Mutagenetix > Incidental Mutation

Incidental Mutation 'FR4304:Cd22'

511003

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) question?

Stock #

FR4304 ()

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

30564829-30579767 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 30577507 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Histidine at position 2 (R2H)

Ref Sequence

ENSEMBL: ENSMUSP00000140528 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000019248] [ENSMUST00000108125] [ENSMUST00000186154] [ENSMUST00000190753] [ENSMUST00000187989] [ENSMUST00000190646] [ENSMUST00000190617] [ENSMUST00000188157] [ENSMUST00000189718] [ENSMUST00000214289]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000019248
AA Change: R2H

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000019248
Gene: ENSMUSG00000030577
AA Change: R2H

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

possibly damaging
Transcript: ENSMUST00000108125
AA Change: R2H

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000103760
Gene: ENSMUSG00000030577
AA Change: R2H

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

possibly damaging
Transcript: ENSMUST00000186154
AA Change: R2H

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000139685
Gene: ENSMUSG00000030577
AA Change: R2H

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: ENSMUST00000187436

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000187585

Predicted Effect

unknown
Transcript: ENSMUST00000190753
AA Change: R2H

Predicted Effect

unknown
Transcript: ENSMUST00000187989
AA Change: R2H

Predicted Effect

possibly damaging
Transcript: ENSMUST00000190646
AA Change: R2H

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000140528
Gene: ENSMUSG00000030577
AA Change: R2H

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

possibly damaging
Transcript: ENSMUST00000190617
AA Change: R2H

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000139871
Gene: ENSMUSG00000030577
AA Change: R2H

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

possibly damaging
Transcript: ENSMUST00000188157
AA Change: R2H

PolyPhen 2 Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000140450
Gene: ENSMUSG00000030577
AA Change: R2H

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
IG	31	147	1.1e-3	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000189718
AA Change: R2H

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000140521
Gene: ENSMUSG00000030577
AA Change: R2H

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: ENSMUST00000189996

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000190170

Predicted Effect

unknown
Transcript: ENSMUST00000214289
AA Change: R2H

Predicted Effect

probably benign
Transcript: ENSMUST00000190455

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.8%
3x: 99.6%
10x: 98.6%
20x: 96.4%

