ZMP

hdhd1

Ensembl ID:

ENSDARG00000027826

ZFIN ID:

ZDB-GENE-050522-36

Description:

haloacid dehalogenase-like hydrolase domain-containing protein 1A [Source:RefSeq peptide;Acc:NP_001

Human Orthologue:

HDHD1

Human Description:

haloacid dehalogenase-like hydrolase domain containing 1 [Source:HGNC Symbol;Acc:16818]

Mouse Orthologue:

Hdhd1a

Mouse Description:

haloacid dehalogenase-like hydrolase domain containing 1A Gene [Source:MGI Symbol;Acc:MGI:1914615]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa19523	Nonsense	Available for shipment	Available now
sa25611	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa19523

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000037293	Nonsense	26	214	2	4
ENSDART00000135078	Nonsense	38	170	2	3
ENSDART00000137156	Nonsense	38	226	2	4

Genomic Location (Zv9):

Chromosome 1 (position 31883254)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	31609579
GRCz11	1	32342147

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGATTGTACACAGTCTCGTTCCAGGAAGTTTGTGACAGGTTTAATAAG[C/T]AGTATACTTGGGAAGTGAAGTCCTCTGTTATGGGCAAAAAGGCTCTGGAT

Long Flanking Sequence:

AGCGTGTTGATCTAAATGCAGCGTAACTTTTATCGTCCAGCAGTTTTCGCTTCTCTGTCTCTCTGTCAATGAAGTTTCCGTAGTCACACAGTCGAGCTATCGTATCGCCAAAAACATGTCTTATAAACCAGTAACACACGTGCTCTTTGATATGGACGGGTTGTTACTAGGTAGGTGATAATCTGCTTAAAATAAAATATATTGAAACCTTTTTTATCCAGCTTGTTTTTCTGTTAGTGCCTGCAACAAAATCAGAAGAAAAACTAACTCTGTTTCAGTTAAAATTAAATTAATTGAGATTAAATTCAGTTTCATACCTAATTCACGCCAAAGCAAAGTCATTTATCAACAGTTTCTGTAGGCTATAAATCATTACGTTCAGCAATTCCGTTTTACTAGGCTGTACGCCGCAATATAATGTTTTAATGCATTTGTTTCTTGCAGATACAGAAAGATTGTACACAGTCTCGTTCCAGGAAGTTTGTGACAGGTTTAATAAG[C/T]AGTATACTTGGGAAGTGAAGTCCTCTGTTATGGGCAAAAAGGCTCTGGATGCTGCCAGGATTATAAGAGACAAAATTGGCCTTCCCATGACCCCTGAAGAGCTCCTAGAAGAGACCAGAAAAATTCAGGAGCGTTTGTTCCCCACAACTTCTCTGCTACCAGGTAATGTCCATGTAGACTTGAAAATTCCTGAAGATGATTTTGAAACAGAAGCAGATGTAGGGTGATGTAGTGCATCATCTTGACCATGTTTGTATCAAAGTCACCATATTGTTAAAATAAGTCAGCTCACTTTGTTAGTTTTTATTTCTGGTGTCTGTTTGCAATGTCTTTTCAGGTGTAGAAAAGCTTGTCAATCACCTACACAAGCATGGCATCCCTATTGCTGTTGGCACAAGCTCAGCAGGTCTGACCTTTGAGATGAAGACCAGCCGTCATAAAGAGTTCTTTAGCCTCTTCAGTCACATTGTGCTTGGAGATGATCCGGACGTAAAAAATGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25611

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000037293	Splice Site, Nonsense	156	214	3	4
ENSDART00000135078	Nonsense	168	170	3	3
ENSDART00000137156	Splice Site, Nonsense	168	226	3	4

Genomic Location (Zv9):

Chromosome 1 (position 31883819)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	31610144
GRCz11	1	32342712

KASP Assay ID:

2259-0740.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATACTTTTTTGGTGTGTGCCAAAAGATTCTCTCCCCCAGCCAACCCTAAA[C/T]AGGTAGGATGAAGCTACTCAGCTATTGCATTCTATTTCAGTCTAGTCTAA

Long Flanking Sequence:

AAGAGACAAAATTGGCCTTCCCATGACCCCTGAAGAGCTCCTAGAAGAGACCAGAAAAATTCAGGAGCGTTTGTTCCCCACAACTTCTCTGCTACCAGGTAATGTCCATGTAGACTTGAAAATTCCTGAAGATGATTTTGAAACAGAAGCAGATGTAGGGTGATGTAGTGCATCATCTTGACCATGTTTGTATCAAAGTCACCATATTGTTAAAATAAGTCAGCTCACTTTGTTAGTTTTTATTTCTGGTGTCTGTTTGCAATGTCTTTTCAGGTGTAGAAAAGCTTGTCAATCACCTACACAAGCATGGCATCCCTATTGCTGTTGGCACAAGCTCAGCAGGTCTGACCTTTGAGATGAAGACCAGCCGTCATAAAGAGTTCTTTAGCCTCTTCAGTCACATTGTGCTTGGAGATGATCCGGACGTAAAAAATGGCAAGCCACTCCCTGATACTTTTTTGGTGTGTGCCAAAAGATTCTCTCCCCCAGCCAACCCTAAA[C/T]AGGTAGGATGAAGCTACTCAGCTATTGCATTCTATTTCAGTCTAGTCTAATAATTTTATGGAAGCAGTGCAGAAAACCCACAAAATCAAGGAATCAATTTGTACATGAACAAAGACATGCACAAATACAACATGAAGTATTTTGTTACATATTACAAATACATGCTTATCAAATTTATTTAAATAAAATACTAAATGCAGATTTGTGAAGTGTAGGCTTTGATTGAAATACATGTAATGTGTAGCAGTTGTTTCAACATAAGCAGTGGGCACTATGCAGTGTCATTGCTTTTTTGTTTATGATGCTATAATGATGACAATCTTCACATCTGGTGTCTCTGTGATTCTGCATTTGGCTGTTATTGGGCAAAGATTAGAACTGCATCGGATACTTTTTCACTTCTTATTGCAGATTCAATGCTTTATTTCTTAGATTTAGATTTAGAATATGCATTTGACATGTTTATAAGAGAAATATTTTTGTAAAGAAGATATTTTTAA

Associated Phenotype:

Not determined