Incidental Mutation 'R7432:Lmo7'
ID |
576588 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Lmo7
|
Ensembl Gene |
ENSMUSG00000033060 |
Gene Name |
LIM domain only 7 |
Synonyms |
FBXO20, LOC380928 |
MMRRC Submission |
045510-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.133)
|
Stock # |
R7432 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
101967393-102172146 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 102139551 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Lysine
at position 945
(Q945K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000097910
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100337]
[ENSMUST00000159026]
[ENSMUST00000159258]
[ENSMUST00000159314]
[ENSMUST00000159597]
|
AlphaFold |
E9PYF4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000100337
AA Change: Q945K
PolyPhen 2
Score 0.421 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000097910 Gene: ENSMUSG00000033060 AA Change: Q945K
Domain | Start | End | E-Value | Type |
CH
|
14 |
124 |
2.57e-13 |
SMART |
low complexity region
|
200 |
211 |
N/A |
INTRINSIC |
Pfam:DUF4757
|
242 |
348 |
2.2e-14 |
PFAM |
low complexity region
|
448 |
462 |
N/A |
INTRINSIC |
Pfam:DUF4757
|
568 |
735 |
1.8e-46 |
PFAM |
low complexity region
|
861 |
879 |
N/A |
INTRINSIC |
low complexity region
|
979 |
991 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1015 |
N/A |
INTRINSIC |
PDZ
|
1047 |
1119 |
1.05e-8 |
SMART |
coiled coil region
|
1222 |
1275 |
N/A |
INTRINSIC |
coiled coil region
|
1319 |
1411 |
N/A |
INTRINSIC |
low complexity region
|
1585 |
1596 |
N/A |
INTRINSIC |
low complexity region
|
1599 |
1617 |
N/A |
INTRINSIC |
LIM
|
1629 |
1687 |
6.54e-10 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159026
|
SMART Domains |
Protein: ENSMUSP00000124605 Gene: ENSMUSG00000033060
Domain | Start | End | E-Value | Type |
low complexity region
|
215 |
229 |
N/A |
INTRINSIC |
coiled coil region
|
435 |
471 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159258
|
SMART Domains |
Protein: ENSMUSP00000125465 Gene: ENSMUSG00000033060
Domain | Start | End | E-Value | Type |
low complexity region
|
215 |
229 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000159314
AA Change: Q712K
PolyPhen 2
Score 0.657 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000124349 Gene: ENSMUSG00000033060 AA Change: Q712K
Domain | Start | End | E-Value | Type |
low complexity region
|
215 |
229 |
N/A |
INTRINSIC |
coiled coil region
|
435 |
492 |
N/A |
INTRINSIC |
low complexity region
|
628 |
646 |
N/A |
INTRINSIC |
low complexity region
|
746 |
758 |
N/A |
INTRINSIC |
low complexity region
|
770 |
782 |
N/A |
INTRINSIC |
PDZ
|
814 |
886 |
1.05e-8 |
SMART |
coiled coil region
|
989 |
1042 |
N/A |
INTRINSIC |
coiled coil region
|
1086 |
1178 |
N/A |
INTRINSIC |
low complexity region
|
1352 |
1363 |
N/A |
INTRINSIC |
low complexity region
|
1366 |
1384 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000159597
AA Change: Q823K
PolyPhen 2
Score 0.526 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000123706 Gene: ENSMUSG00000033060 AA Change: Q823K
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
89 |
N/A |
INTRINSIC |
internal_repeat_1
|
111 |
141 |
6.96e-5 |
PROSPERO |
internal_repeat_1
|
218 |
248 |
6.96e-5 |
PROSPERO |
low complexity region
|
