Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,259,013 (GRCm39) |
|
probably benign |
Het |
Abcg5 |
T |
A |
17: 84,978,575 (GRCm39) |
E294D |
probably benign |
Het |
Actrt2 |
C |
T |
4: 154,751,551 (GRCm39) |
R195Q |
probably benign |
Het |
Adamts12 |
C |
T |
15: 11,310,665 (GRCm39) |
T974I |
probably damaging |
Het |
Ankrd65 |
A |
G |
4: 155,876,530 (GRCm39) |
T239A |
probably benign |
Het |
Ano7 |
G |
T |
1: 93,329,855 (GRCm39) |
|
probably benign |
Het |
Apc |
A |
T |
18: 34,409,654 (GRCm39) |
E198V |
probably damaging |
Het |
Arhgef10 |
A |
G |
8: 14,984,820 (GRCm39) |
D200G |
probably damaging |
Het |
Atp9a |
A |
T |
2: 168,495,457 (GRCm39) |
V583E |
probably damaging |
Het |
Bicral |
C |
T |
17: 47,135,741 (GRCm39) |
A490T |
probably benign |
Het |
C1rl |
C |
T |
6: 124,485,672 (GRCm39) |
P348S |
probably damaging |
Het |
Cog1 |
T |
C |
11: 113,540,424 (GRCm39) |
L13P |
probably damaging |
Het |
Cx3cr1 |
T |
A |
9: 119,880,749 (GRCm39) |
T218S |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,736,071 (GRCm39) |
*493W |
probably null |
Het |
Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
E2f4 |
A |
G |
8: 106,026,973 (GRCm39) |
Y179C |
probably damaging |
Het |
Endod1 |
T |
C |
9: 14,268,949 (GRCm39) |
N179D |
probably benign |
Het |
Epc2 |
C |
T |
2: 49,437,621 (GRCm39) |
|
probably benign |
Het |
Ets2 |
G |
T |
16: 95,519,977 (GRCm39) |
R401L |
probably benign |
Het |
Fgd4 |
C |
T |
16: 16,243,692 (GRCm39) |
C614Y |
probably benign |
Het |
Fgf18 |
A |
C |
11: 33,068,003 (GRCm39) |
F129C |
probably damaging |
Het |
Frem3 |
A |
T |
8: 81,342,086 (GRCm39) |
T1460S |
probably benign |
Het |
H2-M1 |
T |
G |
17: 36,980,929 (GRCm39) |
T336P |
possibly damaging |
Het |
Ikbkb |
T |
C |
8: 23,157,233 (GRCm39) |
|
probably benign |
Het |
Ipo7 |
G |
T |
7: 109,648,838 (GRCm39) |
D704Y |
probably damaging |
Het |
Jaml |
T |
A |
9: 45,012,362 (GRCm39) |
I283N |
probably damaging |
Het |
Jarid2 |
G |
T |
13: 45,059,812 (GRCm39) |
M681I |
probably benign |
Het |
Kif4-ps |
T |
C |
12: 101,113,956 (GRCm39) |
L695P |
probably damaging |
Het |
Kmt2d |
A |
G |
15: 98,737,410 (GRCm39) |
|
probably benign |
Het |
Krt25 |
T |
C |
11: 99,212,023 (GRCm39) |
T205A |
probably benign |
Het |
Lif |
T |
C |
11: 4,219,051 (GRCm39) |
V110A |
possibly damaging |
Het |
Ltbp1 |
T |
A |
17: 75,617,154 (GRCm39) |
V1031E |
possibly damaging |
Het |
Ltbr |
A |
G |
6: 125,286,440 (GRCm39) |
S249P |
probably benign |
Het |
Man2b1 |
A |
G |
8: 85,819,653 (GRCm39) |
|
probably benign |
Het |
Med16 |
A |
T |
10: 79,738,916 (GRCm39) |
M290K |
possibly damaging |
Het |
Mov10l1 |
C |
A |
15: 88,891,830 (GRCm39) |
Q562K |
probably benign |
Het |
Msantd2 |
C |
T |
9: 37,434,227 (GRCm39) |
R357W |
probably damaging |
Het |
Mtcl2 |
T |
C |
2: 156,875,245 (GRCm39) |
E835G |
probably damaging |
Het |
Mtmr6 |
T |
C |
14: 60,534,108 (GRCm39) |
F449L |
probably damaging |
Het |
Myt1l |
A |
T |
12: 29,833,618 (GRCm39) |
|
probably null |
Het |
Neb |
A |
G |
2: 52,154,076 (GRCm39) |
F2345S |
probably damaging |
Het |
Nlrp6 |
T |
C |
7: 140,506,357 (GRCm39) |
V766A |
probably benign |
Het |
Or11g27 |
T |
C |
14: 50,771,403 (GRCm39) |
I178T |
probably damaging |
Het |
Or4k36 |
A |
G |
2: 111,145,844 (GRCm39) |
T7A |
probably benign |
Het |
Or6d13 |
A |
T |
6: 116,517,416 (GRCm39) |
M1L |
probably null |
Het |
Or8k22 |
