Incidental Mutation 'R7419:Cspg4'
ID |
575543 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cspg4
|
Ensembl Gene |
ENSMUSG00000032911 |
Gene Name |
chondroitin sulfate proteoglycan 4 |
Synonyms |
Cspg4a, AN2, NG2, 4732461B14Rik |
MMRRC Submission |
045497-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7419 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
9 |
Chromosomal Location |
56772388-56807154 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 56795727 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Glutamic Acid
at position 1154
(V1154E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000038909
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035661]
|
AlphaFold |
Q8VHY0 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000035661
AA Change: V1154E
PolyPhen 2
Score 0.941 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000038909 Gene: ENSMUSG00000032911 AA Change: V1154E
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
99% (93/94) |
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: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,226,959 (GRCm39) |
S572P |
probably damaging |
Het |
Abca13 |
T |
C |
11: 9,247,833 (GRCm39) |
Y2527H |
probably damaging |
Het |
Abcc5 |
A |
G |
16: 20,241,173 (GRCm39) |
I4T |
possibly damaging |
Het |
Adamts12 |
C |
T |
15: 11,317,365 (GRCm39) |
T1355I |
probably benign |
Het |
Aloxe3 |
A |
G |
11: 69,018,353 (GRCm39) |
T117A |
probably benign |
Het |
Asb15 |
A |
G |
6: 24,556,555 (GRCm39) |
I17V |
probably benign |
Het |
Atf2 |
A |
G |
2: 73,672,777 (GRCm39) |
V194A |
probably benign |
Het |
Capn7 |
T |
C |
14: 31,071,779 (GRCm39) |
V221A |
probably benign |
Het |
Ccdc107 |
A |
T |
4: 43,493,512 (GRCm39) |
S28C |
probably benign |
Het |
Cct4 |
C |
T |
11: 22,946,420 (GRCm39) |
T162I |
probably benign |
Het |
Cdc40 |
A |
T |
10: 40,717,439 (GRCm39) |
H417Q |
probably damaging |
Het |
Celf1 |
A |
G |
2: 90,833,588 (GRCm39) |
I115V |
probably benign |
Het |
Ces3a |
A |
G |
8: 105,783,056 (GRCm39) |
Y395C |
probably damaging |
Het |
Cfh |
C |
A |
1: 140,033,204 (GRCm39) |
C798F |
probably damaging |
Het |
Clstn3 |
T |
C |
6: 124,435,088 (GRCm39) |
T313A |
probably benign |
Het |
Crmp1 |
T |
A |
5: 37,436,229 (GRCm39) |
M329K |
probably benign |
Het |
Csf2ra |
C |
T |
19: 61,215,491 (GRCm39) |
A76T |
possibly damaging |
Het |
Cyp2a4 |
A |
T |
7: 26,014,188 (GRCm39) |
N455I |
probably benign |
Het |
Cyp4a32 |
T |
G |
4: 115,468,234 (GRCm39) |
M268R |
probably benign |
Het |
Dcaf13 |
T |
A |
15: 38,993,615 (GRCm39) |
I236N |
probably damaging |
Het |
Dennd2a |
A |
G |
6: 39,500,397 (GRCm39) |
I56T |
probably damaging |
Het |
Eif2d |
T |
A |
1: 131,098,793 (GRCm39) |
S530R |
probably benign |
Het |
Ep300 |
T |
A |
15: 81,532,715 (GRCm39) |
M1651K |
