ZMP
hkdc1
Ensembl ID:
ZFIN ID:
Description:
putative hexokinase HKDC1 [Source:RefSeq peptide;Acc:NP_001108597]
Human Orthologue:
HKDC1
Human Description:
hexokinase domain containing 1 [Source:HGNC Symbol;Acc:23302]
Mouse Orthologue:
Hkdc1
Mouse Description:
hexokinase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2384910]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42190 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42189 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42188 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22286 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42190
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056523 | Nonsense | 401 | 919 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 23163887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22893225 |
GRCz11 | 13 | 23023675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGGTGGCTGCAGCTTTGGCTGCCATCCTAACACGGATCAGAGAAAAC[A/T]AAAAGCTGAAGACCCTTCGGACTACTGTAGGAGTGGATGGGACGGTCTAC
Long Flanking Sequence:
ATGAAAAGAAGATGGACAAATGAGAACCTTTCTGTCATACACTATAGTAAAACAGCTTGTCAAAAGCTGTGAACAGATTACATACAGGAATAGAGAAAAGAGCCCTCTTTAATTATCAGCTGTTAGTCAGCGCCCACTCTTTTTTCCTGGTGATTGCGCCTTTGCCGTGTGCTGTGTAAGTGCAGACGATCGGATACGAGTCCCTTTTAAAAGATGATGTAAGCAGGTCATCAAAAAAATCGGATACAGTCCCAAAATCGAAATTGACCATCAAGATCTGCAGTGTAAATGCAGCCCTATATGTGCATATTCTAATTGAGGATTTTTCCAGGTATAAAAGCGGTTTGGAAAACACCAAGGAGATCCTGGAGGACCTAGGACTAAATCCCAGTGACGATGACTGTATTGCAGTCCAGCATGTCTGCACCATCGTGTCCTTCAGGTCAGCTAATCTGGTGGCTGCAGCTTTGGCTGCCATCCTAACACGGATCAGAGAAAAC[A/T]AAAAGCTGAAGACCCTTCGGACTACTGTAGGAGTGGATGGGACGGTCTACAGAACACATCCACAGTACGTCAGTTCTCCTCAAATGTAAAATCCAAGGAGATTAATTTAAAATCAGAAGCGGCTAAATACTTTTATCTGATATTTAAAGGTACCCCAAAAGGCTCCACAAGGTGGTCCGCCATCTGGTGCCAGACTGCCATGTGCGTTTTGTGCTGTCTGAAAGTGGCAGTGCCAAAGGTGCCGCTATGGTGACCGCCGTGGCTCAGCGATTAGCCTCCCAGCGGAAAGAGATTGATGATACCCTTGCAGCTTTTGCTTTGACTTCCACACAGCTCCAGGAAGTGAAGCAGAAGATGCATGTTGAGTTGGAACGAGGCCTGAAAAAAGAAACCCATCCCACTGCTTCAGTAAAAATGCTGCCCACATATGTTTACAGGACACCAGATGGGACAGGTAATAGAAAATACCTACTTATTTATTTATTTGTTTGTTTATTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42189
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 |
---|---|---|---|---|---|
ENSDART00000056523 | Nonsense | 581 | 919 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 23162961)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22892299 |
GRCz11 | 13 | 23022749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTATTTATTTCCGTTTAATTTCAGCTGTTTGACCACATCGTTCAGTG[T/A]ATCTCAGATTTCTTGGACTATATGGGAATGAAGAACACTCGTCTGCCACT
Long Flanking Sequence:
ATATGTTTACAGGACACCAGATGGGACAGGTAATAGAAAATACCTACTTATTTATTTATTTGTTTGTTTATTTGCTTGTTTGTTTGAAGTCTAAGCATGATGATAACTGAGTAATTAGGATGTAAATTTTACTTTCACAGAAAGGGGAAAGTACCTTGCTTTGGATCTTGGTGGAACCAATTTCCGCGTGTTGGTGGTTAAGATTCGGACTGGCATGCGAAATTCAGTCCGGATGTACAACAAAATTTATGCCATCCCACTGGAGATTATGCAGGGCACAGGAGAGGAGGTAAAACACTATAAACAAATATGTTTTCATTATTTTTGTACAGTTAACGATGTATGTATATTATAATAATGTATATTATTACCATAATATACCCTATTTCATTTTAACACAATTTATATAGTCCAAAAAACTCAGCACAATAACAAGAATTTATACTGACCTATTTATTTATTTCCGTTTAATTTCAGCTGTTTGACCACATCGTTCAGTG[T/A]ATCTCAGATTTCTTGGACTATATGGGAATGAAGAACACTCGTCTGCCACTTGGCTTCACCTTCTCTTTCCCGTGCAATCAGACAGGTATTGATAAGGTAAAAAAGCATCTACCTCCAGTTATCAGTTTCTTTAATTGTCTATAAAAATAAATGAACGTATACTCAACCTGTTAAAACACACAGATAAACCCTGTGCTCAAATGATTGTCAAAGTCATTTTTCTTGCCCATTTGTTCAGGGAGATCTGGTCTGCTGGACAAAGGGCTTCAAAGCGACAGACTGTGAAGGGTATGATGTTGTGGACATGCTGAGAGAGGCCATCAAAAGACGAAATGTGAGCAGAAAGCAAACATAGTAAAGTAGTTTTACAGATCACACTCCTACACTTAAAGCGTAGCAGCACTATCATCAATACTAATGAATTGGGTTACATTTTCATGCATTCAGAGATTTGATTTAAAACAATAATAACGATTTATCTTATTTCTAACTGGAGCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42188
