Incidental Mutation 'R4674:Cspg4'
| ID |
348715 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cspg4
|
| Ensembl Gene |
ENSMUSG00000032911 |
| Gene Name |
chondroitin sulfate proteoglycan 4 |
| Synonyms |
Cspg4a, AN2, NG2, 4732461B14Rik |
| MMRRC Submission |
041929-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4674 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
56772388-56807154 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 56805489 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 2100
(V2100A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000038909
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035661]
|
| AlphaFold |
Q8VHY0 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000035661
AA Change: V2100A
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000038909
Gene: ENSMUSG00000032911
AA Change: V2100A
| 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: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.6%
|
| 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: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb1b |
T |
C |
5: 8,860,615 (GRCm39) |
I112T |
probably benign |
Het |
| Acvr1b |
T |
C |
15: 101,100,939 (GRCm39) |
I367T |
possibly damaging |
Het |
| Akr1b8 |
G |
A |
6: 34,333,359 (GRCm39) |
|
probably null |
Het |
| Ash1l |
T |
C |
3: 88,979,783 (GRCm39) |
V2769A |
possibly damaging |
Het |
| Asxl3 |
A |
T |
18: 22,650,795 (GRCm39) |
D928V |
probably damaging |
Het |
| Atp1a4 |
A |
T |
1: 172,085,223 (GRCm39) |
V66E |
possibly damaging |
Het |
| Cald1 |
AAGAGAGAGAGAGAG |
AAGAGAGAGAGAG |
6: 34,723,108 (GRCm39) |
|
probably null |
Het |
| Cbx2 |
T |
A |
11: 118,919,935 (GRCm39) |
I500N |
probably damaging |
Het |
| Ccdc82 |
A |
T |
9: 13,252,260 (GRCm39) |
H184L |
probably benign |
Het |
| Cd84 |
A |
T |
1: 171,700,887 (GRCm39) |
H216L |
possibly damaging |
Het |
| Ceacam15 |
T |
C |
7: 16,407,410 (GRCm39) |
T36A |
probably benign |
Het |
| Cebpd |
A |
G |
16: 15,705,385 (GRCm39) |
D66G |
probably damaging |
Het |
| Clec1b |
C |
A |
6: 129,377,097 (GRCm39) |
L47I |
probably damaging |
Het |
| Cracr2b |
A |
G |
7: 141,043,451 (GRCm39) |
D43G |
probably damaging |
Het |
| Crbn |
T |
A |
6: 106,767,932 (GRCm39) |
Q173L |
possibly damaging |
Het |
| Cyp46a1 |
T |
C |
12: 108,324,345 (GRCm39) |
L374P |
probably damaging |
Het |
| Dhx16 |
T |
A |
17: 36,196,831 (GRCm39) |
V607E |
probably damaging |
Het |
| Dido1 |
A |
G |
2: 180,329,352 (GRCm39) |
S357P |
probably damaging |
Het |
| Dnah6 |
T |
A |
6: 73,169,405 (GRCm39) |
I399F |
probably benign |
Het |
| Dock10 |
T |
C |
1: 80,584,337 (GRCm39) |
E123G |
possibly damaging |
Het |
| Dstyk |
A |
G |
1: 132,391,128 (GRCm39) |
D843G |
probably benign |
Het |
| Efcab12 |
C |
A |
6: 115,800,610 (GRCm39) |
V138F |
probably damaging |
Het |
| Egf |
A |
G |
3: 129,511,689 (GRCm39) |
F493L |
probably damaging |
Het |
| Ephx1 |
A |
G |
1: 180,822,256 (GRCm39) |
F220S |
probably damaging |
Het |
| Exoc6 |
T |
C |
19: 37,597,530 (GRCm39) |
F644L |
probably damaging |
Het |
| F13b |
A |
G |
1: 139,429,542 (GRCm39) |
Y20C |
unknown |
Het |
| Fam184b |
T |
A |
5: 45,740,230 (GRCm39) |
K319* |
probably null |
Het |
| Flrt2 |
T |
A |
12: 95,747,462 (GRCm39) |
L600* |
probably null |
Het |
| Gbgt1 |
T |
C |
2: 28,388,453 (GRCm39) |
F46S |
possibly damaging |
Het |
| Gli2 |
T |
C |
1: 118,763,759 (GRCm39) |
E1464G |
probably damaging |
Het |
| Hdac9 |
A |
G |
12: 34,423,959 (GRCm39) |
V501A |
possibly damaging |
Het |
| Heca |
T |
C |
10: 17,791,057 (GRCm39) |
H333R |
probably benign |
Het |
| Hirip3 |
G |
A |
7: 126,463,834 (GRCm39) |
|
probably null |
Het |
| Igsf8 |
G |
A |
1: 172,146,479 (GRCm39) |
W51* |
probably null |
Het |
| Kif21a |
C |
A |
15: 90,824,748 (GRCm39) |
R1342L |
possibly damaging |
Het |
| Krt73 |
T |
C |
15: 101,710,510 (GRCm39) |
N75D |
probably benign |
Het |
| Macf1 |
T |
A |
4: 123,366,190 (GRCm39) |
Y1292F |
probably benign |
Het |
| Macroh2a1 |
A |
C |
13: 56,230,997 (GRCm39) |
