Incidental Mutation 'R0238:Plxnd1'
| ID |
66091 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Plxnd1
|
| Ensembl Gene |
ENSMUSG00000030123 |
| Gene Name |
plexin D1 |
| Synonyms |
b2b553Clo, 6230425C21Rik, b2b1863Clo |
| MMRRC Submission |
038476-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R0238 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
115954811-115995005 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 115968793 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 906
(D906E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000015511
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000015511]
|
| AlphaFold |
Q3UH93 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000015511
AA Change: D906E
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000015511
Gene: ENSMUSG00000030123
AA Change: D906E
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
48 |
N/A |
INTRINSIC |
|
Sema
|
61 |
531 |
6.52e-90 |
SMART |
|
PSI
|
550 |
603 |
6.06e-12 |
SMART |
|
PSI
|
703 |
755 |
1.06e-2 |
SMART |
|
Blast:PSI
|
850 |
891 |
9e-20 |
BLAST |
|
IPT
|
892 |
981 |
4.43e-20 |
SMART |
|
IPT
|
982 |
1068 |
6.61e-19 |
SMART |
|
IPT
|
1070 |
1149 |
6.13e-14 |
SMART |
|
transmembrane domain
|
1271 |
1293 |
N/A |
INTRINSIC |
|
Pfam:Plexin_cytopl
|
1345 |
1888 |
5e-238 |
PFAM |
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000115650
Gene: ENSMUSG00000030123
AA Change: D48E
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:PSI
|
2 |
34 |
1e-13 |
BLAST |
|
IPT
|
35 |
124 |
4.43e-20 |
SMART |
|
Blast:IPT
|
125 |
177 |
3e-30 |
BLAST |
|
Pfam:TIG
|
180 |
233 |
4.6e-6 |
PFAM |
|
| Meta Mutation Damage Score |
0.0964 |
| Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.4%
- 10x: 92.6%
- 20x: 76.9%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Homozygous null mice display neonatal lethality, thin-walled atria, and vascular abnormalities including abnormal branchial arch artery development, cardiac outflow tract abnormalities, and reduced vascular smooth muscle around some vessels. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aar2 |
T |
G |
2: 156,550,973 (GRCm38) |
V94G |
probably benign |
Het |
| Acp5 |
A |
T |
9: 22,129,922 (GRCm38) |
S70T |
possibly damaging |
Het |
| Adcy1 |
C |
G |
11: 7,139,162 (GRCm38) |
N525K |
possibly damaging |
Het |
| Aknad1 |
A |
G |
3: 108,781,239 (GRCm38) |
M628V |
probably benign |
Het |
| Alg8 |
A |
T |
7: 97,383,684 (GRCm38) |
|
probably null |
Het |
| Cacna1d |
A |
G |
14: 30,123,496 (GRCm38) |
V572A |
probably benign |
Het |
| Ccdc158 |
A |
C |
5: 92,662,118 (GRCm38) |
M177R |
probably benign |
Het |
| Ccdc191 |
A |
T |
16: 43,947,496 (GRCm38) |
R678* |
probably null |
Het |
| Cdkn2d |
C |
A |
9: 21,290,992 (GRCm38) |
|
probably benign |
Het |
| Cdx2 |
G |
T |
5: 147,303,287 (GRCm38) |
T193K |
probably damaging |
Het |
| Cfap44 |
T |
A |
16: 44,422,318 (GRCm38) |
M695K |
probably benign |
Het |
| Cfap70 |
A |
C |
14: 20,448,605 (GRCm38) |
S5A |
probably benign |
Het |
| Chd9 |
T |
C |
8: 90,932,828 (GRCm38) |
S139P |
probably damaging |
Het |
| Chmp7 |
A |
G |
14: 69,720,997 (GRCm38) |
V241A |
probably damaging |
Het |
| Cnga1 |
A |
G |
5: 72,605,031 (GRCm38) |
I380T |
probably damaging |
Het |
| Cts6 |
T |
A |
13: 61,201,819 (GRCm38) |
E53D |
probably damaging |
Het |
| Dclk3 |
A |
T |
9: 111,482,628 (GRCm38) |
N646I |
probably damaging |
Het |
| Dnhd1 |
A |
G |
7: 105,721,531 (GRCm38) |
S4673G |
probably benign |
Het |
