Incidental Mutation 'R6258:Eml2'
ID |
506473 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Eml2
|
Ensembl Gene |
ENSMUSG00000040811 |
Gene Name |
echinoderm microtubule associated protein like 2 |
Synonyms |
1600029N02Rik |
MMRRC Submission |
044375-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R6258 (G1)
|
Quality Score |
185.009 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
18910346-18940407 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to G
at 18913289 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000146046
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048502]
[ENSMUST00000117338]
[ENSMUST00000120595]
[ENSMUST00000141718]
[ENSMUST00000144054]
[ENSMUST00000148246]
|
AlphaFold |
Q7TNG5 |
Predicted Effect |
probably null
Transcript: ENSMUST00000048502
|
SMART Domains |
Protein: ENSMUSP00000037654 Gene: ENSMUSG00000040811
Domain | Start | End | E-Value | Type |
Pfam:HELP
|
17 |
65 |
4.6e-14 |
PFAM |
WD40
|
113 |
162 |
8.36e-2 |
SMART |
WD40
|
165 |
210 |
9.21e0 |
SMART |
WD40
|
213 |
252 |
7.99e-1 |
SMART |
WD40
|
258 |
298 |
3.7e0 |
SMART |
WD40
|
301 |
341 |
3.58e-1 |
SMART |
WD40
|
385 |
424 |
5.52e-2 |
SMART |
WD40
|
427 |
465 |
1.1e1 |
SMART |
WD40
|
468 |
507 |
4.95e-4 |
SMART |
WD40
|
514 |
553 |
4.62e-4 |
SMART |
WD40
|
579 |
620 |
4.75e1 |
SMART |
WD40
|
626 |
666 |
2.67e-1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000083609
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000117338
AA Change: C96G
PolyPhen 2
Score 0.919 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000112491 Gene: ENSMUSG00000040811 AA Change: C96G
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
32 |
N/A |
INTRINSIC |
coiled coil region
|
59 |
106 |
N/A |
INTRINSIC |
low complexity region
|
183 |
191 |
N/A |
INTRINSIC |
Pfam:HELP
|
211 |
285 |
3.5e-29 |
PFAM |
WD40
|
286 |
335 |
5.5e-4 |
SMART |
WD40
|
338 |
383 |
5.8e-2 |
SMART |
WD40
|
386 |
425 |
5.2e-3 |
SMART |
WD40
|
431 |
471 |
2.4e-2 |
SMART |
WD40
|
474 |
514 |
2.3e-3 |
SMART |
WD40
|
558 |
597 |
3.6e-4 |
SMART |
WD40
|
600 |
638 |
7.1e-2 |
SMART |
WD40
|
641 |
680 |
3.1e-6 |
SMART |
WD40
|
687 |
726 |
3.1e-6 |
SMART |
WD40
|
752 |
793 |
3e-1 |
SMART |
WD40
|
799 |
839 |
1.7e-3 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000120595
|
SMART Domains |
Protein: ENSMUSP00000112447 Gene: ENSMUSG00000040811
Domain | Start | End | E-Value | Type |
WD40
|
94 |
154 |
2.48e0 |
SMART |
WD40
|
157 |
196 |
7.99e-1 |
SMART |
WD40
|
202 |
242 |
3.7e0 |
SMART |
WD40
|
245 |
285 |
3.58e-1 |
SMART |
WD40
|
329 |
368 |
5.52e-2 |
SMART |
WD40
|
371 |
409 |
1.1e1 |
SMART |
WD40
|
412 |
451 |
4.95e-4 |
SMART |
WD40
|
458 |
497 |
4.62e-4 |
SMART |
WD40
|
523 |
564 |
4.75e1 |
SMART |
WD40
|
570 |
610 |
2.67e-1 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000141718
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141792
|
Predicted Effect |
probably null
Transcript: ENSMUST00000144054
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146095
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000148246
|
SMART Domains |
Protein: ENSMUSP00000115466 Gene: ENSMUSG00000040811
Domain | Start | End | E-Value | Type |
WD40
|
94 |
143 |
8.36e-2 |
SMART |
WD40
|
146 |
191 |
9.21e0 |
