Incidental Mutation 'R2144:Ralgapa2'
ID |
236585 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ralgapa2
|
Ensembl Gene |
ENSMUSG00000037110 |
Gene Name |
Ral GTPase activating protein, alpha subunit 2 (catalytic) |
Synonyms |
AS250, A230067G21Rik, RGC2 |
MMRRC Submission |
040147-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.250)
|
Stock # |
R2144 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
146081799-146354264 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 146230524 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Leucine
at position 1014
(V1014L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153734
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000109986]
[ENSMUST00000131824]
[ENSMUST00000228797]
|
AlphaFold |
A3KGS3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109986
AA Change: V967L
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000105613 Gene: ENSMUSG00000037110 AA Change: V967L
Domain | Start | End | E-Value | Type |
low complexity region
|
469 |
480 |
N/A |
INTRINSIC |
low complexity region
|
1017 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1296 |
1301 |
N/A |
INTRINSIC |
Pfam:Rap_GAP
|
1701 |
1877 |
6.8e-48 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000131824
AA Change: V929L
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000122039 Gene: ENSMUSG00000037110 AA Change: V929L
Domain | Start | End | E-Value | Type |
low complexity region
|
469 |
480 |
N/A |
INTRINSIC |
low complexity region
|
979 |
990 |
N/A |
INTRINSIC |
low complexity region
|
1258 |
1263 |
N/A |
INTRINSIC |
Pfam:Rap_GAP
|
1663 |
1842 |
1.3e-66 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000146307
|
SMART Domains |
Protein: ENSMUSP00000114547 Gene: ENSMUSG00000037110
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
17 |
N/A |
INTRINSIC |
low complexity region
|
285 |
290 |
N/A |
INTRINSIC |
Pfam:Rap_GAP
|
690 |
830 |
4.9e-39 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148784
|
Predicted Effect |
unknown
Transcript: ENSMUST00000149499
AA Change: V599L
|
SMART Domains |
Protein: ENSMUSP00000122017 Gene: ENSMUSG00000037110 AA Change: V599L
Domain | Start | End | E-Value | Type |
low complexity region
|
140 |
151 |
N/A |
INTRINSIC |
low complexity region
|
650 |
661 |
N/A |
INTRINSIC |
low complexity region
|
929 |
934 |
N/A |
INTRINSIC |
Pfam:Rap_GAP
|
1334 |
1511 |
2.4e-48 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000228797
AA Change: V1014L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.1%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased incidence and severity of induced urothelial bladder tumors. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
T |
A |
4: 88,786,412 (GRCm39) |
T69S |
unknown |
Het |
4930553M12Rik |
G |
A |
4: 88,786,411 (GRCm39) |
T69I |
unknown |
Het |
Acsl6 |
A |
T |
11: 54,232,604 (GRCm39) |
Q485L |
probably damaging |
Het |
Adam5 |
C |
A |
8: 25,305,496 (GRCm39) |
V81F |
probably benign |
Het |
Aoc1l1 |
A |
G |
6: 48,952,225 (GRCm39) |
H50R |
probably benign |
