Incidental Mutation 'R0539:Arhgap21'
ID |
49661 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arhgap21
|
Ensembl Gene |
ENSMUSG00000036591 |
Gene Name |
Rho GTPase activating protein 21 |
Synonyms |
ARHGAP10, 5530401C11Rik |
MMRRC Submission |
038731-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.570)
|
Stock # |
R0539 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
20852730-20973692 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 20919610 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Stop codon
at position 32
(K32*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133851
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000114594]
[ENSMUST00000125783]
[ENSMUST00000140230]
[ENSMUST00000141298]
[ENSMUST00000154230]
[ENSMUST00000173194]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000114594
AA Change: K26*
|
SMART Domains |
Protein: ENSMUSP00000110241 Gene: ENSMUSG00000036591 AA Change: K26*
Domain | Start | End | E-Value | Type |
PDZ
|
58 |
159 |
1.03e-16 |
SMART |
low complexity region
|
351 |
362 |
N/A |
INTRINSIC |
low complexity region
|
445 |
459 |
N/A |
INTRINSIC |
low complexity region
|
625 |
635 |
N/A |
INTRINSIC |
low complexity region
|
911 |
925 |
N/A |
INTRINSIC |
PH
|
930 |
1040 |
2.09e-16 |
SMART |
RhoGAP
|
1157 |
1334 |
3.26e-62 |
SMART |
low complexity region
|
1381 |
1399 |
N/A |
INTRINSIC |
low complexity region
|
1448 |
1466 |
N/A |
INTRINSIC |
low complexity region
|
1533 |
1565 |
N/A |
INTRINSIC |
low complexity region
|
1573 |
1593 |
N/A |
INTRINSIC |
low complexity region
|
1891 |
1900 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000125783
|
Predicted Effect |
probably null
Transcript: ENSMUST00000140230
AA Change: K33*
|
SMART Domains |
Protein: ENSMUSP00000122271 Gene: ENSMUSG00000036591 AA Change: K33*
Domain | Start | End | E-Value | Type |
PDZ
|
65 |
145 |
3.4e-1 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000141298
AA Change: K32*
|
SMART Domains |
Protein: ENSMUSP00000120357 Gene: ENSMUSG00000036591 AA Change: K32*
Domain | Start | End | E-Value | Type |
PDZ
|
64 |
165 |
1.03e-16 |
SMART |
low complexity region
|
357 |
368 |
N/A |
INTRINSIC |
low complexity region
|
451 |
465 |
N/A |
INTRINSIC |
low complexity region
|
631 |
641 |
N/A |
INTRINSIC |
low complexity region
|
917 |
931 |
N/A |
INTRINSIC |
PH
|
936 |
1046 |
2.09e-16 |
SMART |
RhoGAP
|
1163 |
1340 |
3.26e-62 |
SMART |
low complexity region
|
1387 |
1405 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1472 |
N/A |
INTRINSIC |
low complexity region
|
1539 |
1571 |
N/A |
INTRINSIC |
low complexity region
|
1579 |
1599 |
N/A |
INTRINSIC |
low complexity region
|
1897 |
1906 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000154230
AA Change: K32*
|
SMART Domains |
Protein: ENSMUSP00000122497 Gene: ENSMUSG00000036591 AA Change: K32*
Domain | Start | End | E-Value | Type |
PDZ
|
64 |
165 |
1.03e-16 |
SMART |
low complexity region
|
357 |
368 |
N/A |
INTRINSIC |
low complexity region
|
451 |
465 |
N/A |
INTRINSIC |
low complexity region
|
631 |
641 |
N/A |
INTRINSIC |
low complexity region
|
917 |
931 |
N/A |
