ZMP
ahcyl2
Ensembl ID:
ZFIN ID:
Description:
putative adenosylhomocysteinase 3 [Source:RefSeq peptide;Acc:NP_958497]
Human Orthologue:
AHCYL2
Human Description:
adenosylhomocysteinase-like 2 [Source:HGNC Symbol;Acc:22204]
Mouse Orthologue:
Ahcyl2
Mouse Description:
S-adenosylhomocysteine hydrolase-like 2 Gene [Source:MGI Symbol;Acc:MGI:1921590]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33371 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8809 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10583 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33371
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
Founder:
SL6_09_F2
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130453 | Nonsense | 156 | 623 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 4 (position 4922108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5040289 |
GRCz11 | 4 | 5048859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGAAGCAAGAGTTCAACAAACGTCCCACCAAGATCGGCCGCAGGTCTT[T/A]GTCCCGCTCCATCTCACAATCTTCAACGGACAGTTACAGCTCAGGTACGC
Long Flanking Sequence:
CAGTACCGGGAAACACTCATACACTCTCGCATTCACACACACTCATACACAATTTAGGACATTAACATATGGACAATTTAGTTTATTCAATTTACCTGTAGCGCATACCTTTGGACTGTGGGGGAAACCGGAAAACCCAGAGAAAACCCACGCCAACATGGGGAGAACATACAAACTCCTCACAGAAATGCCTACTTGCCCTGCTTAGACTCAAACCAGCGACCTTCTTGCTCTGGAGCGACGGTGCTAACTGAGTACTTTCCCAGTACTGGGTTGCAGCTCCAAGGGCATCCATTGTGTAAAACATATGCTGGAGTTGTTGTCGGTTCATGACCTCTGATAAATCAGAGACTAAGCTGAAGGAAAATAAATGAAGGAAGGAATTTAGCCACTTCAAGGAGTCTCACCCGAGACTTTCTCTCTTTTTTCCACACAGATTCAGTTTGCAGACCAGAAGCAAGAGTTCAACAAACGTCCCACCAAGATCGGCCGCAGGTCTT[T/A]GTCCCGCTCCATCTCACAATCTTCAACGGACAGTTACAGCTCAGGTACGCCATAATACATACATACATGCGGCTGTTTTACTTTACGTCAGGGGTCTCGTGTAGAGTGTCAGCATGTGAGCAACGTCTTTCCTGTGTGGCAGGATTTTAAAGAGGATTAAACTGATGAAGCAGAGCAGATTTTAGGAGGGGAAGTAAAATCTACATTCCTGCGGGACTCTCACAGGACACTATATTAGTAGAAGTCAAAATTATTTGCTGTCCTGTGAATTATTTTTTTTAACTTATATATATTTCCCAAATGATGTTTAACAGAGCAAGGTAGAGATCGATTCGGCCACGTTTTAGGATAATAAACGGTAATGTTTTAACGTAATAAAAACAATAATAAACAGTATATTTACAATGATTCATTGACACTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTTGTTGTAGTTTTGTAAAAGCAAAAATAACTTAAATAGATGTTATTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8809
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
Founder:
SL4_01_D5
KASP Assay Location:
Project 554.47, Plate 2, Well C09
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130453 | Essential Splice Site | 581 | 623 | 15 | 17 |
Genomic Location (Zv9):
Chromosome 4 (position 4901791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5019972 |
GRCz11 | 4 | 5028542 |
KASP Assay ID:
2259-4423.1 (used for ordering genotyping assays)
KASP Sequence:
TCCCGAGGGCCGCTACAAACAGGACGTCTACCTGCTGCCGAAGAAAATGG[G/A]TGGGATATTTKTTTTNAGAAATACATGCACAGTAAGATGCTTTGTGTAAAC
