ENSDARG00000055817

Ensembl ID:: ENSDARG00000055817
Human Orthologues:: CD207, CD209, CLEC4F, CLEC4M, FCER2
Human Descriptions:: C-type lectin domain family 4, member F [Source:HGNC Symbol;Acc:25357]; C-type lectin domain family 4, member M [Source:HGNC Symbol;Acc:13523]; CD207 molecule, langerin [Source:HGNC Symbol;Acc:17935]; CD209 molecule [Source:HGNC Symbol;Acc:1641]; Fc fragment of IgE, low affinity II, receptor for (CD23) [Source:HGNC Symbol;Acc:3612]
Mouse Orthologues:: Cd207, Cd209a, Cd209b, Cd209c, Cd209d, Cd209e, Cd209f, Cd209g, Clec4f, Fcer2a
Mouse Descriptions:: C-type lectin domain family 4, member f Gene [Source:MGI Symbol;Acc:MGI:1859834]; CD207 antigen Gene [Source:MGI Symbol;Acc:MGI:2180021]; CD209a antigen Gene [Source:MGI Symbol;Acc:MGI:2157942]; CD209b antigen Gene [Source:MGI Symbol;Acc:MGI:1916415]; CD209c antigen Gene [Source:MGI Symbol;Acc:MGI:2157945]; CD209d antigen Gene [Source:MGI Symbol;Acc:MGI:2157947]; CD209e antigen Gene [Source:MGI Symbol;Acc:MGI:2157948]; CD209f antigen Gene [Source:MGI Symbol;Acc:MGI:1916392]; CD209g antigen Gene [Source:MGI Symbol;Acc:MGI:1917442]; Fc receptor, IgE, low affinity II, alpha polypeptide Gene [Source:MGI Symbol;Acc:MGI:95497]

Alleles

There is 1 allele of this gene:

Allele name	Consequence	Status	Availability Estimate
sa7220	Essential Splice Site	Mutation detected in F1 DNA	During 2015

Mutation Details

Allele Name:: sa7220
Current Status:: Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:: We currently estimate that this allele will be available during 2015.
Mutation:: T > C
Consequence:: Essential Splice Site

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078218	Essential Splice Site	67	408	1	7

Genomic Location:: Chromosome 10 (position 25307769)
KASP Assay ID:: 554-5136.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:: CTAATAATYAACATAACCAGCCTCWTRGAAGAGAGAGACCAGCTACTAAC[T/C]AACATTGTCAATATAACAGAAGAGAGAGATCAGCTACTAWCYAACATTGT
Associated Phenotype:: Not determined

OMIM

OMIM information for FCER2

More OMIM information for CD209

Birbeck granule deficiency

More OMIM information for CD207

OMIM information for CLEC4M

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