Incidental Mutation 'R7196:Nebl'
ID |
559897 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nebl
|
Ensembl Gene |
ENSMUSG00000053702 |
Gene Name |
nebulette |
Synonyms |
Lnebl, D830029A09Rik, A630080F05Rik, 1200007O21Rik |
MMRRC Submission |
045275-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7196 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
17348720-17736275 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 17457329 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Glutamic Acid
at position 77
(V77E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118525
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028080]
[ENSMUST00000124270]
[ENSMUST00000131957]
[ENSMUST00000132418]
[ENSMUST00000145492]
|
AlphaFold |
Q0II04 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000028080
|
SMART Domains |
Protein: ENSMUSP00000028080 Gene: ENSMUSG00000053702
Domain | Start | End | E-Value | Type |
LIM
|
4 |
56 |
6.95e-14 |
SMART |
NEBU
|
62 |
92 |
3.35e-8 |
SMART |
NEBU
|
98 |
128 |
4.88e-10 |
SMART |
NEBU
|
134 |
164 |
3.82e-3 |
SMART |
SH3
|
213 |
270 |
2.12e-20 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000124270
AA Change: V77E
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000117805 Gene: ENSMUSG00000053702 AA Change: V77E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
25 |
N/A |
INTRINSIC |
NEBU
|
30 |
60 |
1.21e-5 |
SMART |
NEBU
|
65 |
95 |
5.4e-3 |
SMART |
NEBU
|
102 |
132 |
4.46e-4 |
SMART |
NEBU
|
139 |
169 |
1.31e-1 |
SMART |
NEBU
|
173 |
203 |
5.4e-3 |
SMART |
NEBU
|
207 |
237 |
2.74e-4 |
SMART |
NEBU
|
245 |
275 |
1.57e0 |
SMART |
NEBU
|
280 |
310 |
9.67e-1 |
SMART |
NEBU
|
315 |
345 |
6.25e-8 |
SMART |
NEBU
|
351 |
381 |
5.97e-5 |
SMART |
NEBU
|
387 |
418 |
2.56e-4 |
SMART |
NEBU
|
425 |
455 |
8.91e-4 |
SMART |
NEBU
|
462 |
492 |
4.92e-6 |
SMART |
NEBU
|
499 |
529 |
2.33e-7 |
SMART |
NEBU
|
536 |
566 |
1.84e-5 |
SMART |
NEBU
|
571 |
601 |
2.23e-4 |
SMART |
NEBU
|
602 |
632 |
1.24e-2 |
SMART |
NEBU
|
664 |
694 |
6.6e-7 |
SMART |
NEBU
|
695 |
725 |
6.86e-5 |
SMART |
NEBU
|
726 |
756 |
2.03e-7 |
SMART |
NEBU
|
761 |
791 |
1.74e-6 |
SMART |
NEBU
|
797 |
827 |
3.82e-3 |
SMART |
SH3
|
957 |
1014 |
2.12e-20 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000124611
|
SMART Domains |
Protein: ENSMUSP00000116065 Gene: ENSMUSG00000053702
Domain | Start | End | E-Value | Type |
NEBU
|
3 |
33 |
4.88e-10 |
SMART |
NEBU
|
39 |
69 |
3.82e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000131957
AA Change: V77E
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000118525 Gene: ENSMUSG00000053702 AA Change: V77E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
25 |
N/A |
INTRINSIC |
NEBU
|
30 |
60 |
1.21e-5 |
SMART |
NEBU
|
65 |
95 |
5.4e-3 |
SMART |
NEBU
|
102 |
132 |
4.46e-4 |
SMART |
NEBU
|
139 |
169 |
1.31e-1 |
SMART |
NEBU
|
173 |
203 |
5.4e-3 |
SMART |
NEBU
|
207 |
237 |
2.74e-4 |
SMART |
NEBU
|
245 |
275 |
7.35e0 |
SMART |
NEBU
|
280 |
310 |
6.25e-8 |
SMART |
NEBU
|
316 |
346 |
5.97e-5 |
SMART |
NEBU
|
352 |
383 |
2.56e-4 |
SMART |
NEBU
|
390 |
420 |
8.91e-4 |
SMART |
NEBU
|
427 |
457 |
4.92e-6 |
SMART |
NEBU
|
464 |
494 |
2.33e-7 |
SMART |
NEBU
|
501 |
525 |
1.02e2 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000132418
AA Change: V77E
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000122024 Gene: ENSMUSG00000053702 AA Change: V77E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
25 |
N/A |
INTRINSIC |
NEBU
|
30 |
60 |
1.21e-5 |
SMART |
NEBU
|
65 |
95 |
5.4e-3 |
SMART |
NEBU
|
102 |
132 |
4.46e-4 |
SMART |
NEBU
|
139 |
169 |
1.31e-1 |
SMART |
NEBU
|
173 |
203 |
5.4e-3 |
SMART |
NEBU
|
207 |
