Incidental Mutation 'R1511:Eml6'
ID |
168345 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Eml6
|
Ensembl Gene |
ENSMUSG00000044072 |
Gene Name |
echinoderm microtubule associated protein like 6 |
Synonyms |
2900083P10Rik, C230094A16Rik |
MMRRC Submission |
039558-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.228)
|
Stock # |
R1511 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
29693048-29976033 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 29768374 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Leucine
at position 771
(H771L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000051080
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058902]
[ENSMUST00000104962]
|
AlphaFold |
Q5SQM0 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000058902
AA Change: H771L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000051080 Gene: ENSMUSG00000044072 AA Change: H771L
Domain | Start | End | E-Value | Type |
low complexity region
|
36 |
47 |
N/A |
INTRINSIC |
WD40
|
49 |
91 |
1.79e-1 |
SMART |
WD40
|
94 |
136 |
1.42e-4 |
SMART |
WD40
|
139 |
178 |
5.31e-4 |
SMART |
WD40
|
184 |
224 |
8.84e1 |
SMART |
WD40
|
225 |
263 |
3.75e-4 |
SMART |
WD40
|
313 |
353 |
4.69e-5 |
SMART |
WD40
|
356 |
394 |
2.22e0 |
SMART |
WD40
|
397 |
436 |
1.72e0 |
SMART |
WD40
|
505 |
546 |
1.7e2 |
SMART |
WD40
|
552 |
592 |
4.55e-3 |
SMART |
low complexity region
|
613 |
625 |
N/A |
INTRINSIC |
Pfam:HELP
|
653 |
715 |
1.9e-22 |
PFAM |
WD40
|
716 |
757 |
9.24e-1 |
SMART |
WD40
|
760 |
802 |
6.53e-4 |
SMART |
WD40
|
805 |
844 |
2.98e-1 |
SMART |
WD40
|
856 |
891 |
8.52e1 |
SMART |
WD40
|
892 |
929 |
2.09e-2 |
SMART |
WD40
|
986 |
1026 |
1.18e-1 |
SMART |
WD40
|
1032 |
1068 |
3.44e0 |
SMART |
WD40
|
1071 |
1111 |
2.58e-1 |
SMART |
WD40
|
1180 |
1221 |
9.24e-1 |
SMART |
WD40
|
1227 |
1267 |
3.85e-1 |
SMART |
low complexity region
|
1280 |
1291 |
N/A |
INTRINSIC |
Pfam:HELP
|
1329 |
1402 |
5e-15 |
PFAM |
WD40
|
1404 |
1447 |
2.66e0 |
SMART |
WD40
|
1450 |
1492 |
1.85e0 |
SMART |
WD40
|
1495 |
1534 |
2.97e0 |
SMART |
WD40
|
1543 |
1582 |
7.1e1 |
SMART |
WD40
|
1584 |
1629 |
9.51e1 |
SMART |
WD40
|
1675 |
1715 |
3.05e-4 |
SMART |
WD40
|
1718 |
1758 |
8.84e1 |
SMART |
WD40
|
1759 |
1798 |
7.16e-1 |
SMART |
WD40
|
1869 |
1910 |
1.53e1 |
SMART |
WD40
|
1916 |
1956 |
4.62e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000104962
|
SMART Domains |
Protein: ENSMUSP00000100568 Gene: ENSMUSG00000078157
Domain | Start | End | E-Value | Type |
ANK
|
19 |
50 |
1.53e3 |
SMART |
ANK
|
57 |
87 |
1.7e-3 |
SMART |
ANK
|
99 |
128 |
3.6e-2 |
SMART |
ANK
|
132 |
162 |
3.31e-1 |
SMART |
ANK
|
166 |
195 |
8.19e-6 |
SMART |
ANK
|
199 |
228 |
7.83e-3 |
SMART |
ANK
|
231 |
260 |
1.8e-2 |
SMART |
low complexity region
|
297 |
306 |
N/A |
INTRINSIC |
low complexity region
|
434 |
445 |
N/A |
INTRINSIC |
low complexity region
|
496 |
507 |
N/A |
INTRINSIC |
ANK
|
536 |
578 |
8.39e-3 |
SMART |
ANK
|
582 |
611 |
3.91e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000109452
|
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.0%
- 10x: 95.4%
- 20x: 89.7%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
