Incidental Mutation 'R1912:Loxhd1'
ID |
210464 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Loxhd1
|
Ensembl Gene |
ENSMUSG00000032818 |
Gene Name |
lipoxygenase homology domains 1 |
Synonyms |
1700096C21Rik, sba |
MMRRC Submission |
039930-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.163)
|
Stock # |
R1912 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
18 |
Chromosomal Location |
77369654-77530626 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 77427833 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 468
(F468L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000094294
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035501]
[ENSMUST00000096547]
[ENSMUST00000148341]
|
AlphaFold |
C8YR32 |
Predicted Effect |
unknown
Transcript: ENSMUST00000035501
AA Change: F235L
|
SMART Domains |
Protein: ENSMUSP00000045450 Gene: ENSMUSG00000032818 AA Change: F235L
Domain | Start | End | E-Value | Type |
Pfam:PLAT
|
1 |
53 |
3.2e-7 |
PFAM |
LH2
|
63 |
176 |
1.1e-4 |
SMART |
LH2
|
192 |
306 |
4.02e-4 |
SMART |
LH2
|
320 |
442 |
3.79e-6 |
SMART |
LH2
|
451 |
567 |
5.92e-6 |
SMART |
LH2
|
581 |
696 |
7.67e-3 |
SMART |
LH2
|
793 |
913 |
1.47e-11 |
SMART |
low complexity region
|
922 |
931 |
N/A |
INTRINSIC |
SCOP:d1lox_2
|
949 |
974 |
1e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000096547
AA Change: F468L
PolyPhen 2
Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000094294 Gene: ENSMUSG00000032818 AA Change: F468L
Domain | Start | End | E-Value | Type |
LH2
|
43 |
158 |
5.64e-5 |
SMART |
LH2
|
172 |
290 |
1.64e-9 |
SMART |
LH2
|
296 |
409 |
1.1e-4 |
SMART |
LH2
|
425 |
539 |
4.02e-4 |
SMART |
LH2
|
553 |
675 |
3.79e-6 |
SMART |
LH2
|
684 |
800 |
5.92e-6 |
SMART |
LH2
|
814 |
936 |
6.91e-8 |
SMART |
low complexity region
|
945 |
954 |
N/A |
INTRINSIC |
LH2
|
970 |
1086 |
4.81e-7 |
SMART |
LH2
|
1101 |
1228 |
5.73e-3 |
SMART |
LH2
|
1255 |
1375 |
8.82e-5 |
SMART |
Pfam:PLAT
|
1424 |
1540 |
5.4e-10 |
PFAM |
LH2
|
1553 |
1666 |
6.41e-3 |
SMART |
LH2
|
1680 |
1799 |
6.76e-6 |
SMART |
Pfam:PLAT
|
1813 |
1929 |
3.8e-9 |
PFAM |
LH2
|
1949 |
2067 |
7.23e-11 |
SMART |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000148341
AA Change: F149L
|
SMART Domains |
Protein: ENSMUSP00000114988 Gene: ENSMUSG00000032818 AA Change: F149L
Domain | Start | End | E-Value | Type |
Pfam:PLAT
|
1 |
91 |
1.7e-11 |
PFAM |
LH2
|
106 |
220 |
4.02e-4 |
SMART |
LH2
|
234 |
356 |
3.79e-6 |
SMART |
LH2
|
365 |
481 |
5.92e-6 |
SMART |
LH2
|
495 |
610 |
7.67e-3 |
SMART |
LH2
|
707 |
827 |
1.47e-11 |
SMART |
low complexity region
|
836 |
845 |
N/A |
INTRINSIC |
LH2
|
861 |
977 |
4.81e-7 |
SMART |
LH2
|
992 |
1119 |
5.73e-3 |
SMART |
LH2
|
1146 |
1266 |
8.82e-5 |
SMART |
Pfam:PLAT
|
1384 |
1469 |
8.9e-14 |
PFAM |
|
Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.8%
- 10x: 95.3%
- 20x: 92.8%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice honozygous for an ENU-induced mutation exhibit hearing loss associated with hair cell and spiral ganglion degeneration. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
A |
G |
7: 12,288,582 (GRCm39) |
M132V |
probably benign |
Het |
4921524L21Rik |
T |
A |
18: 6,620,205 (GRCm39) |
I45N |
possibly damaging |
Het |
Abcb6 |
A |
G |
1: 75,156,599 (GRCm39) |
V55A |
probably benign |
Het |
Adam28 |
A |
T |
14: 68,881,780 (GRCm39) |
D105E |
probably benign |
Het |
Ahnak |
T |
C |
19: 8,995,245 (GRCm39) |
S5510P |
probably damaging |
Het |
