Incidental Mutation 'R9653:Clasp2'
| ID |
727204 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Clasp2
|
| Ensembl Gene |
ENSMUSG00000033392 |
| Gene Name |
CLIP associating protein 2 |
| Synonyms |
CLASP2alpha, 1500004F14Rik, CLASP2gamma, CLASP2, CLASP2beta, 8030404L10Rik |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R9653 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
113570541-113748750 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 113670993 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Arginine
at position 365
(W365R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150741
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000111838]
[ENSMUST00000163895]
[ENSMUST00000166734]
[ENSMUST00000213663]
[ENSMUST00000214522]
[ENSMUST00000215022]
[ENSMUST00000216817]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111838
|
| SMART Domains |
Protein: ENSMUSP00000107469
Gene: ENSMUSG00000033392
| Domain | Start | End | E-Value | Type |
|---|
|
TOG
|
90 |
323 |
1.17e-8 |
SMART |
|
low complexity region
|
382 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
459 |
472 |
N/A |
INTRINSIC |
|
low complexity region
|
473 |
484 |
N/A |
INTRINSIC |
|
low complexity region
|
562 |
572 |
N/A |
INTRINSIC |
|
low complexity region
|
614 |
634 |
N/A |
INTRINSIC |
|
TOG
|
640 |
877 |
2.03e-1 |
SMART |
|
low complexity region
|
995 |
1009 |
N/A |
INTRINSIC |
|
TOG
|
1043 |
1274 |
1.49e-24 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000163895
|
| SMART Domains |
Protein: ENSMUSP00000128460
Gene: ENSMUSG00000033392
| Domain | Start | End | E-Value | Type |
|---|
|
TOG
|
90 |
323 |
1.17e-8 |
SMART |
|
low complexity region
|
382 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
459 |
472 |
N/A |
INTRINSIC |
|
low complexity region
|
473 |
484 |
N/A |
INTRINSIC |
|
low complexity region
|
583 |
593 |
N/A |
INTRINSIC |
|
low complexity region
|
635 |
655 |
N/A |
INTRINSIC |
|
TOG
|
661 |
898 |
2.03e-1 |
SMART |
|
low complexity region
|
1016 |
1030 |
N/A |
INTRINSIC |
|
TOG
|
1064 |
1295 |
1.49e-24 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000166734
|
| SMART Domains |
Protein: ENSMUSP00000130201
Gene: ENSMUSG00000033392
| Domain | Start | End | E-Value | Type |
|---|
|
TOG
|
90 |
323 |
1.17e-8 |
SMART |
|
low complexity region
|
382 |
395 |
N/A |
INTRINSIC |
|
low complexity region
|
459 |
472 |
N/A |
INTRINSIC |
|
low complexity region
|
473 |
484 |
N/A |
INTRINSIC |
|
low complexity region
|
562 |
572 |
N/A |
INTRINSIC |
|
low complexity region
|
614 |
634 |
N/A |
INTRINSIC |
|
TOG
|
640 |
878 |
7.51e-1 |
SMART |
|
low complexity region
|
996 |
1010 |
N/A |
INTRINSIC |
|
TOG
|
1044 |
1275 |
1.49e-24 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213663
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214522
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215022
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216817
AA Change: W365R
PolyPhen 2
Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Targeted deletion of this gene leads to impaired formation of stable microtubules in a wound healing assay, and results in a 2-fold reduction of directionally persistent migration in mutant embryonic fibroblasts. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 89 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
C |
T |
11: 9,243,741 (GRCm39) |
P1868L |
probably benign |
Het |
| Abcc1 |
T |
C |
16: 14,214,257 (GRCm39) |
