Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl1 |
T |
A |
8: 84,661,401 (GRCm39) |
S933T |
probably benign |
Het |
Adgrl2 |
G |
A |
3: 148,544,884 (GRCm39) |
T737I |
probably damaging |
Het |
Adra2c |
T |
A |
5: 35,438,386 (GRCm39) |
V386E |
probably damaging |
Het |
Agbl5 |
C |
A |
5: 31,060,589 (GRCm39) |
T761N |
unknown |
Het |
Ahnak |
T |
A |
19: 8,990,965 (GRCm39) |
M4083K |
possibly damaging |
Het |
Aldh1l1 |
A |
T |
6: 90,575,241 (GRCm39) |
I843F |
probably damaging |
Het |
Ankhd1 |
GGCGGC |
GGCGGCTGCGGC |
18: 36,693,962 (GRCm39) |
|
probably benign |
Het |
Arid1b |
GCG |
GCGCCG |
17: 5,045,869 (GRCm39) |
|
probably benign |
Het |
B4galnt4 |
T |
C |
7: 140,650,609 (GRCm39) |
|
probably null |
Het |
Blm |
C |
CTCCTCCTCCTAG |
7: 80,162,681 (GRCm39) |
|
probably null |
Het |
Btg3 |
A |
G |
16: 78,129,836 (GRCm39) |
*52W |
probably null |
Het |
Cc2d1a |
T |
C |
8: 84,861,298 (GRCm39) |
T796A |
probably damaging |
Het |
Cd200r1 |
T |
C |
16: 44,610,374 (GRCm39) |
S161P |
possibly damaging |
Het |
Cenpj |
A |
G |
14: 56,767,505 (GRCm39) |
|
probably null |
Het |
Cfap251 |
G |
GGAT |
5: 123,392,317 (GRCm39) |
|
probably benign |
Het |
Chd9 |
A |
G |
8: 91,760,578 (GRCm39) |
T2108A |
possibly damaging |
Het |
Cherp |
TGGAGCG |
T |
8: 73,215,903 (GRCm39) |
|
probably benign |
Het |
Cnot11 |
T |
C |
1: 39,581,575 (GRCm39) |
V372A |
probably damaging |
Het |
Cntnap5b |
T |
C |
1: 100,091,795 (GRCm39) |
C179R |
probably damaging |
Het |
Cntrl |
T |
A |
2: 35,060,512 (GRCm39) |
N1901K |
probably benign |
Het |
Coil |
CTGG |
C |
11: 88,872,656 (GRCm39) |
|
probably benign |
Het |
Col1a1 |
A |
G |
11: 94,833,866 (GRCm39) |
D488G |
probably damaging |
Het |
Coro1a |
T |
C |
7: 126,301,024 (GRCm39) |
H130R |
probably damaging |
Het |
Crybg3 |
A |
C |
16: 59,377,067 (GRCm39) |
S1396A |
possibly damaging |
Het |
Csf2rb2 |
A |
G |
15: 78,176,126 (GRCm39) |
I259T |
probably benign |
Het |
Cyp1a2 |
G |
T |
9: 57,589,253 (GRCm39) |
P187Q |
probably damaging |
Het |
Cyp3a13 |
CATTATT |
CATT |
5: 137,892,525 (GRCm39) |
|
probably null |
Het |
Dcun1d3 |
T |
C |
7: 119,458,726 (GRCm39) |
E103G |
possibly damaging |
Het |
Dmkn |
T |
A |
7: 30,469,129 (GRCm39) |
|
probably null |
Het |
Dna2 |
T |
C |
10: 62,802,474 (GRCm39) |
L864P |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,513,374 (GRCm39) |
M1909K |
probably benign |
Het |
Dspp |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
5: 104,326,227 (GRCm39) |
|
probably benign |
Het |
Ecrg4 |
TTCTGTA |
T |
1: 43,776,352 (GRCm39) |
|
probably benign |
Het |
Efna5 |
T |
C |
17: 62,920,389 (GRCm39) |
S163G |
probably benign |
Het |
Entpd2 |
CTT |
CTTT |
2: 25,290,907 (GRCm39) |
|
probably null |
Het |
Ercc4 |
C |
T |
16: 12,941,371 (GRCm39) |
S253L |
possibly damaging |
Het |
Flywch1 |
ACCCA |
ACCCAATTCTGGTGTGGGGAGGCTACGTACTCTCCCA |
17: 23,981,138 (GRCm39) |
|
probably null |
Het |
Flywch1 |
CCTGGTGT |
CCTGGTGTGGGGAGGCTACGTACTCACCCACTTCTGGTGT |
17: 23,981,145 (GRCm39) |
|
probably null |
Het |
Folh1 |
T |
C |
7: 86,424,895 (GRCm39) |
T25A |
probably benign |
Het |
Foxi3 |
C |
A |
6: 70,937,845 (GRCm39) |
T359K |
possibly damaging |
Het |
Gab3 |
TTC |
TTCATC |
X: 74,043,631 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,602 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,617 (GRCm39) |
|
probably benign |
Het |
Gba2 |
G |
T |
4: 43,569,894 (GRCm39) |
L440M |
probably damaging |
Het |
Gm14412 |
T |
A |
