Incidental Mutation 'R7196:Lmo7'
ID |
559967 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Lmo7
|
Ensembl Gene |
ENSMUSG00000033060 |
Gene Name |
LIM domain only 7 |
Synonyms |
FBXO20, LOC380928 |
MMRRC Submission |
045275-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.141)
|
Stock # |
R7196 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
101967393-102172146 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 102133936 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 660
(D660E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000097910
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100337]
[ENSMUST00000159026]
[ENSMUST00000159258]
[ENSMUST00000159314]
[ENSMUST00000159597]
|
AlphaFold |
E9PYF4 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000100337
AA Change: D660E
PolyPhen 2
Score 0.754 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000097910 Gene: ENSMUSG00000033060 AA Change: D660E
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
AA Change: D427E
PolyPhen 2
Score 0.089 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000124605 Gene: ENSMUSG00000033060 AA Change: D427E
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: D427E
PolyPhen 2
Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000124349 Gene: ENSMUSG00000033060 AA Change: D427E
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: D538E
PolyPhen 2
Score 0.662 (Sensitivity: 0.86; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000123706 Gene: ENSMUSG00000033060 AA Change: D538E
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 |
possibly damaging
Transcript: ENSMUST00000159806
AA Change: D149E
PolyPhen 2
Score 0.687 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000124300 Gene: ENSMUSG00000033060 AA Change: D149E
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: 99.9%
- 10x: 99.6%
- 20x: 98.5%
|
Validation Efficiency |
99% (94/95) |
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: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
AGCTTCCCTGCTT |
AGCTT |
9: 57,165,505 (GRCm39) |
|
probably null |
Het |
4921504E06Rik |
A |
C |
2: 19,498,806 (GRCm39) |
S396A |
probably benign |
Het |
Actr6 |
C |
A |
10: 89,550,784 (GRCm39) |
V337F |
possibly damaging |
Het |
Agtpbp1 |
T |
C |
13: 59,680,994 (GRCm39) |
T73A |
possibly damaging |
Het |
AI182371 |
A |
T |
2: 34,976,441 (GRCm39) |
|
probably null |
Het |
Apob |
A |
G |
12: 8,033,893 (GRCm39) |
E202G |
possibly damaging |
Het |
Asb4 |
A |
T |
6: 5,423,356 (GRCm39) |
M168L |
probably benign |
Het |
AU018091 |
T |
C |
7: 3,213,788 (GRCm39) |
Y152C |
probably damaging |
Het |
Casp3 |
G |
A |
8: 47,088,498 (GRCm39) |
G132R |
possibly damaging |
Het |
Cbfa2t3 |
C |
A |
8: 123,365,729 (GRCm39) |
A229S |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,143,759 (GRCm39) |
Y2949N |
probably damaging |
Het |
Ceacam3 |
T |
C |
7: 16,888,881 (GRCm39) |
Y217H |
|
Het |
Cldn5 |
A |
T |
16: 18,595,630 (GRCm39) |
|
probably benign |
Het |
Cltc |
T |
C |
11: 86,597,657 (GRCm39) |
D1093G |
probably damaging |
Het |
Cnn3 |
G |
A |
3: 121,248,437 (GRCm39) |
|
probably null |
