ZMP
zgc:158222
Ensembl ID:
ZFIN ID:
Description:
adenosylhomocysteinase [Source:RefSeq peptide;Acc:NP_001074118]
Human Orthologues:
AHCYL1, AHCYL2
Human Descriptions:
adenosylhomocysteinase-like 1 [Source:HGNC Symbol;Acc:344]
adenosylhomocysteinase-like 2 [Source:HGNC Symbol;Acc:22204]
adenosylhomocysteinase-like 2 [Source:HGNC Symbol;Acc:22204]
Mouse Orthologues:
Ahcyl1, Ahcyl2
Mouse Descriptions:
S-adenosylhomocysteine hydrolase-like 1 Gene [Source:MGI Symbol;Acc:MGI:2385184]
S-adenosylhomocysteine hydrolase-like 2 Gene [Source:MGI Symbol;Acc:MGI:1921590]
S-adenosylhomocysteine hydrolase-like 2 Gene [Source:MGI Symbol;Acc:MGI:1921590]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa3295 | Essential Splice Site | F2 line generated | Not yet available |
| sa38074 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa3295
Status:
F2 line generated
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073580 | Essential Splice Site | 286 | 516 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 25 (position 22477843)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 21709719 |
| GRCz11 | 25 | 21807267 |
KASP Assay ID:
554-2689.1 (used for ordering genotyping assays)
KASP Sequence:
AAACAGAAGTTTGACAACTTGTACTGCTGYAGGGAGTCCATTTTGGATAG[G/A]TAGGATGATACWAGTACTGTATGTRTCCCTAAGTTAATACTAATTTTAAA
Long Flanking Sequence:
ATAAGGTGGCATTTATAAGTTCTGTGTTAAAGCTTATAATACTGCAACACCAATTAAATCATTTCAAACAACAAAATTATTAATTCTAAATTTTATATTTCTAAGTTAAATCCACTGTTGGACGTTGTTGCCACACTTCAACATTTCATGAAGTACCTTAAAAAAGATTTTTTCCATTTTTTTTTTTACAGCACTTCAAGTTAAGCCATTTTAAGAAAAGAAAAACAGTCAAATATTCTCGGAAGCTATAGAAATTTAAAAAATATATTAGGACCACTATTTTTGTTTACATCCCTTAAAATGGTCTATAGATAATTTGACTGCATTGACACTAGGGTGTTTGCGTGATGAAATGTTATATTCTTTTATACTACATATATTAGGCTTCATCACCTCTCCAAAGCTGGAAAGTTATGCGTACCAGCCATAAATGTGAATGACTCTGTCACCAAACAGAAGTTTGACAACTTGTACTGCTGCAGGGAGTCCATTTTGGATAG[G/A]TAGGATGATACAAGTACTGTATGTATCCCTAAGTTAATACTAATTTTAAAAACTAAACCTACACTCAGTGTCATTCCTGTTCCCTCAGCCTTAAAAAGACTGCTGACATCATGTTTGGAGGAAAACAAGTGGTTGTGTGTGGATACGGAGAAGTAAGTTAATTAATTTTGGTTTCTACTGTCAACAACATGCCACCTGAGAACAATGTACGTCACTGCATTAGCTTAGCATAAGCCTTTGTTTTTTTGTGCGTAAATGTAAATATTGGTGCCCACAGGTGGGAAAAGGCTGTTCTGCTGCTCTGAAAGCAATGGGATCTATTGTGTATGTCACTGAAATTGACCCCATATGTGCTCTGCAAGCATGGTAAGGCAATAGAGCTCTACTGAAAGTTAGCATAATGTTAAATCAGCATCACACATAACACTGCGTTATATTTTGACTAGCATGGATGGCTTTCGATTGACCAAACTTAGTGATGTTGTTAGACAAGTGGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38074
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073580 | Nonsense | 324 | 516 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 25 (position 22477515)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 21709391 |
| GRCz11 | 25 | 21806939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGGAAAAGGCTGTTCTGCTGCTCTGAAAGCAATGGGATCTATTGTGTA[T/A]GTCACTGAAATTGACCCCATATGTGCTCTGCAAGCATGGTAAGGCAATAG
Long Flanking Sequence:
ACACTAGGGTGTTTGCGTGATGAAATGTTATATTCTTTTATACTACATATATTAGGCTTCATCACCTCTCCAAAGCTGGAAAGTTATGCGTACCAGCCATAAATGTGAATGACTCTGTCACCAAACAGAAGTTTGACAACTTGTACTGCTGCAGGGAGTCCATTTTGGATAGGTAGGATGATACAAGTACTGTATGTATCCCTAAGTTAATACTAATTTTAAAAACTAAACCTACACTCAGTGTCATTCCTGTTCCCTCAGCCTTAAAAAGACTGCTGACATCATGTTTGGAGGAAAACAAGTGGTTGTGTGTGGATACGGAGAAGTAAGTTAATTAATTTTGGTTTCTACTGTCAACAACATGCCACCTGAGAACAATGTACGTCACTGCATTAGCTTAGCATAAGCCTTTGTTTTTTTGTGCGTAAATGTAAATATTGGTGCCCACAGGTGGGAAAAGGCTGTTCTGCTGCTCTGAAAGCAATGGGATCTATTGTGTA[T/A]GTCACTGAAATTGACCCCATATGTGCTCTGCAAGCATGGTAAGGCAATAGAGCTCTACTGAAAGTTAGCATAATGTTAAATCAGCATCACACATAACACTGCGTTATATTTTGACTAGCATGGATGGCTTTCGATTGACCAAACTTAGTGATGTTGTTAGACAAGTGGACATGGTCATCACCTGTACAGGCGAGTAGTAAATAAAACACACTATACTATTAATCACACTTTGTTATTTACGTTAACAACTTAATTTTAAACAGGTAACAAAAACGTTGTTGTGCGGGAACACATGGATGTAATGAAGAATGGCTGTGTTGTCTGCAATATGGGGCGCTCCAATACAGAAATCAATGTTGTAAGTGGTTTTGTAACCTACAGATATTGACAACGACAGCTTGTGGTTTTGGGAATTCTAGACTACATTTTGTATTCTCAGAGTGCTCTGAAAACTCCTGACTTAACATGGCAGCATGTAAGAGCACAAGTGGATCACATTA
Associated Phenotype:
Not determined