ZMP
adka
Ensembl ID:
ZFIN ID:
Description:
adenosine kinase [Source:RefSeq peptide;Acc:NP_997956]
Human Orthologue:
ADK
Human Description:
adenosine kinase [Source:HGNC Symbol;Acc:257]
Mouse Orthologue:
Adk
Mouse Description:
adenosine kinase Gene [Source:MGI Symbol;Acc:MGI:87930]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42205 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9944 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42205
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057605 | Essential Splice Site | 19 | 359 | None | 11 |
ENSDART00000144227 | None | None | 131 | None | 5 |
The following transcripts of ENSDARG00000039429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 25423003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25068663 |
GRCz11 | 13 | 25199113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGATGAACCTAAAGCAAAGAGGATTAAACTCGAGGAAAAAAAGCTCAGG[T/C]ACAGTAAACACAAGCATCGGTTGAGCATTGTAGATCAACCGAGTCAGAAG
Long Flanking Sequence:
CTATTGAATGATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTAACTGTATGCCATGTTGTATTTGTTTTTTTATTGTGATTCACTGAACACATATTTGCTGACTCTGTGAACAGAGAATTGTTTATTCAAAATAATTTTTATCAGTTCATTTTGAAGCTGATAGTCATCAGAAAAGATAAATATTCGTTCGGTAAATTTGTGAGAAGTGCTCGGACCGTTTTAGCTCCACGAACGAATAGTTATGAACAGTTACACGAATCGACTCACTGAAAAGATTCGACTCAAATGAACAGCATCCACCACCCTCACCGCCAGATGCTTCATTCGCTCAACAAGGTGCCAGGAGCGTATTTGATTGAGCACTATCACTGTACAGCATGGCGTCCGATGAACCTAAAGCAAAGAGGATTAAACTCGAGGAAAAAAAGCTCAGG[T/C]ACAGTAAACACAAGCATCGGTTGAGCATTGTAGATCAACCGAGTCAGAAGTGTGTTGGTGCTTTTATTAAACACAGGGCGGTTTGCTTGCGAGCGCTTTTGGGTCAGAGGTCTTGATGCTTGTCACATAAAGTCCATGTGCTGTCAACTCAGTGATTTTCCTCAAAAGCGTATTGTTGTTGCACCGGAGAGGAATGTATCGGGTATTTTCTCATTACCTCTGACCAATGCCGATGAATGCAGCTCATGCATTTCCTGCAAGGCGTAAATCGCAGACTCGTGATCGAGGCTTTTTTATCATTAGTGAACAATATAAAAAGTTTTACAGTCACTTTAACGTTACTTCCACATGACCGAGTGCATGTATGCTTCATGCTTTTGATCACCCGTTGTCCTTGAGTGATTTATATTGACCACTGGAGTCCGTCCCTCTGGCTCCACGTGTCTTTTGTTGTGCAGTCGAGCACTGCTGCACAAAAAGTCTTCCTGCTGCACGTTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9944
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057605 | Nonsense | 230 | 359 | 7 | 11 |
ENSDART00000144227 | None | None | 131 | None | 5 |
The following transcripts of ENSDARG00000039429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 25210108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24855768 |
GRCz11 | 13 | 24986218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTTCATCTGCGAGTTTTTCAAGGAGGCCMTGATGAAGGTGATGCCCTA[T/A]GTCGAYATCCTTTTYGGCAATGAAACGGTAAGTGTATGCRTGTATTCTTC
Long Flanking Sequence:
GTATTTATGGATTGATAATTAGAGATTCCCAAAAACATTTGCCACCAATATGTCAAAAAAAGACACAAAAAACTTGAACTTGTCCCGACTTTAACAAATGTTAAGATTTTTGTGTTTGAATAAAATGCAAATTAGCACATATTTAATGAAACAATGTGTCATTTGCACGTTTGAAAATTACATTTTGGAAAACGTGTGATACAAAAAAAAAAATATTAGCACTTCTTAATGTAATCAGCTGTGGAAGAGCTGTGAGAATAACTTTTTAATAAACCCAAACTAAGCGATTAATCATCTTGTGTGTTCGAGTCTTCAAAATCTTCATGTTTTGACCACCATTTTTGTCTTGTTCCATAGGGCTTCTTTCTGACCGTGTCCTTGGAGTCGATCCTAAAGGTGGCCAAACACGCTTCTGAAAACAACAAGATCTTCTGCTTGAATCTGTCAGCTCCGTTCATCTGCGAGTTTTTCAAGGAGGCCCTGATGAAGGTGATGCCCTA[T/A]GTCGACATCCTTTTCGGCAATGAAACGGTAAGTGTATGCATGTATTCTTCTATAAGCTTATCTGATCATGTAACCACTTATCAGTACATCAATCATATCACTCTTTCAATCGTACACTTAAGATGAAGGATTGCACATAGCCTTGAACAGACAAGGAACTCAAATTCACTTCTTTTGCATTTATTCTGTACATTGAATAGCCTTCTCATCTTAAATGCATTGTGGTCCAGCTGTGACTGTATTCATTGTGAAAGTAAGAGCCTGCAGACTGGACCATTTACAGACTTTACCTCAGTCTGTTCTTAGTCATTGTGGTCGATCTTTCTCTATGCGCGGTACAGATGTGTTAAAGCCTTGAAGTGTGGGTTAAGTGTGTTTGACTTGTGCTGAGAGTCAGACTTAACATGTTAAAGCTTTATTTGTTTTTTATCGGAATATCTTCAGGGTGTAGGGGTTGGTAGTATGACCCAGAACTTTAGTGAGTAATTTGATTTCAGAGA
Associated Phenotype:
Not determined