Incidental Mutation 'R4751:Cd109'
ID |
397143 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cd109
|
Ensembl Gene |
ENSMUSG00000046186 |
Gene Name |
CD109 antigen |
Synonyms |
Gov platelet alloantigens, 9930012E15Rik |
MMRRC Submission |
041970-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4751 (G1)
|
Quality Score |
174 |
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: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.4%
|
Validation Efficiency |
95% (124/131) |
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: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130023H24Rik |
A |
T |
7: 127,836,258 (GRCm39) |
C112S |
probably benign |
Het |
Abca13 |
G |
A |
11: 9,227,973 (GRCm39) |
|
probably null |
Het |
Abca14 |
A |
G |
7: 119,911,400 (GRCm39) |
E1328G |
probably benign |
Het |
Abca9 |
T |
A |
11: 110,021,396 (GRCm39) |
I1105F |
probably benign |
Het |
Abr |
T |
C |
11: 76,347,434 (GRCm39) |
N396D |
possibly damaging |
Het |
Aftph |
A |
C |
11: 20,677,074 (GRCm39) |
C178W |
probably damaging |
Het |
Akr1c14 |
T |
C |
13: 4,115,338 (GRCm39) |
F89S |
possibly damaging |
Het |
Ank3 |
C |
T |
10: 69,822,036 (GRCm39) |
A1518V |
probably benign |
Het |
Arfgap2 |
T |
G |
2: 91,097,713 (GRCm39) |
S143R |
probably benign |
Het |
Aspdh |
T |
A |
7: 44,116,629 (GRCm39) |
C107* |
probably null |
Het |
Asphd2 |
C |
A |
5: 112,539,612 (GRCm39) |
G74W |
probably damaging |
Het |
AU040320 |
G |
A |
4: 126,748,259 (GRCm39) |
|
probably null |
Het |
B3glct |
T |
A |
5: 149,648,867 (GRCm39) |
|
probably null |
Het |
Bcl9l |
A |
G |
9: 44,418,100 (GRCm39) |
K646R |
probably damaging |
Het |
Brat1 |
T |
G |
5: 140,704,051 (GRCm39) |
L768R |
probably damaging |
Het |
Btbd18 |
T |
A |
2: 84,498,265 (GRCm39) |
Y634* |
probably null |
Het |
Bub1 |
T |
A |
2: 127,665,858 (GRCm39) |
|
probably benign |
Het |
Carns1 |
A |
T |
19: 4,216,417 (GRCm39) |
D588E |
probably damaging |
Het |
Cast |
T |
C |
13: 74,894,166 (GRCm39) |
K141E |
probably damaging |
Het |
Chsy3 |
T |
C |
18: 59,308,872 (GRCm39) |
S42P |
possibly damaging |
Het |
Clca3a1 |
A |
T |
3: 144,710,609 (GRCm39) |
F865I |
possibly damaging |
Het |
Clec4f |
T |
A |
6: 83,622,264 (GRCm39) |
M526L |
possibly damaging |
Het |
Clnk |
T |
C |
5: 38,878,256 (GRCm39) |
E301G |
probably benign |
Het |
Colgalt2 |
T |
A |
1: 152,365,627 (GRCm39) |
I309N |
probably benign |
Het |
Cyp2e1 |
A |
T |
7: 140,354,629 (GRCm39) |
K326* |
probably null |
Het |
Dagla |
T |
A |
19: 10,227,758 (GRCm39) |
T717S |
probably benign |
Het |
Dnajc11 |
G |
A |
4: 152,052,999 (GRCm39) |
R141H |
probably benign |
Het |
Dst |
A |
G |
1: 34,230,965 (GRCm39) |
K2853E |
probably benign |
Het |
Eif4g1 |
A |
G |
16: 20,505,265 (GRCm39) |
K1208E |
possibly damaging |
Het |
Elane |
A |
G |
10: 79,722,625 (GRCm39) |
R48G |
probably benign |
Het |
Fbxo30 |
T |
A |
10: 11,165,939 (GRCm39) |
N220K |
probably benign |
Het |
Fbxo33 |
A |
T |
12: 59,247,714 (GRCm39) |
|
probably benign |
Het |
Fetub |
G |
A |
16: 22,756,645 (GRCm39) |
V169I |
probably benign |
Het |
Gpx6 |
A |
C |
13: 21,501,234 (GRCm39) |
Q107H |
probably damaging |
Het |
H2bc18 |
A |
T |
3: 96,176,467 (GRCm39) |
|
