Incidental Mutation 'R2378:Nbeal2'
ID | 248354 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nbeal2
|
Ensembl Gene |
ENSMUSG00000056724 |
Gene Name | neurobeachin-like 2 |
Synonyms | 1110014F23Rik |
Accession Numbers | |
Is this an essential gene? |
Possibly non essential (E-score: 0.252)
|
Stock # | R2378 (G1)
|
Quality Score | 168 |
Status |
Not validated
|
Chromosome | 9 |
Chromosomal Location | 110624789-110654161 bp(-) (GRCm38) |
Type of Mutation | missense |
DNA Base Change (assembly) |
T to C
at 110630808 bp
|
Zygosity | Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 1175
(E1175G)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000133191]
[ENSMUST00000167320]
[ENSMUST00000196488]
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123996
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126088
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000129095
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000130024
AA Change: E1175G
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000118061 Gene: ENSMUSG00000056724 AA Change: E1175G
Domain | Start | End | E-Value | Type |
low complexity region
|
1 |
13 |
N/A |
INTRINSIC |
low complexity region
|
236 |
248 |
N/A |
INTRINSIC |
Pfam:DUF4704
|
345 |
607 |
2.5e-29 |
PFAM |
low complexity region
|
649 |
664 |
N/A |
INTRINSIC |
low complexity region
|
804 |
819 |
N/A |
INTRINSIC |
Pfam:DUF4800
|
872 |
1138 |
9.9e-113 |
PFAM |
low complexity region
|
1164 |
1193 |
N/A |
INTRINSIC |
Pfam:PH_BEACH
|
1204 |
1291 |
2.2e-21 |
PFAM |
Beach
|
1343 |
1623 |
5.2e-205 |
SMART |
WD40
|
1721 |
1766 |
1.03e1 |
SMART |
WD40
|
1769 |
1808 |
6.19e-5 |
SMART |
WD40
|
1820 |
1859 |
1.02e-5 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000131017
AA Change: E246G
PolyPhen 2
Score 0.889 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000114660 Gene: ENSMUSG00000056724 AA Change: E246G
Domain | Start | End | E-Value | Type |
Pfam:DUF4800
|
1 |
209 |
7.5e-97 |
PFAM |
low complexity region
|
235 |
264 |
N/A |
INTRINSIC |
Pfam:PH_BEACH
|
275 |
362 |
1e-21 |
PFAM |
Beach
|
414 |
694 |
5.2e-205 |
SMART |
WD40
|
762 |
807 |
1.03e1 |
SMART |
WD40
|
810 |
849 |
6.19e-5 |
SMART |
WD40
|
861 |
900 |
1.02e-5 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000133191
AA Change: E1887G
PolyPhen 2
Score 0.488 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000121373 Gene: ENSMUSG00000056724 AA Change: E1887G
Domain | Start | End | E-Value | Type |
low complexity region
|
56 |
84 |
N/A |
INTRINSIC |
low complexity region
|
192 |
201 |
N/A |
INTRINSIC |
low complexity region
|
227 |
238 |
N/A |
INTRINSIC |
low complexity region
|
514 |
522 |
N/A |
INTRINSIC |
low complexity region
|
527 |
542 |
N/A |
INTRINSIC |
Pfam:Laminin_G_3
|
578 |
818 |
5.9e-8 |
PFAM |
low complexity region
|
1014 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1128 |