C |
A |
5: 125,592,041 (GRCm39) |
N576K |
probably benign |
Het |
Abca5 |
G |
T |
11: 110,190,804 (GRCm39) |
L769M |
probably damaging |
Het |
Abca5 |
T |
A |
11: 110,190,812 (GRCm39) |
H766L |
possibly damaging |
Het |
Acvr1c |
A |
G |
2: 58,177,896 (GRCm39) |
I191T |
probably damaging |
Het |
Agps |
A |
T |
2: 75,697,123 (GRCm39) |
E314D |
probably damaging |
Het |
Agxt |
G |
A |
1: 93,063,490 (GRCm39) |
G131R |
probably damaging |
Het |
Ak8 |
A |
G |
2: 28,632,758 (GRCm39) |
T326A |
probably benign |
Het |
Aldoart2 |
T |
A |
12: 55,613,062 (GRCm39) |
I329N |
probably benign |
Het |
Apaf1 |
T |
C |
10: 90,896,047 (GRCm39) |
I342V |
possibly damaging |
Het |
Arhgap40 |
T |
C |
2: 158,369,081 (GRCm39) |
S68P |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
AU022252 |
C |
T |
4: 119,085,294 (GRCm39) |
R71Q |
possibly damaging |
Het |
Baz1b |
T |
C |
5: 135,246,636 (GRCm39) |
L695P |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,792,368 (GRCm39) |
S587T |
probably benign |
Het |
Cep76 |
T |
C |
18: 67,758,028 (GRCm39) |
M421V |
probably benign |
Het |
Clk2 |
A |
G |
3: 89,076,010 (GRCm39) |
D60G |
probably damaging |
Het |
Clstn3 |
G |
T |
6: 124,439,128 (GRCm39) |
T6K |
probably damaging |
Het |
Cluap1 |
T |
A |
16: 3,737,422 (GRCm39) |
D180E |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,606,834 (GRCm39) |
I530V |
probably benign |
Het |
Cpt1a |
T |
C |
19: 3,415,788 (GRCm39) |
|
probably benign |
Het |
Cr2 |
T |
G |
1: 194,837,580 (GRCm39) |
K797Q |
possibly damaging |
Het |
Crybg3 |
C |
A |
16: 59,374,475 (GRCm39) |
V2260L |
probably benign |
Het |
Csnk1a1 |
T |
A |
18: 61,718,321 (GRCm39) |
|
probably benign |
Het |
Cxcr1 |
T |
C |
1: 74,231,929 (GRCm39) |
D31G |
probably benign |
Het |
Cyp2a5 |
G |
T |
7: 26,535,361 (GRCm39) |
D108Y |
probably damaging |
Het |
Dnajc1 |
A |
G |
2: 18,227,538 (GRCm39) |
V376A |
possibly damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,186,278 (GRCm39) |
V462A |
probably benign |
Het |
Elmo1 |
A |
G |
13: 20,474,647 (GRCm39) |
K357R |
possibly damaging |
Het |
Epb41l4a |
A |
G |
18: 33,965,717 (GRCm39) |
I370T |
probably benign |
Het |
Esp36 |
A |
T |
17: 38,728,172 (GRCm39) |
N79K |
possibly damaging |
Het |
Fam229b |
A |
G |
10: 38,994,915 (GRCm39) |
*81Q |
probably null |
Het |
Fat4 |
T |
C |
3: 39,037,225 (GRCm39) |
Y3626H |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,148,205 (GRCm39) |
F2681Y |
probably benign |
Het |
Gad1-ps |
A |
G |
10: 99,281,331 (GRCm39) |
|
noncoding transcript |
Het |
Galm |
C |
A |
17: 80,490,696 (GRCm39) |
N284K |
probably damaging |
Het |
Gtf3c2 |
A |
T |
5: 31,316,446 (GRCm39) |
S735T |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,553,848 (GRCm39) |
S207T |
probably benign |
Het |
Il33 |
C |
T |
19: 29,932,615 (GRCm39) |
R159C |
probably damaging |
Het |
Invs |
A |
G |
4: 48,382,148 (GRCm39) |
N106S |
possibly damaging |
Het |
Kif21b |
G |
T |
1: 136,097,062 (GRCm39) |
|
probably null |
Het |
Kirrel2 |
A |
G |
7: 30,155,923 (GRCm39) |
C42R |
probably damaging |
Het |
Letm1 |
A |
C |
5: 33,909,899 (GRCm39) |