Het |
Bag2 |
A |
G |
1: 33,785,912 (GRCm39) |
S137P |
possibly damaging |
Het |
Birc6 |
A |
T |
17: 74,967,408 (GRCm39) |
Q4103L |
possibly damaging |
Het |
Camta2 |
A |
G |
11: 70,562,401 (GRCm39) |
F999L |
probably benign |
Het |
Cap2 |
A |
T |
13: 46,713,978 (GRCm39) |
|
probably null |
Het |
Ccnk |
T |
A |
12: 108,155,349 (GRCm39) |
L102Q |
probably null |
Het |
Cd52 |
T |
C |
4: 133,821,048 (GRCm39) |
|
probably benign |
Het |
Cdc123 |
A |
T |
2: 5,815,617 (GRCm39) |
I160K |
probably benign |
Het |
Cep85l |
T |
C |
10: 53,234,222 (GRCm39) |
N52S |
probably benign |
Het |
Cntnap5a |
C |
T |
1: 116,029,440 (GRCm39) |
T298I |
probably benign |
Het |
Cpsf4 |
G |
T |
5: 145,115,572 (GRCm39) |
S192I |
probably benign |
Het |
Cpxm1 |
A |
G |
2: 130,239,330 (GRCm39) |
S33P |
probably benign |
Het |
Cyp2a12 |
A |
T |
7: 26,734,194 (GRCm39) |
T376S |
possibly damaging |
Het |
Cyp3a16 |
A |
G |
5: 145,392,894 (GRCm39) |
F137S |
probably damaging |
Het |
Des |
A |
G |
1: 75,343,448 (GRCm39) |
T444A |
probably benign |
Het |
Dgcr8 |
C |
T |
16: 18,102,120 (GRCm39) |
G54D |
probably damaging |
Het |
Dmac2l |
A |
G |
12: 69,787,828 (GRCm39) |
Q88R |
probably damaging |
Het |
Dsc3 |
A |
G |
18: 20,113,743 (GRCm39) |
F393S |
possibly damaging |
Het |
Dstyk |
T |
A |
1: 132,391,113 (GRCm39) |
M838K |
probably damaging |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Eml5 |
A |
C |
12: 98,776,864 (GRCm39) |
F1417C |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,851,384 (GRCm39) |
M1366K |
unknown |
Het |
Epg5 |
G |
T |
18: 77,997,412 (GRCm39) |
C425F |
possibly damaging |
Het |
Epha3 |
C |
G |
16: 63,593,680 (GRCm39) |
R136P |
possibly damaging |
Het |
Extl1 |
C |
A |
4: 134,098,355 (GRCm39) |
E225D |
probably benign |
Het |
Fam186b |
A |
G |
15: 99,178,538 (GRCm39) |
Y263H |
probably benign |
Het |
Fbn2 |
A |
G |
18: 58,186,065 (GRCm39) |
V1761A |
possibly damaging |
Het |
Fer1l6 |
T |
A |
15: 58,499,383 (GRCm39) |
M1251K |
probably benign |
Het |
Gart |
A |
T |
16: 91,426,969 (GRCm39) |
I555N |
probably damaging |
Het |
Gm11596 |
A |
T |
11: 99,683,789 (GRCm39) |
C110* |
probably null |
Het |
Gnptab |
C |
T |
10: 88,264,368 (GRCm39) |
S262L |
possibly damaging |
Het |
Gpr21 |
T |
C |
2: 37,408,243 (GRCm39) |
V263A |
probably benign |
Het |
Gxylt1 |
T |
C |
15: 93,152,361 (GRCm39) |
I224V |
probably benign |
Het |
H2-Aa |
A |
G |
17: 34,502,801 (GRCm39) |
S122P |
probably damaging |
Het |
Hsph1 |
A |
C |
5: 149,553,802 (GRCm39) |
|
probably null |
Het |
Hunk |
G |
A |
16: 90,229,420 (GRCm39) |
D94N |
probably damaging |
Het |
Ikbke |
C |
A |
1: 131,201,211 (GRCm39) |
V176L |
probably damaging |
Het |
Inpp5k |
A |
T |
11: 75,538,017 (GRCm39) |
|
probably null |
Het |
Ints10 |
A |
G |
8: 69,249,457 (GRCm39) |
T96A |
probably damaging |
Het |
Kansl2 |
A |
T |
15: 98,424,512 (GRCm39) |
V306E |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,758,657 (GRCm39) |
D42G |
possibly damaging |
Het |
Klhl7 |
A |
T |
5: 24,305,861 (GRCm39) |
M37L |
probably benign |
Het |
Krtap1-5 |