1136 |
N/A |
INTRINSIC |
low complexity region
|
1149 |
1163 |
N/A |
INTRINSIC |
low complexity region
|
1359 |
1375 |
N/A |
INTRINSIC |
low complexity region
|
1515 |
1530 |
N/A |
INTRINSIC |
low complexity region
|
1621 |
1647 |
N/A |
INTRINSIC |
low complexity region
|
1875 |
1904 |
N/A |
INTRINSIC |
Pfam:PH_BEACH
|
1908 |
2002 |
6.2e-28 |
PFAM |
Beach
|
2054 |
2334 |
5.2e-205 |
SMART |
WD40
|
2432 |
2477 |
1.03e1 |
SMART |
WD40
|
2480 |
2519 |
6.19e-5 |
SMART |
WD40
|
2531 |
2570 |
1.02e-5 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138072
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153960
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000167320
AA Change: E1894G
PolyPhen 2
Score 0.100 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000128586 Gene: ENSMUSG00000056724 AA Change: E1894G
Domain | Start | End | E-Value | Type |
low complexity region
|
56 |
84 |
N/A |
INTRINSIC |
low complexity region
|
192 |
201 |
N/A |
INTRINSIC |
low complexity region
|
227 |
238 |
N/A |
INTRINSIC |
low complexity region
|
514 |
522 |
N/A |
INTRINSIC |
low complexity region
|
527 |
542 |
N/A |
INTRINSIC |
low complexity region
|
763 |
775 |
N/A |
INTRINSIC |
Pfam:DUF4704
|
872 |
1148 |
9.2e-32 |
PFAM |
low complexity region
|
1149 |
1163 |
N/A |
INTRINSIC |
low complexity region
|
1366 |
1382 |
N/A |
INTRINSIC |
low complexity region
|
1522 |
1537 |
N/A |
INTRINSIC |
Pfam:DUF4800
|
1590 |
1856 |
1.5e-112 |
PFAM |
low complexity region
|
1882 |
1911 |
N/A |
INTRINSIC |
Pfam:PH_BEACH
|
1922 |
2009 |
3.1e-21 |
PFAM |
Beach
|
2061 |
2341 |
5.2e-205 |
SMART |
WD40
|
2439 |
2484 |
1.03e1 |
SMART |
WD40
|
2487 |
2526 |
6.19e-5 |
SMART |
WD40
|
2538 |
2577 |
1.02e-5 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000196488
AA Change: E1860G
PolyPhen 2
Score 0.349 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000143265 Gene: ENSMUSG00000056724 AA Change: E1860G
Domain | Start | End | E-Value | Type |
low complexity region
|
56 |
84 |
N/A |
INTRINSIC |
low complexity region
|
192 |
201 |
N/A |
INTRINSIC |
low complexity region
|
227 |
238 |
N/A |
INTRINSIC |
low complexity region
|
487 |
495 |
N/A |
INTRINSIC |
low complexity region
|
500 |
515 |
N/A |
INTRINSIC |
Pfam:Laminin_G_3
|
551 |
791 |
5.3e-6 |
PFAM |
low complexity region
|
987 |
1001 |
N/A |
INTRINSIC |
low complexity region
|
1101 |
1109 |
N/A |
INTRINSIC |
low complexity region
|
1122 |
1136 |
N/A |
INTRINSIC |
low complexity region
|
1332 |
1348 |
N/A |
INTRINSIC |
low complexity region
|
1488 |
1503 |
N/A |
INTRINSIC |
low complexity region
|
1594 |
1620 |
N/A |
INTRINSIC |
low complexity region
|
1848 |
1877 |
N/A |
INTRINSIC |
Pfam:PH_BEACH
|
1881 |
1975 |
3.1e-25 |
PFAM |
Beach
|
2027 |
2307 |
3.8e-209 |
SMART |
WD40
|
2405 |
2450 |
6.3e-2 |
SMART |
WD40
|
2453 |
2492 |
3.8e-7 |
SMART |
WD40
|
2504 |
2543 |