Y191H |
probably damaging |
Het |
| Adamtsl5 |
C |
T |
10: 80,180,763 (GRCm39) |
G100R |
probably damaging |
Het |
| Adgrg5 |
C |
T |
8: 95,663,864 (GRCm39) |
P235S |
|
Het |
| Anks1b |
T |
G |
10: 90,346,524 (GRCm39) |
L608R |
probably damaging |
Het |
| Ano10 |
C |
G |
9: 122,080,221 (GRCm39) |
A597P |
possibly damaging |
Het |
| Calb2 |
T |
C |
8: 110,881,374 (GRCm39) |
M58V |
probably benign |
Het |
| Ccdc180 |
T |
C |
4: 45,923,495 (GRCm39) |
I1092T |
probably damaging |
Het |
| Ces3b |
G |
T |
8: 105,812,257 (GRCm39) |
A169S |
probably damaging |
Het |
| Chmp2a |
A |
T |
7: 12,766,456 (GRCm39) |
F129I |
probably damaging |
Het |
| Col12a1 |
T |
C |
9: 79,584,556 (GRCm39) |
K1344R |
probably benign |
Het |
| Col3a1 |
A |
G |
1: 45,360,728 (GRCm39) |
I53V |
unknown |
Het |
| Coro2b |
T |
C |
9: 62,335,259 (GRCm39) |
Y309C |
probably damaging |
Het |
| Cramp1 |
C |
A |
17: 25,201,783 (GRCm39) |
K566N |
probably damaging |
Het |
| Crygs |
T |
A |
16: 22,625,304 (GRCm39) |
T46S |
probably benign |
Het |
| Ctbp2 |
C |
G |
7: 132,615,933 (GRCm39) |
R334P |
probably damaging |
Het |
| Dcstamp |
A |
T |
15: 39,623,792 (GRCm39) |
D469V |
probably benign |
Het |
| Dhdh |
T |
C |
7: 45,128,551 (GRCm39) |
D209G |
probably damaging |
Het |
| Dnah7b |
T |
C |
1: 46,252,544 (GRCm39) |
V1742A |
possibly damaging |
Het |
| Dnaja2 |
T |
C |
8: 86,265,982 (GRCm39) |
T368A |
probably benign |
Het |
| Dscaml1 |
T |
C |
9: 45,643,466 (GRCm39) |
|
probably null |
Het |
| Eps8l1 |
A |
T |
7: 4,481,886 (GRCm39) |
K704M |
unknown |
Het |
| Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
| Fgd4 |
T |
A |
16: 16,254,461 (GRCm39) |
H524L |
probably benign |
Het |
| Fktn |
T |
A |
4: 53,731,273 (GRCm39) |
F103I |
probably benign |
Het |
| Gcc2 |
T |
C |
10: 58,110,822 (GRCm39) |
M1001T |
possibly damaging |
Het |
| Gm4847 |
T |
C |
1: 166,467,582 (GRCm39) |
S205G |
possibly damaging |
Het |
| Grid2 |
A |
T |
6: 63,907,968 (GRCm39) |
N203Y |
possibly damaging |
Het |
| Hif3a |
G |
A |
7: 16,782,641 (GRCm39) |
A308V |
probably damaging |
Het |
| Htr5a |
A |
G |
5: 28,047,838 (GRCm39) |
N131S |
possibly damaging |
Het |
| Igfn1 |
G |
A |
1: 135,883,323 (GRCm39) |
Q2728* |
probably null |
Het |
| Ighv5-16 |
C |
A |
12: 113,802,313 (GRCm39) |
K62N |
possibly damaging |
Het |
| Ip6k3 |
A |
T |
17: 27,367,588 (GRCm39) |
Y203N |
possibly damaging |
Het |
| Itga2 |
G |
A |
13: 115,020,991 (GRCm39) |
P120L |
probably benign |
Het |
| Itpkb |
G |
T |
1: 180,160,056 (GRCm39) |
E61* |
probably null |
Het |
| Kcnj3 |
G |
A |
2: 55,484,864 (GRCm39) |
V321M |
probably damaging |
Het |
| Kmt2c |
A |
G |
5: 25,507,819 (GRCm39) |
L3206P |
probably damaging |
Het |
| Krtap5-4 |
T |
C |
7: 141,857,908 (GRCm39) |
C193R |
unknown |
Het |
| Large1 |
G |
T |
8: 73,564,106 (GRCm39) |
H553Q |
probably benign |
Het |
| Lrfn5 |
T |
A |
12: 61,890,418 (GRCm39) |
V569D |
probably damaging |
Het |
| Luzp2 |
A |
G |
7: 54,702,580 (GRCm39) |
T48A |
probably damaging |
Het |
| Lypd6 |
A |
T |
2: 50,080,758 (GRCm39) |
T149S |
probably benign |
Het |
| Map3k1 |
T |
C |
13: 111,890,296 (GRCm39) |
N1301S |
possibly damaging |
Het |
| Ndufv2 |
C |
T |
17: 66,396,251 (GRCm39) |
W91* |
probably null |
Het |
| Nisch |
A |
T |
14: 30,893,628 (GRCm39) |
V1315E |
probably damaging |
Het |
| Npas1 |
T |
C |
7: 16,190,146 (GRCm39) |
I467V |
probably benign |
Het |
| Nucb1 |
A |
G |
7: 45,144,202 (GRCm39) |
M337T |
probably benign |
Het |