probably benign |
Het |
Homer3 |
A |
T |
8: 70,738,084 (GRCm39) |
I19F |
probably damaging |
Het |
Hspa4 |
C |
T |
11: 53,175,026 (GRCm39) |
V144I |
probably benign |
Het |
Icos |
C |
T |
1: 61,032,876 (GRCm39) |
S25L |
probably benign |
Het |
Ifna4 |
A |
G |
4: 88,760,185 (GRCm39) |
T30A |
probably benign |
Het |
Ino80b |
C |
T |
6: 83,101,731 (GRCm39) |
G46D |
probably damaging |
Het |
Kpna2 |
T |
G |
11: 106,883,490 (GRCm39) |
I100L |
possibly damaging |
Het |
Krt71 |
C |
T |
15: 101,643,901 (GRCm39) |
G446R |
probably damaging |
Het |
Krtap31-2 |
A |
G |
11: 99,827,402 (GRCm39) |
N78S |
possibly damaging |
Het |
Lman1 |
A |
G |
18: 66,131,505 (GRCm39) |
S132P |
probably benign |
Het |
Lmna |
T |
C |
3: 88,393,840 (GRCm39) |
Q246R |
possibly damaging |
Het |
Lrp10 |
T |
A |
14: 54,706,049 (GRCm39) |
V413E |
probably damaging |
Het |
Macf1 |
A |
C |
4: 123,365,443 (GRCm39) |
I1541S |
probably benign |
Het |
Med24 |
A |
G |
11: 98,597,258 (GRCm39) |
L874P |
probably damaging |
Het |
Mgll |
T |
A |
6: 88,702,093 (GRCm39) |
|
probably benign |
Het |
Mrpl37 |
A |
T |
4: 106,914,672 (GRCm39) |
L364Q |
probably damaging |
Het |
Mrpl47 |
C |
T |
3: 32,782,590 (GRCm39) |
R209H |
probably benign |
Het |
Muc5ac |
T |
C |
7: 141,371,338 (GRCm39) |
F3285L |
probably benign |
Het |
Mylk |
A |
G |
16: 34,699,539 (GRCm39) |
R301G |
probably benign |
Het |
Nacad |
A |
G |
11: 6,555,726 (GRCm39) |
L8P |
unknown |
Het |
Ncf1 |
T |
A |
5: 134,258,399 (GRCm39) |
H8L |
probably damaging |
Het |
Ncoa3 |
T |
A |
2: 165,911,823 (GRCm39) |
M1383K |
possibly damaging |
Het |
Necab2 |
C |
T |
8: 120,194,337 (GRCm39) |
S271L |
probably benign |
Het |
Nme8 |
A |
T |
13: 19,859,808 (GRCm39) |
|
probably null |
Het |
Nsrp1 |
T |
G |
11: 76,967,545 (GRCm39) |
T16P |
possibly damaging |
Het |
Obox3 |
A |
T |
7: 15,359,617 (GRCm39) |
|
probably null |
Het |
Or1l8 |
T |
C |
2: 36,817,595 (GRCm39) |
H177R |
probably damaging |
Het |
Or4c108 |
A |
G |
2: 88,803,477 (GRCm39) |
C253R |
probably damaging |
Het |
Or4c15 |
T |
A |
2: 88,760,258 (GRCm39) |
I134F |
probably damaging |
Het |
Or4d6 |
T |
A |
19: 12,086,541 (GRCm39) |
Y123F |
probably damaging |
Het |
Or52n2b |
A |
T |
7: 104,565,617 (GRCm39) |
Y295* |
probably null |
Het |
Or6b2 |
C |
A |
1: 92,407,705 (GRCm39) |
A213S |
probably benign |
Het |
Osbpl3 |
C |
G |
6: 50,277,977 (GRCm39) |
E790Q |
possibly damaging |
Het |
Osmr |
A |
T |
15: 6,872,333 (GRCm39) |
W254R |
probably damaging |
Het |
Otoa |
T |
C |
7: 120,732,147 (GRCm39) |
|
probably benign |
Het |
Pagr1a |
A |
T |
7: 126,614,551 (GRCm39) |
L218H |
probably damaging |
Het |
Pcdha11 |
G |
A |
18: 37,139,997 (GRCm39) |
G542D |
probably damaging |
Het |
Pck2 |
T |
A |
14: 55,780,018 (GRCm39) |
I54N |
probably damaging |
Het |
Ppif |
T |
C |
14: 25,699,923 (GRCm39) |
V173A |
probably damaging |
Het |
Ptgs2 |
T |
A |
1: 149,979,771 (GRCm39) |
L292H |
probably damaging |
Het |
Ptpru |
A |
G |
4: 131,529,897 (GRCm39) |
S604P |
probably damaging |
Het |
Qrfpr |
T |
C |
3: 36,236,771 (GRCm39) |
H210R |
possibly damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,792,171 (GRCm39) |
T41A |