Aldh3b1 |
T |
G |
19: 3,971,187 (GRCm39) |
D159A |
probably damaging |
Het |
Alx1 |
A |
G |
10: 102,861,222 (GRCm39) |
L102P |
probably damaging |
Het |
Ankrd50 |
C |
T |
3: 38,510,925 (GRCm39) |
V481I |
probably benign |
Het |
Aox4 |
G |
T |
1: 58,303,561 (GRCm39) |
G1200W |
probably damaging |
Het |
Arhgap45 |
A |
C |
10: 79,856,524 (GRCm39) |
D24A |
probably benign |
Het |
Arhgef16 |
A |
T |
4: 154,364,780 (GRCm39) |
|
probably null |
Het |
Asic4 |
A |
T |
1: 75,445,876 (GRCm39) |
Y235F |
possibly damaging |
Het |
Asph |
T |
C |
4: 9,453,335 (GRCm39) |
E646G |
probably damaging |
Het |
Atg4d |
A |
G |
9: 21,183,935 (GRCm39) |
D350G |
probably damaging |
Het |
Auts2 |
T |
C |
5: 131,472,412 (GRCm39) |
T347A |
probably damaging |
Het |
Bsnd |
A |
T |
4: 106,345,227 (GRCm39) |
L73* |
probably null |
Het |
Cachd1 |
A |
T |
4: 100,810,366 (GRCm39) |
S323C |
probably damaging |
Het |
Cacna1e |
A |
G |
1: 154,312,195 (GRCm39) |
I1290T |
probably damaging |
Het |
Cdh8 |
T |
A |
8: 99,825,502 (GRCm39) |
N498Y |
probably damaging |
Het |
Cdkn3 |
A |
G |
14: 47,007,291 (GRCm39) |
|
probably null |
Het |
Celf2 |
A |
T |
2: 6,620,564 (GRCm39) |
M40K |
probably damaging |
Het |
Cfap57 |
A |
C |
4: 118,472,207 (GRCm39) |
S57R |
probably damaging |
Het |
Cfh |
A |
G |
1: 140,063,879 (GRCm39) |
|
probably null |
Het |
Chdh |
A |
G |
14: 29,754,745 (GRCm39) |
S252G |
probably benign |
Het |
Col8a1 |
T |
A |
16: 57,448,287 (GRCm39) |
I408F |
unknown |
Het |
Corin |
C |
T |
5: 72,515,746 (GRCm39) |
C303Y |
probably damaging |
Het |
Crlf2 |
C |
T |
5: 109,705,007 (GRCm39) |
C66Y |
possibly damaging |
Het |
Csmd1 |
C |
T |
8: 16,284,012 (GRCm39) |
|
probably null |
Het |
Cyp4f16 |
T |
C |
17: 32,764,018 (GRCm39) |
V270A |
probably damaging |
Het |
Defa29 |
T |
A |
8: 21,816,028 (GRCm39) |
H113L |
possibly damaging |
Het |
Dhx35 |
A |
T |
2: 158,684,227 (GRCm39) |
N501Y |
probably damaging |
Het |
Dipk1b |
A |
G |
2: 26,522,716 (GRCm39) |
E55G |
probably damaging |
Het |
Dst |
A |
G |
1: 34,330,931 (GRCm39) |
R4690G |
probably damaging |
Het |
Elac2 |
T |
A |
11: 64,885,089 (GRCm39) |
D439E |
probably benign |
Het |
Ercc6 |
A |
G |
14: 32,298,760 (GRCm39) |
R1383G |
probably damaging |
Het |
Fat3 |
T |
A |
9: 15,881,284 (GRCm39) |
Y3196F |
probably damaging |
Het |
Fbxw13 |
A |
T |
9: 109,010,611 (GRCm39) |
D342E |
probably benign |
Het |
Fmod |
A |
G |
1: 133,968,458 (GRCm39) |
N166S |
possibly damaging |
Het |
Folh1 |
A |
G |
7: 86,412,175 (GRCm39) |
S199P |
possibly damaging |
Het |
Fv1 |
A |
G |
4: 147,954,235 (GRCm39) |
N267S |
possibly damaging |
Het |
Fyn |
T |
C |
10: 39,402,828 (GRCm39) |
V200A |
possibly damaging |
Het |
Gfus |
A |
T |
15: 75,797,498 (GRCm39) |
D278E |
possibly damaging |
Het |
Ggnbp2 |
T |
C |
11: 84,753,122 (GRCm39) |
N39S |
probably benign |
Het |
Gm10509 |
A |
T |
17: 21,909,831 (GRCm39) |
I53F |
possibly damaging |
Het |
Gpr139 |
A |
T |
7: 118,744,102 (GRCm39) |
I161N |
possibly damaging |
Het |
Grhl2 |
C |
T |
15: 37,358,651 (GRCm39) |
T148I |
probably damaging |
Het |
Hmcn1 |
C |
A |
1: 150,480,633 (GRCm39) |
M4514I |
probably benign |
Het |
Igsf10 |
T |
G |
3: 59,236,993 (GRCm39) |
T1063P |
probably benign |
Het |
Itgav |
A |
G |
2: 83,625,830 (GRCm39) |
Y792C |
possibly damaging |
Het |
Itgb2l |
T |
C |
16: 96,228,135 (GRCm39) |
Q456R |
probably benign |
Het |
Jph4 |
G |
A |
14: 55,345,818 (GRCm39) |
A613V |
probably benign |
Het |
Kcna2 |
A |
G |
3: 107,012,717 (GRCm39) |
