Incidental Mutation 'R4700:Cd109'
ID |
394789 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cd109
|
Ensembl Gene |
ENSMUSG00000046186 |
Gene Name |
CD109 antigen |
Synonyms |
Gov platelet alloantigens, 9930012E15Rik |
MMRRC Submission |
041948-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4700 (G1)
|
Quality Score |
217 |
Status
|
Validated
|
Chromosome |
9 |
Chromosomal Location |
78522828-78623535 bp(+) (GRCm39) |
Type of Mutation |
critical splice acceptor site |
DNA Base Change (assembly) |
CATTTATTTATTTATTTATTTATTTATTTATTTAT to CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT
at 78619782 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000091330
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000093812]
|
AlphaFold |
Q8R422 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000093812
|
SMART Domains |
Protein: ENSMUSP00000091330 Gene: ENSMUSG00000046186
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
Pfam:A2M_N
|
129 |
220 |
1.5e-16 |
PFAM |
A2M_N_2
|
470 |
601 |
8.89e-32 |
SMART |
A2M
|
695 |
786 |
2.07e-32 |
SMART |
Pfam:Thiol-ester_cl
|
912 |
941 |
2.6e-20 |
PFAM |
Pfam:A2M_comp
|
961 |
1197 |
1.9e-65 |
PFAM |
low complexity region
|
1265 |
1275 |
N/A |
INTRINSIC |
A2M_recep
|
1311 |
1395 |
2.06e-27 |
SMART |
low complexity region
|
1422 |
1437 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.8%
- 20x: 94.0%
|
Validation Efficiency |
97% (127/131) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a glycosyl phosphatidylinositol (GPI)-linked glycoprotein that localizes to the surface of platelets, activated T-cells, and endothelial cells. The protein binds to and negatively regulates signalling by transforming growth factor beta (TGF-beta). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014] PHENOTYPE: Mice homozygous for a null mutation display epidermal hyperplasia and thickening, sebaceous gland hyperplasia and transient impairment of hair growth. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530084C06Rik |
A |
G |
13: 31,742,795 (GRCm39) |
|
probably benign |
Het |
Abca13 |
A |
G |
11: 9,242,306 (GRCm39) |
T1390A |
possibly damaging |
Het |
Abca14 |
T |
A |
7: 119,911,928 (GRCm39) |
|
probably null |
Het |
Abca8a |
A |
C |
11: 109,961,308 (GRCm39) |
V538G |
probably damaging |
Het |
Acy1 |
C |
T |
9: 106,310,782 (GRCm39) |
G329R |
probably benign |
Het |
Adamts17 |
T |
C |
7: 66,691,636 (GRCm39) |
C607R |
probably damaging |
Het |
Adamts20 |
A |
T |
15: 94,292,503 (GRCm39) |
C202* |
probably null |
Het |
Adcy5 |
A |
G |
16: 35,099,586 (GRCm39) |
N712S |
possibly damaging |
Het |
Ahnak |
A |
G |
19: 8,982,045 (GRCm39) |
K1110E |
probably benign |
Het |
Anks6 |
T |
A |
4: 47,033,127 (GRCm39) |
H578L |
possibly damaging |
Het |
Appl1 |
C |
A |
14: 26,647,928 (GRCm39) |
L626F |
probably benign |
Het |
Arl1 |
A |
G |
10: 88,566,499 (GRCm39) |
|
probably benign |
Het |
Atf4 |
T |
A |
15: 80,141,618 (GRCm39) |
I336K |
probably damaging |
Het |
Atp7b |
A |
T |
8: 22,490,137 (GRCm39) |
S1044T |
probably benign |
Het |
Carm1 |
A |
G |
9: 21,498,480 (GRCm39) |
N466S |
probably benign |
Het |
Cbl |
A |
G |
9: 44,084,677 (GRCm39) |
S153P |
probably damaging |
Het |
Ccdc159 |
A |
G |
9: 21,839,027 (GRCm39) |