C378W |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,652,791 (GRCm39) |
K160N |
probably benign |
Het |
Lrrtm3 |
A |
G |
10: 63,924,804 (GRCm39) |
I121T |
probably damaging |
Het |
Lztr1 |
T |
A |
16: 17,327,534 (GRCm39) |
V79E |
probably damaging |
Het |
Mmp8 |
T |
G |
9: 7,566,279 (GRCm39) |
D378E |
probably damaging |
Het |
Mpzl3 |
A |
G |
9: 44,977,827 (GRCm39) |
E145G |
probably damaging |
Het |
Mrps2 |
C |
T |
2: 28,359,676 (GRCm39) |
L178F |
probably damaging |
Het |
Mzb1 |
A |
G |
18: 35,780,875 (GRCm39) |
|
probably null |
Het |
Nckap1 |
T |
C |
2: 80,383,759 (GRCm39) |
D135G |
probably damaging |
Het |
Ndst1 |
A |
G |
18: 60,830,242 (GRCm39) |
F623L |
possibly damaging |
Het |
Nlrp5 |
A |
T |
7: 23,112,772 (GRCm39) |
D143V |
probably damaging |
Het |
Or14a260 |
T |
C |
7: 85,985,553 (GRCm39) |
D17G |
possibly damaging |
Het |
Or4a69 |
T |
C |
2: 89,312,592 (GRCm39) |
M296V |
probably null |
Het |
Or4b1d |
A |
G |
2: 89,968,748 (GRCm39) |
V245A |
probably benign |
Het |
Or4c120 |
A |
G |
2: 89,001,281 (GRCm39) |
S92P |
probably damaging |
Het |
Or4f58 |
A |
G |
2: 111,851,749 (GRCm39) |
V150A |
probably benign |
Het |
Or52b4i |
T |
C |
7: 102,191,332 (GRCm39) |
L63P |
probably damaging |
Het |
Or8b44 |
A |
G |
9: 38,410,114 (GRCm39) |
I50V |
probably benign |
Het |
Or8g17 |
T |
C |
9: 38,930,321 (GRCm39) |
D172G |
probably benign |
Het |
Parp14 |
T |
G |
16: 35,677,594 (GRCm39) |
E791D |
probably benign |
Het |
Pcdh8 |
C |
T |
14: 80,006,829 (GRCm39) |
R578H |
possibly damaging |
Het |
Phrf1 |
T |
A |
7: 140,839,714 (GRCm39) |
|
probably benign |
Het |
Polr3b |
C |
A |
10: 84,516,249 (GRCm39) |
H626N |
probably benign |
Het |
Ppp1r12a |
A |
G |
10: 108,087,720 (GRCm39) |
T58A |
probably benign |
Het |
Ppp4r3b |
T |
A |
11: 29,132,460 (GRCm39) |
V33D |
probably damaging |
Het |
Ppp5c |
A |
G |
7: 16,743,907 (GRCm39) |
Y176H |
probably damaging |
Het |
R3hdm1 |
A |
G |
1: 128,124,742 (GRCm39) |
Y343C |
probably damaging |
Het |
Rabac1 |
C |
T |
7: 24,671,555 (GRCm39) |
V122M |
probably damaging |
Het |
Rasef |
G |
T |
4: 73,653,985 (GRCm39) |
Q561K |
probably damaging |
Het |
Rbl1 |
A |
G |
2: 157,037,554 (GRCm39) |
S198P |
probably damaging |
Het |
Rbm12 |
A |
T |
2: 155,939,456 (GRCm39) |
M272K |
probably damaging |
Het |
Rexo1 |
T |
G |
10: 80,385,884 (GRCm39) |
K391N |
possibly damaging |
Het |
Rnf43 |
T |
C |
11: 87,622,173 (GRCm39) |
S384P |
probably benign |
Het |
Rpsa |
A |
T |
9: 119,960,066 (GRCm39) |
I210F |
possibly damaging |
Het |
Rslcan18 |
A |
G |
13: 67,247,016 (GRCm39) |
Y75H |
possibly damaging |
Het |
Scn9a |
T |
A |
2: 66,357,157 (GRCm39) |
D1048V |
probably benign |
Het |
Sec11a |
T |
C |
7: 80,577,482 (GRCm39) |
|
probably null |
Het |
Sidt2 |
A |
G |
9: 45,861,387 (GRCm39) |
V19A |
probably damaging |
Het |
Snx14 |
G |
A |
9: 88,280,417 (GRCm39) |
Q522* |
probably null |
Het |
Stx1b |
A |
G |
7: 127,414,144 (GRCm39) |
L74S |
probably damaging |
Het |
Tm7sf3 |
A |
T |
6: 146,511,376 (GRCm39) |
M371K |
probably benign |
Het |
Tmem115 |
T |
C |
9: 107,412,174 (GRCm39) |
V166A |
probably benign |
Het |
Traf5 |
T |
A |
1: 191,731,912 (GRCm39) |
T310S |
