Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A330008L17Rik |
A |
G |
8: 100,450,057 (GRCm39) |
|
noncoding transcript |
Het |
Aff2 |
C |
A |
X: 68,791,141 (GRCm39) |
|
probably benign |
Het |
Aldh1a1 |
C |
A |
19: 20,604,010 (GRCm39) |
|
probably benign |
Het |
Anxa7 |
C |
T |
14: 20,519,479 (GRCm39) |
G113E |
probably damaging |
Het |
Apba2 |
A |
T |
7: 64,271,908 (GRCm39) |
|
probably benign |
Het |
Apc2 |
G |
C |
10: 80,135,808 (GRCm39) |
|
probably benign |
Het |
App |
C |
G |
16: 84,822,300 (GRCm39) |
|
probably benign |
Het |
Asic2 |
C |
A |
11: 80,876,570 (GRCm39) |
|
probably benign |
Het |
Btk |
T |
C |
X: 133,479,574 (GRCm39) |
|
probably benign |
Het |
Car12 |
C |
A |
9: 66,668,958 (GRCm39) |
|
probably benign |
Het |
Ccdc121 |
GAGAAG |
GAG |
5: 31,644,717 (GRCm39) |
|
probably benign |
Het |
Ccdc191 |
G |
A |
16: 43,742,164 (GRCm39) |
|
probably benign |
Het |
Ccdc34 |
N |
|
2: 110,016,318 (GRCm38) |
|
probably benign |
Het |
Cd164 |
G |
T |
10: 41,397,922 (GRCm39) |
A59S |
probably benign |
Het |
Cd22 |
C |
T |
7: 30,577,507 (GRCm39) |
R2H |
possibly damaging |
Het |
Cdv3 |
C |
A |
9: 103,242,553 (GRCm39) |
|
probably benign |
Het |
Cdv3 |
A |
T |
9: 103,242,542 (GRCm39) |
|
probably benign |
Het |
Celf2 |
N |
|
2: 6,779,076 (GRCm38) |
|
probably benign |
Het |
Cfap299 |
G |
A |
5: 98,855,367 (GRCm39) |
|
probably benign |
Het |
Clec18a |
C |
A |
8: 111,802,768 (GRCm39) |
|
probably benign |
Het |
Cnpy3 |
GGATGGAT |
GGATAGATAGATAGATAGATGGAT |
17: 47,048,462 (GRCm39) |
|
probably benign |
Het |
Cntn4 |
A |
G |
6: 106,530,901 (GRCm39) |
|
probably benign |
Het |
Cntnap5c |
G |
C |
17: 58,469,155 (GRCm39) |
|
probably benign |
Het |
Col2a1 |
C |
A |
15: 97,886,862 (GRCm39) |
|
probably null |
Het |
Cpne3 |
G |
T |
4: 19,563,382 (GRCm39) |
|
probably benign |
Het |
Cracd |
GGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
GGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
5: 76,806,589 (GRCm39) |
|
probably benign |
Het |
Dab1 |
T |
G |
4: 103,903,769 (GRCm39) |
|
probably benign |
Het |
Dapp1 |
G |
A |
3: 137,645,161 (GRCm39) |
|
probably benign |
Het |
Dcc |
G |
A |
18: 72,430,518 (GRCm39) |
|
probably benign |
Het |
Dcun1d1 |
GAAAAAAAAA |
GAAAAAAAAAA |
3: 35,992,154 (GRCm39) |
|
probably benign |
Het |
Dhdds |
TAA |
TA |
4: 133,697,674 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,571,342 (GRCm39) |
G2817V |
probably damaging |
Het |
Dnm3 |
CATATATATATATATATATATATA |
CATATATATATATATATATATA |
1: 162,234,130 (GRCm39) |
|
probably benign |
Het |
Dock10 |
N |
|
1: 80,716,623 (GRCm38) |
|
probably benign |
Het |
Dusp10 |
G |
T |
1: 183,769,253 (GRCm39) |
C73F |
probably damaging |
Het |
Fgf20 |
A |
C |
8: 40,745,359 (GRCm39) |
|
probably benign |
Het |
Ftsj3 |
G |
T |
11: 106,140,885 (GRCm39) |
|