T |
C |
11: 99,471,644 (GRCm39) |
I50V |
probably benign |
Het |
Ktn1 |
A |
G |
14: 47,952,109 (GRCm39) |
E983G |
probably damaging |
Het |
Lrrk1 |
G |
A |
7: 65,945,911 (GRCm39) |
S566L |
probably damaging |
Het |
M6pr |
A |
G |
6: 122,292,326 (GRCm39) |
M174V |
probably benign |
Het |
Man2a2 |
A |
G |
7: 80,013,264 (GRCm39) |
S510P |
probably damaging |
Het |
Mmrn1 |
G |
A |
6: 60,922,059 (GRCm39) |
S172N |
possibly damaging |
Het |
Mpv17 |
A |
G |
5: 31,311,533 (GRCm39) |
|
probably null |
Het |
Mrgpra9 |
T |
C |
7: 46,885,211 (GRCm39) |
E152G |
probably benign |
Het |
Mst1r |
T |
C |
9: 107,790,367 (GRCm39) |
V660A |
probably benign |
Het |
Myof |
A |
G |
19: 37,969,669 (GRCm39) |
|
probably null |
Het |
Myrf |
G |
A |
19: 10,206,038 (GRCm39) |
P126L |
probably benign |
Het |
Nckap1l |
C |
T |
15: 103,384,103 (GRCm39) |
A567V |
probably damaging |
Het |
Nphs1 |
A |
G |
7: 30,160,395 (GRCm39) |
E169G |
probably benign |
Het |
Npy1r |
T |
A |
8: 67,157,836 (GRCm39) |
V382D |
probably benign |
Het |
Nrl |
A |
T |
14: 55,758,307 (GRCm39) |
M140K |
possibly damaging |
Het |
Odad2 |
C |
T |
18: 7,127,229 (GRCm39) |
E995K |
probably damaging |
Het |
Or14c39 |
T |
A |
7: 86,344,488 (GRCm39) |
F275I |
probably damaging |
Het |
Or2ag1b |
A |
T |
7: 106,288,164 (GRCm39) |
M258K |
probably damaging |
Het |
Or4f56 |
A |
G |
2: 111,703,768 (GRCm39) |
I144T |
probably damaging |
Het |
Or5ac17 |
C |
T |
16: 59,036,389 (GRCm39) |
V196M |
probably benign |
Het |
Or8d2 |
C |
T |
9: 38,759,635 (GRCm39) |
T75I |
probably damaging |
Het |
Orc5 |
T |
A |
5: 22,752,925 (GRCm39) |
L36F |
possibly damaging |
Het |
Osbpl1a |
A |
T |
18: 13,004,230 (GRCm39) |
S396T |
probably benign |
Het |
Pappa |
T |
A |
4: 65,099,186 (GRCm39) |
Y568* |
probably null |
Het |
Pask |
C |
T |
1: 93,249,019 (GRCm39) |
A794T |
probably benign |
Het |
Pclo |
C |
T |
5: 14,908,766 (GRCm39) |
L5025F |
unknown |
Het |
Pde3a |
T |
C |
6: 141,435,837 (GRCm39) |
V924A |
probably benign |
Het |
Pdpr |
A |
G |
8: 111,844,668 (GRCm39) |
N355S |
probably damaging |
Het |
Pepd |
A |
T |
7: 34,620,843 (GRCm39) |
K36M |
probably benign |
Het |
Pet100 |
T |
G |
8: 3,672,355 (GRCm39) |
L14R |
probably damaging |
Het |
Pfkfb2 |
T |
C |
1: 130,626,460 (GRCm39) |
T438A |
probably benign |
Het |
Pik3r6 |
T |
A |
11: 68,434,437 (GRCm39) |
L546* |
probably null |
Het |
Pira2 |
A |
T |
7: 3,847,344 (GRCm39) |
L115Q |
probably damaging |
Het |
Plxdc1 |
T |
C |
11: 97,824,838 (GRCm39) |
Y339C |
probably damaging |
Het |
Primpol |
A |
T |
8: 47,039,378 (GRCm39) |
M414K |
probably damaging |
Het |
Prol1 |
A |
T |
5: 88,476,254 (GRCm39) |
T215S |
unknown |
Het |
Prss22 |
A |
G |
17: 24,213,656 (GRCm39) |
Y212H |
probably damaging |
Het |
Rap1gap2 |
G |
A |
11: 74,316,802 (GRCm39) |
T245M |
probably damaging |
Het |
Rbm26 |
T |
A |
14: 105,352,638 (GRCm39) |
R1009* |
probably null |
Het |
Rbm42 |
A |
G |
7: 30,340,535 (GRCm39) |
*450Q |
probably null |
Het |
Rere |
T |
C |
4: 150,701,388 (GRCm39) |
V1256A |
probably damaging |
Het |
Rmi1 |
G |
T |
