Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810408A11Rik |
C |
T |
11: 69,791,403 (GRCm39) |
V59I |
possibly damaging |
Het |
4930544M13Rik |
T |
G |
13: 114,744,183 (GRCm39) |
|
noncoding transcript |
Het |
Abca13 |
A |
T |
11: 9,492,077 (GRCm39) |
K4373* |
probably null |
Het |
Abtb2 |
A |
T |
2: 103,513,820 (GRCm39) |
T410S |
probably benign |
Het |
Adamts13 |
T |
C |
2: 26,873,142 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
C |
G |
12: 112,742,183 (GRCm39) |
D630H |
probably damaging |
Het |
Aox3 |
T |
C |
1: 58,191,725 (GRCm39) |
S426P |
probably damaging |
Het |
Atxn10 |
C |
T |
15: 85,271,260 (GRCm39) |
S266F |
probably benign |
Het |
B4galnt4 |
G |
T |
7: 140,647,634 (GRCm39) |
M407I |
probably damaging |
Het |
B4galnt4 |
T |
A |
7: 140,644,470 (GRCm39) |
|
probably null |
Het |
Bclaf1 |
T |
A |
10: 20,197,872 (GRCm39) |
|
probably benign |
Het |
C4b |
C |
T |
17: 34,955,864 (GRCm39) |
|
probably null |
Het |
Cdc42bpg |
T |
C |
19: 6,361,365 (GRCm39) |
F297S |
probably damaging |
Het |
Cdh10 |
A |
T |
15: 19,013,664 (GRCm39) |
T755S |
probably benign |
Het |
Ceacam12 |
T |
A |
7: 17,811,305 (GRCm39) |
|
probably null |
Het |
Cfap65 |
C |
A |
1: 74,956,454 (GRCm39) |
V1042F |
possibly damaging |
Het |
Cfap77 |
T |
C |
2: 28,875,844 (GRCm39) |
I89V |
probably benign |
Het |
Cfh |
T |
C |
1: 140,014,125 (GRCm39) |
D688G |
probably benign |
Het |
Clip1 |
C |
G |
5: 123,721,664 (GRCm39) |
A1182P |
probably damaging |
Het |
Cyp2b10 |
T |
A |
7: 25,614,921 (GRCm39) |
Y309* |
probably null |
Het |
Dcaf5 |
T |
C |
12: 80,385,858 (GRCm39) |
E756G |
probably benign |
Het |
Dennd1c |
T |
A |
17: 57,373,428 (GRCm39) |
R682* |
probably null |
Het |
Eml6 |
C |
A |
11: 29,727,052 (GRCm39) |
E1319* |
probably null |
Het |
Erap1 |
T |
C |
13: 74,838,766 (GRCm39) |
I904T |
probably damaging |
Het |
Eri1 |
A |
T |
8: 35,943,673 (GRCm39) |
I207N |
possibly damaging |
Het |
Farp1 |
G |
A |
14: 121,514,469 (GRCm39) |
A933T |
probably damaging |
Het |
Fcna |
T |
A |
2: 25,515,353 (GRCm39) |
Q210L |
probably benign |
Het |
Fhad1 |
A |
T |
4: 141,643,378 (GRCm39) |
|
probably null |
Het |
Fut8 |
T |
G |
12: 77,440,603 (GRCm39) |
Y197D |
probably damaging |
Het |
Garem1 |
G |
A |
18: 21,262,825 (GRCm39) |
T663I |
probably benign |
Het |
Gfm2 |
T |
C |
13: 97,301,546 (GRCm39) |
S450P |
probably damaging |
Het |
Gstk1 |
T |
G |
6: 42,222,938 (GRCm39) |
|
probably benign |
Het |
Helz2 |
C |
T |
2: 180,879,210 (GRCm39) |
A803T |
probably damaging |
Het |
Igsf9 |
T |
A |
1: 172,319,455 (GRCm39) |
I280N |
probably damaging |
Het |
Klhl10 |
A |
G |
11: 100,336,669 (GRCm39) |
K219E |
probably benign |
Het |
L3mbtl4 |
T |
A |
17: 68,768,558 (GRCm39) |
V222D |
probably damaging |
Het |
Lrrc9 |
A |
T |
12: 72,546,453 (GRCm39) |
N1214Y |
probably damaging |
Het |
Ltbp2 |
C |
T |
12: 84,840,414 (GRCm39) |
E1051K |
possibly damaging |
Het |
Mettl17 |
T |
C |
14: 52,122,440 (GRCm39) |
F13S |
probably benign |
Het |
Mettl24 |
C |
A |
10: 40,559,413 (GRCm39) |
A21D |
possibly damaging |
Het |
