ZMP
hk2
Ensembl ID:
ZFIN ID:
Description:
hexokinase-2 [Source:RefSeq peptide;Acc:NP_998231]
Human Orthologue:
HK2
Human Description:
hexokinase 2 [Source:HGNC Symbol;Acc:4923]
Mouse Orthologue:
Hk2
Mouse Description:
hexokinase 2 Gene [Source:MGI Symbol;Acc:MGI:1315197]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40376 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33551 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40376
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032042 | Nonsense | 688 | 919 | 15 | 18 |
ENSDART00000057637 | Nonsense | 688 | 919 | 15 | 18 |
ENSDART00000128401 | Nonsense | 691 | 922 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 15367913)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 13478738 |
GRCz11 | 5 | 13978955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTAAATGCGTTATGTCTATCCTATAGGTACGGGAACTAATGCGTGCTA[C/A]ATGGAGGAGATGTCAAACGTTGAGCTGGTGGATGGAGATGAAGGCCGCAT
Long Flanking Sequence:
ATCCTTGGCAAAGAAACTTTTCAGAGTCATCTGTTTCTTTCTCATTTTTGCTTTCTTGTGGGTTAAATGTTGGCCCTTAAATGACTGTGAATGTAACCGAGAGAATACAGTCATTTTTCAAAATAAAAGATCGTTCAGACCCAGATAATAAATAAAACTTAAATATTCAATGATTTCCTGTACAGCTCAGTACCAATTAGCCTGGGGGTTGGGGATCACTGTACTAGCTGATAGATGTAGATTGATAATAACATCTAATAAAAATAAAAATAACTATTATATATTGATTATTATATATAACAAATTTTATTTTTTTACTGAAATGTGTTCTATCTTTCATCTGCTGTCATTAAATGCAATATTATTTGTTATTTAATAATCTAACATGGCATTAATTTTTAAATTGGTATATTTTATATGTTTACGTGTGCATCAGACATCATGATGTGTAGTTAAATGCGTTATGTCTATCCTATAGGTACGGGAACTAATGCGTGCTA[C/A]ATGGAGGAGATGTCAAACGTTGAGCTGGTGGATGGAGATGAAGGCCGCATGTGTGTGAACATGGAGTGGGGGGCATTCGGGGACCAAGGGGAGCTGGATGACATTTGGACAGAGTTTGATCGAGCTGTCGATGACCAGTCTACTTACCCAGGGAAACAACGGTGAGAGTTCAGACTCAGATCTTTCATGCAATGTTCATGTCATCTTTCCCATTCCAGTCCTGTGGGCTTTTAGATTTGAGCTTCAGAATGGCGAATCTCCTCTGAAAGTCTGATGTTTGAATCTGTTCAGAATCATCACTTCATTTTTTTTTTTCTGGCTTCCAGTCACACATCAAATAGATTTTTAAAGTGCTATTACTTATTTATAGAGGAGTCAATAAAAATAAATTATGGCTATGCTCACGGAATGTAAAGCTAATGGATCTGAGATTATTCCATTCAGGTCAGCTTAGTATAATGCTTTGGGTTCGTTTTAAATATGATGAAACAGCGTTTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33551
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032042 | Nonsense | 913 | 919 | 18 | 18 |
ENSDART00000057637 | Nonsense | 913 | 919 | 18 | 18 |
ENSDART00000128401 | Nonsense | 916 | 922 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 15393698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 13503626 |
GRCz11 | 5 | 14003843 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAGACGGCAGTGGAAAAGGTGCTGCCCTCATCACAGCGGTGGCCTGT[C/T]GATTAAGAGATGCGGGGAAGTAGTGACTGAGTGAAATGATCTAAAGGGCA
Long Flanking Sequence:
TTTCGTGATCTTGATATTGTGATATTGATATTGTGATCTTGATATCGGGATCTTGATATCGTGATATTGATATTGTGATGTTTTTATAATTTTTTGTTGTTTTATGCCGAAAATGATTTAATTTTTGGCCTAAAGTGTCAATGTCAGTTGATGCCAAATGTCATCAGTAGTTAACAGAATAAAACAGTATTGTTTGATTTACTCAAAGACAATATAAATAGCACAAAAGGCACTAATGGAGTTCTGAAAAAGTTGGGCAATTTTGTGAAAAAAAAACAAAACAAAAAATAATTAAATATATCAGATTTAGCTCATGCTCTGATTTCCTCTCTCAGAAGTGTCATTTTTCAAGCACGAATGCTCTCCTCTTTTGTCTCATCAGCTTTGCCACCATCATGCGGGAGACCCTTAGAGACCTGGCACCCAATTGTGAGGTCAGTCTCGTCCAGTCAGAAGACGGCAGTGGAAAAGGTGCTGCCCTCATCACAGCGGTGGCCTGT[C/T]GATTAAGAGATGCGGGGAAGTAGTGACTGAGTGAAATGATCTAAAGGGCAAAAGATAATGAGGAGGAAAGAAAAAGTGATGTTCTGAGCTTCCTAAGATTTTCAGTGTATGTGTGTGTTTGTGTGTGTGCGCCACAATGTGACCTTACTGAACCAACACTCCTGTTTTGTCCAAGAATGTATCTTATTTATTTTTCTCCATTTTATGCTTTTGATCACACTTTGCAAAGACTCAGCGTGTGCTGGTGGGGGGGTTATATGAAGACAAGGGAAAAAAGGAAAGCAAATAACTAGACTACATCCTTTCATGGTTATATTATATATTTGTATAGTTACTGGTTTGAATCATTGTACTTTCTATAAAAAAAAAAAATGCACCTTAGAGCTGTGAATGGTGTCGTTTGTGCTTGCACCTACTAATACATGCATGGTTCTGATTGAAAAGTTTGTTCATTTATTTACACAGTCATGGAAGTAGGTGAGTAAACAGTTTTATTTTTA
Associated Phenotype:
Not determined