6.5e-8 |
SMART |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a beige and Chediak-Higashi (BEACH) domain and multiple WD40 domains, and may play a role in megakaryocyte alpha-granule biogenesis. Mutations in this gene are a cause of gray platelet syndrome. [provided by RefSeq, Dec 2011] PHENOTYPE: Homozygous null mice exhibit megakaryocyte and platelet abnormalities resulting in impaired arterial thrombus formation and protection from infarction following cerebral ischemia. Wound repair is impaired. These abnormalities result in a bleeding disorder similiar to Gray Platelet Syndrome. [provided by MGI curators]
|
Allele List at MGI | |
Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AK157302 |
T |
C |
13: 21,495,562 |
I86T |
possibly damaging |
Het |
Akr1cl |
A |
T |
1: 65,021,988 |
M124K |
probably benign |
Het |
Asap2 |
T |
C |
12: 21,254,318 |
L745P |
possibly damaging |
Het |
B3gnt9 |
G |
A |
8: 105,254,484 |
R91C |
probably damaging |
Het |
Capg |
C |
T |
6: 72,555,491 |
P13L |
probably benign |
Het |
Eif3c |
C |
T |
7: 126,552,325 |
R609H |
probably damaging |
Het |
Ephb3 |
A |
G |
16: 21,218,243 |
H152R |
probably benign |
Het |
Gbp9 |
T |
C |
5: 105,080,176 |
D580G |
probably benign |
Het |
Gm884 |
A |
G |
11: 103,619,711 |
|
probably benign |
Het |
Iars2 |
A |
G |
1: 185,327,721 |
Y97H |
probably damaging |
Het |
Ip6k2 |
A |
G |
9: 108,796,301 |
|
probably null |
Het |
Itih2 |
T |
A |
2: 10,094,887 |
D907V |
probably damaging |
Het |
Msh4 |
A |
G |
3: 153,863,477 |
C732R |
probably damaging |
Het |
Mtss1l |
T |
C |
8: 110,738,349 |
F474L |
probably damaging |
Het |
Pgm3 |
A |
T |
9: 86,562,667 |
C272S |
probably damaging |
Het |
R3hcc1l |
T |
A |
19: 42,563,473 |
I303N |
probably damaging |
Het |
Sla2 |
G |
A |
2: 156,875,942 |
R137C |
probably damaging |
Het |
Spsb3 |
A |
G |
17: 24,886,950 |
|
probably benign |
Het |
Tgfbr2 |
G |
A |
9: 116,129,950 |
T132I |
probably benign |
Het |
Tpp2 |
A |
T |
1: 43,999,765 |
E223V |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,889,450 |
|
probably benign |
Het |
Vmn2r102 |
T |
G |
17: 19,694,668 |
L832V |
probably damaging |
Het |
|
Other mutations in Nbeal2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Nbeal2
|
APN |
9 |
110635869 |
missense |
probably damaging |
1.00 |
IGL00784:Nbeal2
|
APN |
9 |
110629763 |
splice site |
probably benign |
|
IGL00826:Nbeal2
|
APN |
9 |
110626903 |
missense |
probably benign |
|
IGL00885:Nbeal2
|
APN |
9 |
110638661 |
missense |
probably damaging |
1.00 |
IGL01348:Nbeal2
|
APN |
9 |
110629146 |
missense |
probably damaging |
0.99 |
IGL01511:Nbeal2
|
APN |
9 |
110629234 |
missense |
probably damaging |
1.00 |
IGL01571:Nbeal2
|
APN |
9 |
110632758 |
missense |
possibly damaging |
0.63 |
IGL01612:Nbeal2
|
APN |
9 |
110644678 |
missense |
probably damaging |
1.00 |
IGL01924:Nbeal2
|
APN |
9 |
