Incidental Mutation 'R9526:Plxna1'
ID |
719222 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Plxna1
|
Ensembl Gene |
ENSMUSG00000030084 |
Gene Name |
plexin A1 |
Synonyms |
NOV, PlexA1, Plxn1, 2600013D04Rik |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.888)
|
Stock # |
R9526 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
89293295-89339595 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 89319633 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 557
(D557E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000063066
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049845]
[ENSMUST00000163139]
|
AlphaFold |
P70206 |
PDB Structure |
The Plexin A1 intracellular region in complex with Rac1 [X-RAY DIFFRACTION]
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000049845
AA Change: D557E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000063066 Gene: ENSMUSG00000030084 AA Change: D557E
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
Sema
|
49 |
494 |
7.43e-126 |
SMART |
PSI
|
512 |
562 |
6.4e-11 |
SMART |
PSI
|
658 |
705 |
9.78e-7 |
SMART |
low complexity region
|
759 |
772 |
N/A |
INTRINSIC |
PSI
|
806 |
860 |
7.24e-10 |
SMART |
IPT
|
861 |
957 |
3.2e-26 |
SMART |
IPT
|
958 |
1043 |
1.59e-21 |
SMART |
IPT
|
1045 |
1145 |
6.86e-26 |
SMART |
IPT
|
1147 |
1242 |
1.64e-5 |
SMART |
transmembrane domain
|
1243 |
1265 |
N/A |
INTRINSIC |
Pfam:Plexin_cytopl
|
1316 |
1864 |
8.8e-263 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000163139
AA Change: D557E
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000131840 Gene: ENSMUSG00000030084 AA Change: D557E
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
Sema
|
49 |
494 |
7.43e-126 |
SMART |
PSI
|
512 |
562 |
6.4e-11 |
SMART |
PSI
|
658 |
705 |
9.78e-7 |
SMART |
low complexity region
|
759 |
772 |
N/A |
INTRINSIC |
PSI
|
806 |
860 |
7.24e-10 |
SMART |
IPT
|
861 |
957 |
3.2e-26 |
SMART |
IPT
|
958 |
1043 |
1.59e-21 |
SMART |
IPT
|
1045 |
1145 |
6.86e-26 |
SMART |
IPT
|
1147 |
1242 |
1.64e-5 |
SMART |
transmembrane domain
|
1243 |
1265 |
N/A |
INTRINSIC |
Pfam:Plexin_cytopl
|
1315 |
1864 |
2.5e-264 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000205121
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a null allele exhibit bone cellularity abnormalities, altered dendritic cell physiology, abnormal proprioceptive and oligodendrocyte morphology, and increased lymphatic branching complexity and LEC numbers. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn1 |
A |
G |
12: 80,230,393 (GRCm39) |
L287S |
probably damaging |
Het |
Adgrf1 |
A |
T |
17: 43,616,237 (GRCm39) |
Q292L |
possibly damaging |
Het |
Arhgap32 |
A |
G |
9: 32,172,026 (GRCm39) |
D1602G |
probably benign |
Het |
Atrnl1 |
C |
T |
19: 57,617,551 (GRCm39) |
P109S |
probably damaging |
Het |
Camsap1 |
G |
A |
2: 25,843,962 (GRCm39) |
H230Y |
probably benign |
Het |
Capns1 |
C |
T |
7: 29,891,612 (GRCm39) |
C144Y |
probably damaging |
Het |
Ccdc17 |
G |
A |
4: 116,455,994 (GRCm39) |
V341I |
possibly damaging |
Het |
Cd36 |
T |
C |
5: 18,002,033 (GRCm39) |
T323A |
probably damaging |
Het |
Cdc14a |
CGCTGCTGCTGCTGCTGCTG |
CGCTGCTGCTGCTGCTG |
3: 116,087,509 (GRCm39) |
|
probably benign |
Het |
Ckap2l |
G |
A |
2: 129,111,161 (GRCm39) |
Q679* |
probably null |
Het |
Clec4g |
T |
A |
8: 3,768,565 (GRCm39) |
N93I |
probably benign |
Het |
Cntnap2 |
T |
A |
6: 45,992,165 (GRCm39) |
L364Q |
probably damaging |
Het |
Cul9 |
A |
G |
17: 46,841,026 (GRCm39) |
M748T |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,150,711 (GRCm39) |
I349N |
probably damaging |
Het |
Dnajc14 |
