Incidental Mutation 'R4754:Cd109'
| ID |
404219 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cd109
|
| Ensembl Gene |
ENSMUSG00000046186 |
| Gene Name |
CD109 antigen |
| Synonyms |
Gov platelet alloantigens, 9930012E15Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4754 (G1)
|
| Quality Score |
164 |
|
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: 98.6%
- 10x: 97.1%
- 20x: 94.7%
|
| Validation Efficiency |
98% (107/109) |
| 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: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A130010J15Rik |
A |
G |
1: 192,856,837 (GRCm39) |
Y63C |
probably damaging |
Het |
| Abcb4 |
C |
A |
5: 8,960,717 (GRCm39) |
F266L |
probably damaging |
Het |
| Adam8 |
A |
T |
7: 139,564,693 (GRCm39) |
I681N |
possibly damaging |
Het |
| Adgrf3 |
T |
A |
5: 30,402,615 (GRCm39) |
|
probably null |
Het |
| Ang2 |
A |
G |
14: 51,432,974 (GRCm39) |
V136A |
probably damaging |
Het |
| Ankar |
C |
T |
1: 72,737,853 (GRCm39) |
G110R |
probably damaging |
Het |
| Ap3b1 |
T |
C |
13: 94,540,468 (GRCm39) |
L130P |
probably damaging |
Het |
| Apc2 |
T |
G |
10: 80,150,192 (GRCm39) |
W1749G |
probably benign |
Het |
| Asb2 |
T |
C |
12: 103,290,096 (GRCm39) |
N565S |
possibly damaging |
Het |
| B3gnt7 |
C |
A |
1: 86,233,279 (GRCm39) |
T58K |
probably benign |
Het |
| Bltp1 |
C |
T |
3: 37,076,615 (GRCm39) |
Q3663* |
probably null |
Het |
| Brpf1 |
T |
A |
6: 113,297,408 (GRCm39) |
N876K |
possibly damaging |
Het |
| Ccdc157 |
T |
C |
11: 4,098,994 (GRCm39) |
I69V |
possibly damaging |
Het |
| Cdh20 |
A |
T |
1: 104,912,410 (GRCm39) |
I555F |
probably damaging |
Het |
| Cfap73 |
T |
C |
5: 120,767,729 (GRCm39) |
D274G |
probably damaging |
Het |
| Chd5 |
T |
A |
4: 152,462,203 (GRCm39) |
I1310N |
probably damaging |
Het |
| Ckap2 |
T |
A |
8: 22,658,911 (GRCm39) |
I611F |
possibly damaging |
Het |
| Cpeb2 |
A |
G |
5: 43,443,200 (GRCm39) |
I964V |
possibly damaging |
Het |
| Ctbp2 |
C |
A |
7: 132,625,287 (GRCm39) |
|
probably null |
Het |
| Dhrs2 |
A |
T |
14: 55,476,205 (GRCm39) |
I142F |
probably damaging |
Het |
| Dnah5 |
T |
A |
15: 28,421,101 (GRCm39) |
|
probably null |
Het |
| Dst |
T |
C |
1: 34,251,390 (GRCm39) |
S1822P |
probably damaging |
Het |
| Ect2 |
T |
C |
3: 27,181,112 (GRCm39) |
K581E |
probably damaging |
Het |
| Edem1 |
C |
T |
6: 108,818,658 (GRCm39) |
T222M |
probably damaging |
Het |
| Eif2ak1 |
A |
G |
5: 143,838,621 (GRCm39) |
M592V |
probably damaging |
Het |
| Endou |
T |
G |
15: 97,624,420 (GRCm39) |
D49A |
probably damaging |
Het |
| Ensa |
A |
G |
3: 95,529,865 (GRCm39) |
|
probably benign |
Het |
| Evc2 |
G |
T |
5: 37,544,375 (GRCm39) |
R708L |
