Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,057,789 (GRCm39) |
|
probably benign |
Het |
4732465J04Rik |
GATCTATCTATCTATCTATCTATCTATCTATCTATCTATC |
GATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATC |
10: 95,630,440 (GRCm39) |
|
probably null |
Het |
4930522L14Rik |
T |
C |
5: 109,884,713 (GRCm39) |
K382E |
probably damaging |
Het |
Adck1 |
A |
G |
12: 88,422,280 (GRCm39) |
E297G |
probably damaging |
Het |
Ahrr |
G |
A |
13: 74,431,143 (GRCm39) |
|
probably benign |
Het |
Aldh3a2 |
C |
T |
11: 61,139,714 (GRCm39) |
V473I |
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,523,663 (GRCm39) |
I369K |
possibly damaging |
Het |
Atl2 |
A |
G |
17: 80,161,260 (GRCm39) |
|
probably benign |
Het |
Atp1b3 |
T |
C |
9: 96,220,762 (GRCm39) |
I178V |
possibly damaging |
Het |
Axdnd1 |
T |
C |
1: 156,205,956 (GRCm39) |
E520G |
possibly damaging |
Het |
Bahcc1 |
A |
T |
11: 120,175,900 (GRCm39) |
|
probably benign |
Het |
BB019430 |
A |
T |
10: 58,540,093 (GRCm39) |
|
noncoding transcript |
Het |
BC028528 |
A |
T |
3: 95,794,646 (GRCm39) |
|
probably benign |
Het |
Btbd1 |
T |
A |
7: 81,450,751 (GRCm39) |
Q343L |
probably benign |
Het |
Catsper1 |
A |
G |
19: 5,389,503 (GRCm39) |
T473A |
possibly damaging |
Het |
Ccn4 |
T |
C |
15: 66,791,059 (GRCm39) |
L287P |
probably damaging |
Het |
Cstdc7 |
T |
A |
18: 42,306,608 (GRCm39) |
D58E |
probably damaging |
Het |
D130040H23Rik |
T |
C |
8: 69,755,195 (GRCm39) |
V200A |
possibly damaging |
Het |
D830013O20Rik |
C |
T |
12: 73,411,105 (GRCm39) |
|
noncoding transcript |
Het |
Dcaf1 |
T |
A |
9: 106,721,344 (GRCm39) |
S379T |
possibly damaging |
Het |
Dcaf4 |
G |
A |
12: 83,582,762 (GRCm39) |
|
probably benign |
Het |
Dhx58 |
T |
C |
11: 100,586,150 (GRCm39) |
I624V |
probably benign |
Het |
Disp3 |
T |
C |
4: 148,338,708 (GRCm39) |
E821G |
probably damaging |
Het |
Dlc1 |
T |
A |
8: 37,066,594 (GRCm39) |
E464V |
probably damaging |
Het |
Dnah10 |
G |
A |
5: 124,860,898 (GRCm39) |
V2151I |
probably damaging |
Het |
Dnah6 |
C |
T |
6: 73,165,518 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,639 (GRCm39) |
G2617D |
probably benign |
Het |
Dnah9 |
C |
A |
11: 65,809,630 (GRCm39) |
E872* |
probably null |
Het |
Dock9 |
T |
C |
14: 121,835,077 (GRCm39) |
Y99C |
probably damaging |
Het |
Dpy19l3 |
T |
A |
7: 35,416,071 (GRCm39) |
I310F |
probably damaging |
Het |
Fggy |
A |
T |
4: 95,725,891 (GRCm39) |
I137F |
probably damaging |
Het |
Gli2 |
A |
G |
1: 118,818,013 (GRCm39) |
|
probably benign |
Het |
Gm14421 |
A |
T |
2: 176,748,515 (GRCm39) |
|
noncoding transcript |
Het |
Grin2a |
A |
G |
16: 9,812,685 (GRCm39) |
|
probably null |
Het |
Grin2b |
A |
G |
6: 135,755,646 (GRCm39) |
|
probably benign |
Het |
Incenp |
A |
G |
