ZMP
si:ch211-215l11.5
Ensembl ID:
ZFIN ID:
Description:
im:6895556 [Source:RefSeq peptide;Acc:NP_001157278]
Human Orthologue:
G6PC
Human Description:
glucose-6-phosphatase, catalytic subunit [Source:HGNC Symbol;Acc:4056]
Mouse Orthologue:
G6pc
Mouse Description:
glucose-6-phosphatase, catalytic Gene [Source:MGI Symbol;Acc:MGI:95607]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27878 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa22025 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27878
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 > G
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091868 | Missense | 149 | 355 | 3 | 5 |
ENSDART00000130087 | Essential Splice Site | 138 | 352 | None | 6 |
The following transcripts of ENSDARG00000013721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 6727972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 6010892 |
GRCz11 | 12 | 6044476 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCATCCTCGCCATAATGCTTAGCAAAGGGAAGAAATCAACATCCAAT[A/G]GCCTGTAAGTCAATCCCTATCATACAATAAAGTCATTTGACATCACCTGG
Long Flanking Sequence:
ATGACCCCATTAAACCGGGAAAGGTCCTCAAACAAAACAAGTCAGCTTATAGGCCTATAAGTCGACAAAAATGTAAACTAATATTCACAGAAATCTTCGTGATGGATTTAACTTACACAAGGTTAAAATGTTTCAAATTGTTTCCTTCATTAGTTTCGGTTTTATATCGATTCTTATGTTGTTAAATGAACGTATATTGTATTATCTTTGTATAACTATGATGTACTTTTAAATTTGTGTTTATGACACCAATAATTTGACTATTTTGCTTAACTTTAACGTGGTTTTCCCTTTGCTTACTGTGTGGCAATTAGCATATAAGAAATTAGCATCTTCAAAGCTATTTCATCTTATAGCAAAAATCCCTCACTCAACTTGATCTTCTTCTTGATACAGGTAGCCCATCAGGTCATGCTATGGGTGCTGCTGGTGTTTACTACACACTGGTCACCTCCATCCTCGCCATAATGCTTAGCAAAGGGAAGAAATCAACATCCAAT[A/G]GCCTGTAAGTCAATCCCTATCATACAATAAAGTCATTTGACATCACCTGGAGCTTTGGTTTCAAATTAGTGGCTTTGTGCAATGCATTCATACTGTTTGTTTTCTTCTCAGATACTTGCGTGGCTCACTTTGGACACTCTTCTGGACGGTCCAGATCTGTGTTTGTCTCTCTCGGGTCTTCATCGCCGCTCATTTCCCACATCAAGTTTTCGCTGGTGTCATTTCAGGTAAGCATTTTTAGATGAAACTGAAGTTTTTCACTGCATGTAAAAAGATGTTTGTGACAGAATAGGGCATCAATGGAAATTGAACCCATGACCAGTAATAGCTGTTGGAAAAATCAGGAATAAATAAATTTTTTAAATACATTACAACAGAAAATGGTTATAATGGTTGTAATATAAATGGTTGCAATAATACTACTGGCTGTACATAAGTGAAAATAGATTACTTCTTGAAAAAACCAGCTTAAACCAGCCTAGGTTTTAGGTTTTAGTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22025
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091868 | Nonsense | 157 | 355 | 4 | 5 |
ENSDART00000130087 | Nonsense | 154 | 352 | 5 | 6 |
The following transcripts of ENSDARG00000013721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 6728104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 6011024 |
GRCz11 | 12 | 6044608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCATTCATACTGTTTGTTTTCTTCTCAGATACTTGCGTGGCTCACTTT[G/A]GACACTCTTCTGGACGGTCCAGATCTGTGTTTGTCTCTCTCGGGTCTTCA
Long Flanking Sequence:
TCAAATTGTTTCCTTCATTAGTTTCGGTTTTATATCGATTCTTATGTTGTTAAATGAACGTATATTGTATTATCTTTGTATAACTATGATGTACTTTTAAATTTGTGTTTATGACACCAATAATTTGACTATTTTGCTTAACTTTAACGTGGTTTTCCCTTTGCTTACTGTGTGGCAATTAGCATATAAGAAATTAGCATCTTCAAAGCTATTTCATCTTATAGCAAAAATCCCTCACTCAACTTGATCTTCTTCTTGATACAGGTAGCCCATCAGGTCATGCTATGGGTGCTGCTGGTGTTTACTACACACTGGTCACCTCCATCCTCGCCATAATGCTTAGCAAAGGGAAGAAATCAACATCCAATAGCCTGTAAGTCAATCCCTATCATACAATAAAGTCATTTGACATCACCTGGAGCTTTGGTTTCAAATTAGTGGCTTTGTGCAATGCATTCATACTGTTTGTTTTCTTCTCAGATACTTGCGTGGCTCACTTT[G/A]GACACTCTTCTGGACGGTCCAGATCTGTGTTTGTCTCTCTCGGGTCTTCATCGCCGCTCATTTCCCACATCAAGTTTTCGCTGGTGTCATTTCAGGTAAGCATTTTTAGATGAAACTGAAGTTTTTCACTGCATGTAAAAAGATGTTTGTGACAGAATAGGGCATCAATGGAAATTGAACCCATGACCAGTAATAGCTGTTGGAAAAATCAGGAATAAATAAATTTTTTAAATACATTACAACAGAAAATGGTTATAATGGTTGTAATATAAATGGTTGCAATAATACTACTGGCTGTACATAAGTGAAAATAGATTACTTCTTGAAAAAACCAGCTTAAACCAGCCTAGGTTTTAGGTTTTAGTTGGTCGACCTAGCTGATTTTAGCTTGTCATTTGACCCTGACCAGCTAAGACCAGGCTGGAAATGGCTGGAAACCAGCCTGGAAATGGCCAAAACCCCTCTAAAACCAGGCTGGTTTGGAAAAATCCAGCTTAAAC
Associated Phenotype:
Not determined