Mfsd6l |
T |
A |
11: 68,447,331 (GRCm39) |
C61S |
probably benign |
Het |
Mob4 |
T |
G |
1: 55,191,899 (GRCm39) |
D204E |
probably benign |
Het |
Mtus1 |
C |
G |
8: 41,536,189 (GRCm39) |
R509T |
probably damaging |
Het |
Nlrp4a |
T |
A |
7: 26,149,844 (GRCm39) |
F484I |
possibly damaging |
Het |
Nsrp1 |
T |
C |
11: 76,941,444 (GRCm39) |
N88S |
probably benign |
Het |
Odad2 |
G |
T |
18: 7,222,564 (GRCm39) |
H568Q |
possibly damaging |
Het |
Or10d5 |
C |
T |
9: 39,861,408 (GRCm39) |
V220I |
probably benign |
Het |
Or2g25 |
T |
A |
17: 37,970,969 (GRCm39) |
H85L |
probably benign |
Het |
Or51b6b |
T |
C |
7: 103,309,678 (GRCm39) |
T260A |
probably benign |
Het |
Or6c2 |
T |
A |
10: 129,362,449 (GRCm39) |
Y118N |
probably damaging |
Het |
Parg |
A |
G |
14: 31,924,408 (GRCm39) |
N69S |
probably benign |
Het |
Pcdh9 |
A |
C |
14: 94,125,377 (GRCm39) |
N264K |
probably damaging |
Het |
Pcdhb22 |
G |
T |
18: 37,653,615 (GRCm39) |
L694F |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,248,335 (GRCm39) |
E928G |
probably damaging |
Het |
Pdzk1 |
G |
A |
3: 96,775,751 (GRCm39) |
G373D |
probably benign |
Het |
Pea15a |
A |
G |
1: 172,026,740 (GRCm39) |
I89T |
probably damaging |
Het |
Phc1 |
T |
A |
6: 122,313,964 (GRCm39) |
|
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,235,900 (GRCm39) |
C191S |
probably damaging |
Het |
Pitpnm1 |
T |
A |
19: 4,158,130 (GRCm39) |
D573E |
probably damaging |
Het |
Pld5 |
A |
G |
1: 176,102,450 (GRCm39) |
|
probably benign |
Het |
Plscr2 |
A |
T |
9: 92,173,130 (GRCm39) |
N89I |
possibly damaging |
Het |
Pm20d2 |
A |
C |
4: 33,179,293 (GRCm39) |
N315K |
probably damaging |
Het |
Pnpla1 |
T |
A |
17: 29,097,518 (GRCm39) |
M228K |
probably benign |
Het |
Prim2 |
T |
C |
1: 33,709,217 (GRCm39) |
|
probably benign |
Het |
Ralgapa2 |
A |
G |
2: 146,246,987 (GRCm39) |
|
probably benign |
Het |
Rgs22 |
G |
T |
15: 36,050,294 (GRCm39) |
H719N |
probably benign |
Het |
Ror2 |
C |
T |
13: 53,272,880 (GRCm39) |
D250N |
probably damaging |
Het |
Saal1 |
A |
G |
7: 46,349,071 (GRCm39) |
V281A |
probably benign |
Het |
Selenof |
A |
T |
3: 144,296,411 (GRCm39) |
K94N |
probably damaging |
Het |
Slamf9 |
T |
A |
1: 172,304,831 (GRCm39) |
C148* |
probably null |
Het |
Slc4a7 |
T |
C |
14: 14,772,699 (GRCm38) |
|
probably null |
Het |
Slco1a5 |
A |
G |
6: 142,180,431 (GRCm39) |
I657T |
probably benign |
Het |
St3gal2 |
A |
T |
8: 111,684,480 (GRCm39) |
H46L |
probably benign |
Het |
Sucnr1 |
T |
G |
3: 59,994,069 (GRCm39) |
M199R |
probably damaging |
Het |
Taok1 |
T |
A |
11: 77,444,500 (GRCm39) |
E525V |
probably null |
Het |
Tbc1d10c |
T |
A |
19: 4,235,445 (GRCm39) |
E298V |
probably damaging |
Het |
Tll2 |
T |
A |
19: 41,118,951 (GRCm39) |
H259L |
probably damaging |
Het |
Tpcn1 |
A |
T |
5: 120,691,554 (GRCm39) |
F300Y |
probably damaging |
Het |
Uba6 |
T |
A |
5: 86,279,197 (GRCm39) |
I642L |
probably benign |
Het |
Ubqln5 |
T |
A |
7: 103,778,829 (GRCm39) |
|
probably benign |
Het |
Vmn1r27 |
A |
T |
6: 58,192,827 (GRCm39) |
L9Q |
possibly damaging |