13: 58,555,797 (GRCm39) |
L15F |
probably damaging |
Het |
Rnf213 |
T |
C |
11: 119,334,516 (GRCm39) |
S3242P |
probably damaging |
Het |
Rtel1 |
T |
A |
2: 180,965,499 (GRCm39) |
V167E |
probably damaging |
Het |
Scgb1b2 |
G |
T |
7: 30,991,188 (GRCm39) |
|
probably benign |
Het |
Sin3b |
T |
C |
8: 73,457,893 (GRCm39) |
L203P |
probably damaging |
Het |
Skint6 |
T |
C |
4: 113,093,457 (GRCm39) |
S229G |
possibly damaging |
Het |
Slco1a4 |
T |
C |
6: 141,755,104 (GRCm39) |
Y566C |
probably damaging |
Het |
Smgc |
T |
G |
15: 91,728,624 (GRCm39) |
D121E |
possibly damaging |
Het |
Sned1 |
T |
A |
1: 93,199,406 (GRCm39) |
F495L |
probably damaging |
Het |
St7 |
A |
T |
6: 17,886,006 (GRCm39) |
N52I |
possibly damaging |
Het |
Sycn |
C |
A |
7: 28,240,494 (GRCm39) |
Q54K |
probably benign |
Het |
Syngr4 |
A |
G |
7: 45,536,464 (GRCm39) |
V186A |
probably benign |
Het |
Tars3 |
G |
A |
7: 65,305,539 (GRCm39) |
M254I |
possibly damaging |
Het |
Tcaf2 |
A |
T |
6: 42,619,738 (GRCm39) |
H96Q |
probably benign |
Het |
Tcp11l2 |
T |
C |
10: 84,449,363 (GRCm39) |
Y443H |
probably damaging |
Het |
Tmem200c |
A |
T |
17: 69,149,244 (GRCm39) |
Q609L |
possibly damaging |
Het |
Tmx3 |
G |
A |
18: 90,535,614 (GRCm39) |
G83R |
probably damaging |
Het |
Tpgs2 |
A |
C |
18: 25,301,598 (GRCm39) |
V23G |
possibly damaging |
Het |
Trhr |
T |
C |
15: 44,060,579 (GRCm39) |
V33A |
probably benign |
Het |
Trim66 |
A |
T |
7: 109,074,320 (GRCm39) |
I647N |
probably damaging |
Het |
Trnt1 |
A |
G |
6: 106,755,000 (GRCm39) |
K244E |
probably damaging |
Het |
Tsfm |
G |
A |
10: 126,864,314 (GRCm39) |
Q134* |
probably null |
Het |
Ttll9 |
A |
G |
2: 152,844,927 (GRCm39) |
T432A |
probably benign |
Het |
Vmn2r78 |
C |
T |
7: 86,603,690 (GRCm39) |
L623F |
probably damaging |
Het |
Wdr55 |
A |
G |
18: 36,895,419 (GRCm39) |
N132S |
possibly damaging |
Het |
Wipf2 |
A |
T |
11: 98,787,040 (GRCm39) |
R356S |
possibly damaging |
Het |
Wnk1 |
A |
G |
6: 119,925,949 (GRCm39) |
|
probably benign |
Het |
Zfp260 |
A |
G |
7: 29,804,765 (GRCm39) |
K222E |
probably damaging |
Het |
Zfp300 |
A |
G |
X: 20,948,190 (GRCm39) |
S525P |
possibly damaging |
Het |
Zfp592 |
A |
G |
7: 80,687,950 (GRCm39) |
T959A |
probably benign |
Het |
|
Other mutations in Ralgapa2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00666:Ralgapa2
|
APN |
2 |
146,327,056 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL00915:Ralgapa2
|
APN |
2 |
146,184,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01012:Ralgapa2
|
APN |
2 |
146,263,659 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01018:Ralgapa2
|
APN |
2 |
146,252,112 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01018:Ralgapa2
|
APN |
2 |
146,252,113 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01902:Ralgapa2
|
APN |
2 |
146,156,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Ralgapa2
|
APN |
2 |
146,190,360 (GRCm39) |
splice site |
probably benign |
|
IGL02321:Ralgapa2
|
APN |
2 |
146,254,736 (GRCm39) |
nonsense |
probably null |
|
IGL02412:Ralgapa2
|
