Incidental Mutation 'R0335:Arhgap32'
ID |
26200 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Arhgap32
|
Ensembl Gene |
ENSMUSG00000041444 |
Gene Name |
Rho GTPase activating protein 32 |
Synonyms |
p200RhoGAP, Grit, PX-RICS, GC-GAP, 3426406O18Rik |
MMRRC Submission |
038544-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0335 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
9 |
Chromosomal Location |
32027432-32179742 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 32171056 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Alanine
at position 1279
(S1279A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138145
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000168954]
[ENSMUST00000174641]
[ENSMUST00000182802]
|
AlphaFold |
Q811P8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000168954
AA Change: S1279A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000128448 Gene: ENSMUSG00000041444 AA Change: S1279A
Domain | Start | End | E-Value | Type |
RhoGAP
|
34 |
215 |
9.6e-60 |
SMART |
Blast:RhoGAP
|
232 |
298 |
7e-31 |
BLAST |
low complexity region
|
518 |
533 |
N/A |
INTRINSIC |
low complexity region
|
669 |
689 |
N/A |
INTRINSIC |
low complexity region
|
696 |
710 |
N/A |
INTRINSIC |
low complexity region
|
913 |
926 |
N/A |
INTRINSIC |
low complexity region
|
960 |
974 |
N/A |
INTRINSIC |
low complexity region
|
997 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1076 |
1093 |
N/A |
INTRINSIC |
low complexity region
|
1304 |
1317 |
N/A |
INTRINSIC |
low complexity region
|
1691 |
1700 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174641
AA Change: S1628A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000133898 Gene: ENSMUSG00000041444 AA Change: S1628A
Domain | Start | End | E-Value | Type |
Pfam:PX
|
132 |
226 |
5.6e-7 |
PFAM |
SH3
|
262 |
320 |
7.4e-11 |
SMART |
RhoGAP
|
383 |
564 |
9.6e-60 |
SMART |
Blast:RhoGAP
|
581 |
647 |
9e-31 |
BLAST |
low complexity region
|
867 |
882 |
N/A |
INTRINSIC |
low complexity region
|
1018 |
1038 |
N/A |
INTRINSIC |
low complexity region
|
1045 |
1059 |
N/A |
INTRINSIC |
low complexity region
|
1262 |
1275 |
N/A |
INTRINSIC |
low complexity region
|
1309 |
1323 |
N/A |
INTRINSIC |
low complexity region
|
1346 |
1357 |
N/A |
INTRINSIC |
low complexity region
|
1425 |
1442 |
N/A |
INTRINSIC |
low complexity region
|
1653 |
1666 |
N/A |
INTRINSIC |
low complexity region
|
2040 |
2049 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182802
AA Change: S1279A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000138145 Gene: ENSMUSG00000041444 AA Change: S1279A
Domain | Start | End | E-Value | Type |
RhoGAP
|
34 |
215 |
9.6e-60 |
SMART |
Blast:RhoGAP
|
232 |
298 |
7e-31 |
BLAST |
low complexity region
|
518 |
533 |
N/A |
INTRINSIC |
low complexity region
|
669 |
689 |
N/A |
INTRINSIC |
low complexity region
|
696 |
710 |
N/A |
INTRINSIC |
low complexity region
|
913 |
926 |
N/A |
INTRINSIC |
low complexity region
|
960 |
974 |
N/A |
INTRINSIC |
low complexity region
|
997 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1076 |
1093 |