T433A |
probably benign |
Het |
Kmt2e |
A |
G |
5: 23,697,393 (GRCm39) |
K97R |
probably benign |
Het |
Krba1 |
C |
A |
6: 48,392,699 (GRCm39) |
A871E |
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,596,728 (GRCm39) |
V713A |
probably damaging |
Het |
Ltbp2 |
T |
A |
12: 84,832,637 (GRCm39) |
I67F |
probably damaging |
Het |
Mdc1 |
G |
A |
17: 36,155,430 (GRCm39) |
R35H |
probably benign |
Het |
Mdc1 |
A |
G |
17: 36,161,703 (GRCm39) |
D872G |
probably benign |
Het |
Mgam |
C |
T |
6: 40,741,119 (GRCm39) |
Q959* |
probably null |
Het |
Mttp |
T |
A |
3: 137,821,788 (GRCm39) |
T260S |
probably benign |
Het |
Naalad2 |
A |
T |
9: 18,287,831 (GRCm39) |
D266E |
probably benign |
Het |
Nans |
T |
A |
4: 46,500,162 (GRCm39) |
L182H |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,616,145 (GRCm39) |
C2228S |
probably benign |
Het |
Nfix |
A |
T |
8: 85,448,306 (GRCm39) |
V407E |
probably damaging |
Het |
Nktr |
T |
A |
9: 121,579,306 (GRCm39) |
|
probably benign |
Het |
Nlrp10 |
G |
A |
7: 108,524,602 (GRCm39) |
R293* |
probably null |
Het |
Nrxn3 |
T |
C |
12: 88,762,112 (GRCm39) |
F53S |
probably damaging |
Het |
Or11h4 |
G |
A |
14: 50,974,235 (GRCm39) |
P128L |
probably damaging |
Het |
Or12e7 |
T |
C |
2: 87,287,727 (GRCm39) |
S73P |
probably damaging |
Het |
Or1e21 |
A |
T |
11: 73,344,820 (GRCm39) |
F73I |
probably damaging |
Het |
Or2f2 |
T |
C |
6: 42,767,411 (GRCm39) |
I146T |
probably benign |
Het |
Or3a1c |
T |
C |
11: 74,046,711 (GRCm39) |
C244R |
probably damaging |
Het |
Or5ak24 |
T |
A |
2: 85,260,604 (GRCm39) |
N190Y |
probably damaging |
Het |
Or5p68 |
A |
G |
7: 107,946,014 (GRCm39) |
L58P |
probably damaging |
Het |
Or6d12 |
A |
G |
6: 116,492,950 (GRCm39) |
T71A |
probably benign |
Het |
Oxld1 |
A |
G |
11: 120,347,732 (GRCm39) |
V155A |
probably damaging |
Het |
Pamr1 |
T |
A |
2: 102,472,645 (GRCm39) |
F648Y |
probably damaging |
Het |
Parg |
T |
C |
14: 31,932,497 (GRCm39) |
W446R |
probably damaging |
Het |
Pate13 |
A |
T |
9: 35,819,915 (GRCm39) |
T23S |
probably benign |
Het |
Phf3 |
A |
T |
1: 30,843,426 (GRCm39) |
H1844Q |
probably damaging |
Het |
Phf7 |
T |
C |
14: 30,962,281 (GRCm39) |
I175V |
possibly damaging |
Het |
Pibf1 |
G |
A |
14: 99,425,245 (GRCm39) |
|
probably null |
Het |
Plcxd1 |
A |
G |
5: 110,251,308 (GRCm39) |
I295V |
probably benign |
Het |
Pole2 |
A |
C |
12: 69,256,764 (GRCm39) |
Y254D |
probably damaging |
Het |
Ppm1e |
T |
A |
11: 87,135,196 (GRCm39) |
I225F |
probably benign |
Het |
Pttg1ip2 |
C |
A |
5: 5,502,019 (GRCm39) |
W144C |
probably benign |
Het |
Rem1 |
G |
A |
2: 152,476,455 (GRCm39) |
V238M |
probably damaging |
Het |
Resf1 |
T |
A |
6: 149,230,342 (GRCm39) |
D1129E |
possibly damaging |
Het |
Rnase2b |
T |
G |
14: 51,400,357 (GRCm39) |
V146G |
probably damaging |
Het |
Rnf169 |
G |
A |
7: 99,575,461 (GRCm39) |
T378I |
probably damaging |
Het |
Rpf2 |
A |
G |
10: 40,112,197 (GRCm39) |
F80L |
probably benign |
Het |
Sec11c |
T |
A |
18: 65,947,945 (GRCm39) |
D128E |
probably damaging |
Het |
Septin12 |
A |
G |
16: 4,806,417 (GRCm39) |
V248A |
probably damaging |
Het |
Serinc1 |
T |
C |
10: 57,401,547 (GRCm39) |
N82S |
probably benign |
Het |
Serpina9 |
A |
C |
12: 103,967,508 (GRCm39) |
W296G |
probably damaging |
Het |
Sgo2b |
A |
C |
8: 64,384,503 (GRCm39) |
D164E |
probably damaging |
Het |
Slc15a3 |
A |
G |
19: 10,825,977 (GRCm39) |
N223D |
probably damaging |
Het |
Slc44a3 |
A |
G |
3: 121,325,815 (GRCm39) |
