Incidental Mutation 'R8171:Plxna1'
ID |
634105 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Plxna1
|
Ensembl Gene |
ENSMUSG00000030084 |
Gene Name |
plexin A1 |
Synonyms |
NOV, PlexA1, Plxn1, 2600013D04Rik |
MMRRC Submission |
067597-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.888)
|
Stock # |
R8171 (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 A
at 89334102 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Serine
at position 176
(P176S)
|
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: P176S
PolyPhen 2
Score 0.198 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000063066 Gene: ENSMUSG00000030084 AA Change: P176S
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: P176S
PolyPhen 2
Score 0.198 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000131840 Gene: ENSMUSG00000030084 AA Change: P176S
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 97.9%
|
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: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
G |
T |
14: 32,383,982 (GRCm39) |
A661E |
probably benign |
Het |
Abhd14a |
T |
A |
9: 106,317,960 (GRCm39) |
T142S |
probably benign |
Het |
Actn1 |
A |
G |
12: 80,243,167 (GRCm39) |
|
probably null |
Het |
Adss2 |
T |
C |
1: 177,623,917 (GRCm39) |
N15S |
probably benign |
Het |
Alpk2 |
A |
G |
18: 65,439,054 (GRCm39) |
S780P |
probably benign |
Het |
Asap1 |
G |
T |
15: 63,982,815 (GRCm39) |
L830M |
probably damaging |
Het |
Atic |
T |
C |
1: 71,609,032 (GRCm39) |
V319A |
possibly damaging |
Het |
Atp8a2 |
A |
T |
14: 60,283,493 (GRCm39) |
I87N |
probably damaging |
Het |
Bace2 |
G |
T |
16: 97,225,786 (GRCm39) |
V407L |
possibly damaging |
Het |
Bltp1 |
T |
C |
3: 37,029,862 (GRCm39) |
V2423A |
probably benign |
Het |
Bmp3 |
A |
T |
5: 99,020,528 (GRCm39) |
Y317F |
probably damaging |
Het |
Ccdc159 |
A |
G |
9: 21,845,007 (GRCm39) |
E291G |
possibly damaging |
Het |
Cct8l1 |
T |
A |
5: 25,721,552 (GRCm39) |
L89Q |
probably damaging |
Het |
Cep83 |
T |
A |
10: 94,604,797 (GRCm39) |
N503K |
possibly damaging |
Het |
Ces4a |
A |
G |
8: 105,873,839 (GRCm39) |
Y436C |
probably damaging |
Het |
Cftr |
T |
A |
6: 18,258,287 (GRCm39) |
D579E |
probably damaging |
Het |
Chd9 |
T |
A |
8: 91,752,015 (GRCm39) |
V1751D |
possibly damaging |
Het |
Clasp2 |
A |
T |
9: 113,732,974 (GRCm39) |
T937S |
possibly damaging |
Het |
Clock |
T |
A |
5: 76,414,261 (GRCm39) |
D17V |
possibly damaging |
Het |
Cpm |
T |
C |
10: 117,519,220 (GRCm39) |
L376P |
probably damaging |
Het |
Crocc2 |
T |
C |
1: 93,116,723 (GRCm39) |
|
probably null |
Het |
Csnk1g2 |
A |
G |
10: 80,475,636 (GRCm39) |
D401G |
probably damaging |
Het |
Cyb5r4 |
C |
T |
9: 86,924,863 (GRCm39) |
L206F |
possibly damaging |
Het |
Cyp1a1 |
T |
A |
9: 57,607,479 (GRCm39) |
W36R |
probably benign |
Het |
Cyp3a59 |
A |
T |