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: 137 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001K19Rik	CTT	CTTTTT	12: 110,634,883 (GRCm39)		probably benign	Homo
1700001K19Rik	TTC	TTCGTC	12: 110,634,884 (GRCm39)		probably benign	Homo
4930433I11Rik	ACCTC	AC	7: 40,642,480 (GRCm39)		probably benign	Het
4930447C04Rik	AAGT	A	12: 72,928,061 (GRCm39)		probably benign	Homo
Acbd4	CAG	CAGACTAG	11: 102,994,931 (GRCm39)		probably null	Homo
Ahdc1	CT	CTCTT	4: 132,790,070 (GRCm39)		probably benign	Homo
Alpk3	TCT	TCTGCT	7: 80,727,510 (GRCm39)		probably benign	Het
Anapc4	C	T	5: 53,021,868 (GRCm39)	T650M	probably damaging	Homo
Ankhd1	GGCGGC	GGCGGCTGCGGC	18: 36,693,977 (GRCm39)		probably benign	Het
Ankrd35	TAGC	TAGCAGC	3: 96,591,163 (GRCm39)		probably benign	Homo
Apc	GCCAATAAA	GCCAATAAAACCAATAAA	18: 34,415,050 (GRCm39)		probably benign	Het
Apol6	TTGT	TTGTCTGT	15: 76,935,636 (GRCm39)		probably null	Het
Arhgap30	TGGCCC	TGGCCCTGGCCCAGGCCTTGGCCCCGGCCC	1: 171,232,736 (GRCm39)		probably benign	Het
Arpc1b	GCC	GCCTGTCC	5: 145,063,601 (GRCm39)		probably null	Het
Blm	CT	CTACGT	7: 80,113,521 (GRCm39)		probably null	Homo
Blm	TCCTCCTCCTCC	TCCTCCTCCTCCACCTCCTCCTCC	7: 80,162,667 (GRCm39)		probably benign	Het
Btnl10	GA	GAATA	11: 58,814,756 (GRCm39)		probably benign	Homo
Cacna1f	AGG	AGGCGG	X: 7,486,300 (GRCm39)		probably benign	Het
Calhm3	CG	CGG	19: 47,140,335 (GRCm39)		probably null	Homo
Catsper2	C	CTTTTACTTTTTA	2: 121,228,023 (GRCm39)		probably null	Homo
Catsper2	CAT	CATTAT	2: 121,228,263 (GRCm39)		probably benign	Het
Ccdc121	GAGAAG	GAG	5: 31,644,717 (GRCm39)		probably benign	Homo
Ccdc15	AC	ACTTTCC	9: 37,226,453 (GRCm39)		probably null	Het
Ccdc162	T	C	10: 41,432,117 (GRCm39)	D1792G	possibly damaging	Het
Ccdc170	CCA	CCATCA	10: 4,511,021 (GRCm39)		probably benign	Het
Ccdc73	TAAG	T	2: 104,822,185 (GRCm39)		probably benign	Homo
Ccdc85c	GCC	GCCCCC	12: 108,240,871 (GRCm39)		probably benign	Het
Cd80	AGA	AGAGGA	16: 38,306,677 (GRCm39)		probably benign	Homo
Cep89	GACT	G	7: 35,109,066 (GRCm39)		probably benign	Het
Cfap74	A	G	4: 155,500,217 (GRCm39)	D21G	possibly damaging	Homo
Cgref1	T	TCTA	5: 31,091,124 (GRCm39)		probably benign	Homo
Chd4	GCC	GCCACTCCC	6: 125,099,107 (GRCm39)		probably benign	Het
Cnpy3	TCC	TCCCCC	17: 47,047,669 (GRCm39)		probably benign	Het
Cnpy3	TCC	TCCACC	17: 47,047,672 (GRCm39)		probably benign	Het
Cntnap1	AGCCCC	AGCCCCCGCCCC	11: 101,080,407 (GRCm39)		probably benign	Het
Cntnap1	CCCCAG	CCCCAGACCCAG	11: 101,080,415 (GRCm39)		probably benign	Het
Col2a1	C	A	15: 97,886,862 (GRCm39)		probably null	Homo
Cpeb4	T	TGA	11: 31,877,638 (GRCm39)		probably benign	Homo
Cpne1	AGA	AGAGAGA	2: 155,913,945 (GRCm39)		probably null	Homo
Cttnbp2	ATTGCTG	ATTGCTGTTGCTG	6: 18,367,457 (GRCm39)		probably benign	Het
Dhx37	CTGG	C	5: 125,504,594 (GRCm39)		probably benign	Het
Dhx8	CGAGAC	CGAGACGGAGAC	11: 101,629,014 (GRCm39)		probably benign	Homo
Dnaaf9	TCC	TCCCCC	2: 130,612,668 (GRCm39)		probably benign	Het
Dnah12	G	T	14: 26,571,342 (GRCm39)	G2817V	probably damaging	Homo
Dst	C	A	1: 34,240,045 (GRCm39)	S1798Y	probably damaging	Het
Eif3a	TA	TATTTCA	19: 60,763,728 (GRCm39)		probably benign	Homo
Ermn	TTC	TTCCTC	2: 57,938,090 (GRCm39)		probably benign	Het
Ermn	CTT	CTTGTT	2: 57,938,098 (GRCm39)		probably benign	Het
