ZMP

si:dkeyp-20e4.1

Ensembl ID:

ENSDARG00000053375

ZFIN ID:

ZDB-GENE-050208-595

Description:

neuronal pentraxin receptor [Source:RefSeq peptide;Acc:NP_001037779]

Human Orthologues:

CBX6, NPTXR

Human Descriptions:

chromobox homolog 6 [Source:HGNC Symbol;Acc:1556]
neuronal pentraxin receptor [Source:HGNC Symbol;Acc:7954]

Mouse Orthologues:

Cbx6, Npcd, Nptxr

Mouse Descriptions:

chromobox homolog 6 Gene [Source:MGI Symbol;Acc:MGI:3512628]
neuronal pentraxin chromo domain Gene [Source:MGI Symbol;Acc:MGI:3845555]
neuronal pentraxin receptor Gene [Source:MGI Symbol;Acc:MGI:1920590]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43856	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43856

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:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124220	Nonsense	320	527	3	5

Genomic Location (Zv9):

Chromosome 22 (position 25501323)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	25001229
GRCz11	22	25028853

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTACTGTTTGCTTTCCAGGTCTTACAGATTACAGTTATCCACAAGGGTA[T/G]AAACTTTCCTTCCCTGTGAGGACAAACTACATGTACGGGCTTGTCAGGCG

Long Flanking Sequence:

CATGTATTTACAACTAGCCTAGGCTGATTAAATTTGATTCAAGAAAAAATCACTCTTTCGAAGTCCTATAATGCAAATTAATATAGTCAACAGGATGGATTAGGTTTGTTATAATGACTTATTGCATCATTCCCTCTCAGATGGAAATAGGCCCTGCAGCGATAAACCACACTGAACATACTGTGAGCACACTGGGGAGCATAGTGGTGGGCGAGCCAGGCAGGCCTGTGGAGGATCTGGAGGGAGAGCTGGAAAAGAAGATTCGGCTGCTGGAGAAGGAGAGGAAGAACCTCCGCAAAGAGACCCAGAGCCACCACCAGCATATTGACCAGGGAATCAACACCCTGCAGGAGCGTATTGCAGAGCTGGAACAAAGTAAAGAGAAATGCTGTGTCAAACTCAAGGAAGTTACAGTGTATAAAAAATAAGTCTCTTCATTTTCAACTCTCCCTTACTGTTTGCTTTCCAGGTCTTACAGATTACAGTTATCCACAAGGGTA[T/G]AAACTTTCCTTCCCTGTGAGGACAAACTACATGTACGGGCTTGTCAGGCGGAATATTCCAGAAATGTATGCCTTCACAGCGTGTCTGTGGCTTAAGCCTGCTGAGAGTGGAATTGGTACACCATTCTCTTATGCTGTACCAGAACAACCCAATCAACTCGTGCTGTTGCAGGGCATTCATAATCCTGCAGAACTACTCATCAATGATAAGGTAAGACCCACTACACCTTCAGTCTGCAGCTACCTTGCAAAAAACAGTTGATGGGTTTAACAATTCCCTCCATTTTCAGGTGGCACAGTTGCCTCTATCTTTGCCAAAAGGCATCTGGCAGCACATATGTGTGAGCTGGACTCTACGGGATGGAGTTTGGAAAGCATATCAAGGTGGAAAGATGAGAGGACGGGGTGACGGTTTGTCTGCATGGCACCCGATCAAATCTGGGGGCGTCTTGGTGTTGGGACAGGAACAGGTACGACGCAGAAACCTAAAAGTTTGAATAC

Associated Phenotype:

Not determined