2: 177,007,494 (GRCm39) |
N134Y |
possibly damaging |
Het |
Gpr88 |
A |
G |
3: 116,046,018 (GRCm39) |
S98P |
probably benign |
Het |
Il1r1 |
A |
G |
1: 40,352,438 (GRCm39) |
Y539C |
probably damaging |
Het |
Iqcf4 |
TTTCCTTTTCCTTTT |
TTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTCTTCCTTTTCCTTTT |
9: 106,447,808 (GRCm39) |
|
probably benign |
Het |
Lce1m |
CTGCT |
CTGCTTCCACTGTTGCT |
3: 92,925,451 (GRCm39) |
|
probably benign |
Het |
Lkaaear1 |
T |
TATCTCCAGCTCC |
2: 181,339,352 (GRCm39) |
|
probably benign |
Het |
Lkaaear1 |
CAGCTCCAGCTCCAGCTCCAGCTC |
CAGCTCCAGCTCTAGCTCCAGCTCCAGCTCCAGCTC |
2: 181,339,370 (GRCm39) |
|
probably benign |
Het |
Ltb4r1 |
T |
A |
14: 56,005,426 (GRCm39) |
L243Q |
possibly damaging |
Het |
Man2a1 |
T |
A |
17: 65,019,248 (GRCm39) |
V704D |
probably damaging |
Het |
Map1a |
CTCCAGCTCCA |
CTCCAGCTCCAGCTCCAGCTCCAGCTCCAGTTCCAGCTCCA |
2: 121,136,789 (GRCm39) |
|
probably benign |
Het |
Mcu |
G |
T |
10: 59,326,938 (GRCm39) |
A63E |
probably benign |
Het |
Mrps31 |
A |
T |
8: 22,909,880 (GRCm39) |
D182V |
possibly damaging |
Het |
Naip1 |
A |
T |
13: 100,562,642 (GRCm39) |
M841K |
probably benign |
Het |
Ndufab1 |
T |
C |
7: 121,695,861 (GRCm39) |
K88E |
possibly damaging |
Het |
Nlrp5 |
A |
C |
7: 23,117,586 (GRCm39) |
I437L |
probably benign |
Het |
Nnt |
C |
T |
13: 119,533,393 (GRCm39) |
V91M |
probably damaging |
Het |
Nusap1 |
TACACGTTAGCAGTGAGGAGCAAGCTGAGA |
TACACGTTAGCAGTGAGGAGCAAGCTGAGAGACACGTTAGCAGTGAGGAGCAAGCTGAGA |
2: 119,458,062 (GRCm39) |
|
probably benign |
Het |
Nynrin |
T |
G |
14: 56,103,658 (GRCm39) |
|
probably null |
Het |
Or12k5 |
T |
G |
2: 36,895,186 (GRCm39) |
T147P |
probably damaging |
Het |
Or5ak22 |
C |
A |
2: 85,230,137 (GRCm39) |
A247S |
probably damaging |
Het |
Or6c204 |
T |
A |
10: 129,022,562 (GRCm39) |
I243F |
probably damaging |
Het |
Osbpl8 |
A |
G |
10: 111,112,328 (GRCm39) |
K481R |
possibly damaging |
Het |
Padi6 |
T |
C |
4: 140,457,054 (GRCm39) |
D540G |
probably damaging |
Het |
Pcmtd1 |
T |
C |
1: 7,225,329 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
TTTTTGTTTT |
TTTTTGTTTTGGTTTTGTTTT |
4: 134,006,679 (GRCm39) |
|
probably null |
Het |
Phospho1 |
T |
C |
11: 95,721,881 (GRCm39) |
Y184H |
probably damaging |
Het |
Pi4ka |
T |
A |
16: 17,115,097 (GRCm39) |
R1431W |
|
Het |
Plxdc1 |
T |
A |
11: 97,869,504 (GRCm39) |
H28L |
probably benign |
Het |
Pnma8a |
ACCTCATGATGCACCTGCTTCAACA |
ACCTCATGATGCACCTGCTTCAACACCTCATGATGCACCTGCTTCAACA |
7: 16,695,349 (GRCm39) |
|
probably benign |
Het |
Ppp1r7 |
T |
C |
1: 93,274,011 (GRCm39) |
|
probably null |
Het |
Ppp1r9a |
T |
A |
6: 4,906,657 (GRCm39) |
V404E |
probably damaging |
Het |
Scfd1 |
T |
A |
12: 51,469,756 (GRCm39) |
S434T |
probably benign |
Het |
Six5 |
A |
G |
7: 18,828,862 (GRCm39) |
S101G |
probably benign |
Het |
Slc6a4 |
C |
A |
11: 76,910,008 (GRCm39) |
T421K |
probably damaging |
Het |
Smarcd3 |
C |
A |
5: 24,801,068 (GRCm39) |
R113L |
probably damaging |
Het |
Son |
T |
A |
16: 91,456,257 (GRCm39) |
M1668K |
possibly damaging |
Het |
Spmap2l |
CTCCCCAGTCCCGCAAGGCCAG |
CTCCCCAGTCCCGCAAGGCCAGCGATCGTCCCCAGTCCCGCAAGGCCAG |
5: 77,164,255 (GRCm39) |
|
probably benign |
Het |
Tcf25 |
A |
G |
8: 124,122,369 (GRCm39) |
D434G |
probably benign |
Het |
Tcof1 |
CCAGAGATCCCC |
CCAGAGATCCCCGTGGCTGCCGAGATGGGCACTTTCACAGAGATCCCC |
18: 60,966,640 (GRCm39) |
|
probably benign |
Het |
Tep1 |
A |
G |
14: 51,098,402 (GRCm39) |
V463A |
