ZMP
si:ch211-214k5.3
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate CD209 antigen (CD209) [Source:UniProtKB/TrEMBL;Acc:Q5RGH7]
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]
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]
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 |
---|---|---|---|
sa21735 | Nonsense | Available for shipment | Available now |
sa27611 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27612 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21735
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037303 | Nonsense | 37 | 222 | 1 | 6 |
ENSDART00000064459 | Nonsense | 54 | 230 | 2 | 5 |
ENSDART00000130402 | Nonsense | 76 | 236 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 10 (position 25743400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 24967941 |
GRCz11 | 10 | 24937393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTGCTGTGTTTTCTTCTACTGACTGCAGTCATAGTGCTGAGCGTCTA[C/A]ACCCATACAAACTACACACAAGAGAACAGAATTACAAGCCTCACAGAAGA
Long Flanking Sequence:
GAATTTGACACAGTTAGACTCTCATTTCCTCTTTGTTTCTTTAGTTGTTGGAGATAAATGTGTGAAACTGAAAGGCACACTAAGAACATTCAGCATTAGCAGTTTATTATCTTGTAAAAGAGTAAAAATGTCTAAAGATGTTTATGAGAATGTGTTTAGCTCAGAGTCTGGGGAAAGGAACAGTGAGCAAGTGGAGATGATGGTGGCTATTTATGAGAGTGCAAACTGTGTGAGAGATCAAGACTTCAGGATTAACACACAACAACCAATTCAACAAACAGGTAATTACACATTTTGCACATTTAATCATTTAGTATTAAGTTCATGCAGAGCTTTTATTCAAATAAAAATGTCACAGTTTGCACATTAAATTATGTAACATCATATTGGTCTTCATCAGGAAGTGACTCAGTAAATACAAGAATCTTCAGAGCTTATCCAGTGTGTTTGGTGCTGCTGTGTTTTCTTCTACTGACTGCAGTCATAGTGCTGAGCGTCTA[C/A]ACCCATACAAACTACACACAAGAGAACAGAATTACAAGCCTCACAGAAGAGAGAGACCAGCTACTAATCAACATAACCAACCTCATAGAAGAGAGAGACCAACTACTAATCAATATCAATGCTGGGAATGCTCAGAACCAAAACTTGACAAAAGAAAAGAATGAATTATTATCTAAGAATGATGATCTGATAATACAAAACGTGCAGTTACAGCAGGTGGAAAACAACCTGCAGGAGTGTCGTAATAAACTAGGTACTTCATCTTTGGTTACAACCTTTTATTCACATATAGTGTCGTTTAGTGTGATGGAAATAAATTACTTCTACTTTGTTGTGTTTACAGATGGATGGTTTAACTATCAGTCCAGCTTTTACTTCATTTCTTCAGAGAAAAAGAACTGGTCTGAGAGCACAAGAAACTGTAGAGACAGAGGAGCAGATCTGATCATCATAAACAACAAAGAAGAACAAGTGAGTGAAAAACTCTCTCTCCCCCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27611
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037303 | Nonsense | 84 | 222 | 1 | 6 |
ENSDART00000064459 | Nonsense | 101 | 230 | 2 | 5 |
ENSDART00000130402 | None | None | 236 | None | 5 |
Genomic Location (Zv9):
Chromosome 10 (position 25743539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 24967802 |
GRCz11 | 10 | 24937254 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGAGAGACCAACTACTAATCAATATCAATGCTGGGAATGCTCAGAAC[C/T]AAAACTTGACAAAAGAAAAGAATGAATTATTATCTAAGAATGATGATCTG
Long Flanking Sequence:
GTTTATGAGAATGTGTTTAGCTCAGAGTCTGGGGAAAGGAACAGTGAGCAAGTGGAGATGATGGTGGCTATTTATGAGAGTGCAAACTGTGTGAGAGATCAAGACTTCAGGATTAACACACAACAACCAATTCAACAAACAGGTAATTACACATTTTGCACATTTAATCATTTAGTATTAAGTTCATGCAGAGCTTTTATTCAAATAAAAATGTCACAGTTTGCACATTAAATTATGTAACATCATATTGGTCTTCATCAGGAAGTGACTCAGTAAATACAAGAATCTTCAGAGCTTATCCAGTGTGTTTGGTGCTGCTGTGTTTTCTTCTACTGACTGCAGTCATAGTGCTGAGCGTCTACACCCATACAAACTACACACAAGAGAACAGAATTACAAGCCTCACAGAAGAGAGAGACCAGCTACTAATCAACATAACCAACCTCATAGAAGAGAGAGACCAACTACTAATCAATATCAATGCTGGGAATGCTCAGAAC[C/T]AAAACTTGACAAAAGAAAAGAATGAATTATTATCTAAGAATGATGATCTGATAATACAAAACGTGCAGTTACAGCAGGTGGAAAACAACCTGCAGGAGTGTCGTAATAAACTAGGTACTTCATCTTTGGTTACAACCTTTTATTCACATATAGTGTCGTTTAGTGTGATGGAAATAAATTACTTCTACTTTGTTGTGTTTACAGATGGATGGTTTAACTATCAGTCCAGCTTTTACTTCATTTCTTCAGAGAAAAAGAACTGGTCTGAGAGCACAAGAAACTGTAGAGACAGAGGAGCAGATCTGATCATCATAAACAACAAAGAAGAACAAGTGAGTGAAAAACTCTCTCTCCCCCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTTTGTGTGTGTGCGTATTCTGGTATATGTGGTTTACAATTGTACAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27612
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037303 | Essential Splice Site | 148 | 222 | None | 6 |
ENSDART00000064459 | Essential Splice Site | 156 | 230 | None | 5 |
ENSDART00000130402 | Essential Splice Site | 162 | 236 | None | 5 |
Genomic Location (Zv9):
Chromosome 10 (position 25743873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 24967468 |
GRCz11 | 10 | 24936920 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAGACAGAGGAGCAGATCTGATCATCATAAACAACAAAGAAGAACAAG[T/A]GAGTGAAAAACTCTCTCTCCCCCTGTGTGTGTGTGTGTGTGTGTGTGTGT
Long Flanking Sequence:
GACTGCAGTCATAGTGCTGAGCGTCTACACCCATACAAACTACACACAAGAGAACAGAATTACAAGCCTCACAGAAGAGAGAGACCAGCTACTAATCAACATAACCAACCTCATAGAAGAGAGAGACCAACTACTAATCAATATCAATGCTGGGAATGCTCAGAACCAAAACTTGACAAAAGAAAAGAATGAATTATTATCTAAGAATGATGATCTGATAATACAAAACGTGCAGTTACAGCAGGTGGAAAACAACCTGCAGGAGTGTCGTAATAAACTAGGTACTTCATCTTTGGTTACAACCTTTTATTCACATATAGTGTCGTTTAGTGTGATGGAAATAAATTACTTCTACTTTGTTGTGTTTACAGATGGATGGTTTAACTATCAGTCCAGCTTTTACTTCATTTCTTCAGAGAAAAAGAACTGGTCTGAGAGCACAAGAAACTGTAGAGACAGAGGAGCAGATCTGATCATCATAAACAACAAAGAAGAACAAG[T/A]GAGTGAAAAACTCTCTCTCCCCCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTTTGTGTGTGTGCGTATTCTGGTATATGTGGTTTACAATTGTACAGTGACATGAGTATGACCTTGTTATTGCACTTTTTAAAGTGGTTATTGAGGACATGCTCTGTGTCATCATAATTTAAAATGATGGTTGGGTTAAGGGTAAGTCCCTATAATAAGTGGTTTATACAGTATAAAATAGATTCATCCTAAAGGTCCTAATAATCTACATATTTGTGTGTGTCTGAAAAAAATCACTTATTAATTATGCTAAATATAATTGTTGTTATTTTGTTTGCTTTGTACTGTATGGATTTACAAGTGTTACTGTTACTGTACACCCTGAATGGTTAGTCACAAGTGTAACATTGTAGAAGGAGACTCGTTATTAGAGCAGTTTAACTT
Associated Phenotype:
Not determined