Incidental Mutation 'R9605:Cspg4b'
| ID |
726457 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cspg4b
|
| Ensembl Gene |
ENSMUSG00000021763 |
| Gene Name |
chondroitin sulfate proteoglycan 4B |
| Synonyms |
BC067074 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.201)
|
| Stock # |
R9605 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
13 |
| Chromosomal Location |
113429570-113507049 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 113456503 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 850
(S850P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000119993
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000136755]
|
| AlphaFold |
F6RXI4 |
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000119993
Gene: ENSMUSG00000021763
AA Change: S850P
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
26 |
N/A |
INTRINSIC |
|
LamG
|
44 |
177 |
1.28e-20 |
SMART |
|
LamG
|
229 |
371 |
4.66e-14 |
SMART |
|
low complexity region
|
407 |
420 |
N/A |
INTRINSIC |
|
Pfam:Cadherin_3
|
492 |
644 |
2.1e-35 |
PFAM |
|
Pfam:Cadherin_3
|
647 |
759 |
1e-7 |
PFAM |
|
Pfam:Cadherin_3
|
741 |
873 |
1.2e-8 |
PFAM |
|
Pfam:Cadherin_3
|
861 |
989 |
4.1e-14 |
PFAM |
|
Pfam:Cadherin_3
|
958 |
1114 |
1.2e-20 |
PFAM |
|
Pfam:Cadherin_3
|
1117 |
1223 |
1.6e-10 |
PFAM |
|
Pfam:Cadherin_3
|
1212 |
1341 |
5.6e-12 |
PFAM |
|
Pfam:Cadherin_3
|
1347 |
1438 |
3.8e-8 |
PFAM |
|
Pfam:Cadherin_3
|
1419 |
1562 |
2.3e-45 |
PFAM |
|
Pfam:Cadherin_3
|
1576 |
1679 |
2.1e-9 |
PFAM |
|
low complexity region
|
1732 |
1740 |
N/A |
INTRINSIC |
|
Pfam:Cadherin_3
|
1773 |
1926 |
3e-35 |
PFAM |
|
transmembrane domain
|
2267 |
2289 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
|
| Allele List at MGI |
All alleles(2) : Targeted(2)
|
| Other mutations in this stock |
Total: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 6430548M08Rik |
G |
A |
8: 120,872,380 (GRCm39) |
V103I |
possibly damaging |
Het |
| Aatk |
T |
C |
11: 119,902,209 (GRCm39) |
E729G |
possibly damaging |
Het |
| Acaa2 |
A |
G |
18: 74,932,230 (GRCm39) |
T290A |
probably benign |
Het |
| Acaca |
C |
T |
11: 84,183,842 (GRCm39) |
T1240I |
probably benign |
Het |
| Adgre1 |
A |
G |
17: 57,718,083 (GRCm39) |
N365S |
probably benign |
Het |
| Adipor1 |
A |
G |
1: 134,352,553 (GRCm39) |
D108G |
probably damaging |
Het |
| Aebp2 |
A |
G |
6: 140,593,736 (GRCm39) |
Q462R |
probably damaging |
Het |
| Afg2a |
C |
T |
3: 37,505,930 (GRCm39) |
P670S |
probably damaging |
Het |
| Arhgef4 |
A |
G |
1: 34,761,745 (GRCm39) |
T334A |
unknown |
Het |
| Art5 |
T |
C |
7: 101,746,412 (GRCm39) |
E280G |
probably benign |
Het |
| Bloc1s3 |
A |
G |
7: 19,241,457 (GRCm39) |
S24P |
possibly damaging |
Het |
| C2 |
T |
A |
17: 35,081,958 (GRCm39) |
N720I |
possibly damaging |
Het |
| Caprin2 |
T |
C |
6: 148,744,332 (GRCm39) |
D1031G |
probably damaging |
Het |
| Catsper1 |
A |
G |
19: 5,387,785 (GRCm39) |
T355A |
probably benign |
Het |
| Cd19 |
T |
A |
7: 126,010,057 (GRCm39) |
E398D |
possibly damaging |
Het |
| Cdca8 |
T |
C |
4: 124,830,384 (GRCm39) |
E31G |
probably damaging |
Het |
| Ceacam5 |
G |
A |
7: 17,493,520 (GRCm39) |
V848M |