Y12H |
probably benign |
Het |
Slco3a1 |
A |
G |
7: 74,154,359 (GRCm39) |
F42S |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Snx7 |
A |
T |
3: 117,623,317 (GRCm39) |
|
probably null |
Het |
Sorl1 |
A |
T |
9: 41,993,246 (GRCm39) |
D259E |
probably damaging |
Het |
Stpg2 |
G |
A |
3: 139,228,742 (GRCm39) |
|
probably null |
Het |
Strn |
T |
A |
17: 78,991,824 (GRCm39) |
Y165F |
probably damaging |
Het |
Sval2 |
T |
A |
6: 41,841,254 (GRCm39) |
*106R |
probably null |
Het |
Tcaf3 |
A |
G |
6: 42,573,622 (GRCm39) |
S197P |
possibly damaging |
Het |
Tespa1 |
C |
A |
10: 130,190,592 (GRCm39) |
T73N |
probably benign |
Het |
Tex10 |
C |
T |
4: 48,456,800 (GRCm39) |
R637Q |
probably benign |
Het |
Thoc5 |
C |
A |
11: 4,865,561 (GRCm39) |
T380K |
probably benign |
Het |
Tmprss7 |
T |
A |
16: 45,476,911 (GRCm39) |
R784* |
probably null |
Het |
Trank1 |
A |
T |
9: 111,219,777 (GRCm39) |
L2171F |
probably benign |
Het |
Trpm2 |
T |
G |
10: 77,781,710 (GRCm39) |
K303T |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,549,784 (GRCm39) |
V681M |
probably damaging |
Het |
Usp40 |
A |
G |
1: 87,874,368 (GRCm39) |
F1131L |
probably benign |
Het |
Vmn1r215 |
A |
T |
13: 23,260,673 (GRCm39) |
I238F |
possibly damaging |
Het |
Vwa3a |
A |
T |
7: 120,394,850 (GRCm39) |
Y890F |
probably damaging |
Het |
Zdhhc18 |
A |
G |
4: 133,341,171 (GRCm39) |
L234P |
probably damaging |
Het |
Zfp109 |
A |
G |
7: 23,927,676 (GRCm39) |
S578P |
probably damaging |
Het |
Zfp704 |
T |
C |
3: 9,674,418 (GRCm39) |
D121G |
unknown |
Het |
Zgrf1 |
G |
T |
3: 127,356,786 (GRCm39) |
V671L |
probably benign |
Het |
Zkscan8 |
A |
T |
13: 21,704,927 (GRCm39) |
C265* |
probably null |
Het |
Zscan26 |
T |
C |
13: 21,629,310 (GRCm39) |
I398V |
possibly damaging |
Het |
|
Other mutations in Loxhd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Loxhd1
|
APN |
18 |
77,483,146 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00490:Loxhd1
|
APN |
18 |
77,518,770 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00507:Loxhd1
|
APN |
18 |
77,420,263 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00546:Loxhd1
|
APN |
18 |
77,493,672 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01369:Loxhd1
|
APN |
18 |
77,416,897 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01767:Loxhd1
|
APN |
18 |
77,374,120 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02245:Loxhd1
|
APN |
18 |
77,427,797 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02388:Loxhd1
|
APN |
18 |
77,456,833 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02410:Loxhd1
|
APN |
18 |
77,490,648 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02593:Loxhd1
|
APN |
18 |
77,498,235 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02632:Loxhd1
|
APN |
18 |
77,493,628 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02692:Loxhd1
|
APN |
18 |
77,444,609 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02796:Loxhd1
|
APN |
18 |
77,456,811 (GRCm39) |
splice site |
probably benign |
|
IGL03032:Loxhd1
|
APN |
18 |
77,374,169 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03074:Loxhd1
|
APN |
18 |
77,529,480 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03094:Loxhd1
|
APN |
18 |
77,518,809 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03118:Loxhd1
|
APN |
18 |
77,468,160 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03232:Loxhd1
|
APN |
18 |
77,496,446 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03377:Loxhd1