|
probably null |
Het |
Cdc7 |
T |
C |
5: 107,121,707 (GRCm39) |
F207L |
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,304,547 (GRCm39) |
R2271G |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,088,915 (GRCm39) |
Q989R |
probably damaging |
Het |
Cep89 |
A |
G |
7: 35,137,862 (GRCm39) |
T749A |
probably benign |
Het |
Clcn5 |
T |
C |
X: 7,032,591 (GRCm39) |
|
probably null |
Het |
Clu |
A |
T |
14: 66,217,313 (GRCm39) |
Y382F |
probably benign |
Het |
Cnih4 |
A |
G |
1: 180,993,808 (GRCm39) |
|
probably benign |
Het |
Crb1 |
A |
G |
1: 139,126,509 (GRCm39) |
L1340P |
probably damaging |
Het |
Ddx4 |
T |
C |
13: 112,750,269 (GRCm39) |
T421A |
probably damaging |
Het |
Dennd5a |
T |
C |
7: 109,520,405 (GRCm39) |
E484G |
probably benign |
Het |
Dsg4 |
G |
T |
18: 20,589,965 (GRCm39) |
V372L |
possibly damaging |
Het |
Dyrk2 |
T |
C |
10: 118,704,191 (GRCm39) |
D21G |
probably benign |
Het |
E2f1 |
C |
G |
2: 154,405,942 (GRCm39) |
G144R |
probably damaging |
Het |
Epb41l4a |
A |
T |
18: 33,935,560 (GRCm39) |
|
probably null |
Het |
F10 |
G |
T |
8: 13,089,621 (GRCm39) |
V67F |
possibly damaging |
Het |
Fat3 |
A |
G |
9: 15,942,469 (GRCm39) |
I1301T |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,391,058 (GRCm39) |
T549A |
probably benign |
Het |
Flt4 |
C |
A |
11: 49,517,271 (GRCm39) |
|
probably benign |
Het |
Fndc1 |
G |
A |
17: 7,990,312 (GRCm39) |
T1128I |
unknown |
Het |
Fos |
T |
C |
12: 85,522,936 (GRCm39) |
S283P |
probably benign |
Het |
Fryl |
T |
C |
5: 73,222,881 (GRCm39) |
Y1900C |
possibly damaging |
Het |
Fsip2 |
C |
A |
2: 82,817,373 (GRCm39) |
Q4369K |
probably benign |
Het |
Gad2 |
A |
T |
2: 22,563,982 (GRCm39) |
H395L |
probably damaging |
Het |
Grm2 |
T |
A |
9: 106,531,130 (GRCm39) |
I120F |
probably benign |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Igsf10 |
A |
T |
3: 59,227,751 (GRCm39) |
I1974N |
probably damaging |
Het |
Il23r |
T |
C |
6: 67,450,834 (GRCm39) |
N215S |
probably damaging |
Het |
Jph1 |
T |
A |
1: 17,161,928 (GRCm39) |
M245L |
possibly damaging |
Het |
Loxl4 |
G |
A |
19: 42,596,052 (GRCm39) |
H147Y |
probably benign |
Het |
Lsg1 |
A |
G |
16: 30,384,267 (GRCm39) |
I521T |
probably damaging |
Het |
Ltc4s |
C |
T |
11: 50,127,908 (GRCm39) |
G83R |
probably damaging |
Het |
Map2 |
A |
G |
1: 66,449,796 (GRCm39) |
E173G |
probably damaging |
Het |
Med29 |
T |
A |
7: 28,086,352 (GRCm39) |
D152V |
possibly damaging |
Het |
Megf8 |
A |
G |
7: 25,062,940 (GRCm39) |
D2432G |
probably damaging |
Het |
Mrpl38 |
G |
A |
11: 116,025,978 (GRCm39) |
|
probably benign |
Het |
Myh7 |
A |
G |
14: 55,225,778 (GRCm39) |
I521T |
possibly damaging |
Het |
Mylk |
G |
T |
16: 34,742,805 (GRCm39) |
V1106L |
probably benign |
Het |
Myo15b |
A |
T |
11: 115,752,761 (GRCm39) |
D753V |
possibly damaging |
Het |
Myo1g |
T |
C |
11: 6,466,785 (GRCm39) |
|
probably null |
Het |
Myrfl |
A |
G |
10: 116,613,247 (GRCm39) |
|
probably null |
Het |
Naip5 |
A |
G |
13: 100,359,922 (GRCm39) |
V438A |
possibly damaging |
Het |
Nav3 |
A |
G |
10: 109,600,796 (GRCm39) |
V1277A |
probably benign |
Het |
Nek10 |
T |
A |
14: 14,842,841 (GRCm38) |
V182E |
possibly damaging |
Het |
Ngly1 |
T |
C |
14: 16,281,809 (GRCm38) |
V355A |