| Dock4 |
G |
T |
12: 40,737,540 (GRCm38) |
S818I |
probably damaging |
Het |
| Dysf |
C |
T |
6: 84,064,479 (GRCm38) |
Q156* |
probably null |
Het |
| Fam163b |
T |
C |
2: 27,112,634 (GRCm38) |
N117S |
probably damaging |
Het |
| Fam89a |
A |
G |
8: 124,741,232 (GRCm38) |
Y114H |
probably damaging |
Het |
| Flcn |
T |
C |
11: 59,801,076 (GRCm38) |
N249S |
probably benign |
Het |
| Gm20422 |
T |
C |
8: 69,766,715 (GRCm38) |
Y53C |
probably damaging |
Het |
| Gnai1 |
A |
G |
5: 18,273,550 (GRCm38) |
S206P |
probably damaging |
Het |
| H1f6 |
G |
T |
13: 23,696,324 (GRCm38) |
K153N |
possibly damaging |
Het |
| Hal |
T |
C |
10: 93,503,482 (GRCm38) |
S478P |
possibly damaging |
Het |
| Haus3 |
G |
A |
5: 34,166,256 (GRCm38) |
P337S |
possibly damaging |
Het |
| Hectd1 |
T |
A |
12: 51,769,318 (GRCm38) |
M1324L |
possibly damaging |
Het |
| Hspa9 |
A |
T |
18: 34,946,646 (GRCm38) |
Y243* |
probably null |
Het |
| Htr3a |
T |
C |
9: 48,906,386 (GRCm38) |
T96A |
probably benign |
Het |
| Ift140 |
C |
A |
17: 25,045,523 (GRCm38) |
C557* |
probably null |
Het |
| Jph3 |
A |
G |
8: 121,753,720 (GRCm38) |
Q379R |
possibly damaging |
Het |
| Kcnb1 |
A |
G |
2: 167,104,969 (GRCm38) |
V653A |
probably benign |
Het |
| Kif14 |
A |
G |
1: 136,527,393 (GRCm38) |
E1551G |
probably damaging |
Het |
| Krt17 |
G |
A |
11: 100,260,878 (GRCm38) |
R30* |
probably null |
Het |
| Lamb3 |
A |
T |
1: 193,321,053 (GRCm38) |
D100V |
probably damaging |
Het |
| Map2 |
A |
G |
1: 66,416,106 (GRCm38) |
D1385G |
probably damaging |
Het |
| Map3k21 |
A |
G |
8: 125,944,970 (GRCm38) |
D999G |
possibly damaging |
Het |
| Marf1 |
T |
C |
16: 14,151,283 (GRCm38) |
I109V |
probably benign |
Het |
| Mcam |
T |
G |
9: 44,140,205 (GRCm38) |
|
probably null |
Het |
| Med18 |
T |
C |
4: 132,460,026 (GRCm38) |
H99R |
probably damaging |
Het |
| Mettl25 |
C |
T |
10: 105,826,525 (GRCm38) |
V195I |
probably damaging |
Het |
| Myh8 |
A |
G |
11: 67,301,692 (GRCm38) |
T1466A |
probably benign |
Het |
| Myo1e |
A |
T |
9: 70,342,126 (GRCm38) |
I503F |
possibly damaging |
Het |
| Myo3b |
T |
A |
2: 70,105,425 (GRCm38) |
C61S |
probably benign |
Het |
| Myorg |
A |
T |
4: 41,498,912 (GRCm38) |
N239K |
probably benign |
Het |
| Nf1 |
A |
T |
11: 79,418,574 (GRCm38) |
K438M |
possibly damaging |
Het |
| Nlrp9c |
A |
G |
7: 26,378,012 (GRCm38) |
S727P |
possibly damaging |
Het |
| Nmbr |
C |
T |
10: 14,770,395 (GRCm38) |
Q338* |
probably null |
Het |
| Nt5e |
A |
G |
9: 88,367,332 (GRCm38) |
S440G |
possibly damaging |
Het |
| Nubp2 |
T |
C |
17: 24,884,471 (GRCm38) |
E144G |
probably damaging |
Het |
| Or12e7 |
T |
C |
2: 87,458,037 (GRCm38) |
F291L |
probably benign |
Het |
| Or2ag1b |
A |
G |
7: 106,689,255 (GRCm38) |
Y159H |
probably benign |
Het |
| Or52s1 |
G |
A |
7: 103,212,726 (GRCm38) |
V289M |
possibly damaging |
Het |
| Otogl |
T |
A |
10: 107,806,696 (GRCm38) |
N1291I |
probably damaging |
Het |
| Pa2g4 |
T |
C |
10: 128,563,642 (GRCm38) |
K51R |
probably benign |
Het |
| Pcdhb12 |
A |
G |
18: 37,436,727 (GRCm38) |
I309V |
probably benign |
Het |
| Pck1 |
T |
G |
2: 173,157,068 (GRCm38) |
I373S |
possibly damaging |
Het |
| Pga5 |
A |
G |
19: 10,669,453 (GRCm38) |
Y305H |
probably damaging |
Het |
| Ppfia4 |
T |
C |
1: 134,329,189 (GRCm38) |
E98G |
possibly damaging |
Het |
| Rab39 |
G |
A |
9: 53,706,030 (GRCm38) |
T29I |
probably damaging |
Het |
| Raet1e |
C |
A |
10: 22,180,862 (GRCm38) |
H112Q |
possibly damaging |
Het |