19: 9,872,243 (GRCm39) |
S72P |
probably benign |
Het |
Ipo11 |
A |
G |
13: 107,046,702 (GRCm39) |
|
probably benign |
Het |
Klc3 |
T |
A |
7: 19,128,851 (GRCm39) |
N469Y |
possibly damaging |
Het |
Lrrc42 |
A |
G |
4: 107,104,702 (GRCm39) |
S88P |
probably benign |
Het |
Lrrc49 |
G |
A |
9: 60,587,883 (GRCm39) |
T93I |
probably benign |
Het |
Ltn1 |
G |
A |
16: 87,202,407 (GRCm39) |
|
probably benign |
Het |
Mlycd |
A |
T |
8: 120,134,380 (GRCm39) |
Q294L |
probably damaging |
Het |
Mmrn1 |
T |
A |
6: 60,952,799 (GRCm39) |
|
probably benign |
Het |
Mrpl22 |
T |
A |
11: 58,062,647 (GRCm39) |
I19N |
probably benign |
Het |
Msh3 |
T |
A |
13: 92,485,717 (GRCm39) |
K202N |
probably damaging |
Het |
N4bp2 |
T |
C |
5: 65,960,916 (GRCm39) |
|
probably benign |
Het |
Ncam1 |
C |
T |
9: 49,479,709 (GRCm39) |
D90N |
probably damaging |
Het |
Nckap5 |
A |
T |
1: 125,952,144 (GRCm39) |
D1405E |
possibly damaging |
Het |
Ncoa2 |
A |
G |
1: 13,256,955 (GRCm39) |
|
probably null |
Het |
Ncoa6 |
TGC |
TGCGC |
2: 155,250,211 (GRCm39) |
|
probably null |
Het |
Nlrp1b |
A |
T |
11: 71,054,925 (GRCm39) |
W844R |
probably damaging |
Het |
Nmnat1 |
G |
T |
4: 149,553,607 (GRCm39) |
N168K |
possibly damaging |
Het |
Or5b96 |
A |
G |
19: 12,867,809 (GRCm39) |
L44P |
probably damaging |
Het |
Ost4 |
T |
C |
5: 31,064,803 (GRCm39) |
H26R |
probably damaging |
Het |
Otog |
G |
A |
7: 45,953,655 (GRCm39) |
V2638M |
probably damaging |
Het |
Otogl |
A |
T |
10: 107,710,391 (GRCm39) |
I566N |
probably damaging |
Het |
Pcyt1a |
T |
C |
16: 32,289,004 (GRCm39) |
S282P |
probably damaging |
Het |
Prkcg |
G |
A |
7: 3,377,635 (GRCm39) |
E581K |
probably damaging |
Het |
Ralgps2 |
A |
G |
1: 156,714,659 (GRCm39) |
|
probably null |
Het |
Rnf157 |
A |
G |
11: 116,245,636 (GRCm39) |
|
probably benign |
Het |
Scmh1 |
T |
C |
4: 120,387,062 (GRCm39) |
|
probably benign |
Het |
Sgo2b |
T |
C |
8: 64,391,417 (GRCm39) |
H150R |
possibly damaging |
Het |
Sh2b3 |
T |
G |
5: 121,967,100 (GRCm39) |
T5P |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,848,433 (GRCm39) |
|
probably benign |
Het |
Slfn10-ps |
T |
C |
11: 82,926,128 (GRCm39) |
|
noncoding transcript |
Het |
Sspo |
T |
A |
6: 48,471,128 (GRCm39) |
|
probably benign |
Het |
Tcp1 |
T |
A |
17: 13,141,634 (GRCm39) |
|
probably benign |
Het |
Tdp2 |
A |
G |
13: 25,022,222 (GRCm39) |
M214V |
probably damaging |
Het |
Tenm4 |
T |
G |
7: 96,378,547 (GRCm39) |
|
probably benign |
Het |
Tmem144 |
G |
A |
3: 79,746,580 (GRCm39) |
|
probably benign |
Het |
Tmem204 |
A |
G |
17: 25,277,324 (GRCm39) |
I187T |
probably damaging |
Het |
Tmem208 |
T |
G |
8: 106,061,326 (GRCm39) |
D117E |
probably benign |
Het |
Tnks1bp1 |
C |
T |
2: 84,889,565 (GRCm39) |
P631S |
possibly damaging |