unknown |
Het |
Epha3 |
G |
A |
16: 63,418,657 (GRCm39) |
T596I |
probably damaging |
Het |
Fam171a2 |
C |
T |
11: 102,329,628 (GRCm39) |
C377Y |
possibly damaging |
Het |
Fat4 |
T |
A |
3: 39,054,385 (GRCm39) |
N4142K |
probably damaging |
Het |
Galnt5 |
C |
A |
2: 57,904,937 (GRCm39) |
S500Y |
probably damaging |
Het |
Gas6 |
A |
G |
8: 13,521,456 (GRCm39) |
V431A |
probably benign |
Het |
Gm7544 |
C |
T |
1: 82,933,502 (GRCm39) |
C56Y |
unknown |
Het |
Golgb1 |
T |
A |
16: 36,733,281 (GRCm39) |
L884I |
possibly damaging |
Het |
Gpatch2l |
T |
G |
12: 86,312,025 (GRCm39) |
|
probably null |
Het |
Gpr33 |
T |
C |
12: 52,070,050 (GRCm39) |
T330A |
probably benign |
Het |
H2bw2 |
G |
A |
X: 135,828,471 (GRCm39) |
R120K |
unknown |
Het |
Ifi205 |
A |
G |
1: 173,855,874 (GRCm39) |
M52T |
possibly damaging |
Het |
Ino80 |
A |
T |
2: 119,210,495 (GRCm39) |
D1346E |
probably benign |
Het |
Ino80c |
T |
C |
18: 24,241,836 (GRCm39) |
K183R |
unknown |
Het |
Itgal |
G |
T |
7: 126,906,047 (GRCm39) |
R379L |
probably benign |
Het |
Itih3 |
T |
A |
14: 30,636,730 (GRCm39) |
T582S |
probably benign |
Het |
Kcnb2 |
T |
C |
1: 15,781,251 (GRCm39) |
S708P |
possibly damaging |
Het |
Kcnt1 |
A |
T |
2: 25,806,011 (GRCm39) |
Y1200F |
probably benign |
Het |
L3mbtl4 |
G |
A |
17: 68,948,537 (GRCm39) |
D473N |
probably benign |
Het |
Lama1 |
T |
G |
17: 68,024,169 (GRCm39) |
I89R |
|
Het |
Lama2 |
A |
G |
10: 27,142,630 (GRCm39) |
I616T |
probably benign |
Het |
Lipm |
A |
C |
19: 34,093,881 (GRCm39) |
D266A |
probably benign |
Het |
Lrrc4c |
A |
T |
2: 97,460,106 (GRCm39) |
H244L |
probably benign |
Het |
Lrrtm3 |
T |
C |
10: 63,923,925 (GRCm39) |
E414G |
probably damaging |
Het |
Ltbp4 |
A |
G |
7: 27,029,192 (GRCm39) |
V231A |
unknown |
Het |
Me3 |
G |
T |
7: 89,385,927 (GRCm39) |
R92L |
probably damaging |
Het |
Mroh7 |
T |
G |
4: 106,541,115 (GRCm39) |
I1175L |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,553,258 (GRCm39) |
M4345T |
probably benign |
Het |
Mug2 |
A |
G |
6: 122,017,529 (GRCm39) |
Y422C |
possibly damaging |
Het |
N6amt1 |
T |
G |
16: 87,164,454 (GRCm39) |
S214A |
possibly damaging |
Het |
Ogfrl1 |
G |
A |
1: 23,422,063 (GRCm39) |
Q24* |
probably null |
Het |
Or12e14 |
A |
T |
2: 87,677,406 (GRCm39) |
T264S |
probably benign |
Het |
Or1ad6 |
T |
A |
11: 50,860,152 (GRCm39) |
Y102* |
probably null |
Het |
Or2ag2b |
T |
C |
7: 106,417,551 (GRCm39) |
L87P |
possibly damaging |
Het |
Or4f14 |
G |
A |
2: 111,742,435 (GRCm39) |
P280L |
probably damaging |
Het |
Or4k6 |
A |
C |
14: 50,475,448 (GRCm39) |
V298G |
possibly damaging |
Het |
Or4x13 |
A |
G |
2: 90,231,803 (GRCm39) |
D266G |
probably damaging |
Het |
Or6b6 |
A |
G |
7: 106,571,353 (GRCm39) |
M66T |
probably benign |
Het |
Or7g23 |
A |
C |
9: 19,086,642 (GRCm39) |
M110R |