N/A |
INTRINSIC |
low complexity region
|
1304 |
1317 |
N/A |
INTRINSIC |
low complexity region
|
1691 |
1700 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.0605 |
Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.6%
- 10x: 94.6%
- 20x: 87.5%
|
Validation Efficiency |
100% (89/89) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] RICS is a neuron-associated GTPase-activating protein that may regulate dendritic spine morphology and strength by modulating Rho GTPase (see RHOA; MIM 165390) activity (Okabe et al., 2003 [PubMed 12531901]).[supplied by OMIM, Mar 2008] PHENOTYPE: Mice homozygous for a null mutation are fertile but display abnormal neurite growth. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
G |
T |
15: 11,311,144 (GRCm39) |
D1134Y |
possibly damaging |
Het |
Add3 |
A |
G |
19: 53,225,259 (GRCm39) |
T460A |
probably benign |
Het |
Amer3 |
A |
C |
1: 34,618,381 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
C |
T |
14: 33,081,065 (GRCm39) |
|
probably benign |
Het |
Bcas1 |
G |
A |
2: 170,260,601 (GRCm39) |
T26M |
probably damaging |
Het |
Begain |
A |
T |
12: 109,004,860 (GRCm39) |
F256I |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,023,301 (GRCm39) |
V2210A |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,492,883 (GRCm39) |
I1804N |
probably damaging |
Het |
Cad |
G |
A |
5: 31,231,329 (GRCm39) |
|
probably benign |
Het |
Carmil1 |
G |
A |
13: 24,257,966 (GRCm39) |
S762L |
probably damaging |
Het |
Ccdc93 |
T |
A |
1: 121,420,706 (GRCm39) |
L529Q |
probably damaging |
Het |
Cdh12 |
T |
A |
15: 21,578,635 (GRCm39) |
|
probably null |
Het |
Cep15 |
A |
G |
14: 12,301,266 (GRCm38) |
E124G |
possibly damaging |
Het |
Clip2 |
T |
A |
5: 134,564,069 (GRCm39) |
|
probably benign |
Het |
Cmip |
T |
C |
8: 118,172,105 (GRCm39) |
I480T |
probably damaging |
Het |
Cnot1 |
A |
T |
8: 96,498,628 (GRCm39) |
I203K |
probably benign |
Het |
Col18a1 |
G |
A |
10: 76,895,197 (GRCm39) |
P1155S |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,531,956 (GRCm39) |
|
probably benign |
Het |
Crybg3 |
A |
T |
16: 59,364,503 (GRCm39) |
L2373Q |
probably damaging |
Het |
D130043K22Rik |
A |
T |
13: 25,071,860 (GRCm39) |
I935F |
probably damaging |
Het |
Dapl1 |
T |
A |
2: 59,326,938 (GRCm39) |
D61E |
possibly damaging |
Het |
Def6 |
A |
G |
17: 28,447,043 (GRCm39) |
D558G |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,046,382 (GRCm39) |
|
probably benign |
Het |
Dvl2 |
G |
A |
11: 69,891,861 (GRCm39) |
|
probably benign |
Het |
Ecd |
A |
C |
14: 20,370,802 (GRCm39) |
V639G |
probably benign |
Het |
Epg5 |
C |
T |
18: 78,029,687 (GRCm39) |
T1350M |
probably benign |
Het |
Erbb4 |
C |
A |
1: 68,298,418 (GRCm39) |
M657I |
probably benign |
Het |
Evi5 |
T |
C |
5: 107,960,277 (GRCm39) |
R431G |
probably benign |
Het |
Fbxo11 |
G |
A |
17: 88,323,041 (GRCm39) |
A115V |
possibly damaging |
Het |
Fgfr2 |
T |
C |
7: 129,797,979 (GRCm39) |
T192A |
probably benign |
Het |
Gas7 |
C |
T |
11: 67,552,878 (GRCm39) |
A146V |
possibly damaging |
Het |
Gatad2b |
T |
A |
3: 90,263,489 (GRCm39) |
S529T |
