ZMP
tigara
Ensembl ID:
ZFIN ID:
Description:
Probable fructose-2,6-bisphosphatase TIGAR A [Source:UniProtKB/Swiss-Prot;Acc:Q29RA5]
Human Orthologue:
C12orf5
Human Description:
chromosome 12 open reading frame 5 [Source:HGNC Symbol;Acc:1185]
Mouse Orthologue:
9630033F20Rik
Mouse Description:
RIKEN cDNA 9630033F20 gene Gene [Source:MGI Symbol;Acc:MGI:2442752]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38041 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38040 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24639 | Essential Splice Site | Available for shipment | Available now |
sa44263 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38041
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111158 | Essential Splice Site | 11 | 256 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 25 (position 17326786)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 16873330 |
GRCz11 | 25 | 16969730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGACGCGTCTGCGACATGCTCGCCTTTGGTTTAACAGTAGTCCGACAG[T/C]AAGTTCTGTTTTGTTTGCTTTATGAAAGTGATTTGTTCTATTCATAGTTA
Long Flanking Sequence:
TATGAATTTTATCATACCAAGGCAAGAGAGATGGCCTAAACAAATGACAGTTTAATAAACCAAGAAGCGGCGTATGTGAATGATTTTGTTTCAGCGTCAACAAACTAAAGAGCACAAAATTAACCAATTGGTTAAATACAAAATGTATTTAATAAAAAAACTATGATTAACAACGTTAGCTGTATCGGTAAAACTTGAGTACAAGCCTTGAATCTATAGGATCTCTGAAGTGTTGATTGAACCGTTCAAAAAGAATCAATTTGTAAAATTGAATCGGATCTCAACGCATGCGTACACATTTCCGGCTTGTCAAACACCGGGATAAGAGCTGTCAGAGAGCTGTGACCCAAAATCAGCAACAACTGGCGGCTATTTGAAAACGTAAAAAGGGCTGAAAGCTTGTTATTGACTCCGAGTTGGATATCAACGGTGAAGATATTGTATTATTTTCACGACGCGTCTGCGACATGCTCGCCTTTGGTTTAACAGTAGTCCGACAG[T/C]AAGTTCTGTTTTGTTTGCTTTATGAAAGTGATTTGTTCTATTCATAGTTATTTACACTGCACAATTGGTTAAGTAATTGTAAATAAAAGTGATTTGAGCAGTTTAGAAGTTGTTAGTTCTAACGTATGTAAAGCGCTGTATACAGTATAGTAGCCTATAAGTTAACTAAAATCACGCCACAGATTGAGTAACCTAGGTAATGTAATGTAAGTAACATTAGAGCTTCTCTAGAGGCAATAAGGGTTCCTCATATTGTATTTCTCGTGTTGTTGTAGCTTATGCCTAAAGGTCAATACGAATCCATCTTTAGTGAAAGGTCAGAGGTAAACTTACTCAAACGGCAACTTCTACATTCACTATATATGTTAAATAGACAGATAGGCTACATATATTTAAAATATATTATATTTTAACATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATTTATATACACATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38040
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111158 | Essential Splice Site | 24 | 256 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 25 (position 17325082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 16871626 |
GRCz11 | 25 | 16968026 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTGCCAGTGGTGAGACGCAGTGCAACAAAGATGGCCTTTTACAAGG[T/G]AATTGTTTAGAGAGAAAATTAAAACATATGTTATCTCTACGCATTGAGGT
Long Flanking Sequence:
TCAATAGGGACCTTTTAGGCACAAATCTTTACAAAAAAAGGTACCATCCCAGTGACAGATCAAGTACCTTTAGTTCTGAGAGTGTAGAGGGGCAGTCAAAAGGTTATTATGATGATAATGATAATAATAATAATAATTGCAAAAAAACAAGGCTCACCCAATTTTTTAAATTTATTATTAAGTTTCTCAACCTCATATTTATTTATACATAATAATAAGCAGCATATAATGTAAATAAAAAAAATCATAAACACCATAATTCATTTCAGTCATTGCTTCTGATGATACATGAAGAAAAATGAATATGTTTGAGAAAAAAGTATTACATATAATCCACAGCCTTGGCAAAAGGTCCTCTTTTTATTCAACAACAAAGGTGTGCTGGCTTGCAGTGTATAATGAAGGGTAATGAAGTGTGTAATAAAGCTTTTATTGATTACTTGTGATGTGTTTTTTGCCAGTGGTGAGACGCAGTGCAACAAAGATGGCCTTTTACAAGG[T/G]AATTGTTTAGAGAGAAAATTAAAACATATGTTATCTCTACGCATTGAGGTTTATTATTAGCCTATTTAAATTTCCACATTGTGACCACATCTATCATTTCAACTTTAGGTCAGAAAATAGACTCTCTGCTTTCTGACATTGGCATACAGCAGTCTGAGGCTGCTGGACAATACCTCAGGGATGTGAAATTTACAAATGTGTTTGTCAGCAACATGAAACGTGCCAAGCAGGTAAACAGAAACACACCAGTAACTAAAACATTCAATCTGTTTACCAGTAGAGGGAGATGTTTCTCTACAAATCAAACAACCACTTTTTAGGTTATTCTGTTCAGAAATAAGATGGTAATGCTGAAAAAGCTTGATTAAGTATTTAATAAGTGAGTATTGATAAGAATATCAAATAAGATAAAGATACTATCTTTCCACATGATTTGCATCAGACAATTTCTATATATTGCAATGTAGTTATAAGGTTGCACATGCCCACTGAATTTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24639