probably benign |
Het |
Gls |
T |
G |
1: 52,222,526 (GRCm39) |
|
probably benign |
Het |
Gm12130 |
T |
C |
11: 38,397,750 (GRCm39) |
|
noncoding transcript |
Het |
Gm14936 |
G |
A |
X: 111,908,447 (GRCm39) |
|
noncoding transcript |
Het |
Gm16630 |
C |
T |
6: 48,118,203 (GRCm39) |
|
noncoding transcript |
Het |
Gm22194 |
AGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
AGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
10: 11,816,707 (GRCm39) |
|
noncoding transcript |
Het |
Gm26917 |
C |
G |
17: 40,154,862 (GRCm39) |
|
noncoding transcript |
Het |
Gm35048 |
GACACACACACACACACACACACACACACACACACACAC |
GACACACACACACACACACACACACACACACACACAC |
1: 90,449,248 (GRCm39) |
|
noncoding transcript |
Het |
Gm37311 |
G |
A |
16: 77,415,169 (GRCm39) |
|
noncoding transcript |
Het |
Gm37928 |
AACACACACACACACACACACACACACACACACA |
AACACACACACACACACACACACACACACACACACA |
3: 118,328,206 (GRCm39) |
|
noncoding transcript |
Het |
Gm4302 |
T |
C |
10: 100,177,306 (GRCm39) |
W197R |
probably benign |
Het |
H2-Q4 |
G |
A |
17: 35,599,381 (GRCm39) |
D155N |
probably damaging |
Het |
H2-T23 |
T |
C |
17: 36,342,108 (GRCm39) |
|
probably benign |
Het |
Hgs |
CTTTTTTT |
CTTTTTT |
11: 120,360,404 (GRCm39) |
|
probably benign |
Het |
Ighv5-9 |
C |
T |
12: 113,625,497 (GRCm39) |
S82N |
probably benign |
Het |
Il1rap |
C |
A |
16: 26,450,343 (GRCm39) |
|
probably benign |
Het |
Inhbc |
N |
|
10: 127,367,140 (GRCm38) |
|
probably benign |
Het |
Inpp4b |
C |
T |
8: 82,419,639 (GRCm39) |
|
probably benign |
Het |
Kars1 |
N |
|
8: 111,993,708 (GRCm38) |
|
probably benign |
Het |
Kcng4 |
G |
T |
8: 120,360,258 (GRCm39) |
Y39* |
probably null |
Het |
Kcnh7 |
A |
G |
2: 62,880,143 (GRCm39) |
|
probably benign |
Het |
Klhl1 |
G |
C |
14: 96,555,166 (GRCm39) |
|
probably benign |
Het |
Lrch1 |
C |
T |
14: 75,142,461 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
G |
C |
2: 42,127,574 (GRCm39) |
|
probably benign |
Het |
Lsm8 |
G |
A |
6: 18,844,315 (GRCm39) |
|
probably benign |
Het |
Lsm8 |
G |
A |
6: 18,854,320 (GRCm39) |
|
probably benign |
Het |
Magi2 |
T |
C |
5: 20,159,509 (GRCm39) |
|
probably benign |
Het |
Matcap2 |
N |
|
9: 22,442,083 (GRCm38) |
|
probably benign |
Het |
Mef2c |
G |
A |
13: 83,753,942 (GRCm39) |
|
probably benign |
Het |
Mei4 |
A |
G |
9: 82,069,012 (GRCm39) |
|
probably benign |
Het |
Mid1 |
T |
A |
X: 168,788,560 (GRCm39) |
|
probably benign |
Het |
Mndal |
G |
C |
1: 173,707,784 (GRCm39) |
|
probably benign |
Het |
Mpped2 |
C |
A |
2: 106,551,773 (GRCm39) |
|
probably benign |
Het |
Mtarc2 |
TAGGCAGCCAATCAGAGCACTGCCTCTCAGCGCCAGGCAGCCAATCAGAGCACTGCCTCTCAGCGCCAGGCA |
TAGGCAGCCAATCAGAGCACTGCCTCTCAGCGCCAGGCA |
1: 184,554,985 (GRCm39) |
|
probably benign |
Het |
Mtf1 |
A |
G |
4: 124,723,109 (GRCm39) |
|
probably benign |
Het |
Mxd1 |