probably benign |
Het |
Gm10722 |
G |
T |
9: 3,001,048 (GRCm39) |
Q41H |
probably null |
Het |
Gm10801 |
G |
C |
2: 98,494,352 (GRCm39) |
R143T |
possibly damaging |
Het |
Gm7535 |
A |
G |
17: 18,131,374 (GRCm39) |
|
probably benign |
Het |
Gstm1 |
T |
A |
3: 107,920,012 (GRCm39) |
N193I |
possibly damaging |
Het |
Heatr5b |
G |
A |
17: 79,135,375 (GRCm39) |
P252L |
probably benign |
Het |
Hmgb1 |
A |
G |
5: 148,987,441 (GRCm39) |
V36A |
probably benign |
Het |
Hrh1 |
G |
T |
6: 114,457,193 (GRCm39) |
W158L |
probably damaging |
Het |
Ighv6-4 |
T |
C |
12: 114,370,294 (GRCm39) |
M53V |
probably benign |
Het |
Iqgap2 |
T |
A |
13: 95,772,141 (GRCm39) |
D1346V |
probably damaging |
Het |
Kcng3 |
A |
T |
17: 83,895,166 (GRCm39) |
N433K |
possibly damaging |
Het |
Kif1a |
T |
A |
1: 92,980,288 (GRCm39) |
|
probably benign |
Het |
Lctl |
C |
A |
9: 64,026,169 (GRCm39) |
Q75K |
probably benign |
Het |
Ldb3 |
T |
A |
14: 34,300,608 (GRCm39) |
I89F |
possibly damaging |
Het |
Lrrc49 |
A |
T |
9: 60,584,378 (GRCm39) |
L156Q |
probably damaging |
Het |
Mark2 |
G |
T |
19: 7,259,193 (GRCm39) |
T83K |
probably benign |
Het |
Ms4a15 |
A |
T |
19: 10,957,574 (GRCm39) |
D170E |
probably damaging |
Het |
Msantd2 |
A |
G |
9: 37,434,056 (GRCm39) |
S99G |
possibly damaging |
Het |
Nemf |
G |
T |
12: 69,400,577 (GRCm39) |
T124N |
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,093,561 (GRCm39) |
F35I |
possibly damaging |
Het |
Nwd2 |
A |
G |
5: 63,962,116 (GRCm39) |
I567V |
probably benign |
Het |
Optn |
C |
T |
2: 5,028,926 (GRCm39) |
G526R |
probably damaging |
Het |
Or11l3 |
T |
C |
11: 58,516,566 (GRCm39) |
Y102C |
probably damaging |
Het |
Or13p8 |
A |
G |
4: 118,584,367 (GRCm39) |
I308V |
probably null |
Het |
Or5v1b |
A |
C |
17: 37,841,533 (GRCm39) |
I222L |
probably benign |
Het |
Or7g16 |
T |
A |
9: 18,727,290 (GRCm39) |
Q100L |
probably damaging |
Het |
Pdk4 |
T |
C |
6: 5,491,138 (GRCm39) |
E209G |
probably benign |
Het |
Plch1 |
T |
C |
3: 63,618,399 (GRCm39) |
Q712R |
probably damaging |
Het |
Pnpla1 |
T |
A |
17: 29,105,852 (GRCm39) |
V569E |
possibly damaging |
Het |
Prkar2a |
A |
T |
9: 108,596,457 (GRCm39) |
D134V |
probably damaging |
Het |
Ptov1 |
T |
A |
7: 44,514,046 (GRCm39) |
Q40L |
possibly damaging |
Het |
Ptprq |
T |
C |
10: 107,544,589 (GRCm39) |
I314V |
probably benign |
Het |
Rabl2 |
T |
C |
15: 89,468,169 (GRCm39) |
K66E |
probably damaging |
Het |
Rnf38 |
A |
G |
4: 44,152,507 (GRCm39) |
V19A |
possibly damaging |
Het |
Scn2a |
T |
A |
2: 65,512,435 (GRCm39) |
W191R |
probably damaging |
Het |
Sec22b |
T |
A |
3: 97,828,572 (GRCm39) |
F212I |
possibly damaging |
Het |
Sec24c |
T |
A |
14: 20,738,783 (GRCm39) |
|
probably null |
Het |
Septin2 |
T |
C |
1: 93,423,321 (GRCm39) |
S51P |
probably damaging |
Het |
Serpinb1a |
T |
C |
13: 33,032,639 (GRCm39) |
N90S |
probably damaging |
Het |
Slc1a2 |
C |
T |
2: 102,574,208 (GRCm39) |
T206I |
probably benign |
Het |
Slc25a19 |
C |
A |
11: 115,515,032 (GRCm39) |
R42L |
probably damaging |
Het |
St14 |
G |
A |
9: 31,002,620 (GRCm39) |
|
probably benign |
Het |
Stxbp1 |
C |
T |