Het |
Col4a2 |
A |
G |
8: 11,448,693 (GRCm39) |
Y71C |
probably damaging |
Het |
Csf1 |
T |
C |
3: 107,661,214 (GRCm39) |
D77G |
possibly damaging |
Het |
Cyp2j7 |
T |
A |
4: 96,103,651 (GRCm39) |
T295S |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,724,000 (GRCm39) |
M133K |
probably benign |
Het |
Dock5 |
G |
A |
14: 67,993,919 (GRCm39) |
P1852L |
probably damaging |
Het |
Dpysl3 |
T |
A |
18: 43,462,910 (GRCm39) |
D489V |
probably damaging |
Het |
Dsg4 |
T |
C |
18: 20,599,537 (GRCm39) |
Y718H |
probably damaging |
Het |
Dync2h1 |
G |
A |
9: 7,147,715 (GRCm39) |
Q972* |
probably null |
Het |
Epn1 |
G |
A |
7: 5,096,380 (GRCm39) |
D225N |
possibly damaging |
Het |
Esp4 |
A |
G |
17: 40,913,256 (GRCm39) |
E41G |
probably benign |
Het |
Fam171a2 |
T |
C |
11: 102,329,172 (GRCm39) |
D529G |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,691,301 (GRCm39) |
I694N |
probably damaging |
Het |
Fshr |
C |
T |
17: 89,292,897 (GRCm39) |
A594T |
probably damaging |
Het |
Galnt3 |
A |
G |
2: 65,921,268 (GRCm39) |
Y533H |
probably damaging |
Het |
Gja5 |
C |
A |
3: 96,958,422 (GRCm39) |
R160S |
probably damaging |
Het |
Gm12353 |
A |
T |
4: 19,608,938 (GRCm39) |
D7V |
unknown |
Het |
Gm17669 |
T |
C |
18: 67,695,572 (GRCm39) |
F39S |
probably damaging |
Het |
Gm7145 |
T |
A |
1: 117,913,791 (GRCm39) |
N224K |
possibly damaging |
Het |
Gpd1 |
G |
T |
15: 99,619,936 (GRCm39) |
G245C |
probably benign |
Het |
Gpr4 |
G |
A |
7: 18,957,089 (GRCm39) |
G337D |
probably benign |
Het |
Hgd |
G |
A |
16: 37,409,078 (GRCm39) |
C14Y |
probably benign |
Het |
Ibtk |
A |
T |
9: 85,625,709 (GRCm39) |
S14T |
probably damaging |
Het |
Ifi205 |
G |
T |
1: 173,854,109 (GRCm39) |
N181K |
probably damaging |
Het |
Inppl1 |
G |
A |
7: 101,477,993 (GRCm39) |
A673V |
probably benign |
Het |
Itgb3 |
C |
A |
11: 104,524,438 (GRCm39) |
Y191* |
probably null |
Het |
Jrkl |
G |
T |
9: 13,244,162 (GRCm39) |
P500T |
probably benign |
Het |
Kcnq1 |
G |
A |
7: 142,912,478 (GRCm39) |
V515I |
possibly damaging |
Het |
Kifc3 |
A |
G |
8: 95,833,239 (GRCm39) |
V453A |
probably benign |
Het |
Krt10 |
C |
T |
11: 99,278,371 (GRCm39) |
E263K |
probably damaging |
Het |
Lingo1 |
A |
T |
9: 56,527,903 (GRCm39) |
F235I |
probably damaging |
Het |
Magi3 |
A |
C |
3: 103,956,484 (GRCm39) |
C661W |
probably benign |
Het |
Mmp1a |
C |
T |
9: 7,476,018 (GRCm39) |
Q428* |
probably null |
Het |
Msrb1 |
A |
T |
17: 24,958,556 (GRCm39) |
T47S |
probably benign |
Het |
Naip6 |
A |
T |
13: 100,436,666 (GRCm39) |
I619K |
probably benign |
Het |
Ndfip2 |
T |
C |
14: 105,535,472 (GRCm39) |
S253P |
probably damaging |
Het |
Nebl |
A |
T |
2: 17,457,329 (GRCm39) |
V77E |
probably damaging |
Het |
Nit1 |
T |
C |
1: 171,172,003 (GRCm39) |
E65G |
probably benign |
Het |
Ntn4 |
C |
T |
10: 93,569,576 (GRCm39) |
H430Y |
probably benign |
Het |
Nxpe5 |
A |
T |
5: 138,237,586 (GRCm39) |
I49F |
probably benign |
Het |
Or10a2 |
A |
G |
7: 106,673,935 (GRCm39) |
N300S |
probably benign |
Het |
Or10c1 |
A |
G |
17: 37,522,084 (GRCm39) |
I220T |
probably damaging |
Het |
Or14c46 |
A |
T |
7: 85,918,649 (GRCm39) |