Het |
Vmn2r100 |
C |
T |
17: 19,741,672 (GRCm39) |
T128I |
probably benign |
Het |
Vmn2r109 |
C |
T |
17: 20,761,494 (GRCm39) |
G621D |
probably benign |
Het |
Vmn2r49 |
C |
T |
7: 9,720,352 (GRCm39) |
D380N |
probably benign |
Het |
Vps13a |
C |
T |
19: 16,655,356 (GRCm39) |
V1891I |
probably benign |
Het |
Wbp2 |
G |
T |
11: 115,971,463 (GRCm39) |
Y147* |
probably null |
Het |
Wdr46 |
T |
A |
17: 34,160,810 (GRCm39) |
N191K |
probably benign |
Het |
Wdr46 |
T |
C |
17: 34,168,373 (GRCm39) |
|
probably benign |
Het |
Wnt2 |
A |
C |
6: 18,023,285 (GRCm39) |
F121L |
probably benign |
Het |
Xpnpep1 |
T |
A |
19: 53,003,053 (GRCm39) |
D100V |
probably benign |
Het |
Xpo4 |
T |
C |
14: 57,827,559 (GRCm39) |
Y879C |
probably damaging |
Het |
Zswim4 |
A |
T |
8: 84,938,948 (GRCm39) |
V978D |
probably damaging |
Het |
|
Other mutations in Dctn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01113:Dctn1
|
APN |
6 |
83,156,879 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01450:Dctn1
|
APN |
6 |
83,171,092 (GRCm39) |
unclassified |
probably benign |
|
IGL01876:Dctn1
|
APN |
6 |
83,174,903 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Dctn1
|
APN |
6 |
83,168,326 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02554:Dctn1
|
APN |
6 |
83,159,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02668:Dctn1
|
APN |
6 |
83,168,030 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02814:Dctn1
|
APN |
6 |
83,166,896 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02818:Dctn1
|
APN |
6 |
83,169,496 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03007:Dctn1
|
APN |
6 |
83,159,690 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03065:Dctn1
|
APN |
6 |
83,169,475 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03083:Dctn1
|
APN |
6 |
83,174,466 (GRCm39) |
splice site |
probably benign |
|
IGL03394:Dctn1
|
APN |
6 |
83,168,266 (GRCm39) |
missense |
possibly damaging |
0.61 |
E0374:Dctn1
|
UTSW |
6 |
83,171,156 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03014:Dctn1
|
UTSW |
6 |
83,174,351 (GRCm39) |
intron |
probably benign |
|
PIT4812001:Dctn1
|
UTSW |
6 |
83,176,744 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0044:Dctn1
|
UTSW |
6 |
83,168,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Dctn1
|
UTSW |
6 |
83,159,614 (GRCm39) |
nonsense |
probably null |
|
R0047:Dctn1
|
UTSW |
6 |
83,159,614 (GRCm39) |
nonsense |
probably null |
|
R0057:Dctn1
|
UTSW |
6 |
83,156,874 (GRCm39) |
missense |
probably benign |
0.14 |
R0731:Dctn1
|
UTSW |
6 |
83,160,071 (GRCm39) |
missense |
probably damaging |
0.98 |
R0738:Dctn1
|
UTSW |
6 |
83,167,089 (GRCm39) |
critical splice donor site |
probably null |
|
R0755:Dctn1
|
UTSW |
6 |
83,166,059 (GRCm39) |
missense |
probably damaging |
0.96 |
R0839:Dctn1
|
UTSW |
6 |
83,167,459 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1035:Dctn1
|
UTSW |
6 |
83,167,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Dctn1
|
UTSW |
6 |
83,174,490 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1469:Dctn1