probably damaging |
Het |
| Chd8 |
A |
T |
14: 52,457,055 (GRCm39) |
L971Q |
probably damaging |
Het |
| Ciao1 |
G |
A |
2: 127,087,684 (GRCm39) |
T217I |
probably damaging |
Het |
| Cldn1 |
A |
T |
16: 26,181,924 (GRCm39) |
I95N |
probably damaging |
Het |
| Clip2 |
C |
T |
5: 134,533,616 (GRCm39) |
R487Q |
probably benign |
Het |
| Cluh |
C |
T |
11: 74,558,772 (GRCm39) |
R1253C |
possibly damaging |
Het |
| Cngb3 |
A |
T |
4: 19,505,187 (GRCm39) |
Q640L |
probably benign |
Het |
| Cyp2c40 |
A |
T |
19: 39,766,443 (GRCm39) |
V384D |
probably damaging |
Het |
| Cyp2d26 |
T |
A |
15: 82,674,672 (GRCm39) |
M437L |
probably benign |
Het |
| D430041D05Rik |
A |
G |
2: 104,087,189 (GRCm39) |
S596P |
probably benign |
Het |
| Dagla |
A |
T |
19: 10,233,053 (GRCm39) |
V448D |
probably damaging |
Het |
| Ddx59 |
A |
T |
1: 136,344,594 (GRCm39) |
E88D |
probably benign |
Het |
| Dock1 |
T |
A |
7: 134,384,141 (GRCm39) |
F671I |
possibly damaging |
Het |
| Dtna |
T |
A |
18: 23,764,454 (GRCm39) |
V541D |
probably damaging |
Het |
| Eef2k |
T |
C |
7: 120,491,170 (GRCm39) |
F552S |
probably damaging |
Het |
| Erbb2 |
T |
C |
11: 98,311,746 (GRCm39) |
V94A |
possibly damaging |
Het |
| Etl4 |
A |
T |
2: 20,771,345 (GRCm39) |
I607F |
possibly damaging |
Het |
| Ets2 |
G |
T |
16: 95,516,121 (GRCm39) |
E234* |
probably null |
Het |
| Fbp1 |
A |
C |
13: 63,019,023 (GRCm39) |
V175G |
probably damaging |
Het |
| Fmn2 |
C |
T |
1: 174,436,194 (GRCm39) |
Q722* |
probably null |
Het |
| Fnip1 |
G |
T |
11: 54,381,713 (GRCm39) |
R288L |
probably benign |
Het |
| Ghr |
G |
A |
15: 3,362,993 (GRCm39) |
P160S |
probably damaging |
Het |
| Glipr1 |
A |
G |
10: 111,832,801 (GRCm39) |
S46P |
probably damaging |
Het |
| Kif19b |
A |
T |
5: 140,455,461 (GRCm39) |
T356S |
probably benign |
Het |
| Kif9 |
G |
A |
9: 110,346,710 (GRCm39) |
R616H |
probably benign |
Het |
| Krt87 |
G |
T |
15: 101,336,484 (GRCm39) |
C56* |
probably null |
Het |
| Ldlr |
A |
G |
9: 21,646,626 (GRCm39) |
D264G |
probably damaging |
Het |
| Lrrk2 |
A |
T |
15: 91,621,420 (GRCm39) |
D998V |
probably benign |
Het |
| Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
| Mrc1 |
A |
G |
2: 14,324,110 (GRCm39) |
N1149S |
probably benign |
Het |
| Myo1c |
T |
A |
11: 75,559,899 (GRCm39) |
V661E |
probably benign |
Het |
| N4bp2 |
T |
C |
5: 65,963,879 (GRCm39) |
S643P |
probably benign |
Het |
| Nbl1 |
T |
A |
4: 138,812,608 (GRCm39) |
T75S |
probably benign |
Het |
| Ndn |
C |
T |
7: 61,998,337 (GRCm39) |
P61L |
possibly damaging |
Het |
| Nqo2 |
T |
A |
13: 34,156,361 (GRCm39) |
V25E |
possibly damaging |
Het |
| Oma1 |
G |
T |
4: 103,210,726 (GRCm39) |
V411L |
possibly damaging |
Het |
| Or12e13 |
T |
G |
2: 87,663,478 (GRCm39) |
F32V |
probably benign |
Het |
| Or5v1 |
T |
A |
17: 37,810,331 (GRCm39) |
I263N |
probably damaging |
Het |
| Or8b12i |
A |
G |
9: 20,082,093 (GRCm39) |
V258A |
probably damaging |
Het |
| Osgin2 |
G |
T |
4: 15,998,427 (GRCm39) |
H398Q |
probably damaging |
Het |
| Pepd |
A |
C |
7: 34,743,218 (GRCm39) |
D419A |
probably benign |
Het |
| Pikfyve |
A |
T |
1: 65,303,561 (GRCm39) |
S1694C |
probably benign |