326 |
340 |
N/A |
INTRINSIC |
coiled coil region
|
546 |
603 |
N/A |
INTRINSIC |
low complexity region
|
739 |
757 |
N/A |
INTRINSIC |
low complexity region
|
857 |
869 |
N/A |
INTRINSIC |
low complexity region
|
881 |
893 |
N/A |
INTRINSIC |
PDZ
|
925 |
997 |
1.05e-8 |
SMART |
coiled coil region
|
1127 |
1180 |
N/A |
INTRINSIC |
coiled coil region
|
1224 |
1316 |
N/A |
INTRINSIC |
low complexity region
|
1490 |
1501 |
N/A |
INTRINSIC |
low complexity region
|
1504 |
1522 |
N/A |
INTRINSIC |
LIM
|
1534 |
1592 |
6.54e-10 |
SMART |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000124300 Gene: ENSMUSG00000033060 AA Change: Q434K
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
45 |
N/A |
INTRINSIC |
Pfam:DUF4757
|
76 |
225 |
4.5e-53 |
PFAM |
low complexity region
|
351 |
369 |
N/A |
INTRINSIC |
low complexity region
|
469 |
481 |
N/A |
INTRINSIC |
low complexity region
|
493 |
505 |
N/A |
INTRINSIC |
PDZ
|
537 |
609 |
1.05e-8 |
SMART |
internal_repeat_1
|
620 |
691 |
9.31e-5 |
PROSPERO |
coiled coil region
|
711 |
764 |
N/A |
INTRINSIC |
coiled coil region
|
808 |
900 |
N/A |
INTRINSIC |
internal_repeat_1
|
921 |
976 |
9.31e-5 |
PROSPERO |
low complexity region
|
1075 |
1086 |
N/A |
INTRINSIC |
low complexity region
|
1089 |
1107 |
N/A |
INTRINSIC |
LIM
|
1119 |
1177 |
6.54e-10 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing a calponin homology (CH) domain, a PDZ domain, and a LIM domain, and may be involved in protein-protein interactions. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene, however, the full-length nature of some variants is not known. [provided by RefSeq, Jan 2009] PHENOTYPE: Targeted mutations in this gene result in postnatal lethality, growth defects, skeletal muscle abnormalities and retinal defects reflective of retinal degeneration. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
T |
C |
11: 23,468,839 (GRCm39) |
I31V |
probably benign |
Het |
Adamts17 |
A |
G |
7: 66,701,665 (GRCm39) |
K40E |
|
Het |
Akr1c14 |
G |
A |
13: 4,138,952 (GRCm39) |
D312N |
probably benign |
Het |
Alg6 |
T |
C |
4: 99,641,295 (GRCm39) |
V398A |
probably benign |
Het |
Ankmy1 |
A |
T |
1: 92,823,801 (GRCm39) |
M155K |
probably benign |
Het |
Arid5b |
C |
A |
10: 67,954,096 (GRCm39) |
R396L |
probably damaging |
Het |
Armt1 |
C |
A |
10: 4,382,706 (GRCm39) |
D12E |
probably benign |
Het |
Arrb2 |
T |
A |
11: 70,328,796 (GRCm39) |
N217K |
probably benign |
Het |
Atg2b |
A |
T |
12: 105,627,463 (GRCm39) |
L508Q |
probably damaging |
Het |
Atg2b |
A |
T |
12: 105,630,957 (GRCm39) |
S323T |
probably benign |
Het |
Atp1a3 |
G |
A |
7: 24,705,300 (GRCm39) |
|
probably benign |
Het |
Atp6v0e |
T |
C |
17: 26,901,672 (GRCm39) |
V42A |
probably benign |
Het |
Atp9b |
A |
G |
18: 80,809,056 (GRCm39) |
V621A |
|
Het |
Atrnl1 |
A |
C |
19: 57,743,956 (GRCm39) |
D1186A |
probably damaging |
Het |
Atxn2l |
A |
T |
7: 126,093,046 (GRCm39) |
M821K |
possibly damaging |
Het |
Blnk |
G |
A |
19: 40,948,301 (GRCm39) |
R123* |
probably null |
Het |
Bud13 |
T |
A |
9: 46,198,372 (GRCm39) |
S98T |
probably benign |
Het |
Ccdc183 |
T |
C |
2: 25,499,469 (GRCm39) |
M455V |
probably benign |
Het |
Cd109 |
A |
G |
9: 78,622,225 (GRCm39) |
Y1405C |
possibly damaging |
Het |
Cdan1 |
A |
T |
2: 120,553,236 (GRCm39) |
L989Q |
probably damaging |
Het |