SMART |
WD40
|
194 |
233 |
7.99e-1 |
SMART |
WD40
|
239 |
279 |
3.7e0 |
SMART |
WD40
|
282 |
322 |
3.58e-1 |
SMART |
WD40
|
366 |
405 |
5.52e-2 |
SMART |
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.5%
- 20x: 95.7%
|
Validation Efficiency |
99% (74/75) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl3 |
T |
C |
7: 82,178,191 (GRCm39) |
|
probably null |
Het |
Alms1 |
A |
T |
6: 85,605,717 (GRCm39) |
K2456* |
probably null |
Het |
Alppl2 |
A |
T |
1: 87,016,184 (GRCm39) |
M225K |
probably damaging |
Het |
AU041133 |
A |
G |
10: 81,986,992 (GRCm39) |
E215G |
probably damaging |
Het |
Carmil3 |
T |
A |
14: 55,737,889 (GRCm39) |
L815Q |
probably damaging |
Het |
Casr |
A |
G |
16: 36,337,971 (GRCm39) |
C60R |
probably damaging |
Het |
Cdc7 |
A |
G |
5: 107,117,093 (GRCm39) |
K84E |
probably damaging |
Het |
Cdc73 |
G |
A |
1: 143,567,211 (GRCm39) |
T104I |
probably benign |
Het |
Clcc1 |
G |
A |
3: 108,580,624 (GRCm39) |
V313I |
possibly damaging |
Het |
Cntn3 |
A |
G |
6: 102,254,178 (GRCm39) |
|
probably null |
Het |
Crocc2 |
A |
G |
1: 93,141,360 (GRCm39) |
K1171R |
possibly damaging |
Het |
Ctsa |
T |
C |
2: 164,676,281 (GRCm39) |
V86A |
probably damaging |
Het |
Cyp2s1 |
ACAGCAGCAGCAGCAGCAGCAGCAG |
ACAGCAGCAGCAGCAGCAGCAG |
7: 25,515,867 (GRCm39) |
|
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dnah17 |
C |
A |
11: 118,017,148 (GRCm39) |
W197C |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 118,017,150 (GRCm39) |
W197R |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 118,017,149 (GRCm39) |
W197* |
probably null |
Het |
Egflam |
T |
A |
15: 7,263,773 (GRCm39) |
T726S |
probably damaging |
Het |
Ercc6 |
T |
A |
14: 32,279,813 (GRCm39) |
D609E |
probably benign |
Het |
Erg |
C |
A |
16: 95,181,100 (GRCm39) |
R147L |
probably damaging |
Het |
Faiml |
T |
C |
9: 99,114,513 (GRCm39) |
I125M |
possibly damaging |
Het |
Fbxo41 |
A |
T |
6: 85,455,537 (GRCm39) |
L549H |
probably damaging |
Het |
Fbxw2 |
A |
T |
2: 34,702,825 (GRCm39) |
|
probably null |
Het |
Fgd6 |
T |
A |
10: 93,880,161 (GRCm39) |
N338K |
probably benign |
Het |
Gaa |
C |
A |
11: 119,171,997 (GRCm39) |
A700D |
probably benign |
Het |
Gm32742 |
T |
A |
9: 51,068,862 (GRCm39) |
I200F |
probably damaging |
Het |
Gm4924 |
T |
G |
10: 82,213,307 (GRCm39) |
|
probably benign |
Het |
Gm8369 |
G |
A |
19: 11,488,973 (GRCm39) |
A87T |
possibly damaging |
Het |
H2-M10.1 |
T |
A |
17: 36,634,994 (GRCm39) |
I304F |
unknown |
Het |
Ighv5-8 |
A |
G |
12: 113,618,611 (GRCm39) |
T9A |
possibly damaging |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Jakmip1 |
G |
T |
5: 37,299,104 (GRCm39) |
E775* |
probably null |
Het |
Klhl40 |
T |
C |
9: 121,607,026 (GRCm39) |
F62S |
probably damaging |
Het |
Krtcap3 |
A |
T |
5: 31,409,572 (GRCm39) |
R84W |
probably damaging |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Lins1 |
T |
C |
7: 66,360,496 (GRCm39) |
|
probably null |
Het |
Magi3 |
A |
G |
3: 103,996,912 (GRCm39) |
L211P |
probably damaging |
Het |
Map2k5 |
T |
A |
9: 63,124,647 (GRCm39) |
I359F |
probably benign |
Het |
Map4k5 |
C |
A |
12: 69,878,336 (GRCm39) |
R355L |
probably benign |
Het |
Mef2c |
T |
A |
13: 83,801,057 (GRCm39) |
D252E |
probably damaging |
Het |
Methig1 |
T |
