Incidental Mutation 'R1386:Plxnb1'
ID |
160605 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Plxnb1
|
Ensembl Gene |
ENSMUSG00000053646 |
Gene Name |
plexin B1 |
Synonyms |
2900002G15Rik |
MMRRC Submission |
039448-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1386 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
108924457-108948985 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 108930091 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Proline
at position 316
(S316P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000071966
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072093]
[ENSMUST00000130366]
[ENSMUST00000131462]
|
AlphaFold |
Q8CJH3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000072093
AA Change: S316P
PolyPhen 2
Score 0.272 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000071966 Gene: ENSMUSG00000053646 AA Change: S316P
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
Sema
|
35 |
463 |
5.84e-101 |
SMART |
PSI
|
481 |
534 |
1.17e-13 |
SMART |
PSI
|
628 |
678 |
6.97e-3 |
SMART |
low complexity region
|
691 |
706 |
N/A |
INTRINSIC |
low complexity region
|
752 |
771 |
N/A |
INTRINSIC |
PSI
|
1019 |
1066 |
2.06e-5 |
SMART |
IPT
|
1067 |
1158 |
7.48e-18 |
SMART |
IPT
|
1159 |
1247 |
3.97e-22 |
SMART |
IPT
|
1249 |
1359 |
6.09e-9 |
SMART |
low complexity region
|
1483 |
1494 |
N/A |
INTRINSIC |
Pfam:Plexin_cytopl
|
1546 |
2086 |
6.5e-230 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000130366
|
SMART Domains |
Protein: ENSMUSP00000114358 Gene: ENSMUSG00000053646
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
Pfam:Sema
|
35 |
138 |
7.5e-11 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000131462
|
SMART Domains |
Protein: ENSMUSP00000115265 Gene: ENSMUSG00000053646
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
Pfam:Sema
|
35 |
138 |
7.5e-11 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134690
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192117
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000192988
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000195364
|
Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.8%
- 10x: 94.5%
- 20x: 87.0%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Homozygous null mutants are viable and fertile and show no apparent defects in development, adult histology or basic functional parameters. However, a transitory renal phenotype, characterized by increased ureteric branching and enlarged kidneys, is noted over early stages of renal development. [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 |
Abca6 |
T |
C |
11: 110,135,081 (GRCm39) |
I235V |
probably benign |
Het |
Acsm4 |
T |
C |
7: 119,297,801 (GRCm39) |
I146T |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,676,984 (GRCm39) |
N1949S |
probably benign |
Het |
Afdn |
T |
C |
17: 14,066,798 (GRCm39) |
V630A |
probably damaging |
Het |
Amfr |
A |
G |
8: 94,712,027 (GRCm39) |
V301A |
possibly damaging |
Het |
Anapc16 |
T |
C |
10: 59,832,279 (GRCm39) |
M45V |
probably benign |
Het |
Ankrd12 |
T |
C |
17: 66,290,375 (GRCm39) |
E1686G |
possibly damaging |
Het |
Ap2m1 |
T |
G |
16: 20,359,979 (GRCm39) |
H193Q |
probably damaging |
Het |
Aplnr |
T |
C |
2: 84,967,805 (GRCm39) |
W277R |
possibly damaging |