INTRINSIC |
PH
|
936 |
1046 |
2.09e-16 |
SMART |
RhoGAP
|
1163 |
1340 |
3.26e-62 |
SMART |
low complexity region
|
1387 |
1405 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1472 |
N/A |
INTRINSIC |
low complexity region
|
1539 |
1571 |
N/A |
INTRINSIC |
low complexity region
|
1579 |
1599 |
N/A |
INTRINSIC |
low complexity region
|
1897 |
1906 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156142
|
Predicted Effect |
probably null
Transcript: ENSMUST00000173194
AA Change: K32*
|
SMART Domains |
Protein: ENSMUSP00000133851 Gene: ENSMUSG00000036591 AA Change: K32*
Domain | Start | End | E-Value | Type |
PDZ
|
64 |
165 |
1.03e-16 |
SMART |
low complexity region
|
347 |
358 |
N/A |
INTRINSIC |
low complexity region
|
441 |
455 |
N/A |
INTRINSIC |
low complexity region
|
621 |
631 |
N/A |
INTRINSIC |
low complexity region
|
907 |
921 |
N/A |
INTRINSIC |
PH
|
926 |
1036 |
2.09e-16 |
SMART |
RhoGAP
|
1153 |
1330 |
3.26e-62 |
SMART |
low complexity region
|
1377 |
1395 |
N/A |
INTRINSIC |
low complexity region
|
1444 |
1462 |
N/A |
INTRINSIC |
low complexity region
|
1529 |
1561 |
N/A |
INTRINSIC |
low complexity region
|
1569 |
1589 |
N/A |
INTRINSIC |
low complexity region
|
1887 |
1896 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.3%
|
Validation Efficiency |
100% (107/107) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] ARHGAP21 functions preferentially as a GTPase-activating protein (GAP) for CDC42 (MIM 116952) and regulates the ARP2/3 complex (MIM 604221) and F-actin dynamics at the Golgi through control of CDC42 activity (Dubois et al., 2005 [PubMed 15793564]).[supplied by OMIM, Mar 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730480H06Rik |
T |
A |
5: 48,536,692 (GRCm39) |
H129Q |
probably damaging |
Het |
Abca14 |
G |
A |
7: 119,807,020 (GRCm39) |
R22Q |
probably damaging |
Het |
Abcg5 |
T |
A |
17: 84,976,503 (GRCm39) |
M445L |
probably benign |
Het |
Abhd3 |
T |
A |
18: 10,645,208 (GRCm39) |
N357I |
possibly damaging |
Het |
Adamts5 |
C |
T |
16: 85,665,580 (GRCm39) |
G574S |
probably damaging |
Het |
Adgrg5 |
T |
A |
8: 95,665,260 (GRCm39) |
N389K |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,329,330 (GRCm39) |
V80A |
probably benign |
Het |
Arhgap20 |
A |
G |
9: 51,761,455 (GRCm39) |
Q1066R |
probably benign |
Het |
AW209491 |
T |
C |
13: 14,812,317 (GRCm39) |
F390S |
probably damaging |
Het |
Axl |
A |
T |
7: 25,478,142 (GRCm39) |
|
probably benign |
Het |
Bri3bp |
A |
G |
5: 125,531,603 (GRCm39) |
Y183C |
probably damaging |
Het |
Cad |
T |
C |
5: 31,232,801 (GRCm39) |
|
probably benign |
Het |
Capns2 |
A |
G |
8: 93,628,360 (GRCm39) |
Q83R |
possibly damaging |
Het |
Ccdc180 |
G |
T |
4: 45,922,010 (GRCm39) |
R1028L |
probably damaging |
Het |
Cdh19 |
C |
A |
1: 110,852,892 (GRCm39) |
V348F |
possibly damaging |
Het |
Chrm2 |
T |
C |
6: 36,500,641 (GRCm39) |
V166A |
possibly damaging |
Het |
Clmp |
A |
G |
9: 40,693,782 (GRCm39) |
Y333C |
probably benign |
Het |
Cntn3 |
A |
G |
6: 102,254,178 (GRCm39) |
|
probably null |
Het |
Copz1 |
A |
G |
15: 103,199,792 (GRCm39) |
Y69C |
probably damaging |
Het |
Crybg1 |
T |