2: 32,692,917 (GRCm39) |
|
probably benign |
Het |
Tas2r131 |
C |
T |
6: 132,934,792 (GRCm39) |
V6I |
probably benign |
Het |
Tdo2 |
T |
A |
3: 81,871,307 (GRCm39) |
M235L |
probably benign |
Het |
Tenm3 |
T |
G |
8: 48,685,140 (GRCm39) |
H2432P |
probably damaging |
Het |
Tmprss15 |
C |
T |
16: 78,821,630 (GRCm39) |
|
probably benign |
Het |
Tmx1 |
A |
G |
12: 70,500,030 (GRCm39) |
N30D |
probably benign |
Het |
Tom1 |
A |
G |
8: 75,791,020 (GRCm39) |
|
probably null |
Het |
Top2a |
T |
C |
11: 98,913,781 (GRCm39) |
N20S |
probably benign |
Het |
Ttc23l |
T |
A |
15: 10,540,049 (GRCm39) |
T145S |
probably benign |
Het |
Unc13b |
T |
A |
4: 43,236,983 (GRCm39) |
M3351K |
possibly damaging |
Het |
Vmn1r47 |
T |
C |
6: 89,999,641 (GRCm39) |
S258P |
probably damaging |
Het |
Vmn2r8 |
T |
G |
5: 108,945,317 (GRCm39) |
|
probably null |
Het |
Vps11 |
T |
C |
9: 44,265,135 (GRCm39) |
Q641R |
probably null |
Het |
Wapl |
T |
A |
14: 34,414,281 (GRCm39) |
I381N |
probably damaging |
Het |
Zmym6 |
G |
A |
4: 127,016,601 (GRCm39) |
G794E |
probably damaging |
Het |
|
Other mutations in Arhgap32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01020:Arhgap32
|
APN |
9 |
32,168,657 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01317:Arhgap32
|
APN |
9 |
32,168,260 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01614:Arhgap32
|
APN |
9 |
32,171,801 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01791:Arhgap32
|
APN |
9 |
32,158,486 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02318:Arhgap32
|
APN |
9 |
32,170,627 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02542:Arhgap32
|
APN |
9 |
32,166,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02568:Arhgap32
|
APN |
9 |
32,158,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02627:Arhgap32
|
APN |
9 |
32,157,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02927:Arhgap32
|
APN |
9 |
32,172,431 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03157:Arhgap32
|
APN |
9 |
32,170,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Arhgap32
|
APN |
9 |
32,170,816 (GRCm39) |
missense |
probably benign |
0.06 |
PIT4445001:Arhgap32
|
UTSW |
9 |
32,172,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Arhgap32
|
UTSW |
9 |
32,063,294 (GRCm39) |
missense |
probably damaging |
0.98 |
R0380:Arhgap32
|
UTSW |
9 |
32,157,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Arhgap32
|
UTSW |
9 |
32,156,551 (GRCm39) |
critical splice donor site |
probably null |
|
R0494:Arhgap32
|
UTSW |
9 |
32,170,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R0508:Arhgap32
|
UTSW |
9 |
32,101,364 (GRCm39) |
splice site |
probably benign |
|
R0856:Arhgap32
|
UTSW |
9 |
32,171,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R0990:Arhgap32
|
UTSW |
9 |
32,166,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R1312:Arhgap32
|
UTSW |
9 |
32,166,608 (GRCm39) |
missense |
probably benign |
|
R1455:Arhgap32
|
UTSW |
9 |
32,171,381 (GRCm39) |
missense |
probably benign |
0.08 |
R1515:Arhgap32
|
UTSW |
9 |
32,027,498 (GRCm39) |
missense |
probably benign |
|
R1523:Arhgap32