| Rars2 |
T |
C |
4: 34,645,838 (GRCm38) |
Y252H |
probably damaging |
Het |
| Rars2 |
A |
C |
4: 34,656,030 (GRCm38) |
Q421P |
probably benign |
Het |
| Rasa2 |
A |
T |
9: 96,568,407 (GRCm38) |
D479E |
probably damaging |
Het |
| Rbl2 |
A |
T |
8: 91,106,507 (GRCm38) |
T689S |
probably damaging |
Het |
| Rims4 |
C |
T |
2: 163,864,025 (GRCm38) |
V230M |
probably benign |
Het |
| Skp2 |
A |
C |
15: 9,127,884 (GRCm38) |
|
probably null |
Het |
| Slc35f4 |
A |
T |
14: 49,304,256 (GRCm38) |
I347N |
possibly damaging |
Het |
| Slc4a2 |
A |
T |
5: 24,436,274 (GRCm38) |
|
probably null |
Het |
| Slc52a3 |
T |
C |
2: 152,008,156 (GRCm38) |
*461Q |
probably null |
Het |
| Slc6a1 |
G |
A |
6: 114,302,800 (GRCm38) |
V142I |
probably benign |
Het |
| Susd5 |
A |
G |
9: 114,096,909 (GRCm38) |
*620W |
probably null |
Het |
| Timm21 |
T |
C |
18: 84,947,666 (GRCm38) |
N239S |
probably damaging |
Het |
| Tmem63c |
T |
C |
12: 87,075,639 (GRCm38) |
W404R |
probably damaging |
Het |
| Tnrc6b |
A |
G |
15: 80,887,864 (GRCm38) |
D1118G |
probably damaging |
Het |
| Traf2 |
G |
C |
2: 25,537,126 (GRCm38) |
A71G |
possibly damaging |
Het |
| Trim54 |
A |
G |
5: 31,134,119 (GRCm38) |
M195V |
probably benign |
Het |
| Trip11 |
C |
T |
12: 101,884,728 (GRCm38) |
E741K |
probably damaging |
Het |
| Trp73 |
AGCTGCTGCTGCTGCTGCTG |
AGCTGCTGCTGCTGCTG |
4: 154,062,524 (GRCm38) |
|
probably benign |
Het |
| Trpm5 |
G |
T |
7: 143,082,958 (GRCm38) |
T414N |
probably damaging |
Het |
| Vps51 |
G |
T |
19: 6,071,437 (GRCm38) |
S185* |
probably null |
Het |
| Zfp329 |
G |
T |
7: 12,810,829 (GRCm38) |
T256K |
probably damaging |
Het |
| Zfp729b |
A |
G |
13: 67,591,903 (GRCm38) |
Y748H |
probably damaging |
Het |
| Zfp777 |
T |
C |
6: 48,024,969 (GRCm38) |
E773G |
probably damaging |
Het |
|
| Other mutations in Plxnd1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00764:Plxnd1
|
APN |
6 |
115,967,972 (GRCm38) |
missense |
possibly damaging |
0.51 |
|
IGL01099:Plxnd1
|
APN |
6 |
115,969,945 (GRCm38) |
missense |
probably benign |
|
|
IGL01323:Plxnd1
|
APN |
6 |
115,966,799 (GRCm38) |
missense |
possibly damaging |
0.81 |
|
IGL01382:Plxnd1
|
APN |
6 |
115,960,527 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01786:Plxnd1
|
APN |
6 |
115,959,935 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02244:Plxnd1
|
APN |
6 |
115,978,257 (GRCm38) |
missense |
probably benign |
0.39 |
|
IGL02272:Plxnd1
|
APN |
6 |
115,993,628 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02293:Plxnd1
|
APN |
6 |
115,963,913 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02465:Plxnd1
|
APN |
6 |
115,955,742 (GRCm38) |
makesense |
probably null |
|
|
IGL02873:Plxnd1
|
APN |
6 |
115,959,976 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03209:Plxnd1
|
APN |
6 |
115,962,357 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Hiss
|
UTSW |
6 |
115,969,929 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
murmer
|
UTSW |
6 |
115,968,793 (GRCm38) |
missense |
probably benign |
0.00 |
|
mutter
|
UTSW |
6 |
115,968,044 (GRCm38) |
missense |
probably benign |
0.27 |
|
rattle
|
UTSW |
6 |
115,959,794 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R0238:Plxnd1
|
UTSW |
6 |
115,968,793 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0239:Plxnd1
|
UTSW |
6 |
115,968,793 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0239:Plxnd1
|
UTSW |
6 |
115,968,793 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0357:Plxnd1
