ZMP
si:ch211-234p6.7
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC100124600 [Source:RefSeq peptide;Acc:NP_001096097]
Human Orthologues:
APCS, CRP
Human Descriptions:
C-reactive protein, pentraxin-related [Source:HGNC Symbol;Acc:2367]
amyloid P component, serum [Source:HGNC Symbol;Acc:584]
amyloid P component, serum [Source:HGNC Symbol;Acc:584]
Mouse Orthologues:
1810030J14Rik, Apcs, Crp, Gm11062
Mouse Descriptions:
C-reactive protein, pentraxin-related Gene [Source:MGI Symbol;Acc:MGI:88512]
RIKEN cDNA 1810030J14 gene Gene [Source:MGI Symbol;Acc:MGI:1913539]
predicted gene 11062 Gene [Source:MGI Symbol;Acc:MGI:3779286]
serum amyloid P-component Gene [Source:MGI Symbol;Acc:MGI:98229]
RIKEN cDNA 1810030J14 gene Gene [Source:MGI Symbol;Acc:MGI:1913539]
predicted gene 11062 Gene [Source:MGI Symbol;Acc:MGI:3779286]
serum amyloid P-component Gene [Source:MGI Symbol;Acc:MGI:98229]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|
Mutation Details
This allele has been removed from public view.
Allele Name:
sa6780
Status:
Less stringent filtering
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:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109975 | Nonsense | 35 | 225 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 39641094)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38250183 |
GRCz11 | 24 | 38138080 |
KASP Assay ID:
554-4539.1 (used for ordering genotyping assays)
KASP Sequence:
GGTCTTGGTGGAAAAGTTCTTCTGTTTCCAAYCSAAASTGCTACCAGCTA[T/A]GTTAAACTGACTCCTGATAAACYCCTGARTCTGTCAGCRTTTACTCTCTG
Long Flanking Sequence:
ATGTATTAAAATATCTGTTAGGTGTTTAACACTTGGATCCGCCTATTCTGCCTATAAATAATAGACAGACATCAGGCTAAGAGCATCTTGGAGACTAACAAGTGATCATCTGTCTGACAACAGTTGTTGAACATTAAATTTGGTAAATATTATTTACAGTATTGTGAAGACTTTGTGTATTAGTCTCTGAAAACTGTTTGTTATAAGCAGATGTCTTTAAAGCTGAAAGTTAAAGCAGTGAAGAATGTTTTCTATGGGTATTTTTGCATTATTTTCTTTCAGACCTGCAGCAAAAGATGTTGGGCTTTATTTTCACTCTGCTCATTCTGACACCAGCAGCTGCTGAAGGTAAAACTCTTAAATCAACAGAGCACACAGTTAGCTTTAATGCAGAATTTAGCTTGTTTGCTTCATTATTTTTAATGCATATTTTAATTTTCTCTCACAGTGGGTCTTGGTGGAAAAGTTCTTCTGTTTCCAACCCAAAGTGCTACCAGCTA[T/A]GTTAAACTGACTCCTGATAAACTCCTGAGTCTGTCAGCGTTTACTCTCTGCATGCGTGTGGCGACCGAGCTCCAGGGCGGGCGGGAAGTCATTCTGTTCGCCTACCGCACTTCTGAAGTTGATGAACTCAATGTGTGGAGAGAGAACGATGGCCGTTTGTCCATGTATATTCAGTCTAGTAGCGATGCAGCACGTTTCTATCTTCCCCCTCTCTCCACATTTCAGACACATCTGTGTGTGTCCTGGGAGTCTGCAACTGGTCTTACTGCTTTTTGGGTGGACGGGCGTCGCAGTTTGTACCAGATCTATAAGAAAGACGCCTCTGTCAGACCTGGCGGCACCGTACTGCTCGGACAGGACCCTGATTCATATGTAGGTTCGTTTGACGCAAATCAGTGCTTTATTGGTGAAATTACAGATGTGAAACTGTGGGATTATGTTCTGTCTGAGATCCAGATTAAGGCTTTGTATTCAAACCAGGATCCGTTGGTGCCAGCGGG
Associated Phenotype:
Not determined