M116K |
probably damaging |
Het |
Or1e23 |
A |
G |
11: 73,407,957 (GRCm39) |
Y23H |
probably benign |
Het |
Or1m1 |
A |
T |
9: 18,666,886 (GRCm39) |
L15* |
probably null |
Het |
Or4k49 |
T |
G |
2: 111,495,042 (GRCm39) |
L157W |
probably damaging |
Het |
Or52s6 |
A |
T |
7: 103,092,204 (GRCm39) |
M42K |
probably benign |
Het |
Or7e178 |
A |
G |
9: 20,225,494 (GRCm39) |
Y241H |
probably benign |
Het |
Oxct2a |
T |
A |
4: 123,217,165 (GRCm39) |
N72I |
probably damaging |
Het |
Pappa |
G |
A |
4: 65,242,128 (GRCm39) |
|
probably null |
Het |
Pcnx1 |
G |
A |
12: 82,042,312 (GRCm39) |
R34H |
possibly damaging |
Het |
Plekha5 |
G |
T |
6: 140,489,648 (GRCm39) |
V236L |
possibly damaging |
Het |
Prdm1 |
A |
G |
10: 44,332,988 (GRCm39) |
S44P |
probably benign |
Het |
Prss46 |
T |
A |
9: 110,680,533 (GRCm39) |
L226Q |
probably benign |
Het |
Prss47 |
C |
A |
13: 65,192,640 (GRCm39) |
W380C |
probably benign |
Het |
Ptch2 |
T |
G |
4: 116,971,946 (GRCm39) |
V1156G |
probably benign |
Het |
Rab3gap2 |
T |
C |
1: 185,013,864 (GRCm39) |
F1190S |
probably damaging |
Het |
Raver2 |
T |
G |
4: 100,960,056 (GRCm39) |
Y179D |
probably damaging |
Het |
Rgl2 |
C |
T |
17: 34,152,403 (GRCm39) |
R367W |
probably damaging |
Het |
Ripor2 |
T |
G |
13: 24,888,808 (GRCm39) |
I629S |
possibly damaging |
Het |
Robo4 |
T |
A |
9: 37,314,001 (GRCm39) |
M84K |
possibly damaging |
Het |
Rps6ka5 |
A |
T |
12: 100,562,123 (GRCm39) |
S252T |
possibly damaging |
Het |
Rtl1 |
C |
T |
12: 109,559,221 (GRCm39) |
V873M |
possibly damaging |
Het |
Sla |
T |
A |
15: 66,703,420 (GRCm39) |
R4W |
probably benign |
Het |
Smco1 |
A |
G |
16: 32,092,620 (GRCm39) |
D97G |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,676,753 (GRCm39) |
T414A |
probably benign |
Het |
Syt14 |
A |
G |
1: 192,717,936 (GRCm39) |
I3T |
probably benign |
Het |
Tnpo2 |
G |
A |
8: 85,773,766 (GRCm39) |
V303M |
possibly damaging |
Het |
Tstd2 |
A |
C |
4: 46,119,955 (GRCm39) |
S332R |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,582,386 (GRCm39) |
A22836S |
possibly damaging |
Het |
Ufl1 |
A |
G |
4: 25,250,669 (GRCm39) |
V728A |
probably benign |
Het |
Usp33 |
A |
T |
3: 152,089,828 (GRCm39) |
K789N |
possibly damaging |
Het |
Usp54 |
T |
A |
14: 20,638,438 (GRCm39) |
Q214L |
probably damaging |
Het |
Vmn2r7 |
T |
G |
3: 64,623,198 (GRCm39) |
N374T |
probably benign |
Het |
Zbtb7a |
T |
A |
10: 80,980,434 (GRCm39) |
N209K |
probably damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,306,207 (GRCm39) |
V615A |
probably benign |
Het |
Zdhhc20 |
A |
G |
14: 58,111,348 (GRCm39) |
|
probably null |
Het |
Zfp90 |
G |
T |
8: 107,151,780 (GRCm39) |
V498L |
probably damaging |
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 |
|
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 |
R7432:Lmo7
|
UTSW |
14 |
102,139,551 (GRCm39) |
missense |
probably benign |
0.42 |
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'- TGTGGCGCTATTTCAGGGAC -3'
(R):5'- AGACATAGGACAGAACTTTGGTC -3'
Sequencing Primer
(F):5'- GCGCTATTTCAGGGACACTATCAG -3'
(R):5'- AGGACAGAACTTTGGTCTCATTCTC -3'
|
Posted On |
2019-06-26 |