Het |
Tomm70a |
T |
C |
16: 56,968,184 (GRCm39) |
V517A |
probably damaging |
Het |
Ttc7 |
T |
C |
17: 87,687,323 (GRCm39) |
V801A |
probably damaging |
Het |
Txndc5 |
A |
T |
13: 38,691,929 (GRCm39) |
C146S |
probably damaging |
Het |
Ubac2 |
A |
G |
14: 122,246,329 (GRCm39) |
|
probably benign |
Het |
Ube4b |
G |
T |
4: 149,444,781 (GRCm39) |
T493K |
probably damaging |
Het |
Ufl1 |
A |
T |
4: 25,256,008 (GRCm39) |
Y504N |
probably benign |
Het |
Ugt1a6a |
T |
C |
1: 88,066,992 (GRCm39) |
V266A |
possibly damaging |
Het |
Ugt1a6b |
T |
A |
1: 88,035,189 (GRCm39) |
C176S |
probably damaging |
Het |
Ulk3 |
T |
A |
9: 57,497,969 (GRCm39) |
I90N |
probably damaging |
Het |
Unc13c |
T |
C |
9: 73,602,174 (GRCm39) |
I1357M |
probably benign |
Het |
Vmn1r28 |
G |
A |
6: 58,242,702 (GRCm39) |
A182T |
probably benign |
Het |
Vmn2r114 |
A |
G |
17: 23,528,800 (GRCm39) |
|
probably null |
Het |
Vmn2r91 |
A |
C |
17: 18,326,399 (GRCm39) |
N228T |
probably benign |
Het |
Wdr43 |
T |
G |
17: 71,938,992 (GRCm39) |
|
probably benign |
Het |
Zbtb6 |
G |
T |
2: 37,319,600 (GRCm39) |
Y109* |
probably null |
Het |
Zfp980 |
A |
G |
4: 145,428,567 (GRCm39) |
D432G |
probably benign |
Het |
|
Other mutations in Chmp6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01767:Chmp6
|
APN |
11 |
119,807,812 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03405:Chmp6
|
APN |
11 |
119,806,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Chmp6
|
UTSW |
11 |
119,807,508 (GRCm39) |
missense |
probably damaging |
0.99 |
R0164:Chmp6
|
UTSW |
11 |
119,806,349 (GRCm39) |
critical splice donor site |
probably null |
|
R0345:Chmp6
|
UTSW |
11 |
119,808,872 (GRCm39) |
unclassified |
probably benign |
|
R1528:Chmp6
|
UTSW |
11 |
119,807,541 (GRCm39) |
missense |
probably benign |
0.04 |
R2187:Chmp6
|
UTSW |
11 |
119,807,562 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5026:Chmp6
|
UTSW |
11 |
119,809,469 (GRCm39) |
missense |
probably damaging |
0.98 |
R5799:Chmp6
|
UTSW |
11 |
119,807,517 (GRCm39) |
missense |
probably benign |
0.41 |
R7059:Chmp6
|
UTSW |
11 |
119,806,866 (GRCm39) |
missense |
probably damaging |
0.98 |
R7486:Chmp6
|
UTSW |
11 |
119,807,783 (GRCm39) |
missense |
probably benign |
0.38 |
R7490:Chmp6
|
UTSW |
11 |
119,806,269 (GRCm39) |
nonsense |
probably null |
|
R7862:Chmp6
|
UTSW |
11 |
119,807,836 (GRCm39) |
critical splice donor site |
probably null |
|
R7908:Chmp6
|
UTSW |
11 |
119,804,656 (GRCm39) |
unclassified |
probably benign |
|
R9390:Chmp6
|
UTSW |
11 |
119,806,288 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9677:Chmp6
|
UTSW |
11 |
119,806,459 (GRCm39) |
nonsense |
probably null |
|
X0025:Chmp6
|
UTSW |
11 |
119,806,942 (GRCm39) |
splice site |
probably null |
|
|