Incidental Mutation 'R4796:Cd22'
ID |
369048 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cd22
|
Ensembl Gene |
ENSMUSG00000030577 |
Gene Name |
CD22 antigen |
Synonyms |
Lyb8, Lyb-8 |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4796 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
30564829-30579767 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to T
at 30572381 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000139871
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000019248]
[ENSMUST00000108125]
[ENSMUST00000186154]
[ENSMUST00000187989]
[ENSMUST00000189718]
[ENSMUST00000190646]
[ENSMUST00000190617]
[ENSMUST00000190753]
[ENSMUST00000188157]
[ENSMUST00000214289]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000019248
|
SMART Domains |
Protein: ENSMUSP00000019248 Gene: ENSMUSG00000030577
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
IG
|
31 |
147 |
2.75e-1 |
SMART |
IG_like
|
156 |
254 |
4.07e1 |
SMART |
IGc2
|
269 |
337 |
2.68e-4 |
SMART |
IGc2
|
365 |
424 |
4.52e-11 |
SMART |
IG
|
448 |
523 |
1.21e-2 |
SMART |
IGc2
|
541 |
599 |
6.75e-10 |
SMART |
IGc2
|
628 |
687 |
2.68e-4 |
SMART |
transmembrane domain
|
709 |
726 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000108125
|
SMART Domains |
Protein: ENSMUSP00000103760 Gene: ENSMUSG00000030577
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
IG
|
31 |
147 |
2.75e-1 |
SMART |
IG_like
|
156 |
254 |
4.07e1 |
SMART |
IGc2
|
269 |
337 |
2.68e-4 |
SMART |
IGc2
|
365 |
424 |
4.52e-11 |
SMART |
IG
|
448 |
523 |
1.21e-2 |
SMART |
IGc2
|
541 |
599 |
6.75e-10 |
SMART |
IGc2
|
628 |
687 |
2.68e-4 |
SMART |
transmembrane domain
|
709 |
726 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000186154
|
SMART Domains |
Protein: ENSMUSP00000139685 Gene: ENSMUSG00000030577
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
IG
|
31 |
147 |
2.75e-1 |
SMART |
IG_like
|
156 |
254 |
4.07e1 |
SMART |
IGc2
|
269 |
337 |
2.68e-4 |
SMART |
IGc2
|
365 |
424 |
4.52e-11 |
SMART |
IG
|
448 |
523 |
1.21e-2 |
SMART |
IGc2
|
541 |
599 |
6.75e-10 |
SMART |
IGc2
|
628 |
687 |
2.68e-4 |
SMART |
transmembrane domain
|
709 |
726 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186333
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186354
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000187585
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000187989
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000189996
|
Predicted Effect |
probably null
Transcript: ENSMUST00000189718
|
SMART Domains |
Protein: ENSMUSP00000140521 Gene: ENSMUSG00000030577
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
IG
|
31 |
147 |
2.75e-1 |
SMART |
IG_like
|
156 |
254 |
4.07e1 |
SMART |
IGc2
|
269 |
337 |
2.68e-4 |
SMART |
IGc2
|
365 |
424 |
4.52e-11 |
SMART |
IG
|
448 |
523 |
1.21e-2 |
SMART |
IGc2
|
541 |
599 |
6.75e-10 |
SMART |
IGc2
|
628 |
687 |
2.68e-4 |
SMART |
transmembrane domain
|
709 |
726 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000190646
|
