ZMP
si:dkey-96f10.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
PFKFB1
Human Description:
6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 [Source:HGNC Symbol;Acc:8872]
Mouse Orthologue:
Pfkfb1
Mouse Description:
6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 Gene [Source:MGI Symbol;Acc:MGI:107816]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18547 | Nonsense | Available for shipment | Available now |
sa14640 | Nonsense | Available for shipment | Available now |
sa32429 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18547
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 |
---|---|---|---|---|---|
ENSDART00000012724 | None | None | 99 | None | 3 |
ENSDART00000103231 | Nonsense | 153 | 304 | 3 | 8 |
ENSDART00000139166 | Nonsense | 192 | 342 | 5 | 10 |
ENSDART00000146640 | None | None | 227 | None | 5 |
The following transcripts of ENSDARG00000074457 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12816318)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 12948251 |
GRCz11 | 23 | 12704328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCACATGAGGAGAACAATCCAGACTGCAGAAGCGGTTGGAGTGCCATA[T/A]GAACAATGGAAAGCTCTGAATGAGATTGATGCTGTGAGWACAGTCCTGTA
Long Flanking Sequence:
TTGTTTGGTTGTTGTTTGTTTTGAAATTTGCGAATCAGAAGTTGTCTAATAATAAACCCGAAACACATGTGGTTGTTGTCATGGAGTGAACTTGGCCAATCGTGTAATATCGGTGTCGTCATCAGAGCTTGAGCAGTAGATCTTCAGATGCTGCACAGTCTGAATCAGTCGTCTGATCTGAGCACTTTCGCGGTACTTTGATGCCACATGTGACAGTCACGTGGTGTTGGTGCAGGATCAATCCGGACAAAATTTCTTACCAGCATGCACCGCTTTAAAACAGATTTCTATCCGTCTCCACAGCGCTGCATGAAGTTGAACGCACCTATTTTCTTAAATACATAGACCAGTATCCATACAACTATCCAATGACCACATTTGTGTCAGTTTGCTGCAGCTTTAGGCACCTATATCAGGGGTCAGCATATCCTGGACCTGAAGATCTGGACCAGTCACATGAGGAGAACAATCCAGACTGCAGAAGCGGTTGGAGTGCCATA[T/A]GAACAATGGAAAGCTCTGAATGAGATTGATGCTGTGAGTACAGTCCTGTATATAGTTGCAGATGATATTCACAGCACTACCCATTGGGCCATTTGTTTTGCTTCTTTCTCAAAATGTGCTTTTGTTATGAAGGGATTTGTTAGAGATTCTATATAAATTGTCTTCATCTGCAGGGTGTATGTGAGGAGATGACATATGAAGAGATTCAAGAACACTTTCCTGAGGAGTTTGCCCTCAGAGACCAAGACAAATATCGTTATCGATACCCAAAGGGAGAAGTGAGTGTGTTTAAATATGTTACTCATCACTATGGTTTCGTCCACTGTGCTGTCGCATCACAGCAAAAAGGTCACTAGGTGGGTTCGAACCTCGGCTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCCTTCACGTGGGTTTCCTCTAGGTGCTCTGGTTTCCCCCACAGTTCAAAGACATGTGGTACAGGTGCATTGGGTAGGCTAAATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14640
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 |
---|---|---|---|---|---|
ENSDART00000012724 | None | None | 99 | None | 3 |
ENSDART00000103231 | Nonsense | 193 | 304 | 4 | 8 |
ENSDART00000139166 | Nonsense | 232 | 342 | 6 | 10 |
ENSDART00000146640 | None | None | 227 | None | 5 |
The following transcripts of ENSDARG00000074457 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12816058)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 12947991 |
GRCz11 | 23 | 12704068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACACTTTCCTGAGGAGTTTGCCCTCAGAGACCAAGACAAATATCGTTA[T/A]CGATACCCAAAGGGAGAAGTGAGTGTGTTTAAATATGTTACTCATCACTA
