Incidental Mutation 'R4884:Cspg4'
ID |
375552 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cspg4
|
Ensembl Gene |
ENSMUSG00000032911 |
Gene Name |
chondroitin sulfate proteoglycan 4 |
Synonyms |
Cspg4a, AN2, NG2, 4732461B14Rik |
MMRRC Submission |
041978-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4884 (G1)
|
Quality Score |
153 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
56772388-56807154 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 56805353 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tryptophan to Arginine
at position 2055
(W2055R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000038909
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035661]
|
AlphaFold |
Q8VHY0 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000035661
AA Change: W2055R
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000038909 Gene: ENSMUSG00000032911 AA Change: W2055R
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
29 |
N/A |
INTRINSIC |
LamG
|
47 |
179 |
9.16e-22 |
SMART |
LamG
|
223 |
364 |
3.52e-23 |
SMART |
low complexity region
|
384 |
397 |
N/A |
INTRINSIC |
Pfam:Cadherin_3
|
495 |
646 |
1e-36 |
PFAM |
Pfam:Cadherin_3
|
732 |
885 |
7.9e-14 |
PFAM |
Pfam:Cadherin_3
|
868 |
996 |
7e-15 |
PFAM |
Pfam:Cadherin_3
|
972 |
1115 |
9e-26 |
PFAM |
Pfam:Cadherin_3
|
1116 |
1223 |
1.1e-10 |
PFAM |
Pfam:Cadherin_3
|
1225 |
1344 |
3.3e-12 |
PFAM |
Pfam:Cadherin_3
|
1425 |
1568 |
6.3e-52 |
PFAM |
Pfam:Cadherin_3
|
1578 |
1684 |
9.7e-9 |
PFAM |
Pfam:Cadherin_3
|
1674 |
1809 |
3.2e-9 |
PFAM |
Pfam:Cadherin_3
|
1779 |
1929 |
1.6e-31 |
PFAM |
transmembrane domain
|
2229 |
2251 |
N/A |
INTRINSIC |
low complexity region
|
2295 |
2305 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000215666
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000217052
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] A human melanoma-associated chondroitin sulfate proteoglycan plays a role in stabilizing cell-substratum interactions during early events of melanoma cell spreading on endothelial basement membranes. CSPG4 represents an integral membrane chondroitin sulfate proteoglycan expressed by human malignant melanoma cells. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a null mutation display abnormal dentate gyrus morphology and abnormal smooth muscle cell physiology. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Aadat |
C |
T |
8: 60,979,663 (GRCm39) |
P175L |
probably damaging |
Het |
Acot7 |
G |
T |
4: 152,270,664 (GRCm39) |
|
probably benign |
Het |
Adad1 |
T |
G |
3: 37,130,813 (GRCm39) |
F259V |
possibly damaging |
Het |
Adora2a |
A |
G |
10: 75,161,879 (GRCm39) |
Y6C |
probably null |
Het |
Ahnak |
A |
G |
19: 8,990,118 (GRCm39) |
|
probably benign |
Het |
Ankar |
A |
T |
1: 72,737,966 (GRCm39) |
M72K |
probably damaging |
Het |
Ankrd45 |
A |
G |
1: 160,988,270 (GRCm39) |
K176R |
possibly damaging |
Het |
Ap3m2 |
T |
C |
8: 23,293,997 (GRCm39) |
K18E |
probably damaging |
Het |
Apol10b |
C |
T |
15: 77,473,006 (GRCm39) |
R16Q |
possibly damaging |
Het |
Atp2b2 |
T |
A |
6: 113,819,147 (GRCm39) |
T49S |
possibly damaging |
Het |
B3gntl1 |
T |
G |
11: 121,520,795 (GRCm39) |
Y206S |
possibly damaging |
Het |
BC061237 |
G |
A |