APN |
2 |
146,254,052 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03026:Ralgapa2
|
APN |
2 |
146,302,695 (GRCm39) |
splice site |
probably benign |
|
IGL03115:Ralgapa2
|
APN |
2 |
146,266,734 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03256:Ralgapa2
|
APN |
2 |
146,302,632 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03379:Ralgapa2
|
APN |
2 |
146,199,907 (GRCm39) |
missense |
probably benign |
0.01 |
Chow
|
UTSW |
2 |
146,188,638 (GRCm39) |
nonsense |
probably null |
|
purina
|
UTSW |
2 |
146,175,406 (GRCm39) |
missense |
probably damaging |
1.00 |
P4748:Ralgapa2
|
UTSW |
2 |
146,188,731 (GRCm39) |
nonsense |
probably null |
|
R0012:Ralgapa2
|
UTSW |
2 |
146,254,672 (GRCm39) |
missense |
probably benign |
|
R0012:Ralgapa2
|
UTSW |
2 |
146,254,672 (GRCm39) |
missense |
probably benign |
|
R0165:Ralgapa2
|
UTSW |
2 |
146,230,407 (GRCm39) |
splice site |
probably benign |
|
R0344:Ralgapa2
|
UTSW |
2 |
146,188,714 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0402:Ralgapa2
|
UTSW |
2 |
146,276,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R0419:Ralgapa2
|
UTSW |
2 |
146,270,592 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0638:Ralgapa2
|
UTSW |
2 |
146,184,112 (GRCm39) |
missense |
probably benign |
0.00 |
R0704:Ralgapa2
|
UTSW |
2 |
146,293,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R0722:Ralgapa2
|
UTSW |
2 |
146,230,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R0866:Ralgapa2
|
UTSW |
2 |
146,277,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1065:Ralgapa2
|
UTSW |
2 |
146,292,478 (GRCm39) |
missense |
probably benign |
0.00 |
R1212:Ralgapa2
|
UTSW |
2 |
146,199,902 (GRCm39) |
missense |
probably benign |
0.00 |
R1395:Ralgapa2
|
UTSW |
2 |
146,230,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1614:Ralgapa2
|
UTSW |
2 |
146,230,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R1686:Ralgapa2
|
UTSW |
2 |
146,199,920 (GRCm39) |
missense |
probably benign |
0.09 |
R1799:Ralgapa2
|
UTSW |
2 |
146,184,648 (GRCm39) |
missense |
probably benign |
0.02 |
R1905:Ralgapa2
|
UTSW |
2 |
146,229,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1956:Ralgapa2
|
UTSW |
2 |
146,302,679 (GRCm39) |
missense |
probably benign |
0.00 |
R2148:Ralgapa2
|
UTSW |
2 |
146,273,807 (GRCm39) |
missense |
probably benign |
0.02 |
R2219:Ralgapa2
|
UTSW |
2 |
146,263,599 (GRCm39) |
missense |
probably benign |
0.09 |
R2220:Ralgapa2
|
UTSW |
2 |
146,263,599 (GRCm39) |
missense |
probably benign |
0.09 |
R2261:Ralgapa2
|
UTSW |
2 |
146,184,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2402:Ralgapa2
|
UTSW |
2 |
146,195,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2495:Ralgapa2
|
UTSW |
2 |
146,203,320 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3752:Ralgapa2
|
UTSW |
2 |
146,263,551 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3953:Ralgapa2
|
UTSW |
2 |
146,277,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R3956:Ralgapa2
|
UTSW |
2 |
146,277,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R4177:Ralgapa2