probably benign |
Het |
Trdn |
A |
G |
10: 33,342,448 (GRCm39) |
K619E |
probably benign |
Het |
Trmt10a |
T |
A |
3: 137,857,945 (GRCm39) |
|
probably null |
Het |
Txk |
A |
C |
5: 72,865,014 (GRCm39) |
I287R |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,389,344 (GRCm39) |
D452G |
probably damaging |
Het |
Ube2f |
G |
A |
1: 91,190,023 (GRCm39) |
|
probably null |
Het |
Ubtfl1 |
T |
G |
9: 18,321,489 (GRCm39) |
I339R |
probably benign |
Het |
Upf1 |
A |
G |
8: 70,791,155 (GRCm39) |
I529T |
probably damaging |
Het |
Vmn1r197 |
A |
G |
13: 22,512,823 (GRCm39) |
D248G |
possibly damaging |
Het |
Vmn1r5 |
A |
T |
6: 56,962,771 (GRCm39) |
T149S |
probably benign |
Het |
Vmn1r83 |
C |
T |
7: 12,055,197 (GRCm39) |
V287I |
possibly damaging |
Het |
Vmn2r118 |
G |
A |
17: 55,915,496 (GRCm39) |
R485* |
probably null |
Het |
Vmn2r130 |
A |
G |
17: 23,282,775 (GRCm39) |
T152A |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,840,121 (GRCm39) |
F2448L |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,841,719 (GRCm39) |
N2583S |
probably benign |
Het |
Wscd1 |
C |
T |
11: 71,679,501 (GRCm39) |
P458L |
probably damaging |
Het |
Xylt2 |
T |
A |
11: 94,561,259 (GRCm39) |
D168V |
probably damaging |
Het |
Zdhhc2 |
A |
G |
8: 40,921,013 (GRCm39) |
T306A |
probably benign |
Het |
Zfp804b |
A |
T |
5: 6,819,771 (GRCm39) |
D1097E |
possibly damaging |
Het |
Zfp93 |
T |
A |
7: 23,975,156 (GRCm39) |
C380* |
probably null |
Het |
Zfp960 |
T |
A |
17: 17,308,518 (GRCm39) |
C411S |
probably damaging |
Het |
Zmynd15 |
T |
A |
11: 70,355,619 (GRCm39) |
V430E |
probably damaging |
Het |
|
Other mutations in Eml6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01071:Eml6
|
APN |
11 |
29,800,816 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01407:Eml6
|
APN |
11 |
29,705,021 (GRCm39) |
nonsense |
probably null |
|
IGL01434:Eml6
|
APN |
11 |
29,769,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01578:Eml6
|
APN |
11 |
29,800,870 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01780:Eml6
|
APN |
11 |
29,755,175 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01821:Eml6
|
APN |
11 |
29,771,699 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01837:Eml6
|
APN |
11 |
29,727,055 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01904:Eml6
|
APN |
11 |
29,788,613 (GRCm39) |
nonsense |
probably null |
|
IGL01972:Eml6
|
APN |
11 |
29,788,451 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02134:Eml6
|
APN |
11 |
29,709,066 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02192:Eml6
|
APN |
11 |
29,755,743 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02377:Eml6
|
APN |
11 |
29,727,282 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02584:Eml6
|
APN |
11 |
29,699,387 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02587:Eml6
|
APN |
11 |
29,734,236 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02810:Eml6
|
APN |
11 |
29,799,016 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02873:Eml6
|
APN |
11 |
29,830,700 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02880:Eml6
|
APN |
11 |
29,699,959 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03289:Eml6
