ZMP

zgc:77228

Ensembl ID:

ENSDARG00000026762

ZFIN ID:

ZDB-GENE-040426-1806

Description:

Hyccin [Source:UniProtKB/Swiss-Prot;Acc:Q6P121]

Human Orthologue:

FAM126A

Human Description:

family with sequence similarity 126, member A [Source:HGNC Symbol;Acc:24587]

Mouse Orthologue:

Fam126a

Mouse Description:

family with sequence similarity 126, member A Gene [Source:MGI Symbol;Acc:MGI:2149839]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15394	Essential Splice Site	Available for shipment	Available now
sa8406	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15394

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
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Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000033132	Essential Splice Site	111	518	4	11

Genomic Location (Zv9):

Chromosome 19 (position 3062743)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	2708721
GRCz11	19	2639605

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCACTGCAGCGGCTGCATAGAGGCGCTACTTCTCGGCATCTACAACCTGG[T/C]CAGTGCCTCTYYACATTACATTAGACATGGGCTGGTATAAYATTCACATA

Long Flanking Sequence:

TAAATTAAATCTTCTTTTTTCTATTAATACCTTTTAAAATATTTCCATGTGCTGTTTAATGGCGAGATTATACATTATAGTTTTAAAAACTAATTTCTAGCAGCTAATTTCTTTTGTCTATGCAATAATGGCATAGTATTCAGCTTAAAATGTCATTTAAAGGCTTAACTAGGTTAATTAGGCAAGTCATTGGACAACAGTGGTTTGTTCTGTAGTGAATCGAGGAAAAAATCTTAAGGGGGCTAATAATATTGACCTTAAAAATATGCTTTGAATCTAAACCAAGAGTAATCATGATTGAATGATGATTGTGTTTCAGCTTCTGGAGCCGGTGTGTCATCAGCTGTTTGAGTTTTACCGCAGCGGTGAGCCTCGTCTCCAGCGCTTCACCCTGCAGTTTCTGCCAGAGCTGGTGTGGAGTTATCTGTCTGTGACGGCGGCTCGTGATCCGCACTGCAGCGGCTGCATAGAGGCGCTACTTCTCGGCATCTACAACCTGG[T/C]CAGTGCCTCTTCACATTACATTAGACATGGGCTGGTATAACATTCACATATTGAAAACTATTGAAAAAGACACAGCCATCTGAATAGAAAAGTCTCTCAGCGAGCATCTTCTGTGAGCTTTAGCTGAAGCCGGAAACAGAGATGGGAAAGCCGGCTGTCTGCTCCGCCGATGGTCTTTCAAGGGTTTTTACGCCCCGCAAACTCGCTCTCGCTCCCGAATATCAGAGTAGGTCATCTGTCAGTCGCATGTCATCGTGGTGTCAGCGAGCGTTTGATCATCCTGCCGTTATCGGCTCTGAATCCACCGCAGGCTGATGGAGGACAGCAGGCTGGTGGGCGAATGCTACACAAACACACACACACACACACACACACTTGAATCTCACTTCATCTGCTGTGTTTTTACACCTGAAAAACTCCTGAGTCGTCTTCAGCCAGAACAGCTTCATCGTCCCTCAGCTGAAAGAGTTCAACTTTATACTAACTCAGCTGCATTTTCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8406

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000033132	Nonsense	413	518	11	11

Genomic Location (Zv9):

Chromosome 19 (position 3086787)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	2732765
GRCz11	19	2663649

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGAAGGATAARGAGAAGGACGCGGCCACCGGCATGGACCAGYTAACCCGC[A/T]AACAAGCAGCCGTCCGCGCCATGAGTGAAAACCTAGAGCTGCTGTCACTC

Long Flanking Sequence:

CGACATACAACTCTGTTCGCATACTGTTTTTTGAATACTATGAATTTCCACATACTACTTGGTTTGCATTCTGTTTTTCCCAATAATATGAATTTCCACATACTACTCGGCTCGCATACTGTTTTAATCGTACTATATGGTATGGAAGTATACTATTGCGGTCCGCCAGGTTCATGGTTGAGAAACACTAGTCTAAGAGGAGTAGTTTTACCTCTCAGATCTTAGAATAAATGTGCGCTCTTCTCTCTCCTGCAGATGCAGTGGATTTGGGTTCCCCGGATGAGCTGACGGAGATCGCGGAGGTTGATGAGGGCATCTGTACGCAGGCGTCCGGCGCTCAGAGCAGCCCTCCGACCATCGTGATCAGCAGCAGCGCTGGAGGAGCCGCAGCCGGAGCTGGAAAGCTGGCGGGGAAAGGTCTGCGCCGCCTGACTGGACGATCCAGCAAGGAGAAGGATAAAGAGAAGGACGCGGCCACCGGCATGGACCAGCTAACCCGC[A/T]AACAAGCAGCCGTCCGCGCCATGAGTGAAAACCTAGAGCTGCTGTCACTCAAACGGCTGACGCTGACGGCCAGCCAATCAGTGCCTAAGAGCGGCTCGCTTAGCCTGTCGCGCACCGCTAGCGCCGTCTTCTCTCGCTCCTTCGAGCAGGTCAGCAACGTCTTCTCCGGAAACCAGCCGTCCAGTCGTGCGTCAAGTCCAACGTCCAATCACGTCGCTGAACAAGATGAGGGTGTGGCTTATCTGGATCACATAAGCCCCGCCCACCAGCATCGGCAGCGTTCTCCTACCATCAGTATCCATGTGACCTCTGACCTGTGAACTTAAAAACTGGCCGCCATCTTGTGGCACACAACTGCAGCACCTTACAGGACGTCTGTTTGTTTCCCTAAGTCGTGTTTAATGACCAAAGTCGTGTATTTTTTTGAAGTACGTGTTTTTAAGGACGTCTCCCAGTTTGCTCATGAAGTTTACAGGCGGTGTTGTGTATTTTTTAATGCT

Associated Phenotype:

Not determined