G |
A |
2: 86,163,689 (GRCm39) |
R4C |
probably benign |
Het |
Patj |
T |
A |
4: 98,344,462 (GRCm39) |
D591E |
probably benign |
Het |
Pde6d |
A |
G |
1: 86,473,524 (GRCm39) |
F91L |
probably benign |
Het |
Pitpnm2 |
G |
A |
5: 124,265,332 (GRCm39) |
P757L |
probably damaging |
Het |
Plcd4 |
A |
G |
1: 74,603,584 (GRCm39) |
T662A |
probably benign |
Het |
Podn |
C |
T |
4: 107,880,558 (GRCm39) |
A31T |
probably damaging |
Het |
Prss37 |
G |
A |
6: 40,492,294 (GRCm39) |
R186* |
probably null |
Het |
Psg20 |
T |
A |
7: 18,414,947 (GRCm39) |
Y316F |
probably benign |
Het |
Psmd1 |
T |
A |
1: 86,006,422 (GRCm39) |
S263T |
possibly damaging |
Het |
Pum1 |
C |
A |
4: 130,396,581 (GRCm39) |
T112K |
possibly damaging |
Het |
Rab3gap2 |
A |
T |
1: 184,993,564 (GRCm39) |
D782V |
possibly damaging |
Het |
Rasgrp2 |
T |
A |
19: 6,454,425 (GRCm39) |
M156K |
probably benign |
Het |
Reln |
G |
A |
5: 22,174,083 (GRCm39) |
H2007Y |
probably damaging |
Het |
Rhbdl2 |
T |
A |
4: 123,718,712 (GRCm39) |
I222K |
probably damaging |
Het |
Rimbp2 |
A |
G |
5: 128,865,582 (GRCm39) |
S582P |
probably damaging |
Het |
Rpe |
T |
C |
1: 66,754,387 (GRCm39) |
M153T |
probably damaging |
Het |
Sars1 |
T |
C |
3: 108,341,472 (GRCm39) |
I114V |
probably benign |
Het |
Scamp5 |
C |
A |
9: 57,354,508 (GRCm39) |
V49F |
possibly damaging |
Het |
Sec14l1 |
C |
T |
11: 117,039,358 (GRCm39) |
|
probably benign |
Het |
Serpinb8 |
A |
G |
1: 107,533,617 (GRCm39) |
E224G |
probably damaging |
Het |
Setd2 |
A |
G |
9: 110,378,932 (GRCm39) |
S632G |
probably benign |
Het |
Slco6c1 |
C |
T |
1: 96,993,808 (GRCm39) |
R645H |
possibly damaging |
Het |
Srgn |
T |
A |
10: 62,343,413 (GRCm39) |
|
probably benign |
Het |
Stk40 |
C |
T |
4: 126,022,640 (GRCm39) |
T138I |
probably benign |
Het |
Syt10 |
C |
T |
15: 89,674,979 (GRCm39) |
D456N |
probably damaging |
Het |
Tada3 |
T |
C |
6: 113,347,976 (GRCm39) |
I263V |
possibly damaging |
Het |
Tas2r106 |
A |
T |
6: 131,655,317 (GRCm39) |
L178H |
probably damaging |
Het |
Tas2r115 |
T |
A |
6: 132,714,470 (GRCm39) |
R160S |
possibly damaging |
Het |
Trak1 |
T |
A |
9: 121,302,063 (GRCm39) |
*940R |
probably null |
Het |
Trp53bp2 |
A |
G |
1: 182,269,204 (GRCm39) |
M223V |
probably benign |
Het |
Ttc21b |
C |
T |
2: 66,057,098 (GRCm39) |
V625I |
probably benign |
Het |
Txnrd1 |
T |
A |
10: 82,723,067 (GRCm39) |
C421S |
possibly damaging |
Het |
Unc45a |
T |
C |
7: 79,989,846 (GRCm39) |
T8A |
probably benign |
Het |
Usp6nl |
T |
A |
2: 6,445,748 (GRCm39) |
V552E |
probably damaging |
Het |
Vmn2r115 |
T |
G |
17: 23,578,297 (GRCm39) |
L590R |
probably damaging |
Het |
Vmn2r88 |
A |
T |
14: 51,650,665 (GRCm39) |
H126L |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,826,616 (GRCm39) |
D1419G |
possibly damaging |
Het |
Vwa3a |
A |
G |
7: 120,391,641 (GRCm39) |
T776A |
probably benign |
Het |
Zfp580 |
T |
C |
7: 5,056,008 (GRCm39) |
Y123H |
probably damaging |
Het |
|
Other mutations in Ecel1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01161:Ecel1
|
APN |
1 |
87,080,915 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01431:Ecel1
|
APN |
1 |
87,079,226 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01992:Ecel1
|
APN |
1 |
87,077,577 (GRCm39) |
splice site |
probably benign |
|
IGL02040:Ecel1
|
APN |
1 |
87,082,645 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02230:Ecel1