|
APN |
11 |
29,745,328 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03301:Eml6
|
APN |
11 |
29,714,083 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03386:Eml6
|
APN |
11 |
29,699,934 (GRCm39) |
missense |
probably benign |
|
IGL03407:Eml6
|
APN |
11 |
29,856,330 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Eml6
|
UTSW |
11 |
29,752,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Eml6
|
UTSW |
11 |
29,832,088 (GRCm39) |
missense |
probably benign |
0.19 |
R0240:Eml6
|
UTSW |
11 |
29,742,367 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0240:Eml6
|
UTSW |
11 |
29,742,367 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0271:Eml6
|
UTSW |
11 |
29,798,949 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0304:Eml6
|
UTSW |
11 |
29,727,441 (GRCm39) |
missense |
probably benign |
0.00 |
R0415:Eml6
|
UTSW |
11 |
29,699,392 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0449:Eml6
|
UTSW |
11 |
29,843,213 (GRCm39) |
missense |
probably benign |
0.01 |
R0538:Eml6
|
UTSW |
11 |
29,710,010 (GRCm39) |
splice site |
probably benign |
|
R0671:Eml6
|
UTSW |
11 |
29,755,065 (GRCm39) |
missense |
probably benign |
0.00 |
R0766:Eml6
|
UTSW |
11 |
29,781,219 (GRCm39) |
splice site |
probably benign |
|
R0800:Eml6
|
UTSW |
11 |
29,699,877 (GRCm39) |
missense |
probably benign |
0.08 |
R0841:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R0879:Eml6
|
UTSW |
11 |
29,800,816 (GRCm39) |
critical splice donor site |
probably null |
|
R1061:Eml6
|
UTSW |
11 |
29,727,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R1145:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R1172:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1173:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1174:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1199:Eml6
|
UTSW |
11 |
29,705,044 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1311:Eml6
|
UTSW |
11 |
29,781,088 (GRCm39) |
splice site |
probably benign |
|
R1312:Eml6
|
UTSW |
11 |
29,781,219 (GRCm39) |
splice site |
probably benign |
|
R1355:Eml6
|
UTSW |
11 |
29,783,085 (GRCm39) |
missense |
probably benign |
0.03 |
R1370:Eml6
|
UTSW |
11 |
29,783,085 (GRCm39) |
missense |
probably benign |
0.03 |
R1457:Eml6
|
UTSW |
11 |
29,974,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1486:Eml6
|
UTSW |
11 |
29,755,114 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1532:Eml6
|
UTSW |
11 |
29,742,256 (GRCm39) |
splice site |
probably null |
|
R1642:Eml6
|
UTSW |
11 |
29,727,001 (GRCm39) |
critical splice donor site |
probably null |
|
R1682:Eml6
|
UTSW |
11 |
29,709,065 (GRCm39) |
missense |
probably benign |
0.13 |
R1687:Eml6
|
UTSW |
11 |
29,783,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Eml6
|
UTSW |
11 |
29,696,282 (GRCm39) |
nonsense |
probably null |
|
R1796:Eml6
|
UTSW |
11 |
29,831,975 (GRCm39) |
missense |
probably benign |
0.19 |
R1797:Eml6
|
UTSW |
11 |
29,832,041 (GRCm39) |
missense |
probably benign |
0.09 |
R1837:Eml6
|
UTSW |
11 |
29,699,802 (GRCm39) |
splice site |
probably null |
|
R1874:Eml6
|
UTSW |
11 |