possibly damaging |
Het |
Trav15-2-dv6-2 |
GGGAG |
GGGAGGAG |
14: 53,887,207 (GRCm39) |
|
probably benign |
Het |
Trav15-2-dv6-2 |
AAG |
AAGCAG |
14: 53,887,212 (GRCm39) |
|
probably benign |
Het |
Trav15-2-dv6-2 |
GGAG |
GGAGGAG |
14: 53,887,208 (GRCm39) |
|
probably benign |
Het |
Trim24 |
A |
G |
6: 37,930,471 (GRCm39) |
K642E |
possibly damaging |
Het |
Trim33 |
GGCCCCCGC |
GGC |
3: 103,187,533 (GRCm39) |
|
probably benign |
Het |
Triobp |
CTCCCTGTGCCCAACGG |
CTCCCTGTGCCCAACGGAACAACCCCAGGATTCCCTGTGCCCAACGG |
15: 78,851,244 (GRCm39) |
|
probably benign |
Het |
Trmu |
G |
T |
15: 85,776,770 (GRCm39) |
V161L |
possibly damaging |
Het |
Try4 |
T |
A |
6: 41,282,297 (GRCm39) |
C206S |
probably damaging |
Het |
Usp2 |
TTCACTTAC |
TTCACTTACTCATGTGACCTGTTCGTCACTTAC |
9: 44,000,418 (GRCm39) |
|
probably benign |
Het |
Vmn1r62 |
A |
T |
7: 5,678,669 (GRCm39) |
M117L |
probably benign |
Het |
Vmn2r104 |
A |
T |
17: 20,268,302 (GRCm39) |
Y56N |
probably benign |
Het |
Xxylt1 |
C |
T |
16: 30,869,498 (GRCm39) |
D201N |
possibly damaging |
Het |
Zfp563 |
T |
A |
17: 33,323,999 (GRCm39) |
I198K |
probably benign |
Het |
Zfp612 |
T |
A |
8: 110,816,174 (GRCm39) |
C460* |
probably null |
Het |
Zfp691 |
G |
A |
4: 119,027,932 (GRCm39) |
T100M |
probably benign |
Het |
Zfp773 |
A |
T |
7: 7,135,689 (GRCm39) |
C302* |
probably null |
Het |
Zmat2 |
A |
G |
18: 36,930,936 (GRCm39) |
E154G |
probably damaging |
Het |
Zw10 |
T |
A |
9: 48,972,220 (GRCm39) |
I132N |
possibly damaging |
Het |
|
Other mutations in Mslnl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:Mslnl
|
APN |
17 |
25,962,641 (GRCm39) |
unclassified |
probably benign |
|
IGL01629:Mslnl
|
APN |
17 |
25,963,749 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02084:Mslnl
|
APN |
17 |
25,965,125 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02408:Mslnl
|
APN |
17 |
25,966,972 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02726:Mslnl
|
APN |
17 |
25,963,077 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03387:Mslnl
|
APN |
17 |
25,963,051 (GRCm39) |
missense |
probably benign |
0.06 |
R0561:Mslnl
|
UTSW |
17 |
25,962,177 (GRCm39) |
nonsense |
probably null |
|
R0881:Mslnl
|
UTSW |
17 |
25,961,939 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1295:Mslnl
|
UTSW |
17 |
25,962,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Mslnl
|
UTSW |
17 |
25,962,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R1582:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1629:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1630:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1631:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1632:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1794:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1850:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1866:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1876:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1914:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2166:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2241:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2243:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2247:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2282:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2284:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2852:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2867:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2867:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2877:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2878:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2919:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R2920:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3026:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3405:Mslnl