|
APN |
18 |
77,529,369 (GRCm39) |
missense |
possibly damaging |
0.91 |
H8562:Loxhd1
|
UTSW |
18 |
77,429,627 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4494001:Loxhd1
|
UTSW |
18 |
77,529,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R0003:Loxhd1
|
UTSW |
18 |
77,427,196 (GRCm39) |
missense |
probably damaging |
0.98 |
R0003:Loxhd1
|
UTSW |
18 |
77,427,196 (GRCm39) |
missense |
probably damaging |
0.98 |
R0048:Loxhd1
|
UTSW |
18 |
77,496,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R0049:Loxhd1
|
UTSW |
18 |
77,468,256 (GRCm39) |
splice site |
probably benign |
|
R0049:Loxhd1
|
UTSW |
18 |
77,468,256 (GRCm39) |
splice site |
probably benign |
|
R0206:Loxhd1
|
UTSW |
18 |
77,492,562 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0206:Loxhd1
|
UTSW |
18 |
77,492,562 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0208:Loxhd1
|
UTSW |
18 |
77,492,562 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0323:Loxhd1
|
UTSW |
18 |
77,456,833 (GRCm39) |
missense |
probably benign |
0.18 |
R0332:Loxhd1
|
UTSW |
18 |
77,471,526 (GRCm39) |
splice site |
probably null |
|
R0367:Loxhd1
|
UTSW |
18 |
77,513,453 (GRCm39) |
splice site |
probably benign |
|
R0709:Loxhd1
|
UTSW |
18 |
77,492,665 (GRCm39) |
missense |
probably benign |
0.23 |
R0783:Loxhd1
|
UTSW |
18 |
77,517,680 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1132:Loxhd1
|
UTSW |
18 |
77,517,639 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1232:Loxhd1
|
UTSW |
18 |
77,493,699 (GRCm39) |
critical splice donor site |
probably null |
|
R1331:Loxhd1
|
UTSW |
18 |
77,490,632 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1465:Loxhd1
|
UTSW |
18 |
77,468,269 (GRCm39) |
splice site |
probably null |
|
R1465:Loxhd1
|
UTSW |
18 |
77,468,269 (GRCm39) |
splice site |
probably null |
|
R1501:Loxhd1
|
UTSW |
18 |
77,444,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Loxhd1
|
UTSW |
18 |
77,490,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1656:Loxhd1
|
UTSW |
18 |
77,409,364 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1671:Loxhd1
|
UTSW |
18 |
77,492,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Loxhd1
|
UTSW |
18 |
77,380,937 (GRCm39) |
missense |
probably benign |
0.32 |
R1735:Loxhd1
|
UTSW |
18 |
77,492,585 (GRCm39) |
missense |
probably damaging |
0.98 |
R1796:Loxhd1
|
UTSW |
18 |
77,513,335 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1796:Loxhd1
|
UTSW |
18 |
77,493,603 (GRCm39) |
missense |
probably damaging |
0.96 |
R1800:Loxhd1
|
UTSW |
18 |
77,490,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Loxhd1
|
UTSW |
18 |
77,369,667 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1945:Loxhd1
|
UTSW |
18 |
77,492,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1978:Loxhd1
|
UTSW |
18 |
77,409,338 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1997:Loxhd1
|
UTSW |
18 |
77,383,465 (GRCm39) |
missense |
probably damaging |
0.98 |
R2086:Loxhd1
|
UTSW |
18 |
77,472,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Loxhd1
|
UTSW |
18 |
77,443,862 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3124:Loxhd1
|
UTSW |
18 |
77,518,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R3896:Loxhd1
|
UTSW |
18 |
77,469,719 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3907:Loxhd1
|
UTSW |
18 |
77,496,464 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3980:Loxhd1
|
UTSW |
18 |
77,501,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R4165:Loxhd1
