Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500015O10Rik |
TTCTGTA |
T |
1: 43,737,192 |
|
probably benign |
Het |
Adgrl1 |
T |
A |
8: 83,934,772 |
S933T |
probably benign |
Het |
Adgrl2 |
G |
A |
3: 148,839,248 |
T737I |
probably damaging |
Het |
Adra2c |
T |
A |
5: 35,281,042 |
V386E |
probably damaging |
Het |
Agbl5 |
C |
A |
5: 30,903,245 |
T761N |
unknown |
Het |
Ahnak |
T |
A |
19: 9,013,601 |
M4083K |
possibly damaging |
Het |
Aldh1l1 |
A |
T |
6: 90,598,259 |
I843F |
probably damaging |
Het |
Ankhd1 |
GGCGGC |
GGCGGCTGCGGC |
18: 36,560,909 |
|
probably benign |
Het |
Arid1b |
GCG |
GCGCCG |
17: 4,995,594 |
|
probably benign |
Het |
B4galnt4 |
T |
C |
7: 141,070,696 |
|
probably null |
Het |
Blm |
C |
CTCCTCCTCCTAG |
7: 80,512,933 |
|
probably null |
Het |
Btg3 |
A |
G |
16: 78,332,948 |
*52W |
probably null |
Het |
Cc2d1a |
T |
C |
8: 84,134,669 |
T796A |
probably damaging |
Het |
Cd200r1 |
T |
C |
16: 44,790,011 |
S161P |
possibly damaging |
Het |
Cenpj |
A |
G |
14: 56,530,048 |
|
probably null |
Het |
Chd9 |
A |
G |
8: 91,033,950 |
T2108A |
possibly damaging |
Het |
Cherp |
TGGAGCG |
T |
8: 72,462,059 |
|
probably benign |
Het |
Cnot11 |
T |
C |
1: 39,542,494 |
V372A |
probably damaging |
Het |
Cntnap5b |
T |
C |
1: 100,164,070 |
C179R |
probably damaging |
Het |
Cntrl |
T |
A |
2: 35,170,500 |
N1901K |
probably benign |
Het |
Coil |
CTGG |
C |
11: 88,981,830 |
|
probably benign |
Het |
Col1a1 |
A |
G |
11: 94,943,040 |
D488G |
probably damaging |
Het |
Coro1a |
T |
C |
7: 126,701,852 |
H130R |
probably damaging |
Het |
Crybg3 |
A |
C |
16: 59,556,704 |
S1396A |
possibly damaging |
Het |
Csf2rb2 |
A |
G |
15: 78,291,926 |
I259T |
probably benign |
Het |
Cyp1a2 |
G |
T |
9: 57,681,970 |
P187Q |
probably damaging |
Het |
Cyp3a13 |
CATTATT |
CATT |
5: 137,894,263 |
|
probably null |
Het |
Dcun1d3 |
T |
C |
7: 119,859,503 |
E103G |
possibly damaging |
Het |
Dmkn |
T |
A |
7: 30,769,704 |
|
probably null |
Het |
Dna2 |
T |
C |
10: 62,966,695 |
L864P |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,685,809 |
M1909K |
probably benign |
Het |
Dspp |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
5: 104,178,361 |
|
probably benign |
Het |
Efna5 |
T |
C |
17: 62,613,394 |
S163G |
probably benign |
Het |
Entpd2 |
CTT |
CTTT |
2: 25,400,895 |
|
probably null |
Het |
Ercc4 |
C |
T |
16: 13,123,507 |
S253L |
possibly damaging |
Het |
Flywch1 |
ACCCA |
ACCCAATTCTGGTGTGGGGAGGCTACGTACTCTCCCA |
17: 23,762,164 |
|
probably null |