possibly damaging |
Het |
Or8g23 |
T |
A |
9: 38,971,465 (GRCm39) |
I166L |
probably benign |
Het |
Or8k3 |
C |
T |
2: 86,058,557 (GRCm39) |
G253R |
probably damaging |
Het |
Oser1 |
A |
T |
2: 163,253,364 (GRCm39) |
D48E |
probably benign |
Het |
Piwil4 |
G |
A |
9: 14,613,691 (GRCm39) |
P867L |
probably damaging |
Het |
Pla2g6 |
C |
T |
15: 79,189,898 (GRCm39) |
|
probably null |
Het |
Plxna1 |
A |
G |
6: 89,334,584 (GRCm39) |
L15P |
unknown |
Het |
Ppan |
C |
T |
9: 20,803,140 (GRCm39) |
T404I |
probably benign |
Het |
Pros1 |
C |
A |
16: 62,748,433 (GRCm39) |
Y635* |
probably null |
Het |
Rabep2 |
G |
A |
7: 126,043,342 (GRCm39) |
R414Q |
probably benign |
Het |
Rbms3 |
T |
A |
9: 116,651,894 (GRCm39) |
E201V |
probably damaging |
Het |
Robo4 |
A |
C |
9: 37,314,105 (GRCm39) |
I119L |
probably benign |
Het |
S100b |
A |
T |
10: 76,095,820 (GRCm39) |
D66V |
probably damaging |
Het |
Serpina1f |
A |
G |
12: 103,656,101 (GRCm39) |
S376P |
probably damaging |
Het |
Slc24a4 |
T |
C |
12: 102,193,350 (GRCm39) |
|
probably null |
Het |
Slc30a6 |
T |
C |
17: 74,730,424 (GRCm39) |
V438A |
probably benign |
Het |
Sobp |
A |
G |
10: 42,897,804 (GRCm39) |
S594P |
probably benign |
Het |
Tcstv1b |
A |
G |
13: 120,634,994 (GRCm39) |
E92G |
probably damaging |
Het |
Tmem45b |
T |
C |
9: 31,339,334 (GRCm39) |
D213G |
probably benign |
Het |
Topbp1 |
T |
A |
9: 103,200,543 (GRCm39) |
D525E |
probably benign |
Het |
Trim30c |
G |
T |
7: 104,037,472 (GRCm39) |
L165I |
probably benign |
Het |
Unc13b |
A |
T |
4: 43,174,023 (GRCm39) |
D1617V |
unknown |
Het |
Ush1c |
A |
G |
7: 45,878,679 (GRCm39) |
L112P |
probably damaging |
Het |
Vipr1 |
T |
A |
9: 121,490,539 (GRCm39) |
I195N |
probably damaging |
Het |
Vmn2r38 |
A |
C |
7: 9,078,354 (GRCm39) |
V676G |
probably damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,307,992 (GRCm39) |
Y749N |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,842,073 (GRCm39) |
S2615R |
|
Het |
Whrn |
A |
G |
4: 63,334,330 (GRCm39) |
V828A |
possibly damaging |
Het |
Zbp1 |
A |
G |
2: 173,050,958 (GRCm39) |
V304A |
probably benign |
Het |
Zeb2 |
A |
T |
2: 44,886,359 (GRCm39) |
N899K |
probably benign |
Het |
Zfp148 |
T |
C |
16: 33,317,511 (GRCm39) |
S728P |
possibly damaging |
Het |
Zfp518a |
T |
A |
19: 40,902,207 (GRCm39) |
I712N |
possibly damaging |
Het |
Zfp683 |
T |
C |
4: 133,786,211 (GRCm39) |
V446A |
probably benign |
Het |
Zranb3 |
A |
T |
1: 127,891,588 (GRCm39) |
V796D |
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 |
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 |
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'- AAGTCCTGTTTGTGCACTCGG -3'
(R):5'- TTAGTGTGTACTGGCCCTGC -3'
Sequencing Primer
(F):5'- TTTGTGCACTCGGGGGCC -3'
(R):5'- AAACGCCAGGGTGTCTTG -3'
|
Posted On |
2019-10-07 |