|
UTSW |
6 |
115,969,460 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0646:Plxnd1
|
UTSW |
6 |
115,958,699 (GRCm38) |
splice site |
probably benign |
|
|
R0648:Plxnd1
|
UTSW |
6 |
115,994,001 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R0718:Plxnd1
|
UTSW |
6 |
115,966,638 (GRCm38) |
missense |
possibly damaging |
0.68 |
|
R1116:Plxnd1
|
UTSW |
6 |
115,967,005 (GRCm38) |
splice site |
probably null |
|
|
R1292:Plxnd1
|
UTSW |
6 |
115,962,683 (GRCm38) |
unclassified |
probably benign |
|
|
R1715:Plxnd1
|
UTSW |
6 |
115,968,681 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1760:Plxnd1
|
UTSW |
6 |
115,967,779 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R1799:Plxnd1
|
UTSW |
6 |
115,994,057 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1817:Plxnd1
|
UTSW |
6 |
115,980,601 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R1848:Plxnd1
|
UTSW |
6 |
115,966,546 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1851:Plxnd1
|
UTSW |
6 |
115,963,914 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1864:Plxnd1
|
UTSW |
6 |
115,969,441 (GRCm38) |
splice site |
probably null |
|
|
R1865:Plxnd1
|
UTSW |
6 |
115,969,441 (GRCm38) |
splice site |
probably null |
|
|
R1875:Plxnd1
|
UTSW |
6 |
115,978,084 (GRCm38) |
splice site |
probably null |
|
|
R1899:Plxnd1
|
UTSW |
6 |
115,969,363 (GRCm38) |
missense |
probably benign |
|
|
R1913:Plxnd1
|
UTSW |
6 |
115,978,017 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
R1970:Plxnd1
|
UTSW |
6 |
115,962,517 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2007:Plxnd1
|
UTSW |
6 |
115,967,255 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2134:Plxnd1
|
UTSW |
6 |
115,957,548 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2202:Plxnd1
|
UTSW |
6 |
115,962,764 (GRCm38) |
missense |
probably benign |
0.45 |
|
R2230:Plxnd1
|
UTSW |
6 |
115,964,144 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2267:Plxnd1
|
UTSW |
6 |
115,962,743 (GRCm38) |
missense |
probably benign |
0.29 |
|
R2427:Plxnd1
|
UTSW |
6 |
115,967,748 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4108:Plxnd1
|
UTSW |
6 |
115,959,315 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4233:Plxnd1
|
UTSW |
6 |
115,965,953 (GRCm38) |
missense |
probably benign |
0.30 |
|
R4280:Plxnd1
|
UTSW |
6 |
115,956,095 (GRCm38) |
splice site |
probably null |
|
|
R4280:Plxnd1
|
UTSW |
6 |
115,956,094 (GRCm38) |
splice site |
probably benign |
|
|
R4346:Plxnd1
|
UTSW |
6 |
115,977,980 (GRCm38) |
missense |
probably benign |
0.16 |
|
R4439:Plxnd1
|
UTSW |
6 |
115,993,976 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4572:Plxnd1
|
UTSW |
6 |
115,955,756 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4576:Plxnd1
|
UTSW |
6 |
115,968,044 (GRCm38) |
missense |
probably benign |
0.27 |
|
R4599:Plxnd1
|
UTSW |
6 |
115,994,276 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4614:Plxnd1
|
UTSW |
6 |
115,972,525 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R4700:Plxnd1
|
UTSW |
6 |
115,958,615 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4705:Plxnd1
|
UTSW |
6 |
115,958,620 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4806:Plxnd1
|
UTSW |
6 |
115,960,855 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4944:Plxnd1
|
UTSW |
6 |
115,955,765 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4977:Plxnd1
|
UTSW |
6 |
115,994,376 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5069:Plxnd1
|
UTSW |