Het |
Flywch1 |
CCTGGTGT |
CCTGGTGTGGGGAGGCTACGTACTCACCCACTTCTGGTGT |
17: 23,762,171 |
|
probably null |
Het |
Folh1 |
T |
C |
7: 86,775,687 |
T25A |
probably benign |
Het |
Foxi3 |
C |
A |
6: 70,960,861 |
T359K |
possibly damaging |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,999,996 |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 75,000,011 |
|
probably benign |
Het |
Gab3 |
TTC |
TTCATC |
X: 75,000,025 |
|
probably benign |
Het |
Gba2 |
G |
T |
4: 43,569,894 |
L440M |
probably damaging |
Het |
Gm14412 |
T |
A |
2: 177,315,701 |
N134Y |
possibly damaging |
Het |
Gpr88 |
A |
G |
3: 116,252,369 |
S98P |
probably benign |
Het |
Il1r1 |
A |
G |
1: 40,313,278 |
Y539C |
probably damaging |
Het |
Iqcf4 |
TTTCCTTTTCCTTTT |
TTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTCTTCCTTTTCCTTTT |
9: 106,570,609 |
|
probably benign |
Het |
Lce1m |
CTGCT |
CTGCTTCCACTGTTGCT |
3: 93,018,144 |
|
probably benign |
Het |
Lkaaear1 |
T |
TATCTCCAGCTCC |
2: 181,697,559 |
|
probably benign |
Het |
Lkaaear1 |
CAGCTCCAGCTCCAGCTCCAGCTC |
CAGCTCCAGCTCTAGCTCCAGCTCCAGCTCCAGCTC |
2: 181,697,577 |
|
probably benign |
Het |
Ltb4r1 |
T |
A |
14: 55,767,969 |
L243Q |
possibly damaging |
Het |
Man2a1 |
T |
A |
17: 64,712,253 |
V704D |
probably damaging |
Het |
Map1a |
CTCCAGCTCCA |
CTCCAGCTCCAGCTCCAGCTCCAGCTCCAGTTCCAGCTCCA |
2: 121,306,308 |
|
probably benign |
Het |
Mcu |
G |
T |
10: 59,491,116 |
A63E |
probably benign |
Het |
Mrps31 |
A |
T |
8: 22,419,864 |
D182V |
possibly damaging |
Het |
Naip1 |
A |
T |
13: 100,426,134 |
M841K |
probably benign |
Het |
Ndufab1 |
T |
C |
7: 122,096,638 |
K88E |
possibly damaging |
Het |
Nlrp5 |
A |
C |
7: 23,418,161 |
I437L |
probably benign |
Het |
Nnt |
C |
T |
13: 119,396,857 |
V91M |
probably damaging |
Het |
Nusap1 |
TACACGTTAGCAGTGAGGAGCAAGCTGAGA |
TACACGTTAGCAGTGAGGAGCAAGCTGAGAGACACGTTAGCAGTGAGGAGCAAGCTGAGA |
2: 119,627,581 |
|
probably benign |
Het |
Nynrin |
T |
G |
14: 55,866,201 |
|
probably null |
Het |
Olfr358 |
T |
G |
2: 37,005,174 |
T147P |
probably damaging |
Het |
Olfr773 |
T |
A |
10: 129,186,693 |
I243F |
probably damaging |
Het |
Olfr992 |
C |
A |
2: 85,399,793 |
A247S |
probably damaging |
Het |
Osbpl8 |
A |
G |
10: 111,276,467 |
K481R |
possibly damaging |
Het |
Padi6 |
T |
C |
4: 140,729,743 |
D540G |
probably damaging |
Het |
Pcmtd1 |
T |
C |
1: 7,155,105 |
|
probably benign |
Het |
Pdik1l |
TTTTTGTTTT |
TTTTTGTTTTGGTTTTGTTTT |
4: 134,279,368 |
|
probably null |
Het |
Phospho1 |
T |
C |
11: 95,831,055 |