14: 44,738,666 (GRCm39) |
E22K |
possibly damaging |
Het |
Bmp1 |
A |
G |
14: 70,712,655 (GRCm39) |
V959A |
probably benign |
Het |
Cep295 |
T |
C |
9: 15,263,056 (GRCm39) |
E169G |
probably damaging |
Het |
Cfap20dc |
G |
A |
14: 8,578,394 (GRCm38) |
T116I |
probably damaging |
Het |
Cfap65 |
T |
G |
1: 74,942,283 (GRCm39) |
E1757A |
possibly damaging |
Het |
Cgrrf1 |
T |
A |
14: 47,090,912 (GRCm39) |
I216N |
possibly damaging |
Het |
Clstn2 |
T |
A |
9: 97,681,448 (GRCm39) |
D64V |
probably damaging |
Het |
Col27a1 |
T |
A |
4: 63,194,197 (GRCm39) |
D851E |
possibly damaging |
Het |
Coq9 |
C |
T |
8: 95,579,822 (GRCm39) |
P259L |
probably benign |
Het |
Cps1 |
A |
G |
1: 67,216,183 (GRCm39) |
N836S |
probably benign |
Het |
Cracd |
A |
T |
5: 76,996,682 (GRCm39) |
I47F |
probably damaging |
Het |
Crebbp |
T |
C |
16: 3,906,239 (GRCm39) |
K1588E |
probably damaging |
Het |
Cyp3a44 |
A |
T |
5: 145,714,792 (GRCm39) |
M453K |
probably damaging |
Het |
Dhx36 |
T |
G |
3: 62,391,681 (GRCm39) |
D555A |
probably damaging |
Het |
Dock2 |
A |
T |
11: 34,216,248 (GRCm39) |
Y1219N |
probably damaging |
Het |
Dpy19l2 |
A |
T |
9: 24,539,476 (GRCm39) |
C492* |
probably null |
Het |
Dusp22 |
A |
G |
13: 30,852,813 (GRCm39) |
N16S |
probably benign |
Het |
Epha1 |
A |
G |
6: 42,337,668 (GRCm39) |
M805T |
probably damaging |
Het |
Espl1 |
C |
T |
15: 102,232,505 (GRCm39) |
A2071V |
possibly damaging |
Het |
Fbxo11 |
T |
A |
17: 88,299,761 (GRCm39) |
D863V |
probably damaging |
Het |
Fbxo7 |
T |
A |
10: 85,865,014 (GRCm39) |
Y106N |
probably damaging |
Het |
Fhip1a |
A |
C |
3: 85,590,918 (GRCm39) |
C178G |
probably damaging |
Het |
Fst |
A |
G |
13: 114,590,920 (GRCm39) |
V282A |
probably damaging |
Het |
Gfra3 |
T |
A |
18: 34,844,304 (GRCm39) |
M79L |
probably benign |
Het |
Glp1r |
T |
C |
17: 31,155,240 (GRCm39) |
V409A |
probably damaging |
Het |
Gm10799 |
T |
A |
2: 103,898,552 (GRCm39) |
D51V |
probably damaging |
Het |
Gm572 |
C |
A |
4: 148,751,819 (GRCm39) |
T228N |
possibly damaging |
Het |
Grip1 |
C |
T |
10: 119,911,211 (GRCm39) |
T643M |
probably damaging |
Het |
Hdgfl2 |
C |
T |
17: 56,403,265 (GRCm39) |
R222C |
possibly damaging |
Het |
Hecw2 |
T |
A |
1: 53,990,000 (GRCm39) |
I125F |
probably benign |
Het |
Hipk1 |
A |
G |
3: 103,651,338 (GRCm39) |
S1153P |
possibly damaging |
Het |
Insm2 |
T |
C |
12: 55,646,546 (GRCm39) |
S97P |
probably damaging |
Het |
Iqca1 |
A |
G |
1: 90,067,759 (GRCm39) |
V164A |
probably benign |
Het |
Kcna6 |
T |
C |
6: 126,715,689 (GRCm39) |
D400G |
probably benign |
Het |
Kctd1 |
T |
C |
18: 15,107,311 (GRCm39) |
Y122C |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Klra2 |
T |
C |
6: 131,207,165 (GRCm39) |
Y148C |
probably damaging |
Het |
Krtap31-1 |
G |
A |
11: 99,799,310 (GRCm39) |
C171Y |
unknown |
Het |
Ldlrap1 |
C |
T |
4: 134,486,282 (GRCm39) |
R59Q |
probably benign |
Het |
Ltb |
T |
C |
17: 35,414,234 (GRCm39) |
I3T |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,348,802 (GRCm39) |
I2477V |
probably benign |
Het |
Mpdz |
A |
T |
4: 81,279,713 (GRCm39) |
I39N |
probably damaging |
Het |
Mtcl3 |
A |
T |
10: 29,072,537 (GRCm39) |
N610Y |
probably damaging |
Het |
Mycbp2 |
A |
G |
14: 103,448,731 (GRCm39) |
I1776T |
