Other mutations in this stock |
Total: 127 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921536K21Rik |
A |
G |
11: 3,840,067 (GRCm39) |
L110P |
probably damaging |
Het |
6030458C11Rik |
T |
C |
15: 12,817,993 (GRCm39) |
D168G |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,242,134 (GRCm39) |
E1332D |
probably benign |
Het |
Abhd11 |
A |
G |
5: 135,040,471 (GRCm39) |
Y168C |
probably damaging |
Het |
Actr5 |
A |
C |
2: 158,480,643 (GRCm39) |
T554P |
probably damaging |
Het |
Adam34l |
A |
T |
8: 44,078,132 (GRCm39) |
Y697* |
probably null |
Het |
Adamts16 |
A |
G |
13: 70,883,866 (GRCm39) |
L1103P |
probably damaging |
Het |
Adgrb3 |
A |
T |
1: 25,865,519 (GRCm39) |
I108K |
possibly damaging |
Het |
Agbl4 |
T |
A |
4: 111,423,826 (GRCm39) |
M284K |
possibly damaging |
Het |
Aoc3 |
T |
A |
11: 101,222,293 (GRCm39) |
Y176* |
probably null |
Het |
Aox1 |
A |
G |
1: 58,115,262 (GRCm39) |
E749G |
probably damaging |
Het |
Ap4b1 |
T |
A |
3: 103,728,184 (GRCm39) |
Y399* |
probably null |
Het |
Arhgef5 |
A |
T |
6: 43,265,616 (GRCm39) |
I1553F |
probably damaging |
Het |
Bag6 |
T |
C |
17: 35,361,802 (GRCm39) |
V541A |
probably benign |
Het |
Bdp1 |
A |
C |
13: 100,178,709 (GRCm39) |
V1879G |
probably damaging |
Het |
Bod1l |
G |
A |
5: 41,991,018 (GRCm39) |
S179F |
possibly damaging |
Het |
Bsnd |
C |
T |
4: 106,343,833 (GRCm39) |
V158I |
probably benign |
Het |
Cachd1 |
C |
A |
4: 100,840,587 (GRCm39) |
H880N |
probably damaging |
Het |
Ccdc27 |
T |
C |
4: 154,111,220 (GRCm39) |
|
probably null |
Het |
Cd74 |
C |
T |
18: 60,943,484 (GRCm39) |
P190S |
probably benign |
Het |
Cep68 |
A |
T |
11: 20,190,217 (GRCm39) |
L265Q |
probably damaging |
Het |
Cfap70 |
G |
A |
14: 20,458,678 (GRCm39) |
Q772* |
probably null |
Het |
CK137956 |
T |
A |
4: 127,864,327 (GRCm39) |
S101C |
possibly damaging |
Het |
Clca3a2 |
G |
A |
3: 144,512,164 (GRCm39) |
T524M |
probably benign |
Het |
Cxcr6 |
T |
C |
9: 123,639,022 (GRCm39) |
S15P |
probably benign |
Het |
Cyfip2 |
T |
A |
11: 46,114,995 (GRCm39) |
Y904F |
probably benign |
Het |
D130040H23Rik |
T |
A |
8: 69,755,354 (GRCm39) |
I253N |
probably benign |
Het |
Ddx56 |
C |
T |
11: 6,213,993 (GRCm39) |
V389M |
possibly damaging |
Het |
Dmp1 |
A |
T |
5: 104,359,942 (GRCm39) |
D206V |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 117,938,015 (GRCm39) |
C3350* |
probably null |
Het |
Dst |
A |
T |
1: 34,291,913 (GRCm39) |
S877C |
probably damaging |
Het |
Ermp1 |
A |
G |
19: 29,623,415 (GRCm39) |
S192P |
possibly damaging |
Het |
F13b |
G |
A |
1: 139,438,672 (GRCm39) |
D359N |
probably benign |
Het |
Fam171a1 |
A |
T |
2: 3,227,189 (GRCm39) |
Q769L |
possibly damaging |
Het |
Fap |
T |
C |
2: 62,359,071 (GRCm39) |
R411G |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,193,947 (GRCm39) |
V1340A |
probably benign |
Het |
Fbxw19 |
T |
C |
9: 109,311,100 (GRCm39) |
I370V |
probably benign |
Het |
Foxi1 |
A |
T |
11: 34,157,937 (GRCm39) |
N29K |
possibly damaging |
Het |
Frem2 |
T |
G |