Clec16a |
T |
C |
16: 10,506,419 (GRCm39) |
I713T |
possibly damaging |
Het |
Clta |
T |
A |
4: 44,032,419 (GRCm39) |
F168L |
possibly damaging |
Het |
Cnnm1 |
A |
T |
19: 43,456,710 (GRCm39) |
H583L |
probably benign |
Het |
Cyp4f18 |
A |
G |
8: 72,749,906 (GRCm39) |
Y248H |
probably benign |
Het |
Dsg4 |
G |
T |
18: 20,579,323 (GRCm39) |
G20* |
probably null |
Het |
Dusp12 |
T |
A |
1: 170,707,345 (GRCm39) |
K248* |
probably null |
Het |
Eeig2 |
C |
T |
3: 108,910,723 (GRCm39) |
A51T |
probably damaging |
Het |
Elp1 |
C |
T |
4: 56,776,925 (GRCm39) |
G624D |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,134,966 (GRCm39) |
D359G |
possibly damaging |
Het |
Frmpd2 |
C |
A |
14: 33,229,510 (GRCm39) |
F365L |
probably damaging |
Het |
Gab1 |
A |
G |
8: 81,515,298 (GRCm39) |
I340T |
probably benign |
Het |
Gabpa |
C |
T |
16: 84,654,408 (GRCm39) |
Q362* |
probably null |
Het |
Gcnt2 |
A |
T |
13: 41,040,688 (GRCm39) |
|
probably benign |
Het |
Gm12728 |
T |
A |
4: 105,651,486 (GRCm39) |
L32Q |
probably damaging |
Het |
Gpatch4 |
A |
G |
3: 87,959,003 (GRCm39) |
N35D |
probably damaging |
Het |
Grid2 |
G |
T |
6: 64,252,854 (GRCm39) |
V441L |
possibly damaging |
Het |
H2-M2 |
A |
G |
17: 37,792,361 (GRCm39) |
|
probably null |
Het |
Hip1r |
T |
C |
5: 124,129,829 (GRCm39) |
F180L |
probably benign |
Het |
Il17re |
T |
C |
6: 113,439,332 (GRCm39) |
F81L |
probably benign |
Het |
Il3ra |
T |
C |
14: 14,350,691 (GRCm38) |
V235A |
possibly damaging |
Het |
Krtap6-2 |
C |
T |
16: 89,216,761 (GRCm39) |
G69S |
unknown |
Het |
Lmln |
T |
C |
16: 32,909,738 (GRCm39) |
L373P |
probably damaging |
Het |
Loxhd1 |
G |
T |
18: 77,383,547 (GRCm39) |
V149L |
possibly damaging |
Het |
Lrrc73 |
T |
C |
17: 46,566,709 (GRCm39) |
|
probably null |
Het |
Mapkapk5 |
G |
A |
5: 121,675,234 (GRCm39) |
H112Y |
possibly damaging |
Het |
Maz |
A |
G |
7: 126,622,220 (GRCm39) |
V467A |
probably benign |
Het |
Med13l |
T |
G |
5: 118,890,003 (GRCm39) |
V1884G |
probably damaging |
Het |
Nlrp12 |
A |
C |
7: 3,271,213 (GRCm39) |
N1033K |
probably benign |
Het |
Nos3 |
T |
A |
5: 24,572,613 (GRCm39) |
V184E |
probably damaging |
Het |
Npr2 |
T |
C |
4: 43,647,155 (GRCm39) |
V737A |
probably damaging |
Het |
Nsd1 |
A |
G |
13: 55,361,187 (GRCm39) |
T52A |
probably benign |
Het |
Obscn |
C |
T |
11: 58,919,733 (GRCm39) |
R108Q |
|
Het |
Or4k50-ps1 |
A |
G |
2: 111,522,401 (GRCm39) |
*179W |
probably null |
Het |
Or4x11 |
A |
T |
2: 89,867,528 (GRCm39) |
K88N |
probably damaging |
Het |
Or5t5 |
G |
T |
2: 86,616,565 (GRCm39) |
G164* |
probably null |
Het |
Or5w22 |
T |
C |
2: 87,362,784 (GRCm39) |
S136P |
probably damaging |
Het |
Or6c70 |
T |
C |
10: 129,709,719 (GRCm39) |
I302M |
probably benign |
Het |
Or9a4 |
C |
A |
6: 40,549,240 (GRCm39) |
R307S |
probably benign |
Het |
Ovol2 |
A |
G |
2: 144,159,792 (GRCm39) |
V116A |
probably benign |
Het |
Pcdha5 |
C |
A |
18: 37,095,379 (GRCm39) |
S629R |
probably benign |
Het |
Pde4dip |
T |
A |
3: 97,602,408 (GRCm39) |
M2274L |
probably benign |
Het |
Pdpk1 |
T |
C |
17: 24,320,643 (GRCm39) |
T185A |
probably benign |
Het |
Pip5k1a |
T |
G |
3: 94,981,431 (GRCm39) |
T67P |
probably benign |
Het |
Plat |
G |
T |
8: 23,263,667 (GRCm39) |
V189F |
probably damaging |
Het |
Ppm1a |
C |
T |
12: 72,830,916 (GRCm39) |
S147L |
probably damaging |
