Busch Lab

ZMP

ENSDARG00000026805

Ensembl ID:
ENSDARG00000026805
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 are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa27603 Nonsense Mutation detected in F1 DNA Not yet available
sa45406 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa27603
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124081 Nonsense 34 226 2 5
Genomic Location (Zv9):
Chromosome 10 (position 23772204)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 23543531
GRCz11 10 23512983
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACAGTATATTCATGTCTGTCATCTCCAGGAAGTGATTCAGTGAAGACG[A/T]GATTCTCCAGAGCAGCTCCGGTGTGTTTGGTGCTGTTGTGTTTCCTTCTG
Long Flanking Sequence:
TGTGATGAATAAACATAAATAAAAAAATAAATATATAAATAAATTAAGATAAAGATGACTTTTCCTCATGAATAAATTTACTGTGCTTATTTTATCGACAATTTTCTCTACATCTACAGTGACCACACAACCACAGTGGAGACCTTTAGTGAGACTTTTCTGTATGCATGTGAACAGATACAGGATGTCACATGGTTGTATACATTGGCATGTTTGCCACATTAGCTTCAATTGCTAATATTAGCGACTCAACAGCACATGACTAGACAGTAGAAACAGACTGCATTAATTTACCATTTATAGATGACCAGCAAAATAAAAATGTCTCAGCCTATTTATGGTAACATAAACACTGATTCAAGACTGAAGATGGACAGGTCCTCTCATAGAAATCAAACAGGTACTGTACAAATACAAACACACTTTCATTTTTGTCAGATAAAGAAACATTTACAGTATATTCATGTCTGTCATCTCCAGGAAGTGATTCAGTGAAGACG[A/T]GATTCTCCAGAGCAGCTCCGGTGTGTTTGGTGCTGTTGTGTTTCCTTCTGCTGACTGCAGTCATAGTGCTGAGTGTCTTCATCTATACAAACAACACAAACTACACTGAAGAGAGACGCCAGCTAATAACTAACATCACCAACCTCACAGGAGCCAAAGACGAGCTGACAAACCTTCTATATGACAAAGACCAACTAATAAAGTGGCTTCAGATTTTTGGTCAAGAAGGTAAATGACCTTAATCTGCAGTTAAAGCAAATTTGAGCTGCTTGTAGACTTGCAATGCTTCAGTGTATACTCTATATAAGTGTACTTTACCTGCTGTAAGTAACAGCTGTGGGATTGTAAATCGAGCTAATAAATTAACAGCTAAACTTGTTGTGTTAACAGCTGGATGGTTTTACTATCAATCCAGTTTTTACTACTTTTCCAATGAGACAAAAAGCTGGACTGAGAGCAGAAGATACTGTAGAGACAAAAGAGCAGACCTGATCATCATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45406
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124081 Essential Splice Site 100 226 3 5
Genomic Location (Zv9):
Chromosome 10 (position 23772593)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 23543920
GRCz11 10 23513372
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGATTGTAAATCGAGCTAATAAATTAACAGCTAAACTTGTTGTGTTAAC[A/G]GCTGGATGGTTTTACTATCAATCCAGTTTTTACTACTTTTCCAATGAGAC
Long Flanking Sequence:
AAATCAAACAGGTACTGTACAAATACAAACACACTTTCATTTTTGTCAGATAAAGAAACATTTACAGTATATTCATGTCTGTCATCTCCAGGAAGTGATTCAGTGAAGACGAGATTCTCCAGAGCAGCTCCGGTGTGTTTGGTGCTGTTGTGTTTCCTTCTGCTGACTGCAGTCATAGTGCTGAGTGTCTTCATCTATACAAACAACACAAACTACACTGAAGAGAGACGCCAGCTAATAACTAACATCACCAACCTCACAGGAGCCAAAGACGAGCTGACAAACCTTCTATATGACAAAGACCAACTAATAAAGTGGCTTCAGATTTTTGGTCAAGAAGGTAAATGACCTTAATCTGCAGTTAAAGCAAATTTGAGCTGCTTGTAGACTTGCAATGCTTCAGTGTATACTCTATATAAGTGTACTTTACCTGCTGTAAGTAACAGCTGTGGGATTGTAAATCGAGCTAATAAATTAACAGCTAAACTTGTTGTGTTAAC[A/G]GCTGGATGGTTTTACTATCAATCCAGTTTTTACTACTTTTCCAATGAGACAAAAAGCTGGACTGAGAGCAGAAGATACTGTAGAGACAAAAGAGCAGACCTGATCATCATAAACAACAAACAGGAACAAGTGAGTGAGCGATTGTGTGTGTTTGTGGTGCTTAGAAGAAGATAAAATGTGAATATTGTCTATTGATTAAATAAATGTCGCATTGTTTCATCTGCTCAGGACTTTATTATGAAGATCACTTGTAACAATGAATTCTGGATTGGTCTGACTGACATTAAAAAAGAGGGCACTTGGAAATGGGTTGATGGCAGTATACTGACCTCTGGGTGAGAAATCACTGAACGGAACTGATCATGATCTAATAAATGATTCTTCACGACCAGTAGCATATCACAAAGCAGCACTGAACATCTAATGTTGATTTGTTCATGCAGGTTCTGGGCTTCCTCTGGATCAATAAATGAGCCCAATGGAGGGAAAACAGAGAACTG
Associated Phenotype:
Not determined