Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921536K21Rik |
T |
A |
11: 3,844,933 (GRCm39) |
E52V |
probably benign |
Het |
4930516K23Rik |
G |
A |
7: 103,708,083 (GRCm39) |
T242M |
probably damaging |
Het |
Abcg5 |
T |
A |
17: 84,990,253 (GRCm39) |
I17F |
probably benign |
Het |
Adam25 |
T |
A |
8: 41,207,710 (GRCm39) |
Y325* |
probably null |
Het |
Adamts16 |
C |
T |
13: 70,939,910 (GRCm39) |
|
probably benign |
Het |
Akr1b1 |
A |
T |
6: 34,289,639 (GRCm39) |
V57E |
probably benign |
Het |
Api5 |
A |
G |
2: 94,255,374 (GRCm39) |
L267P |
probably damaging |
Het |
Asap3 |
T |
C |
4: 135,963,726 (GRCm39) |
Y329H |
probably benign |
Het |
Atp13a4 |
C |
T |
16: 29,273,592 (GRCm39) |
R442K |
|
Het |
Cadps2 |
T |
C |
6: 23,302,300 (GRCm39) |
D1129G |
probably benign |
Het |
Cd79b |
T |
A |
11: 106,203,632 (GRCm39) |
Q145L |
probably benign |
Het |
Cdh23 |
C |
T |
10: 60,140,908 (GRCm39) |
E3147K |
probably damaging |
Het |
Cfap251 |
A |
G |
5: 123,424,481 (GRCm39) |
D722G |
possibly damaging |
Het |
Col4a4 |
A |
G |
1: 82,431,533 (GRCm39) |
W1584R |
unknown |
Het |
Cops8 |
T |
C |
1: 90,532,155 (GRCm39) |
L46P |
probably damaging |
Het |
Cpne1 |
T |
C |
2: 155,913,965 (GRCm39) |
Y146C |
probably benign |
Het |
Ctdnep1 |
T |
A |
11: 69,875,311 (GRCm39) |
V80E |
probably damaging |
Het |
Cyp4a32 |
T |
C |
4: 115,468,460 (GRCm39) |
V314A |
probably damaging |
Het |
Dlgap3 |
C |
A |
4: 127,127,463 (GRCm39) |
H710Q |
probably damaging |
Het |
Dnah9 |
T |
C |
11: 65,802,747 (GRCm39) |
M3448V |
probably benign |
Het |
E030018B13Rik |
C |
A |
7: 63,569,727 (GRCm39) |
Q84K |
unknown |
Het |
Efna5 |
A |
G |
17: 63,188,053 (GRCm39) |
S25P |
possibly damaging |
Het |
Egfl8 |
T |
G |
17: 34,833,751 (GRCm39) |
T76P |
probably damaging |
Het |
Endod1 |
A |
G |
9: 14,268,942 (GRCm39) |
L181P |
probably damaging |
Het |
Epha3 |
A |
G |
16: 63,472,838 (GRCm39) |
L349P |
possibly damaging |
Het |
Fam161b |
T |
A |
12: 84,395,056 (GRCm39) |
T553S |
probably benign |
Het |
Fmnl1 |
T |
C |
11: 103,087,967 (GRCm39) |
F981L |
unknown |
Het |
Galr2 |
T |
A |
11: 116,173,973 (GRCm39) |
V201E |
probably damaging |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Greb1l |
T |
C |
18: 10,541,825 (GRCm39) |
S1191P |
probably benign |
Het |
Hmg20b |
T |
C |
10: 81,184,821 (GRCm39) |
R84G |
probably damaging |
Het |
Inppl1 |
T |
C |
7: 101,472,593 (GRCm39) |
D1234G |
possibly damaging |
Het |
Insl5 |
A |
G |
4: 102,883,760 (GRCm39) |
S54P |
probably damaging |
Het |
Itpr1 |
T |
A |
6: 108,355,159 (GRCm39) |
F483L |
possibly damaging |
Het |
Kif21a |
T |
C |
15: 90,855,930 (GRCm39) |
E609G |
probably benign |
Het |
Kpna7 |
A |
T |
5: 144,941,840 (GRCm39) |
V150D |
probably damaging |
Het |
L1td1 |
T |
A |
4: 98,622,175 (GRCm39) |
C246S |
possibly damaging |
Het |
Laptm4a |
T |
A |
12: 8,988,139 (GRCm39) |
M292K |
possibly damaging |
Het |
Lefty2 |
C |
G |
1: 180,725,043 (GRCm39) |
P258A |
possibly damaging |
Het |
Map4k1 |
G |
A |
7: 28,701,052 (GRCm39) |
V719M |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,463,590 (GRCm39) |
H1292Q |
probably benign |
Het |
Nfkbia |
C |
T |
12: 55,537,340 (GRCm39) |
G250S |
probably damaging |
Het |
Nkain3 |
T |
C |
4: 20,245,902 (GRCm39) |
T163A |
unknown |
Het |
Npcd |
T |
C |
15: 79,713,163 (GRCm39) |
E88G |
probably benign |
Het |
Oas1f |
A |
T |
5: 120,989,556 (GRCm39) |
Y165F |
probably benign |
Het |
Or10d4 |
T |
A |
9: 39,580,737 (GRCm39) |
L128* |
probably null |
Het |
Or51aa5 |
A |
G |
7: 103,167,030 (GRCm39) |
I187T |
possibly damaging |
Het |
Or52e2 |
T |
C |
7: 102,804,660 (GRCm39) |
D98G |
probably benign |
Het |
Phtf2 |
T |
C |
5: 21,008,275 (GRCm39) |
I135M |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,125,604 (GRCm39) |
E1177G |
|
Het |
Polr3gl |
A |
T |