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 |
---|---|---|---|---|---|
ENSDART00000056523 | Nonsense | 644 | 919 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 23162632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22891970 |
GRCz11 | 13 | 23022420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTGAAGGGTATGATGTTGTGGACATGCTGAGAGAGGCCATCAAAAGA[C/T]GAAATGTGAGCAGAAAGCAAACATAGTAAAGTAGTTTTACAGATCACACT
Long Flanking Sequence:
CAGTTAACGATGTATGTATATTATAATAATGTATATTATTACCATAATATACCCTATTTCATTTTAACACAATTTATATAGTCCAAAAAACTCAGCACAATAACAAGAATTTATACTGACCTATTTATTTATTTCCGTTTAATTTCAGCTGTTTGACCACATCGTTCAGTGTATCTCAGATTTCTTGGACTATATGGGAATGAAGAACACTCGTCTGCCACTTGGCTTCACCTTCTCTTTCCCGTGCAATCAGACAGGTATTGATAAGGTAAAAAAGCATCTACCTCCAGTTATCAGTTTCTTTAATTGTCTATAAAAATAAATGAACGTATACTCAACCTGTTAAAACACACAGATAAACCCTGTGCTCAAATGATTGTCAAAGTCATTTTTCTTGCCCATTTGTTCAGGGAGATCTGGTCTGCTGGACAAAGGGCTTCAAAGCGACAGACTGTGAAGGGTATGATGTTGTGGACATGCTGAGAGAGGCCATCAAAAGA[C/T]GAAATGTGAGCAGAAAGCAAACATAGTAAAGTAGTTTTACAGATCACACTCCTACACTTAAAGCGTAGCAGCACTATCATCAATACTAATGAATTGGGTTACATTTTCATGCATTCAGAGATTTGATTTAAAACAATAATAACGATTTATCTTATTTCTAACTGGAGCACTAAAACATTTTGTTTTTTTTAACAAATAACTAACGTTACTTTTCAGTTGTGTTGCTTGATTTAACATGCCATCCTGTTTGGTAATGGTAGCATGAATTGAAACTTTGCTAATAAGTTTAGAAGCAAAGATTAACATCGCTAACCTGTTTTAAAGCATTGTTTCAATGCACTACTAGCATGTTTATCGCTTACTTTAGCACATTGTTAGCATGTTCAACTGGTTTTTTTAATAATTGTTAGCATATGCTATGCTAGTCGCTAATCTTTGCTCATGATAGATAGCTACAGTAGAACTGTTTAAATCCTGTAAGATTTACTGTTTGAAAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22286
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056523 | Nonsense | 739 | 919 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 23161155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22890493 |
GRCz11 | 13 | 23020943 |
KASP Assay ID:
2260-6353.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACCAGATATGACAGAGAGGTCGACAGCGGCTCACTCAATGCTGGGAAA[C/T]AAAGGTAAATATTACAATGTTTCGATAGTTTTATTATAACATTTTTAATA
Long Flanking Sequence:
TTCATTTAAAGCACTTTGAATTACCCTTGTGTATGAAATGTGCTATATACAGTAAACAAACTTGCCTTGCATTGATAACATGTTAACATAATAACTTGTTTTTACAGGAGTTTGATCTCGATATCGTAGCTATAGTTAATGACACAGTTGGCACAATGATGACCTGTGCATATGAGGACCCTAAATGTCAGATTGGTCTTATTGCTGGTATGTATTAATGCATTTCTGTGGTATTTTAGGCTACCTTACTCCTCATTACAAACCAAAATATGTACAGAAAGAAATATAATTTTCAAACATGCATGATTCTTAACTCTACAGGAACAGGAAGCAATGTGTGTTACATGGAGGAGATGAAGAACATTGAGATTGTTGAGGGTGATGAAGGACAGATGTGTGTAAACACTGAGTGGGGAGGTTTTGGAGAAAATGATAATATTGAGGACATCCGGACCAGATATGACAGAGAGGTCGACAGCGGCTCACTCAATGCTGGGAAA[C/T]AAAGGTAAATATTACAATGTTTCGATAGTTTTATTATAACATTTTTAATATTATGTATTTATACTGTATAGTTTATATAGTTTTATTTTTTTATGGTTATCTACACAATTGTGCAAGGTAAATGCAATGCAAGGTTTCTGCGTTTGTCCACATGGAGGCAGCATACTATAATGATTCCCTTAAAACATAGGAATGGTGTTAGCAACCTGTTGTAATACACAAAAAAAAATGTCTTTAAATAGCAAAAAATATATATAATTTTTATTTGACGCTTTTTTTTTTGTTTTTTGCTACTAAATACAAATGTAATTTTACTATTGTTGTTATTAAATATTTAATCAATTAAAATATACTAAACATTAAAATATACAATATATACTATAATTCACTCATTTATTTTCTTTTCGGCTTAGTCCTTTTATTTATCTGGGGTCGCCAGAGCAGAATGAACCGACAACTTATCCAGCATATGAAATTAAGCAAGTTTACACAGTGGATGT
Associated Phenotype:
Not determined