Het |
| Pirb |
G |
A |
7: 3,720,617 (GRCm39) |
R294C |
possibly damaging |
Het |
| Plec |
A |
T |
15: 76,065,213 (GRCm39) |
L1619Q |
unknown |
Het |
| Polq |
A |
G |
16: 36,843,173 (GRCm39) |
I236V |
probably benign |
Het |
| Pphln1-ps1 |
A |
G |
16: 13,495,087 (GRCm39) |
D62G |
probably benign |
Het |
| Prkag3 |
T |
G |
1: 74,786,378 (GRCm39) |
Q189P |
probably damaging |
Het |
| Prkcg |
A |
T |
7: 3,359,360 (GRCm39) |
M136L |
probably benign |
Het |
| Ptprn2 |
T |
C |
12: 117,125,278 (GRCm39) |
L604P |
probably benign |
Het |
| Rab6b |
A |
T |
9: 103,017,601 (GRCm39) |
T31S |
probably benign |
Het |
| Rnf213 |
A |
G |
11: 119,359,879 (GRCm39) |
N4424S |
|
Het |
| Ryr3 |
A |
T |
2: 112,491,966 (GRCm39) |
L3795Q |
probably damaging |
Het |
| Scg2 |
A |
G |
1: 79,412,936 (GRCm39) |
Y556H |
probably damaging |
Het |
| Serpina3j |
A |
G |
12: 104,286,093 (GRCm39) |
N416S |
probably damaging |
Het |
| Sik3 |
T |
A |
9: 46,120,117 (GRCm39) |
H735Q |
probably benign |
Het |
| Slain1 |
A |
C |
14: 103,902,112 (GRCm39) |
T60P |
|
Het |
| Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
| Slc46a2 |
A |
T |
4: 59,914,056 (GRCm39) |
V289E |
probably damaging |
Het |
| Sorcs3 |
A |
T |
19: 48,711,364 (GRCm39) |
Y643F |
probably damaging |
Het |
| Sox30 |
A |
G |
11: 45,875,640 (GRCm39) |
N464S |
possibly damaging |
Het |
| Spta1 |
A |
G |
1: 174,035,880 (GRCm39) |
Y1062C |
probably damaging |
Het |
| Srrm3 |
A |
G |
5: 135,881,105 (GRCm39) |
D135G |
probably damaging |
Het |
| Stat5b |
T |
A |
11: 100,699,276 (GRCm39) |
H25L |
possibly damaging |
Het |
| Synj2 |
A |
G |
17: 6,063,794 (GRCm39) |
I513V |
probably benign |
Het |
| Syt11 |
T |
A |
3: 88,669,325 (GRCm39) |
Q189L |
probably benign |
Het |
| Tbc1d1 |
G |
A |
5: 64,443,350 (GRCm39) |
R523Q |
probably damaging |
Het |
| Traf3ip2 |
T |
A |
10: 39,521,772 (GRCm39) |
D443E |
probably benign |
Het |
| Traf6 |
G |
T |
2: 101,524,625 (GRCm39) |
C235F |
probably damaging |
Het |
| Treh |
A |
G |
9: 44,592,416 (GRCm39) |
D47G |
probably damaging |
Het |
| Trpc4 |
C |
A |
3: 54,225,550 (GRCm39) |
H966Q |
probably benign |
Het |
| Ttbk1 |
A |
T |
17: 46,784,516 (GRCm39) |
D316E |
possibly damaging |
Het |
| Txndc16 |
A |
T |
14: 45,442,799 (GRCm39) |
F132Y |
probably damaging |
Het |
| Uggt1 |
A |
T |
1: 36,273,886 (GRCm39) |
|
probably null |
Het |
| Usp25 |
A |
T |
16: 76,874,046 (GRCm39) |
I541F |
probably damaging |
Het |
| Xirp1 |
A |
T |
9: 119,847,274 (GRCm39) |
D536E |
possibly damaging |
Het |
| Zfp51 |
A |
G |
17: 21,684,291 (GRCm39) |
E302G |
probably damaging |
Het |
| Zfp648 |
A |
T |
1: 154,080,110 (GRCm39) |
T90S |
probably benign |
Het |
| Zfp84 |
A |
G |
7: 29,476,264 (GRCm39) |
T319A |
possibly damaging |
Het |
|
| Other mutations in Cspg4b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01723:Cspg4b
|
APN |
13 |
113,504,091 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL03023:Cspg4b
|
APN |
13 |
113,488,275 (GRCm39) |
missense |
probably benign |
0.03 |
|
cumpleanos
|
UTSW |
13 |
113,504,870 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
Sorpresa
|
UTSW |
13 |
113,454,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|