SMART Domains |
Protein: ENSMUSP00000140528 Gene: ENSMUSG00000030577
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
IG
|
31 |
147 |
1.1e-3 |
SMART |
IG_like
|
166 |
245 |
1.6e-2 |
SMART |
IGc2
|
269 |
337 |
1.1e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000190455
|
Predicted Effect |
probably null
Transcript: ENSMUST00000190617
|
SMART Domains |
Protein: ENSMUSP00000139871 Gene: ENSMUSG00000030577
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
IG
|
31 |
147 |
2.75e-1 |
SMART |
IG_like
|
156 |
254 |
4.07e1 |
SMART |
IGc2
|
269 |
337 |
2.68e-4 |
SMART |
IGc2
|
365 |
424 |
4.52e-11 |
SMART |
IG
|
448 |
523 |
1.21e-2 |
SMART |
IGc2
|
541 |
599 |
6.75e-10 |
SMART |
IGc2
|
628 |
687 |
2.68e-4 |
SMART |
transmembrane domain
|
709 |
726 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000190170
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000190753
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000188157
|
SMART Domains |
Protein: ENSMUSP00000140450 Gene: ENSMUSG00000030577
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
IG
|
31 |
147 |
1.1e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000214289
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.8%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Homozygous null mice have reduced mature B cell numbers with altered proliferation kinetics and reduced antibody production to T cell independent antigens. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,303,350 (GRCm39) |
W132* |
probably null |
Het |
Atp8b3 |
A |
G |
10: 80,360,188 (GRCm39) |
V961A |
probably damaging |
Het |
Bglap |
A |
C |
3: 88,291,712 (GRCm39) |
I4S |
unknown |
Het |
Bmp1 |
T |
C |
14: 70,729,513 (GRCm39) |
|
probably null |
Het |
Brd10 |
G |
A |
19: 29,731,018 (GRCm39) |
H665Y |
probably benign |
Het |
Btaf1 |
T |
C |
19: 36,933,828 (GRCm39) |
L152P |
possibly damaging |
Het |
Cacna1b |
T |
A |
2: 24,527,499 (GRCm39) |
T1621S |
possibly damaging |
Het |
Capn3 |
A |
T |
2: 120,333,479 (GRCm39) |
N621I |
probably damaging |
Het |
Ccdc121rt3 |
A |
G |
5: 112,503,165 (GRCm39) |
S180P |
possibly damaging |
Het |
Ccdc59 |
T |
C |
10: 105,677,429 (GRCm39) |
S23P |
probably benign |
Het |
Cdh20 |
A |
G |
1: 104,868,989 (GRCm39) |
D160G |
probably damaging |
Het |
Cep112 |
T |
C |
11: 108,377,818 (GRCm39) |
|
probably null |
Het |
Clock |
T |
C |
5: 76,413,763 (GRCm39) |
K44R |
probably damaging |
Het |
Coq10b |
A |
G |
1: 55,110,957 (GRCm39) |
T242A |
probably damaging |
Het |
Cstdc2 |
A |
G |
2: 148,692,658 (GRCm39) |
F48S |
probably damaging |
Het |
Ctnnd1 |
G |
T |
2: 84,450,270 (GRCm39) |
R317S |
probably damaging |
Het |
Dlg5 |
G |
A |
14: 24,194,451 (GRCm39) |
H1674Y |
probably damaging |
Het |
Drc3 |
C |
A |
11: 60,254,354 (GRCm39) |
N75K |
probably damaging |
Het |
Efna4 |
T |
C |
3: 89,242,555 (GRCm39) |
E113G |
probably damaging |
Het |
Egr3 |
C |
A |
14: 70,315,024 (GRCm39) |
A44D |
probably benign |
Het |
Ercc3 |
T |
C |
18: 32,381,363 (GRCm39) |
F393S |
probably damaging |