Het |
Aspm |
C |
T |
1: 139,406,710 (GRCm39) |
H1866Y |
possibly damaging |
Het |
Aspm |
A |
G |
1: 139,385,361 (GRCm39) |
E335G |
probably benign |
Het |
Atp8b4 |
T |
A |
2: 126,220,664 (GRCm39) |
D578V |
probably benign |
Het |
Ccr1 |
T |
A |
9: 123,763,999 (GRCm39) |
E177V |
probably benign |
Het |
Cecr2 |
A |
G |
6: 120,739,092 (GRCm39) |
E1245G |
probably damaging |
Het |
Cep162 |
A |
T |
9: 87,103,255 (GRCm39) |
C638S |
probably benign |
Het |
Ces1b |
A |
T |
8: 93,794,705 (GRCm39) |
I298N |
probably benign |
Het |
Cfap47 |
C |
T |
X: 78,553,507 (GRCm39) |
V323I |
possibly damaging |
Het |
Chdh |
T |
A |
14: 29,753,391 (GRCm39) |
L100Q |
probably damaging |
Het |
Chrnd |
T |
C |
1: 87,120,312 (GRCm39) |
I156T |
probably damaging |
Het |
Clpx |
G |
A |
9: 65,234,170 (GRCm39) |
R605Q |
probably null |
Het |
Cnga1 |
T |
A |
5: 72,769,526 (GRCm39) |
K135* |
probably null |
Het |
Col6a4 |
A |
T |
9: 105,940,144 (GRCm39) |
V1262E |
probably benign |
Het |
Cracr2b |
T |
C |
7: 141,043,481 (GRCm39) |
L53P |
probably damaging |
Het |
Crhr1 |
T |
C |
11: 104,065,220 (GRCm39) |
S372P |
possibly damaging |
Het |
Cyp11b2 |
T |
A |
15: 74,723,624 (GRCm39) |
|
probably null |
Het |
Cyp21a1 |
T |
A |
17: 35,021,184 (GRCm39) |
D373V |
probably damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Ddah1 |
A |
T |
3: 145,594,966 (GRCm39) |
Y242F |
probably benign |
Het |
Dlgap3 |
A |
G |
4: 127,088,719 (GRCm39) |
D105G |
possibly damaging |
Het |
Dtl |
A |
G |
1: 191,301,829 (GRCm39) |
V76A |
probably damaging |
Het |
Dzank1 |
A |
G |
2: 144,333,751 (GRCm39) |
S361P |
probably benign |
Het |
Ehd3 |
T |
A |
17: 74,127,538 (GRCm39) |
I157N |
probably damaging |
Het |
Elk4 |
T |
C |
1: 131,945,568 (GRCm39) |
F149L |
probably damaging |
Het |
Eme2 |
G |
A |
17: 25,111,892 (GRCm39) |
S263F |
probably damaging |
Het |
Fam83a |
A |
G |
15: 57,849,899 (GRCm39) |
R148G |
probably damaging |
Het |
Farp2 |
C |
A |
1: 93,547,873 (GRCm39) |
|
probably null |
Het |
Fbxw25 |
T |
A |
9: 109,483,709 (GRCm39) |
I168F |
possibly damaging |
Het |
Fermt1 |
T |
C |
2: 132,757,978 (GRCm39) |
D479G |
probably damaging |
Het |
Fgf17 |
C |
A |
14: 70,874,210 (GRCm39) |
R193L |
probably damaging |
Het |
Foxred2 |
T |
G |
15: 77,832,721 (GRCm39) |
|
probably null |
Het |
Gad1 |
T |
C |
2: 70,404,467 (GRCm39) |
V119A |
possibly damaging |
Het |
Gas2l3 |
A |
G |
10: 89,250,215 (GRCm39) |
V301A |
possibly damaging |
Het |
Gimap8 |
G |
A |
6: 48,633,587 (GRCm39) |
V469I |
probably benign |
Het |
Gja1 |
A |
T |
10: 56,264,065 (GRCm39) |
E141D |
probably benign |
Het |
Glod4 |
C |
T |
11: 76,112,829 (GRCm39) |
W268* |
probably null |
Het |
Guf1 |
C |
T |
5: 69,720,505 (GRCm39) |
H309Y |
probably benign |
Het |
Hax1 |
A |
G |
3: 89,903,156 (GRCm39) |
V215A |
probably damaging |
Het |
Heatr9 |
T |
C |
11: 83,409,651 (GRCm39) |
D107G |
probably benign |
Het |
Hephl1 |
T |
A |
9: 14,988,050 (GRCm39) |
Y686F |
probably benign |
Het |
Hk3 |
T |
C |
13: 55,154,843 (GRCm39) |
|
probably null |
Het |
Ikbkb |
G |
T |
8: 23,155,633 (GRCm39) |
Q620K |
possibly damaging |
Het |
Il18rap |
C |
T |
1: 40,570,682 (GRCm39) |
A208V |
probably benign |
Het |
Kif26b |
T |
C |
1: 178,743,209 (GRCm39) |
S1102P |
probably benign |
Het |
Kif5b |
A |
T |
18: 6,226,383 (GRCm39) |