Fbxo43	TGTGCC	TGTGCCAGTGCC	15: 36,152,243 (GRCm39)		probably benign	Het
Fbxo43	GCCTGT	GCCTGTCCCTGT	15: 36,152,246 (GRCm39)		probably benign	Het
Fbxo43	GCCTGT	GCCTGTTCCTGT	15: 36,152,240 (GRCm39)		probably benign	Het
Fmn1	TCC	TCCTCCACC	2: 113,356,128 (GRCm39)		probably benign	Homo
Fmn1	TCCTCC	TCCTCCCCCTCC	2: 113,356,119 (GRCm39)		probably benign	Het
Foxd3	GGACCCTACGGCCG	GG	4: 99,545,633 (GRCm39)		probably benign	Homo
Frmpd2	G	T	14: 33,232,978 (GRCm39)	L399F	probably damaging	Homo
Gabre	ACTCCGGCTCCGGCTCAGGCTCAGGCTCCGGCTCAGGCTCCGGCTCCGGCTCCGGCTC	ACTCCGGCTCCGGCTCCGGCTCAGGCTCAGGCTCCGGCTCAGGCTCCGGCTCCGGCTCCGGCTC	X: 71,313,648 (GRCm39)		probably benign	Homo
Gbp2b	A	G	3: 142,309,413 (GRCm39)	I175V	probably benign	Het
Gm4340	CAG	CAGAAG	10: 104,031,933 (GRCm39)		probably benign	Het
Gm4340	AGC	AGCGGC	10: 104,031,943 (GRCm39)		probably benign	Het
Gm5114	T	C	7: 39,060,529 (GRCm39)	R107G	probably benign	Het
Gm5114	A	C	7: 39,060,530 (GRCm39)	H106Q	probably benign	Het
H1f6	GAGAA	GA	13: 23,879,903 (GRCm39)		probably benign	Homo
H2-Q4	G	A	17: 35,599,381 (GRCm39)	D155N	probably damaging	Het
H2-T10	TGTTTCCCACTG	T	17: 36,431,173 (GRCm39)		probably null	Het
Ifi203	C	T	1: 173,755,894 (GRCm39)		probably benign	Het
Ifi208	ATGGTG	ATG	1: 173,505,264 (GRCm39)		probably benign	Homo
Ighv5-9	C	T	12: 113,625,497 (GRCm39)	S82N	probably benign	Homo
Il17rd	CGG	CGGTGG	14: 26,804,637 (GRCm39)		probably benign	Het
Il2	AGTGG	AGTGGGGCTTGAGGTGG	3: 37,179,975 (GRCm39)		probably benign	Het
Ipo9	TCC	TCCGCC	1: 135,314,013 (GRCm39)		probably benign	Het
Ipo9	CCT	CCTACT	1: 135,314,017 (GRCm39)		probably null	Het
Isg20l2	AAG	AAGCAG	3: 87,839,019 (GRCm39)		probably benign	Homo
Kmt2b	TCCTCC	TCCTCCCCCTCC	7: 30,285,788 (GRCm39)		probably benign	Het
Kmt2c	TGCTGCTG	TGCTGCTGCTGCTG	5: 25,520,764 (GRCm39)		probably benign	Homo
Krt10	CGCC	CGCCGCC	11: 99,277,025 (GRCm39)		probably benign	Het
Krt10	CCTCCT	CCTCCTACTCCT	11: 99,280,100 (GRCm39)		probably benign	Het
Las1l	GAG	GAGCAG	X: 94,984,426 (GRCm39)		probably benign	Het
Las1l	AGG	AGGCGG	X: 94,984,427 (GRCm39)		probably benign	Het
Lkaaear1	GCTCCAGCTCCAGCTCCAGCTCCA	GCTCCAGCTCCATCTCCAGCTCCAGCTCCAGCTCCA	2: 181,339,372 (GRCm39)		probably benign	Het
Lrch1	A	T	14: 75,057,005 (GRCm39)	C241S	possibly damaging	Het
Lrit3	G	GCTT	3: 129,582,468 (GRCm39)		probably benign	Het
Maml2	GCAGCAGCAACAGCAGCA	GCAGCAGCA	9: 13,532,755 (GRCm39)		probably benign	Homo
Mast4	T	TTTC	13: 102,871,370 (GRCm39)		probably benign	Het
Med12l	AGC	AGCGGC	3: 59,183,403 (GRCm39)		probably benign	Het
Muc21	T	G	17: 35,933,013 (GRCm39)		probably benign	Homo
Noc2l	TGC	TGCAGC	4: 156,324,553 (GRCm39)		probably benign	Het
Nrg3	G	GACATTT	14: 38,119,230 (GRCm39)		probably benign	Homo
Or51q1	TCC	TCCC	7: 103,629,110 (GRCm39)		probably null	Het
Padi3	TCTCAC	TC	4: 140,520,283 (GRCm39)		probably benign	Homo
Patl2	GCT	GCTTCT	2: 121,956,616 (GRCm39)		probably benign	Het
Pdik1l	TTTT	TTTTGTTTTTGGTTT	4: 134,006,685 (GRCm39)		probably null	Homo
Pik3c2g	AG	AGAGGG	6: 139,612,654 (GRCm39)		probably null	Homo
Plekhs1	T	TTCAGACCTCCCC	19: 56,468,290 (GRCm39)		probably benign	Het
Prkd3	G	T	17: 79,283,249 (GRCm39)		probably null	Homo
Prkn	G	A	17: 12,073,650 (GRCm39)	V323M	probably damaging	Het