Het |
Prim1 |
T |
A |
10: 127,851,885 (GRCm39) |
D52E |
probably damaging |
Het |
Prkab1 |
C |
G |
5: 116,162,221 (GRCm39) |
D30H |
possibly damaging |
Het |
Psma6 |
A |
T |
12: 55,445,613 (GRCm39) |
|
probably benign |
Het |
Psmd2 |
T |
A |
16: 20,473,675 (GRCm39) |
M196K |
probably damaging |
Het |
Ralgapa2 |
G |
T |
2: 146,276,776 (GRCm39) |
T488K |
probably benign |
Het |
Rapgefl1 |
A |
G |
11: 98,741,940 (GRCm39) |
K635E |
probably damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,118,424 (GRCm39) |
I522V |
probably damaging |
Het |
Rcor3 |
C |
A |
1: 191,822,173 (GRCm39) |
G8V |
probably damaging |
Het |
Rgs11 |
G |
A |
17: 26,426,734 (GRCm39) |
V289M |
probably damaging |
Het |
Ro60 |
T |
C |
1: 143,641,548 (GRCm39) |
I304M |
probably benign |
Het |
Scmh1 |
T |
C |
4: 120,386,353 (GRCm39) |
L631P |
probably damaging |
Het |
Sema3e |
T |
G |
5: 14,274,404 (GRCm39) |
D218E |
probably damaging |
Het |
Sh3rf2 |
T |
C |
18: 42,187,091 (GRCm39) |
V70A |
probably damaging |
Het |
Slc12a1 |
G |
T |
2: 125,047,960 (GRCm39) |
V801L |
probably benign |
Het |
Slc25a51 |
C |
G |
4: 45,399,765 (GRCm39) |
A142P |
possibly damaging |
Het |
Slc41a1 |
C |
T |
1: 131,758,694 (GRCm39) |
T112I |
probably damaging |
Het |
Slc44a2 |
T |
C |
9: 21,254,511 (GRCm39) |
M264T |
probably benign |
Het |
Snapc1 |
T |
A |
12: 74,015,068 (GRCm39) |
M134K |
probably benign |
Het |
Snrk |
T |
C |
9: 121,986,276 (GRCm39) |
F215S |
probably damaging |
Het |
Stab2 |
T |
C |
10: 86,721,547 (GRCm39) |
E1526G |
probably damaging |
Het |
Tbc1d10a |
C |
A |
11: 4,163,016 (GRCm39) |
Y260* |
probably null |
Het |
Tdrd5 |
A |
T |
1: 156,130,002 (GRCm39) |
L56Q |
probably damaging |
Het |
Tenm2 |
T |
C |
11: 36,755,768 (GRCm39) |
T77A |
probably benign |
Het |
Tmprss11g |
T |
G |
5: 86,644,366 (GRCm39) |
R159S |
possibly damaging |
Het |
Traj38 |
T |
A |
14: 54,418,034 (GRCm39) |
N1K |
|
Het |
Ttn |
A |
G |
2: 76,596,631 (GRCm39) |
I20094T |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,115,693 (GRCm39) |
L64P |
probably damaging |
Het |
Utp20 |
C |
T |
10: 88,634,260 (GRCm39) |
R812Q |
probably benign |
Het |
Vmn2r57 |
C |
A |
7: 41,076,148 (GRCm39) |
V455L |
probably benign |
Het |
Wdcp |
T |
C |
12: 4,900,246 (GRCm39) |
V34A |
probably damaging |
Het |
Zfp27 |
C |
T |
7: 29,594,784 (GRCm39) |
V394I |
probably benign |
Het |
Zfp512b |
T |
C |
2: 181,231,649 (GRCm39) |
H177R |
probably benign |
Het |
Zfp648 |
T |
A |
1: 154,080,783 (GRCm39) |
M314K |
possibly damaging |
Het |
Zfp811 |
T |
C |
17: 33,017,733 (GRCm39) |
I102M |
possibly damaging |
Het |
Zkscan6 |
A |
G |
11: 65,705,189 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Lmo7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Lmo7
|
APN |
14 |
102,124,487 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00733:Lmo7
|
APN |
14 |
102,153,138 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00778:Lmo7
|
APN |
14 |
102,148,321 (GRCm39) |
splice site |
probably benign |
|
IGL01014:Lmo7
|
APN |
14 |
102,157,993 (GRCm39) |
splice site |
probably benign |
|
IGL01401:Lmo7
|
APN |
14 |
102,031,713 (GRCm39) |
nonsense |
probably null |
|
IGL01550:Lmo7
|
APN |
14 |
102,163,576 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01570:Lmo7
|
APN |
14 |
102,139,807 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01602:Lmo7
