ZMP

zgc:101049

Ensembl ID:

ENSDARG00000071051

ZFIN ID:

ZDB-GENE-040808-26

Description:

chromobox 6 [Source:RefSeq peptide;Acc:NP_001003768]

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]

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]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa45775	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45775

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104812	Nonsense	156	411	5	6
ENSDART00000147480	Nonsense	156	462	5	5

Genomic Location (Zv9):

Chromosome 22 (position 31651793)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	29130871
GRCz11	22	29080066

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCTGCTCATAAATTGAAGAAAGACATACATCGTTGTCACATGATGTCT[C/T]GACGACCTTTGCCACGATCTGACCCTCTGGCCAACTCCACAGGATCCTCG

Long Flanking Sequence:

CATTTGCATTGTTATGGTTTAGACTTGACACCAAAGTGATGTCATATTTTCCCTGGCTTAAATGGTGCTGTTATACAATTCATAGGGAGAGGGAGCAGGAACTTTACGGCCCAAAGAAACGTGGACCCAAACCAAAAAACTTTGTACTAAAGGTTTGAGAACTTCTTTGAATTTCTTTTTTTAATACAATTTTTTTTTTTTGTTTGTTTTGATTGATCTTCTCAAAACTTTCTATTTCAAAGTTAATCTCTTTCACTTACCTTTGTTTTCTGCCTGTCTAGGCACGGGCTCAGTCGGGTGATCGACCTCGGAGCTCATATACTCGACGCACTCCATCTTGCACCACTGCAAAGCCTCCCACCGCTTCCTCCTCTGCAAGTTCAGCTACTCCTCAGCCTTCATCATCCTCTTCCCACTCTACCGCTCCAACCCCTAGAGTGCATTCTCTCGCAGCTGCTCATAAATTGAAGAAAGACATACATCGTTGTCACATGATGTCT[C/T]GACGACCTTTGCCACGATCTGACCCTCTGGCCAACTCCACAGGATCCTCGTCTCGTCACCCCATTTCTCCATTTTCTGAAACTGTCCGCATTCTTAACCGCAGGGTCAAACCACGGGAGGTTAAACGAGGGCGCATAATCTTGAACCTAAAGGTCATTGACAAATCTGAAAATGGTGGAATGACCAGTAGAAGGACACCACAGTCATTTGCAGGGAGGGCGAAAATCCCATCCCGAAATCGAATCATTGGGAAAAAGCATGGGGACATGCCTTACAGGCCGTTCCAGCATCCTATGAAGATGTTAGGTATTCCGATGTATGGCCAACCTTTTGGGCTTAACCCCTCTGGAGGGGCATCCTCTATGGCCAATGAAGGGTCCAACACTAGAGCCAGTCATGGAGGTGGAAGCAGGTGTGGTAGTCAATCTTCTGCGCAGAGGTTTCAGTACCAGCCTACTCCTTCTCCATCCAACTCCAGTGGGTCTAATGGCAGCTCCCCA

Associated Phenotype:

Not determined