|
UTSW |
9 |
32,168,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Arhgap32
|
UTSW |
9 |
32,171,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R1743:Arhgap32
|
UTSW |
9 |
32,170,727 (GRCm39) |
missense |
probably benign |
0.00 |
R1999:Arhgap32
|
UTSW |
9 |
32,027,436 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2098:Arhgap32
|
UTSW |
9 |
32,171,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R2150:Arhgap32
|
UTSW |
9 |
32,027,436 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2256:Arhgap32
|
UTSW |
9 |
32,158,793 (GRCm39) |
missense |
probably damaging |
0.99 |
R2257:Arhgap32
|
UTSW |
9 |
32,158,793 (GRCm39) |
missense |
probably damaging |
0.99 |
R2989:Arhgap32
|
UTSW |
9 |
32,150,694 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3780:Arhgap32
|
UTSW |
9 |
32,063,315 (GRCm39) |
splice site |
probably null |
|
R3793:Arhgap32
|
UTSW |
9 |
32,166,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R3846:Arhgap32
|
UTSW |
9 |
32,101,320 (GRCm39) |
missense |
probably benign |
0.03 |
R4086:Arhgap32
|
UTSW |
9 |
32,158,362 (GRCm39) |
unclassified |
probably benign |
|
R4177:Arhgap32
|
UTSW |
9 |
32,158,510 (GRCm39) |
missense |
probably null |
1.00 |
R4230:Arhgap32
|
UTSW |
9 |
32,168,770 (GRCm39) |
missense |
probably benign |
0.10 |
R4280:Arhgap32
|
UTSW |
9 |
32,171,185 (GRCm39) |
missense |
probably damaging |
0.98 |
R4504:Arhgap32
|
UTSW |
9 |
32,093,135 (GRCm39) |
splice site |
probably null |
|
R4587:Arhgap32
|
UTSW |
9 |
32,172,241 (GRCm39) |
missense |
probably benign |
0.02 |
R4612:Arhgap32
|
UTSW |
9 |
32,170,775 (GRCm39) |
missense |
probably damaging |
0.99 |
R4622:Arhgap32
|
UTSW |
9 |
32,150,644 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4670:Arhgap32
|
UTSW |
9 |
32,081,441 (GRCm39) |
missense |
probably benign |
0.03 |
R4784:Arhgap32
|
UTSW |
9 |
32,172,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Arhgap32
|
UTSW |
9 |
32,040,949 (GRCm39) |
missense |
probably damaging |
0.99 |
R4785:Arhgap32
|
UTSW |
9 |
32,172,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Arhgap32
|
UTSW |
9 |
32,040,949 (GRCm39) |
missense |
probably damaging |
0.99 |
R4906:Arhgap32
|
UTSW |
9 |
32,156,552 (GRCm39) |
critical splice donor site |
probably null |
|
R5046:Arhgap32
|
UTSW |
9 |
32,168,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R5360:Arhgap32
|
UTSW |
9 |
32,170,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R5382:Arhgap32
|
UTSW |
9 |
32,063,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Arhgap32
|
UTSW |
9 |
32,159,678 (GRCm39) |
missense |
probably benign |
0.19 |
R5637:Arhgap32
|
UTSW |
9 |
32,158,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R5659:Arhgap32
|
UTSW |
9 |
32,093,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Arhgap32
|
UTSW |
9 |
32,167,084 (GRCm39) |
missense |
probably benign |
0.01 |
R6002:Arhgap32
|
UTSW |
9 |
32,168,275 (GRCm39) |
missense |
probably benign |
0.00 |
R6109:Arhgap32
|
UTSW |
9 |
32,171,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R6405:Arhgap32
|
UTSW |
9 |
32,159,784 (GRCm39) |
missense |