D147E |
probably damaging |
Het |
Klhl3 |
T |
C |
13: 58,178,247 (GRCm39) |
T348A |
probably damaging |
Het |
Krt10 |
T |
C |
11: 99,276,746 (GRCm39) |
|
probably benign |
Het |
Lama3 |
A |
T |
18: 12,610,427 (GRCm39) |
H1124L |
probably benign |
Het |
Lin7a |
A |
T |
10: 107,247,983 (GRCm39) |
Q96L |
unknown |
Het |
Ly6c2 |
T |
G |
15: 74,982,438 (GRCm39) |
I37L |
probably benign |
Het |
Mov10l1 |
A |
G |
15: 88,895,589 (GRCm39) |
Y585C |
possibly damaging |
Het |
Msr1 |
G |
A |
8: 40,042,334 (GRCm39) |
Q414* |
probably null |
Het |
Myh13 |
T |
C |
11: 67,261,776 (GRCm39) |
C1900R |
possibly damaging |
Het |
Obscn |
T |
A |
11: 59,024,679 (GRCm39) |
N454Y |
probably damaging |
Het |
Olfml2b |
T |
G |
1: 170,508,731 (GRCm39) |
Y530D |
probably damaging |
Het |
Or1ad1 |
T |
C |
11: 50,876,194 (GRCm39) |
F222S |
probably damaging |
Het |
Or4c11 |
T |
A |
2: 88,695,697 (GRCm39) |
F249L |
probably benign |
Het |
Or52s1b |
T |
A |
7: 102,822,574 (GRCm39) |
H90L |
probably benign |
Het |
Or5b24 |
A |
T |
19: 12,912,503 (GRCm39) |
T134S |
probably benign |
Het |
Or7e174 |
T |
A |
9: 20,012,878 (GRCm39) |
N274K |
probably benign |
Het |
Or8j3b |
A |
G |
2: 86,205,265 (GRCm39) |
F164L |
probably damaging |
Het |
Pde10a |
T |
G |
17: 9,172,574 (GRCm39) |
V648G |
probably damaging |
Het |
Pde7b |
T |
A |
10: 20,294,547 (GRCm39) |
H258L |
probably damaging |
Het |
Pik3cb |
A |
G |
9: 98,946,080 (GRCm39) |
V582A |
possibly damaging |
Het |
Pmpca |
C |
T |
2: 26,282,530 (GRCm39) |
T246I |
probably damaging |
Het |
Reep3 |
A |
T |
10: 66,898,788 (GRCm39) |
V32D |
possibly damaging |
Het |
Rfx4 |
A |
G |
10: 84,699,149 (GRCm39) |
M252V |
probably damaging |
Het |
Rnf168 |
C |
A |
16: 32,117,781 (GRCm39) |
D447E |
probably damaging |
Het |
Rnf31 |
T |
C |
14: 55,834,221 (GRCm39) |
V518A |
probably damaging |
Het |
Rnpc3 |
A |
T |
3: 113,407,433 (GRCm39) |
L340* |
probably null |
Het |
Scn2a |
A |
G |
2: 65,519,085 (GRCm39) |
E437G |
probably damaging |
Het |
Scnn1b |
C |
A |
7: 121,501,711 (GRCm39) |
N175K |
possibly damaging |
Het |
Slc39a11 |
T |
A |
11: 113,138,550 (GRCm39) |
I344F |
probably benign |
Het |
Slc9a2 |
T |
A |
1: 40,758,178 (GRCm39) |
L239Q |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,262,978 (GRCm39) |
F794L |
probably damaging |
Het |
Smim13 |
C |
T |
13: 41,426,168 (GRCm39) |
S68L |
possibly damaging |
Het |
Sos2 |
A |
T |
12: 69,661,432 (GRCm39) |
Y680N |
probably damaging |
Het |
Spag6 |
T |
A |
2: 18,739,057 (GRCm39) |
M329K |
possibly damaging |
Het |
Spire2 |
G |
A |
8: 124,088,105 (GRCm39) |
|
probably null |
Het |
Tdrd9 |
T |
A |
12: 112,011,238 (GRCm39) |
V1149D |
probably benign |
Het |
Tns3 |
T |
A |
11: 8,468,261 (GRCm39) |
Y321F |
probably benign |
Het |
Top3b |
T |
C |
16: 16,698,493 (GRCm39) |
V112A |
probably benign |
Het |
Trafd1 |
G |
A |
5: 121,517,715 (GRCm39) |
T26I |
probably damaging |
Het |
Ttc28 |
G |
A |
5: 111,373,543 (GRCm39) |
S962N |
probably damaging |
Het |
Vmn2r78 |
T |
C |
7: 86,564,615 (GRCm39) |
L20S |
unknown |
Het |
Vmn2r82 |
A |
T |
10: 79,214,545 (GRCm39) |
D176V |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,923,458 (GRCm39) |
F3778L |
probably damaging |
Het |
Vwa3b |
T |
C |
1: 37,090,962 (GRCm39) |
|
probably null |
Het |
Vwc2 |
C |