3: 53,442,617 (GRCm39) |
D2640A |
probably benign |
Het |
Fzd4 |
T |
C |
7: 89,056,454 (GRCm39) |
V167A |
probably benign |
Het |
Galnt3 |
T |
C |
2: 65,928,123 (GRCm39) |
I258V |
possibly damaging |
Het |
Galr2 |
T |
C |
11: 116,174,069 (GRCm39) |
V233A |
possibly damaging |
Het |
Gldc |
G |
T |
19: 30,116,732 (GRCm39) |
Q407K |
probably benign |
Het |
Gmcl1 |
T |
C |
6: 86,674,498 (GRCm39) |
D460G |
probably benign |
Het |
Gpr89 |
A |
G |
3: 96,782,975 (GRCm39) |
I325T |
probably benign |
Het |
Grap |
T |
A |
11: 61,555,015 (GRCm39) |
Y61N |
possibly damaging |
Het |
Hbs1l |
G |
T |
10: 21,234,305 (GRCm39) |
|
probably null |
Het |
Hydin |
T |
A |
8: 111,227,337 (GRCm39) |
V1507D |
possibly damaging |
Het |
Igkv8-16 |
C |
A |
6: 70,363,971 (GRCm39) |
G17V |
probably benign |
Het |
Kdm4a |
T |
A |
4: 117,996,068 (GRCm39) |
Q987L |
probably null |
Het |
Krt76 |
A |
G |
15: 101,797,922 (GRCm39) |
|
probably null |
Het |
Lap3 |
T |
C |
5: 45,660,729 (GRCm39) |
S238P |
probably benign |
Het |
Letm2 |
T |
C |
8: 26,071,729 (GRCm39) |
D391G |
probably damaging |
Het |
Lipn |
A |
G |
19: 34,058,139 (GRCm39) |
T287A |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,244,921 (GRCm39) |
S466G |
probably damaging |
Het |
Map3k5 |
C |
A |
10: 20,007,855 (GRCm39) |
S1220* |
probably null |
Het |
Map4 |
T |
A |
9: 109,897,996 (GRCm39) |
S754R |
possibly damaging |
Het |
Map4 |
T |
C |
9: 109,864,032 (GRCm39) |
V419A |
probably benign |
Het |
Mroh9 |
A |
G |
1: 162,854,082 (GRCm39) |
S773P |
probably damaging |
Het |
Mtus1 |
A |
C |
8: 41,529,267 (GRCm39) |
|
probably null |
Het |
Muc1 |
C |
T |
3: 89,139,117 (GRCm39) |
P533S |
probably damaging |
Het |
Muc13 |
A |
T |
16: 33,624,970 (GRCm39) |
I282F |
probably damaging |
Het |
Mucl3 |
A |
G |
17: 35,949,305 (GRCm39) |
L98P |
possibly damaging |
Het |
Myh14 |
T |
A |
7: 44,261,067 (GRCm39) |
Q1816L |
possibly damaging |
Het |
Nalcn |
A |
C |
14: 123,831,965 (GRCm39) |
V103G |
possibly damaging |
Het |
Nlrp9c |
G |
A |
7: 26,084,245 (GRCm39) |
Q445* |
probably null |
Het |
Olfml2b |
A |
G |
1: 170,496,812 (GRCm39) |
D481G |
probably damaging |
Het |
Or13g1 |
T |
A |
7: 85,955,875 (GRCm39) |
I149F |
possibly damaging |
Het |
Or2ag19 |
T |
G |
7: 106,444,301 (GRCm39) |
I161S |
probably benign |
Het |
Or5g23 |
A |
G |
2: 85,438,844 (GRCm39) |
S137P |
probably benign |
Het |
Or8b37 |
T |
A |
9: 37,959,498 (GRCm39) |
|
probably null |
Het |
Or8k3b |
T |
A |
2: 86,520,735 (GRCm39) |
I195F |
probably damaging |
Het |
Pcdhb2 |
A |
T |
18: 37,430,408 (GRCm39) |
|
probably null |
Het |
Pcdhb22 |
A |
C |
18: 37,652,200 (GRCm39) |
T223P |
probably damaging |
Het |
Pcdhga1 |
T |
A |
18: 37,973,143 (GRCm39) |
N907K |
probably damaging |
Het |
Pcnt |
T |
C |
10: 76,215,740 (GRCm39) |
E2347G |
probably null |
Het |
Phax |
T |
A |
18: 56,706,176 (GRCm39) |
V22D |
probably benign |
Het |
Pik3ca |
T |
C |
3: 32,504,499 (GRCm39) |
F667S |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,813,905 (GRCm39) |