C |
10: 43,874,894 (GRCm39) |
D738G |
probably benign |
Het |
Ctnna2 |
T |
A |
6: 76,950,882 (GRCm39) |
I165F |
probably damaging |
Het |
Dcaf7 |
T |
G |
11: 105,942,652 (GRCm39) |
S200A |
probably damaging |
Het |
Deup1 |
T |
A |
9: 15,493,893 (GRCm39) |
R416S |
possibly damaging |
Het |
Dmxl1 |
T |
A |
18: 49,990,497 (GRCm39) |
|
probably benign |
Het |
Dnaaf11 |
A |
T |
15: 66,319,455 (GRCm39) |
V305D |
probably damaging |
Het |
Dnase2b |
A |
T |
3: 146,294,910 (GRCm39) |
|
probably benign |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Eef2 |
C |
CN |
10: 81,014,602 (GRCm39) |
|
probably null |
Het |
Ephb2 |
T |
C |
4: 136,383,287 (GRCm39) |
Y931C |
probably damaging |
Het |
Fam83h |
T |
C |
15: 75,875,076 (GRCm39) |
S754G |
possibly damaging |
Het |
Fibp |
T |
A |
19: 5,513,216 (GRCm39) |
V177D |
probably damaging |
Het |
Gfpt2 |
T |
C |
11: 49,723,725 (GRCm39) |
I571T |
probably damaging |
Het |
Grm7 |
T |
G |
6: 111,336,055 (GRCm39) |
|
probably benign |
Het |
Gsdma3 |
A |
G |
11: 98,526,745 (GRCm39) |
Y335C |
probably damaging |
Het |
H2-T23 |
A |
T |
17: 36,343,033 (GRCm39) |
|
probably benign |
Het |
H4c3 |
A |
G |
13: 23,882,131 (GRCm39) |
F101S |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,249,704 (GRCm39) |
I2216V |
probably benign |
Het |
Ipo8 |
A |
G |
6: 148,719,606 (GRCm39) |
M113T |
probably benign |
Het |
Kdm6a |
A |
G |
X: 18,128,664 (GRCm39) |
E1045G |
probably damaging |
Het |
Kyat1 |
C |
T |
2: 30,078,229 (GRCm39) |
E117K |
probably damaging |
Het |
Lin7b |
A |
G |
7: 45,019,326 (GRCm39) |
|
probably benign |
Het |
Lipn |
G |
A |
19: 34,062,003 (GRCm39) |
|
probably benign |
Het |
Lrfn2 |
C |
A |
17: 49,378,072 (GRCm39) |
N384K |
probably damaging |
Het |
Map1b |
T |
C |
13: 99,570,526 (GRCm39) |
K732E |
unknown |
Het |
Mpl |
A |
G |
4: 118,300,705 (GRCm39) |
M541T |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,631,943 (GRCm39) |
|
probably benign |
Het |
Mrc1 |
T |
C |
2: 14,274,937 (GRCm39) |
|
probably benign |
Het |
Ms4a13 |
T |
C |
19: 11,149,235 (GRCm39) |
|
probably benign |
Het |
Myo18b |
G |
T |
5: 112,871,734 (GRCm39) |
R2116S |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,111,686 (GRCm39) |
T731A |
probably damaging |
Het |
Ncoa6 |
G |
T |
2: 155,257,617 (GRCm39) |
A642D |
probably benign |
Het |
Ndufs7 |
T |
A |
10: 80,090,665 (GRCm39) |
|
probably benign |
Het |
Nfkbiz |
G |
A |
16: 55,638,242 (GRCm39) |
T406M |
probably benign |
Het |
Nr4a1 |
A |
G |
15: 101,168,765 (GRCm39) |
E267G |
probably damaging |
Het |
Nrxn2 |
T |
G |
19: 6,543,434 (GRCm39) |
F1103V |
probably damaging |
Het |
Or10ab4 |
C |
T |
7: 107,655,029 (GRCm39) |
T280I |
probably damaging |
Het |
Or10d3 |
A |
T |
9: 39,461,593 (GRCm39) |
D191E |
probably damaging |
Het |
Or1e22 |
T |
C |
11: 73,376,889 (GRCm39) |
T254A |
probably benign |
Het |
Or5a3 |
C |
T |
19: 12,400,173 (GRCm39) |
L167F |
probably damaging |
Het |
Or5g27 |
T |
A |
2: 85,410,119 (GRCm39) |
C179S |
probably damaging |
Het |
Or5m11 |
G |
T |
2: 85,782,353 (GRCm39) |
M315I |
probably benign |
Het |
Or8u9 |
A |
T |
2: 86,001,387 (GRCm39) |
M258K |
probably damaging |