Het |
Evi2 |
T |
A |
11: 79,406,273 (GRCm39) |
|
probably benign |
Het |
Fam78b |
T |
C |
1: 166,906,216 (GRCm39) |
V125A |
probably benign |
Het |
Fars2 |
A |
T |
13: 36,721,400 (GRCm39) |
E448V |
probably damaging |
Het |
Farsb |
A |
T |
1: 78,401,833 (GRCm39) |
*590R |
probably null |
Het |
Fat3 |
A |
G |
9: 15,911,028 (GRCm39) |
M1658T |
probably benign |
Het |
Fhod3 |
G |
T |
18: 25,118,358 (GRCm39) |
V232F |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Fzd3 |
A |
G |
14: 65,472,607 (GRCm39) |
V387A |
possibly damaging |
Het |
Gm1527 |
A |
G |
3: 28,974,812 (GRCm39) |
I542V |
possibly damaging |
Het |
Gm7964 |
A |
G |
7: 83,405,109 (GRCm39) |
|
probably null |
Het |
Hbs1l |
G |
T |
10: 21,218,405 (GRCm39) |
G301C |
probably damaging |
Het |
Hipk4 |
A |
G |
7: 27,227,995 (GRCm39) |
H247R |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,629,362 (GRCm39) |
V965A |
probably benign |
Het |
Hoxa5 |
C |
T |
6: 52,180,943 (GRCm39) |
A130T |
probably benign |
Het |
Igf2r |
C |
T |
17: 12,903,013 (GRCm39) |
V2346I |
possibly damaging |
Het |
Igsf8 |
T |
C |
1: 172,143,889 (GRCm39) |
V14A |
probably benign |
Het |
Impg1 |
G |
A |
9: 80,301,377 (GRCm39) |
P183L |
probably damaging |
Het |
Isl1 |
T |
C |
13: 116,441,966 (GRCm39) |
N89S |
probably benign |
Het |
Itga1 |
C |
A |
13: 115,171,921 (GRCm39) |
W61C |
probably damaging |
Het |
Itga5 |
T |
C |
15: 103,256,187 (GRCm39) |
R922G |
probably benign |
Het |
Itgb5 |
T |
C |
16: 33,705,391 (GRCm39) |
V227A |
possibly damaging |
Het |
Jph4 |
G |
T |
14: 55,347,165 (GRCm39) |
P461T |
probably damaging |
Het |
Kcnab1 |
T |
A |
3: 65,211,586 (GRCm39) |
|
probably null |
Het |
Klrc1 |
T |
A |
6: 129,654,725 (GRCm39) |
|
probably null |
Het |
Lonrf2 |
A |
T |
1: 38,855,119 (GRCm39) |
L92Q |
probably benign |
Het |
Ly75 |
T |
C |
2: 60,180,284 (GRCm39) |
E631G |
probably benign |
Het |
Mapk13 |
T |
C |
17: 28,994,528 (GRCm39) |
Y140H |
probably damaging |
Het |
Meak7 |
A |
T |
8: 120,495,093 (GRCm39) |
S222T |
probably benign |
Het |
Mgat4d |
A |
G |
8: 84,084,749 (GRCm39) |
E164G |
probably damaging |
Het |
Mrtfa |
C |
T |
15: 80,901,234 (GRCm39) |
S419N |
probably damaging |
Het |
Mtcl2 |
A |
G |
2: 156,862,172 (GRCm39) |
S1586P |
probably benign |
Het |
Mthfs |
A |
T |
9: 89,122,078 (GRCm39) |
H188L |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,417,983 (GRCm39) |
M3643K |
possibly damaging |
Het |
Mylk3 |
T |
C |
8: 86,077,014 (GRCm39) |
Y474C |
probably damaging |
Het |
Myo5b |
A |
G |
18: 74,877,701 (GRCm39) |
T1567A |
possibly damaging |
Het |
Ncaph2 |
T |
G |
15: 89,255,010 (GRCm39) |
V478G |
probably damaging |
Het |
Ncbp1 |
A |
G |
4: 46,152,967 (GRCm39) |
R247G |
possibly damaging |
Het |
Nedd9 |
T |
C |
13: 41,471,376 (GRCm39) |
K208E |
probably benign |
Het |
Nxph2 |
C |
T |
2: 23,289,870 (GRCm39) |
T74M |
probably benign |
Het |
Ogdh |
T |
A |
11: 6,290,570 (GRCm39) |
M385K |
probably benign |
Het |
Or10a5 |
A |
T |
7: 106,636,121 (GRCm39) |
Y253F |
probably benign |
Het |