5: 146,022,584 (GRCm39) |
H30L |
probably damaging |
Het |
Dab2 |
G |
A |
15: 6,453,407 (GRCm39) |
V182I |
probably benign |
Het |
Dnah1 |
G |
T |
14: 31,019,067 (GRCm39) |
F1342L |
probably damaging |
Het |
Draxin |
A |
T |
4: 148,200,123 (GRCm39) |
L109Q |
possibly damaging |
Het |
Elfn1 |
G |
A |
5: 139,957,112 (GRCm39) |
V39M |
probably damaging |
Het |
Erlin1 |
A |
G |
19: 44,057,768 (GRCm39) |
I19T |
probably benign |
Het |
F830016B08Rik |
T |
A |
18: 60,433,150 (GRCm39) |
S78T |
possibly damaging |
Het |
Fer1l4 |
A |
G |
2: 155,890,151 (GRCm39) |
V258A |
probably benign |
Het |
Fgb |
T |
C |
3: 82,949,822 (GRCm39) |
D445G |
probably damaging |
Het |
Fgd6 |
T |
C |
10: 93,910,194 (GRCm39) |
|
probably null |
Het |
Frem3 |
T |
A |
8: 81,341,869 (GRCm39) |
D1387E |
probably damaging |
Het |
Gdf3 |
T |
C |
6: 122,586,862 (GRCm39) |
T22A |
probably benign |
Het |
Glcci1 |
C |
T |
6: 8,593,167 (GRCm39) |
A511V |
probably benign |
Het |
Gldc |
A |
T |
19: 30,111,161 (GRCm39) |
N538K |
probably benign |
Het |
Glipr1l1 |
C |
T |
10: 111,914,289 (GRCm39) |
P217S |
probably benign |
Het |
Gpr161 |
A |
G |
1: 165,134,005 (GRCm39) |
N89S |
probably damaging |
Het |
Gypa |
T |
A |
8: 81,236,092 (GRCm39) |
S166T |
probably benign |
Het |
Hcar1 |
A |
G |
5: 124,017,152 (GRCm39) |
S180P |
probably damaging |
Het |
Hcn1 |
T |
C |
13: 117,739,270 (GRCm39) |
S11P |
unknown |
Het |
Hectd4 |
A |
G |
5: 121,456,819 (GRCm39) |
E728G |
possibly damaging |
Het |
Ints14 |
A |
T |
9: 64,880,532 (GRCm39) |
H213L |
possibly damaging |
Het |
Itih1 |
A |
T |
14: 30,659,047 (GRCm39) |
M323K |
possibly damaging |
Het |
Ivl |
A |
G |
3: 92,479,085 (GRCm39) |
S327P |
probably damaging |
Het |
Kcnt2 |
T |
A |
1: 140,437,203 (GRCm39) |
N545K |
probably benign |
Het |
Kdm4b |
A |
T |
17: 56,696,534 (GRCm39) |
R417W |
probably damaging |
Het |
Kif13a |
T |
C |
13: 46,932,444 (GRCm39) |
E1083G |
probably damaging |
Het |
Klhl40 |
A |
T |
9: 121,607,623 (GRCm39) |
H261L |
probably benign |
Het |
Kpnb1 |
A |
G |
11: 97,066,573 (GRCm39) |
|
probably null |
Het |
Lamc3 |
C |
A |
2: 31,804,983 (GRCm39) |
T621N |
probably benign |
Het |
Lingo3 |
T |
C |
10: 80,670,595 (GRCm39) |
H445R |
probably benign |
Het |
Ly75 |
G |
A |
2: 60,144,572 (GRCm39) |
T1297I |
possibly damaging |
Het |
Lypd6 |
C |
T |
2: 50,080,759 (GRCm39) |
T149M |
possibly damaging |
Het |
Mcrs1 |
A |
T |
15: 99,146,613 (GRCm39) |
D139E |
probably damaging |
Het |
Muc5b |
G |
A |
7: 141,414,737 (GRCm39) |
S2561N |
unknown |
Het |
Mybpc1 |
C |
T |
10: 88,358,865 (GRCm39) |
G1095R |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,093,398 (GRCm39) |
Y163C |
probably damaging |
Het |
Notch4 |
T |
A |
17: 34,801,483 (GRCm39) |
C1110* |
probably null |
Het |
Nt5el |
T |
A |
13: 105,246,291 (GRCm39) |
V284E |
probably benign |
Het |
Or12j2 |
A |
T |