P0018:Cspg4b
|
UTSW |
13 |
113,504,040 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R0003:Cspg4b
|
UTSW |
13 |
113,505,310 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0016:Cspg4b
|
UTSW |
13 |
113,502,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0016:Cspg4b
|
UTSW |
13 |
113,502,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0053:Cspg4b
|
UTSW |
13 |
113,505,023 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0053:Cspg4b
|
UTSW |
13 |
113,505,023 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0158:Cspg4b
|
UTSW |
13 |
113,505,687 (GRCm39) |
nonsense |
probably null |
|
|
R0281:Cspg4b
|
UTSW |
13 |
113,505,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1212:Cspg4b
|
UTSW |
13 |
113,505,951 (GRCm39) |
intron |
probably benign |
|
|
R1300:Cspg4b
|
UTSW |
13 |
113,502,694 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1434:Cspg4b
|
UTSW |
13 |
113,505,026 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R1509:Cspg4b
|
UTSW |
13 |
113,504,790 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1738:Cspg4b
|
UTSW |
13 |
113,504,034 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R1758:Cspg4b
|
UTSW |
13 |
113,505,266 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1828:Cspg4b
|
UTSW |
13 |
113,505,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2061:Cspg4b
|
UTSW |
13 |
113,454,628 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2570:Cspg4b
|
UTSW |
13 |
113,455,121 (GRCm39) |
missense |
probably benign |
0.34 |
|
R2884:Cspg4b
|
UTSW |
13 |
113,457,216 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2884:Cspg4b
|
UTSW |
13 |
113,505,725 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3004:Cspg4b
|
UTSW |
13 |
113,502,688 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3150:Cspg4b
|
UTSW |
13 |
113,488,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3773:Cspg4b
|
UTSW |
13 |
113,454,743 (GRCm39) |
missense |
probably benign |
0.12 |
|
R3864:Cspg4b
|
UTSW |
13 |
113,459,485 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R3971:Cspg4b
|
UTSW |
13 |
113,453,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4004:Cspg4b
|
UTSW |
13 |
113,454,914 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4271:Cspg4b
|
UTSW |
13 |
113,478,904 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R4382:Cspg4b
|
UTSW |
13 |
113,459,288 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4484:Cspg4b
|
UTSW |
13 |
113,455,733 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4570:Cspg4b
|
UTSW |
13 |
113,454,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4600:Cspg4b
|
UTSW |
13 |
113,455,783 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4622:Cspg4b
|
UTSW |
13 |
113,456,615 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4676:Cspg4b
|
UTSW |
13 |
113,505,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4676:Cspg4b
|
UTSW |
13 |
113,505,341 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4677:Cspg4b
|
UTSW |
13 |
113,516,020 (GRCm39) |
missense |
unknown |
|
|
R4775:Cspg4b
|
UTSW |
13 |
113,454,229 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4779:Cspg4b