29,781,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R1967:Eml6
|
UTSW |
11 |
29,974,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Eml6
|
UTSW |
11 |
29,783,075 (GRCm39) |
missense |
probably benign |
|
R2007:Eml6
|
UTSW |
11 |
29,798,814 (GRCm39) |
critical splice donor site |
probably null |
|
R2012:Eml6
|
UTSW |
11 |
29,781,128 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2198:Eml6
|
UTSW |
11 |
29,800,935 (GRCm39) |
missense |
probably benign |
0.01 |
R2217:Eml6
|
UTSW |
11 |
29,768,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R2218:Eml6
|
UTSW |
11 |
29,768,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R2403:Eml6
|
UTSW |
11 |
29,752,434 (GRCm39) |
missense |
probably benign |
0.05 |
R2520:Eml6
|
UTSW |
11 |
29,741,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Eml6
|
UTSW |
11 |
29,783,049 (GRCm39) |
splice site |
probably benign |
|
R2938:Eml6
|
UTSW |
11 |
29,783,049 (GRCm39) |
splice site |
probably benign |
|
R3085:Eml6
|
UTSW |
11 |
29,759,332 (GRCm39) |
missense |
probably damaging |
0.96 |
R3236:Eml6
|
UTSW |
11 |
29,781,097 (GRCm39) |
critical splice donor site |
probably null |
|
R3738:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R3739:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R3752:Eml6
|
UTSW |
11 |
29,759,360 (GRCm39) |
missense |
probably benign |
0.06 |
R3854:Eml6
|
UTSW |
11 |
29,699,905 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3941:Eml6
|
UTSW |
11 |
29,753,167 (GRCm39) |
missense |
probably damaging |
0.98 |
R4034:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R4049:Eml6
|
UTSW |
11 |
29,788,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R4108:Eml6
|
UTSW |
11 |
29,755,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R4657:Eml6
|
UTSW |
11 |
29,755,108 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4662:Eml6
|
UTSW |
11 |
29,727,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Eml6
|
UTSW |
11 |
29,769,007 (GRCm39) |
nonsense |
probably null |
|
R4721:Eml6
|
UTSW |
11 |
29,788,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4729:Eml6
|
UTSW |
11 |
29,783,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Eml6
|
UTSW |
11 |
29,755,757 (GRCm39) |
missense |
probably benign |
0.22 |
R4810:Eml6
|
UTSW |
11 |
29,705,011 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4831:Eml6
|
UTSW |
11 |
29,727,052 (GRCm39) |
nonsense |
probably null |
|
R5035:Eml6
|
UTSW |
11 |
29,804,187 (GRCm39) |
missense |
probably benign |
0.00 |
R5064:Eml6
|
UTSW |
11 |
29,699,300 (GRCm39) |
missense |
probably benign |
0.12 |
R5103:Eml6
|
UTSW |
11 |
29,800,905 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5121:Eml6
|
UTSW |
11 |
29,694,606 (GRCm39) |
missense |
probably benign |
0.03 |
R5161:Eml6
|
UTSW |
11 |
29,974,467 (GRCm39) |
missense |
probably damaging |
0.99 |
R5211:Eml6
|
UTSW |
11 |
29,804,145 (GRCm39) |
missense |
probably benign |
0.02 |
R5268:Eml6
|
UTSW |
11 |
29,753,108 (GRCm39) |
missense |
probably benign |
0.15 |
R5390:Eml6
|
UTSW |
11 |
29,710,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Eml6
|
UTSW |
11 |
29,714,126 (GRCm39) |
missense |