probably damaging |
Het |
Myof |
T |
A |
19: 37,930,805 (GRCm39) |
E994V |
probably damaging |
Het |
Myom3 |
A |
G |
4: 135,510,366 (GRCm39) |
E553G |
possibly damaging |
Het |
Mysm1 |
A |
T |
4: 94,847,185 (GRCm39) |
C504S |
probably damaging |
Het |
Nectin3 |
A |
T |
16: 46,269,249 (GRCm39) |
H384Q |
probably benign |
Het |
Net1 |
G |
A |
13: 3,934,252 (GRCm39) |
R482* |
probably null |
Het |
Nit1 |
T |
C |
1: 171,171,263 (GRCm39) |
K193R |
probably null |
Het |
Nlgn1 |
A |
G |
3: 25,966,838 (GRCm39) |
V205A |
probably damaging |
Het |
Nr3c2 |
A |
T |
8: 77,635,438 (GRCm39) |
I180F |
possibly damaging |
Het |
Nup50l |
A |
T |
6: 96,141,793 (GRCm39) |
M417K |
probably damaging |
Het |
Nup62 |
T |
A |
7: 44,478,289 (GRCm39) |
S101R |
probably damaging |
Het |
Or13c7 |
T |
C |
4: 43,854,890 (GRCm39) |
S194P |
probably damaging |
Het |
Or1l8 |
G |
T |
2: 36,818,024 (GRCm39) |
T34K |
possibly damaging |
Het |
Or4c3 |
A |
G |
2: 89,851,987 (GRCm39) |
V141A |
probably benign |
Het |
Or51b17 |
T |
A |
7: 103,542,862 (GRCm39) |
I27F |
probably benign |
Het |
Or56b2j |
T |
A |
7: 104,353,068 (GRCm39) |
I98N |
probably damaging |
Het |
Or5b111 |
A |
T |
19: 13,291,034 (GRCm39) |
I205N |
probably benign |
Het |
Or5b124 |
A |
T |
19: 13,611,391 (GRCm39) |
K305N |
probably benign |
Het |
Or5p80 |
A |
T |
7: 108,229,819 (GRCm39) |
I207F |
probably damaging |
Het |
Osbpl6 |
A |
T |
2: 76,379,883 (GRCm39) |
I158F |
probably damaging |
Het |
Pcbp4 |
A |
G |
9: 106,339,301 (GRCm39) |
T103A |
probably benign |
Het |
Pcdha2 |
T |
A |
18: 37,073,953 (GRCm39) |
L528Q |
probably damaging |
Het |
Pcdhga5 |
T |
C |
18: 37,827,680 (GRCm39) |
S43P |
probably damaging |
Het |
Pdgfra |
C |
A |
5: 75,349,973 (GRCm39) |
N952K |
probably benign |
Het |
Pla2r1 |
A |
G |
2: 60,365,328 (GRCm39) |
S81P |
probably damaging |
Het |
Rabggtb |
A |
T |
3: 153,617,568 (GRCm39) |
D43E |
possibly damaging |
Het |
Rexo5 |
T |
A |
7: 119,424,774 (GRCm39) |
C43* |
probably null |
Het |
Robo1 |
T |
A |
16: 72,701,639 (GRCm39) |
D168E |
probably damaging |
Het |
Saxo4 |
A |
T |
19: 10,451,865 (GRCm39) |
*428R |
probably null |
Het |
Scimp |
A |
G |
11: 70,688,865 (GRCm39) |
M49T |
unknown |
Het |
Sema3e |
T |
A |
5: 14,275,579 (GRCm39) |
V228E |
probably damaging |
Het |
Sema6d |
A |
G |
2: 124,498,738 (GRCm39) |
|
probably null |
Het |
Serpinb6d |
A |
T |
13: 33,850,428 (GRCm39) |
D85V |
possibly damaging |
Het |
Slc24a2 |
C |
T |
4: 86,909,745 (GRCm39) |
V658I |
probably damaging |
Het |
Snd1 |
T |
C |
6: 28,526,911 (GRCm39) |
I198T |
possibly damaging |
Het |
Snx33 |
C |
T |
9: 56,833,464 (GRCm39) |
V202M |
probably damaging |
Het |
Srcap |
A |
G |
7: 127,121,189 (GRCm39) |
E174G |
probably damaging |
Het |
Srgap2 |
C |
A |
1: 131,220,314 (GRCm39) |
|
probably null |
Het |
Stxbp5 |
A |
T |
10: 9,688,085 (GRCm39) |
Y405* |
probably null |
Het |
Thsd4 |
C |
T |
9: 59,895,320 (GRCm39) |
R710H |
probably benign |
Het |
Trp53inp1 |
T |
A |
4: 11,165,130 (GRCm39) |
D51E |
probably benign |
Het |
Ttc41 |
A |
G |
10: 86,566,882 (GRCm39) |
D516G |
probably benign |
Het |
Tut7 |
A |
T |
13: 59,937,266 (GRCm39) |
L775H |
probably damaging |
Het |
Uap1l1 |
A |
G |
2: 25,252,840 (GRCm39) |
V400A |
probably damaging |