probably benign |
Het |
Nol6 |
T |
C |
4: 41,118,944 (GRCm39) |
E683G |
possibly damaging |
Het |
Obsl1 |
A |
T |
1: 75,480,085 (GRCm39) |
V487E |
probably damaging |
Het |
Oc90 |
T |
A |
15: 65,753,354 (GRCm39) |
R322W |
possibly damaging |
Het |
Or1q1 |
C |
A |
2: 36,887,515 (GRCm39) |
A231D |
probably benign |
Het |
Or4f60 |
A |
G |
2: 111,902,097 (GRCm39) |
V277A |
possibly damaging |
Het |
Or52e4 |
A |
T |
7: 104,705,483 (GRCm39) |
H10L |
possibly damaging |
Het |
Or8b4 |
A |
G |
9: 37,830,217 (GRCm39) |
E93G |
possibly damaging |
Het |
Osbp2 |
T |
C |
11: 3,662,160 (GRCm39) |
H231R |
probably damaging |
Het |
Pate6 |
A |
T |
9: 35,701,021 (GRCm39) |
C22S |
probably damaging |
Het |
Pdzph1 |
T |
C |
17: 59,281,541 (GRCm39) |
H247R |
probably damaging |
Het |
Pidd1 |
T |
C |
7: 141,022,162 (GRCm39) |
N209S |
probably damaging |
Het |
Pknox1 |
C |
T |
17: 31,822,286 (GRCm39) |
A351V |
probably damaging |
Het |
Plxnd1 |
C |
A |
6: 115,935,576 (GRCm39) |
V1737F |
probably damaging |
Het |
Prkdc |
A |
T |
16: 15,519,976 (GRCm39) |
K1138M |
probably damaging |
Het |
Rad54l2 |
T |
C |
9: 106,631,224 (GRCm39) |
D21G |
possibly damaging |
Het |
Recql4 |
C |
T |
15: 76,592,785 (GRCm39) |
C302Y |
probably damaging |
Het |
Scgb2b6 |
T |
C |
7: 31,318,908 (GRCm39) |
|
noncoding transcript |
Het |
Sdc1 |
A |
G |
12: 8,840,541 (GRCm39) |
E106G |
possibly damaging |
Het |
Slc10a5 |
T |
G |
3: 10,400,360 (GRCm39) |
Q100P |
probably damaging |
Het |
Slc10a5 |
C |
A |
3: 10,400,359 (GRCm39) |
Q100H |
probably damaging |
Het |
Slc5a9 |
A |
T |
4: 111,748,134 (GRCm39) |
L226Q |
possibly damaging |
Het |
Slfn1 |
T |
C |
11: 83,012,475 (GRCm39) |
V197A |
probably benign |
Het |
Spire1 |
T |
C |
18: 67,645,935 (GRCm39) |
M244V |
probably benign |
Het |
St3gal3 |
C |
T |
4: 117,817,232 (GRCm39) |
V141I |
probably benign |
Het |
St6galnac4 |
G |
T |
2: 32,477,172 (GRCm39) |
|
probably benign |
Het |
Svep1 |
T |
C |
4: 58,097,323 (GRCm39) |
K1407E |
possibly damaging |
Het |
Tbc1d32 |
A |
G |
10: 56,100,745 (GRCm39) |
C78R |
probably damaging |
Het |
Tcstv5 |
T |
C |
13: 120,411,378 (GRCm39) |
Y76C |
probably benign |
Het |
Tln2 |
A |
G |
9: 67,253,809 (GRCm39) |
V754A |
probably benign |
Het |
Tmeff1 |
A |
T |
4: 48,636,869 (GRCm39) |
Y189F |
possibly damaging |
Het |
Tmem131l |
C |
T |
3: 83,806,519 (GRCm39) |
A1433T |
probably benign |
Het |
Tnfrsf8 |
T |
C |
4: 145,029,692 (GRCm39) |
Y36C |
probably damaging |
Het |
Trp53i11 |
G |
T |
2: 93,030,245 (GRCm39) |
R184L |
probably damaging |
Het |
Trpv1 |
A |
T |
11: 73,142,110 (GRCm39) |
M214L |
possibly damaging |
Het |
Tsnax |
T |
A |
8: 125,755,533 (GRCm39) |
S132T |
probably benign |
Het |
Ttc28 |
T |
C |
5: 111,424,909 (GRCm39) |
L1547P |
probably damaging |
Het |
Ttc3 |
A |
G |
16: 94,240,100 (GRCm39) |
|
probably null |
Het |
Tubal3 |
T |
A |
13: 3,983,514 (GRCm39) |
D431E |
probably damaging |
Het |
Ugt2b36 |
A |
T |
5: 87,240,301 (GRCm39) |
|
probably null |
Het |
Vmn1r23 |
A |
T |
6: 57,903,190 (GRCm39) |
I196K |
probably benign |
Het |
Vmn1r55 |
A |
C |
7: 5,149,586 (GRCm39) |
L279R |
probably damaging |
Het |
Vmn1r55 |
G |
T |
7: 5,149,587 (GRCm39) |
L279M |
probably damaging |
Het |
Vmn2r89 |
G |
A |
14: 51,694,942 (GRCm39) |