Het |
Phf1 |
A |
G |
17: 27,153,432 (GRCm39) |
|
probably null |
Het |
Pip |
C |
T |
6: 41,826,819 (GRCm39) |
Q53* |
probably null |
Het |
Ppp2ca |
T |
C |
11: 52,008,989 (GRCm39) |
|
probably null |
Het |
Prl2c5 |
A |
G |
13: 13,363,906 (GRCm39) |
|
probably null |
Het |
Psph |
T |
A |
5: 129,843,641 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
C |
T |
13: 63,691,294 (GRCm39) |
|
probably benign |
Het |
Ptprs |
C |
T |
17: 56,765,255 (GRCm39) |
V10M |
probably damaging |
Het |
Rarg |
T |
C |
15: 102,147,312 (GRCm39) |
R358G |
probably damaging |
Het |
Rbl2 |
T |
C |
8: 91,839,133 (GRCm39) |
|
probably benign |
Het |
Robo2 |
A |
T |
16: 73,782,462 (GRCm39) |
|
probably benign |
Het |
Scin |
A |
T |
12: 40,131,765 (GRCm39) |
D256E |
possibly damaging |
Het |
Scn8a |
T |
C |
15: 100,914,449 (GRCm39) |
Y1152H |
probably damaging |
Het |
Sh2b2 |
T |
G |
5: 136,254,155 (GRCm39) |
|
probably benign |
Het |
Slc13a2 |
G |
A |
11: 78,289,964 (GRCm39) |
P450L |
probably damaging |
Het |
Slc2a12 |
A |
G |
10: 22,568,129 (GRCm39) |
I519V |
probably benign |
Het |
Slc30a9 |
C |
T |
5: 67,491,953 (GRCm39) |
T260M |
probably damaging |
Het |
Slc9a7 |
A |
T |
X: 20,069,001 (GRCm39) |
F184Y |
probably damaging |
Het |
Smc2 |
G |
T |
4: 52,458,558 (GRCm39) |
K466N |
probably benign |
Het |
Snx16 |
T |
C |
3: 10,491,278 (GRCm39) |
E209G |
probably damaging |
Het |
Sp3 |
A |
T |
2: 72,800,876 (GRCm39) |
I423N |
possibly damaging |
Het |
Ssh2 |
G |
T |
11: 77,345,620 (GRCm39) |
V1202F |
probably benign |
Het |
Stam2 |
A |
T |
2: 52,593,268 (GRCm39) |
|
probably benign |
Het |
Stox2 |
T |
C |
8: 47,647,070 (GRCm39) |
Y194C |
probably damaging |
Het |
Sult3a1 |
A |
G |
10: 33,742,519 (GRCm39) |
T49A |
probably damaging |
Het |
Supt3 |
A |
T |
17: 45,314,018 (GRCm39) |
I136F |
possibly damaging |
Het |
Syne2 |
A |
T |
12: 76,070,895 (GRCm39) |
R103S |
possibly damaging |
Het |
Synj2 |
T |
A |
17: 6,047,163 (GRCm39) |
M1K |
probably null |
Het |
Tas2r110 |
T |
C |
6: 132,845,334 (GRCm39) |
S122P |
possibly damaging |
Het |
Tln1 |
A |
G |
4: 43,543,434 (GRCm39) |
|
probably null |
Het |
Tmem117 |
A |
G |
15: 94,612,793 (GRCm39) |
T110A |
possibly damaging |
Het |
Tmem247 |
A |
G |
17: 87,224,906 (GRCm39) |
D5G |
probably benign |
Het |
Tmem39a |
T |
A |
16: 38,411,337 (GRCm39) |
F363I |
probably benign |
Het |
Tmem80 |
G |
A |
7: 140,915,808 (GRCm39) |
A73T |
possibly damaging |
Het |
Trpm4 |
C |
T |
7: 44,954,896 (GRCm39) |
G901S |
probably damaging |
Het |
Upk3bl |
T |
C |
5: 136,092,840 (GRCm39) |
|
probably benign |
Het |
Vmn1r120 |
A |
T |
7: 20,787,397 (GRCm39) |
C105S |
probably damaging |
Het |
Vmn1r69 |
A |
T |
7: 10,314,874 (GRCm39) |
|
probably benign |
Het |
Vmn2r95 |
T |
C |
17: 18,672,362 (GRCm39) |
F700L |
probably damaging |
Het |
Wdr70 |
G |
A |
15: 7,915,118 (GRCm39) |
T550M |
possibly damaging |
Het |
Zbtb22 |
A |
G |
17: 34,137,118 (GRCm39) |
D421G |
possibly damaging |
Het |
Zbtb45 |
G |
A |
7: 12,740,260 (GRCm39) |
R452C |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,527,141 (GRCm39) |
Y1013H |
probably damaging |
Het |
Zfp329 |
C |
T |
7: 12,540,520 (GRCm39) |