|
UTSW |
18 |
77,460,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R4166:Loxhd1
|
UTSW |
18 |
77,460,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R4176:Loxhd1
|
UTSW |
18 |
77,418,755 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4345:Loxhd1
|
UTSW |
18 |
77,486,697 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4354:Loxhd1
|
UTSW |
18 |
77,483,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Loxhd1
|
UTSW |
18 |
77,460,607 (GRCm39) |
missense |
probably damaging |
0.99 |
R4402:Loxhd1
|
UTSW |
18 |
77,529,456 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4404:Loxhd1
|
UTSW |
18 |
77,518,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4456:Loxhd1
|
UTSW |
18 |
77,486,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R4525:Loxhd1
|
UTSW |
18 |
77,444,608 (GRCm39) |
missense |
probably damaging |
0.98 |
R4605:Loxhd1
|
UTSW |
18 |
77,493,642 (GRCm39) |
missense |
probably benign |
0.00 |
R4661:Loxhd1
|
UTSW |
18 |
77,490,581 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4698:Loxhd1
|
UTSW |
18 |
77,459,987 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4725:Loxhd1
|
UTSW |
18 |
77,483,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Loxhd1
|
UTSW |
18 |
77,472,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Loxhd1
|
UTSW |
18 |
77,449,432 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5288:Loxhd1
|
UTSW |
18 |
77,451,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Loxhd1
|
UTSW |
18 |
77,498,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R5329:Loxhd1
|
UTSW |
18 |
77,420,378 (GRCm39) |
missense |
probably damaging |
0.98 |
R5347:Loxhd1
|
UTSW |
18 |
77,454,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R5589:Loxhd1
|
UTSW |
18 |
77,429,751 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5616:Loxhd1
|
UTSW |
18 |
77,492,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5703:Loxhd1
|
UTSW |
18 |
77,444,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R5837:Loxhd1
|
UTSW |
18 |
77,374,105 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5888:Loxhd1
|
UTSW |
18 |
77,490,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R6021:Loxhd1
|
UTSW |
18 |
77,499,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Loxhd1
|
UTSW |
18 |
77,469,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Loxhd1
|
UTSW |
18 |
77,469,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R6153:Loxhd1
|
UTSW |
18 |
77,383,454 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6174:Loxhd1
|
UTSW |
18 |
77,499,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Loxhd1
|
UTSW |
18 |
77,449,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R6377:Loxhd1
|
UTSW |
18 |
77,468,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6530:Loxhd1
|
UTSW |
18 |
77,499,847 (GRCm39) |
missense |
probably benign |
0.30 |
R6555:Loxhd1
|
UTSW |
18 |
77,380,965 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6782:Loxhd1
|
UTSW |
18 |
77,518,873 (GRCm39) |
missense |
probably damaging |
0.99 |
R6834:Loxhd1
|
UTSW |
18 |
77,529,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:Loxhd1
|
UTSW |
18 |
77,460,129 (GRCm39) |
critical splice donor site |
probably null |
|
R7112:Loxhd1
|
UTSW |
18 |
77,476,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Loxhd1
|
UTSW |
18 |
77,501,892 (GRCm39) |
missense |
probably damaging |
0.97 |
R7206:Loxhd1
|
UTSW |
18 |
77,529,513 (GRCm39) |
missense |