Het |
Vit |
T |
C |
17: 78,932,182 (GRCm39) |
S430P |
probably damaging |
Het |
Vmn1r9 |
T |
A |
6: 57,048,294 (GRCm39) |
M123K |
possibly damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,369,384 (GRCm39) |
|
probably null |
Het |
Vwa3a |
A |
G |
7: 120,390,924 (GRCm39) |
T746A |
probably benign |
Het |
Wdfy4 |
G |
T |
14: 32,710,852 (GRCm39) |
Y2578* |
probably null |
Het |
Wdr53 |
A |
T |
16: 32,075,796 (GRCm39) |
K334* |
probably null |
Het |
Xpot |
G |
T |
10: 121,442,713 (GRCm39) |
H495Q |
probably damaging |
Het |
Zfp109 |
T |
C |
7: 23,928,570 (GRCm39) |
T288A |
probably benign |
Het |
Zfp277 |
T |
A |
12: 40,413,152 (GRCm39) |
E276V |
probably damaging |
Het |
Zfp703 |
A |
G |
8: 27,468,729 (GRCm39) |
D131G |
probably benign |
Het |
Zfp985 |
T |
A |
4: 147,667,801 (GRCm39) |
I223N |
probably benign |
Het |
Zrsr2-ps1 |
T |
C |
11: 22,923,805 (GRCm39) |
V193A |
possibly damaging |
Het |
Zscan20 |
A |
G |
4: 128,481,958 (GRCm39) |
I568T |
possibly damaging |
Het |
|
Other mutations in Cspg4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01074:Cspg4
|
APN |
9 |
56,806,149 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01322:Cspg4
|
APN |
9 |
56,805,872 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01922:Cspg4
|
APN |
9 |
56,795,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01993:Cspg4
|
APN |
9 |
56,805,762 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02379:Cspg4
|
APN |
9 |
56,799,893 (GRCm39) |
splice site |
probably benign |
|
IGL02398:Cspg4
|
APN |
9 |
56,793,970 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02503:Cspg4
|
APN |
9 |
56,804,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02504:Cspg4
|
APN |
9 |
56,793,056 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02692:Cspg4
|
APN |
9 |
56,794,738 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02728:Cspg4
|
APN |
9 |
56,793,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02806:Cspg4
|
APN |
9 |
56,797,543 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02886:Cspg4
|
APN |
9 |
56,804,672 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03005:Cspg4
|
APN |
9 |
56,795,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Cspg4
|
APN |
9 |
56,805,759 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03202:Cspg4
|
APN |
9 |
56,805,023 (GRCm39) |
missense |
possibly damaging |
0.93 |
chiclets
|
UTSW |
9 |
56,792,506 (GRCm39) |
splice site |
probably null |
|
R0066:Cspg4
|
UTSW |
9 |
56,795,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Cspg4
|
UTSW |
9 |
56,795,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Cspg4
|
UTSW |
9 |
56,804,694 (GRCm39) |
missense |
probably damaging |
0.98 |
R0284:Cspg4
|
UTSW |
9 |
56,793,423 (GRCm39) |
missense |
probably damaging |
0.96 |
R0513:Cspg4
|
UTSW |
9 |
56,805,375 (GRCm39) |
missense |
probably benign |
0.03 |
R0602:Cspg4
|
UTSW |
9 |
56,795,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:Cspg4
|
UTSW |
9 |
56,797,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R1005:Cspg4
|
UTSW |
9 |
56,796,020 (GRCm39) |
missense |
probably benign |
0.13 |
R1421:Cspg4
|
UTSW |
9 |
56,803,910 (GRCm39) |
missense |
probably benign |
0.00 |
R1443:Cspg4
|
UTSW |
9 |