|
probably null |
Het |
Zfp532 |
T |
A |
18: 65,756,837 (GRCm39) |
S257T |
probably benign |
Het |
Zfp933 |
G |
A |
4: 147,911,005 (GRCm39) |
T197I |
probably benign |
Het |
Zgrf1 |
T |
A |
3: 127,408,841 (GRCm39) |
N1649K |
probably damaging |
Het |
|
Other mutations in Arhgap21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01382:Arhgap21
|
APN |
2 |
20,860,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01472:Arhgap21
|
APN |
2 |
20,854,392 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01634:Arhgap21
|
APN |
2 |
20,919,455 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01766:Arhgap21
|
APN |
2 |
20,854,448 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02097:Arhgap21
|
APN |
2 |
20,884,813 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02197:Arhgap21
|
APN |
2 |
20,885,117 (GRCm39) |
missense |
probably benign |
|
IGL02264:Arhgap21
|
APN |
2 |
20,864,850 (GRCm39) |
splice site |
probably null |
|
IGL02346:Arhgap21
|
APN |
2 |
20,884,762 (GRCm39) |
splice site |
probably benign |
|
IGL02418:Arhgap21
|
APN |
2 |
20,885,711 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02605:Arhgap21
|
APN |
2 |
20,860,399 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02701:Arhgap21
|
APN |
2 |
20,896,902 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03019:Arhgap21
|
APN |
2 |
20,865,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03085:Arhgap21
|
APN |
2 |
20,919,532 (GRCm39) |
missense |
probably benign |
|
IGL03265:Arhgap21
|
APN |
2 |
20,854,439 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03379:Arhgap21
|
APN |
2 |
20,885,500 (GRCm39) |
missense |
probably benign |
0.41 |
R0304:Arhgap21
|
UTSW |
2 |
20,864,612 (GRCm39) |
splice site |
probably benign |
|
R0363:Arhgap21
|
UTSW |
2 |
20,885,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R0498:Arhgap21
|
UTSW |
2 |
20,867,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0633:Arhgap21
|
UTSW |
2 |
20,860,198 (GRCm39) |
nonsense |
probably null |
|
R0905:Arhgap21
|
UTSW |
2 |
20,854,745 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1550:Arhgap21
|
UTSW |
2 |
20,886,576 (GRCm39) |
nonsense |
probably null |
|
R1570:Arhgap21
|
UTSW |
2 |
20,885,651 (GRCm39) |
missense |
probably benign |
|
R1686:Arhgap21
|
UTSW |
2 |
20,886,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R1746:Arhgap21
|
UTSW |
2 |
20,865,910 (GRCm39) |
missense |
probably damaging |
0.99 |
R1864:Arhgap21
|
UTSW |
2 |
20,866,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Arhgap21
|
UTSW |
2 |
20,866,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R2209:Arhgap21
|
UTSW |
2 |
20,854,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Arhgap21
|
UTSW |
2 |
20,886,451 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2276:Arhgap21
|
UTSW |
2 |
20,868,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2277:Arhgap21
|
UTSW |
2 |
20,868,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2279:Arhgap21
|
UTSW |
2 |
20,868,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2336:Arhgap21
|
UTSW |
2 |
20,884,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Arhgap21