Or3a1c |
A |
T |
11: 74,046,417 (GRCm39) |
I146F |
probably benign |
Het |
Or4a2 |
T |
C |
2: 89,248,235 (GRCm39) |
H174R |
probably damaging |
Het |
Or6a2 |
C |
T |
7: 106,600,542 (GRCm39) |
G175D |
probably damaging |
Het |
Or7g18 |
T |
C |
9: 18,787,475 (GRCm39) |
V284A |
probably damaging |
Het |
Or8b54 |
T |
A |
9: 38,686,670 (GRCm39) |
F40I |
probably benign |
Het |
Pcsk2 |
A |
C |
2: 143,655,345 (GRCm39) |
I510L |
probably benign |
Het |
Pdgfra |
A |
G |
5: 75,349,972 (GRCm39) |
N952S |
probably benign |
Het |
Pex26 |
T |
C |
6: 121,170,516 (GRCm39) |
F287S |
probably damaging |
Het |
Pick1 |
G |
C |
15: 79,139,810 (GRCm39) |
|
probably benign |
Het |
Plxnb1 |
G |
T |
9: 108,943,663 (GRCm39) |
V1917L |
probably damaging |
Het |
Polk |
T |
C |
13: 96,625,764 (GRCm39) |
T347A |
probably benign |
Het |
Ppp1r10 |
T |
G |
17: 36,234,979 (GRCm39) |
I61R |
probably damaging |
Het |
Prex1 |
A |
T |
2: 166,434,211 (GRCm39) |
L503Q |
probably damaging |
Het |
Ptp4a1 |
A |
C |
1: 30,983,019 (GRCm39) |
I133R |
probably damaging |
Het |
Rassf10 |
G |
T |
7: 112,553,735 (GRCm39) |
R112L |
probably damaging |
Het |
Ripor3 |
T |
A |
2: 167,823,260 (GRCm39) |
I884F |
probably damaging |
Het |
Rnft2 |
A |
G |
5: 118,339,311 (GRCm39) |
Y369H |
probably damaging |
Het |
Rtp3 |
A |
T |
9: 110,815,522 (GRCm39) |
V281E |
probably benign |
Het |
Runx1t1 |
T |
A |
4: 13,837,767 (GRCm39) |
N51K |
probably damaging |
Het |
Selp |
A |
G |
1: 163,972,475 (GRCm39) |
T705A |
probably benign |
Het |
Sgca |
A |
T |
11: 94,861,553 (GRCm39) |
|
probably null |
Het |
Slc22a3 |
T |
C |
17: 12,642,675 (GRCm39) |
E514G |
probably damaging |
Het |
Slc28a2b |
T |
A |
2: 122,344,940 (GRCm39) |
I182N |
probably damaging |
Het |
Slc2a1 |
G |
A |
4: 118,989,642 (GRCm39) |
R61Q |
probably damaging |
Het |
Smarcal1 |
G |
A |
1: 72,636,599 (GRCm39) |
V425I |
probably benign |
Het |
Ssx2ip |
T |
C |
3: 146,124,114 (GRCm39) |
V43A |
probably benign |
Het |
Synpo |
A |
G |
18: 60,737,386 (GRCm39) |
S187P |
probably damaging |
Het |
Thnsl1 |
T |
A |
2: 21,216,856 (GRCm39) |
C203* |
probably null |
Het |
Ttyh3 |
A |
T |
5: 140,620,541 (GRCm39) |
I232N |
probably damaging |
Het |
Upk1b |
T |
C |
16: 38,607,604 (GRCm39) |
H41R |
probably benign |
Het |
Vmn2r76 |
T |
C |
7: 85,879,652 (GRCm39) |
D216G |
possibly damaging |
Het |
Zan |
A |
T |
5: 137,379,112 (GRCm39) |
C5329* |
probably null |
Het |
Zbtb40 |
C |
T |
4: 136,725,953 (GRCm39) |
M535I |
probably benign |
Het |
Zfp383 |
A |
C |
7: 29,614,263 (GRCm39) |
T173P |
possibly damaging |
Het |
Zfp7 |
T |
A |
15: 76,775,546 (GRCm39) |
C529* |
probably null |
Het |
|
Other mutations in Cd22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00714:Cd22
|
APN |
7 |
30,575,572 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02236:Cd22
|
APN |
7 |
30,566,893 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02321:Cd22
|
APN |
7 |
30,569,308 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02335:Cd22
|
APN |
7 |