| Oog3 |
T |
G |
4: 143,884,489 (GRCm39) |
R482S |
probably benign |
Het |
| Or10d4b |
T |
C |
9: 39,535,154 (GRCm39) |
L243P |
probably damaging |
Het |
| Or4f14c |
A |
T |
2: 111,941,261 (GRCm39) |
M112K |
probably damaging |
Het |
| Or51ag1 |
C |
T |
7: 103,155,727 (GRCm39) |
R142H |
probably benign |
Het |
| Or56a42-ps1 |
A |
T |
7: 104,775,985 (GRCm39) |
N164K |
probably benign |
Het |
| Padi2 |
T |
C |
4: 140,662,036 (GRCm39) |
|
probably null |
Het |
| Pam |
C |
T |
1: 97,768,469 (GRCm39) |
V660M |
possibly damaging |
Het |
| Phc2 |
C |
T |
4: 128,641,012 (GRCm39) |
L700F |
probably damaging |
Het |
| Plekha1 |
T |
C |
7: 130,479,494 (GRCm39) |
V4A |
possibly damaging |
Het |
| Rai1 |
A |
G |
11: 60,080,142 (GRCm39) |
E1402G |
probably benign |
Het |
| Recql5 |
G |
A |
11: 115,788,032 (GRCm39) |
A429V |
probably benign |
Het |
| Rere |
A |
G |
4: 150,516,010 (GRCm39) |
N101S |
probably benign |
Het |
| Robo1 |
T |
G |
16: 72,821,330 (GRCm39) |
S1357A |
possibly damaging |
Het |
| Rsl1 |
T |
A |
13: 67,330,106 (GRCm39) |
Y185N |
probably damaging |
Het |
| Rsph3a |
T |
C |
17: 8,165,074 (GRCm39) |
S145P |
possibly damaging |
Het |
| Sall1 |
T |
C |
8: 89,757,506 (GRCm39) |
E866G |
probably damaging |
Het |
| Sall3 |
A |
T |
18: 81,016,228 (GRCm39) |
S567T |
probably benign |
Het |
| Sap30 |
G |
A |
8: 57,938,156 (GRCm39) |
Q154* |
probably null |
Het |
| Sbf2 |
T |
C |
7: 110,040,702 (GRCm39) |
Q375R |
possibly damaging |
Het |
| Scn8a |
A |
G |
15: 100,937,947 (GRCm39) |
E1772G |
probably damaging |
Het |
| Scube3 |
C |
T |
17: 28,375,772 (GRCm39) |
A169V |
probably damaging |
Het |
| Sema6c |
T |
C |
3: 95,080,525 (GRCm39) |
S940P |
probably benign |
Het |
| Sertad4 |
C |
T |
1: 192,528,836 (GRCm39) |
D327N |
probably damaging |
Het |
| Shisal2b |
A |
G |
13: 105,000,296 (GRCm39) |
|
probably benign |
Het |
| Skp1 |
A |
G |
11: 52,134,514 (GRCm39) |
T82A |
possibly damaging |
Het |
| Slc39a14 |
G |
T |
14: 70,547,248 (GRCm39) |
T366K |
probably damaging |
Het |
| Snrnp200 |
G |
T |
2: 127,067,959 (GRCm39) |
V819L |
probably damaging |
Het |
| Sntg1 |
T |
A |
1: 8,433,749 (GRCm39) |
T501S |
unknown |
Het |
| Srsf12 |
T |
C |
4: 33,231,249 (GRCm39) |
S253P |
possibly damaging |
Het |
| Sycp2l |
A |
G |
13: 41,295,381 (GRCm39) |
S315G |
probably benign |
Het |
| Tars2 |
T |
C |
3: 95,655,379 (GRCm39) |
Y337C |
probably damaging |
Het |
| Thbs4 |
T |
C |
13: 92,898,022 (GRCm39) |
D599G |
probably benign |
Het |
| Tmem200c |
A |
G |
17: 69,149,181 (GRCm39) |
H588R |
probably benign |
Het |
| Tmem255b |
T |
A |
8: 13,506,005 (GRCm39) |
V204E |
probably damaging |
Het |
| Usp24 |
T |
A |
4: 106,204,564 (GRCm39) |
M261K |
probably benign |
Het |
| Utrn |
T |
A |
10: 12,497,123 (GRCm39) |
I2429F |
probably benign |
Het |
| Utrn |
C |
T |
10: 12,539,189 (GRCm39) |
A1943T |
probably benign |
Het |
| Vmn2r85 |
A |
T |
10: 130,261,694 (GRCm39) |
D214E |
probably damaging |
Het |
| Wdr81 |
G |
T |
11: 75,340,213 (GRCm39) |
P183T |
|
Het |
| Zfp28 |
G |
A |
7: 6,395,623 (GRCm39) |
R134H |
|
Het |
| Zfp532 |
T |
A |
18: 65,756,308 (GRCm39) |
D80E |
possibly damaging |
Het |
| Zfyve26 |
T |
C |
12: 79,334,418 (GRCm39) |
D200G |
probably benign |
Het |
|
| Other mutations in Clasp2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00772:Clasp2
|
APN |
9 |
113,735,060 (GRCm39) |
splice site |
probably benign |
|
|
IGL00885:Clasp2
|
APN |
9 |
113,740,484 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01314:Clasp2