|
UTSW |
6 |
83,169,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Dctn1
|
UTSW |
6 |
83,169,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1627:Dctn1
|
UTSW |
6 |
83,172,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R1631:Dctn1
|
UTSW |
6 |
83,174,578 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1812:Dctn1
|
UTSW |
6 |
83,169,500 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1928:Dctn1
|
UTSW |
6 |
83,176,166 (GRCm39) |
splice site |
probably benign |
|
R2008:Dctn1
|
UTSW |
6 |
83,166,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R2242:Dctn1
|
UTSW |
6 |
83,176,687 (GRCm39) |
missense |
probably damaging |
0.99 |
R2259:Dctn1
|
UTSW |
6 |
83,174,568 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2422:Dctn1
|
UTSW |
6 |
83,176,782 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2483:Dctn1
|
UTSW |
6 |
83,171,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R4455:Dctn1
|
UTSW |
6 |
83,172,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Dctn1
|
UTSW |
6 |
83,166,920 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4812:Dctn1
|
UTSW |
6 |
83,166,919 (GRCm39) |
missense |
probably benign |
0.24 |
R4819:Dctn1
|
UTSW |
6 |
83,167,501 (GRCm39) |
missense |
probably damaging |
0.97 |
R4928:Dctn1
|
UTSW |
6 |
83,166,189 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5087:Dctn1
|
UTSW |
6 |
83,168,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Dctn1
|
UTSW |
6 |
83,160,108 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5372:Dctn1
|
UTSW |
6 |
83,167,192 (GRCm39) |
missense |
probably damaging |
0.96 |
R5493:Dctn1
|
UTSW |
6 |
83,159,546 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5494:Dctn1
|
UTSW |
6 |
83,159,546 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5732:Dctn1
|
UTSW |
6 |
83,174,931 (GRCm39) |
critical splice donor site |
probably null |
|
R5856:Dctn1
|
UTSW |
6 |
83,174,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Dctn1
|
UTSW |
6 |
83,170,673 (GRCm39) |
splice site |
probably null |
|
R6999:Dctn1
|
UTSW |
6 |
83,168,263 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7052:Dctn1
|
UTSW |
6 |
83,172,262 (GRCm39) |
splice site |
probably null |
|
R7133:Dctn1
|
UTSW |
6 |
83,157,026 (GRCm39) |
splice site |
probably null |
|
R7485:Dctn1
|
UTSW |
6 |
83,166,887 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7607:Dctn1
|
UTSW |
6 |
83,172,051 (GRCm39) |
nonsense |
probably null |
|
R7729:Dctn1
|
UTSW |
6 |
83,160,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R7749:Dctn1
|
UTSW |
6 |
83,163,123 (GRCm39) |
intron |
probably benign |
|
R8282:Dctn1
|
UTSW |
6 |
83,176,738 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8750:Dctn1
|
UTSW |
6 |
83,160,108 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9126:Dctn1
|
UTSW |
6 |
83,169,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R9208:Dctn1
|
UTSW |
6 |
83,176,684 (GRCm39) |
missense |
probably benign |
0.33 |
R9422:Dctn1
|
UTSW |
6 |
83,170,691 (GRCm39) |
missense |
possibly damaging |
0.71 |
|