Long Flanking Sequence:
TTATTTAAATTTTTTTAATTTTTATTGTTAAATTTGTCGTGAAAATAGTCTTCTAATGACACATTATTACTATTTCTTAATCGTTTTAATCACTTATTTGTATATACTTCCAGGGTCGCCTCTTAAACCTGAGCTGCTCCACTGTTCCTACCTTTGTGCTGTCTATCACTGCTACAACCCAGGTGAGAATAGAAGAACAAATGATGAAAAACTAACACAGATGCCTTTATTAAACTGGTTATTAATGTGCTTTATGCAAGAGAATTGGACTTCGCAGTTCAATCAGAGAATAGCTTTCTTGGTCTATTTGCAGTGTGAGAGTATGAACCCCAAGCGTTTCATATATACGTGTGTGTGTGTGTGTGTGTGTCACAGTCCTGCTGTTGTCATGGTGACTGATTTCTTGCTCCTTTTTCCCCAGGCTCTGGCTCTGATAGAGCTCTACAATGCTCCCGAGGGCCGCTACAAACAGGACGTCTACCTGCTGCCGAAGAAAATGG[G/A]TGGGATATTTGTTTTAGAAATACATGCACAGTAAGATGCTTTGTGTAAACCCAGCGAAATGAAGGGTTCTGCATGATGCTCAGTTGCTTATGTTCAACTGAAACAAGCATCAAATGCAGTCAGATCCTCAAATGCGTTAATATTATGGCCGTCTATGGGTTTAATCGCCGCAATATGTTTAGTTTGGAACATGCATGGATGTTTTCCGCCTTTTGCGGTGAGTTTAGCCATGTGGGATCATGCATTGAGCCTGAGGAGCAGGAGACAGCTGAAAATAGGTCACGCTGTCACAAACGGCTGCCACTTTTCACTGCAGACTCTGCTGCATTCTGCTCCGCTCCCTCCACAAACACTCATCCGCTCCACTGCCGTTCATCTGTTCATGCCAAACCCGCAGCTCACACTCATAGACACATGCAGTACAAATATAAGACTGACTGGAGAGATTGAAGCTTGTAATAGAGAGATAAATAATGGCCTGTTCTGATCGGAGAGTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10583
Status:
Available for shipment
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:
Founder:
SL4_03_E3
KASP Assay Location:
Project 554.47, Plate 9, Well A01
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130453 | Nonsense | 584 | 623 | 16 | 17 |
Genomic Location (Zv9):
Chromosome 4 (position 4899827)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5018008 |
GRCz11 | 4 | 5026578 |
KASP Assay ID:
2259-4422.1 (used for ordering genotyping assays)
KASP Sequence:
MATGATTCTAGATGATGTGAATTTGCTTATGCWTTTTCTRCAGATGAGTA[T/A]GTGGCCAGCCTTCATCTCCCTACATTTGATGCACACCTGACTGAACTGTC
Long Flanking Sequence:
GTGATGCAAATTTCTCAATGTTGGCAACATGGTGGCACCTCAGTTTTCCCAATATTTTGGTTTTGTCACACATATGCTTTACACAATTGGCATAAACGATTATCTATTGGTACAAAGTGTGCCCCAAAAAACTAATCATTTTCAAAACCTTACCAAAACCTTACTTTGGCGGGCAGCTATCTACCTACTAATCTCACATGGTCGCCCACTGAAGCTAAGCAGGGCTGCGCCCGGTTAGTACCTGGATGGGAGACCACATGGGAAAACCAGGTTGTTGCTGTTGTTAGTGAAACCAGTGCTTTGAATGTCGAGAAAAATGCTATATAAAATTATTATTATTATTATTATTATTACAATAAAAAATAAAATAAAAGACACTGTTTCCATCCAAAGCAAATCTATAAAACTTGACAATTGTTCCAATTGTTTTTCCAGTGCAGTAATAATATAAATGATTCTAGATGATGTGAATTTGCTTATGCTTTTTCTGCAGATGAGTA[T/A]GTGGCCAGCCTTCATCTCCCTACATTTGATGCACACCTGACTGAACTGTCTGATGAACAGGCCAAATACCTCGGCCTCAACAAAAACGGACCCTTTAAGCCAAACTACTACAGGTCAGTGACTTTTCAGTGAGAGCATTTTTACGTCATATCAATGACTTTCTTAATAATACTAAATAATACTAAATAATAATGTGTCCTTTTTAGGTACTAGACCCAAACTAAAGAAGACTAAAGAAATCACCAAGACTCCATATTTCATACAGACTAAGACGAGCCAGAGCTGTGTGTGTGTCGCAGCCTGCTATTGGAAAGGAGGGAGAATCCCTAATCTGATTGGTCGAGGGTAAAATGGGCGTGGCTAATTAGCGCTACGGCAGTGTTTATTTATTTTACGCTAGAATAACATAGCTAACCTTTTTATGAGCTGCTACTGCCAGTGGTGCAACCTAGCGACGTTTCCATGATCTTTTCTTAGCTTCATGTGTTAGTTGTACGTAA
Associated Phenotype:
Not determined