|
APN |
9 |
113,735,195 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL01344:Clasp2
|
APN |
9 |
113,642,360 (GRCm39) |
splice site |
probably null |
|
|
IGL01567:Clasp2
|
APN |
9 |
113,709,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02238:Clasp2
|
APN |
9 |
113,709,088 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02299:Clasp2
|
APN |
9 |
113,709,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02323:Clasp2
|
APN |
9 |
113,697,794 (GRCm39) |
splice site |
probably benign |
|
|
IGL02635:Clasp2
|
APN |
9 |
113,737,910 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02645:Clasp2
|
APN |
9 |
113,719,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02976:Clasp2
|
APN |
9 |
113,735,204 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03190:Clasp2
|
APN |
9 |
113,673,208 (GRCm39) |
nonsense |
probably null |
|
|
IGL03219:Clasp2
|
APN |
9 |
113,677,545 (GRCm39) |
splice site |
probably benign |
|
|
PIT4810001:Clasp2
|
UTSW |
9 |
113,735,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0067:Clasp2
|
UTSW |
9 |
113,689,209 (GRCm39) |
splice site |
probably benign |
|
|
R0067:Clasp2
|
UTSW |
9 |
113,689,209 (GRCm39) |
splice site |
probably benign |
|
|
R0421:Clasp2
|
UTSW |
9 |
113,683,370 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0432:Clasp2
|
UTSW |
9 |
113,738,487 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0458:Clasp2
|
UTSW |
9 |
113,735,292 (GRCm39) |
splice site |
probably null |
|
|
R0865:Clasp2
|
UTSW |
9 |
113,740,568 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R0972:Clasp2
|
UTSW |
9 |
113,676,773 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R1037:Clasp2
|
UTSW |
9 |
113,725,702 (GRCm39) |
splice site |
probably benign |
|
|
R1925:Clasp2
|
UTSW |
9 |
113,735,265 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R2015:Clasp2
|
UTSW |
9 |
113,740,568 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R2066:Clasp2
|
UTSW |
9 |
113,735,225 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2330:Clasp2
|
UTSW |
9 |
113,705,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2568:Clasp2
|
UTSW |
9 |
113,707,832 (GRCm39) |
missense |
probably benign |
|
|
R3011:Clasp2
|
UTSW |
9 |
113,730,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3879:Clasp2
|
UTSW |
9 |
113,719,029 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3915:Clasp2
|
UTSW |
9 |
113,737,805 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3928:Clasp2
|
UTSW |
9 |
113,735,173 (GRCm39) |
missense |
probably benign |
0.28 |
|
R4323:Clasp2
|
UTSW |
9 |
113,719,027 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4571:Clasp2
|
UTSW |
9 |
113,676,789 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4975:Clasp2
|
UTSW |
9 |
113,732,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5445:Clasp2
|
UTSW |
9 |
113,733,014 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5564:Clasp2
|
UTSW |
9 |
113,641,836 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5697:Clasp2
|
UTSW |
9 |
113,689,190 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5780:Clasp2
|
UTSW |
9 |
113,679,220 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5787:Clasp2
|
UTSW |
9 |
113,691,310 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6011:Clasp2
|
UTSW |
9 |
113,705,315 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6026:Clasp2
|
UTSW |
9 |
113,740,646 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6090:Clasp2
|
UTSW |
9 |
113,681,803 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6262:Clasp2
|
UTSW |
9 |
113,705,420 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6427:Clasp2
|
UTSW |
9 |
113,721,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6464:Clasp2
|
UTSW |
9 |
113,602,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6586:Clasp2
|
UTSW |
9 |
113,642,332 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6628:Clasp2
|
UTSW |
9 |
113,725,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6745:Clasp2
|
UTSW |
9 |
113,704,338 (GRCm39) |
nonsense |
probably null |
|
|
R7032:Clasp2
|
UTSW |
9 |
113,683,391 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7165:Clasp2
|
UTSW |
9 |
113,615,467 (GRCm39) |
splice site |
probably null |
|
|
R7221:Clasp2
|
UTSW |
9 |
113,681,825 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7336:Clasp2
|
UTSW |
9 |
113,705,421 (GRCm39) |
splice site |
probably null |
|
|
R7583:Clasp2
|
UTSW |
9 |
113,737,755 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7774:Clasp2
|
UTSW |
9 |
113,677,804 (GRCm39) |
splice site |
probably null |
|
|
R7895:Clasp2
|
UTSW |
9 |
113,733,016 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8084:Clasp2
|
UTSW |
9 |
113,676,823 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8109:Clasp2
|
UTSW |
9 |
113,740,588 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8171:Clasp2
|
UTSW |
9 |
113,732,974 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8230:Clasp2
|
UTSW |
9 |
113,721,482 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R8810:Clasp2
|
UTSW |
9 |
113,728,649 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8879:Clasp2
|
UTSW |
9 |
113,602,773 (GRCm39) |
missense |
probably benign |
0.39 |
|
R8888:Clasp2
|
UTSW |
9 |
113,732,936 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R8889:Clasp2
|
UTSW |
9 |
113,709,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8892:Clasp2
|
UTSW |
9 |
113,709,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8922:Clasp2
|
UTSW |
9 |
113,725,728 (GRCm39) |
nonsense |
probably null |
|
|
R9042:Clasp2
|
UTSW |
9 |
113,735,065 (GRCm39) |
missense |
probably benign |
|
|
R9195:Clasp2
|
UTSW |
9 |
113,671,045 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9355:Clasp2
|
UTSW |
9 |
113,664,309 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9481:Clasp2
|
UTSW |
9 |
113,670,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9502:Clasp2
|
UTSW |
9 |
113,737,866 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9523:Clasp2
|
UTSW |
9 |
113,705,372 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9525:Clasp2
|
UTSW |
9 |
113,740,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9699:Clasp2
|
UTSW |
9 |
113,738,614 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9738:Clasp2
|
UTSW |
9 |
113,590,665 (GRCm39) |
nonsense |
probably null |
|
|
R9775:Clasp2
|
UTSW |
9 |
113,725,740 (GRCm39) |
missense |
probably benign |
|
|
X0022:Clasp2
|
UTSW |
9 |
113,681,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Clasp2
|
UTSW |
9 |
113,599,289 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Clasp2
|
UTSW |
9 |
113,737,863 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATGCACTCAGCTGTGATGCAG -3'
(R):5'- CCATTCCTAGCTCAAGGATGAC -3'
Sequencing Primer
(F):5'- CAGCTGTGATGCAGGCTGAG -3'
(R):5'- TCCTAGCTCAAGGATGACCAAAAATG -3'
|
| Posted On |
2022-10-06 |
Incidental Mutation