|
APN |
14 |
102,148,192 (GRCm39) |
splice site |
probably benign |
|
IGL01605:Lmo7
|
APN |
14 |
102,148,192 (GRCm39) |
splice site |
probably benign |
|
IGL02012:Lmo7
|
APN |
14 |
102,126,152 (GRCm39) |
intron |
probably benign |
|
IGL02145:Lmo7
|
APN |
14 |
102,139,659 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02236:Lmo7
|
APN |
14 |
102,163,524 (GRCm39) |
splice site |
probably benign |
|
IGL02318:Lmo7
|
APN |
14 |
102,137,502 (GRCm39) |
splice site |
probably benign |
|
IGL02345:Lmo7
|
APN |
14 |
102,124,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02498:Lmo7
|
APN |
14 |
102,044,918 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02583:Lmo7
|
APN |
14 |
102,171,360 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02670:Lmo7
|
APN |
14 |
102,118,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02694:Lmo7
|
APN |
14 |
102,124,606 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03026:Lmo7
|
APN |
14 |
102,166,769 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03062:Lmo7
|
APN |
14 |
102,149,515 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03068:Lmo7
|
APN |
14 |
102,112,928 (GRCm39) |
unclassified |
probably benign |
|
IGL03178:Lmo7
|
APN |
14 |
102,166,696 (GRCm39) |
nonsense |
probably null |
|
IGL03279:Lmo7
|
APN |
14 |
102,137,944 (GRCm39) |
missense |
probably benign |
0.30 |
PIT4458001:Lmo7
|
UTSW |
14 |
102,124,923 (GRCm39) |
nonsense |
probably null |
|
R0029:Lmo7
|
UTSW |
14 |
102,171,357 (GRCm39) |
utr 3 prime |
probably benign |
|
R0112:Lmo7
|
UTSW |
14 |
102,124,629 (GRCm39) |
nonsense |
probably null |
|
R0345:Lmo7
|
UTSW |
14 |
102,114,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R0372:Lmo7
|
UTSW |
14 |
102,155,489 (GRCm39) |
splice site |
probably benign |
|
R0393:Lmo7
|
UTSW |
14 |
102,137,892 (GRCm39) |
missense |
probably benign |
|
R0514:Lmo7
|
UTSW |
14 |
102,133,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Lmo7
|
UTSW |
14 |
102,124,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Lmo7
|
UTSW |
14 |
102,137,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R0615:Lmo7
|
UTSW |
14 |
102,114,295 (GRCm39) |
nonsense |
probably null |
|
R0900:Lmo7
|
UTSW |
14 |
102,124,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R0961:Lmo7
|
UTSW |
14 |
102,031,705 (GRCm39) |
missense |
probably benign |
0.00 |
R0964:Lmo7
|
UTSW |
14 |
102,158,003 (GRCm39) |
splice site |
probably benign |
|
R1078:Lmo7
|
UTSW |
14 |
102,157,910 (GRCm39) |
splice site |
probably benign |
|
R1252:Lmo7
|
UTSW |
14 |
102,138,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R1527:Lmo7
|
UTSW |
14 |
102,114,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1537:Lmo7
|
UTSW |
14 |
102,166,700 (GRCm39) |
utr 3 prime |
probably benign |
|
R1565:Lmo7
|
UTSW |
14 |
102,124,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R1637:Lmo7
|
UTSW |
14 |
102,118,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Lmo7
|
UTSW |
14 |
102,139,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Lmo7
|
UTSW |
14 |
102,137,651 (GRCm39) |
missense |
probably benign |
0.36 |
R2002:Lmo7
|
UTSW |
14 |
102,124,497 (GRCm39) |
missense |
probably benign |
0.13 |
R2057:Lmo7
|
UTSW |
14 |
102,124,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Lmo7
|
UTSW |
14 |
102,137,674 (GRCm39) |