T |
A |
10: 128,642,260 (GRCm39) |
Y61N |
probably benign |
Het |
Dock6 |
A |
T |
9: 21,713,802 (GRCm39) |
Y1909* |
probably null |
Het |
Dock8 |
T |
A |
19: 25,165,739 (GRCm39) |
D1874E |
probably benign |
Het |
Dpm1 |
A |
G |
2: 168,072,210 (GRCm39) |
S22P |
probably benign |
Het |
Dysf |
T |
C |
6: 84,128,885 (GRCm39) |
L1385P |
probably damaging |
Het |
Egf |
T |
C |
3: 129,491,421 (GRCm39) |
T859A |
probably benign |
Het |
Eif2b1 |
A |
T |
5: 124,711,867 (GRCm39) |
S162T |
probably benign |
Het |
Emilin1 |
T |
C |
5: 31,075,484 (GRCm39) |
L575P |
probably damaging |
Het |
Erp27 |
T |
A |
6: 136,886,550 (GRCm39) |
Q161L |
probably benign |
Het |
Fbxw10 |
C |
A |
11: 62,765,945 (GRCm39) |
D738E |
possibly damaging |
Het |
Fcgbp |
T |
G |
7: 27,790,937 (GRCm39) |
C733G |
probably damaging |
Het |
Fgb |
T |
A |
3: 82,957,122 (GRCm39) |
|
probably benign |
Het |
Gata3os |
A |
T |
2: 9,887,634 (GRCm39) |
T12S |
unknown |
Het |
Got1l1 |
G |
T |
8: 27,688,503 (GRCm39) |
Q283K |
probably benign |
Het |
Grk2 |
G |
A |
19: 4,340,871 (GRCm39) |
R226C |
probably damaging |
Het |
Hoxa10 |
T |
C |
6: 52,211,334 (GRCm39) |
D194G |
probably benign |
Het |
Ipcef1 |
G |
A |
10: 6,840,620 (GRCm39) |
T363I |
probably damaging |
Het |
Itga10 |
C |
A |
3: 96,564,273 (GRCm39) |
T922N |
probably damaging |
Het |
Itgad |
T |
C |
7: 127,777,552 (GRCm39) |
I144T |
probably benign |
Het |
Kat6b |
C |
A |
14: 21,567,564 (GRCm39) |
Q208K |
possibly damaging |
Het |
Kidins220 |
T |
G |
12: 25,088,383 (GRCm39) |
L1042R |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,486,355 (GRCm39) |
S4733G |
probably damaging |
Het |
Lrig3 |
A |
G |
10: 125,850,736 (GRCm39) |
I1101V |
probably benign |
Het |
Lrp1 |
T |
A |
10: 127,431,229 (GRCm39) |
N311I |
probably damaging |
Het |
Man2a1 |
A |
T |
17: 64,958,310 (GRCm39) |
K275I |
probably benign |
Het |
Map3k10 |
T |
A |
7: 27,364,434 (GRCm39) |
N318I |
probably damaging |
Het |
Map3k8 |
G |
A |
18: 4,333,869 (GRCm39) |
R408W |
probably damaging |
Het |
Mast1 |
A |
G |
8: 85,647,805 (GRCm39) |
M523T |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,873,593 (GRCm39) |
H1925R |
probably benign |
Het |
Med12l |
C |
T |
3: 58,984,207 (GRCm39) |
S461L |
probably damaging |
Het |
Mfap1a |
T |
C |
2: 121,333,237 (GRCm39) |
K65E |
probably damaging |
Het |
Mical1 |
T |
C |
10: 41,358,602 (GRCm39) |
S507P |
probably benign |
Het |
Miga2 |
T |
C |
2: 30,268,400 (GRCm39) |
V433A |
unknown |
Het |
Mpdz |
T |
C |
4: 81,274,653 (GRCm39) |
T848A |
probably benign |
Het |
Mycn |
A |
G |
12: 12,989,778 (GRCm39) |
V206A |
probably benign |
Het |
Ndst1 |
G |
A |
18: 60,838,220 (GRCm39) |
Q342* |
probably null |
Het |
Nectin1 |
A |
G |
9: 43,702,369 (GRCm39) |
M39V |
probably benign |
Het |
Nectin4 |
A |
T |
1: 171,210,209 (GRCm39) |
R234* |
probably null |
Het |
Ngb |
C |
G |
12: 87,145,317 (GRCm39) |
V113L |
possibly damaging |
Het |
Nphp3 |
T |
A |
9: 103,913,337 (GRCm39) |
Y990N |
probably damaging |
Het |
Nrdc |
T |
C |
4: 108,915,833 (GRCm39) |
|
probably null |
Het |
Or10a2 |
A |
T |
7: 106,673,739 (GRCm39) |
K235* |
probably null |
Het |
Or1e23 |
T |
A |
11: 73,407,351 (GRCm39) |
I225F |
probably damaging |
Het |
Or5p60 |
T |
A |
7: 107,723,801 (GRCm39) |
Y223F |
probably benign |
Het |
Osbpl6 |
A |
G |
2: 76,415,603 (GRCm39) |
Y655C |
probably damaging |
Het |
Pcdhgb4 |
A |
G |
18: 37,855,882 (GRCm39) |
Q759R |
probably benign |
Het |
Pcsk4 |
T |
C |
10: 80,161,800 (GRCm39) |
D164G |
probably damaging |
Het |
Pde4d |
T |
A |
13: 110,071,915 (GRCm39) |
I303N |
probably damaging |
Het |
Pdf |
T |
A |
8: 107,774,972 (GRCm39) |