G474E |
probably damaging |
Het |
Vps26b |
T |
C |
9: 26,926,511 (GRCm39) |
K163E |
probably damaging |
Het |
Zfp142 |
A |
G |
1: 74,609,431 (GRCm39) |
F1352L |
probably damaging |
Het |
Zfp422 |
C |
T |
6: 116,603,844 (GRCm39) |
E52K |
possibly damaging |
Het |
Zfp423 |
T |
A |
8: 88,508,338 (GRCm39) |
|
probably null |
Het |
Zfp493 |
T |
C |
13: 67,934,736 (GRCm39) |
F230L |
probably damaging |
Het |
Zfp760 |
T |
C |
17: 21,941,388 (GRCm39) |
C188R |
probably benign |
Het |
Zfyve28 |
G |
T |
5: 34,375,189 (GRCm39) |
T275K |
probably damaging |
Het |
Znhit3 |
T |
C |
11: 84,807,155 (GRCm39) |
N5D |
probably benign |
Het |
|
Other mutations in Cd109 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Cd109
|
APN |
9 |
78,524,251 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00465:Cd109
|
APN |
9 |
78,568,216 (GRCm39) |
nonsense |
probably null |
|
IGL00667:Cd109
|
APN |
9 |
78,592,159 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01432:Cd109
|
APN |
9 |
78,605,405 (GRCm39) |
missense |
probably benign |
|
IGL01795:Cd109
|
APN |
9 |
78,569,047 (GRCm39) |
splice site |
probably benign |
|
IGL02343:Cd109
|
APN |
9 |
78,596,237 (GRCm39) |
splice site |
probably benign |
|
IGL02450:Cd109
|
APN |
9 |
78,603,132 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02699:Cd109
|
APN |
9 |
78,579,271 (GRCm39) |
splice site |
probably benign |
|
IGL02738:Cd109
|
APN |
9 |
78,598,581 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02797:Cd109
|
APN |
9 |
78,568,995 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03160:Cd109
|
APN |
9 |
78,568,338 (GRCm39) |
splice site |
probably null |
|
IGL03349:Cd109
|
APN |
9 |
78,543,767 (GRCm39) |
missense |
probably benign |
0.34 |
FR4589:Cd109
|
UTSW |
9 |
78,619,811 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R0048:Cd109
|
UTSW |
9 |
78,587,303 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0060:Cd109
|
UTSW |
9 |
78,610,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Cd109
|
UTSW |
9 |
78,610,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R0158:Cd109
|
UTSW |
9 |
78,596,214 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0415:Cd109
|
UTSW |
9 |
78,619,897 (GRCm39) |
missense |
probably benign |
0.13 |
R0659:Cd109
|
UTSW |
9 |
78,587,452 (GRCm39) |
splice site |
probably benign |
|
R0709:Cd109
|
UTSW |
9 |
78,579,260 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0840:Cd109
|
UTSW |
9 |
78,571,612 (GRCm39) |
missense |
probably benign |
0.04 |
R0909:Cd109
|
UTSW |
9 |
78,543,755 (GRCm39) |
missense |
probably benign |
0.01 |
R0945:Cd109
|
UTSW |
9 |
78,596,223 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1344:Cd109
|
UTSW |
9 |
78,579,832 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1471:Cd109
|
UTSW |
9 |
78,561,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R1570:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R1688:Cd109
|
UTSW |
9 |
78,612,373 (GRCm39) |
missense |
probably benign |
0.17 |
R1773:Cd109
|
UTSW |
9 |
78,611,006 (GRCm39) |
missense |
probably benign |
0.21 |
R1813:Cd109
|
UTSW |
9 |
78,524,287 (GRCm39) |
missense |
probably benign |
0.04 |
R2004:Cd109
|
UTSW |
9 |
78,611,044 (GRCm39) |
missense |
probably benign |
0.00 |
R2083:Cd109