missense |
probably damaging |
0.99 |
R2153:Lmo7
|
UTSW |
14 |
102,157,951 (GRCm39) |
utr 3 prime |
probably benign |
|
R2257:Lmo7
|
UTSW |
14 |
102,137,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R2355:Lmo7
|
UTSW |
14 |
102,126,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Lmo7
|
UTSW |
14 |
102,124,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R2898:Lmo7
|
UTSW |
14 |
102,114,350 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3847:Lmo7
|
UTSW |
14 |
102,159,531 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3848:Lmo7
|
UTSW |
14 |
102,159,531 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3849:Lmo7
|
UTSW |
14 |
102,159,531 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3916:Lmo7
|
UTSW |
14 |
102,166,778 (GRCm39) |
utr 3 prime |
probably benign |
|
R4050:Lmo7
|
UTSW |
14 |
102,139,713 (GRCm39) |
nonsense |
probably null |
|
R4326:Lmo7
|
UTSW |
14 |
102,137,510 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4357:Lmo7
|
UTSW |
14 |
102,125,091 (GRCm39) |
missense |
probably null |
1.00 |
R4571:Lmo7
|
UTSW |
14 |
102,125,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R4658:Lmo7
|
UTSW |
14 |
102,124,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Lmo7
|
UTSW |
14 |
102,124,784 (GRCm39) |
splice site |
probably null |
|
R5006:Lmo7
|
UTSW |
14 |
102,163,673 (GRCm39) |
utr 3 prime |
probably benign |
|
R5528:Lmo7
|
UTSW |
14 |
102,139,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Lmo7
|
UTSW |
14 |
102,134,026 (GRCm39) |
splice site |
probably null |
|
R5643:Lmo7
|
UTSW |
14 |
102,166,772 (GRCm39) |
utr 3 prime |
probably benign |
|
R5644:Lmo7
|
UTSW |
14 |
102,166,772 (GRCm39) |
utr 3 prime |
probably benign |
|
R5650:Lmo7
|
UTSW |
14 |
102,136,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R5737:Lmo7
|
UTSW |
14 |
102,124,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R5832:Lmo7
|
UTSW |
14 |
102,121,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R5966:Lmo7
|
UTSW |
14 |
102,137,938 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6026:Lmo7
|
UTSW |
14 |
102,118,426 (GRCm39) |
missense |
probably benign |
0.04 |
R6072:Lmo7
|
UTSW |
14 |
102,166,772 (GRCm39) |
utr 3 prime |
probably benign |
|
R6158:Lmo7
|
UTSW |
14 |
102,137,573 (GRCm39) |
missense |
probably benign |
0.03 |
R6246:Lmo7
|
UTSW |
14 |
102,156,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R6335:Lmo7
|
UTSW |
14 |
102,138,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R6620:Lmo7
|
UTSW |
14 |
102,112,888 (GRCm39) |
missense |
probably benign |
0.29 |
R6658:Lmo7
|
UTSW |
14 |
102,148,281 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6917:Lmo7
|
UTSW |
14 |
102,155,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Lmo7
|
UTSW |
14 |
102,121,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Lmo7
|
UTSW |
14 |
102,136,136 (GRCm39) |
critical splice donor site |
probably null |
|
R7121:Lmo7
|
UTSW |
14 |
102,124,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R7136:Lmo7
|
UTSW |
14 |
102,157,975 (GRCm39) |
missense |
unknown |
|
R7196:Lmo7
|
UTSW |
14 |
102,133,936 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7228:Lmo7
|
UTSW |
14 |
102,133,971 (GRCm39) |
missense |
probably damaging |
0.99 |
R7337:Lmo7
|
UTSW |
14 |
102,121,640 (GRCm39) |
missense |
probably damaging |