3: 96,485,833 (GRCm39) |
D214E |
probably damaging |
Het |
Pramel25 |
C |
T |
4: 143,519,322 (GRCm39) |
Q28* |
probably null |
Het |
Pramel51 |
T |
C |
12: 88,143,952 (GRCm39) |
E295G |
probably benign |
Het |
Prkar1a |
C |
A |
11: 109,556,744 (GRCm39) |
Q275K |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,054,039 (GRCm39) |
|
probably null |
Het |
Pwwp2a |
C |
A |
11: 43,596,344 (GRCm39) |
P503Q |
probably damaging |
Het |
Rad17 |
T |
C |
13: 100,754,192 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
T |
C |
11: 54,570,065 (GRCm39) |
L1146S |
probably benign |
Het |
Rara |
C |
A |
11: 98,864,452 (GRCm39) |
Q460K |
unknown |
Het |
Rassf4 |
C |
T |
6: 116,638,897 (GRCm39) |
|
probably benign |
Het |
Rere |
A |
G |
4: 150,696,471 (GRCm39) |
D492G |
unknown |
Het |
Selenon |
T |
G |
4: 134,268,153 (GRCm39) |
K460T |
possibly damaging |
Het |
Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
Slc35e1 |
T |
C |
8: 73,241,988 (GRCm39) |
T245A |
probably benign |
Het |
Stat4 |
C |
T |
1: 52,144,892 (GRCm39) |
A726V |
probably benign |
Het |
Stim1 |
G |
T |
7: 102,070,597 (GRCm39) |
V277L |
probably damaging |
Het |
Strbp |
A |
G |
2: 37,514,503 (GRCm39) |
|
probably null |
Het |
Tln2 |
T |
C |
9: 67,174,105 (GRCm39) |
Y860C |
probably damaging |
Het |
Tmod4 |
T |
A |
3: 95,033,289 (GRCm39) |
|
probably null |
Het |
Tpm3-rs7 |
T |
C |
14: 113,552,493 (GRCm39) |
V129A |
probably benign |
Het |
Trp53bp2 |
C |
T |
1: 182,273,971 (GRCm39) |
P41S |
|
Het |
Tubal3 |
G |
A |
13: 3,983,428 (GRCm39) |
D403N |
probably damaging |
Het |
Zfp369 |
T |
C |
13: 65,444,044 (GRCm39) |
S396P |
possibly damaging |
Het |
Zfp976 |
G |
A |
7: 42,262,575 (GRCm39) |
H422Y |
possibly damaging |
Het |
|
Other mutations in Cttnbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00954:Cttnbp2
|
APN |
6 |
18,381,061 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01014:Cttnbp2
|
APN |
6 |
18,423,894 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01148:Cttnbp2
|
APN |
6 |
18,382,817 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01903:Cttnbp2
|
APN |
6 |
18,501,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01906:Cttnbp2
|
APN |
6 |
18,378,375 (GRCm39) |
nonsense |
probably null |
|
IGL01994:Cttnbp2
|
APN |
6 |
18,420,814 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02212:Cttnbp2
|
APN |
6 |
18,382,748 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02696:Cttnbp2
|
APN |
6 |
18,434,128 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02813:Cttnbp2
|
APN |
6 |
18,367,537 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02864:Cttnbp2
|
APN |
6 |
18,374,548 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03309:Cttnbp2
|
APN |
6 |
18,381,035 (GRCm39) |
missense |
probably damaging |
0.98 |
Feelers
|
UTSW |
6 |
18,405,278 (GRCm39) |
splice site |
probably null |
|
warning
|
UTSW |
6 |
18,375,952 (GRCm39) |
missense |
probably damaging |
1.00 |
BB009:Cttnbp2
|
UTSW |
6 |
18,427,532 (GRCm39) |
missense |
probably damaging |
1.00 |
BB019:Cttnbp2
|
UTSW |
6 |
18,427,532 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Cttnbp2
|
UTSW |
6 |
18,367,457 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4449:Cttnbp2
|
UTSW |
6 |
18,367,461 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4548:Cttnbp2
|
UTSW |
6 |
18,367,462 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4589:Cttnbp2
|
UTSW |
6 |
18,367,457 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4976:Cttnbp2
|
UTSW |
6 |
18,367,466 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4976:Cttnbp2
|
UTSW |
6 |
18,367,460 (GRCm39) |
utr 3 prime |
probably benign |
|
R0165:Cttnbp2
|
UTSW |
6 |
18,435,409 (GRCm39) |
nonsense |
probably null |
|
R0382:Cttnbp2
|
UTSW |
6 |
18,435,342 (GRCm39) |
missense |