probably damaging |
0.97 |
R7260:Loxhd1
|
UTSW |
18 |
77,420,338 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7432:Loxhd1
|
UTSW |
18 |
77,383,547 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7475:Loxhd1
|
UTSW |
18 |
77,500,001 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7555:Loxhd1
|
UTSW |
18 |
77,483,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R7590:Loxhd1
|
UTSW |
18 |
77,409,330 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7612:Loxhd1
|
UTSW |
18 |
77,517,671 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7626:Loxhd1
|
UTSW |
18 |
77,518,882 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7768:Loxhd1
|
UTSW |
18 |
77,472,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R7791:Loxhd1
|
UTSW |
18 |
77,471,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R7829:Loxhd1
|
UTSW |
18 |
77,496,483 (GRCm39) |
missense |
probably damaging |
0.99 |
R7884:Loxhd1
|
UTSW |
18 |
77,518,909 (GRCm39) |
missense |
probably damaging |
0.98 |
R7960:Loxhd1
|
UTSW |
18 |
77,472,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R7986:Loxhd1
|
UTSW |
18 |
77,462,890 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8042:Loxhd1
|
UTSW |
18 |
77,518,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R8084:Loxhd1
|
UTSW |
18 |
77,427,845 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8088:Loxhd1
|
UTSW |
18 |
77,429,709 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8100:Loxhd1
|
UTSW |
18 |
77,492,512 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8139:Loxhd1
|
UTSW |
18 |
77,468,192 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8152:Loxhd1
|
UTSW |
18 |
77,476,095 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8199:Loxhd1
|
UTSW |
18 |
77,469,334 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8246:Loxhd1
|
UTSW |
18 |
77,451,242 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8263:Loxhd1
|
UTSW |
18 |
77,462,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Loxhd1
|
UTSW |
18 |
77,427,275 (GRCm39) |
critical splice donor site |
probably null |
|
R8342:Loxhd1
|
UTSW |
18 |
77,493,681 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8401:Loxhd1
|
UTSW |
18 |
77,468,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R8480:Loxhd1
|
UTSW |
18 |
77,518,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8490:Loxhd1
|
UTSW |
18 |
77,529,162 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8807:Loxhd1
|
UTSW |
18 |
77,444,468 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8961:Loxhd1
|
UTSW |
18 |
77,472,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R8974:Loxhd1
|
UTSW |
18 |
77,518,899 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9079:Loxhd1
|
UTSW |
18 |
77,490,593 (GRCm39) |
missense |
probably benign |
|
R9284:Loxhd1
|
UTSW |
18 |
77,501,826 (GRCm39) |
missense |
probably damaging |
0.97 |
R9312:Loxhd1
|
UTSW |
18 |
77,498,285 (GRCm39) |
missense |
probably benign |
0.05 |
R9619:Loxhd1
|
UTSW |
18 |
77,443,871 (GRCm39) |
missense |
probably benign |
0.32 |
X0020:Loxhd1
|
UTSW |
18 |
77,427,258 (GRCm39) |
nonsense |
probably null |
|
X0024:Loxhd1
|
UTSW |
18 |
77,483,099 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Loxhd1
|
UTSW |
18 |
77,529,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGAGTTTACAACGCACCG -3'
(R):5'- TGGACTATTTCAGGTGGAAGATC -3'
Sequencing Primer
(F):5'- GTTTACAACGCACCGTGACCTG -3'
(R):5'- TTTCAGGTGGAAGATCAAACATAAGC -3'
|
Posted On |
2014-06-30 |