T |
11: 11,104,262 (GRCm39) |
P265S |
probably damaging |
Het |
Zbtb9 |
T |
A |
17: 27,193,612 (GRCm39) |
I339N |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,740,161 (GRCm39) |
T764A |
probably benign |
Het |
Zfp366 |
T |
A |
13: 99,383,063 (GRCm39) |
V742D |
probably damaging |
Het |
Zfp709 |
A |
T |
8: 72,644,506 (GRCm39) |
Y645F |
probably damaging |
Het |
Zmym2 |
T |
A |
14: 57,150,548 (GRCm39) |
C424S |
probably damaging |
Het |
|
Other mutations in Plxnb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00593:Plxnb1
|
APN |
9 |
108,942,936 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01014:Plxnb1
|
APN |
9 |
108,935,102 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01142:Plxnb1
|
APN |
9 |
108,931,765 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01454:Plxnb1
|
APN |
9 |
108,942,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01469:Plxnb1
|
APN |
9 |
108,934,483 (GRCm39) |
intron |
probably benign |
|
IGL01530:Plxnb1
|
APN |
9 |
108,939,473 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01599:Plxnb1
|
APN |
9 |
108,939,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01968:Plxnb1
|
APN |
9 |
108,930,052 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02175:Plxnb1
|
APN |
9 |
108,929,914 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02216:Plxnb1
|
APN |
9 |
108,929,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02277:Plxnb1
|
APN |
9 |
108,941,201 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02311:Plxnb1
|
APN |
9 |
108,930,190 (GRCm39) |
missense |
probably benign |
|
IGL02645:Plxnb1
|
APN |
9 |
108,943,311 (GRCm39) |
splice site |
probably benign |
|
IGL03076:Plxnb1
|
APN |
9 |
108,935,970 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03107:Plxnb1
|
APN |
9 |
108,934,054 (GRCm39) |
missense |
probably benign |
|
IGL03343:Plxnb1
|
APN |
9 |
108,943,780 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:Plxnb1
|
UTSW |
9 |
108,929,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Plxnb1
|
UTSW |
9 |
108,934,286 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0211:Plxnb1
|
UTSW |
9 |
108,932,731 (GRCm39) |
nonsense |
probably null |
|
R0211:Plxnb1
|
UTSW |
9 |
108,932,731 (GRCm39) |
nonsense |
probably null |
|
R0843:Plxnb1
|
UTSW |
9 |
108,942,769 (GRCm39) |
missense |
probably benign |
0.20 |
R0970:Plxnb1
|
UTSW |
9 |
108,932,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Plxnb1
|
UTSW |
9 |
108,931,210 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1342:Plxnb1
|
UTSW |
9 |
108,929,720 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1419:Plxnb1
|
UTSW |
9 |
108,943,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Plxnb1
|
UTSW |
9 |
108,937,989 (GRCm39) |
missense |
probably null |
|
R1548:Plxnb1
|
UTSW |
9 |
108,929,968 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1621:Plxnb1
|
UTSW |
9 |
108,935,873 (GRCm39) |
missense |
probably benign |
0.04 |
R1658:Plxnb1
|
UTSW |
9 |
108,931,939 (GRCm39) |
nonsense |
probably null |
|
R1727:Plxnb1
|
UTSW |
9 |
108,930,125 (GRCm39) |
splice site |
probably null |
|
R1750:Plxnb1
|
UTSW |
9 |
108,940,836 (GRCm39) |
missense |
probably benign |
0.00 |
R1795:Plxnb1
|
UTSW |
9 |
108,929,813 (GRCm39) |
missense |
probably benign |
|
R1929:Plxnb1
|