110631414 |
missense |
probably benign |
0.23 |
IGL02056:Nbeal2
|
APN |
9 |
110627324 |
missense |
probably benign |
0.17 |
IGL02481:Nbeal2
|
APN |
9 |
110625995 |
nonsense |
probably null |
|
IGL02483:Nbeal2
|
APN |
9 |
110625995 |
nonsense |
probably null |
|
IGL02502:Nbeal2
|
APN |
9 |
110633768 |
missense |
probably damaging |
1.00 |
IGL02631:Nbeal2
|
APN |
9 |
110630208 |
missense |
probably damaging |
0.99 |
IGL02637:Nbeal2
|
APN |
9 |
110625977 |
missense |
possibly damaging |
0.62 |
IGL02727:Nbeal2
|
APN |
9 |
110639285 |
splice site |
probably benign |
|
IGL02887:Nbeal2
|
APN |
9 |
110628276 |
missense |
probably damaging |
1.00 |
IGL02896:Nbeal2
|
APN |
9 |
110639292 |
critical splice donor site |
probably null |
|
IGL03110:Nbeal2
|
APN |
9 |
110631433 |
missense |
probably damaging |
1.00 |
Antonym
|
UTSW |
9 |
110630252 |
missense |
probably damaging |
1.00 |
dog
|
UTSW |
9 |
110635341 |
missense |
possibly damaging |
0.89 |
legion
|
UTSW |
9 |
110629179 |
missense |
probably damaging |
1.00 |
litigious
|
UTSW |
9 |
110628195 |
missense |
probably damaging |
1.00 |
mall
|
UTSW |
9 |
110632886 |
missense |
probably damaging |
1.00 |
Mollusca
|
UTSW |
9 |
110645438 |
splice site |
probably null |
|
Schleuter
|
UTSW |
9 |
110628744 |
missense |
possibly damaging |
0.69 |
shellfish
|
UTSW |
9 |
110628720 |
missense |
probably damaging |
1.00 |
F5770:Nbeal2
|
UTSW |
9 |
110637937 |
missense |
possibly damaging |
0.65 |
R0032:Nbeal2
|
UTSW |
9 |
110637868 |
splice site |
probably benign |
|
R0084:Nbeal2
|
UTSW |
9 |
110643710 |
critical splice donor site |
probably null |
|
R0147:Nbeal2
|
UTSW |
9 |
110642143 |
nonsense |
probably null |
|
R0294:Nbeal2
|
UTSW |
9 |
110632859 |
missense |
probably damaging |
1.00 |
R0310:Nbeal2
|
UTSW |
9 |
110638163 |
missense |
probably damaging |
1.00 |
R0494:Nbeal2
|
UTSW |
9 |
110627187 |
missense |
probably damaging |
1.00 |
R0550:Nbeal2
|
UTSW |
9 |
110642158 |
missense |
probably benign |
0.01 |
R0630:Nbeal2
|
UTSW |
9 |
110636034 |
splice site |
probably benign |
|
R0762:Nbeal2
|
UTSW |
9 |
110643808 |
splice site |
probably benign |
|
R0862:Nbeal2
|
UTSW |
9 |
110628195 |
missense |
probably damaging |
1.00 |
R0864:Nbeal2
|
UTSW |
9 |
110628195 |
missense |
probably damaging |
1.00 |
R1225:Nbeal2
|
UTSW |
9 |
110632886 |
missense |
probably damaging |
1.00 |
R1240:Nbeal2
|
UTSW |
9 |
110627108 |
missense |
probably damaging |
0.98 |
R1450:Nbeal2
|
UTSW |
9 |
110633672 |
splice site |
probably benign |
|
R1519:Nbeal2
|
UTSW |
9 |
110636305 |
missense |
probably damaging |
1.00 |
R1655:Nbeal2
|
UTSW |
9 |
110632872 |
missense |
probably damaging |
1.00 |
R1668:Nbeal2
|
UTSW |
9 |
110638893 |
missense |
probably damaging |
1.00 |
R1705:Nbeal2
|
UTSW |
9 |
110625196 |
missense |
probably damaging |
1.00 |
R1784:Nbeal2
|
UTSW |
9 |
110630857 |
nonsense |