C |
15: 100,251,422 (GRCm39) |
V111A |
possibly damaging |
Het |
Mical3 |
A |
T |
6: 120,985,991 (GRCm39) |
L150Q |
probably damaging |
Het |
Nf1 |
A |
T |
11: 79,456,581 (GRCm39) |
|
probably null |
Het |
Nisch |
T |
A |
14: 30,899,085 (GRCm39) |
|
probably benign |
Het |
Or4f15 |
C |
T |
2: 111,814,396 (GRCm39) |
V8I |
probably benign |
Het |
Or5p61 |
T |
C |
7: 107,758,181 (GRCm39) |
N300D |
probably damaging |
Het |
Pcdhb12 |
T |
C |
18: 37,569,892 (GRCm39) |
V346A |
probably benign |
Het |
Pde7b |
T |
C |
10: 20,316,546 (GRCm39) |
D168G |
possibly damaging |
Het |
Pdzrn4 |
A |
T |
15: 92,655,562 (GRCm39) |
E485V |
probably damaging |
Het |
Pla2g4a |
A |
G |
1: 149,733,238 (GRCm39) |
S504P |
probably benign |
Het |
Plin2 |
G |
T |
4: 86,575,526 (GRCm39) |
A341D |
probably damaging |
Het |
Psma8 |
A |
G |
18: 14,854,324 (GRCm39) |
D68G |
probably damaging |
Het |
Rcor3 |
G |
A |
1: 191,808,559 (GRCm39) |
H207Y |
probably benign |
Het |
Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
Ryr3 |
A |
G |
2: 112,490,449 (GRCm39) |
F3795S |
probably damaging |
Het |
Samm50 |
C |
G |
15: 84,084,512 (GRCm39) |
P150A |
probably damaging |
Het |
Samm50 |
C |
A |
15: 84,084,513 (GRCm39) |
P150H |
probably damaging |
Het |
Slc28a2b |
A |
T |
2: 122,353,963 (GRCm39) |
I530F |
probably damaging |
Het |
Slc6a18 |
A |
T |
13: 73,818,164 (GRCm39) |
C284* |
probably null |
Het |
Smc3 |
T |
A |
19: 53,616,162 (GRCm39) |
|
probably null |
Het |
Snrnp200 |
G |
A |
2: 127,060,343 (GRCm39) |
G529D |
possibly damaging |
Het |
Sord |
T |
A |
2: 122,089,613 (GRCm39) |
|
probably null |
Het |
Spdl1 |
T |
A |
11: 34,710,713 (GRCm39) |
N345I |
probably damaging |
Het |
Sucnr1 |
T |
C |
3: 59,993,778 (GRCm39) |
L102P |
probably damaging |
Het |
Tbc1d9 |
T |
C |
8: 83,937,145 (GRCm39) |
W76R |
probably damaging |
Het |
Tcerg1 |
T |
A |
18: 42,686,530 (GRCm39) |
Y696N |
probably damaging |
Het |
Thsd7b |
A |
G |
1: 129,595,655 (GRCm39) |
T492A |
probably benign |
Het |
Trdmt1 |
T |
A |
2: 13,524,870 (GRCm39) |
Q195L |
probably benign |
Het |
Ubr3 |
A |
G |
2: 69,813,208 (GRCm39) |
|
probably null |
Het |
Ung |
A |
T |
5: 114,275,361 (GRCm39) |
Y250F |
probably benign |
Het |
Vezf1 |
A |
G |
11: 87,972,326 (GRCm39) |
N229S |
probably damaging |
Het |
Wdfy3 |
C |
T |
5: 102,020,831 (GRCm39) |
R2491Q |
possibly damaging |
Het |
Wdr97 |
C |
A |
15: 76,239,895 (GRCm39) |
S277* |
probably null |
Het |
Zfp1007 |
T |
C |
5: 109,824,433 (GRCm39) |
H339R |
probably benign |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zscan4-ps1 |
C |
A |
7: 10,799,829 (GRCm39) |
E353D |
probably benign |
Het |
|
Other mutations in Eml2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00690:Eml2
|
APN |
7 |
18,940,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00786:Eml2
|
APN |
7 |
18,936,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Eml2
|
APN |
7 |
18,924,663 (GRCm39) |
nonsense |
probably null |
|
IGL01132:Eml2
|
APN |
7 |
18,934,464 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01678:Eml2
|
APN |
7 |
18,920,047 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01800:Eml2
|
APN |
7 |
18,935,122 (GRCm39) |
intron |
probably benign |
|
IGL02517:Eml2
|
APN |
7 |