|
UTSW |
9 |
78,574,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Cd109
|
UTSW |
9 |
78,574,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2858:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2859:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2911:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2912:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2914:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2927:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3623:Cd109
|
UTSW |
9 |
78,574,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3760:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3762:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3771:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3772:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3773:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3916:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3917:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4117:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4260:Cd109
|
UTSW |
9 |
78,543,745 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4387:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4389:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4526:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4527:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4528:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4708:Cd109
|
UTSW |
9 |
78,579,871 (GRCm39) |
missense |
probably benign |
0.00 |
R4723:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4750:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4751:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4754:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4755:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4773:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4984:Cd109
|
UTSW |
9 |
78,541,959 (GRCm39) |
critical splice donor site |
probably null |
|
R5259:Cd109
|
UTSW |
9 |
78,617,434 (GRCm39) |
missense |
probably benign |
0.30 |
R5353:Cd109
|
UTSW |
9 |
78,617,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5440:Cd109
|
UTSW |
9 |
78,587,446 (GRCm39) |
critical splice donor site |
probably null |
|
R5559:Cd109
|
UTSW |
9 |
78,568,250 (GRCm39) |
missense |
probably benign |
0.01 |
R5701:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R5995:Cd109
|
UTSW |
9 |
78,607,561 (GRCm39) |
missense |
probably benign |
0.01 |
R5997:Cd109
|
UTSW |
9 |
78,612,344 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6103:Cd109
|
UTSW |
9 |
78,605,596 (GRCm39) |
splice site |
probably null |
|
R6174:Cd109
|
UTSW |
9 |
78,572,828 (GRCm39) |
critical splice donor site |
probably null |
|
R6410:Cd109
|
UTSW |
9 |
78,564,798 (GRCm39) |
missense |
probably benign |
0.01 |
R6529:Cd109
|
UTSW |
9 |
78,619,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R6655:Cd109
|
UTSW |
9 |
78,592,220 (GRCm39) |
missense |
probably benign |
0.44 |
R6704:Cd109
|
UTSW |
9 |
78,587,357 (GRCm39) |
missense |
probably benign |
0.01 |
R6772:Cd109
|
UTSW |
9 |
78,588,092 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6817:Cd109
|
UTSW |
9 |
78,622,237 (GRCm39) |
missense |
probably benign |
0.01 |
R6903:Cd109