F4123S |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,685,491 (GRCm39) |
|
probably null |
Het |
Plcb1 |
G |
A |
2: 135,152,934 (GRCm39) |
R368K |
probably benign |
Het |
Prrc2a |
G |
T |
17: 35,372,284 (GRCm39) |
R1739S |
possibly damaging |
Het |
Psg23 |
A |
T |
7: 18,348,543 (GRCm39) |
M88K |
probably benign |
Het |
Pstk |
T |
A |
7: 130,989,526 (GRCm39) |
Y354N |
probably damaging |
Het |
Rab39 |
A |
G |
9: 53,617,231 (GRCm39) |
I62T |
possibly damaging |
Het |
Ranbp2 |
A |
G |
10: 58,328,383 (GRCm39) |
I2800V |
probably damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,120,828 (GRCm39) |
Y431C |
probably damaging |
Het |
Rest |
T |
A |
5: 77,416,209 (GRCm39) |
V141E |
possibly damaging |
Het |
Rnf167 |
T |
A |
11: 70,540,965 (GRCm39) |
I197N |
possibly damaging |
Het |
Rtn1 |
A |
G |
12: 72,354,942 (GRCm39) |
S335P |
probably damaging |
Het |
Ryr2 |
G |
T |
13: 11,676,961 (GRCm39) |
R3297S |
probably damaging |
Het |
S1pr3 |
A |
C |
13: 51,573,952 (GRCm39) |
K378Q |
probably benign |
Het |
Scgb1b24 |
T |
C |
7: 33,443,469 (GRCm39) |
Y43H |
probably damaging |
Het |
Sh3rf3 |
T |
A |
10: 58,919,335 (GRCm39) |
M484K |
probably damaging |
Het |
Shank1 |
A |
T |
7: 43,991,539 (GRCm39) |
R69* |
probably null |
Het |
Siglecf |
A |
G |
7: 43,004,967 (GRCm39) |
N399S |
probably benign |
Het |
Slc1a7 |
A |
G |
4: 107,865,561 (GRCm39) |
T350A |
probably damaging |
Het |
Slc25a54 |
T |
A |
3: 108,987,932 (GRCm39) |
Y24* |
probably null |
Het |
Slk |
T |
C |
19: 47,613,891 (GRCm39) |
F916L |
probably damaging |
Het |
Snap91 |
T |
A |
9: 86,672,194 (GRCm39) |
|
probably null |
Het |
Snrpb2 |
A |
T |
2: 142,907,106 (GRCm39) |
R25S |
possibly damaging |
Het |
Specc1l |
T |
C |
10: 75,097,659 (GRCm39) |
Y811H |
probably damaging |
Het |
Sprr2h |
A |
G |
3: 92,293,925 (GRCm39) |
|
probably benign |
Het |
Sult2a5 |
A |
T |
7: 13,358,045 (GRCm39) |
I26F |
probably benign |
Het |
Syt13 |
C |
T |
2: 92,776,448 (GRCm39) |
T245I |
possibly damaging |
Het |
Tecrl |
T |
A |
5: 83,502,706 (GRCm39) |
T33S |
probably benign |
Het |
Telo2 |
T |
A |
17: 25,333,968 (GRCm39) |
D93V |
probably benign |
Het |
Tet2 |
A |
T |
3: 133,187,202 (GRCm39) |
|
probably null |
Het |
Tgm7 |
A |
T |
2: 120,931,570 (GRCm39) |
C198S |
probably damaging |
Het |
Ticrr |
T |
C |
7: 79,328,883 (GRCm39) |
F674S |
probably damaging |
Het |
Tmem129 |
C |
A |
5: 33,811,843 (GRCm39) |
C31F |
probably damaging |
Het |
Tmem132a |
T |
A |
19: 10,836,052 (GRCm39) |
D826V |
possibly damaging |
Het |
Tpd52 |
T |
C |
3: 9,018,862 (GRCm39) |
|
probably null |
Het |
Trub2 |
A |
G |
2: 29,667,678 (GRCm39) |
S321P |
probably benign |
Het |
Ttc29 |
A |
G |
8: 79,009,014 (GRCm39) |
T295A |
probably benign |
Het |
Tubb1 |
G |
A |
2: 174,298,482 (GRCm39) |
S89N |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,386,497 (GRCm39) |
F1122L |
probably damaging |
Het |
Ubap2 |
C |
A |
4: 41,233,617 (GRCm39) |
G91V |
probably damaging |
Het |
Ugt2b35 |
A |
G |
5: 87,149,147 (GRCm39) |