18,940,055 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02607:Eml2
|
APN |
7 |
18,940,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02676:Eml2
|
APN |
7 |
18,918,846 (GRCm39) |
nonsense |
probably null |
|
IGL03082:Eml2
|
APN |
7 |
18,935,802 (GRCm39) |
missense |
probably damaging |
1.00 |
puffery
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R0628_Eml2_697
|
UTSW |
7 |
18,935,479 (GRCm39) |
splice site |
probably benign |
|
R0040:Eml2
|
UTSW |
7 |
18,930,539 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0135:Eml2
|
UTSW |
7 |
18,937,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Eml2
|
UTSW |
7 |
18,918,797 (GRCm39) |
nonsense |
probably null |
|
R0240:Eml2
|
UTSW |
7 |
18,918,797 (GRCm39) |
nonsense |
probably null |
|
R0362:Eml2
|
UTSW |
7 |
18,924,731 (GRCm39) |
splice site |
probably null |
|
R0387:Eml2
|
UTSW |
7 |
18,916,184 (GRCm39) |
splice site |
probably null |
|
R0432:Eml2
|
UTSW |
7 |
18,913,456 (GRCm39) |
nonsense |
probably null |
|
R0614:Eml2
|
UTSW |
7 |
18,936,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R0628:Eml2
|
UTSW |
7 |
18,935,479 (GRCm39) |
splice site |
probably benign |
|
R1078:Eml2
|
UTSW |
7 |
18,913,687 (GRCm39) |
missense |
probably benign |
0.24 |
R1531:Eml2
|
UTSW |
7 |
18,930,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Eml2
|
UTSW |
7 |
18,927,986 (GRCm39) |
missense |
probably damaging |
0.97 |
R1864:Eml2
|
UTSW |
7 |
18,935,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Eml2
|
UTSW |
7 |
18,937,889 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2032:Eml2
|
UTSW |
7 |
18,936,480 (GRCm39) |
missense |
probably benign |
0.03 |
R2185:Eml2
|
UTSW |
7 |
18,927,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R2419:Eml2
|
UTSW |
7 |
18,910,620 (GRCm39) |
unclassified |
probably benign |
|
R3821:Eml2
|
UTSW |
7 |
18,936,911 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4199:Eml2
|
UTSW |
7 |
18,913,364 (GRCm39) |
missense |
probably benign |
0.00 |
R4411:Eml2
|
UTSW |
7 |
18,916,326 (GRCm39) |
critical splice donor site |
probably null |
|
R4497:Eml2
|
UTSW |
7 |
18,913,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Eml2
|
UTSW |
7 |
18,937,935 (GRCm39) |
missense |
probably benign |
0.05 |
R4912:Eml2
|
UTSW |
7 |
18,927,924 (GRCm39) |
splice site |
probably null |
|
R5028:Eml2
|
UTSW |
7 |
18,913,372 (GRCm39) |
critical splice donor site |
probably null |
|
R5192:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5196:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5373:Eml2
|
UTSW |
7 |
18,913,188 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5718:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5720:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5727:Eml2
|
UTSW |
7 |
18,924,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R5841:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5842:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5844:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6015:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6017:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6073:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6075:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6126:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