probably null |
|
R1834:Nbeal2
|
UTSW |
9 |
110627129 |
missense |
probably damaging |
1.00 |
R1997:Nbeal2
|
UTSW |
9 |
110632198 |
missense |
probably damaging |
1.00 |
R2013:Nbeal2
|
UTSW |
9 |
110634071 |
missense |
probably benign |
0.09 |
R2014:Nbeal2
|
UTSW |
9 |
110634071 |
missense |
probably benign |
0.09 |
R2055:Nbeal2
|
UTSW |
9 |
110635307 |
missense |
possibly damaging |
0.92 |
R2086:Nbeal2
|
UTSW |
9 |
110634071 |
missense |
probably benign |
0.09 |
R2113:Nbeal2
|
UTSW |
9 |
110625406 |
missense |
probably damaging |
1.00 |
R2167:Nbeal2
|
UTSW |
9 |
110638308 |
missense |
probably damaging |
1.00 |
R2201:Nbeal2
|
UTSW |
9 |
110630250 |
missense |
probably benign |
0.16 |
R2309:Nbeal2
|
UTSW |
9 |
110626570 |
missense |
probably damaging |
1.00 |
R2945:Nbeal2
|
UTSW |
9 |
110628068 |
missense |
possibly damaging |
0.82 |
R3052:Nbeal2
|
UTSW |
9 |
110633085 |
missense |
possibly damaging |
0.93 |
R3076:Nbeal2
|
UTSW |
9 |
110631700 |
missense |
probably damaging |
1.00 |
R3176:Nbeal2
|
UTSW |
9 |
110636887 |
splice site |
probably benign |
|
R3974:Nbeal2
|
UTSW |
9 |
110633846 |
missense |
probably damaging |
1.00 |
R4183:Nbeal2
|
UTSW |
9 |
110636675 |
missense |
probably benign |
|
R4342:Nbeal2
|
UTSW |
9 |
110631793 |
intron |
probably benign |
|
R4654:Nbeal2
|
UTSW |
9 |
110632004 |
missense |
probably damaging |
1.00 |
R4707:Nbeal2
|
UTSW |
9 |
110632055 |
missense |
probably benign |
0.10 |
R4822:Nbeal2
|
UTSW |
9 |
110636315 |
missense |
possibly damaging |
0.82 |
R4854:Nbeal2
|
UTSW |
9 |
110631396 |
missense |
probably damaging |
1.00 |
R4860:Nbeal2
|
UTSW |
9 |
110635194 |
missense |
probably benign |
0.00 |
R4860:Nbeal2
|
UTSW |
9 |
110635194 |
missense |
probably benign |
0.00 |
R4990:Nbeal2
|
UTSW |
9 |
110634803 |
missense |
probably benign |
0.10 |
R4991:Nbeal2
|
UTSW |
9 |
110638767 |
missense |
probably damaging |
1.00 |
R5021:Nbeal2
|
UTSW |
9 |
110637463 |
missense |
probably damaging |
0.99 |
R5057:Nbeal2
|
UTSW |
9 |
110631005 |
missense |
probably damaging |
1.00 |
R5092:Nbeal2
|
UTSW |
9 |
110626728 |
splice site |
probably null |
|
R5161:Nbeal2
|
UTSW |
9 |
110629868 |
missense |
probably benign |
|
R5202:Nbeal2
|
UTSW |
9 |
110644666 |
missense |
probably damaging |
0.99 |
R5217:Nbeal2
|
UTSW |
9 |
110632090 |
missense |
possibly damaging |
0.56 |
R5408:Nbeal2
|
UTSW |
9 |
110637520 |
missense |
possibly damaging |
0.91 |
R5540:Nbeal2
|
UTSW |
9 |
110631733 |
missense |
probably damaging |
1.00 |
R5866:Nbeal2
|
UTSW |
9 |
110631492 |
missense |
probably damaging |
1.00 |
R5925:Nbeal2
|
UTSW |
9 |
110629880 |
missense |
probably benign |
0.00 |
R6057:Nbeal2
|
UTSW |
9 |
110641877 |
missense |
possibly damaging |
0.81 |
R6180:Nbeal2
|
UTSW |
9 |
110625147 |
missense |
probably damaging |
1.00 |
R6191:Nbeal2
|
UTSW |
9 |
110627990 |
critical splice donor site |