T |
C |
6: 86,644,388 (GRCm39) |
|
probably benign |
Het |
Nbea |
G |
T |
3: 55,608,948 (GRCm39) |
|
probably benign |
Het |
Ncor1 |
N |
|
11: 62,419,782 (GRCm38) |
|
probably benign |
Het |
Nox4 |
A |
G |
7: 86,892,275 (GRCm39) |
|
probably benign |
Het |
Ocln |
C |
T |
13: 100,657,075 (GRCm39) |
|
probably benign |
Het |
Ofcc1 |
G |
A |
13: 40,246,443 (GRCm39) |
|
probably benign |
Het |
Or5af2 |
T |
A |
11: 58,708,266 (GRCm39) |
V144D |
possibly damaging |
Het |
Paics |
N |
|
5: 76,956,744 (GRCm38) |
|
probably null |
Het |
Paqr8 |
G |
T |
1: 20,984,882 (GRCm39) |
|
probably benign |
Het |
Pate9 |
T |
C |
9: 36,444,849 (GRCm39) |
|
probably benign |
Het |
Pdss1 |
C |
T |
2: 22,790,980 (GRCm39) |
|
probably benign |
Het |
Piezo1 |
G |
A |
8: 123,222,308 (GRCm39) |
R503W |
probably damaging |
Het |
Pkhd1 |
G |
A |
1: 20,681,638 (GRCm39) |
|
probably benign |
Het |
Ppp1r3f |
C |
A |
X: 7,426,575 (GRCm39) |
G562V |
probably damaging |
Het |
Prr16 |
C |
T |
18: 51,333,396 (GRCm39) |
|
probably benign |
Het |
Prss38 |
T |
G |
11: 59,266,467 (GRCm39) |
|
probably benign |
Het |
Prxl2c |
G |
A |
13: 64,435,099 (GRCm39) |
|
probably benign |
Het |
Ptprk |
T |
C |
10: 28,450,983 (GRCm39) |
|
probably benign |
Het |
Pum1 |
N |
|
4: 130,730,549 (GRCm38) |
|
probably benign |
Het |
Rabgef1 |
N |
|
5: 130,187,586 (GRCm38) |
|
probably null |
Het |
Rgs16 |
G |
A |
1: 153,619,976 (GRCm39) |
|
probably benign |
Het |
Riok3 |
G |
T |
18: 12,263,039 (GRCm39) |
|
probably benign |
Het |
Rn18s-rs5 |
T |
C |
17: 40,159,446 (GRCm39) |
|
noncoding transcript |
Het |
Robo2 |
N |
|
16: 74,055,954 (GRCm38) |
|
probably benign |
Het |
Rps6ka3 |
A |
G |
X: 158,062,211 (GRCm39) |
|
probably benign |
Het |
Rptn |
T |
A |
3: 93,304,848 (GRCm39) |
L727Q |
probably benign |
Het |
Slc25a46 |
C |
A |
18: 31,730,366 (GRCm39) |
|
probably benign |
Het |
Spata31f1e |
T |
C |
4: 42,792,885 (GRCm39) |
T416A |
probably benign |
Het |
Spsb1 |
C |
T |
4: 150,036,943 (GRCm39) |
|
probably benign |
Het |
Tbc1d19 |
A |
C |
5: 53,974,051 (GRCm39) |
|
probably benign |
Het |
Trav7-4 |
C |
T |
14: 53,698,975 (GRCm39) |
L41F |
probably benign |
Het |
Trip12 |
N |
|
1: 84,754,482 (GRCm38) |
|
probably benign |
Het |
Ttc13 |
G |
A |
8: 125,402,605 (GRCm39) |
|
probably benign |
Het |
Ttll6 |
C |
T |
11: 96,046,084 (GRCm39) |
|
probably benign |
Het |
Unc5b |
C |
G |
10: 60,621,950 (GRCm39) |
|
probably benign |
Het |
Vmn2r87 |
C |
T |
10: 130,314,583 (GRCm39) |
M334I |
probably benign |
Het |
Vps13b |
G |
T |
15: 35,847,103 (GRCm39) |
A2629S |
probably damaging |
Het |
Wars2 |
N |
|
3: 99,214,774 (GRCm38) |
|
probably null |
Het |
Zdhhc3 |
AACACACACACACACACACACACACACACACAC |
AACACACACACACACACACACACACACACACACAC |
9: 122,912,087 (GRCm39) |
|
probably benign |
Het |
Zfp26 |
C |
A |