|
UTSW |
17 |
25,965,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R3406:Mslnl
|
UTSW |
17 |
25,965,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R3411:Mslnl
|
UTSW |
17 |
25,963,491 (GRCm39) |
missense |
probably benign |
0.05 |
R3434:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3546:Mslnl
|
UTSW |
17 |
25,963,943 (GRCm39) |
missense |
probably damaging |
0.98 |
R3612:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3729:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3730:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3802:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3804:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3894:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R3895:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4454:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4455:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4456:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4457:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4561:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4562:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4564:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4600:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4601:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4610:Mslnl
|
UTSW |
17 |
25,961,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R4704:Mslnl
|
UTSW |
17 |
25,957,952 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5155:Mslnl
|
UTSW |
17 |
25,957,942 (GRCm39) |
nonsense |
probably null |
|
R5257:Mslnl
|
UTSW |
17 |
25,965,139 (GRCm39) |
missense |
probably benign |
0.00 |
R5456:Mslnl
|
UTSW |
17 |
25,962,133 (GRCm39) |
missense |
probably damaging |
0.98 |
R5645:Mslnl
|
UTSW |
17 |
25,956,816 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6007:Mslnl
|
UTSW |
17 |
25,965,749 (GRCm39) |
missense |
probably benign |
0.00 |
R6083:Mslnl
|
UTSW |
17 |
25,956,876 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6142:Mslnl
|
UTSW |
17 |
25,963,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R6761:Mslnl
|
UTSW |
17 |
25,965,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Mslnl
|
UTSW |
17 |
25,962,186 (GRCm39) |
missense |
probably benign |
0.03 |
R7156:Mslnl
|
UTSW |
17 |
25,962,184 (GRCm39) |
missense |
probably benign |
0.20 |
R7467:Mslnl
|
UTSW |
17 |
25,955,895 (GRCm39) |
start codon destroyed |
probably benign |
0.33 |
R7687:Mslnl
|
UTSW |
17 |
25,962,157 (GRCm39) |
missense |
probably damaging |
0.97 |
R7807:Mslnl
|
UTSW |
17 |
25,965,751 (GRCm39) |
missense |
probably benign |
0.03 |
R8682:Mslnl
|
UTSW |
17 |
25,965,962 (GRCm39) |
missense |
probably benign |
|
R8735:Mslnl
|
UTSW |
17 |
25,964,062 (GRCm39) |
missense |
probably benign |
0.09 |
R8742:Mslnl
|
UTSW |
17 |
25,964,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Mslnl
|
UTSW |
17 |
25,961,694 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9264:Mslnl
|
UTSW |
17 |
25,961,506 (GRCm39) |
intron |
probably benign |
|
|