probably benign |
0.39 |
R0464:Cttnbp2
|
UTSW |
6 |
18,408,690 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0550:Cttnbp2
|
UTSW |
6 |
18,435,308 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0571:Cttnbp2
|
UTSW |
6 |
18,381,102 (GRCm39) |
missense |
probably benign |
|
R0627:Cttnbp2
|
UTSW |
6 |
18,367,372 (GRCm39) |
makesense |
probably null |
|
R0788:Cttnbp2
|
UTSW |
6 |
18,423,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R0826:Cttnbp2
|
UTSW |
6 |
18,405,177 (GRCm39) |
splice site |
probably benign |
|
R1319:Cttnbp2
|
UTSW |
6 |
18,434,629 (GRCm39) |
missense |
probably benign |
0.00 |
R1476:Cttnbp2
|
UTSW |
6 |
18,434,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Cttnbp2
|
UTSW |
6 |
18,375,974 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1596:Cttnbp2
|
UTSW |
6 |
18,408,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R1607:Cttnbp2
|
UTSW |
6 |
18,435,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Cttnbp2
|
UTSW |
6 |
18,435,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Cttnbp2
|
UTSW |
6 |
18,408,656 (GRCm39) |
missense |
probably benign |
0.39 |
R1661:Cttnbp2
|
UTSW |
6 |
18,434,982 (GRCm39) |
missense |
probably benign |
0.20 |
R1665:Cttnbp2
|
UTSW |
6 |
18,434,982 (GRCm39) |
missense |
probably benign |
0.20 |
R1834:Cttnbp2
|
UTSW |
6 |
18,501,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Cttnbp2
|
UTSW |
6 |
18,408,601 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Cttnbp2
|
UTSW |
6 |
18,378,412 (GRCm39) |
missense |
probably benign |
|
R2018:Cttnbp2
|
UTSW |
6 |
18,434,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2169:Cttnbp2
|
UTSW |
6 |
18,426,096 (GRCm39) |
missense |
probably benign |
0.00 |
R2175:Cttnbp2
|
UTSW |
6 |
18,434,828 (GRCm39) |
splice site |
probably null |
|
R2202:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2203:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2204:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2205:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2371:Cttnbp2
|
UTSW |
6 |
18,380,603 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2416:Cttnbp2
|
UTSW |
6 |
18,448,285 (GRCm39) |
missense |
probably damaging |
0.99 |
R3414:Cttnbp2
|
UTSW |
6 |
18,389,204 (GRCm39) |
missense |
probably benign |
|
R3617:Cttnbp2
|
UTSW |
6 |
18,414,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R3861:Cttnbp2
|
UTSW |
6 |
18,423,832 (GRCm39) |
missense |
probably benign |
0.11 |
R3862:Cttnbp2
|
UTSW |
6 |
18,434,905 (GRCm39) |
missense |
probably benign |
0.02 |
R3940:Cttnbp2
|
UTSW |
6 |
18,420,974 (GRCm39) |
missense |
probably benign |
0.34 |
R3941:Cttnbp2
|
UTSW |
6 |
18,427,452 (GRCm39) |
missense |
probably benign |
0.11 |
R4097:Cttnbp2
|
UTSW |
6 |
18,420,871 (GRCm39) |
missense |
probably benign |
|
R4211:Cttnbp2
|
UTSW |
6 |
18,427,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Cttnbp2
|
UTSW |
6 |
18,514,703 (GRCm39) |
missense |
probably benign |
0.00 |
R4367:Cttnbp2
|
UTSW |
6 |
18,405,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Cttnbp2
|
UTSW |
6 |
18,434,037 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4652:Cttnbp2
|
UTSW |
6 |
18,434,037 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4660:Cttnbp2
|
UTSW |
6 |
18,406,536 (GRCm39) |
missense |
probably benign |
0.05 |
R4975:Cttnbp2
|
UTSW |
6 |
18,406,525 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5064:Cttnbp2
|
UTSW |
6 |
18,448,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R5205:Cttnbp2
|
UTSW |
6 |
18,427,432 (GRCm39) |
splice site |
probably benign |
|
R5305:Cttnbp2
|
UTSW |
6 |
18,381,097 (GRCm39) |
missense |
probably benign |
|
R5484:Cttnbp2
|
UTSW |
6 |
18,427,689 (GRCm39) |
intron |
probably benign |
|
R5629:Cttnbp2
|
UTSW |
6 |