|
UTSW |
9 |
78,543,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R7294:Cd109
|
UTSW |
9 |
78,619,917 (GRCm39) |
missense |
probably damaging |
0.97 |
R7432:Cd109
|
UTSW |
9 |
78,622,225 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7566:Cd109
|
UTSW |
9 |
78,588,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Cd109
|
UTSW |
9 |
78,617,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Cd109
|
UTSW |
9 |
78,596,048 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8017:Cd109
|
UTSW |
9 |
78,614,828 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8019:Cd109
|
UTSW |
9 |
78,614,828 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8050:Cd109
|
UTSW |
9 |
78,571,633 (GRCm39) |
missense |
probably benign |
0.28 |
R8225:Cd109
|
UTSW |
9 |
78,568,972 (GRCm39) |
missense |
probably damaging |
0.99 |
R8269:Cd109
|
UTSW |
9 |
78,572,964 (GRCm39) |
missense |
probably benign |
0.06 |
R8479:Cd109
|
UTSW |
9 |
78,574,628 (GRCm39) |
nonsense |
probably null |
|
R8493:Cd109
|
UTSW |
9 |
78,564,801 (GRCm39) |
missense |
probably benign |
0.41 |
R8781:Cd109
|
UTSW |
9 |
78,543,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R8977:Cd109
|
UTSW |
9 |
78,614,810 (GRCm39) |
missense |
probably benign |
0.36 |
R9051:Cd109
|
UTSW |
9 |
78,619,813 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9051:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9228:Cd109
|
UTSW |
9 |
78,577,042 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9366:Cd109
|
UTSW |
9 |
78,622,275 (GRCm39) |
missense |
probably benign |
0.11 |
R9430:Cd109
|
UTSW |
9 |
78,574,698 (GRCm39) |
critical splice donor site |
probably null |
|
R9572:Cd109
|
UTSW |
9 |
78,567,588 (GRCm39) |
missense |
probably benign |
0.16 |
R9691:Cd109
|
UTSW |
9 |
78,611,074 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9736:Cd109
|
UTSW |
9 |
78,619,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Cd109
|
UTSW |
9 |
78,592,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R9751:Cd109
|
UTSW |
9 |
78,605,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R9752:Cd109
|
UTSW |
9 |
78,614,834 (GRCm39) |
missense |
probably benign |
0.00 |
R9789:Cd109
|
UTSW |
9 |
78,541,944 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9797:Cd109
|
UTSW |
9 |
78,579,217 (GRCm39) |
missense |
probably benign |
0.04 |
RF002:Cd109
|
UTSW |
9 |
78,619,810 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF002:Cd109
|
UTSW |
9 |
78,619,805 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF003:Cd109
|
UTSW |
9 |
78,619,813 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF011:Cd109
|
UTSW |
9 |
78,619,810 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF013:Cd109
|
UTSW |
9 |
78,619,813 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF047:Cd109
|
UTSW |
9 |
78,619,809 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF060:Cd109
|
UTSW |
9 |
78,619,807 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1177:Cd109
|
UTSW |
9 |
78,598,595 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- ATCCCTTTAGTAGACGGGGACTAAG -3'
(R):5'- AAATGCCTGCCTTGATTCCC -3'
Sequencing Primer
(F):5'- GGGGACTAAGAACCATTCCTCTG -3'
(R):5'- GCCTTGATTCCCAAAGTCTTAGAAAC -3'
|
Posted On |
2016-06-17 |