ZMP
si:ch211-283g2.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate asialoglycoprotein receptor 2 (ASGR2) [Source:UniProtKB/TrEMBL;A
Human Orthologues:
CLEC4A, CLEC4C, CLEC4D, CLEC4E, CLEC6A
Human Descriptions:
C-type lectin domain family 4, member A [Source:HGNC Symbol;Acc:13257]
C-type lectin domain family 4, member C [Source:HGNC Symbol;Acc:13258]
C-type lectin domain family 4, member D [Source:HGNC Symbol;Acc:14554]
C-type lectin domain family 4, member E [Source:HGNC Symbol;Acc:14555]
C-type lectin domain family 6, member A [Source:HGNC Symbol;Acc:14556]
C-type lectin domain family 4, member C [Source:HGNC Symbol;Acc:13258]
C-type lectin domain family 4, member D [Source:HGNC Symbol;Acc:14554]
C-type lectin domain family 4, member E [Source:HGNC Symbol;Acc:14555]
C-type lectin domain family 6, member A [Source:HGNC Symbol;Acc:14556]
Mouse Orthologues:
Clec4a1, Clec4a2, Clec4a3, Clec4a4, Clec4b1, Clec4b2, Clec4d, Clec4e, Clec4n
Mouse Descriptions:
C-type lectin domain family 4, member a1 Gene [Source:MGI Symbol;Acc:MGI:3036291]
C-type lectin domain family 4, member a2 Gene [Source:MGI Symbol;Acc:MGI:1349412]
C-type lectin domain family 4, member a3 Gene [Source:MGI Symbol;Acc:MGI:1920399]
C-type lectin domain family 4, member a4 Gene [Source:MGI Symbol;Acc:MGI:3624119]
C-type lectin domain family 4, member b1 Gene [Source:MGI Symbol;Acc:MGI:1917060]
C-type lectin domain family 4, member b2 Gene [Source:MGI Symbol;Acc:MGI:3588267]
C-type lectin domain family 4, member d Gene [Source:MGI Symbol;Acc:MGI:1298389]
C-type lectin domain family 4, member e Gene [Source:MGI Symbol;Acc:MGI:1861232]
C-type lectin domain family 4, member n Gene [Source:MGI Symbol;Acc:MGI:1861231]
C-type lectin domain family 4, member a2 Gene [Source:MGI Symbol;Acc:MGI:1349412]
C-type lectin domain family 4, member a3 Gene [Source:MGI Symbol;Acc:MGI:1920399]
C-type lectin domain family 4, member a4 Gene [Source:MGI Symbol;Acc:MGI:3624119]
C-type lectin domain family 4, member b1 Gene [Source:MGI Symbol;Acc:MGI:1917060]
C-type lectin domain family 4, member b2 Gene [Source:MGI Symbol;Acc:MGI:3588267]
C-type lectin domain family 4, member d Gene [Source:MGI Symbol;Acc:MGI:1298389]
C-type lectin domain family 4, member e Gene [Source:MGI Symbol;Acc:MGI:1861232]
C-type lectin domain family 4, member n Gene [Source:MGI Symbol;Acc:MGI:1861231]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6959 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa33522 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6959
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100085 | Missense | 44 | 131 | 1 | 3 |
ENSDART00000145912 | Essential Splice Site | 195 | 280 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 4244393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 3904062 |
