ZMP

asah2

Ensembl ID:

ENSDARG00000012829

ZFIN ID:

ZDB-GENE-041112-1

Description:

Neutral ceramidase [Source:UniProtKB/Swiss-Prot;Acc:Q5W7F1]

Human Orthologues:

ASAH2, ASAH2B, ASAH2C

Human Descriptions:

N-acylsphingosine amidohydrolase (non-lysosomal ceramidase) 2 [Source:HGNC Symbol;Acc:18860]
N-acylsphingosine amidohydrolase (non-lysosomal ceramidase) 2B [Source:HGNC Symbol;Acc:23456]
N-acylsphingosine amidohydrolase (non-lysosomal ceramidase) 2C [Source:HGNC Symbol;Acc:23457]

Mouse Orthologue:

Asah2

Mouse Description:

N-acylsphingosine amidohydrolase 2 Gene [Source:MGI Symbol;Acc:MGI:1859310]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa27879	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa27879

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
ENSDART00000027793	Nonsense	204	743	5	20
ENSDART00000146650	Nonsense	204	743	6	21

Genomic Location (Zv9):

Chromosome 12 (position 6809070)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	6091990
GRCz11	12	6125574

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATTGATATTGCTCATAGGAATTTGAGGCCTGGACGAATATTCATAAAT[A/T]AAGGACAAGTAGCAGACAGCAACTTCAACAGAAGCCCACATTCATACATG

Long Flanking Sequence:

GGCCAGACAGAATCTGGGGACATTTTTTGCTATTTCTGCTGAGAATTTTGTAAAAAAAAAAAAAAAATCTGCAGAATGATTTTATCATAACTAAAAACTTAACACATGAAATAATAAATAATACCTTTTTAACTTTTATTTGATGTTTACTATGCGAATTCAATTAGATCCACTTATTTGGTAAACAAAGCAAGTCTCTCGTATAATAGATTTACTAAAAGACAGAAAATAGTACTTAACAAAATGTATTGTAAACAAATCATATGAACATTATCATATTAGTCAATGATATTACTGAAATTAATTTAAATTAATAAATTTATTTACACACATTTACACAAGAAAATAAATAGACTCATTGATGGTTTTAAAAATCTACATAATACTACAAATTCCTCATGTAAATGGTTTCAGCGGTCACTGATAATATTTTCTATCCTCTGTATCAGAGTATTGATATTGCTCATAGGAATTTGAGGCCTGGACGAATATTCATAAAT[A/T]AAGGACAAGTAGCAGACAGCAACTTCAACAGAAGCCCACATTCATACATGAACAATCCGGAAGAGGAGAGAAACAGGTCTGTTTGTTTTTACTATATGAATATATACTTTGTAAATTGTCGGATGAATAAAAAAATCTCATAAGTGACAGAAATCAAACTATTAAGGGCAAACATTTGCATTCTGAAAAAAAAAATCTTAAAGCTAATAATATTGACCTTAGTTTTATTTATTATTATTATTATTATTTTATTATTATTATTGTTGTTAATATTATTAGTATAGGAGGACATTTGCATTCAGAAAAAAATCTTCTTAATTCCGTTATTTATTTATTTATTTCATTTTTATCTAATAATTTAATTTAATTTTTTACAATTGTTTACTTTTTTTATTCCAGCAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGAAATACTGTTAAATTTTCTTTGCTCT

Associated Phenotype:

Not determined