9: 20,349,842 (GRCm39) |
A241S |
probably benign |
Het |
Zfp442 |
C |
T |
2: 150,261,768 (GRCm39) |
|
probably benign |
Het |
Zfp808 |
C |
T |
13: 62,314,465 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Dennd1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Dennd1b
|
APN |
1 |
138,990,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00510:Dennd1b
|
APN |
1 |
139,029,809 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00671:Dennd1b
|
APN |
1 |
139,061,475 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00937:Dennd1b
|
APN |
1 |
139,097,977 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00959:Dennd1b
|
APN |
1 |
139,071,626 (GRCm39) |
splice site |
probably benign |
|
IGL01446:Dennd1b
|
APN |
1 |
138,950,848 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01610:Dennd1b
|
APN |
1 |
139,097,504 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02275:Dennd1b
|
APN |
1 |
139,008,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Dennd1b
|
APN |
1 |
139,096,705 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02995:Dennd1b
|
APN |
1 |
139,008,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03089:Dennd1b
|
APN |
1 |
139,029,767 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03240:Dennd1b
|
APN |
1 |
139,067,130 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL03267:Dennd1b
|
APN |
1 |
138,990,599 (GRCm39) |
nonsense |
probably null |
|
Dendrite
|
UTSW |
1 |
138,981,155 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4418001:Dennd1b
|
UTSW |
1 |
139,008,999 (GRCm39) |
missense |
|
|
PIT4504001:Dennd1b
|
UTSW |
1 |
138,967,742 (GRCm39) |
missense |
probably benign |
0.28 |
R0426:Dennd1b
|
UTSW |
1 |
139,097,934 (GRCm39) |
missense |
probably benign |
|
R0445:Dennd1b
|
UTSW |
1 |
139,095,503 (GRCm39) |
splice site |
probably benign |
|
R0497:Dennd1b
|
UTSW |
1 |
138,967,724 (GRCm39) |
splice site |
probably benign |
|
R0627:Dennd1b
|
UTSW |
1 |
139,008,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R1027:Dennd1b
|
UTSW |
1 |
138,969,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R1599:Dennd1b
|
UTSW |
1 |
139,095,468 (GRCm39) |
missense |
probably benign |
0.01 |
R1703:Dennd1b
|
UTSW |
1 |
139,097,492 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1844:Dennd1b
|
UTSW |
1 |
139,018,143 (GRCm39) |
splice site |
probably null |
|
R1943:Dennd1b
|
UTSW |
1 |
139,096,690 (GRCm39) |
utr 3 prime |
probably benign |
|
R2504:Dennd1b
|
UTSW |
1 |
139,097,908 (GRCm39) |
utr 3 prime |
probably benign |
|
R2866:Dennd1b
|
UTSW |
1 |
139,098,019 (GRCm39) |
missense |
possibly damaging |
0.58 |
R3109:Dennd1b
|
UTSW |
1 |
138,969,654 (GRCm39) |
splice site |
probably benign |
|
R3843:Dennd1b
|
UTSW |
1 |
138,981,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Dennd1b
|
UTSW |