probably damaging |
Het |
| Fam120b |
T |
A |
17: 15,643,224 (GRCm39) |
C668S |
probably damaging |
Het |
| Fam135a |
A |
T |
1: 24,067,835 (GRCm39) |
C798* |
probably null |
Het |
| Fam135b |
T |
C |
15: 71,334,800 (GRCm39) |
D798G |
probably benign |
Het |
| Fshb |
A |
C |
2: 106,887,627 (GRCm39) |
*131E |
probably null |
Het |
| G3bp2 |
C |
T |
5: 92,202,768 (GRCm39) |
V441M |
possibly damaging |
Het |
| Galnt6 |
A |
T |
15: 100,597,105 (GRCm39) |
F354I |
probably damaging |
Het |
| Gm1123 |
C |
A |
9: 98,905,293 (GRCm39) |
|
probably null |
Het |
| Gm1123 |
A |
T |
9: 98,905,294 (GRCm39) |
|
probably null |
Het |
| Gm15130 |
T |
C |
2: 110,973,207 (GRCm39) |
N115S |
unknown |
Het |
| Gm7104 |
A |
G |
12: 88,252,765 (GRCm39) |
|
noncoding transcript |
Het |
| Gm9762 |
A |
T |
3: 78,873,728 (GRCm39) |
|
noncoding transcript |
Het |
| Grip2 |
T |
C |
6: 91,756,173 (GRCm39) |
T505A |
probably damaging |
Het |
| Grip2 |
A |
G |
6: 91,756,163 (GRCm39) |
V508A |
probably damaging |
Het |
| Haus4 |
A |
G |
14: 54,787,349 (GRCm39) |
|
probably null |
Het |
| Herc1 |
T |
A |
9: 66,408,488 (GRCm39) |
D4571E |
probably benign |
Het |
| Hnrnpk |
T |
A |
13: 58,546,950 (GRCm39) |
|
probably benign |
Het |
| Ica1l |
T |
C |
1: 60,067,321 (GRCm39) |
Y23C |
probably damaging |
Het |
| Kansl2-ps |
A |
G |
7: 72,322,881 (GRCm39) |
|
noncoding transcript |
Het |
| Kcnma1 |
T |
C |
14: 23,413,904 (GRCm39) |
D833G |
probably damaging |
Het |
| Kmt2e |
A |
T |
5: 23,687,439 (GRCm39) |
I430F |
possibly damaging |
Het |
| Lama2 |
C |
A |
10: 26,994,527 (GRCm39) |
R1794L |
possibly damaging |
Het |
| Mcpt1 |
T |
A |
14: 56,256,137 (GRCm39) |
F59I |
probably damaging |
Het |
| Mib2 |
G |
T |
4: 155,739,822 (GRCm39) |
T783K |
possibly damaging |
Het |
| Nlrp4g |
T |
C |
9: 124,349,788 (GRCm38) |
|
noncoding transcript |
Het |
| Nudt16l2 |
A |
T |
9: 105,021,592 (GRCm39) |
F151L |
probably benign |
Het |
| Obscn |
T |
C |
11: 58,926,869 (GRCm39) |
I6352V |
possibly damaging |
Het |
| Or2j6 |
C |
T |
7: 139,980,072 (GRCm39) |
A296T |
probably damaging |
Het |
| Or4a72 |
A |
T |
2: 89,405,391 (GRCm39) |
H226Q |
probably benign |
Het |
| Or4k1 |
T |
A |
14: 50,377,490 (GRCm39) |
N202I |
possibly damaging |
Het |
| Or4k1 |
T |
G |
14: 50,377,491 (GRCm39) |
N202H |
probably benign |
Het |
| Or52a5 |
T |
C |
7: 103,426,875 (GRCm39) |
I226V |
probably benign |
Het |
| Or5b125-ps1 |
T |
A |
19: 13,056,225 (GRCm39) |
|
noncoding transcript |
Het |
| Pcdh10 |
G |
A |
3: 45,335,072 (GRCm39) |
R462H |
probably damaging |
Het |
| Pcdhga12 |
C |
A |
18: 37,899,604 (GRCm39) |
N145K |
probably damaging |
Het |
| Pik3r6 |
T |
A |
11: 68,435,601 (GRCm39) |
L613Q |
probably damaging |