M87L |
probably benign |
Het |
Pigb |
A |
G |
9: 72,941,840 (GRCm39) |
S140P |
probably damaging |
Het |
Plch1 |
T |
A |
3: 63,758,549 (GRCm39) |
|
probably benign |
Het |
Polr2e |
C |
T |
10: 79,872,792 (GRCm39) |
V149M |
probably benign |
Het |
Polr3a |
A |
T |
14: 24,503,313 (GRCm39) |
C1174S |
probably benign |
Het |
Prb1c |
T |
A |
6: 132,338,891 (GRCm39) |
N109I |
unknown |
Het |
Psmd2 |
T |
A |
16: 20,474,369 (GRCm39) |
S308R |
probably benign |
Het |
Ptger1 |
T |
A |
8: 84,396,002 (GRCm39) |
V353E |
probably damaging |
Het |
Ptprc |
A |
G |
1: 137,996,111 (GRCm39) |
M940T |
probably benign |
Het |
Pus7l |
T |
C |
15: 94,425,781 (GRCm39) |
N540S |
probably damaging |
Het |
Rap1gds1 |
T |
A |
3: 138,756,317 (GRCm39) |
I13L |
probably benign |
Het |
Rasl10b |
A |
T |
11: 83,303,590 (GRCm39) |
N49I |
probably damaging |
Het |
Rftn1 |
A |
T |
17: 50,301,237 (GRCm39) |
N537K |
probably benign |
Het |
Rnase4 |
A |
G |
14: 51,342,645 (GRCm39) |
Y123C |
probably damaging |
Het |
Rnf181 |
A |
C |
6: 72,338,302 (GRCm39) |
N26K |
probably benign |
Het |
Rnf31 |
G |
A |
14: 55,836,269 (GRCm39) |
|
probably null |
Het |
Rpusd3 |
C |
G |
6: 113,393,200 (GRCm39) |
C304S |
unknown |
Het |
Rsf1 |
CGGC |
CGGCGGCGGGGGC |
7: 97,229,139 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
C |
A |
2: 112,664,270 (GRCm39) |
V1694L |
probably benign |
Het |
Sanbr |
T |
C |
11: 23,559,098 (GRCm39) |
Y372C |
probably damaging |
Het |
Sephs2 |
T |
C |
7: 126,872,346 (GRCm39) |
D249G |
probably damaging |
Het |
Serpina10 |
A |
G |
12: 103,583,217 (GRCm39) |
I409T |
probably damaging |
Het |
Serpina5 |
C |
T |
12: 104,069,403 (GRCm39) |
A205V |
probably damaging |
Het |
Sfr1 |
T |
A |
19: 47,723,453 (GRCm39) |
V319E |
probably damaging |
Het |
Skil |
T |
A |
3: 31,171,639 (GRCm39) |
Y542N |
probably benign |
Het |
Slc15a5 |
T |
C |
6: 138,049,954 (GRCm39) |
T154A |
probably benign |
Het |
Slc27a2 |
T |
A |
2: 126,429,846 (GRCm39) |
L618Q |
probably damaging |
Het |
Slc6a6 |
A |
T |
6: 91,726,808 (GRCm39) |
Y483F |
probably benign |
Het |
Sprr1b |
T |
C |
3: 92,344,443 (GRCm39) |
I144M |
probably benign |
Het |
Stat5a |
T |
A |
11: 100,771,161 (GRCm39) |
V580E |
|
Het |
Tnk1 |
C |
T |
11: 69,746,011 (GRCm39) |
D305N |
probably damaging |
Het |
Tox2 |
A |
G |
2: 163,164,930 (GRCm39) |
*523W |
probably null |
Het |
Trav12-2 |
A |
G |
14: 53,854,085 (GRCm39) |
N20D |
probably benign |
Het |
Trav16 |
T |
A |
14: 53,981,046 (GRCm39) |
N78K |
probably damaging |
Het |
Trf |
C |
T |
9: 103,104,130 (GRCm39) |
A78T |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,711,543 (GRCm39) |
|
probably benign |
Het |
Vmn2r67 |
T |
A |
7: 84,785,834 (GRCm39) |
M724L |
probably benign |
Het |
Vmn2r94 |
A |
T |
17: 18,477,261 (GRCm39) |
F383L |
probably benign |
Het |
Vwa2 |
T |
C |
19: 56,895,208 (GRCm39) |
S461P |
probably benign |
Het |
Zfp991 |
G |
A |
4: 147,264,327 (GRCm39) |
G568E |
probably damaging |
Het |
Zfpl1 |
A |
G |
19: 6,134,440 (GRCm39) |
F15S |
probably damaging |
Het |
|
Other mutations in Plxna1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Plxna1
|
APN |
6 |
89,297,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01358:Plxna1
|
APN |
6 |
89,299,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01475:Plxna1
|
APN |
6 |
89,331,870 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01480:Plxna1
|
APN |
6 |
89,321,078 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01585:Plxna1
|
APN |
6 |
89,306,538 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01804:Plxna1
|
APN |
6 |
89,306,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01909:Plxna1