N133D |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,314,479 (GRCm39) |
H807R |
probably benign |
Het |
Vmn1r220 |
A |
C |
13: 23,368,457 (GRCm39) |
C80G |
probably damaging |
Het |
Vmn1r79 |
A |
G |
7: 11,910,574 (GRCm39) |
E152G |
probably benign |
Het |
Vmn2r28 |
T |
C |
7: 5,489,345 (GRCm39) |
Y498C |
probably benign |
Het |
Wif1 |
A |
G |
10: 120,920,824 (GRCm39) |
I215M |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,928,050 (GRCm39) |
T1134A |
probably damaging |
Het |
Zfp90 |
A |
G |
8: 107,145,755 (GRCm39) |
H29R |
probably benign |
Het |
Zfp972 |
A |
G |
2: 177,563,480 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Hexb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Hexb
|
APN |
13 |
97,318,437 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02010:Hexb
|
APN |
13 |
97,313,353 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02126:Hexb
|
APN |
13 |
97,314,532 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02303:Hexb
|
APN |
13 |
97,313,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02955:Hexb
|
APN |
13 |
97,317,584 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02988:Hexb
|
UTSW |
13 |
97,334,729 (GRCm39) |
missense |
unknown |
|
R0311:Hexb
|
UTSW |
13 |
97,320,327 (GRCm39) |
unclassified |
probably benign |
|
R0470:Hexb
|
UTSW |
13 |
97,314,507 (GRCm39) |
missense |
probably damaging |
0.97 |
R0520:Hexb
|
UTSW |
13 |
97,317,618 (GRCm39) |
missense |
probably benign |
0.00 |
R0893:Hexb
|
UTSW |
13 |
97,322,135 (GRCm39) |
missense |
probably benign |
0.02 |
R2295:Hexb
|
UTSW |
13 |
97,322,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Hexb
|
UTSW |
13 |
97,320,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R4237:Hexb
|
UTSW |
13 |
97,313,259 (GRCm39) |
intron |
probably benign |
|
R4238:Hexb
|
UTSW |
13 |
97,313,259 (GRCm39) |
intron |
probably benign |
|
R4239:Hexb
|
UTSW |
13 |
97,313,259 (GRCm39) |
intron |
probably benign |
|
R4689:Hexb
|
UTSW |
13 |
97,317,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R5166:Hexb
|
UTSW |
13 |
97,318,512 (GRCm39) |
missense |
probably benign |
0.13 |
R6665:Hexb
|
UTSW |
13 |
97,315,893 (GRCm39) |
missense |
probably benign |
0.01 |
R7379:Hexb
|
UTSW |
13 |
97,317,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7553:Hexb
|
UTSW |
13 |
97,334,681 (GRCm39) |
missense |
probably benign |
0.01 |
R8307:Hexb
|
UTSW |
13 |
97,330,707 (GRCm39) |
missense |
probably benign |
0.02 |
R8830:Hexb
|
UTSW |
13 |
97,330,762 (GRCm39) |
missense |
probably benign |
|
R8980:Hexb
|
UTSW |
13 |
97,330,689 (GRCm39) |
missense |
probably damaging |
0.99 |
R9144:Hexb
|
UTSW |
13 |
97,317,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Hexb
|
UTSW |
13 |
97,314,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R9186:Hexb
|
UTSW |
13 |
97,325,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Hexb
|
UTSW |
13 |
97,313,336 (GRCm39) |
nonsense |
probably null |
|
R9546:Hexb
|
UTSW |
13 |
97,322,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|