Het |
| Pknox2 |
T |
C |
9: 36,821,016 (GRCm39) |
D282G |
probably damaging |
Het |
| Plod2 |
T |
G |
9: 92,488,584 (GRCm39) |
Y624* |
probably null |
Het |
| Prkd3 |
C |
A |
17: 79,264,043 (GRCm39) |
V684F |
probably damaging |
Het |
| Ptpn1 |
T |
A |
2: 167,816,080 (GRCm39) |
V198D |
probably damaging |
Het |
| Ptpn12 |
G |
T |
5: 21,203,587 (GRCm39) |
P397Q |
probably benign |
Het |
| Rad1 |
C |
A |
15: 10,493,212 (GRCm39) |
|
probably benign |
Het |
| Rasl11a |
A |
G |
5: 146,783,825 (GRCm39) |
D90G |
probably benign |
Het |
| Rnf181 |
A |
G |
6: 72,337,543 (GRCm39) |
|
probably benign |
Het |
| Ryr3 |
T |
C |
2: 112,587,984 (GRCm39) |
I2652M |
possibly damaging |
Het |
| Siglecg |
C |
T |
7: 43,061,295 (GRCm39) |
|
probably benign |
Het |
| Slc22a3 |
T |
C |
17: 12,726,082 (GRCm39) |
S44G |
probably benign |
Het |
| Slc38a1 |
A |
T |
15: 96,474,663 (GRCm39) |
F463I |
probably damaging |
Het |
| Smg1 |
A |
T |
7: 117,755,954 (GRCm39) |
|
probably benign |
Het |
| Syk |
T |
C |
13: 52,766,295 (GRCm39) |
|
probably benign |
Het |
| Tasor |
A |
T |
14: 27,183,052 (GRCm39) |
I504L |
probably benign |
Het |
| Tbc1d5 |
T |
C |
17: 51,107,193 (GRCm39) |
I454M |
probably benign |
Het |
| Tmed6 |
C |
A |
8: 107,790,362 (GRCm39) |
D146Y |
probably damaging |
Het |
| Tmem132e |
A |
T |
11: 82,335,677 (GRCm39) |
K828* |
probably null |
Het |
| Tmprss15 |
A |
T |
16: 78,851,012 (GRCm39) |
S294T |
probably damaging |
Het |
| Trp53bp1 |
A |
G |
2: 121,038,360 (GRCm39) |
S1493P |
probably damaging |
Het |
| Tshb |
A |
T |
3: 102,685,491 (GRCm39) |
I46N |
probably damaging |
Het |
| Tspan11 |
T |
C |
6: 127,915,183 (GRCm39) |
V99A |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,545,905 (GRCm39) |
T24176A |
probably benign |
Het |
| Vmn1r8 |
T |
C |
6: 57,012,952 (GRCm39) |
M1T |
probably null |
Het |
| Vmn2r104 |
A |
T |
17: 20,261,030 (GRCm39) |
Y464* |
probably null |
Het |
| Vmn2r110 |
T |
C |
17: 20,816,458 (GRCm39) |
T22A |
probably benign |
Het |
| Vmn2r17 |
T |
A |
5: 109,600,715 (GRCm39) |
I671K |
probably damaging |
Het |
| Zbtb21 |
T |
C |
16: 97,752,466 (GRCm39) |
N606D |
probably damaging |
Het |
| Zfy2 |
A |
T |
Y: 2,121,477 (GRCm39) |
S139T |
probably benign |
Het |
| Zkscan17 |
G |
A |
11: 59,393,851 (GRCm39) |
R156* |
probably null |
Het |
| Zp2 |
A |
G |
7: 119,737,541 (GRCm39) |
V248A |
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 |
|
|
R4751: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'- ATCCCTTTAGTAGACGGGGAC -3'
(R):5'- ATGCCTGCCTTGATTCCCAAAG -3'
Sequencing Primer
(F):5'- GGGGACTAAGAACCATTCCTCTG -3'
(R):5'- GCCTTGATTCCCAAAGTCTTAGAAAC -3'
|
| Posted On |
2016-07-22 |
Incidental Mutation