237 |
2.74e-4 |
SMART |
NEBU
|
245 |
275 |
7.35e0 |
SMART |
NEBU
|
280 |
310 |
6.25e-8 |
SMART |
NEBU
|
316 |
346 |
5.97e-5 |
SMART |
NEBU
|
352 |
383 |
2.56e-4 |
SMART |
NEBU
|
390 |
420 |
4.78e-4 |
SMART |
NEBU
|
427 |
450 |
6.81e1 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000145492
AA Change: V77E
PolyPhen 2
Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000121313 Gene: ENSMUSG00000053702 AA Change: V77E
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
25 |
N/A |
INTRINSIC |
NEBU
|
30 |
60 |
1.21e-5 |
SMART |
NEBU
|
65 |
95 |
5.4e-3 |
SMART |
NEBU
|
102 |
132 |
4.46e-4 |
SMART |
NEBU
|
139 |
169 |
1.31e-1 |
SMART |
NEBU
|
173 |
203 |
5.4e-3 |
SMART |
NEBU
|
207 |
237 |
2.74e-4 |
SMART |
NEBU
|
245 |
275 |
7.35e0 |
SMART |
NEBU
|
280 |
310 |
6.25e-8 |
SMART |
NEBU
|
316 |
346 |
5.97e-5 |
SMART |
NEBU
|
352 |
383 |
2.56e-4 |
SMART |
NEBU
|
390 |
420 |
8.91e-4 |
SMART |
|
Meta Mutation Damage Score |
0.7326 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.5%
|
Validation Efficiency |
99% (94/95) |
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 |
Lmo7 |
T |
A |
14: 102,133,936 (GRCm39) |
D660E |
possibly 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 |
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 Nebl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02146:Nebl
|
APN |
2 |
17,353,679 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02732:Nebl
|
APN |
2 |
17,457,295 (GRCm39) |
splice site |
probably benign |
|
IGL03241:Nebl
|
APN |
2 |
17,397,975 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03334:Nebl
|
APN |
2 |
17,418,522 (GRCm39) |
missense |
probably damaging |
0.98 |
BB008:Nebl
|
UTSW |
2 |
17,381,433 (GRCm39) |
critical splice donor site |
probably null |
|
BB018:Nebl
|
UTSW |
2 |
17,381,433 (GRCm39) |
critical splice donor site |
probably null |
|
R0068:Nebl
|
UTSW |
2 |
17,439,782 (GRCm39) |
nonsense |
probably null |
|
R0127:Nebl
|
UTSW |
2 |
17,397,794 (GRCm39) |
missense |
probably benign |
0.31 |
R0128:Nebl
|
UTSW |
2 |
17,397,834 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0130:Nebl
|
UTSW |
2 |
17,397,834 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0130:Nebl
|
UTSW |
2 |
17,395,737 (GRCm39) |
start gained |
probably benign |
|
R0537:Nebl
|
UTSW |
2 |
17,409,026 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0743:Nebl
|
UTSW |
2 |
17,415,929 (GRCm39) |
missense |
probably benign |
|
R0884:Nebl
|
UTSW |
2 |
17,415,929 (GRCm39) |
missense |
probably benign |
|
R1364:Nebl
|
UTSW |
2 |
17,397,848 (GRCm39) |
unclassified |
probably benign |
|
R1638:Nebl
|
UTSW |
2 |
17,381,462 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1711:Nebl
|
UTSW |
2 |
17,393,565 (GRCm39) |
missense |
probably damaging |
0.96 |
R1933:Nebl
|
UTSW |
2 |
17,380,103 (GRCm39) |
missense |
probably damaging |
0.97 |
R1990:Nebl
|
UTSW |
2 |
17,457,321 (GRCm39) |
missense |
probably damaging |
0.98 |
R1991:Nebl
|
UTSW |
2 |
17,457,321 (GRCm39) |
missense |
probably damaging |
0.98 |
R1992:Nebl
|
UTSW |
2 |
17,457,321 (GRCm39) |
missense |
probably damaging |
0.98 |
R2062:Nebl
|
UTSW |
2 |
17,401,932 (GRCm39) |
missense |
probably benign |
0.39 |
R2183:Nebl
|
UTSW |
2 |
17,409,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R2325:Nebl
|
UTSW |
2 |
17,397,827 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2679:Nebl
|
UTSW |
2 |
17,429,402 (GRCm39) |
missense |
probably benign |
0.03 |
R2877:Nebl
|
UTSW |
2 |
17,439,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R2878:Nebl
|
UTSW |
2 |
17,439,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R3079:Nebl
|
UTSW |
2 |