30,575,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02397:Cd22
|
APN |
7 |
30,577,050 (GRCm39) |
missense |
probably benign |
|
IGL02402:Cd22
|
APN |
7 |
30,576,955 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02538:Cd22
|
APN |
7 |
30,576,985 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02736:Cd22
|
APN |
7 |
30,577,470 (GRCm39) |
splice site |
probably null |
|
blitz
|
UTSW |
7 |
30,569,329 (GRCm39) |
missense |
probably damaging |
1.00 |
crullers
|
UTSW |
7 |
30,569,308 (GRCm39) |
missense |
probably damaging |
1.00 |
gansu
|
UTSW |
7 |
30,569,530 (GRCm39) |
missense |
probably damaging |
1.00 |
lacrima
|
UTSW |
7 |
30,575,578 (GRCm39) |
missense |
probably damaging |
1.00 |
Lluvia
|
UTSW |
7 |
30,569,912 (GRCm39) |
missense |
possibly damaging |
0.48 |
Mist
|
UTSW |
7 |
30,566,083 (GRCm39) |
missense |
probably damaging |
1.00 |
rain
|
UTSW |
7 |
30,576,959 (GRCm39) |
missense |
probably damaging |
1.00 |
well
|
UTSW |
7 |
30,577,212 (GRCm39) |
nonsense |
probably null |
|
Yosemite
|
UTSW |
7 |
30,568,934 (GRCm39) |
critical splice donor site |
probably null |
|
FR4304:Cd22
|
UTSW |
7 |
30,577,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
FR4340:Cd22
|
UTSW |
7 |
30,577,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
FR4342:Cd22
|
UTSW |
7 |
30,577,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
FR4589:Cd22
|
UTSW |
7 |
30,577,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
LCD18:Cd22
|
UTSW |
7 |
30,577,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4142001:Cd22
|
UTSW |
7 |
30,577,224 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0123:Cd22
|
UTSW |
7 |
30,566,533 (GRCm39) |
splice site |
probably benign |
|
R0130:Cd22
|
UTSW |
7 |
30,569,389 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0926:Cd22
|
UTSW |
7 |
30,568,934 (GRCm39) |
critical splice donor site |
probably null |
|
R1245:Cd22
|
UTSW |
7 |
30,569,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1332:Cd22
|
UTSW |
7 |
30,569,912 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1457:Cd22
|
UTSW |
7 |
30,572,595 (GRCm39) |
missense |
probably benign |
0.07 |
R1716:Cd22
|
UTSW |
7 |
30,577,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Cd22
|
UTSW |
7 |
30,572,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R2017:Cd22
|
UTSW |
7 |
30,572,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R2061:Cd22
|
UTSW |
7 |
30,575,581 (GRCm39) |
missense |
probably benign |
0.03 |
R2061:Cd22
|
UTSW |
7 |
30,569,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Cd22
|
UTSW |
7 |
30,569,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R2216:Cd22
|
UTSW |
7 |
30,566,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Cd22
|
UTSW |
7 |
30,569,532 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4599:Cd22
|
UTSW |
7 |
30,575,325 (GRCm39) |
missense |
probably damaging |
0.98 |
R4701:Cd22
|
UTSW |
7 |
30,575,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R5179:Cd22
|
UTSW |
7 |
30,575,299 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5233:Cd22