|
APN |
6 |
89,309,066 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01989:Plxna1
|
APN |
6 |
89,306,396 (GRCm39) |
nonsense |
probably null |
|
IGL02015:Plxna1
|
APN |
6 |
89,319,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Plxna1
|
APN |
6 |
89,334,314 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02668:Plxna1
|
APN |
6 |
89,334,251 (GRCm39) |
nonsense |
probably null |
|
IGL02703:Plxna1
|
APN |
6 |
89,333,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02954:Plxna1
|
APN |
6 |
89,301,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03212:Plxna1
|
APN |
6 |
89,308,885 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4544001:Plxna1
|
UTSW |
6 |
89,334,411 (GRCm39) |
missense |
probably benign |
0.14 |
R0055:Plxna1
|
UTSW |
6 |
89,306,721 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0055:Plxna1
|
UTSW |
6 |
89,306,721 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0147:Plxna1
|
UTSW |
6 |
89,297,692 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0149:Plxna1
|
UTSW |
6 |
89,297,595 (GRCm39) |
missense |
probably null |
0.95 |
R0166:Plxna1
|
UTSW |
6 |
89,310,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Plxna1
|
UTSW |
6 |
89,300,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R0415:Plxna1
|
UTSW |
6 |
89,334,318 (GRCm39) |
missense |
probably benign |
0.12 |
R0841:Plxna1
|
UTSW |
6 |
89,309,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Plxna1
|
UTSW |
6 |
89,319,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Plxna1
|
UTSW |
6 |
89,298,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R1355:Plxna1
|
UTSW |
6 |
89,297,748 (GRCm39) |
unclassified |
probably benign |
|
R1700:Plxna1
|
UTSW |
6 |
89,333,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R1776:Plxna1
|
UTSW |
6 |
89,312,446 (GRCm39) |
missense |
probably benign |
0.00 |
R1957:Plxna1
|
UTSW |
6 |
89,308,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R2314:Plxna1
|
UTSW |
6 |
89,301,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R2968:Plxna1
|
UTSW |
6 |
89,319,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R3118:Plxna1
|
UTSW |
6 |
89,333,958 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3522:Plxna1
|
UTSW |
6 |
89,314,335 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3619:Plxna1
|
UTSW |
6 |
89,334,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R3766:Plxna1
|
UTSW |
6 |
89,311,757 (GRCm39) |
unclassified |
probably benign |
|
R3847:Plxna1
|
UTSW |
6 |
89,333,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3849:Plxna1
|
UTSW |
6 |
89,333,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3872:Plxna1
|
UTSW |
6 |
89,309,674 (GRCm39) |
nonsense |
probably null |
|
R4555:Plxna1
|
UTSW |
6 |
89,300,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R4709:Plxna1
|
UTSW |
6 |
89,311,733 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4726:Plxna1
|
UTSW |
6 |
89,299,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Plxna1
|
UTSW |
6 |
89,309,657 (GRCm39) |
splice site |
probably null |
|
R5053:Plxna1
|
UTSW |
6 |
89,299,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5221:Plxna1
|
UTSW |
6 |
89,297,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5449:Plxna1
|
UTSW |
6 |
89,300,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Plxna1
|
UTSW |
6 |
89,301,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5575:Plxna1
|
UTSW |
6 |
89,301,523 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5743:Plxna1
|
UTSW |
6 |
89,333,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Plxna1
|
UTSW |
6 |