18,405,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Cttnbp2
|
UTSW |
6 |
18,414,298 (GRCm39) |
missense |
probably benign |
0.00 |
R5766:Cttnbp2
|
UTSW |
6 |
18,381,032 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5942:Cttnbp2
|
UTSW |
6 |
18,448,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6073:Cttnbp2
|
UTSW |
6 |
18,448,368 (GRCm39) |
missense |
probably benign |
0.01 |
R6073:Cttnbp2
|
UTSW |
6 |
18,434,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Cttnbp2
|
UTSW |
6 |
18,434,950 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6545:Cttnbp2
|
UTSW |
6 |
18,405,278 (GRCm39) |
splice site |
probably null |
|
R6858:Cttnbp2
|
UTSW |
6 |
18,448,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:Cttnbp2
|
UTSW |
6 |
18,435,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Cttnbp2
|
UTSW |
6 |
18,448,446 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7141:Cttnbp2
|
UTSW |
6 |
18,380,467 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Cttnbp2
|
UTSW |
6 |
18,375,943 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7465:Cttnbp2
|
UTSW |
6 |
18,501,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R7500:Cttnbp2
|
UTSW |
6 |
18,378,419 (GRCm39) |
missense |
probably benign |
0.00 |
R7534:Cttnbp2
|
UTSW |
6 |
18,420,764 (GRCm39) |
critical splice donor site |
probably null |
|
R7646:Cttnbp2
|
UTSW |
6 |
18,375,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Cttnbp2
|
UTSW |
6 |
18,382,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Cttnbp2
|
UTSW |
6 |
18,514,734 (GRCm39) |
start codon destroyed |
possibly damaging |
0.82 |
R7809:Cttnbp2
|
UTSW |
6 |
18,434,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R7816:Cttnbp2
|
UTSW |
6 |
18,448,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7932:Cttnbp2
|
UTSW |
6 |
18,427,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8011:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8014:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8015:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8095:Cttnbp2
|
UTSW |
6 |
18,435,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R8754:Cttnbp2
|
UTSW |
6 |
18,434,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8769:Cttnbp2
|
UTSW |
6 |
18,376,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R8836:Cttnbp2
|
UTSW |
6 |
18,375,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8886:Cttnbp2
|
UTSW |
6 |
18,414,298 (GRCm39) |
missense |
probably benign |
0.00 |
R8931:Cttnbp2
|
UTSW |
6 |
18,434,808 (GRCm39) |
missense |
probably benign |
0.00 |
R8956:Cttnbp2
|
UTSW |
6 |
18,434,165 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9005:Cttnbp2
|
UTSW |
6 |
18,434,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R9141:Cttnbp2
|
UTSW |
6 |
18,429,138 (GRCm39) |
nonsense |
probably null |
|
R9194:Cttnbp2
|
UTSW |
6 |
18,434,850 (GRCm39) |
missense |
probably benign |
0.00 |
R9425:Cttnbp2
|
UTSW |
6 |
18,423,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Cttnbp2
|
UTSW |
6 |
18,427,467 (GRCm39) |
nonsense |
probably null |
|
R9563:Cttnbp2
|
UTSW |
6 |
18,367,382 (GRCm39) |
missense |
probably benign |
0.03 |
R9661:Cttnbp2
|
UTSW |
6 |
18,429,151 (GRCm39) |
missense |
|
|
R9763:Cttnbp2
|
UTSW |
6 |
18,435,240 (GRCm39) |
missense |
probably benign |
|
R9790:Cttnbp2
|
UTSW |
6 |
18,376,027 (GRCm39) |
missense |
probably benign |
0.03 |
R9791:Cttnbp2
|
UTSW |
6 |
18,376,027 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Cttnbp2
|
UTSW |
6 |
18,408,724 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Cttnbp2
|
UTSW |
6 |
18,408,708 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Cttnbp2
|
UTSW |
6 |
18,501,959 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cttnbp2
|
UTSW |
6 |
18,420,835 (GRCm39) |
missense |
possibly damaging |
0.83 |
|