ZMP

si:dkey-24f17.5

Ensembl ID:

ENSDARG00000056723

ZFIN ID:

ZDB-GENE-041210-354

Description:

hypothetical protein LOC100006131 [Source:RefSeq peptide;Acc:NP_001035472]

Human Orthologue:

FHAD1

Human Description:

forkhead-associated (FHA) phosphopeptide binding domain 1 [Source:HGNC Symbol;Acc:29408]

Mouse Orthologue:

Fhad1

Mouse Description:

forkhead-associated (FHA) phosphopeptide binding domain 1 Gene [Source:MGI Symbol;Acc:MGI:1920323]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21276	Essential Splice Site	Available for shipment	Available now
sa27183	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21276

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079263	Essential Splice Site	33	359	3	8
ENSDART00000125695	Essential Splice Site	33	227	3	6
ENSDART00000127545	Essential Splice Site	33	352	3	8
ENSDART00000133601	Essential Splice Site	33	221	3	6

Genomic Location (Zv9):

Chromosome 8 (position 21922597)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	21352494
GRCz11	8	21384579

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAATCACTTGAGAGGACAGTCTTTAAGTGTTTGTCATCTCATGTACTC[A/T]GAACAGTGGGGTGGATGAATATCATGCCACTATTGACTGGTGTGAAGCGG

Long Flanking Sequence:

CCATGCTAATAGTTTATTTTCGACCTTCTTGAAAATAGGCTATGTAAATAAGAGAATAATAGTGAATATTATATCTTGACTTTTGGGTGTTTGACTGGGGCCGAACATTTGGTGCTACTCCTTTGGTAGATATAGCTGTTTACAACAGACTGCAATTAAATGTTAAATATGGGTGAACTAATTAGCAGGGATTTTTTATTTTTTTATTTGTCAGCAGGTTCAAATGAGGGGTTTTCTTAAAACGCCAAACTGGGTATTTAAACTCCAGCCTAAAACCACAACTATAGGAAGACACAAAGACTCTGACCTCTGTCTACAGGTATTAACCCATATTGTCTCCAGTGTTTCCACTCAATATGTCATTTCAATTGGTTATTGATTTAGTATTTAATTATTCATTCTGATTAGCAGATGATTTAATGTTGGATATGAAAGGCCAATTCCTGCTGGATGAATCACTTGAGAGGACAGTCTTTAAGTGTTTGTCATCTCATGTACTC[A/T]GAACAGTGGGGTGGATGAATATCATGCCACTATTGACTGGTGTGAAGCGGACAGCTGCTATGTTATCCGTGACTTAAACTCAGCACACGGGACATACGTTAATGACTGCCGGATCCACAATGCAACAGTGCGTCTCTCTCCAGGAGACCAGCTTCACTTTGGCTATGGAGGATCAACCTATGAGCTGTCCATTGACAACGAGAAATCAGTAAAATTAGCAGTATATTTGAACCTTTGTTGTTGTTTTTGGAAATATAATGGAAGATATAGCAATTAATTCTTTCTAATAAATAATATGATATTTTTATATTAAATAATATAATAAATAACATTCAAATCTTTATAATGAAAAAACTTTTCCTAAACAGTTTCCTCATTTGGCTGCTCAGTCTCCAGTTCCACAGGCCTGGCCACGAGTTCGGACTACCTCTGTTTCACCCCATCCTCCAACCAGACCTCGTCCTATGAGTGCCGGAATGAAACGGGGTTCCACTACAACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa27183

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
ENSDART00000079263	Nonsense	296	359	7	8
ENSDART00000125695	None	None	227	None	6
ENSDART00000127545	Nonsense	289	352	7	8
ENSDART00000133601	None	None	221	None	6

The following genes are also affected by this mutation:

ENSDARG00000094473

Genomic Location (Zv9):

Chromosome 8 (position 21930516)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	21360413
GRCz11	8	21392498

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAGAGATCAGAAGATCAGCGCTTTATTAGAACAGATGGATAAACTCAGG[A/T]GACAAAATTCTTCCTCTACAGGTATGAGGATGCTATTAAGTGGATGACAT

Long Flanking Sequence:

GACAAGATTTTGTCAGGTAGTGTACAGCCATTATCTTAAACACTGCATAAACATTAATTTAATGTTTCACAGAACTTTGAAAGGTTGACGTAAAACATGCATCTTTCACATTATTTATATACTTTTATCAAAATGCCCCAAATCCTTTGCATTAAAATCCATCAACAAATATTGAAAGATCATGGCCACTGAAGTCTGCTATACCAGGAAAAGGCAAAAACACTCATTACAGATAGTAATTATTCAAGTTTCTTTATATTTAAGGTTTAATTTAAGCAATGCTTGCATTTTGGTGAAGCTATTTCTCCACTTTCCAAATTCATCGAAAATCTTTCAAGGGCTAATTAATAATTAACTGCTGCGCCTCATTTCAAGCTTGATCTGTTTAATGGATGCAGATGCTGGAGCTTCAGAGATGTTCTGGAGAGATGCTTGAACAGACTGTGACTGAGAGAGATCAGAAGATCAGCGCTTTATTAGAACAGATGGATAAACTCAGG[A/T]GACAAAATTCTTCCTCTACAGGTATGAGGATGCTATTAAGTGGATGACATGTATAGGTCATTTACATTCCTGTAATGTGGAAAAAAATATATAAATACTTTATCACAGAAAACCATATTTCACACAGGGTTAAACTTAATTTATGTACATTTAAATGTCTAAAAATACACTTTATACTCCATTTATAGTTCATTTATATTCATACTAAACTTCAGTTTGAAGATATTACTACTATTAAACTGTATTTTCTGTATTTTATTTCGTACTTTCTATTCATCCATTTAAATTGTATTTTATATTGTACTTTCTATTGTTTGAGTCATGATTTCAACAAAACAGCAAAATGGTTTATAATAAAAGTTTTTGTGATTAAATTTTGAGTAATATGGATGGAAATACACTGTTTTGTAGTGAAATTACAAATAAATTATTGCATAAATAAAAATATTTTGACATTTTTGTGGCATGTCTGTATAGTGAGTAAGATAACTTGTTGGAGA

Associated Phenotype:

Not determined