17,381,462 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3080:Nebl
|
UTSW |
2 |
17,381,462 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3878:Nebl
|
UTSW |
2 |
17,398,063 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3947:Nebl
|
UTSW |
2 |
17,382,917 (GRCm39) |
critical splice donor site |
probably null |
|
R4983:Nebl
|
UTSW |
2 |
17,380,082 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5006:Nebl
|
UTSW |
2 |
17,393,582 (GRCm39) |
splice site |
probably null |
|
R5256:Nebl
|
UTSW |
2 |
17,438,786 (GRCm39) |
missense |
probably benign |
0.37 |
R5491:Nebl
|
UTSW |
2 |
17,439,783 (GRCm39) |
nonsense |
probably null |
|
R5533:Nebl
|
UTSW |
2 |
17,398,079 (GRCm39) |
nonsense |
probably null |
|
R5597:Nebl
|
UTSW |
2 |
17,382,978 (GRCm39) |
missense |
probably benign |
|
R5658:Nebl
|
UTSW |
2 |
17,353,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Nebl
|
UTSW |
2 |
17,408,998 (GRCm39) |
missense |
probably benign |
|
R6056:Nebl
|
UTSW |
2 |
17,455,045 (GRCm39) |
missense |
probably benign |
0.13 |
R6161:Nebl
|
UTSW |
2 |
17,735,641 (GRCm39) |
missense |
probably benign |
0.26 |
R6646:Nebl
|
UTSW |
2 |
17,381,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R6784:Nebl
|
UTSW |
2 |
17,439,725 (GRCm39) |
nonsense |
probably null |
|
R6935:Nebl
|
UTSW |
2 |
17,353,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7671:Nebl
|
UTSW |
2 |
17,395,727 (GRCm39) |
nonsense |
probably null |
|
R7728:Nebl
|
UTSW |
2 |
17,375,325 (GRCm39) |
missense |
|
|
R7931:Nebl
|
UTSW |
2 |
17,381,433 (GRCm39) |
critical splice donor site |
probably null |
|
R8007:Nebl
|
UTSW |
2 |
17,375,300 (GRCm39) |
missense |
|
|
R8048:Nebl
|
UTSW |
2 |
17,429,333 (GRCm39) |
missense |
probably benign |
0.12 |
R8118:Nebl
|
UTSW |
2 |
17,384,631 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8317:Nebl
|
UTSW |
2 |
17,355,568 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8349:Nebl
|
UTSW |
2 |
17,418,593 (GRCm39) |
missense |
probably damaging |
0.98 |
R8360:Nebl
|
UTSW |
2 |
17,465,298 (GRCm39) |
missense |
probably benign |
0.04 |
R8392:Nebl
|
UTSW |
2 |
17,457,363 (GRCm39) |
missense |
probably benign |
0.36 |
R8449:Nebl
|
UTSW |
2 |
17,418,593 (GRCm39) |
missense |
probably damaging |
0.98 |
R8537:Nebl
|
UTSW |
2 |
17,355,520 (GRCm39) |
missense |
probably benign |
0.02 |
R8778:Nebl
|
UTSW |
2 |
17,409,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R8893:Nebl
|
UTSW |
2 |
17,735,671 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R8894:Nebl
|
UTSW |
2 |
17,380,036 (GRCm39) |
missense |
probably benign |
0.01 |
R8906:Nebl
|
UTSW |
2 |
17,382,928 (GRCm39) |
missense |
probably benign |
0.18 |
R8929:Nebl
|
UTSW |
2 |
17,397,991 (GRCm39) |
nonsense |
probably null |
|
R9054:Nebl
|
UTSW |
2 |
17,415,907 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9119:Nebl
|
UTSW |
2 |
17,405,370 (GRCm39) |
missense |
probably damaging |
0.96 |
R9211:Nebl
|
UTSW |
2 |
17,393,501 (GRCm39) |
critical splice donor site |
probably null |
|
R9225:Nebl
|
UTSW |
2 |
17,405,322 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9296:Nebl
|
UTSW |
2 |
17,429,451 (GRCm39) |
splice site |
probably benign |
|
R9310:Nebl
|
UTSW |
2 |
17,353,678 (GRCm39) |
missense |
probably benign |
0.16 |
R9474:Nebl
|
UTSW |
2 |
17,374,421 (GRCm39) |
nonsense |
probably null |
|
X0012:Nebl
|
UTSW |
2 |
17,448,605 (GRCm39) |
missense |
probably benign |
0.16 |
X0025:Nebl
|
UTSW |
2 |
17,409,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCTCAGTTTGCACATATTAACTTGG -3'
(R):5'- ACCTCAGAAATGGCTGCTTGG -3'
Sequencing Primer
(F):5'- GTGGATATGATCAGTATTTAGTG -3'
(R):5'- GTCAGTCTTCACTTCAACAACTGGG -3'
|
Posted On |
2019-06-26 |