|
UTSW |
2 |
20,859,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R3722:Arhgap21
|
UTSW |
2 |
20,855,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R3877:Arhgap21
|
UTSW |
2 |
20,864,717 (GRCm39) |
missense |
probably damaging |
0.99 |
R4017:Arhgap21
|
UTSW |
2 |
20,896,915 (GRCm39) |
missense |
probably benign |
0.10 |
R4232:Arhgap21
|
UTSW |
2 |
20,891,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4233:Arhgap21
|
UTSW |
2 |
20,891,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Arhgap21
|
UTSW |
2 |
20,891,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Arhgap21
|
UTSW |
2 |
20,891,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4236:Arhgap21
|
UTSW |
2 |
20,891,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4434:Arhgap21
|
UTSW |
2 |
20,972,146 (GRCm39) |
missense |
probably benign |
|
R4686:Arhgap21
|
UTSW |
2 |
20,868,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R4817:Arhgap21
|
UTSW |
2 |
20,854,967 (GRCm39) |
missense |
probably benign |
|
R4834:Arhgap21
|
UTSW |
2 |
20,870,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R4845:Arhgap21
|
UTSW |
2 |
20,885,998 (GRCm39) |
missense |
probably damaging |
0.99 |
R4889:Arhgap21
|
UTSW |
2 |
20,885,279 (GRCm39) |
missense |
probably benign |
0.10 |
R4904:Arhgap21
|
UTSW |
2 |
20,854,872 (GRCm39) |
missense |
probably benign |
0.00 |
R4911:Arhgap21
|
UTSW |
2 |
20,863,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4994:Arhgap21
|
UTSW |
2 |
20,854,701 (GRCm39) |
missense |
probably benign |
0.00 |
R5067:Arhgap21
|
UTSW |
2 |
20,884,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Arhgap21
|
UTSW |
2 |
20,853,645 (GRCm39) |
missense |
probably benign |
0.00 |
R5281:Arhgap21
|
UTSW |
2 |
20,854,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R5364:Arhgap21
|
UTSW |
2 |
20,854,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R5420:Arhgap21
|
UTSW |
2 |
20,885,897 (GRCm39) |
missense |
probably damaging |
0.99 |
R5476:Arhgap21
|
UTSW |
2 |
20,885,497 (GRCm39) |
missense |
probably benign |
0.06 |
R5831:Arhgap21
|
UTSW |
2 |
20,868,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:Arhgap21
|
UTSW |
2 |
20,853,852 (GRCm39) |
missense |
probably damaging |
0.97 |
R5994:Arhgap21
|
UTSW |
2 |
20,886,187 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6014:Arhgap21
|
UTSW |
2 |
20,886,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Arhgap21
|
UTSW |
2 |
20,885,543 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6817:Arhgap21
|
UTSW |
2 |
20,885,107 (GRCm39) |
missense |
probably benign |
0.23 |
R6821:Arhgap21
|
UTSW |
2 |
20,853,659 (GRCm39) |
missense |
probably benign |
|
R6844:Arhgap21
|
UTSW |
2 |
20,886,116 (GRCm39) |
missense |
probably benign |
0.00 |
R6870:Arhgap21
|
UTSW |
2 |
20,885,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R6891:Arhgap21
|
UTSW |
2 |
20,855,142 (GRCm39) |
missense |
probably damaging |
0.97 |
R7011:Arhgap21
|
UTSW |
2 |
20,853,689 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7144:Arhgap21
|
UTSW |
2 |
20,870,198 (GRCm39) |
missense |
probably benign |
|
R7237:Arhgap21
|
UTSW |