6 |
115,965,901 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R5155:Plxnd1
|
UTSW |
6 |
115,958,988 (GRCm38) |
critical splice donor site |
probably null |
|
|
R5460:Plxnd1
|
UTSW |
6 |
115,957,648 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5729:Plxnd1
|
UTSW |
6 |
115,965,877 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5909:Plxnd1
|
UTSW |
6 |
115,968,688 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5992:Plxnd1
|
UTSW |
6 |
115,967,787 (GRCm38) |
critical splice acceptor site |
probably null |
|
|
R6129:Plxnd1
|
UTSW |
6 |
115,978,174 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6254:Plxnd1
|
UTSW |
6 |
115,977,960 (GRCm38) |
missense |
probably benign |
0.01 |
|
R6273:Plxnd1
|
UTSW |
6 |
115,978,492 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6310:Plxnd1
|
UTSW |
6 |
115,976,736 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R6732:Plxnd1
|
UTSW |
6 |
115,969,929 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R6857:Plxnd1
|
UTSW |
6 |
115,993,763 (GRCm38) |
missense |
probably benign |
0.05 |
|
R7243:Plxnd1
|
UTSW |
6 |
115,972,507 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7282:Plxnd1
|
UTSW |
6 |
115,960,837 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7632:Plxnd1
|
UTSW |
6 |
115,976,639 (GRCm38) |
missense |
probably benign |
|
|
R7699:Plxnd1
|
UTSW |
6 |
115,959,794 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R7915:Plxnd1
|
UTSW |
6 |
115,966,918 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8090:Plxnd1
|
UTSW |
6 |
115,956,617 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8382:Plxnd1
|
UTSW |
6 |
115,972,472 (GRCm38) |
missense |
probably benign |
|
|
R8507:Plxnd1
|
UTSW |
6 |
115,966,905 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R8539:Plxnd1
|
UTSW |
6 |
115,962,807 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R8548:Plxnd1
|
UTSW |
6 |
115,957,597 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8963:Plxnd1
|
UTSW |
6 |
115,972,545 (GRCm38) |
nonsense |
probably null |
|
|
R9119:Plxnd1
|
UTSW |
6 |
115,955,871 (GRCm38) |
splice site |
probably benign |
|
|
R9177:Plxnd1
|
UTSW |
6 |
115,966,508 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9182:Plxnd1
|
UTSW |
6 |
115,993,785 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R9185:Plxnd1
|
UTSW |
6 |
115,957,565 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9226:Plxnd1
|
UTSW |
6 |
115,957,563 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9433:Plxnd1
|
UTSW |
6 |
115,968,793 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9449:Plxnd1
|
UTSW |
6 |
115,955,769 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9451:Plxnd1
|
UTSW |
6 |
115,963,316 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R9599:Plxnd1
|
UTSW |
6 |
115,963,313 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
R9627:Plxnd1
|
UTSW |
6 |
115,963,313 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
R9644:Plxnd1
|
UTSW |
6 |
115,963,313 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
R9672:Plxnd1
|
UTSW |
6 |
115,963,313 (GRCm38) |
missense |
possibly damaging |
0.78 |
|
X0024:Plxnd1
|
UTSW |
6 |
115,963,310 (GRCm38) |
missense |
probably benign |
0.02 |
|
X0026:Plxnd1
|
UTSW |
6 |
115,966,784 (GRCm38) |
missense |
possibly damaging |
0.88 |
|
Z1088:Plxnd1
|
UTSW |
6 |
115,967,510 (GRCm38) |
missense |
probably benign |
0.02 |
|
| Predicted Primers |
|
| Posted On |
2013-08-19 |
Incidental Mutation