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111158 | Essential Splice Site | 64 | 256 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 25 (position 17324850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 16871394 |
GRCz11 | 25 | 16967794 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAAATTTACAAATGTGTTTGTCAGCAACATGAAACGTGCCAAGCAGG[T/C]AAACAGAAACACACCAGTAACTAAAACATTCAATCTGTTTACCAGTAGAG
Long Flanking Sequence:
AAATAAAAAAAATCATAAACACCATAATTCATTTCAGTCATTGCTTCTGATGATACATGAAGAAAAATGAATATGTTTGAGAAAAAAGTATTACATATAATCCACAGCCTTGGCAAAAGGTCCTCTTTTTATTCAACAACAAAGGTGTGCTGGCTTGCAGTGTATAATGAAGGGTAATGAAGTGTGTAATAAAGCTTTTATTGATTACTTGTGATGTGTTTTTTGCCAGTGGTGAGACGCAGTGCAACAAAGATGGCCTTTTACAAGGTAATTGTTTAGAGAGAAAATTAAAACATATGTTATCTCTACGCATTGAGGTTTATTATTAGCCTATTTAAATTTCCACATTGTGACCACATCTATCATTTCAACTTTAGGTCAGAAAATAGACTCTCTGCTTTCTGACATTGGCATACAGCAGTCTGAGGCTGCTGGACAATACCTCAGGGATGTGAAATTTACAAATGTGTTTGTCAGCAACATGAAACGTGCCAAGCAGG[T/C]AAACAGAAACACACCAGTAACTAAAACATTCAATCTGTTTACCAGTAGAGGGAGATGTTTCTCTACAAATCAAACAACCACTTTTTAGGTTATTCTGTTCAGAAATAAGATGGTAATGCTGAAAAAGCTTGATTAAGTATTTAATAAGTGAGTATTGATAAGAATATCAAATAAGATAAAGATACTATCTTTCCACATGATTTGCATCAGACAATTTCTATATATTGCAATGTAGTTATAAGGTTGCACATGCCCACTGAATTTATAATCATAATGTTTCTTTTTAAAAGCGATAATTTCTTTTGTGTCTATTTGTTTACAATGTGTATTTGTTGGGACCTTTAAACTTATATCAATATATTAATATTATAATCATATATGAATAGTCATGTCTTTAAAATACAGACTGCTGAGATCATTGTAAGAAACAACAGAACCTGCCATGACTTAGAACTGGTAGCAGATCCATCACTTATAGAAAGGGTAAGTACTGCCTGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44263
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 |
---|---|---|---|---|---|
ENSDART00000111158 | Nonsense | 142 | 256 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 25 (position 17321564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 16868108 |
GRCz11 | 25 | 16964508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCCAGGTGAAGTTGCGAATTAAGGATTTTCTGAAGGCCATGTACCAG[C/T]GAATAGCAAATGACCATCAAGACAAAGTACAAGATGGAGGAACATCCTCA
Long Flanking Sequence:
AAAACACTGCAAAGTTAAATATGTTTTGTTAATAAATTAGATGTAATTTAAATAAATACATAAATGACTGAAGCATGTATTACACAAACTAAAATTACCGAACTAACATACTAACGTTACCCCTCCACCAACCCTAATCGTCAATGTATAATTTGCACACTGCTTTATATACATTTCTTTAAAATGGGTGCATTATAAATTTGAGGATGCAATTTTGGATGTAGACGAAAAGTTGCATTGTTTCTAAATAAATCACTCATTTTGAACAAATCAATTGAATGAATGATTCAGTGAATCGCTTGTTAAAACAAGGACTTGCTGCTACCTACTGGCAGTTTTAGTGTCATATTTTTATCCAAAACAGACATAAACTAACACGCTGATCAATAATGATAAGTGAACAGTTATTTGGTAAGTTATAATTGCACACCACTAATAGAAAGGCCACATTTTTCCAGGTGAAGTTGCGAATTAAGGATTTTCTGAAGGCCATGTACCAG[C/T]GAATAGCAAATGACCATCAAGACAAAGTACAAGATGGAGGAACATCCTCAGCAGACGAAAGCACCGAGGCTCCAGCAGGACTGGCTAATGATGGAGTCTCTAGTGTGCCTGTACATGCACTGGTGGTCGGTCATGGGGCTTATATGAGCATAGCCATGCGCTATTTTTTTGAGGACCTGAAATGCCCAGTGCCTCGTGGTTTAGATCCAGCTCAACAGTTTTCCATCTGCCCGAACACTGGAATGTGCCGATTTATTATCACTTTGAAATGTAGCAGTGTGGATATTGCACTTTCTGACATCAAATGTGTGTTCATCAACAGAAGAGACCACTTCAAGACTAATTAGCATGTAAAAGGAAATGTAAAGTAAAGAGACAAAATGTGTACTGTACGTCTTATGCAAAAGATTGTCATACTGAAGCACTTTTCCTGAGATAAAACTTAAAACATTTTTGAGAATCAACATTTACAGAAATAAGATCAATCTGAATTTACAATA
Associated Phenotype:
Not determined