56,793,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Cspg4
|
UTSW |
9 |
56,795,094 (GRCm39) |
missense |
probably damaging |
0.98 |
R1585:Cspg4
|
UTSW |
9 |
56,806,151 (GRCm39) |
missense |
probably damaging |
0.99 |
R1624:Cspg4
|
UTSW |
9 |
56,795,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1670:Cspg4
|
UTSW |
9 |
56,804,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Cspg4
|
UTSW |
9 |
56,796,027 (GRCm39) |
missense |
probably damaging |
0.98 |
R1728:Cspg4
|
UTSW |
9 |
56,805,821 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Cspg4
|
UTSW |
9 |
56,805,821 (GRCm39) |
missense |
probably benign |
0.00 |
R1763:Cspg4
|
UTSW |
9 |
56,794,263 (GRCm39) |
missense |
probably damaging |
0.97 |
R1772:Cspg4
|
UTSW |
9 |
56,804,776 (GRCm39) |
missense |
probably benign |
0.02 |
R1938:Cspg4
|
UTSW |
9 |
56,794,385 (GRCm39) |
missense |
probably benign |
0.00 |
R1975:Cspg4
|
UTSW |
9 |
56,797,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Cspg4
|
UTSW |
9 |
56,803,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Cspg4
|
UTSW |
9 |
56,794,256 (GRCm39) |
missense |
probably benign |
0.37 |
R2252:Cspg4
|
UTSW |
9 |
56,805,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Cspg4
|
UTSW |
9 |
56,800,027 (GRCm39) |
missense |
probably damaging |
0.96 |
R2329:Cspg4
|
UTSW |
9 |
56,795,834 (GRCm39) |
missense |
probably benign |
0.00 |
R3780:Cspg4
|
UTSW |
9 |
56,795,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R3830:Cspg4
|
UTSW |
9 |
56,804,905 (GRCm39) |
missense |
probably damaging |
0.99 |
R3944:Cspg4
|
UTSW |
9 |
56,793,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R4011:Cspg4
|
UTSW |
9 |
56,794,601 (GRCm39) |
missense |
probably benign |
0.19 |
R4115:Cspg4
|
UTSW |
9 |
56,805,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R4173:Cspg4
|
UTSW |
9 |
56,795,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R4243:Cspg4
|
UTSW |
9 |
56,795,141 (GRCm39) |
missense |
probably benign |
0.12 |
R4329:Cspg4
|
UTSW |
9 |
56,799,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R4544:Cspg4
|
UTSW |
9 |
56,795,913 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4545:Cspg4
|
UTSW |
9 |
56,795,913 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4546:Cspg4
|
UTSW |
9 |
56,795,913 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4649:Cspg4
|
UTSW |
9 |
56,794,149 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4663:Cspg4
|
UTSW |
9 |
56,793,960 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4674:Cspg4
|
UTSW |
9 |
56,805,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4779:Cspg4
|
UTSW |
9 |
56,793,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R5021:Cspg4
|
UTSW |
9 |
56,805,014 (GRCm39) |
missense |
probably benign |
0.01 |
R5051:Cspg4
|
UTSW |
9 |
56,793,020 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5328:Cspg4
|
UTSW |
9 |
56,793,140 (GRCm39) |
missense |
probably benign |
0.01 |
R5394:Cspg4
|
UTSW |
9 |
56,797,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Cspg4
|
UTSW |
9 |
56,793,932 (GRCm39) |
missense |
probably benign |
0.00 |
R5682:Cspg4
|
UTSW |
9 |
56,793,480 (GRCm39) |
missense |
probably benign |
0.14 |
R5690:Cspg4
|
UTSW |
9 |
56,806,019 (GRCm39) |
missense |
probably benign |
0.01 |
