ZMP
gc2
Ensembl ID:
ZFIN ID:
Description:
guanylyl cyclase 2 [Source:RefSeq peptide;Acc:NP_001103165]
Human Orthologue:
GUCY2F
Human Description:
guanylate cyclase 2F, retinal [Source:HGNC Symbol;Acc:4691]
Mouse Orthologue:
Gucy2f
Mouse Description:
guanylate cyclase 2f Gene [Source:MGI Symbol;Acc:MGI:105119]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34182 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41018 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34182
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 |
---|---|---|---|---|---|
ENSDART00000098648 | Nonsense | 330 | 1107 | 2 | 18 |
ENSDART00000098649 | Nonsense | 322 | 1099 | 3 | 19 |
ENSDART00000125807 | None | None | 259 | None | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 52746023)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51015773 |
GRCz11 | 7 | 51290843 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCTGTGCTCACGATCACTATTGAGTCTCCAAAGGAACAGTCTTTTTA[T/A]CAAGCTTTTGAAAAGGCACAGGAGGATGGAGAGTTACCCAAACACCTCAA
Long Flanking Sequence:
TTTCAACATTTTACTTGTACGCTATTCTAAAACTTACAATGCCAAATTTCTTTTATCCTAGTAATTTAAGAGTTTTGCTGCTTATATAAACTACCTATTTAAAATGAGCTGAAACAACACATTTCTTGAGATTTTATTGGGACAACTTAATTGTGTTCAATGCATTTACTACAGTGCATGTATACTTTCTCAGCATCACACTCAAGCATTTAAAAGTCTGAACTGTCCTTTCCTCTTCTCAATGCTTTGTTTGCAGTGGTCATCTTGGTCATGCACTCTGTGTTAATTGGTGGAAGAACCCAGAAGCTGCTGCTGGAAACGGCACATGACATGCGGATGACAGACGGCTCGTTGGTGTTTATGTCCTACGATACTCTCTTTTACAGTCTGCCCTACCATCACGTTACTCAACCAGCCCTGCGCTATAACAGCAAGCTGCTACGTGCCTATGATGCTGTGCTCACGATCACTATTGAGTCTCCAAAGGAACAGTCTTTTTA[T/A]CAAGCTTTTGAAAAGGCACAGGAGGATGGAGAGTTACCCAAACACCTCAAACCACAGCAGGTACAAAGACTGTTTACATATGGCGTTACTTTTTTTGTACTAAGTTAATGGCTAATATCACCATCATGCATGTTCTGGTTTTGGAGAGTTATGCTTCTGGGTAAGTTTATTATAGTTTTAAAATGAATTTTAAAAGCAATAAACAGCAACACGGTGGCTCAGTGGTTAGCACTGTTGCCTCACAGCAAGAAGGTTGCTGGTTCAAGCCCGGCTGGGTCAGTTGGCATTTCTGTGTGCAGTTTGCATGTTCTCCCTGTGTTTGCGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAAGAGATGCGCTATAGGTAAATTTAGTGAGCTAAATTGGCCGAAGTGTATATGTGTAAATGAGTGTGTATGGGTGTTTCCCCATAATGGGTTGCATCTGGAAGGGCATCCGCTGTGTACAACATATTGAATTATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41018
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 |
---|---|---|---|---|---|
ENSDART00000098648 | Essential Splice Site | 350 | 1107 | 2 | 18 |
ENSDART00000098649 | Essential Splice Site | 342 | 1099 | 3 | 19 |
ENSDART00000125807 | None | None | 259 | None | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 52745961)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51015711 |
GRCz11 | 7 | 51290781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGCACAGGAGGATGGAGAGTTACCCAAACACCTCAAACCACAGCAGG[T/C]ACAAAGACTGTTTACATATGGCGTTACTTTTTTTGTACTAAGTTAATGGC
Long Flanking Sequence:
AATTTAAGAGTTTTGCTGCTTATATAAACTACCTATTTAAAATGAGCTGAAACAACACATTTCTTGAGATTTTATTGGGACAACTTAATTGTGTTCAATGCATTTACTACAGTGCATGTATACTTTCTCAGCATCACACTCAAGCATTTAAAAGTCTGAACTGTCCTTTCCTCTTCTCAATGCTTTGTTTGCAGTGGTCATCTTGGTCATGCACTCTGTGTTAATTGGTGGAAGAACCCAGAAGCTGCTGCTGGAAACGGCACATGACATGCGGATGACAGACGGCTCGTTGGTGTTTATGTCCTACGATACTCTCTTTTACAGTCTGCCCTACCATCACGTTACTCAACCAGCCCTGCGCTATAACAGCAAGCTGCTACGTGCCTATGATGCTGTGCTCACGATCACTATTGAGTCTCCAAAGGAACAGTCTTTTTATCAAGCTTTTGAAAAGGCACAGGAGGATGGAGAGTTACCCAAACACCTCAAACCACAGCAGG[T/C]ACAAAGACTGTTTACATATGGCGTTACTTTTTTTGTACTAAGTTAATGGCTAATATCACCATCATGCATGTTCTGGTTTTGGAGAGTTATGCTTCTGGGTAAGTTTATTATAGTTTTAAAATGAATTTTAAAAGCAATAAACAGCAACACGGTGGCTCAGTGGTTAGCACTGTTGCCTCACAGCAAGAAGGTTGCTGGTTCAAGCCCGGCTGGGTCAGTTGGCATTTCTGTGTGCAGTTTGCATGTTCTCCCTGTGTTTGCGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAAGAGATGCGCTATAGGTAAATTTAGTGAGCTAAATTGGCCGAAGTGTATATGTGTAAATGAGTGTGTATGGGTGTTTCCCCATAATGGGTTGCATCTGGAAGGGCATCCGCTGTGTACAACATATTGAATTATAAGGTTCTATCTGACATTTTTGTCAAAATTAAGTTACTGACATATTCTTATTAAATGACAACTTA
Associated Phenotype:
Not determined