ZMP
asah2
Ensembl ID:
ZFIN ID:
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]
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.
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