Prr13	TCC	TCCCCC	15: 102,370,612 (GRCm39)		probably benign	Homo
Prrc2b	G	A	2: 32,111,179 (GRCm39)	A1852T	probably damaging	Homo
Ptms	CTT	CTTTTT	6: 124,891,421 (GRCm39)		probably benign	Homo
Rtl1	TTCCTCTTCCTCCTC	TTCCTC	12: 109,557,632 (GRCm39)		probably benign	Homo
Scaf4	TGCGGC	TGC	16: 90,026,742 (GRCm39)		probably benign	Homo
Serac1	T	A	17: 6,121,083 (GRCm39)	K70N	probably damaging	Homo
Six3	CGG	CGGTGG	17: 85,928,796 (GRCm39)		probably benign	Het
Sry	GTG	GTGCTG	Y: 2,662,837 (GRCm39)		probably benign	Homo
Stard8	GGAAGA	GGAAGAAGA	X: 98,110,111 (GRCm39)		probably benign	Het
Supt20	TTCAGCA	TTCAGCATCAGCA	3: 54,635,068 (GRCm39)		probably benign	Het
Supt20	CAGCAG	CAGCAGTAGCAG	3: 54,635,085 (GRCm39)		probably null	Het
Supt20	AGCAGC	AGCAGCGGCAGC	3: 54,635,083 (GRCm39)		probably benign	Het
Sytl1	CTCT	C	4: 132,984,304 (GRCm39)		probably benign	Homo
Tcof1	AGC	AGCGGC	18: 60,968,814 (GRCm39)		probably benign	Het
Tdpoz2	T	TCA	3: 93,558,922 (GRCm39)		probably null	Homo
Tert	GCC	GCCAAGGGTTCC	13: 73,796,421 (GRCm39)		probably benign	Homo
Tfeb	GCA	GCAACA	17: 48,097,019 (GRCm39)		probably benign	Het
Ticrr	ATT	ATTTTT	7: 79,344,059 (GRCm39)		probably benign	Homo
Tnfaip8	ACACACACTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	AC	18: 50,179,906 (GRCm39)		probably null	Homo
Tnfrsf9	T	TGCC	4: 151,018,852 (GRCm39)		probably benign	Homo
Tob1	GCA	GCAACA	11: 94,105,290 (GRCm39)		probably benign	Het
Tob1	CA	CAGTA	11: 94,105,303 (GRCm39)		probably null	Het
Trav15-2-dv6-2	GGGAG	GGGAGGAG	14: 53,887,207 (GRCm39)		probably benign	Homo
Triobp	TCGTCG	TCGTCGTCG	15: 78,877,587 (GRCm39)		probably benign	Homo
Tsbp1	A	AGCC	17: 34,679,029 (GRCm39)		probably benign	Het
Tsbp1	GC	GCATC	17: 34,679,051 (GRCm39)		probably benign	Het
Tsen2	AGG	AGGGGG	6: 115,537,030 (GRCm39)		probably benign	Het
Ubtf	TCC	TCCGCC	11: 102,197,782 (GRCm39)		probably benign	Het
Ubtf	CTCGTCGTC	CTCGTCGTCGTC	11: 102,197,784 (GRCm39)		probably benign	Het
Vars1	TGG	TGGAGTCCTGGGCGG	17: 35,234,965 (GRCm39)		probably benign	Homo
Vmn1r171	C	T	7: 23,332,105 (GRCm39)	A110V	probably benign	Het
Vmn2r31	G	T	7: 7,387,607 (GRCm39)	Q655K	probably damaging	Het
Vmn2r87	C	T	10: 130,314,583 (GRCm39)	M334I	probably benign	Homo
Zc3h13	CG	CGAGATGTGTG	14: 75,561,050 (GRCm39)		probably benign	Het
Zc3h13	AGATGTGCG	AGATGTGCGGGATGTGCG	14: 75,561,043 (GRCm39)		probably benign	Het
Zfp282	GGC	GGCCGC	6: 47,881,731 (GRCm39)		probably benign	Het
Zfp384	AGGC	AGGCCCAGGCCCCGGC	6: 125,013,456 (GRCm39)		probably benign	Het
Zfp459	TGA	TGAGCGA	13: 67,556,393 (GRCm39)		probably null	Homo
Zfp462	GCCACC	GCCACCTCAGCCACAACCACC	4: 55,009,757 (GRCm39)		probably benign	Het
Zfp462	CCACC	CCACCTCAGCCACAGTCACC	4: 55,009,758 (GRCm39)		probably benign	Het
Zfp598	CACCAC	CACCACAACCAC	17: 24,899,749 (GRCm39)		probably benign	Het
Zfp831	CCT	CCTGCT	2: 174,487,274 (GRCm39)		probably benign	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
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
R4796:Cd22	UTSW	7	30,572,381 (GRCm39)	splice site	probably null
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'- ACTGAGGGGTGAGAACTTCC -3'
(R):5'- CAACAAGATGGCTCAAAGGC -3'

Sequencing Primer
(F):5'- GGGTGAGAACTTCCACTGG -3'
(R):5'- AAGGCAAATTCCTTTTGTTGTTCTTG -3'

Posted On

2018-04-05