probably damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,894,919 (GRCm39) |
H1113R |
probably damaging |
Het |
Rhoc |
T |
A |
3: 104,699,963 (GRCm39) |
I80N |
probably damaging |
Het |
Riok3 |
A |
G |
18: 12,287,040 (GRCm39) |
N472S |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,336,571 (GRCm39) |
Y3314C |
probably benign |
Het |
Shank2 |
C |
T |
7: 143,963,205 (GRCm39) |
T264I |
probably damaging |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Sipa1l1 |
A |
G |
12: 82,387,968 (GRCm39) |
I65V |
probably benign |
Het |
Slc22a19 |
T |
C |
19: 7,668,510 (GRCm39) |
K291R |
possibly damaging |
Het |
Slc22a20 |
T |
C |
19: 6,030,488 (GRCm39) |
I315V |
probably benign |
Het |
Slc44a1 |
A |
T |
4: 53,560,973 (GRCm39) |
D563V |
probably damaging |
Het |
Smchd1 |
A |
T |
17: 71,698,463 (GRCm39) |
H1104Q |
probably benign |
Het |
Spcs2 |
A |
T |
7: 99,493,976 (GRCm39) |
|
probably null |
Het |
Speer1e |
T |
A |
5: 11,236,458 (GRCm39) |
Y138N |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,673,884 (GRCm39) |
E301G |
probably benign |
Het |
Stum |
T |
C |
1: 180,270,234 (GRCm39) |
D86G |
probably damaging |
Het |
Sufu |
A |
T |
19: 46,472,088 (GRCm39) |
D449V |
probably benign |
Het |
Sun5 |
T |
C |
2: 153,707,936 (GRCm39) |
|
probably null |
Het |
Tbc1d15 |
T |
A |
10: 115,038,492 (GRCm39) |
I574F |
probably damaging |
Het |
Tert |
G |
A |
13: 73,776,182 (GRCm39) |
S311N |
possibly damaging |
Het |
Tiparp |
T |
C |
3: 65,460,225 (GRCm39) |
Y507H |
probably damaging |
Het |
Tnk2 |
T |
C |
16: 32,498,675 (GRCm39) |
C158R |
probably damaging |
Het |
Tpgs1 |
T |
C |
10: 79,511,454 (GRCm39) |
S199P |
possibly damaging |
Het |
Trdmt1 |
G |
T |
2: 13,549,464 (GRCm39) |
|
probably benign |
Het |
Trp53bp1 |
T |
A |
2: 121,058,290 (GRCm39) |
D944V |
probably damaging |
Het |
Tsc1 |
T |
A |
2: 28,569,093 (GRCm39) |
I720N |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,539,949 (GRCm39) |
T34346A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,727,925 (GRCm39) |
|
probably benign |
Het |
Uba7 |
T |
A |
9: 107,857,004 (GRCm39) |
C686S |
possibly damaging |
Het |
Ush2a |
T |
A |
1: 188,582,284 (GRCm39) |
F3782L |
probably damaging |
Het |
Vars2 |
A |
T |
17: 35,970,235 (GRCm39) |
H745Q |
possibly damaging |
Het |
Vgf |
T |
A |
5: 137,061,255 (GRCm39) |
D472E |
probably damaging |
Het |
Vmn2r15 |
T |
C |
5: 109,434,620 (GRCm39) |
M695V |
probably benign |
Het |
Vps41 |
A |
T |
13: 18,995,792 (GRCm39) |
D208V |
probably damaging |
Het |
Vta1 |
C |
T |
10: 14,531,560 (GRCm39) |
A272T |
probably benign |
Het |
Wnk4 |
G |
A |
11: 101,167,188 (GRCm39) |
|
probably benign |
Het |
Zfp507 |
T |
C |
7: 35,493,807 (GRCm39) |
K412R |
probably damaging |
Het |
Zfp768 |
A |
G |
7: 126,943,934 (GRCm39) |
F65L |
possibly damaging |
Het |
Zfp956 |
T |
C |
6: 47,940,510 (GRCm39) |
S290P |
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 |
|
R4700: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 |
|
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'- AGCATCCCTTTAGTAGACGGG -3'
(R):5'- GCCTGCCTTGATTCCCAAAG -3'
Sequencing Primer
(F):5'- GGGGACTAAGAACCATTCCTCTG -3'
(R):5'- GCCTTGATTCCCAAAGTCTTAGAAAC -3'
|
Posted On |
2016-06-24 |