UTSW |
9 |
108,931,776 (GRCm39) |
splice site |
probably null |
|
R1935:Plxnb1
|
UTSW |
9 |
108,924,715 (GRCm39) |
critical splice donor site |
probably null |
|
R1936:Plxnb1
|
UTSW |
9 |
108,924,715 (GRCm39) |
critical splice donor site |
probably null |
|
R2014:Plxnb1
|
UTSW |
9 |
108,935,687 (GRCm39) |
splice site |
probably benign |
|
R2057:Plxnb1
|
UTSW |
9 |
108,938,294 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2102:Plxnb1
|
UTSW |
9 |
108,944,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Plxnb1
|
UTSW |
9 |
108,931,776 (GRCm39) |
splice site |
probably null |
|
R2422:Plxnb1
|
UTSW |
9 |
108,937,506 (GRCm39) |
missense |
probably benign |
0.02 |
R2881:Plxnb1
|
UTSW |
9 |
108,943,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R3409:Plxnb1
|
UTSW |
9 |
108,935,681 (GRCm39) |
splice site |
probably null |
|
R3417:Plxnb1
|
UTSW |
9 |
108,929,828 (GRCm39) |
missense |
probably damaging |
0.97 |
R3756:Plxnb1
|
UTSW |
9 |
108,942,526 (GRCm39) |
unclassified |
probably benign |
|
R3788:Plxnb1
|
UTSW |
9 |
108,938,355 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3789:Plxnb1
|
UTSW |
9 |
108,938,355 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4042:Plxnb1
|
UTSW |
9 |
108,934,241 (GRCm39) |
missense |
probably benign |
0.00 |
R4289:Plxnb1
|
UTSW |
9 |
108,943,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Plxnb1
|
UTSW |
9 |
108,929,291 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4564:Plxnb1
|
UTSW |
9 |
108,942,488 (GRCm39) |
missense |
probably benign |
0.10 |
R4676:Plxnb1
|
UTSW |
9 |
108,939,503 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4706:Plxnb1
|
UTSW |
9 |
108,941,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Plxnb1
|
UTSW |
9 |
108,939,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Plxnb1
|
UTSW |
9 |
108,943,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R4835:Plxnb1
|
UTSW |
9 |
108,934,442 (GRCm39) |
missense |
probably damaging |
0.96 |
R4901:Plxnb1
|
UTSW |
9 |
108,934,027 (GRCm39) |
missense |
probably benign |
0.01 |
R4952:Plxnb1
|
UTSW |
9 |
108,943,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5005:Plxnb1
|
UTSW |
9 |
108,935,647 (GRCm39) |
missense |
probably benign |
0.00 |
R5015:Plxnb1
|
UTSW |
9 |
108,929,498 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5029:Plxnb1
|
UTSW |
9 |
108,943,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R5180:Plxnb1
|
UTSW |
9 |
108,940,761 (GRCm39) |
splice site |
probably null |
|
R5256:Plxnb1
|
UTSW |
9 |
108,943,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Plxnb1
|
UTSW |
9 |
108,937,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R5431:Plxnb1
|
UTSW |
9 |
108,929,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R5444:Plxnb1
|
UTSW |
9 |
108,935,521 (GRCm39) |
missense |
probably benign |
0.22 |
R5546:Plxnb1
|
UTSW |
9 |
108,929,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5852:Plxnb1
|
UTSW |
9 |
108,935,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Plxnb1
|
UTSW |
9 |
108,940,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:Plxnb1
|
UTSW |
9 |
108,945,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R6053:Plxnb1
|
UTSW |
9 |
108,940,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6177:Plxnb1
|
UTSW |
9 |