1 |
139,071,697 (GRCm39) |
missense |
probably benign |
0.00 |
R4258:Dennd1b
|
UTSW |
1 |
138,990,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R4504:Dennd1b
|
UTSW |
1 |
139,013,665 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4805:Dennd1b
|
UTSW |
1 |
138,981,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Dennd1b
|
UTSW |
1 |
139,013,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R4954:Dennd1b
|
UTSW |
1 |
138,981,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5098:Dennd1b
|
UTSW |
1 |
139,061,459 (GRCm39) |
missense |
probably damaging |
0.97 |
R5205:Dennd1b
|
UTSW |
1 |
138,982,306 (GRCm39) |
missense |
probably benign |
0.00 |
R5240:Dennd1b
|
UTSW |
1 |
138,990,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5383:Dennd1b
|
UTSW |
1 |
139,095,409 (GRCm39) |
missense |
probably benign |
|
R5504:Dennd1b
|
UTSW |
1 |
139,018,246 (GRCm39) |
missense |
probably benign |
0.07 |
R5702:Dennd1b
|
UTSW |
1 |
139,061,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Dennd1b
|
UTSW |
1 |
138,967,727 (GRCm39) |
splice site |
probably null |
|
R6144:Dennd1b
|
UTSW |
1 |
139,008,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Dennd1b
|
UTSW |
1 |
139,061,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Dennd1b
|
UTSW |
1 |
139,095,456 (GRCm39) |
missense |
probably benign |
0.00 |
R6289:Dennd1b
|
UTSW |
1 |
139,096,683 (GRCm39) |
utr 3 prime |
probably benign |
|
R6453:Dennd1b
|
UTSW |
1 |
139,071,686 (GRCm39) |
missense |
probably benign |
0.07 |
R6479:Dennd1b
|
UTSW |
1 |
138,969,698 (GRCm39) |
intron |
probably benign |
|
R6940:Dennd1b
|
UTSW |
1 |
138,981,155 (GRCm39) |
critical splice donor site |
probably null |
|
R6954:Dennd1b
|
UTSW |
1 |
139,096,683 (GRCm39) |
utr 3 prime |
probably benign |
|
R7183:Dennd1b
|
UTSW |
1 |
139,097,990 (GRCm39) |
missense |
unknown |
|
R7710:Dennd1b
|
UTSW |
1 |
138,990,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7796:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7921:Dennd1b
|
UTSW |
1 |
138,990,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7991:Dennd1b
|
UTSW |
1 |
139,013,634 (GRCm39) |
missense |
|
|
R8025:Dennd1b
|
UTSW |
1 |
139,038,158 (GRCm39) |
missense |
|
|
R8239:Dennd1b
|
UTSW |
1 |
138,969,673 (GRCm39) |
missense |
probably benign |
0.02 |
R8526:Dennd1b
|
UTSW |
1 |
138,950,858 (GRCm39) |
nonsense |
probably null |
|
R8532:Dennd1b
|
UTSW |
1 |
139,097,912 (GRCm39) |
utr 3 prime |
probably benign |
|
R8691:Dennd1b
|
UTSW |
1 |
138,969,774 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9229:Dennd1b
|
UTSW |
1 |
138,981,100 (GRCm39) |
nonsense |
probably null |
|
R9577:Dennd1b
|
UTSW |
1 |
139,018,196 (GRCm39) |
missense |
|
|
RF008:Dennd1b
|
UTSW |
1 |
138,981,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|