2 |
20,854,783 (GRCm39) |
nonsense |
probably null |
|
R7261:Arhgap21
|
UTSW |
2 |
20,885,177 (GRCm39) |
missense |
probably benign |
|
R7558:Arhgap21
|
UTSW |
2 |
20,860,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R7566:Arhgap21
|
UTSW |
2 |
20,917,102 (GRCm39) |
missense |
probably benign |
0.17 |
R7738:Arhgap21
|
UTSW |
2 |
20,855,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7738:Arhgap21
|
UTSW |
2 |
20,854,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7820:Arhgap21
|
UTSW |
2 |
20,867,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7822:Arhgap21
|
UTSW |
2 |
20,885,524 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7965:Arhgap21
|
UTSW |
2 |
20,854,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Arhgap21
|
UTSW |
2 |
20,867,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R8028:Arhgap21
|
UTSW |
2 |
20,885,216 (GRCm39) |
missense |
probably benign |
0.02 |
R8209:Arhgap21
|
UTSW |
2 |
20,876,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R8226:Arhgap21
|
UTSW |
2 |
20,876,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Arhgap21
|
UTSW |
2 |
20,854,221 (GRCm39) |
missense |
probably benign |
|
R8486:Arhgap21
|
UTSW |
2 |
20,865,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8487:Arhgap21
|
UTSW |
2 |
20,886,116 (GRCm39) |
missense |
probably benign |
0.08 |
R8508:Arhgap21
|
UTSW |
2 |
20,858,991 (GRCm39) |
missense |
probably benign |
0.17 |
R8835:Arhgap21
|
UTSW |
2 |
20,972,144 (GRCm39) |
nonsense |
probably null |
|
R9140:Arhgap21
|
UTSW |
2 |
20,886,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Arhgap21
|
UTSW |
2 |
20,858,983 (GRCm39) |
missense |
probably null |
0.04 |
R9204:Arhgap21
|
UTSW |
2 |
20,885,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Arhgap21
|
UTSW |
2 |
20,860,469 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9230:Arhgap21
|
UTSW |
2 |
20,860,469 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9308:Arhgap21
|
UTSW |
2 |
20,854,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R9374:Arhgap21
|
UTSW |
2 |
20,886,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Arhgap21
|
UTSW |
2 |
20,885,464 (GRCm39) |
missense |
probably benign |
|
R9454:Arhgap21
|
UTSW |
2 |
20,870,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R9499:Arhgap21
|
UTSW |
2 |
20,886,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9544:Arhgap21
|
UTSW |
2 |
20,858,938 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9552:Arhgap21
|
UTSW |
2 |
20,886,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Arhgap21
|
UTSW |
2 |
20,896,953 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9588:Arhgap21
|
UTSW |
2 |
20,858,938 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9749:Arhgap21
|
UTSW |
2 |
20,854,026 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Arhgap21
|
UTSW |
2 |
20,886,283 (GRCm39) |
missense |
probably benign |
0.30 |
|
Predicted Primers |
PCR Primer
(F):5'- CACACTGACCCTTTTCAGACAGGC -3'
(R):5'- GGGTGGTTATAATGCATCTAACGCTAGG -3'
Sequencing Primer
(F):5'- CATGGTCTGCTCAGAGAATAAATAC -3'
(R):5'- GCTAGGAACAAATATACATCCTGTC -3'
|
Posted On |
2013-06-12 |