ZMP
si:ch211-234p6.14
Ensembl ID:
ZFIN ID:
Description:
Novel pentaxin family domain containing protein [Source:UniProtKB/TrEMBL;Acc:A3KPG7]
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 are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15702 | Nonsense | Available for shipment | Available now |
sa3267 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15702
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105662 | Nonsense | 74 | 225 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 24 (position 39576695)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38185784 |
GRCz11 | 24 | 38073681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGGCCACAGAGCTCCARGGMGAGCGGCAGATCATCCTGTTYGCCTAC[C/T]GAACAYCCGACTTTGATGAACTGAAYTTGTGGAGRGAGAAAGAMGGCCGT
Long Flanking Sequence:
ACAACGACAGACATTCTGACGTGGAAAGCACATTTTCAAAGGAGAATAACTTAACATTGTTAATCGGATAAACAAGCATGTTTACTTCACGTGTTTCTGAAATATCTGCAAACATGTTATGGTATTTTAATAATTAAGAAGAGTCAAAAACTTACAGCACCTGTCGATTTGATGACTTGTCTAGTTTTGGACTTTTGTTAGTTTGATGTCATTCACACACACACACACACACACACACACCCACACGCATGCACACACACACACACACGCACACACAAACACACACACACACACACACACACACATGCTTGTTTGGTGTTTATCAGTCGTTTTGTCTTGCAGTGGGTCTTGCTGGTAAAGTTCTTCTGTTCCCGTACGAGACAGACTTCAGCTACGTCAAACTCACTCCTAAGAAGCCTCTGGGTCTTTCAGCGTTTACTCTCTGCATGCGTGTGGCCACAGAGCTCCAGGGCGAGCGGCAGATCATCCTGTTCGCCTAC[C/T]GAACACCCGACTTTGATGAACTGAATTTGTGGAGGGAGAAAGACGGCCGTGTGTCTTTCTACCTCAGCGGTGATGGGGCGTTTTTCAACCTGCCGCCTCTGTCCACCTTCCGGACGCACCTGTGCCTGTCCTGGAGCTCTCGCACCGGGCTCGCTGCCTTCTGGGTGGACGGACGCCGCAGTGCGTTTCAGCTTTATAAACCGGGCCACAGCATCCGCCCGCAGGGCACTGCTCTGCTTGGACAGGACCCTGATAAACTCCTGGGCGACTTCGAGACGGTGCAGAGTTTCGCCGGTGAACTCACAGACCTGAACATGTGGGATTATGTGCTCACCGGGAACCAGATTAAAGCGCTGTATTTCAACCATGCGCAGCGCGTGCCCAAGGCAAACGTGTTTGAGTGGAGCTCCATCGAGTATGAGATTAAGGGGAATGTGCTTGTCACGCAAGACGATTGATAATATTCAGTATGATACTACACGTATAACATTTACAGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3267
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105662 | Nonsense | 159 | 225 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 24 (position 39576440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38185529 |
GRCz11 | 24 | 38073426 |
KASP Assay ID:
554-3037.1 (used for ordering genotyping assays)
KASP Sequence:
GCCACAGCATCCGCCCGCAGGGCACTGCTCTGCTYGGACAGGACCCTGAT[A/T]AACTCCTGGGCGACTTCGAGACGGTGCAGAGTTTCGCCGGTGAACTCACA
Long Flanking Sequence:
CACACACACACACGCACACACAAACACACACACACACACACACACACACATGCTTGTTTGGTGTTTATCAGTCGTTTTGTCTTGCAGTGGGTCTTGCTGGTAAAGTTCTTCTGTTCCCGTACGAGACAGACTTCAGCTACGTCAAACTCACTCCTAAGAAGCCTCTGGGTCTTTCAGCGTTTACTCTCTGCATGCGTGTGGCCACAGAGCTCCAGGGCGAGCGGCAGATCATCCTGTTCGCCTACCGAACACCCGACTTTGATGAACTGAATTTGTGGAGGGAGAAAGACGGCCGTGTGTCTTTCTACCTCAGCGGTGATGGGGCGTTTTTCAACCTGCCGCCTCTGTCCACCTTCCGGACGCACCTGTGCCTGTCCTGGAGCTCTCGCACCGGGCTCGCTGCCTTCTGGGTGGACGGACGCCGCAGTGCGTTTCAGCTTTATAAACCGGGCCACAGCATCCGCCCGCAGGGCACTGCTCTGCTTGGACAGGACCCTGAT[A/T]AACTCCTGGGCGACTTCGAGACGGTGCAGAGTTTCGCCGGTGAACTCACAGACCTGAACATGTGGGATTATGTGCTCACCGGGAACCAGATTAAAGCGCTGTATTTCAACCATGCGCAGCGCGTGCCCAAGGCAAACGTGTTTGAGTGGAGCTCCATCGAGTATGAGATTAAGGGGAATGTGCTTGTCACGCAAGACGATTGATAATATTCAGTATGATACTACACGTATAACATTTACAGTTATTTTCTGCATAACACGTACTTTATAGTTCACCACTGTAATATGCACTGCATTGTGGGTCATTTTAAAACTTTTACAGTAACTTACTGCATATTAGGAACTTGCAGTATTCTACTGTAATGAAAATAATCTAAAAATAATAAGTACTGCGACTGTAGTTGAAGACTAAAATGAAAAGGTTGATTAAAATGTACTAAATTTAATAGTAAATACTAAGGGTGCTTTCACACCTACACTTTTGTTTCGGAACCTGTCTCG
Associated Phenotype:
Not determined