GRCz11 | 5 | 4237097 |
KASP Assay ID:
554-5024.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAGGCGCATGGCTCTTAAAAATTGAAGATGACTCTGAGGATGAGTGGG[T/A]GCGTAATGAATGTACATAGACACATGGTTTTCCTTATCACAGGGCTCTAG
Long Flanking Sequence:
TCAAGAACGCATGATTATATGCTCTTATGGCTTTGCAATCAATAAATGTGATTATAAATGGAAGTCAGTGGGGCAAAAACAGCCACCAACATAACCAAAGGGTAGTACTCAGTGTATTGTTGACTTTTTAAAAAAAATTCCAAAGCATTTTCCCAAATTATGTGTCAAAACAAGATTTGTCAGCAAAGATCATCCCATTTGCTGAGACTCAAAATCACATCAGCTTGGATGAAAACATCCCCAACAGCACATGAGGGTTAATTCGATTTTTTTTCATCTGACATAAATGCATTGAACAAAAGCATAAAAACATTCTGCATTCTTTCTCTCCTATGCAGAAGAACTTGAATCAGGCTGCAGTGATTCTGCTTGGGTTCCTTTCGGCAACAGCTGTTACCTCTTCTCTCGTGATAAAATGAACTGGACAGAAGCAAAAGATTACTGCGAAGAGAAAGGCGCATGGCTCTTAAAAATTGAAGATGACTCTGAGGATGAGTGGG[T/A]GCGTAATGAATGTACATAGACACATGGTTTTCCTTATCACAGGGCTCTAGATTAGAACTGCCCAACATCCAGCAAGATAGATGTTTAAAAATGTTGAGATTATTGACATAAACACAAAAGATTATTGCCACTCACCCGTATAGAGGTGCTGACAAAAAAACACAATAGAAGTCAGACTGACAGCCAGTTCTGTACAACAGGCAATTGTGTTATATTCAAATTCATTCATATATGTTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATACAGTTCTCATCATAATTGAGTACAGCCCATTTTGAAAATAAATATCTGTATCTATTTCTCAGTGAATATAGGTAATGCATTTTGGTGCATTTAAACATTCATTCATTCATTTTCTTTTCGGCTTAGTCCCCCATTATTAATTAGGGGTCGCCACAGCGGAATGAACCGTCAACTTATCCAGCATATGTTTTACGCAGCGGATGCCCTTCCAGCTGCAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33522
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100085 | Essential Splice Site | 47 | 131 | 2 | 3 |
ENSDART00000145912 | Essential Splice Site | 196 | 280 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 4243170)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 3902839 |
GRCz11 | 5 | 4235874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTATGTGCCCATTCTGTCTTTAAGTGAGCCTTTGGTCTCTTTTACTA[G/T]CAATTTGTAACTGATTTTGCCAATCCAACTCATTACTGGATCGGCTTAAC
Long Flanking Sequence:
CTTTACCACGGGGAGCTCCCATCTGATCTCGTACTCCCCTTACATGCTCAATTGACTAGGCGGGAGCCCGGGCTCAATTATTTCCGAACTCAGGGCTCTCTCCCGAGACAGCATGCCAACATGGCTAATAGCGTCATGCAATATCTAAGTGTAAACTCTTGAAGGACAATTTAGCCTACCCGATTACCTAACTAAAACTTTCAATTCTTTGTTTCTCTTGATTTTTCCTCTTTTTAAATTTTTTTATTTAATATTTTTCTATAACAAATCAATTTGGCTGTGCTAGTTTTTGAATCGTTATTGTGAGTTATTTTGTTAGACAAGCTCCATTTGGCTTTAGTACTGACTAATCTAATGTATATGTACAAATATACTATTGTACAGCTTCCTATTAAAAATATGAATTTAAAAGAGTTTCGTATGGGGTGTACTTATATGAGCACTGTATATACAGTATGTGCCCATTCTGTCTTTAAGTGAGCCTTTGGTCTCTTTTACTA[G/T]CAATTTGTAACTGATTTTGCCAATCCAACTCATTACTGGATCGGCTTAACGGATCAGAACACAGGCCAGTGGAGATGGGCAGATGGAACTAATTACACCATGAACAAAGAGTGAGATGAACACACAAATATACAGAACACTTTTTACTAAGTCTGATTTAAGAGAATTCACATTTATAACCAGACATATTTTATTGTTGCAGACACTGGGGACCTGGACAGCCGGATGAGTGGACTGAGCATAGCTTGGGAGAGGAAGGAGAGGACTGTGCGGAAATTACATATGAATCTCTGCTCAATGACCTGCACTGCTCCTCCAAAATAAAGTTCATTTGTGAAATGAAAACATAGGACTGAGAATGGAAACACTTGAGTGTGGTCAAAACTCTAAATATGGAATTTTAAATAAACAACTTTTGAGTATTGAGAATTTGTAAAAGGACATTTTGTTAAAATTGTTATATTGGTTTAAGCTTGTAAATTTAAATGAATCATTTATCA
Associated Phenotype:
Not determined