ZMP

A2AVI5_DANRE

Ensembl ID:

ENSDARG00000063451

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:A2AVI5]

Human Orthologue:

CCDC13

Human Description:

coiled-coil domain containing 13 [Source:HGNC Symbol;Acc:26358]

Mouse Orthologue:

Ccdc13

Mouse Description:

coiled-coil domain containing 13 Gene [Source:MGI Symbol;Acc:MGI:1920144]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25097	Nonsense	Mutation detected in F1 DNA	Not yet available
sa1826	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa25097

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
ENSDART00000092763	Nonsense	262	666	6	14

Genomic Location (Zv9):

Chromosome 2 (position 1995705)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	1850791
GRCz11	2	2193597

KASP Assay ID:

554-7771.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATTCAGCAGATTCTGTGTAACCCAGGAGGCTGGAGAGGGCGATCGCAG[C/T]AGATCCTCGCCCTGCAGAACCGAGTGAGTGTCCGCTGAGTGTTCAGCTTT

Long Flanking Sequence:

AAAACACTATGAAAAAGTGAAAACCTCAGGTACTCGGACTCTGATTGGCTGTTGTCATTTTTCTCGCTCATCTCGACTCCACCCATTAGTGTTTATTTTCAGCTCTGGGTTCAGCTTTGTGTCGCTCCAGCCAACAGCAGAGCAGCAGCTACTGGGGAGGCGGAGATAAAGATAGCAAGGCCCCATCTGATTGGTCAAATTTAGATTTTTGATTTTAAATTTAAATTTTAACAACCAATGCATAAAGTAAATATAATGTATCGCACGTCTGCAATATTTTGCATATACTATTATCGTGATAACAATAATATTGCGATATATTGTGCAGCCTTAATTTGTTCTCAACAGATCTTTTCATGTGTTATTGAGCTGTATAGTATATAGTGCTATAGTAGGCATCATTTTAACGTGTTTTCCAGGTGTTGAGCTGCGAGGTCGGTGAGGACGTCAGTATTCAGCAGATTCTGTGTAACCCAGGAGGCTGGAGAGGGCGATCGCAG[C/T]AGATCCTCGCCCTGCAGAACCGAGTGAGTGTCCGCTGAGTGTTCAGCTTTAGTTAACTAGTGTGCTTTTTCATTATTTTAAATGACTGTTCACATTTTCCCCAAAAAATAAGAAAAGATGTTTTAAAAGCACATCTTTTTCCTCTTGCTTTTGAACATGCTTTATAGCAACACAATCAGGAAAATGTTCCCAGGGATACAATTCTAAGAACCGAGAAATATGGGCTGCATTTCGTGTGTAAACCGAACAGGGCTACCGGGTAGTTCCGCTCACTGTTTACCTCTGTATGGGCGATGTTTCCTGTATGACTGGTTTGCTTGGTAGCTCAACACAAATTAAGGACAGTTCCAAAAACCAGGTAAAACAAAACCCAAAACAAAGAGCAGTGTGATAGAAGCAAGCGTCCACCATAGCTTTTCTCTTCCCAACTGAAAAATCCAGCTTGAAGCCTAGGCTGGTGGGCTGGTTTTAGCTGGTCGACCAGGCTGGTTTTAGAGGGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1826

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092763	Nonsense	495	666	11	14

Genomic Location (Zv9):

Chromosome 2 (position 2004488)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	1859574
GRCz11	2	2202380

KASP Assay ID:

554-1818.1 (used for ordering genotyping assays)

KASP Sequence:

TTTCAGAGATGCACWAGTGGCCTGTCCAGAGTGWGCTGTTAAAGTCCCCT[C/A]GCTCCAGGCGCAGTGTGCAGAGTATAAAACCCTTTACCAAAGCGCAAGTG

Long Flanking Sequence:

TCTGCAGTTCAACAAGCACTTCAACAAGCCTGCTTTTTCCTGCTTGGCAAGCCAAGCTGATGTGACATGGGGGCGTGGCAGCATCGACCATTCTATTTTTTGATTCGATAATCGAAATTGAGCATAAATTTCTATCGATTTCCATTAAAAATCGAAATCGTGACACCCCTAGTTAAAATCAAATACAGAATTACAATATGTAACTCAAAATCCAGAGAACAAATATATGAATTGTGATATACATCTGACATAAATATAAGTTTATAACTCGCAATACTGAGAAATAAAGTCTCAGAAAAGTTGAACTGTGTAAGAAAAAAAAAGTTTTTAATTACCCCATTTTTACTTCCCTGGAAAAAGCAAGCTTCCACACTGCACTGAATTTCAGACACAGCCTGCATTATGCCCTGCTGTCTAATACAGCAACATGAGTGAAAGAGTTGCATATTATTTCAGAGATGCACTAGTGGCCTGTCCAGAGTGTGCTGTTAAAGTCCCCT[C/A]GCTCCAGGCGCAGTGTGCAGAGTATAAAACCCTTTACCAAAGCGCAAGTGTGGAGAGAGACAGACTGCTGGAGCTGACCAAAGTGCAGCACGCCAGGTAGGAGACAATTAATAATCCCTCTCTACACAACATCTTCATCTGTGTTCTATCATTTATAAAGGCATTGAACAATCCTTTAAGTTGTATATTCTCCCTTGTAATTTTGTTCAAATTCACCATTACATTTGATTGGATTATTCATATCACAATCATGAATTTAGAGCAAGTAATGAAGCAGACTGATTTAAATGATATAAAGGGGACCTATTATGCAAAAAACACTTTTATAAGGGGTTTACACACAGTTGTGTGTCAGCAGTGTGTGAATATAAGCAACCTCTAATGGTAAAAATTTGTTAATTCTATTGTTTATAATCATACTTGATTAAAACAGTCTGCAGAAACACTTTGATTGACATTCTCCCTTTGTATGATGTCATCAGAGGGGGAAAGTCCCGCCC

Associated Phenotype:

Not determined