|
APN |
1 |
87,079,916 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Ecel1
|
APN |
1 |
87,079,725 (GRCm39) |
missense |
probably damaging |
1.00 |
Capulin
|
UTSW |
1 |
87,081,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R0139:Ecel1
|
UTSW |
1 |
87,082,248 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1723:Ecel1
|
UTSW |
1 |
87,082,143 (GRCm39) |
missense |
probably benign |
0.37 |
R2118:Ecel1
|
UTSW |
1 |
87,075,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2119:Ecel1
|
UTSW |
1 |
87,075,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Ecel1
|
UTSW |
1 |
87,075,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R3815:Ecel1
|
UTSW |
1 |
87,080,622 (GRCm39) |
missense |
probably damaging |
0.97 |
R3836:Ecel1
|
UTSW |
1 |
87,078,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Ecel1
|
UTSW |
1 |
87,079,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R4685:Ecel1
|
UTSW |
1 |
87,080,668 (GRCm39) |
splice site |
probably null |
|
R4841:Ecel1
|
UTSW |
1 |
87,081,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R4842:Ecel1
|
UTSW |
1 |
87,081,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R4888:Ecel1
|
UTSW |
1 |
87,076,449 (GRCm39) |
splice site |
probably benign |
|
R4976:Ecel1
|
UTSW |
1 |
87,078,861 (GRCm39) |
missense |
probably benign |
0.17 |
R5032:Ecel1
|
UTSW |
1 |
87,081,975 (GRCm39) |
missense |
probably damaging |
0.97 |
R5119:Ecel1
|
UTSW |
1 |
87,078,861 (GRCm39) |
missense |
probably benign |
0.17 |
R5393:Ecel1
|
UTSW |
1 |
87,080,598 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5798:Ecel1
|
UTSW |
1 |
87,079,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R5862:Ecel1
|
UTSW |
1 |
87,077,318 (GRCm39) |
missense |
probably benign |
0.19 |
R5874:Ecel1
|
UTSW |
1 |
87,075,731 (GRCm39) |
missense |
probably benign |
0.24 |
R6341:Ecel1
|
UTSW |
1 |
87,078,193 (GRCm39) |
splice site |
probably null |
|
R6351:Ecel1
|
UTSW |
1 |
87,077,231 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6534:Ecel1
|
UTSW |
1 |
87,082,564 (GRCm39) |
missense |
probably benign |
0.13 |
R7405:Ecel1
|
UTSW |
1 |
87,081,238 (GRCm39) |
critical splice donor site |
probably null |
|
R7422:Ecel1
|
UTSW |
1 |
87,077,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7850:Ecel1
|
UTSW |
1 |
87,079,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7939:Ecel1
|
UTSW |
1 |
87,077,256 (GRCm39) |
missense |
probably benign |
0.19 |
R7950:Ecel1
|
UTSW |
1 |
87,075,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R8022:Ecel1
|
UTSW |
1 |
87,081,052 (GRCm39) |
missense |
probably benign |
0.34 |
R8856:Ecel1
|
UTSW |
1 |
87,079,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Ecel1
|
UTSW |
1 |
87,076,349 (GRCm39) |
nonsense |
probably null |
|
R8967:Ecel1
|
UTSW |
1 |
87,078,862 (GRCm39) |
missense |
probably damaging |
0.98 |
R9248:Ecel1
|
UTSW |
1 |
87,081,112 (GRCm39) |
missense |
probably benign |
0.00 |
R9395:Ecel1
|
UTSW |
1 |
87,082,350 (GRCm39) |
missense |
probably damaging |
0.99 |
R9487:Ecel1
|
UTSW |
1 |
87,075,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R9620:Ecel1
|
UTSW |
1 |
87,080,853 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9676:Ecel1
|
UTSW |
1 |
87,079,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Ecel1
|
UTSW |
1 |
87,080,853 (GRCm39) |
missense |
possibly damaging |
0.65 |
|