probably benign |
0.04 |
R6239:Eml6
|
UTSW |
11 |
29,699,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Eml6
|
UTSW |
11 |
29,769,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Eml6
|
UTSW |
11 |
29,759,321 (GRCm39) |
missense |
probably benign |
0.00 |
R6476:Eml6
|
UTSW |
11 |
29,741,971 (GRCm39) |
critical splice donor site |
probably null |
|
R6483:Eml6
|
UTSW |
11 |
29,699,875 (GRCm39) |
missense |
probably benign |
0.00 |
R6701:Eml6
|
UTSW |
11 |
29,735,748 (GRCm39) |
missense |
probably damaging |
0.98 |
R6753:Eml6
|
UTSW |
11 |
29,704,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Eml6
|
UTSW |
11 |
29,753,161 (GRCm39) |
missense |
probably benign |
0.23 |
R6847:Eml6
|
UTSW |
11 |
29,768,447 (GRCm39) |
missense |
probably benign |
0.00 |
R6855:Eml6
|
UTSW |
11 |
29,701,381 (GRCm39) |
splice site |
probably null |
|
R7168:Eml6
|
UTSW |
11 |
29,788,529 (GRCm39) |
missense |
probably benign |
0.01 |
R7175:Eml6
|
UTSW |
11 |
29,734,231 (GRCm39) |
missense |
probably benign |
0.00 |
R7305:Eml6
|
UTSW |
11 |
29,727,258 (GRCm39) |
missense |
probably benign |
0.01 |
R7615:Eml6
|
UTSW |
11 |
29,752,501 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7692:Eml6
|
UTSW |
11 |
29,703,085 (GRCm39) |
missense |
probably damaging |
0.98 |
R7980:Eml6
|
UTSW |
11 |
29,783,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R8026:Eml6
|
UTSW |
11 |
29,699,973 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8046:Eml6
|
UTSW |
11 |
29,708,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R8049:Eml6
|
UTSW |
11 |
29,843,201 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8114:Eml6
|
UTSW |
11 |
29,704,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8425:Eml6
|
UTSW |
11 |
29,705,008 (GRCm39) |
missense |
probably benign |
0.00 |
R8799:Eml6
|
UTSW |
11 |
29,708,981 (GRCm39) |
missense |
probably benign |
0.11 |
R8945:Eml6
|
UTSW |
11 |
29,703,110 (GRCm39) |
missense |
probably damaging |
0.98 |
R8977:Eml6
|
UTSW |
11 |
29,734,182 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8986:Eml6
|
UTSW |
11 |
29,755,181 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9088:Eml6
|
UTSW |
11 |
29,768,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R9150:Eml6
|
UTSW |
11 |
29,755,791 (GRCm39) |
missense |
probably benign |
0.15 |
R9209:Eml6
|
UTSW |
11 |
29,781,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Eml6
|
UTSW |
11 |
29,788,641 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9467:Eml6
|
UTSW |
11 |
29,769,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R9481:Eml6
|
UTSW |
11 |
29,788,641 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9534:Eml6
|
UTSW |
11 |
29,734,155 (GRCm39) |
missense |
possibly damaging |
0.45 |
RF037:Eml6
|
UTSW |
11 |
29,702,549 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF039:Eml6
|
UTSW |
11 |
29,702,551 (GRCm39) |
critical splice acceptor site |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- GCCACATTCTCTTGGTGAGGTGTTC -3'
(R):5'- GATGACATTCTCAGCCTGACCATCC -3'
Sequencing Primer
(F):5'- GTGTTCACATGTGGCTTCCA -3'
(R):5'- gccagaccaggttatttccag -3'
|
Posted On |
2014-04-13 |