ZMP
ak5
Ensembl ID:
ZFIN ID:
Description:
adenylate kinase isoenzyme 5 [Source:RefSeq peptide;Acc:NP_001093554]
Human Orthologue:
AK5
Human Description:
adenylate kinase 5 [Source:HGNC Symbol;Acc:365]
Mouse Orthologue:
Ak5
Mouse Description:
adenylate kinase 5 Gene [Source:MGI Symbol;Acc:MGI:2677491]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32844 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25759 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18317 | Essential Splice Site | Available for shipment | Available now |
sa2067 | Nonsense | F2 line generated | Not yet available |
sa32843 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32844
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_10_E3
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022768 | Nonsense | 291 | 563 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 8780355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 9198009 |
GRCz11 | 2 | 8996014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGCTTGACTAATTTCAAACAGAATGCCATCCCCCTGGTTAAATACTTC[C/T]AAGAAAAAGGCCTCATCGTCACAGTAAGGAATATGTTTGAATATTTATTG
Long Flanking Sequence:
ATAATGCACAATGGATCTTATAATGTGTCATTACATATAATCTTATAAATAATCTCATGAATAATTATGTAATTGTAATGTGAGGCATGTTGACAACAGAGATAAGGATATACGGAGTGTCTCTCCTGCTTCAGCAGCGTGTCCCGCTGGTTATAAACGATGAGGCGGAGGCCTTTTCAATTAACATTTCATTAGGCCCAAAGTTTCTCTTAATATCCATATATCCAGAGATCACTGCAGCCTCAAGTCTTTTTGATCTTACCCATCAGTATCAACTTCAACTGAGACATTAGTATTTAAAAACCCTCACTTCCTTTCTTCTGTTTCCGTAGGTCTGTACTCCAGACTTGGTGGTGTTTCTGGCTTGTTCTAATCAGCGTCTGAAGGAGCGCCTGGAGAAACGAGCAGAACAGCAGGGTCGCCCAGACGACAACCCTAAAGCTATCGATCGACGCTTGACTAATTTCAAACAGAATGCCATCCCCCTGGTTAAATACTTC[C/T]AAGAAAAAGGCCTCATCGTCACAGTAAGGAATATGTTTGAATATTTATTGTCACAAACTTAAAAGAGAACGTAGGCTTGGGTAGAACTCTTTAATAAAATAATGTGCTGAAGGAATTCGAGAACTGCCTTCTAAAAAGACAAGTAACACTTGTTCATGAGGTCCTGGAAAGTGCTTTGAAATGTGCATTTTTGTTCTGTGTTCGACGTCATTATAACTGAAACAAGAAGACAGAACATGATATAGAATAGCCCCTCCCATTTAAAAAAAACAGCCAATAGTAATTTGTTTTCATCCCAGCTCTGCCAGTAAGAGTGGTTGACCTTAAACGCATTAAATGAAAAGCAAATGAAAAGCTTTATGAAGTGGGCAGGACATGTCAGATACTAGAGAGCGTTTGATTGGTTGAAGGATTTGATGAGAAACTAAAATATGAGGTGACCTGGGAAAAAAATATTGATTGATTTTTGACAAACTGAGGGCATTGAGTGTTTATATCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25759
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_B10, SL4_01_B3
KASP Assay Location:
Unknown
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022768 | Essential Splice Site | 299 | 563 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 8708027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 9125681 |
GRCz11 | 2 | 8923686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATATATATTGTACTGATTGTCTGACATGAGTGATTTTTCTTTTATGCA[G/T]CTTGATGCAGATCGAGATGAAGAGGAAGTCTTCTATGACATCAGCATGAC
Long Flanking Sequence:
ATCTATTTGATCTATTTAGTATTTTTTATTGGATTCAAGTCAAGTGATTGTCTGGGCCATTATACATTATGTTTCTCTGAAAGCATTTAAGTGTTTCCTTGGATGTGATTTGGATCATTGTCTTGCTGAAATGCCCACCCTTGTTTCATCTTTATCATCTTGGTAATGTACGTGTTAGACTGAAGCAGCTAATATTTATTTACAATAAGGAAGGGCAGAGGGTTGCTGAAGAACTACTTAGAGATTTCAGCTGCTGCCTGGGCTTTCACTGCCTTTCCACACCTAGCTTTCTTCATATATTAAATACCTTTTCCCTGCATCATTTCATTTTATTACACGTAACTTAATTTGTAAACTATCCAGATTTGTTTTCTCTGCACATATTATTTTCTTTGGTTGTTATCAATGAATTTTCAAGTCAATAGCACCTTTAGAACTGTTTTCTGAGAAATATATATATTGTACTGATTGTCTGACATGAGTGATTTTTCTTTTATGCA[G/T]CTTGATGCAGATCGAGATGAAGAGGAAGTCTTCTATGACATCAGCATGACAGTTGACAACAAACTGTTCCCCACCAAAGAACCTGTGGCAGGTAAGCATATATAAATACTACTTAATTTGGTTAAAAATATATAAGATTTTTTATAAGAATTTACAGTGTGATAACAATGTAATGGCCTAATTAAAGTACTGTAATATAATTACACACATGTTAGGTAAGGGTTTAAGCTAGGGATGTCCCGAGTCCGAGTCATTTTATTTTGAGTATCTATCGATACCCGATCCGATACTTCTATAATACATTTTTAAAAATTAAGAAGAGTGAAGAAAAAGATCCAAGATGTTATTTATTATTTAATTCACCTTATTTTAACATTCAACAACTCTGTTAAGAAGCAGAGCATTTATGTAAGGTAGCTTAAACAATCGTGCAATAAATAACATAAATTCTTCACTTTTGGACTGTAGTGCAATAGTAAATATATAAAAAAAAAATCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18317
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_10_F3
KASP Assay Location:
Unknown
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022768 | Essential Splice Site | 369 | 563 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 8654363)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 9072017 |
GRCz11 | 2 | 8870022 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCAGGCTGATGAAGAGGYGGCTGAATATGCAGAGGCGATTGGAGAAAG[T/C]GAGTGCAGTCTTTTNCAATGTATCTTCWTGCACTGTATTTGTGTGTGGGTT
Long Flanking Sequence:
CGAAGGAAACCACGTCATCACGTGGAGAACATGCAAACTCGACACAGGAATGCCAACTTACCCAGCTGCGGCTAGAACCAGCAACTTTCTTGCTGGGAGTACACAGTGCTACCATGTTGGCACTGTTAGTTGGTTGGTTGGTTGGTTGCTTGGTTGGCTGGCTGACAAACTGGTTGGTTGATTGATGATTGAGTGCCATTGCTCTCATGGCAGTGACATTTCTTAAAATACTTTTTCTTATTTGTACTTTCTAGTTTTTTACTTATTTATCTGTTACTCACCCCCCCCCCCCCTTTCTCTCATCTGTTATTTGTTCGAAATATAATCTTCAATTAATGTATTTCACATCATTCTAAGGGCAACAGGAGGCATATTTAATAATTAATTTACAGTTTTCCTGTACTTAACAGTTAACTTTATGAAAGTAAGAGCTTTTCATGTGTATCTCTGTGTCAGGCTGATGAAGAGGTGGCTGAATATGCAGAGGCGATTGGAGAAAG[T/C]GAGTGCAGTCTTTTCAATGTATCTTCTTGCACTGTATTTGTGTGTGGGTTTATTTTTTTCTTATGTTTTTTTTTATGGAGGAGTTTTTTATCTCTGTAAAGTGGCATTAATCTTAAAGGAACACTTCAATTTTCATTTACTGTCAGCCTTAGTACACGATGAAACTACAGAAGAGTCAATCTTTAAATAGGAAAATTACCAAAAAAAAGATTTAGATGCTAATGGTCTAATCCAATTCAATGATTTATGCTAAGCTAAGCTAAGCTAAAAGTGCTCCTGCCAGACCTGGAGATTGGTTGAATCTCTTAAAAAATGGTAAAACTCTACTGTTTAGCTTTAGGGCACTAGCCTATTTCCCAAAAAAGTGTGTTGTTCCTTTAAATAATGCTGTAATCAAAATAGGACAATATACTCAAATGATGTTGCACTAAGCAATATTTGAAAAATGCTTTGACCGTAGTGTCCCAAACACACTTGCAGCCAATCATCAGTAACTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2067
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
Founder:
mrf328
KASP Assay Location:
Project 554.26, Plate 64, Well B01
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022768 | Nonsense | 427 | 563 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 8647528)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 9065182 |
