Busch Lab

ZMP

ENSDARG00000091455

Ensembl ID:
ENSDARG00000091455
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa738 Essential Splice Site Available for shipment Available now
sa27559 Nonsense Mutation detected in F1 DNA Not yet available
sa8841 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa738
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122010 Essential Splice Site 110 374 1 4
Genomic Location (Zv9):
Chromosome 10 (position 7530355)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 8551630
GRCz11 10 8510330
KASP Assay ID:
554-0645.1 (used for ordering genotyping assays)
KASP Sequence:
CCTTAATCGCAACAATGACCTGACGAAAGAAAGAGAGCAGATAYTGAAAA[G/A]CAAGAATGACCTTACGAAAGAAAGRGAGCAGATACTAAAAAACAACAATG
Long Flanking Sequence:
TTATCAAAAAATAAATACAGAAGATACTGAAGGATGTCTAGATCTGAAGACAGAGAAACACCAGACACCTCAACTCACAGGTATGTAAGTGTAAATTCAGGTTTATACTGTTATAAGAGACAATGAAAAAGTCAAAAGCTTGTTTTCTTCATCCTCAGGAAGCATCTCAGTGAAGAGCAGAAAGCAGAGAGCAATTGGAGTGTGTTTGTGTTTGCTTTGTGCTCTTCTGCTGACAGCTGTAATAGTGCTCTGTGTGTATTTCACCATCGAGAGAAGACACTTACCAACAAACATCACTAACCTCAATGAAGAAAGAGAAAAGATACTAAAGCGCAGCAATGAACTGACTGAAGAAAGAGAGCAGTTACTTACTAATATCACTAACCTCAAAGGAGAAAGAGAGCGGTTACTGAACCACAACAATGACCTGACTAAAGAAAGAGAGCAGATCCTTAATCGCAACAATGACCTGACGAAAGAAAGAGAGCAGATACTGAAAA[G/A]CAAGAATGACCTTACGAAAGAAAGGGAGCAGATACTAAAAAACAACAATGACCTGACTAAAGAAAGAGAGCAGATACTGAAACGCAACAATGACCTGACGAAAGAAAAAGAGCAGATACTGAAACGCAACAATGACCTGACGAAAGAAAGAGAGCAGATACTAAAAAACAACAATGACCTGACTAAAGAAAGAGAGCAGTTACTGAAACGCAACAATGACCTGACGAAAGAAAAAGAGCAGATACTGAAACGCAACAATGACCTTACGAAAGAAAGAGAGCAGATACTAAAAAACAACAATGACCTGACGAAAGAAAAAGAGCAGATACTGAAACGCAACAATGACCTGACGAAAGAAAAAGAGCAGATACTGAAACGTAACAATGACCTGACTAAAGAAAGAGAGCAGATACTGAAACGCAACAATGACCTGACGAAAGAAAAAGAGCAGATACTAAAAAACAACAATGACCTGACTAAAGAAAGAGAGCAGATACTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27559
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122010 Nonsense 183 374 2 4
Genomic Location (Zv9):
Chromosome 10 (position 7531221)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 8552496
GRCz11 10 8511196
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAAAAGAGCAGATACTGACACGCAACAATGAGCTGACTAAAGAAAAA[G/T]AGCAGATACTGAAACGTAACAATGACCTGACTAAAGAAAAAGAGCAGATA
Long Flanking Sequence:
AGATACTGAAACGTAACAATGACCTGACTAAAGAAAGAGAGCAGATACTGAAACGCAACAATGACCTGACGAAAGAAAAAGAGCAGATACTAAAAAACAACAATGACCTGACTAAAGAAAGAGAGCAGATACTGAAACGCAACAATGACCTGACGAAAGAAAGAGAGCAGATACTAAAAAACAACAATGACCTGACGAAAGAAAAAGAGCAAATACTGAAACGCAACAATGACCTGACGAAAGAAAAAGAGCAGATGCTGAAACGCAACAATGACATAACTAAAGAAAAAGAGCAGATACTGACACGCAACAATGAGCTGACTAAAGAAAAAGAGCAGATACTGAAACGTAACAATGACCTGACTAAAGAAAAAGAGCAGATACTGAAACGCAACAATGACCTGACGAAAGAAAAAGAGCAGATACTGAAACGCAACAATGACATAACTAAAGAAAAAGAGCAGATACTGACACGCAACAATGAGCTGACTAAAGAAAAA[G/T]AGCAGATACTGAAACGTAACAATGACCTGACTAAAGAAAAAGAGCAGATACTGAAACGTAACAATGACCTGACTAAAGAAAAAGAGCAGATTCTGAAACGTAACAATGACCTGACGAAAGAAAAAGAGCAGATACTGAAACGCAACAATGACTTAACTAAAGAAAAAGAGCAGATACTGAAAAGCAACAATGACCTGACTAAAGAAAGAGAGCAGATACTGAAACGCAACAATGACCTGACTAAAGAAAAAGAGCAGATACTGAAAAGCAACAATGACCTGACTAAAGAAAGAGACAAGATAAGGAATGAGCAGAACCAGCTGCGTCATTGGCTTCATGAACAGGGTAAAGTTCTCTTTAATTGCCTGTACTTTTTTTGTCTACAACACAGTCTACTTTCTTTTTTATACAACTCATTTCATTTTAATACATAACCATAATTTAAAGGCATTTTCACTCCTGAGAAATGTTTTCAAAACTCCTAGAAATAGCTAGAAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8841
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122010 Nonsense 370 374 4 4
Genomic Location (Zv9):
Chromosome 10 (position 7534748)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 8556023
GRCz11 10 8514723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGAATAACAATTTATGGGTTGGCTGGAGACAGACAAATGGAGAMAATT[G/A]GATATGGATTGATGACCCTTYWGTGGCAAATGGGTGAGTGATCACCAATT
Long Flanking Sequence:
CTTCTTTCCCTGTGAAAAATTCACAAAGGATTCTGTTTTTGACTTTTGACTTCTCATATTCTGCACAAAATAAATTAAATACTACCTTCTTATATACTAAAGCTTTTGCAGTTTAGGCAATTGTCATGGTACATGATTGCTTGTGGGTCAGGAGGTGGGAGATCTTGTCATTTTTTTTATGCATTTTATGTGTATTTCTGTATTTCTGATATTGTTCTTGTTTTTTTATTATTATTAAAATGTAATTTAGTAATTTTCTTTTAATCATCCTACCATCTTGCATTCTGCTATTTTTTCTGAGGTTTGAACCTCCGATCTACCCTAATGCAAATCATTTACTTTATTTAATTGAACATAAAAAGGTGGTCAAGTGAATTGTAATCATGTTTTATGCAGAAATAAAATATAGACCTATAATTTATCATTACAGACATTTTTGCAAAAGGTTCTTCAGAATAACAATTTATGGGTTGGCTGGAGACAGACAAATGGAGACAATT[G/A]GATATGGATTGATGACCCTTTAGTGGCAAATGGGTGAGTGATCACCAATTTACTATATACAGTTAGTATCATATGATAAACAGAGTATAACAGTTACTAAAGTAACCCTCATTCCCCGAGGGGGGGAATGTAAATGCTATGTGGAAATATATGATAAAAAACACAACAATTGAAACTTACCACGTCTCTGGTGACATGTTATGCCAAGCTCCAGCATGACCGCACCTGCCTCACCAGAGGTGCAGCCTTCTAACATGTCCCCTGACCCTTACTTACCTCACTTACCTAAGAAGATTTATTTGTTTAGATATATTTTTCGGGAGTCGTAAAAATACACATAGTTAAGTTCTAGAAATTTTAAACATGACAATACGCTTGAAAAGATCCGACAGGGAGGACACCGTGGAGGCCACCTGCTACCTCAATGGGAAGACCTGGTGGCAAGAAGGCATATGGACTAGCCCTGAGAAGGGGGAGTGCTCATATGAGAAGATGGTTAG
Associated Phenotype:
Not determined