Busch Lab

ZMP

gc2

Ensembl ID:
ENSDARG00000018329
ZFIN ID:
ZDB-GENE-011128-8
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.
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.
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