probably benign |
0.31 |
R6922:Arhgap32
|
UTSW |
9 |
32,063,983 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7009:Arhgap32
|
UTSW |
9 |
32,157,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R7137:Arhgap32
|
UTSW |
9 |
32,063,232 (GRCm39) |
missense |
probably benign |
0.32 |
R7183:Arhgap32
|
UTSW |
9 |
32,097,679 (GRCm39) |
missense |
probably benign |
0.15 |
R7251:Arhgap32
|
UTSW |
9 |
32,119,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7287:Arhgap32
|
UTSW |
9 |
32,063,993 (GRCm39) |
missense |
|
|
R7289:Arhgap32
|
UTSW |
9 |
32,168,234 (GRCm39) |
missense |
probably benign |
0.02 |
R7289:Arhgap32
|
UTSW |
9 |
32,168,233 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7391:Arhgap32
|
UTSW |
9 |
32,093,235 (GRCm39) |
missense |
probably benign |
0.00 |
R7408:Arhgap32
|
UTSW |
9 |
32,157,220 (GRCm39) |
missense |
probably benign |
0.06 |
R7566:Arhgap32
|
UTSW |
9 |
32,162,018 (GRCm39) |
missense |
probably benign |
0.10 |
R7584:Arhgap32
|
UTSW |
9 |
32,168,263 (GRCm39) |
missense |
probably benign |
0.16 |
R7653:Arhgap32
|
UTSW |
9 |
32,168,441 (GRCm39) |
missense |
probably benign |
|
R7884:Arhgap32
|
UTSW |
9 |
32,171,810 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8087:Arhgap32
|
UTSW |
9 |
32,168,324 (GRCm39) |
missense |
probably benign |
0.00 |
R8109:Arhgap32
|
UTSW |
9 |
32,093,150 (GRCm39) |
missense |
probably benign |
0.09 |
R8131:Arhgap32
|
UTSW |
9 |
32,158,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R8155:Arhgap32
|
UTSW |
9 |
32,093,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R8232:Arhgap32
|
UTSW |
9 |
32,168,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R8303:Arhgap32
|
UTSW |
9 |
32,172,205 (GRCm39) |
missense |
probably benign |
0.00 |
R8304:Arhgap32
|
UTSW |
9 |
32,167,233 (GRCm39) |
nonsense |
probably null |
|
R8696:Arhgap32
|
UTSW |
9 |
32,159,799 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8832:Arhgap32
|
UTSW |
9 |
32,172,115 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9112:Arhgap32
|
UTSW |
9 |
32,157,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R9170:Arhgap32
|
UTSW |
9 |
32,162,039 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9279:Arhgap32
|
UTSW |
9 |
32,168,655 (GRCm39) |
missense |
probably benign |
0.01 |
R9431:Arhgap32
|
UTSW |
9 |
32,170,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9522:Arhgap32
|
UTSW |
9 |
32,027,450 (GRCm39) |
missense |
probably benign |
|
R9526:Arhgap32
|
UTSW |
9 |
32,172,026 (GRCm39) |
missense |
probably benign |
0.28 |
R9661:Arhgap32
|
UTSW |
9 |
32,168,531 (GRCm39) |
missense |
probably benign |
0.01 |
X0027:Arhgap32
|
UTSW |
9 |
32,161,937 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0063:Arhgap32
|
UTSW |
9 |
32,172,365 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arhgap32
|
UTSW |
9 |
32,171,976 (GRCm39) |
missense |
probably damaging |
0.97 |
|
Predicted Primers |
PCR Primer
(F):5'- CTCGGTTAGGAATCCTTGTTGCCC -3'
(R):5'- AGAAATAGCCAGTTGCATTGGCCC -3'
Sequencing Primer
(F):5'- GAATCCTTGTTGCCCTGAAGAC -3'
(R):5'- ACCAGCATAGTTGTACACGTTC -3'
|
Posted On |
2013-04-16 |