
9 |
34,924,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Kirrel3
|
UTSW |
9 |
34,919,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6449:Kirrel3
|
UTSW |
9 |
34,902,269 (GRCm39) |
missense |
probably benign |
|
R6908:Kirrel3
|
UTSW |
9 |
34,924,697 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6967:Kirrel3
|
UTSW |
9 |
34,946,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R7578:Kirrel3
|
UTSW |
9 |
34,850,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Kirrel3
|
UTSW |
9 |
34,931,419 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8383:Kirrel3
|
UTSW |
9 |
34,941,179 (GRCm39) |
missense |
probably null |
0.89 |
R8494:Kirrel3
|
UTSW |
9 |
34,902,341 (GRCm39) |
missense |
probably benign |
0.03 |
R8878:Kirrel3
|
UTSW |
9 |
34,850,561 (GRCm39) |
splice site |
probably benign |
|
R8955:Kirrel3
|
UTSW |
9 |
34,855,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R9140:Kirrel3
|
UTSW |
9 |
34,924,596 (GRCm39) |
missense |
probably benign |
0.00 |
|