|
UTSW |
2 |
146,327,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R4182:Ralgapa2
|
UTSW |
2 |
146,277,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4193:Ralgapa2
|
UTSW |
2 |
146,184,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R4332:Ralgapa2
|
UTSW |
2 |
146,102,288 (GRCm39) |
missense |
probably benign |
0.10 |
R4507:Ralgapa2
|
UTSW |
2 |
146,195,168 (GRCm39) |
missense |
probably benign |
0.11 |
R4574:Ralgapa2
|
UTSW |
2 |
146,277,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Ralgapa2
|
UTSW |
2 |
146,156,944 (GRCm39) |
missense |
probably damaging |
0.99 |
R4627:Ralgapa2
|
UTSW |
2 |
146,203,373 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4647:Ralgapa2
|
UTSW |
2 |
146,229,549 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4677:Ralgapa2
|
UTSW |
2 |
146,187,387 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4724:Ralgapa2
|
UTSW |
2 |
146,187,453 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4760:Ralgapa2
|
UTSW |
2 |
146,188,669 (GRCm39) |
missense |
probably benign |
0.00 |
R4831:Ralgapa2
|
UTSW |
2 |
146,246,987 (GRCm39) |
intron |
probably benign |
|
R4962:Ralgapa2
|
UTSW |
2 |
146,276,754 (GRCm39) |
nonsense |
probably null |
|
R4993:Ralgapa2
|
UTSW |
2 |
146,289,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R5041:Ralgapa2
|
UTSW |
2 |
146,327,071 (GRCm39) |
missense |
probably benign |
0.00 |
R5120:Ralgapa2
|
UTSW |
2 |
146,254,004 (GRCm39) |
missense |
probably benign |
0.26 |
R5185:Ralgapa2
|
UTSW |
2 |
146,230,406 (GRCm39) |
splice site |
probably null |
|
R5393:Ralgapa2
|
UTSW |
2 |
146,187,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R5428:Ralgapa2
|
UTSW |
2 |
146,176,414 (GRCm39) |
missense |
probably damaging |
0.96 |
R5439:Ralgapa2
|
UTSW |
2 |
146,184,430 (GRCm39) |
missense |
probably benign |
0.08 |
R5476:Ralgapa2
|
UTSW |
2 |
146,289,356 (GRCm39) |
missense |
probably benign |
|
R5695:Ralgapa2
|
UTSW |
2 |
146,175,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R5705:Ralgapa2
|
UTSW |
2 |
146,291,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R5718:Ralgapa2
|
UTSW |
2 |
146,295,326 (GRCm39) |
splice site |
probably null |
|
R5817:Ralgapa2
|
UTSW |
2 |
146,175,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Ralgapa2
|
UTSW |
2 |
146,230,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:Ralgapa2
|
UTSW |
2 |
146,203,373 (GRCm39) |
missense |
probably benign |
0.00 |
R6048:Ralgapa2
|
UTSW |
2 |
146,276,765 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6158:Ralgapa2
|
UTSW |
2 |
146,266,596 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6169:Ralgapa2
|
UTSW |
2 |
146,292,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6280:Ralgapa2
|
UTSW |
2 |
146,184,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Ralgapa2
|
UTSW |
2 |
146,169,331 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6650:Ralgapa2
|
UTSW |
2 |
146,230,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Ralgapa2
|
UTSW |
2 |
146,184,621 (GRCm39) |
missense |