0.98 |
R7341:Lmo7
|
UTSW |
14 |
102,122,948 (GRCm39) |
missense |
probably benign |
0.30 |
R7408:Lmo7
|
UTSW |
14 |
102,118,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R7470:Lmo7
|
UTSW |
14 |
102,138,040 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7506:Lmo7
|
UTSW |
14 |
102,157,045 (GRCm39) |
missense |
unknown |
|
R7559:Lmo7
|
UTSW |
14 |
102,124,662 (GRCm39) |
nonsense |
probably null |
|
R7565:Lmo7
|
UTSW |
14 |
102,122,737 (GRCm39) |
missense |
probably damaging |
0.98 |
R7788:Lmo7
|
UTSW |
14 |
102,136,012 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8095:Lmo7
|
UTSW |
14 |
102,124,855 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8100:Lmo7
|
UTSW |
14 |
102,137,899 (GRCm39) |
missense |
probably benign |
0.33 |
R8121:Lmo7
|
UTSW |
14 |
102,163,736 (GRCm39) |
missense |
unknown |
|
R8308:Lmo7
|
UTSW |
14 |
102,139,807 (GRCm39) |
critical splice donor site |
probably null |
|
R8371:Lmo7
|
UTSW |
14 |
102,124,444 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8403:Lmo7
|
UTSW |
14 |
102,139,800 (GRCm39) |
missense |
probably benign |
0.03 |
R8690:Lmo7
|
UTSW |
14 |
102,168,644 (GRCm39) |
missense |
unknown |
|
R8778:Lmo7
|
UTSW |
14 |
102,156,655 (GRCm39) |
missense |
probably benign |
0.24 |
R8778:Lmo7
|
UTSW |
14 |
102,149,503 (GRCm39) |
missense |
probably damaging |
0.98 |
R8822:Lmo7
|
UTSW |
14 |
102,121,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R8849:Lmo7
|
UTSW |
14 |
102,163,543 (GRCm39) |
missense |
unknown |
|
R8923:Lmo7
|
UTSW |
14 |
102,137,679 (GRCm39) |
missense |
probably benign |
0.31 |
R9006:Lmo7
|
UTSW |
14 |
102,155,072 (GRCm39) |
small deletion |
probably benign |
|
R9135:Lmo7
|
UTSW |
14 |
102,118,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R9154:Lmo7
|
UTSW |
14 |
102,122,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R9178:Lmo7
|
UTSW |
14 |
102,044,906 (GRCm39) |
nonsense |
probably null |
|
R9375:Lmo7
|
UTSW |
14 |
102,136,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R9428:Lmo7
|
UTSW |
14 |
102,155,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R9488:Lmo7
|
UTSW |
14 |
102,122,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9493:Lmo7
|
UTSW |
14 |
102,137,907 (GRCm39) |
missense |
probably benign |
0.01 |
R9594:Lmo7
|
UTSW |
14 |
102,156,136 (GRCm39) |
missense |
probably null |
0.98 |
R9674:Lmo7
|
UTSW |
14 |
102,078,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Lmo7
|
UTSW |
14 |
102,157,929 (GRCm39) |
missense |
unknown |
|
X0066:Lmo7
|
UTSW |
14 |
102,124,897 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Lmo7
|
UTSW |
14 |
102,124,369 (GRCm39) |
splice site |
probably null |
|
Z1176:Lmo7
|
UTSW |
14 |
102,156,717 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Lmo7
|
UTSW |
14 |
102,121,742 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Lmo7
|
UTSW |
14 |
102,166,664 (GRCm39) |
missense |
unknown |
|
Z1176:Lmo7
|
UTSW |
14 |
102,156,879 (GRCm39) |
missense |
unknown |
|
Z1177:Lmo7
|
UTSW |
14 |
102,135,993 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lmo7
|
UTSW |
14 |
102,133,954 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCATGTGTTTCTGTGCACG -3'
(R):5'- CGTGGCTTTGGAAGAGACTG -3'
Sequencing Primer
(F):5'- GGAACACACTCCAGGCCTTTG -3'
(R):5'- TTTGGAAGAGACTGCCCGGTC -3'
|
Posted On |
2019-10-07 |