7: 139,916,143 (GRCm39) |
I123F |
probably damaging |
Het |
Or2ag1 |
C |
T |
7: 106,313,825 (GRCm39) |
S21N |
probably benign |
Het |
Or2ag1 |
T |
A |
7: 106,313,826 (GRCm39) |
S21C |
|
Het |
Or4c10b |
A |
G |
2: 89,711,409 (GRCm39) |
I80V |
probably benign |
Het |
Pcsk1 |
T |
A |
13: 75,238,210 (GRCm39) |
C10* |
probably null |
Het |
Pdlim5 |
A |
T |
3: 142,017,948 (GRCm39) |
S107T |
probably benign |
Het |
Plac8l1 |
T |
A |
18: 42,313,445 (GRCm39) |
D99V |
probably damaging |
Het |
Plin2 |
A |
T |
4: 86,575,349 (GRCm39) |
V400E |
probably damaging |
Het |
Pnn |
A |
G |
12: 59,117,223 (GRCm39) |
K238R |
probably damaging |
Het |
Pou5f1 |
A |
G |
17: 35,820,933 (GRCm39) |
E231G |
probably benign |
Het |
Ppara |
A |
T |
15: 85,682,077 (GRCm39) |
M258L |
probably benign |
Het |
Prune2 |
G |
A |
19: 17,097,882 (GRCm39) |
D1129N |
probably damaging |
Het |
Rai14 |
G |
A |
15: 10,633,249 (GRCm39) |
T47M |
probably damaging |
Het |
Rdh5 |
T |
C |
10: 128,753,969 (GRCm39) |
I117V |
probably benign |
Het |
Rpain |
G |
A |
11: 70,864,724 (GRCm39) |
C137Y |
probably damaging |
Het |
Scn3a |
A |
G |
2: 65,361,154 (GRCm39) |
V126A |
possibly damaging |
Het |
Senp7 |
G |
T |
16: 55,932,089 (GRCm39) |
L129F |
probably damaging |
Het |
Setd1a |
A |
G |
7: 127,390,399 (GRCm39) |
D1025G |
unknown |
Het |
Sirt4 |
A |
T |
5: 115,621,082 (GRCm39) |
V30E |
probably damaging |
Het |
Slit1 |
C |
A |
19: 41,715,512 (GRCm39) |
R113L |
probably damaging |
Het |
Stxbp5l |
G |
A |
16: 37,028,416 (GRCm39) |
T549I |
noncoding transcript |
Het |
Sytl2 |
A |
G |
7: 90,058,678 (GRCm39) |
M926V |
probably damaging |
Het |
Tgfbr2 |
C |
T |
9: 115,959,074 (GRCm39) |
W113* |
probably null |
Het |
Tmem86a |
A |
G |
7: 46,703,512 (GRCm39) |
Y213C |
probably damaging |
Het |
Tpo |
T |
A |
12: 30,154,045 (GRCm39) |
Y220F |
probably damaging |
Het |
Ttc6 |
C |
A |
12: 57,720,096 (GRCm39) |
A889E |
probably damaging |
Het |
Tyw1 |
A |
G |
5: 130,328,855 (GRCm39) |
D547G |
probably benign |
Het |
Ubtfl1 |
A |
G |
9: 18,320,523 (GRCm39) |
K17R |
probably benign |
Het |
Usp46 |
T |
A |
5: 74,163,354 (GRCm39) |
I331F |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,792,073 (GRCm39) |
H61R |
probably benign |
Het |
Wdr75 |
T |
A |
1: 45,861,706 (GRCm39) |
N715K |
probably benign |
Het |
Wdr97 |
C |
A |
15: 76,247,819 (GRCm39) |
F1614L |
|
Het |
Zfp772 |
A |
T |
7: 7,207,096 (GRCm39) |
C198* |
probably null |
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 |
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 |
R9526:Plxna1
|
UTSW |
6 |
89,319,633 (GRCm39) |
missense |
probably benign |
|
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'- TGCGGAAACTGTACACATAGTAG -3'
(R):5'- TACTGCTGGACTATGCAGCC -3'
Sequencing Primer
(F):5'- CTGTACACATAGTAGATGTCAAAGGC -3'
(R):5'- TGGACTATGCAGCCAACCG -3'
|
Posted On |
2020-07-13 |