probably damaging |
0.98 |
R7020:Ralgapa2
|
UTSW |
2 |
146,188,638 (GRCm39) |
nonsense |
probably null |
|
R7035:Ralgapa2
|
UTSW |
2 |
146,353,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R7167:Ralgapa2
|
UTSW |
2 |
146,190,374 (GRCm39) |
missense |
probably benign |
|
R7186:Ralgapa2
|
UTSW |
2 |
146,230,406 (GRCm39) |
splice site |
probably null |
|
R7252:Ralgapa2
|
UTSW |
2 |
146,184,671 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7266:Ralgapa2
|
UTSW |
2 |
146,176,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R7371:Ralgapa2
|
UTSW |
2 |
146,189,046 (GRCm39) |
missense |
probably benign |
0.05 |
R7432:Ralgapa2
|
UTSW |
2 |
146,276,776 (GRCm39) |
missense |
probably benign |
0.41 |
R7470:Ralgapa2
|
UTSW |
2 |
146,266,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Ralgapa2
|
UTSW |
2 |
146,260,335 (GRCm39) |
missense |
probably benign |
0.01 |
R7780:Ralgapa2
|
UTSW |
2 |
146,184,334 (GRCm39) |
missense |
probably benign |
0.14 |
R7973:Ralgapa2
|
UTSW |
2 |
146,230,481 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8018:Ralgapa2
|
UTSW |
2 |
146,182,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R8063:Ralgapa2
|
UTSW |
2 |
146,285,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Ralgapa2
|
UTSW |
2 |
146,195,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R8264:Ralgapa2
|
UTSW |
2 |
146,175,370 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8309:Ralgapa2
|
UTSW |
2 |
146,246,786 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8409:Ralgapa2
|
UTSW |
2 |
146,086,897 (GRCm39) |
missense |
|
|
R8474:Ralgapa2
|
UTSW |
2 |
146,266,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8487:Ralgapa2
|
UTSW |
2 |
146,230,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Ralgapa2
|
UTSW |
2 |
146,184,524 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8733:Ralgapa2
|
UTSW |
2 |
146,266,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8856:Ralgapa2
|
UTSW |
2 |
146,184,139 (GRCm39) |
missense |
probably benign |
0.30 |
R8858:Ralgapa2
|
UTSW |
2 |
146,102,285 (GRCm39) |
critical splice donor site |
probably null |
|
R8862:Ralgapa2
|
UTSW |
2 |
146,266,731 (GRCm39) |
missense |
probably benign |
0.41 |
R9146:Ralgapa2
|
UTSW |
2 |
146,184,252 (GRCm39) |
missense |
probably benign |
|
R9324:Ralgapa2
|
UTSW |
2 |
146,302,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R9439:Ralgapa2
|
UTSW |
2 |
146,254,058 (GRCm39) |
missense |
probably benign |
|
R9457:Ralgapa2
|
UTSW |
2 |
146,176,474 (GRCm39) |
missense |
probably damaging |
0.99 |
RF019:Ralgapa2
|
UTSW |
2 |
146,203,423 (GRCm39) |
missense |
possibly damaging |
0.53 |
X0019:Ralgapa2
|
UTSW |
2 |
146,230,572 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1088:Ralgapa2
|
UTSW |
2 |
146,276,825 (GRCm39) |
missense |
probably benign |
0.20 |
|
Predicted Primers |
PCR Primer
(F):5'- GGACTAAATGAAATAACTCTCAGGC -3'
(R):5'- AATCTTCACATGATCACCCCATTG -3'
Sequencing Primer
(F):5'- CGTCTAATTTGCATTTCAGAAATGG -3'
(R):5'- CTTGTTGGGCATTCAATTTGAAAG -3'
|
Posted On |
2014-10-01 |