Long Flanking Sequence:
CAGCATGCACCGCTTTAAAACAGATTTCTATCCGTCTCCACAGCGCTGCATGAAGTTGAACGCACCTATTTTCTTAAATACATAGACCAGTATCCATACAACTATCCAATGACCACATTTGTGTCAGTTTGCTGCAGCTTTAGGCACCTATATCAGGGGTCAGCATATCCTGGACCTGAAGATCTGGACCAGTCACATGAGGAGAACAATCCAGACTGCAGAAGCGGTTGGAGTGCCATATGAACAATGGAAAGCTCTGAATGAGATTGATGCTGTGAGTACAGTCCTGTATATAGTTGCAGATGATATTCACAGCACTACCCATTGGGCCATTTGTTTTGCTTCTTTCTCAAAATGTGCTTTTGTTATGAAGGGATTTGTTAGAGATTCTATATAAATTGTCTTCATCTGCAGGGTGTATGTGAGGAGATGACATATGAAGAGATTCAAGAACACTTTCCTGAGGAGTTTGCCCTCAGAGACCAAGACAAATATCGTTA[T/A]CGATACCCAAAGGGAGAAGTGAGTGTGTTTAAATATGTTACTCATCACTATGGTTTCGTCCACTGTGCTGTCGCATCACAGCAAAAAGGTCACTAGGTGGGTTCGAACCTCGGCTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCCTTCACGTGGGTTTCCTCTAGGTGCTCTGGTTTCCCCCACAGTTCAAAGACATGTGGTACAGGTGCATTGGGTAGGCTAAATTGTCCGTAGTGTATGAGAGTGTGTGTGAATATGTGTGTGGATGTTTCCCAGAGATGGTTTGCGGCTGGAAGGGCGTCTGCTGCGTAAAAACTTGCTGGATAAGTTGGAGGTTCATTCCGCTGTGGCGACCCTGGATTAATAAAGGGACTAAGCCAACAAGAAAATGAATGAATGAATGAATAAATAATGCATGTCACTTCGGGTTGCATTATGAATTATGAAGTTTATGCTCCGACATACAGATTATATCTTTCCAGAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32429
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 |
---|---|---|---|---|---|
ENSDART00000012724 | None | None | 99 | None | 3 |
ENSDART00000103231 | Nonsense | 218 | 304 | 5 | 8 |
ENSDART00000139166 | Nonsense | 257 | 342 | 7 | 10 |
ENSDART00000146640 | None | None | 227 | None | 5 |
The following transcripts of ENSDARG00000074457 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 12800563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 12932496 |
GRCz11 | 23 | 12688573 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGGATCTGGTTCATCGTTTAGAACCGGTAATCATGGAGCTTGAGCGC[C/T]AGGAGAATGTTCTGGTCATTTGCCATCAGGCTGTCATGCGCTGTCTGCTG
Long Flanking Sequence:
TTGTGGAGCTAGCTCATTGGCTGCAGAGAAAACAGCAACCAAACTTCTGTGCCATGTAGTTAATGACATAGGGGCAGATTAAGCGTTTAAGCCTGCACATACATATTATGACATAACTTTGTATTTACCCTTCAAGTATGAGAAGGAGGCAACAAGAAGGCAAAAAAACAACCTTCATTTGCAGCCAAACATATGACACTTACCTTATGAAATTGAATTGCACCAACTCCAACTCCCCAACATCACCATCATATCAAAGAGGAGGTTGATGCTCAGTTTTCATGGAATTGCGAAAGTATTTCAGGCAAGAAAAAGAAGCAATAAACACATTTACTTTTGTCATAACAAACCTATATGGATAAACTATATTTTGAGAAACAATTAACTTTGTCATGTTTAAGAATATTTTGTTCACTCAGTAAAAATCAGTGTGTATGTGTGTTCAGTCCTATGAGGATCTGGTTCATCGTTTAGAACCGGTAATCATGGAGCTTGAGCGC[C/T]AGGAGAATGTTCTGGTCATTTGCCATCAGGCTGTCATGCGCTGTCTGCTGGCATACTTCCTGGACAAAACTGCAGGTAGAGAGTTTTTTAGAACACATTGCACTTATTTTTAAATAGATTTTAAATGCTAAAAAACTTGGTCAAAGTCTAAAAAAAACTATTATTTGTGAACATTTGGGAATGATGTCAATCTGAATATTACACAGTTAGAAAAATATTGTCTACACATGGAGAAATTATTAAATGTTGCTACTAAGACATTCTGAAAAAATGTTCAATATGCAATTCTAAAAGAAATGATTTACCTCAAGAAAACTTGAGGTAATTGCAAATATCTTTGTTTAGAGTAACTTAAAGTTTTTTTACTTTGCACTCTTTTGTATTGTTATTTATTTTATTTTGGACTTTTAAATTAGATCAATTTATAATATAATCTAATGCAAGATTTTCATGAGTCAGGCAAGTTTAACAACTTTTTTACTTCAGTTCAAATCTCGCAA
Associated Phenotype:
Not determined