|
UTSW |
7 |
30,576,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R5456:Cd22
|
UTSW |
7 |
30,575,464 (GRCm39) |
missense |
probably benign |
0.02 |
R5511:Cd22
|
UTSW |
7 |
30,569,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R5513:Cd22
|
UTSW |
7 |
30,566,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R5611:Cd22
|
UTSW |
7 |
30,577,575 (GRCm39) |
unclassified |
probably benign |
|
R5656:Cd22
|
UTSW |
7 |
30,569,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5966:Cd22
|
UTSW |
7 |
30,566,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Cd22
|
UTSW |
7 |
30,577,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R6356:Cd22
|
UTSW |
7 |
30,577,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Cd22
|
UTSW |
7 |
30,575,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6550:Cd22
|
UTSW |
7 |
30,576,977 (GRCm39) |
missense |
probably benign |
0.00 |
R6656:Cd22
|
UTSW |
7 |
30,577,182 (GRCm39) |
missense |
probably benign |
0.11 |
R6688:Cd22
|
UTSW |
7 |
30,572,389 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6844:Cd22
|
UTSW |
7 |
30,572,856 (GRCm39) |
splice site |
probably null |
|
R6957:Cd22
|
UTSW |
7 |
30,566,999 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7068:Cd22
|
UTSW |
7 |
30,577,504 (GRCm39) |
missense |
probably benign |
0.03 |
R7083:Cd22
|
UTSW |
7 |
30,567,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R7225:Cd22
|
UTSW |
7 |
30,577,059 (GRCm39) |
missense |
not run |
|
R7732:Cd22
|
UTSW |
7 |
30,569,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R8686:Cd22
|
UTSW |
7 |
30,569,494 (GRCm39) |
missense |
probably benign |
0.03 |
R8851:Cd22
|
UTSW |
7 |
30,577,084 (GRCm39) |
missense |
probably benign |
0.01 |
R8987:Cd22
|
UTSW |
7 |
30,577,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Cd22
|
UTSW |
7 |
30,575,449 (GRCm39) |
missense |
probably benign |
|
R9098:Cd22
|
UTSW |
7 |
30,567,391 (GRCm39) |
missense |
probably benign |
0.00 |
R9124:Cd22
|
UTSW |
7 |
30,572,662 (GRCm39) |
missense |
probably benign |
0.01 |
R9167:Cd22
|
UTSW |
7 |
30,575,430 (GRCm39) |
missense |
probably benign |
0.07 |
R9319:Cd22
|
UTSW |
7 |
30,569,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Cd22
|
UTSW |
7 |
30,576,999 (GRCm39) |
missense |
probably benign |
0.09 |
X0025:Cd22
|
UTSW |
7 |
30,572,844 (GRCm39) |
splice site |
probably null |
|
Z1176:Cd22
|
UTSW |
7 |
30,568,955 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cd22
|
UTSW |
7 |
30,567,388 (GRCm39) |
missense |
probably benign |
0.03 |
Z1186:Cd22
|
UTSW |
7 |
30,566,891 (GRCm39) |
missense |
probably benign |
|
Z1186:Cd22
|
UTSW |
7 |
30,566,478 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Cd22
|
UTSW |
7 |
30,575,292 (GRCm39) |
missense |
probably damaging |
0.97 |
|
Predicted Primers |
PCR Primer
(F):5'- GGACATCCAGCTTAGCTTCC -3'
(R):5'- CACTGTGAGTTTCCTTGAAGC -3'
Sequencing Primer
(F):5'- ATCTTTCCATGACCCAGACGG -3'
(R):5'- CCTTGAAGCTGGTGAGGGAG -3'
|
Posted On |
2016-02-04 |