|
UTSW |
13 |
113,504,870 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R4780:Cspg4b
|
UTSW |
13 |
113,454,392 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4829:Cspg4b
|
UTSW |
13 |
113,504,696 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4841:Cspg4b
|
UTSW |
13 |
113,502,724 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4879:Cspg4b
|
UTSW |
13 |
113,456,321 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4930:Cspg4b
|
UTSW |
13 |
113,464,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4934:Cspg4b
|
UTSW |
13 |
113,504,882 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4987:Cspg4b
|
UTSW |
13 |
113,454,635 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5065:Cspg4b
|
UTSW |
13 |
113,457,453 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5216:Cspg4b
|
UTSW |
13 |
113,478,947 (GRCm39) |
missense |
probably benign |
0.20 |
|
R5236:Cspg4b
|
UTSW |
13 |
113,502,754 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5247:Cspg4b
|
UTSW |
13 |
113,455,993 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5250:Cspg4b
|
UTSW |
13 |
113,456,305 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5337:Cspg4b
|
UTSW |
13 |
113,455,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5342:Cspg4b
|
UTSW |
13 |
113,502,803 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5426:Cspg4b
|
UTSW |
13 |
113,505,587 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5472:Cspg4b
|
UTSW |
13 |
113,455,703 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5526:Cspg4b
|
UTSW |
13 |
113,504,427 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5543:Cspg4b
|
UTSW |
13 |
113,457,407 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5589:Cspg4b
|
UTSW |
13 |
113,454,484 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5623:Cspg4b
|
UTSW |
13 |
113,483,168 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5668:Cspg4b
|
UTSW |
13 |
113,453,701 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R5793:Cspg4b
|
UTSW |
13 |
113,457,556 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R5824:Cspg4b
|
UTSW |
13 |
113,505,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6038:Cspg4b
|
UTSW |
13 |
113,455,153 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R6038:Cspg4b
|
UTSW |
13 |
113,455,153 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R6053:Cspg4b
|
UTSW |
13 |
113,457,260 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R6125:Cspg4b
|
UTSW |
13 |
113,454,217 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6129:Cspg4b
|
UTSW |
13 |
113,505,340 (GRCm39) |
nonsense |
probably null |
|
|
R6290:Cspg4b
|
UTSW |
13 |
113,456,492 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6291:Cspg4b
|
UTSW |
13 |
113,456,981 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6302:Cspg4b
|
UTSW |
13 |
113,504,646 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6317:Cspg4b
|
UTSW |
13 |
113,504,802 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6395:Cspg4b
|
UTSW |
13 |
113,506,003 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6673:Cspg4b
|
UTSW |
13 |
113,504,366 (GRCm39) |
nonsense |
probably null |