GRCz11 | 2 | 8863187 |
KASP Assay ID:
554-3371.1 (used for ordering genotyping assays)
KASP Sequence:
ACATCCTGTGCAGTGAGCTGCAGTCTCACAGCGAGAGAGGACGCTTTCTC[C/T]GAGACCTTCTGGAAAGAGGAGAGCAGCTTCCCGAGGTGCACAATCTTGTT
Long Flanking Sequence:
AGCATTCTTACATGATTCCAAGACTCACCATCAGTATTTAGACTATTGACTGTTTGCTGTGTATAAGCATTTTGCCTTAGGGAAATCTGCCTGTAGACTTGTGCTGTAGATAAGGGCTGCCCTGAGCTGTGTACAGAATCTTAATGAAAGCCTGTGGGAGTTCAGCCAGAAGGTAGGGTCGGGGATAGACCAACACATGTGTGTAGTATTGGCTATATACAATACATGCTGATAATCCATCTCACATCTCCCAAGACACTCAATTACTGAAGAGTTGGCCCCTTATCCCAACAGTTAACAGCACTTTCTGTCATCCATTTAATTTACTGCTTTTTAAAATTCTATTCTTCGATTTTCTCATTGTGAATATAGGTGGGCCAGGATCAGGGAAAGCTCTCCAGTCAGAAAAGATAGAAGAGCGGTACAGTTTGAAGCGGCTGTGTCCCGGGGACATCCTGTGCAGTGAGCTGCAGTCTCACAGCGAGAGAGGACGCTTTCTC[C/T]GAGACCTTCTGGAAAGAGGAGAGCAGCTTCCCGAGGTGCACAATCTTGTTAAAATCCATTACTGGAAGAAATTACAATGACCGGCTTCTCCTTAACTGAATTGAATGCTTTTGCTGCAAACACACACTGTAGACACACGATTTCGTAACACGTCTGAGTGCTTTTAACCTTTGAAGGATGCTTTATTTAATAGCCTGGTCAGTAATAAATACTGGCTTTAGGGAAAAGAATGGGACAAGAAGTTTGGGAAGTCCCAGCTAACAACGAACGTTCTTGTAATTTTAGTTATATCAAAGTTGTTTGTAGAAAGTTTCCTTAAATGTTATCTGTAATTAATATATGTTCTAAAAAAATGTTATTAATGTGTTGTTGGGGGAATGTTTTAAAAACGTTTGCATTATAAACGTTACAATTAAATTATGAATGGAACACGCTGAAAACGGTTTAATTTTAGTCTTTAGACTAAAATTCAATTTTAATTTAGGTAATTTTTTAGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32843
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_11_C12
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022768 | Nonsense | 480 | 563 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 8640822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 9058476 |
GRCz11 | 2 | 8856481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATCTGCTTGTGTGTGTGTGTATGTGTGTGTGTGTGTTTCAGATGGGC[C/T]AGCCAGACATAGTTCTGCTACTTGAATGTTCTGCAGACATCATGAGTCGA
Long Flanking Sequence:
CTTGAATTAACTTCACAACAAATACATCAAATAATCATTGGGAATGTTCTTACTTAAGTATTTCTCACAAACATTACGTGAGATCTGCTTCCTTCATGTCTGTCACTGTGCTGTTTATCTGACGCAGCCAGTAAGGAGGACACTCTGGGGACACTCTGATTCTCATGTGGGAACAGTGGTCAGGTAGAACTAGCAATAAAGGCACAAGCAACAAAAACTACTTTGTGTTCAAAGCAGAAAATTCCAATGTTCTGAAAGCTATAATAAATAATCTGATGGGTGTTTTAACCTGGAACTTTACAGACACATTCTGGAGACATAAAAGACTTATCTTAAATCTAGTAGAAGAGGTAAAAAGTCAATGCCTGTTTAGTTTTTGAGTAAAAATTTGACAGTTATTGCTTCTTTTTTAACTCTTTCAATCACTGTAATTTGTGTCACAAGATCTGACAGATCTGCTTGTGTGTGTGTGTATGTGTGTGTGTGTGTTTCAGATGGGC[C/T]AGCCAGACATAGTTCTGCTACTTGAATGTTCTGCAGACATCATGAGTCGACGGCTACAGCAGAGGGCCACCTGCAGCCTGCACAGTAAAGAAGCCCGAGACAGAGATACTCGCCGTAGAGTAGACGGGTTCTGCAGCCTGATCAATCCTGTGGTCGCTCACTATCAACACAGAGAATTTTTCCATAAGGTTGGTGCATGTGTTAAAGCACAGCTACACTGAGGTTACAGCATAATACTCACATAATCTGGTAATGAGTTTGGACAAACACTTCCTGTTTACTTCACCTCTAGCTGTGGTTGAGACAGCTCTCTGCGTTCATAGCCACCAAGCAATTTTGTGTTTAACAATAGTCCAAGAATAGAGCAGGCATCAAATAGACAGGAGTGAAGAGTTGTTGCCATTTACCTATTTTTAATTGGATTTTGGAATTCTGCATAAAAAATGCTTAATGCATACATTTTGAAAATAAAAACTCATAAGTGGGATAAACTTTTTATT
Associated Phenotype:
Not determined