probably null |
|
R6232:Nbeal2
|
UTSW |
9 |
110638734 |
missense |
probably damaging |
1.00 |
R6372:Nbeal2
|
UTSW |
9 |
110628744 |
missense |
possibly damaging |
0.69 |
R6423:Nbeal2
|
UTSW |
9 |
110625994 |
missense |
probably damaging |
1.00 |
R6543:Nbeal2
|
UTSW |
9 |
110644458 |
missense |
probably benign |
|
R6648:Nbeal2
|
UTSW |
9 |
110637642 |
missense |
probably damaging |
1.00 |
R6722:Nbeal2
|
UTSW |
9 |
110632992 |
missense |
probably damaging |
1.00 |
R6738:Nbeal2
|
UTSW |
9 |
110636905 |
missense |
possibly damaging |
0.93 |
R6916:Nbeal2
|
UTSW |
9 |
110626108 |
missense |
probably damaging |
1.00 |
R6935:Nbeal2
|
UTSW |
9 |
110639391 |
missense |
probably damaging |
1.00 |
R7022:Nbeal2
|
UTSW |
9 |
110638618 |
missense |
probably damaging |
1.00 |
R7023:Nbeal2
|
UTSW |
9 |
110638618 |
missense |
probably damaging |
1.00 |
R7050:Nbeal2
|
UTSW |
9 |
110628720 |
missense |
probably damaging |
1.00 |
R7072:Nbeal2
|
UTSW |
9 |
110626051 |
missense |
probably benign |
0.01 |
R7073:Nbeal2
|
UTSW |
9 |
110626109 |
missense |
probably damaging |
0.99 |
R7099:Nbeal2
|
UTSW |
9 |
110645438 |
splice site |
probably null |
|
R7354:Nbeal2
|
UTSW |
9 |
110629179 |
missense |
probably damaging |
1.00 |
R7394:Nbeal2
|
UTSW |
9 |
110630189 |
critical splice donor site |
probably null |
|
R7397:Nbeal2
|
UTSW |
9 |
110628032 |
missense |
possibly damaging |
0.78 |
R7552:Nbeal2
|
UTSW |
9 |
110653917 |
missense |
probably benign |
0.16 |
R7619:Nbeal2
|
UTSW |
9 |
110625818 |
missense |
probably benign |
0.19 |
R7821:Nbeal2
|
UTSW |
9 |
110630252 |
missense |
probably damaging |
1.00 |
R7902:Nbeal2
|
UTSW |
9 |
110637547 |
missense |
probably benign |
|
R7923:Nbeal2
|
UTSW |
9 |
110631446 |
nonsense |
probably null |
|
R8018:Nbeal2
|
UTSW |
9 |
110629157 |
unclassified |
probably benign |
|
R8190:Nbeal2
|
UTSW |
9 |
110626090 |
missense |
probably benign |
0.04 |
R8297:Nbeal2
|
UTSW |
9 |
110635341 |
missense |
possibly damaging |
0.89 |
R8404:Nbeal2
|
UTSW |
9 |
110634389 |
missense |
possibly damaging |
0.48 |
R8502:Nbeal2
|
UTSW |
9 |
110634389 |
missense |
possibly damaging |
0.48 |
V7583:Nbeal2
|
UTSW |
9 |
110637937 |
missense |
possibly damaging |
0.65 |
X0017:Nbeal2
|
UTSW |
9 |
110644278 |
missense |
probably benign |
0.02 |
X0065:Nbeal2
|
UTSW |
9 |
110644413 |
splice site |
probably benign |
|
Z1088:Nbeal2
|
UTSW |
9 |
110632372 |
missense |
possibly damaging |
0.51 |
Z1176:Nbeal2
|
UTSW |
9 |
110625816 |
missense |
probably benign |
0.01 |
Z1176:Nbeal2
|
UTSW |
9 |
110638835 |
missense |
probably benign |
|
Z1177:Nbeal2
|
UTSW |
9 |
110629854 |
missense |
probably benign |
0.03 |
|
Predicted Primers |
PCR Primer
(F):5'- GGTGCTTAGCTACTAAAGAGCAC -3'
(R):5'- TAGCGCCCTACGTGACAATC -3'
Sequencing Primer
(F):5'- GAGCACCCACCCTTTTTAAATAAC -3'
(R):5'- CCTACGTGACAATCTCGGTAAGTG -3'
|
Posted On | 2014-11-11 |