|
|
R6783:Cspg4b
|
UTSW |
13 |
113,456,743 (GRCm39) |
nonsense |
probably null |
|
|
R6800:Cspg4b
|
UTSW |
13 |
113,504,686 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6857:Cspg4b
|
UTSW |
13 |
113,456,492 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6889:Cspg4b
|
UTSW |
13 |
113,454,912 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6934:Cspg4b
|
UTSW |
13 |
113,505,800 (GRCm39) |
missense |
probably benign |
|
|
R7019:Cspg4b
|
UTSW |
13 |
113,488,284 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7100:Cspg4b
|
UTSW |
13 |
113,455,501 (GRCm39) |
missense |
|
|
|
R7115:Cspg4b
|
UTSW |
13 |
113,457,310 (GRCm39) |
missense |
|
|
|
R7152:Cspg4b
|
UTSW |
13 |
113,455,384 (GRCm39) |
missense |
|
|
|
R7195:Cspg4b
|
UTSW |
13 |
113,504,463 (GRCm39) |
missense |
|
|
|
R7213:Cspg4b
|
UTSW |
13 |
113,454,475 (GRCm39) |
missense |
|
|
|
R7250:Cspg4b
|
UTSW |
13 |
113,455,349 (GRCm39) |
missense |
|
|
|
R7341:Cspg4b
|
UTSW |
13 |
113,454,706 (GRCm39) |
missense |
|
|
|
R7358:Cspg4b
|
UTSW |
13 |
113,456,501 (GRCm39) |
missense |
|
|
|
R7359:Cspg4b
|
UTSW |
13 |
113,478,964 (GRCm39) |
missense |
|
|
|
R7396:Cspg4b
|
UTSW |
13 |
113,455,524 (GRCm39) |
missense |
|
|
|
R7632:Cspg4b
|
UTSW |
13 |
113,457,420 (GRCm39) |
missense |
|
|
|
R7689:Cspg4b
|
UTSW |
13 |
113,515,948 (GRCm39) |
missense |
|
|
|
R7713:Cspg4b
|
UTSW |
13 |
113,483,075 (GRCm39) |
missense |
|
|
|
R7892:Cspg4b
|
UTSW |
13 |
113,456,140 (GRCm39) |
missense |
|
|
|
R7975:Cspg4b
|
UTSW |
13 |
113,455,841 (GRCm39) |
missense |
|
|
|
R8017:Cspg4b
|
UTSW |
13 |
113,456,157 (GRCm39) |
missense |
|
|
|
R8019:Cspg4b
|
UTSW |
13 |
113,456,157 (GRCm39) |
missense |
|
|
|
R8034:Cspg4b
|
UTSW |
13 |
113,479,045 (GRCm39) |
missense |
|
|
|
R8101:Cspg4b
|
UTSW |
13 |
113,457,425 (GRCm39) |
missense |
|
|
|
R8104:Cspg4b
|
UTSW |
13 |
113,456,263 (GRCm39) |
missense |
|
|
|
R8122:Cspg4b
|
UTSW |
13 |
113,455,442 (GRCm39) |
missense |
|
|
|
R8126:Cspg4b
|
UTSW |
13 |
113,504,697 (GRCm39) |
missense |
|
|
|
R8272:Cspg4b
|
UTSW |
13 |
113,504,889 (GRCm39) |
missense |
|
|
|
R8679:Cspg4b
|
UTSW |
13 |
113,488,163 (GRCm39) |
missense |
|
|
|
R8973:Cspg4b
|
UTSW |
13 |
113,456,293 (GRCm39) |
missense |
|
|
|
R9123:Cspg4b
|
UTSW |
13 |
113,505,374 (GRCm39) |
missense |
|
|
|
R9125:Cspg4b
|
UTSW |
13 |
113,505,374 (GRCm39) |
missense |
|
|
|
R9182:Cspg4b
|
UTSW |
13 |
113,457,358 (GRCm39) |
missense |
|
|
|
R9233:Cspg4b
|
UTSW |
13 |
113,502,754 (GRCm39) |
missense |
|
|
|
R9264:Cspg4b
|
UTSW |
13 |
113,456,014 (GRCm39) |
missense |
|
|
|
R9306:Cspg4b
|
UTSW |
13 |
113,506,010 (GRCm39) |
missense |
unknown |
|
|
R9327:Cspg4b
|
UTSW |
13 |
113,453,710 (GRCm39) |
missense |
|
|
|
R9411:Cspg4b
|
UTSW |
13 |
113,504,767 (GRCm39) |
missense |
|
|
|
R9516:Cspg4b
|
UTSW |
13 |
113,455,649 (GRCm39) |
missense |
|
|
|
R9562:Cspg4b
|
UTSW |
13 |
113,504,574 (GRCm39) |
missense |
|
|
|
| Predicted Primers |
PCR Primer
(F):5'- AACAAGAAAGTATTGGATTCTGGCC -3'
(R):5'- ATGCTGAGGACTCTTGGTGAC -3'
Sequencing Primer
(F):5'- AAAGTATTGGATTCTGGCCATCTGC -3'
(R):5'- GGAAGACATGATTATCCAGTGTTTG -3'
|
| Posted On |
2022-10-06 |
Incidental Mutation