ZMP

abhd2b

Ensembl ID:

ENSDARG00000045804

ZFIN ID:

ZDB-GENE-061027-74

Description:

Abhydrolase domain-containing protein 2-B [Source:UniProtKB/Swiss-Prot;Acc:Q05AK6]

Human Orthologue:

ABHD2

Human Description:

abhydrolase domain containing 2 [Source:HGNC Symbol;Acc:18717]

Mouse Orthologue:

Abhd2

Mouse Description:

abhydrolase domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1914344]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24656	Essential Splice Site	Available for shipment	Available now
sa25225	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa44278	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24656

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067327	Essential Splice Site	130	422	4	11
ENSDART00000127577	Essential Splice Site	130	422	3	10

Genomic Location (Zv9):

Chromosome 25 (position 19623149)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	19035126
GRCz11	25	19133077

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACAGCTACCTTTGACCTGTTTGAGCCGCAGGGGGTCCACAGCACTGGAGG[T/C]GAGCTTGGGTTCACTGAAACAAAATGTATTTTTACGCAACAAAATTTAAA

Long Flanking Sequence:

AAGAAAAAGCTTTCAAATCAAAAGATTAATGTACTGTATATGTAAGACACAGAAAAGAAAAGAAGAAAAATCATACAGATTTTTCTTGTAGAATGCTTGTGCAAGTATACATTTATTATTGATTAAATGGTCTTAGTAATGCACTTTTCTAAAAACAAAAAAAAAATGACATTAACTAAATATCTTCATGAAACATTATCTTTGCTCAAATCCCTTACAATCATTTTGACCCATACGAATGTGCTTCTGGCTATTGCAAATATTAGTTTTCAGCACTTGAATACATTTGAGCTACTCTTTGCACCATGTTCCCTTGTCTCCAGGTACATCCCTCCTTTGTTATGGGGAAAGAGTGGTCATCTGCAGACGGCGCTCTATGGAAAGATTGGACGAGTGAAATCACCTAAACCCTGCGGGCTTCGTAAGTTTCTGCCCATGCAAGACGGAGCCACAGCTACCTTTGACCTGTTTGAGCCGCAGGGGGTCCACAGCACTGGAGG[T/C]GAGCTTGGGTTCACTGAAACAAAATGTATTTTTACGCAACAAAATTTAAATAGGGTAAAATAACAAATTTATTCACTTGGTTGATTACATAAATAATTGCAAACTTTTTAAATTATGAGATTTCTAAAATGTGTGAATTTTCAAATGATACATTTTATAAGATTACACCAATATGCATACATTTTTGACACAAAAACCTGAACTTTGGATAAAGTTGCATTCAAAATAGGTTTTTTTTTTTTTTTTTTTACATATTGACAAAATATCAGGCAACTTGTTTATGACTGAACCACTCTTTTAAAAAGTGAAGTTTGGTGTCTGTAAGGGCCTTTAAAAAATTGTATTATAACTGAAATCTACAGACACAATTTGATATAGAGTGCAATGAATCACACTGTATTTTAGATGGGGCTGGATGACATGGCAAAAATACAATCTTGATAACTATTTTCCATGTTGAATGATGATGATATATATTTCGATATAAGTTGTTAATGCTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25225

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067327	Essential Splice Site	312	422	8	11
ENSDART00000127577	Essential Splice Site	312	422	7	10

Genomic Location (Zv9):

Chromosome 25 (position 19617707)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	19029684
GRCz11	25	19127635

KASP Assay ID:

554-7711.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTCTATACAGCCACCTCTCTCATGCAGATTGATGACAACATTATGAGG[T/A]TCTGGAAAAACCTTCATCGCACTATTTTGCTTTTAGATGTCAGATAGCTC

Long Flanking Sequence:

CACAGATGAATTGTTCACCACACAACCAACAATGAGAGCTAACAAAATCAACTTAGTTAGTTTTGAATTCATGTGTACATTAAAACTGTATATACACTGCATTATCCACAGCTATAAACATGCCAATGTATAAAATATGTCTCTTGAACAGGTACATTGATACATTATTAGTTTATACAATATTTTAATTCAATTATAATTAATCTAGAACTAAGGTAACTGAGTTTTAATGATAGAAAATCAAAGTGAATTCAAATGAATTTTCACTAACCCAAAGATAAAATGTTAGTTTACTCAAATGTTTTGCAGCAATACCTTTCCACAAACATTTTGAGTAAGCTGGACTTATGAAATGTTCCAGTGCTGTTGTAATGAGTGACCTGAATGTGTCTTGTAGGGGAAGTTTATTTGGTATGAACTCCAGCAGAATGGAGTTTGCTGACCTCAGCCGTCTCTATACAGCCACCTCTCTCATGCAGATTGATGACAACATTATGAGG[T/A]TCTGGAAAAACCTTCATCGCACTATTTTGCTTTTAGATGTCAGATAGCTCTGGCTTTCATTTGCTGTAAGTGGCTAAGACAGTAATAGACTACAGCTCGTGTTCATATTTTGTCTCTTTTAGGAAGTTTCATGGACACAACTCGCTAAAGGAGTACTATGAGAAGGAAAGCTGCGTGCATTACATTCATAATGTAAGTAAAATTGTGGAAAACAGCTCAAAAGTCCTACATGATTTCATGAGAGAGCAATCTTAGCTGCATCCAATGCACTCAACTCACCCCACCCATAACCCTACCCCTCACAGTGATGTTACTAGCTCCATTGAGCGTATTGTGTCTGACATGGTATTACCAAGCAATGCAATTTCAGCTTGCATCATAAAGGCTGCATCCAGATACTATTGGATTTCATAGCAATTTATTGCTGCGTTTGGAAAAAATAGAGTCTAAGCCTGTATAATCTATTAAAGGGCACCAATTTTACCCCTTTTAAAGATTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44278

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067327	Essential Splice Site	336	422	10	11
ENSDART00000127577	Essential Splice Site	336	422	9	10

Genomic Location (Zv9):

Chromosome 25 (position 19615308)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	19027285
GRCz11	25	19125236

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAGCATAATTGATATATTTTATGGTAACACTAATATTTGTCATTTATTTC[A/T]GATCAGCGTTCCTCTCCTCTTGGTGAACTCTTCAGATGATCCATTAGTCC

Long Flanking Sequence:

AAATTTACAGTTTATGACAAGGCTTTTGTACTGTAATATACAACACCAACCCAGACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATATCTTTAAACTATTAAAAATGTTAATAAAAGTCAAGCTTTTCAAACTTTTAAAGGTTAAAAATTTTTGGAAGAAAGATTGACGTCCCATAATGCAGTTCAAAAGCATAAATGAATGGCAAAAAATGAAAACATGAATCACAAAATATGGTAAACCCTTAATTTAAGGATATTTTTACAGTGTAAGTTTGGGTAAAGTTTTGTAGATTTTTATATGAATAAATACTTACACTGTAATATACACAGTATTACCGTATATGAACTACCCACTAATTTACTAAAACCTAATACAGTTACATTTTACAAGTTAATTTAGCATAATTGATATATTTTATGGTAACACTAATATTTGTCATTTATTTC[A/T]GATCAGCGTTCCTCTCCTCTTGGTGAACTCTTCAGATGATCCATTAGTCCACCAGTCTCTGCTGACGATACCTCGAACACTAGCAGGTATTTATTAACTAAACTAAATCAACTGGACATACAGTACAATAGACATGGAAATGCACTATGCAAACTCAGATGTTTGTAATTCCGAAATGCCTGGATAAAAAGCTTCGTCTATTTTAAACTAATGGTAAGAGAGGGTATTATGCAATTGCTATGGAAACCCTGAGGTTGACATCACATCGATAGCTCAACAGAAGCAAATGGTCAGACTTTCATTCACTGTAAAAAGCGGTTAGTAGATTTTACTTAAATAAAGAGAGTAAACTCACTGCCTTATAAATATTAAATAAACAAACAGTTTACTGACTTTTTATAAGTAAAATAAATTTGTTGCTTTTAAGGCAACGGGTCTACTGACTTTTTAAAACTAAACACTGTAGCATTTTAGATTTAATGTGACTTTAAAGTGTTACC

Associated Phenotype:

Not determined