89,311,664 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5754:Plxna1
|
UTSW |
6 |
89,310,087 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5868:Plxna1
|
UTSW |
6 |
89,299,704 (GRCm39) |
splice site |
probably benign |
|
R5988:Plxna1
|
UTSW |
6 |
89,334,522 (GRCm39) |
nonsense |
probably null |
|
R6190:Plxna1
|
UTSW |
6 |
89,333,586 (GRCm39) |
nonsense |
probably null |
|
R6425:Plxna1
|
UTSW |
6 |
89,311,647 (GRCm39) |
missense |
probably benign |
0.00 |
R6561:Plxna1
|
UTSW |
6 |
89,333,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R6623:Plxna1
|
UTSW |
6 |
89,299,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R6638:Plxna1
|
UTSW |
6 |
89,301,382 (GRCm39) |
missense |
probably damaging |
0.97 |
R6701:Plxna1
|
UTSW |
6 |
89,296,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R6825:Plxna1
|
UTSW |
6 |
89,297,597 (GRCm39) |
missense |
probably benign |
0.01 |
R6911:Plxna1
|
UTSW |
6 |
89,297,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R7073:Plxna1
|
UTSW |
6 |
89,334,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R7177:Plxna1
|
UTSW |
6 |
89,300,311 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7235:Plxna1
|
UTSW |
6 |
89,317,573 (GRCm39) |
missense |
probably damaging |
0.97 |
R7419:Plxna1
|
UTSW |
6 |
89,334,584 (GRCm39) |
missense |
unknown |
|
R7511:Plxna1
|
UTSW |
6 |
89,318,889 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7543:Plxna1
|
UTSW |
6 |
89,299,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R7665:Plxna1
|
UTSW |
6 |
89,301,520 (GRCm39) |
critical splice donor site |
probably null |
|
R7678:Plxna1
|
UTSW |
6 |
89,308,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R7748:Plxna1
|
UTSW |
6 |
89,314,335 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7748:Plxna1
|
UTSW |
6 |
89,314,334 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7877:Plxna1
|
UTSW |
6 |
89,300,241 (GRCm39) |
missense |
probably damaging |
0.99 |
R8025:Plxna1
|
UTSW |
6 |
89,308,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Plxna1
|
UTSW |
6 |
89,334,102 (GRCm39) |
missense |
probably benign |
0.20 |
R8277:Plxna1
|
UTSW |
6 |
89,334,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Plxna1
|
UTSW |
6 |
89,300,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Plxna1
|
UTSW |
6 |
89,310,079 (GRCm39) |
missense |
probably benign |
0.00 |
R9245:Plxna1
|
UTSW |
6 |
89,314,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R9253:Plxna1
|
UTSW |
6 |
89,334,522 (GRCm39) |
nonsense |
probably null |
|
R9269:Plxna1
|
UTSW |
6 |
89,306,541 (GRCm39) |
missense |
probably null |
1.00 |
R9273:Plxna1
|
UTSW |
6 |
89,296,364 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9281:Plxna1
|
UTSW |
6 |
89,300,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R9368:Plxna1
|
UTSW |
6 |
89,314,138 (GRCm39) |
missense |
probably benign |
|
R9440:Plxna1
|
UTSW |
6 |
89,318,912 (GRCm39) |
missense |
probably benign |
0.00 |
R9601:Plxna1
|
UTSW |
6 |
89,308,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R9714:Plxna1
|
UTSW |
6 |
89,296,440 (GRCm39) |
missense |
probably damaging |
0.99 |
R9782:Plxna1
|
UTSW |
6 |
89,333,817 (GRCm39) |
missense |
probably benign |
0.01 |
S24628:Plxna1
|
UTSW |
6 |
89,334,318 (GRCm39) |
missense |
probably benign |
0.12 |
V8831:Plxna1
|
UTSW |
6 |
89,334,119 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Plxna1
|
UTSW |
6 |
89,298,034 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGAGAGGTCAGGCACATTCC -3'
(R):5'- CTCATTTGACCCCACTGACAAG -3'
Sequencing Primer
(F):5'- GGCACATTCCAAGCCTGCAG -3'
(R):5'- CTGACAAGTGATGGGAGTGTTAAC -3'
|
Posted On |
2022-07-18 |