C297G |
possibly damaging |
Het |
| Mapk14 |
A |
G |
17: 28,963,996 (GRCm39) |
|
probably null |
Het |
| Mgat5 |
T |
A |
1: 127,318,495 (GRCm39) |
V330D |
probably damaging |
Het |
| Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
| Naip1 |
A |
T |
13: 100,580,682 (GRCm39) |
F188L |
probably damaging |
Het |
| Ncoa3 |
T |
C |
2: 165,901,731 (GRCm39) |
S1035P |
probably benign |
Het |
| Ndn |
T |
A |
7: 61,998,570 (GRCm39) |
W139R |
probably damaging |
Het |
| Nes |
T |
C |
3: 87,879,102 (GRCm39) |
V198A |
possibly damaging |
Het |
| Or4c107 |
G |
T |
2: 88,789,216 (GRCm39) |
M135I |
probably damaging |
Het |
| Or4c35 |
A |
G |
2: 89,808,250 (GRCm39) |
I43V |
possibly damaging |
Het |
| Or51ab3 |
T |
G |
7: 103,201,183 (GRCm39) |
L64V |
probably damaging |
Het |
| Or52p1 |
T |
A |
7: 104,267,631 (GRCm39) |
C248* |
probably null |
Het |
| Or5b111 |
T |
A |
19: 13,291,178 (GRCm39) |
H157L |
probably benign |
Het |
| Or5p72 |
T |
C |
7: 108,022,309 (GRCm39) |
V177A |
possibly damaging |
Het |
| Pcf11 |
G |
A |
7: 92,308,985 (GRCm39) |
|
probably benign |
Het |
| Pde1a |
TCC |
TC |
2: 79,728,525 (GRCm39) |
|
probably benign |
Het |
| Pipox |
T |
G |
11: 77,784,596 (GRCm39) |
Q4P |
probably benign |
Het |
| Pla2g4c |
C |
T |
7: 13,077,439 (GRCm39) |
T327I |
probably null |
Het |
| Plppr1 |
C |
T |
4: 49,323,384 (GRCm39) |
R225W |
probably damaging |
Het |
| Pnpla6 |
T |
A |
8: 3,571,412 (GRCm39) |
V145D |
probably damaging |
Het |
| Pnpla7 |
T |
C |
2: 24,942,329 (GRCm39) |
Y83H |
probably damaging |
Het |
| Rif1 |
T |
A |
2: 51,996,954 (GRCm39) |
L970Q |
probably null |
Het |
| Rimklb |
C |
A |
6: 122,433,242 (GRCm39) |
E303* |
probably null |
Het |
| Rpl13a |
A |
T |
7: 44,776,242 (GRCm39) |
|
probably benign |
Het |
| Rttn |
T |
A |
18: 89,029,135 (GRCm39) |
|
probably null |
Het |
| Sf3b3 |
G |
A |
8: 111,571,137 (GRCm39) |
R10W |
probably damaging |
Het |
| Skint4 |
G |
A |
4: 111,975,430 (GRCm39) |
C130Y |
probably damaging |
Het |
| Snap91 |
A |
G |
9: 86,674,070 (GRCm39) |
S593P |
possibly damaging |
Het |
| Ssb |
A |
G |
2: 69,699,194 (GRCm39) |
Q209R |
probably benign |
Het |
| Stap1 |
A |
T |
5: 86,229,044 (GRCm39) |
I71L |
probably benign |
Het |
| Syna |
C |
A |
5: 134,587,209 (GRCm39) |
R580L |
probably damaging |
Het |
| Tacc2 |
T |
A |
7: 130,226,591 (GRCm39) |
M1111K |
possibly damaging |
Het |
| Tanc2 |
T |
C |
11: 105,758,306 (GRCm39) |
L689P |
probably damaging |
Het |
| Tasor2 |
T |
C |
13: 3,623,686 (GRCm39) |
E1406G |
possibly damaging |
Het |
| Tcstv7b |
T |
C |
13: 120,702,362 (GRCm39) |
W53R |
probably damaging |
Het |
| Tdrd5 |
A |
C |
1: 156,105,005 (GRCm39) |
C463W |
probably damaging |
Het |
| Tet1 |
A |
G |
10: 62,674,627 (GRCm39) |
F1150L |
probably damaging |
Het |
| Tia1 |
T |
A |
6: 86,397,382 (GRCm39) |
F118L |
probably damaging |
Het |
| Trav3-1 |
A |
T |
14: 52,818,460 (GRCm39) |
T45S |
possibly damaging |
Het |
| Uaca |
A |
T |
9: 60,761,711 (GRCm39) |
Y235F |
possibly damaging |
Het |
| Ube4b |
T |
C |
4: 149,415,827 (GRCm39) |
N44S |
possibly damaging |
Het |
| Vmn2r93 |
T |
A |
17: 18,525,255 (GRCm39) |
H304Q |
probably benign |
Het |
| Wdr18 |
A |
G |
10: 79,801,069 (GRCm39) |
I161V |
probably benign |
Het |
| Zfp112 |
A |
G |
7: 23,826,399 (GRCm39) |
H789R |
probably damaging |
Het |
| Zfp873 |
A |
G |
10: 81,895,814 (GRCm39) |
T182A |
possibly damaging |
Het |
| Zscan2 |
T |
A |
7: 80,525,150 (GRCm39) |
S290R |
probably damaging |
Het |
| Zup1 |
A |
T |
10: 33,824,980 (GRCm39) |
D167E |
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 |
|
R4779:Cspg4
|
UTSW |
9 |
56,793,092 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4884:Cspg4
|
UTSW |
9 |
56,805,353 (GRCm39) |
missense |
probably benign |
0.00 |
|
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'- TAAATGTCACAGTGCAGGCTC -3'
(R):5'- CTGTAGGATTTGGCCGCATG -3'
Sequencing Primer
(F):5'- ACAGTGCAGGCTCTGTTGC -3'
(R):5'- TCAGTGGCAAAGTCCAGC -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation