Incidental Mutation 'R4941:Arap2'
ID |
383076 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arap2
|
Ensembl Gene |
ENSMUSG00000037999 |
Gene Name |
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 |
Synonyms |
Centd1 |
MMRRC Submission |
042539-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4941 (G1)
|
Quality Score |
107 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
62759788-62923502 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 62906821 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Threonine
at position 66
(M66T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124743
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076623]
[ENSMUST00000159470]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000076623
AA Change: M66T
PolyPhen 2
Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
|
SMART Domains |
Protein: ENSMUSP00000075924 Gene: ENSMUSG00000037999 AA Change: M66T
Domain | Start | End | E-Value | Type |
SAM
|
3 |
70 |
3.69e-7 |
SMART |
low complexity region
|
222 |
233 |
N/A |
INTRINSIC |
PH
|
481 |
574 |
6.45e-17 |
SMART |
PH
|
586 |
679 |
9.05e-12 |
SMART |
ArfGap
|
684 |
805 |
9.2e-33 |
SMART |
PH
|
891 |
1003 |
1.51e-8 |
SMART |
PH
|
1013 |
1112 |
9.21e-4 |
SMART |
RhoGAP
|
1124 |
1300 |
1.36e-50 |
SMART |
Pfam:RA
|
1325 |
1416 |
2.1e-7 |
PFAM |
PH
|
1429 |
1533 |
2.68e-14 |
SMART |
coiled coil region
|
1561 |
1590 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159470
AA Change: M66T
PolyPhen 2
Score 0.205 (Sensitivity: 0.92; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000124743 Gene: ENSMUSG00000037999 AA Change: M66T
Domain | Start | End | E-Value | Type |
SAM
|
3 |
70 |
3.69e-7 |
SMART |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 98.9%
- 3x: 98.0%
- 10x: 95.4%
- 20x: 89.0%
|
Validation Efficiency |
97% (112/116) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, and pleckstrin homology domains. The protein is a phosphatidylinositol (3,4,5)-trisphosphate-dependent Arf6 GAP that binds RhoA-GTP, but it lacks the predicted catalytic arginine in the RHO-GAP domain and does not have RHO-GAP activity. The protein associates with focal adhesions and functions downstream of RhoA to regulate focal adhesion dynamics. [provided by RefSeq, Sep 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4galt |
T |
A |
15: 83,112,529 (GRCm39) |
I85F |
probably damaging |
Het |
Abcc6 |
T |
A |
7: 45,661,947 (GRCm39) |
I435F |
probably benign |
Het |
Adam3 |
T |
C |
8: 25,167,332 (GRCm39) |
|
probably benign |
Het |
Adrb3 |
T |
C |
8: 27,717,450 (GRCm39) |
Y333C |
probably damaging |
Het |
Ago4 |
A |
T |
4: 126,419,847 (GRCm39) |
D43E |
probably benign |
Het |
Agt |
T |
A |
8: 125,283,727 (GRCm39) |
Q464L |
probably benign |
Het |
Amdhd1 |
A |
T |
10: 93,367,463 (GRCm39) |
D230E |
probably damaging |
Het |
Aplf |
A |
G |
6: 87,645,405 (GRCm39) |
I33T |
probably damaging |
Het |
Aplf |
A |
T |
6: 87,623,331 (GRCm39) |
N249K |
probably benign |
Het |
Atf4 |
T |
C |
15: 80,140,434 (GRCm39) |
|
probably benign |
Het |
Bahcc1 |
A |
C |
11: 120,177,491 (GRCm39) |
H2068P |
probably benign |
Het |
Bcor |
C |
T |
X: 11,906,725 (GRCm39) |
R1551Q |
probably damaging |
Het |
Bltp1 |
A |
C |
3: 36,971,851 (GRCm39) |
H528P |
probably damaging |
Het |
Bltp1 |
G |
A |
3: 36,974,050 (GRCm39) |
S600N |
probably benign |
Het |
Catsper1 |
C |
A |
19: 5,391,466 (GRCm39) |
A616D |
possibly damaging |
Het |
Cdkn3 |
A |
G |
14: 47,007,320 (GRCm39) |
D159G |
possibly damaging |
Het |
Cep162 |
T |
C |
9: 87,108,022 (GRCm39) |
|
probably benign |
Het |
Clca3a1 |
T |
A |
3: 144,721,414 (GRCm39) |
I386L |
probably damaging |
Het |
Cldn10 |
G |
A |
14: 119,025,725 (GRCm39) |
G53S |
possibly damaging |
Het |
Cmtm3 |
T |
C |
8: 105,070,460 (GRCm39) |
L73P |
probably damaging |
Het |
Cnksr3 |
A |
C |
10: 7,102,925 (GRCm39) |
L149R |
probably benign |
Het |
Cope |
T |
C |
8: 70,755,584 (GRCm39) |
|
probably null |
Het |
Cpa6 |
T |
A |
1: 10,479,562 (GRCm39) |
M224L |
probably benign |
Het |
Cyp2d41-ps |
T |
C |
15: 82,666,154 (GRCm39) |
|
noncoding transcript |
Het |
Ddx55 |
T |
A |
5: 124,706,779 (GRCm39) |
L592* |
probably null |
Het |
Deup1 |
T |
C |
9: 15,499,323 (GRCm39) |
M333V |
probably benign |
Het |
Eif4a1 |
T |
C |
11: 69,558,640 (GRCm39) |
|
probably benign |
Het |
Eif4g3 |
A |
C |
4: 137,897,876 (GRCm39) |
D1026A |
probably damaging |
Het |
Eif5b |
T |
C |
1: 38,090,280 (GRCm39) |
V1153A |
probably damaging |
Het |
Ercc8 |
G |
T |
13: 108,297,301 (GRCm39) |
|
probably benign |
Het |
Fam227a |
C |
A |
15: 79,524,204 (GRCm39) |
|
probably null |
Het |
Fat1 |
A |
G |
8: 45,489,312 (GRCm39) |
I3505V |
probably benign |
Het |
Fat3 |
T |
G |
9: 16,286,448 (GRCm39) |
E1025A |
probably damaging |
Het |
Fat4 |
C |
T |
3: 39,011,601 (GRCm39) |
R2234W |
probably damaging |
Het |
Fer1l4 |
G |
T |
2: 155,887,009 (GRCm39) |
F634L |
probably damaging |
Het |
Fetub |
G |
A |
16: 22,756,624 (GRCm39) |
V162I |
probably benign |
Het |
Fgd4 |
T |
C |
16: 16,302,402 (GRCm39) |
Q51R |
probably benign |
Het |
Fgfr2 |
T |
C |
7: 129,800,175 (GRCm39) |
H140R |
probably benign |
Het |
Flt3 |
T |
A |
5: 147,293,185 (GRCm39) |
|
probably null |
Het |
Gabrb1 |
A |
G |
5: 72,294,121 (GRCm39) |
N465S |
probably damaging |
Het |
Gapdhs |
T |
C |
7: 30,432,691 (GRCm39) |
I206V |
probably benign |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Glp2r |
T |
C |
11: 67,637,529 (GRCm39) |
|
probably null |
Het |
Gm4956 |
T |
A |
1: 21,368,306 (GRCm39) |
|
noncoding transcript |
Het |
Gtf2a1l |
A |
T |
17: 89,022,350 (GRCm39) |
D447V |
probably damaging |
Het |
Hsd3b5 |
A |
G |
3: 98,526,379 (GRCm39) |
W356R |
probably damaging |
Het |
Idh2 |
A |
T |
7: 79,745,847 (GRCm39) |
V335D |
probably damaging |
Het |
Isyna1 |
T |
C |
8: 71,048,146 (GRCm39) |
I184T |
probably damaging |
Het |
Kcnh2 |
A |
G |
5: 24,536,085 (GRCm39) |
S320P |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Kpna6 |
A |
G |
4: 129,541,825 (GRCm39) |
F524S |
probably damaging |
Het |
Lap3 |
A |
T |
5: 45,663,539 (GRCm39) |
M338L |
probably benign |
Het |
Lins1 |
T |
C |
7: 66,359,198 (GRCm39) |
|
probably benign |
Het |
Llgl1 |
C |
T |
11: 60,600,394 (GRCm39) |
P581L |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,639,126 (GRCm39) |
D385G |
probably benign |
Het |
Maf |
T |
C |
8: 116,433,532 (GRCm39) |
D24G |
unknown |
Het |
Nell1 |
T |
C |
7: 49,712,386 (GRCm39) |
S69P |
probably benign |
Het |
Nkapd1 |
G |
T |
9: 50,518,809 (GRCm39) |
Q268K |
probably benign |
Het |
Or13p4 |
C |
T |
4: 118,547,089 (GRCm39) |
V187I |
possibly damaging |
Het |
Or2h1 |
C |
T |
17: 37,404,484 (GRCm39) |
G94E |
probably damaging |
Het |
Or2j6 |
T |
A |
7: 139,980,792 (GRCm39) |
M56L |
probably benign |
Het |
Or51af1 |
T |
C |
7: 103,141,458 (GRCm39) |
D209G |
probably damaging |
Het |
Or5an10 |
A |
G |
19: 12,276,260 (GRCm39) |
S79P |
possibly damaging |
Het |
Or8g54 |
T |
C |
9: 39,707,160 (GRCm39) |
M163T |
possibly damaging |
Het |
Oxld1 |
T |
C |
11: 120,347,862 (GRCm39) |
T112A |
probably benign |
Het |
Parp14 |
T |
C |
16: 35,666,403 (GRCm39) |
N1210S |
probably benign |
Het |
Pcdhb10 |
C |
A |
18: 37,545,887 (GRCm39) |
T321K |
probably benign |
Het |
Pcdhb8 |
C |
T |
18: 37,489,059 (GRCm39) |
L246F |
probably benign |
Het |
Pcdhga1 |
T |
A |
18: 37,795,659 (GRCm39) |
I221K |
probably benign |
Het |
Pcdhga9 |
T |
A |
18: 37,871,185 (GRCm39) |
V338E |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,108,325 (GRCm39) |
S1231P |
probably damaging |
Het |
Pde6c |
A |
T |
19: 38,140,013 (GRCm39) |
L325F |
probably damaging |
Het |
Pnpla7 |
T |
A |
2: 24,887,276 (GRCm39) |
|
probably null |
Het |
Pparg |
T |
A |
6: 115,467,071 (GRCm39) |
V478E |
probably damaging |
Het |
Ppib |
T |
C |
9: 65,967,672 (GRCm39) |
V42A |
probably benign |
Het |
Ppox |
T |
C |
1: 171,105,166 (GRCm39) |
M341V |
probably damaging |
Het |
Proc |
T |
C |
18: 32,258,166 (GRCm39) |
K260E |
possibly damaging |
Het |
Ptpro |
C |
T |
6: 137,369,763 (GRCm39) |
P525L |
probably damaging |
Het |
Rnf14 |
C |
A |
18: 38,441,435 (GRCm39) |
A275E |
probably damaging |
Het |
Scnn1b |
C |
T |
7: 121,511,231 (GRCm39) |
P306L |
probably damaging |
Het |
Sec14l5 |
A |
G |
16: 4,994,364 (GRCm39) |
E386G |
probably damaging |
Het |
Sftpa1 |
T |
A |
14: 40,854,509 (GRCm39) |
I32N |
probably damaging |
Het |
Slc26a5 |
A |
G |
5: 22,025,384 (GRCm39) |
I408T |
probably damaging |
Het |
Slc7a13 |
A |
G |
4: 19,841,467 (GRCm39) |
Y438C |
probably damaging |
Het |
Spire1 |
T |
C |
18: 67,652,384 (GRCm39) |
E231G |
possibly damaging |
Het |
Stab1 |
T |
A |
14: 30,873,528 (GRCm39) |
I1014F |
probably benign |
Het |
Steap2 |
T |
C |
5: 5,727,651 (GRCm39) |
Y228C |
probably damaging |
Het |
Tmem131l |
T |
C |
3: 83,806,546 (GRCm39) |
T1487A |
probably benign |
Het |
Tmem171 |
A |
G |
13: 98,828,803 (GRCm39) |
F116L |
possibly damaging |
Het |
Tmem215 |
T |
C |
4: 40,474,520 (GRCm39) |
V199A |
probably damaging |
Het |
Tmem45a |
T |
C |
16: 56,642,652 (GRCm39) |
N173S |
possibly damaging |
Het |
Uqcrc2 |
C |
T |
7: 120,242,301 (GRCm39) |
R148C |
probably benign |
Het |
Vmn2r116 |
A |
G |
17: 23,620,116 (GRCm39) |
K617E |
probably damaging |
Het |
Xrcc6 |
T |
C |
15: 81,924,013 (GRCm39) |
L229P |
probably damaging |
Het |
Yju2 |
A |
G |
17: 56,271,149 (GRCm39) |
D97G |
possibly damaging |
Het |
Zfp184 |
A |
G |
13: 22,133,891 (GRCm39) |
D46G |
probably damaging |
Het |
Zfp790 |
T |
A |
7: 29,528,916 (GRCm39) |
C534S |
possibly damaging |
Het |
Zfp990 |
A |
T |
4: 145,263,407 (GRCm39) |
N135I |
probably damaging |
Het |
|
Other mutations in Arap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Arap2
|
APN |
5 |
62,793,305 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00642:Arap2
|
APN |
5 |
62,890,401 (GRCm39) |
nonsense |
probably null |
|
IGL00705:Arap2
|
APN |
5 |
62,835,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00942:Arap2
|
APN |
5 |
62,855,732 (GRCm39) |
nonsense |
probably null |
|
IGL01069:Arap2
|
APN |
5 |
62,807,199 (GRCm39) |
missense |
probably benign |
|
IGL01601:Arap2
|
APN |
5 |
62,798,685 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01986:Arap2
|
APN |
5 |
62,779,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02032:Arap2
|
APN |
5 |
62,828,340 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02262:Arap2
|
APN |
5 |
62,800,184 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02331:Arap2
|
APN |
5 |
62,807,025 (GRCm39) |
splice site |
probably benign |
|
IGL02527:Arap2
|
APN |
5 |
62,906,650 (GRCm39) |
missense |
probably benign |
|
IGL02803:Arap2
|
APN |
5 |
62,906,452 (GRCm39) |
missense |
probably benign |
|
IGL02864:Arap2
|
APN |
5 |
62,835,308 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03078:Arap2
|
APN |
5 |
62,890,408 (GRCm39) |
splice site |
probably benign |
|
IGL03154:Arap2
|
APN |
5 |
62,800,268 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03213:Arap2
|
APN |
5 |
62,906,438 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03279:Arap2
|
APN |
5 |
62,779,253 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03288:Arap2
|
APN |
5 |
62,761,959 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4354001:Arap2
|
UTSW |
5 |
62,811,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Arap2
|
UTSW |
5 |
62,840,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Arap2
|
UTSW |
5 |
62,840,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Arap2
|
UTSW |
5 |
62,840,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0166:Arap2
|
UTSW |
5 |
62,833,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R0472:Arap2
|
UTSW |
5 |
62,864,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Arap2
|
UTSW |
5 |
62,763,474 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0551:Arap2
|
UTSW |
5 |
62,798,666 (GRCm39) |
splice site |
probably null |
|
R0607:Arap2
|
UTSW |
5 |
62,763,474 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0617:Arap2
|
UTSW |
5 |
62,807,250 (GRCm39) |
splice site |
probably benign |
|
R0975:Arap2
|
UTSW |
5 |
62,888,229 (GRCm39) |
splice site |
probably benign |
|
R0976:Arap2
|
UTSW |
5 |
62,807,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R1164:Arap2
|
UTSW |
5 |
62,840,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R1268:Arap2
|
UTSW |
5 |
62,887,964 (GRCm39) |
missense |
probably benign |
0.00 |
R1480:Arap2
|
UTSW |
5 |
62,826,472 (GRCm39) |
nonsense |
probably null |
|
R1502:Arap2
|
UTSW |
5 |
62,761,747 (GRCm39) |
missense |
probably benign |
0.00 |
R1543:Arap2
|
UTSW |
5 |
62,763,498 (GRCm39) |
nonsense |
probably null |
|
R1865:Arap2
|
UTSW |
5 |
62,855,606 (GRCm39) |
missense |
probably damaging |
0.97 |
R1962:Arap2
|
UTSW |
5 |
62,834,007 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2040:Arap2
|
UTSW |
5 |
62,906,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R2118:Arap2
|
UTSW |
5 |
62,864,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Arap2
|
UTSW |
5 |
62,835,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Arap2
|
UTSW |
5 |
62,864,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R2215:Arap2
|
UTSW |
5 |
62,834,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R3027:Arap2
|
UTSW |
5 |
62,827,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R3053:Arap2
|
UTSW |
5 |
62,906,200 (GRCm39) |
missense |
probably benign |
0.35 |
R3975:Arap2
|
UTSW |
5 |
62,906,237 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4272:Arap2
|
UTSW |
5 |
62,828,322 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4273:Arap2
|
UTSW |
5 |
62,828,322 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4326:Arap2
|
UTSW |
5 |
62,779,206 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4327:Arap2
|
UTSW |
5 |
62,779,206 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4328:Arap2
|
UTSW |
5 |
62,779,206 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4451:Arap2
|
UTSW |
5 |
62,906,513 (GRCm39) |
missense |
probably benign |
0.06 |
R4659:Arap2
|
UTSW |
5 |
62,811,469 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4665:Arap2
|
UTSW |
5 |
62,827,312 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4715:Arap2
|
UTSW |
5 |
62,906,437 (GRCm39) |
missense |
probably benign |
0.43 |
R4808:Arap2
|
UTSW |
5 |
62,887,984 (GRCm39) |
missense |
probably benign |
0.23 |
R4983:Arap2
|
UTSW |
5 |
62,833,868 (GRCm39) |
missense |
probably damaging |
0.98 |
R5095:Arap2
|
UTSW |
5 |
62,811,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5156:Arap2
|
UTSW |
5 |
62,826,524 (GRCm39) |
nonsense |
probably null |
|
R5201:Arap2
|
UTSW |
5 |
62,840,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Arap2
|
UTSW |
5 |
62,872,089 (GRCm39) |
missense |
probably benign |
0.39 |
R5359:Arap2
|
UTSW |
5 |
62,840,762 (GRCm39) |
nonsense |
probably null |
|
R5426:Arap2
|
UTSW |
5 |
62,800,159 (GRCm39) |
missense |
probably benign |
0.02 |
R5503:Arap2
|
UTSW |
5 |
62,787,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5605:Arap2
|
UTSW |
5 |
62,772,410 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5764:Arap2
|
UTSW |
5 |
62,800,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Arap2
|
UTSW |
5 |
62,834,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5846:Arap2
|
UTSW |
5 |
62,807,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R6084:Arap2
|
UTSW |
5 |
62,828,297 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6173:Arap2
|
UTSW |
5 |
62,906,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Arap2
|
UTSW |
5 |
62,872,074 (GRCm39) |
critical splice donor site |
probably null |
|
R6249:Arap2
|
UTSW |
5 |
62,803,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R6386:Arap2
|
UTSW |
5 |
62,761,865 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6424:Arap2
|
UTSW |
5 |
62,840,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6744:Arap2
|
UTSW |
5 |
62,906,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6766:Arap2
|
UTSW |
5 |
62,834,443 (GRCm39) |
critical splice donor site |
probably null |
|
R6990:Arap2
|
UTSW |
5 |
62,833,860 (GRCm39) |
missense |
probably damaging |
0.96 |
R7067:Arap2
|
UTSW |
5 |
62,811,387 (GRCm39) |
critical splice donor site |
probably null |
|
R7098:Arap2
|
UTSW |
5 |
62,833,293 (GRCm39) |
critical splice donor site |
probably null |
|
R7107:Arap2
|
UTSW |
5 |
62,763,551 (GRCm39) |
missense |
probably damaging |
0.98 |
R7156:Arap2
|
UTSW |
5 |
62,761,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R7174:Arap2
|
UTSW |
5 |
62,761,621 (GRCm39) |
missense |
probably benign |
|
R7187:Arap2
|
UTSW |
5 |
62,826,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R7197:Arap2
|
UTSW |
5 |
62,798,729 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7214:Arap2
|
UTSW |
5 |
62,906,681 (GRCm39) |
missense |
probably benign |
0.00 |
R7317:Arap2
|
UTSW |
5 |
62,807,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Arap2
|
UTSW |
5 |
62,855,728 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7438:Arap2
|
UTSW |
5 |
62,906,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R7452:Arap2
|
UTSW |
5 |
62,833,892 (GRCm39) |
missense |
probably benign |
0.00 |
R7495:Arap2
|
UTSW |
5 |
62,833,893 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7796:Arap2
|
UTSW |
5 |
62,888,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R7936:Arap2
|
UTSW |
5 |
62,888,048 (GRCm39) |
missense |
probably damaging |
0.96 |
R8116:Arap2
|
UTSW |
5 |
62,887,954 (GRCm39) |
missense |
probably benign |
0.00 |
R8172:Arap2
|
UTSW |
5 |
62,779,324 (GRCm39) |
splice site |
probably null |
|
R8277:Arap2
|
UTSW |
5 |
62,771,335 (GRCm39) |
critical splice donor site |
probably null |
|
R8369:Arap2
|
UTSW |
5 |
62,761,669 (GRCm39) |
nonsense |
probably null |
|
R8398:Arap2
|
UTSW |
5 |
62,906,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R8893:Arap2
|
UTSW |
5 |
62,888,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R8973:Arap2
|
UTSW |
5 |
62,855,668 (GRCm39) |
nonsense |
probably null |
|
R9102:Arap2
|
UTSW |
5 |
62,906,341 (GRCm39) |
missense |
probably benign |
0.03 |
R9121:Arap2
|
UTSW |
5 |
62,906,326 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9174:Arap2
|
UTSW |
5 |
62,855,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R9222:Arap2
|
UTSW |
5 |
62,828,421 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9281:Arap2
|
UTSW |
5 |
62,906,848 (GRCm39) |
missense |
probably damaging |
0.97 |
R9399:Arap2
|
UTSW |
5 |
62,763,455 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9450:Arap2
|
UTSW |
5 |
62,855,762 (GRCm39) |
missense |
probably benign |
0.16 |
R9467:Arap2
|
UTSW |
5 |
62,887,900 (GRCm39) |
missense |
probably benign |
0.00 |
R9567:Arap2
|
UTSW |
5 |
62,761,841 (GRCm39) |
missense |
probably benign |
0.01 |
R9577:Arap2
|
UTSW |
5 |
62,769,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R9626:Arap2
|
UTSW |
5 |
62,906,878 (GRCm39) |
missense |
probably benign |
0.00 |
R9688:Arap2
|
UTSW |
5 |
62,872,109 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- CGGAGACTGACAGTTTCCTTC -3'
(R):5'- CAGCGAAGTAAATGCGGACATC -3'
Sequencing Primer
(F):5'- GGAGACTGACAGTTTCCTTCACTAAG -3'
(R):5'- TGCGGACATCAGAGATTTCC -3'
|
Posted On |
2016-04-27 |