108,931,993 (GRCm39) |
splice site |
probably null |
|
R6193:Plxnb1
|
UTSW |
9 |
108,933,971 (GRCm39) |
missense |
probably benign |
|
R6274:Plxnb1
|
UTSW |
9 |
108,941,209 (GRCm39) |
critical splice donor site |
probably null |
|
R6310:Plxnb1
|
UTSW |
9 |
108,938,796 (GRCm39) |
missense |
probably damaging |
0.96 |
R6404:Plxnb1
|
UTSW |
9 |
108,945,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R6422:Plxnb1
|
UTSW |
9 |
108,937,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R6479:Plxnb1
|
UTSW |
9 |
108,940,733 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6555:Plxnb1
|
UTSW |
9 |
108,937,473 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6646:Plxnb1
|
UTSW |
9 |
108,937,895 (GRCm39) |
missense |
probably benign |
|
R6648:Plxnb1
|
UTSW |
9 |
108,933,398 (GRCm39) |
missense |
probably benign |
0.14 |
R6661:Plxnb1
|
UTSW |
9 |
108,933,367 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6674:Plxnb1
|
UTSW |
9 |
108,937,214 (GRCm39) |
missense |
probably benign |
0.00 |
R6734:Plxnb1
|
UTSW |
9 |
108,937,988 (GRCm39) |
nonsense |
probably null |
|
R6859:Plxnb1
|
UTSW |
9 |
108,935,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6948:Plxnb1
|
UTSW |
9 |
108,945,702 (GRCm39) |
missense |
probably damaging |
0.96 |
R7030:Plxnb1
|
UTSW |
9 |
108,941,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R7038:Plxnb1
|
UTSW |
9 |
108,929,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Plxnb1
|
UTSW |
9 |
108,929,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R7427:Plxnb1
|
UTSW |
9 |
108,937,236 (GRCm39) |
missense |
probably benign |
0.01 |
R7428:Plxnb1
|
UTSW |
9 |
108,937,236 (GRCm39) |
missense |
probably benign |
0.01 |
R7443:Plxnb1
|
UTSW |
9 |
108,943,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Plxnb1
|
UTSW |
9 |
108,929,929 (GRCm39) |
missense |
probably damaging |
0.99 |
R7645:Plxnb1
|
UTSW |
9 |
108,943,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R7680:Plxnb1
|
UTSW |
9 |
108,929,571 (GRCm39) |
nonsense |
probably null |
|
R7866:Plxnb1
|
UTSW |
9 |
108,929,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R7898:Plxnb1
|
UTSW |
9 |
108,943,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7905:Plxnb1
|
UTSW |
9 |
108,938,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R8092:Plxnb1
|
UTSW |
9 |
108,929,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8150:Plxnb1
|
UTSW |
9 |
108,941,146 (GRCm39) |
missense |
probably damaging |
0.98 |
R8286:Plxnb1
|
UTSW |
9 |
108,935,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R8290:Plxnb1
|
UTSW |
9 |
108,938,687 (GRCm39) |
missense |
probably benign |
0.00 |
R8987:Plxnb1
|
UTSW |
9 |
108,937,178 (GRCm39) |
splice site |
probably benign |
|
R9176:Plxnb1
|
UTSW |
9 |
108,941,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Plxnb1
|
UTSW |
9 |
108,934,286 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9698:Plxnb1
|
UTSW |
9 |
108,925,251 (GRCm39) |
start gained |
probably benign |
|
Z1177:Plxnb1
|
UTSW |
9 |
108,937,989 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
Predicted Primers |
PCR Primer
(F):5'- TTATGTGGAATTGCCCCTGGCCTG -3'
(R):5'- AGCACCTAACACCTGTCCTGAGAG -3'
Sequencing Primer
(F):5'- CTGCCAGGGTGGTCGTTAC -3'
(R):5'- CCAGACTTTCTGGGCAGGTG -3'
|
Posted On |
2014-03-14 |