Y184H |
probably damaging |
Het |
Pi4ka |
T |
A |
16: 17,297,233 |
R1431W |
|
Het |
Plxdc1 |
T |
A |
11: 97,978,678 |
H28L |
probably benign |
Het |
Pnmal1 |
ACCTCATGATGCACCTGCTTCAACA |
ACCTCATGATGCACCTGCTTCAACACCTCATGATGCACCTGCTTCAACA |
7: 16,961,424 |
|
probably benign |
Het |
Ppp1r7 |
T |
C |
1: 93,346,289 |
|
probably null |
Het |
Ppp1r9a |
T |
A |
6: 4,906,657 |
V404E |
probably damaging |
Het |
Scfd1 |
T |
A |
12: 51,422,973 |
S434T |
probably benign |
Het |
Six5 |
A |
G |
7: 19,094,937 |
S101G |
probably benign |
Het |
Slc6a4 |
C |
A |
11: 77,019,182 |
T421K |
probably damaging |
Het |
Smarcd3 |
C |
A |
5: 24,596,070 |
R113L |
probably damaging |
Het |
Son |
T |
A |
16: 91,659,369 |
M1668K |
possibly damaging |
Het |
Tcf25 |
A |
G |
8: 123,395,630 |
D434G |
probably benign |
Het |
Tcof1 |
CCAGAGATCCCC |
CCAGAGATCCCCGTGGCTGCCGAGATGGGCACTTTCACAGAGATCCCC |
18: 60,833,568 |
|
probably benign |
Het |
Tep1 |
A |
G |
14: 50,860,945 |
V463A |
possibly damaging |
Het |
Thegl |
CTCCCCAGTCCCGCAAGGCCAG |
CTCCCCAGTCCCGCAAGGCCAGCGATCGTCCCCAGTCCCGCAAGGCCAG |
5: 77,016,408 |
|
probably benign |
Het |
Trav15-2-dv6-2 |
GGGAG |
GGGAGGAG |
14: 53,649,750 |
|
probably benign |
Het |
Trav15-2-dv6-2 |
GGAG |
GGAGGAG |
14: 53,649,751 |
|
probably benign |
Het |
Trav15-2-dv6-2 |
AAG |
AAGCAG |
14: 53,649,755 |
|
probably benign |
Het |
Trim24 |
A |
G |
6: 37,953,536 |
K642E |
possibly damaging |
Het |
Trim33 |
GGCCCCCGC |
GGC |
3: 103,280,217 |
|
probably benign |
Het |
Triobp |
CTCCCTGTGCCCAACGG |
CTCCCTGTGCCCAACGGAACAACCCCAGGATTCCCTGTGCCCAACGG |
15: 78,967,044 |
|
probably benign |
Het |
Trmu |
G |
T |
15: 85,892,569 |
V161L |
possibly damaging |
Het |
Try4 |
T |
A |
6: 41,305,363 |
C206S |
probably damaging |
Het |
Usp2 |
TTCACTTAC |
TTCACTTACTCATGTGACCTGTTCGTCACTTAC |
9: 44,089,121 |
|
probably benign |
Het |
Vmn1r62 |
A |
T |
7: 5,675,670 |
M117L |
probably benign |
Het |
Vmn2r104 |
A |
T |
17: 20,048,040 |
Y56N |
probably benign |
Het |
Wdr66 |
G |
GGAT |
5: 123,254,254 |
|
probably benign |
Het |
Xxylt1 |
C |
T |
16: 31,050,680 |
D201N |
possibly damaging |
Het |
Zfp563 |
T |
A |
17: 33,105,025 |
I198K |
probably benign |
Het |
Zfp612 |
T |
A |
8: 110,089,542 |
C460* |
probably null |
Het |
Zfp691 |
G |
A |
4: 119,170,735 |
T100M |
probably benign |
Het |
Zfp773 |
A |
T |
7: 7,132,690 |
C302* |
probably null |
Het |
Zmat2 |
A |
G |
18: 36,797,883 |
E154G |
probably damaging |
Het |
Zw10 |
T |
A |
9: 49,060,920 |
I132N |
possibly damaging |
Het |
|