R5715:Cspg4
|
UTSW |
9 |
56,798,335 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5717:Cspg4
|
UTSW |
9 |
56,793,082 (GRCm39) |
missense |
probably benign |
|
R5726:Cspg4
|
UTSW |
9 |
56,793,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Cspg4
|
UTSW |
9 |
56,792,506 (GRCm39) |
splice site |
probably null |
|
R6140:Cspg4
|
UTSW |
9 |
56,804,508 (GRCm39) |
missense |
probably benign |
0.35 |
R6147:Cspg4
|
UTSW |
9 |
56,796,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R6239:Cspg4
|
UTSW |
9 |
56,795,466 (GRCm39) |
missense |
probably benign |
0.04 |
R6343:Cspg4
|
UTSW |
9 |
56,799,976 (GRCm39) |
missense |
probably benign |
|
R6351:Cspg4
|
UTSW |
9 |
56,799,928 (GRCm39) |
missense |
probably benign |
0.00 |
R6564:Cspg4
|
UTSW |
9 |
56,797,442 (GRCm39) |
missense |
probably benign |
0.02 |
R6814:Cspg4
|
UTSW |
9 |
56,797,624 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6928:Cspg4
|
UTSW |
9 |
56,805,164 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6967:Cspg4
|
UTSW |
9 |
56,797,420 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6981:Cspg4
|
UTSW |
9 |
56,794,385 (GRCm39) |
missense |
probably benign |
0.00 |
R7033:Cspg4
|
UTSW |
9 |
56,795,358 (GRCm39) |
missense |
probably damaging |
0.96 |
R7419:Cspg4
|
UTSW |
9 |
56,795,727 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7809:Cspg4
|
UTSW |
9 |
56,797,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7940:Cspg4
|
UTSW |
9 |
56,795,381 (GRCm39) |
nonsense |
probably null |
|
R8078:Cspg4
|
UTSW |
9 |
56,797,543 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8082:Cspg4
|
UTSW |
9 |
56,793,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8217:Cspg4
|
UTSW |
9 |
56,797,637 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8237:Cspg4
|
UTSW |
9 |
56,799,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Cspg4
|
UTSW |
9 |
56,805,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Cspg4
|
UTSW |
9 |
56,794,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R8691:Cspg4
|
UTSW |
9 |
56,800,280 (GRCm39) |
missense |
probably benign |
|
R8720:Cspg4
|
UTSW |
9 |
56,794,797 (GRCm39) |
missense |
probably benign |
0.25 |
R8907:Cspg4
|
UTSW |
9 |
56,790,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R9063:Cspg4
|
UTSW |
9 |
56,795,687 (GRCm39) |
missense |
probably benign |
0.03 |
R9115:Cspg4
|
UTSW |
9 |
56,797,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R9152:Cspg4
|
UTSW |
9 |
56,795,463 (GRCm39) |
missense |
probably benign |
0.26 |
R9154:Cspg4
|
UTSW |
9 |
56,798,287 (GRCm39) |
missense |
|
|
R9361:Cspg4
|
UTSW |
9 |
56,803,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R9574:Cspg4
|
UTSW |
9 |
56,797,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Cspg4
|
UTSW |
9 |
56,792,836 (GRCm39) |
missense |
probably benign |
|
R9685:Cspg4
|
UTSW |
9 |
56,797,622 (GRCm39) |
missense |
probably benign |
0.05 |
X0065:Cspg4
|
UTSW |
9 |
56,793,020 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Cspg4
|
UTSW |
9 |
56,793,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TAGCTTACCGCCTCACTCAG -3'
(R):5'- TCCACAAGTTGGTTGCTCC -3'
Sequencing Primer
(F):5'- CCTGTATGGGCAGCTACTAGTAG -3'
(R):5'- ACAAGTTGGTTGCTCCTAGATTC -3'
|
Posted On |
2016-03-17 |