6128:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6129:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6189:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6273:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6289:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6381:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6384:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6435:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6436:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6437:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Eml2
|
UTSW |
7 |
18,930,236 (GRCm39) |
missense |
probably benign |
0.26 |
R6550:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6551:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6552:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6572:Eml2
|
UTSW |
7 |
18,930,539 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6598:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6599:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6704:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6705:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6709:Eml2
|
UTSW |
7 |
18,940,136 (GRCm39) |
makesense |
probably null |
|
R6730:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Eml2
|
UTSW |
7 |
18,934,432 (GRCm39) |
missense |
probably benign |
0.35 |
R6742:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6769:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6770:Eml2
|
UTSW |
7 |
18,935,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R6864:Eml2
|
UTSW |
7 |
18,930,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R6878:Eml2
|
UTSW |
7 |
18,934,537 (GRCm39) |
missense |
probably benign |
0.08 |
R7045:Eml2
|
UTSW |
7 |
18,935,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Eml2
|
UTSW |
7 |
18,934,515 (GRCm39) |
missense |
probably benign |
0.45 |
R7478:Eml2
|
UTSW |
7 |
18,940,066 (GRCm39) |
nonsense |
probably null |
|
R7706:Eml2
|
UTSW |
7 |
18,920,035 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7811:Eml2
|
UTSW |
7 |
18,920,047 (GRCm39) |
missense |
probably benign |
0.38 |
R8084:Eml2
|
UTSW |
7 |
18,915,149 (GRCm39) |
critical splice donor site |
probably null |
|
R8337:Eml2
|
UTSW |
7 |
18,930,161 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8414:Eml2
|
UTSW |
7 |
18,913,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R8868:Eml2
|
UTSW |
7 |
18,927,988 (GRCm39) |
missense |
probably benign |
0.03 |
R8934:Eml2
|
UTSW |
7 |
18,913,738 (GRCm39) |
missense |
probably damaging |
0.99 |
R9110:Eml2
|
UTSW |
7 |
18,925,620 (GRCm39) |
missense |
probably benign |
0.07 |
R9131:Eml2
|
UTSW |
7 |
18,918,751 (GRCm39) |
missense |
|
|
R9144:Eml2
|
UTSW |
7 |
18,935,564 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9261:Eml2
|
UTSW |
7 |
18,913,743 (GRCm39) |
missense |
probably benign |
0.45 |
R9285:Eml2
|
UTSW |
7 |
18,925,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R9767:Eml2
|
UTSW |
7 |
18,920,083 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GAGAGACTCTCCTGGTCTTTGG -3'
(R):5'- CTGACACACTGGAGCAATAGGG -3'
Sequencing Primer
(F):5'- CCTGGTCTTTGGAGCGCTC -3'
(R):5'- CACTGGAGCAATAGGGTTAGATATG -3'
|
Posted On |
2018-03-15 |