ZMP

cubn

Ensembl ID:

ENSDARG00000087013

ZFIN ID:

ZDB-GENE-060228-6

Description:

Cubn protein [Source:UniProtKB/TrEMBL;Acc:B0JZN9]

Human Orthologue:

CDCP2

Human Description:

CUB domain containing protein 2 [Source:HGNC Symbol;Acc:27297]

Mouse Orthologue:

Cdcp2

Mouse Description:

CUB domain containing protein 2 Gene [Source:MGI Symbol;Acc:MGI:3045328]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37922	Nonsense	Available for shipment	Available now
sa45836	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa25216	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37922

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124198	Nonsense	135	420	3	8

Genomic Location (Zv9):

Chromosome 24 (position 33279953)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	32159854
GRCz11	24	32074497

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCTGTTGGGGAAACACTGTGGAAACAACCTTCCGGCTCCCATGGATACT[G/T]GAGACAGTTTTGCCTATGTAAAGTTTGTCAGTGATGCTAGCGCGAATGCT

Long Flanking Sequence:

CTGGCACCACCATGTATTTACGATTCCGAACTGATGCTAGTGTCACACATATTGGTTTCAAAGCCAAGTACTCCATTGGTAATCCATTTTGAATCCCACTGACATTCCAATCATTTTTTTTCCAAGCTTCAATGACTAAAAAGGTATTTTGTCCTCCTTAGCTGTATGTGGTGGTACCTACATCGGTCAAAATGGTGTCATCAGAAGCCCTGGTTTTCCTGGCTCAAATTATCCTGACAACTCTAACTGTGAATGGTACCTAGAAGGTCCTACTGGACACTATTTAACTCTCACCTACACTGCCTTCGACTTGCAGAGCTCCGCTAATTGCAACAGTGACTACGTTGAGATACGTGAATACAATGCTTCAGGTTTGGAATCTCCCAACTCAAATCTAGTCTCCTTTTAAATACCCAAGGTAGTAATGTAAGATCTTCTTCTCACCAGGTCGCCTGTTGGGGAAACACTGTGGAAACAACCTTCCGGCTCCCATGGATACT[G/T]GAGACAGTTTTGCCTATGTAAAGTTTGTCAGTGATGCTAGCGCGAATGCTGGAGGGTTTAGCTTATCATTTGAAGCCAGCATTGAAGGCAAGTGTGAAATCCATAAACAAAAACAATCACATAAGCATCACAATTCATTAATAAATATTGGACTCAGTGTTCAAGGTTTCTGTGTCTGACCATTTTTAGGATAACGAATAGGAGACTTTATCTGGTAATAAAAACAAATGGTTTGTCTTGTAGAATGTGGAGGGGATCTGAATGCACCATTCGGGACCATATCATCTCCCAACTACCCCAACCTCTACCCACACAGCCGAATTTGTCGCTGGAGTATCACTGTTCCTCAAGGTCGTAGGGTCACTCTTACAATCAATGACTTGAGGCTGGAGGACCAAAGTACCTGCGCATTTGACTTTGTTGAGGTGAGGTTATCTGTATGTTTTAAAGGGGGTCATCCTGTTAAATACTTTCTGTGGGCATTTTTTAATTCAGAGGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45836

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124198	Essential Splice Site	224	420	4	8

Genomic Location (Zv9):

Chromosome 24 (position 33279527)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	32159428
GRCz11	24	32074071

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGACTTGAGGCTGGAGGACCAAAGTACCTGCGCATTTGACTTTGTTGAG[G/A]TGAGGTTATCTGTATGTTTTAAAGGGGGTCATCCTGTTAAATACTTTCTG

Long Flanking Sequence:

GTAAGATCTTCTTCTCACCAGGTCGCCTGTTGGGGAAACACTGTGGAAACAACCTTCCGGCTCCCATGGATACTGGAGACAGTTTTGCCTATGTAAAGTTTGTCAGTGATGCTAGCGCGAATGCTGGAGGGTTTAGCTTATCATTTGAAGCCAGCATTGAAGGCAAGTGTGAAATCCATAAACAAAAACAATCACATAAGCATCACAATTCATTAATAAATATTGGACTCAGTGTTCAAGGTTTCTGTGTCTGACCATTTTTAGGATAACGAATAGGAGACTTTATCTGGTAATAAAAACAAATGGTTTGTCTTGTAGAATGTGGAGGGGATCTGAATGCACCATTCGGGACCATATCATCTCCCAACTACCCCAACCTCTACCCACACAGCCGAATTTGTCGCTGGAGTATCACTGTTCCTCAAGGTCGTAGGGTCACTCTTACAATCAATGACTTGAGGCTGGAGGACCAAAGTACCTGCGCATTTGACTTTGTTGAG[G/A]TGAGGTTATCTGTATGTTTTAAAGGGGGTCATCCTGTTAAATACTTTCTGTGGGCATTTTTTAATTCAGAGGTTCAGCACAGCCATTTTGGCTCTTGAATTGGTAGATCCTGAATGGTCTGACTCCCAGTGCCCCTCGATTGGATCGTTTATGTGGTACAGTCCCTGCTGGAACCCAGGTCAAGTCTTCAGGGAATACTATGACAGTCATTTTCAGCACAGATTCATCTGTGTCTAATGGTGGATTCACAGCAGACTATTCATCAGAGGAGTCAGCAGGTAGGAAAGAAGAACTTTGGCTTTAAAGTAAACACTTTTGGGGGTCCTGATTTAATTCTTGAGTCTTTGCAGTTTGTGGTGGGATTCTCAATGAACCTGGAAACTTCACCTCACCCGACTTTGGCAATGGCAACTACAGCAACAACCTGAACTGTGAATGGCTGATCCAGAACCCACATCACACAAATTCCTCCATTGTGGTTATTATAGATGAGCTGCATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25216

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124198	Essential Splice Site	224	420	4	8

Genomic Location (Zv9):

Chromosome 24 (position 33279526)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	32159427
GRCz11	24	32074070

KASP Assay ID:

554-7676.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGACTTGAGGCTGGAGGACCAAAGTACCTGCGCATTTGACTTTGTTGAGG[T/C]GAGGTTATCTGTATGTTTTAAAGGGGGTCATCCTGTTAAATACTTTCTGT

Long Flanking Sequence:

TAAGATCTTCTTCTCACCAGGTCGCCTGTTGGGGAAACACTGTGGAAACAACCTTCCGGCTCCCATGGATACTGGAGACAGTTTTGCCTATGTAAAGTTTGTCAGTGATGCTAGCGCGAATGCTGGAGGGTTTAGCTTATCATTTGAAGCCAGCATTGAAGGCAAGTGTGAAATCCATAAACAAAAACAATCACATAAGCATCACAATTCATTAATAAATATTGGACTCAGTGTTCAAGGTTTCTGTGTCTGACCATTTTTAGGATAACGAATAGGAGACTTTATCTGGTAATAAAAACAAATGGTTTGTCTTGTAGAATGTGGAGGGGATCTGAATGCACCATTCGGGACCATATCATCTCCCAACTACCCCAACCTCTACCCACACAGCCGAATTTGTCGCTGGAGTATCACTGTTCCTCAAGGTCGTAGGGTCACTCTTACAATCAATGACTTGAGGCTGGAGGACCAAAGTACCTGCGCATTTGACTTTGTTGAGG[T/C]GAGGTTATCTGTATGTTTTAAAGGGGGTCATCCTGTTAAATACTTTCTGTGGGCATTTTTTAATTCAGAGGTTCAGCACAGCCATTTTGGCTCTTGAATTGGTAGATCCTGAATGGTCTGACTCCCAGTGCCCCTCGATTGGATCGTTTATGTGGTACAGTCCCTGCTGGAACCCAGGTCAAGTCTTCAGGGAATACTATGACAGTCATTTTCAGCACAGATTCATCTGTGTCTAATGGTGGATTCACAGCAGACTATTCATCAGAGGAGTCAGCAGGTAGGAAAGAAGAACTTTGGCTTTAAAGTAAACACTTTTGGGGGTCCTGATTTAATTCTTGAGTCTTTGCAGTTTGTGGTGGGATTCTCAATGAACCTGGAAACTTCACCTCACCCGACTTTGGCAATGGCAACTACAGCAACAACCTGAACTGTGAATGGCTGATCCAGAACCCACATCACACAAATTCCTCCATTGTGGTTATTATAGATGAGCTGCATCT

Associated Phenotype:

Not determined