ZMP
hes2.1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC559147 [Source:RefSeq peptide;Acc:NP_001116717]
Human Orthologue:
HES2
Human Description:
hairy and enhancer of split 2 (Drosophila) [Source:HGNC Symbol;Acc:16005]
Mouse Orthologue:
Hes2
Mouse Description:
hairy and enhancer of split 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1098624]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34488 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7157 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34488
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 |
---|---|---|---|---|---|
ENSDART00000111075 | Essential Splice Site | 63 | 195 | 2 | 5 |
ENSDART00000143321 | Essential Splice Site | 63 | 150 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 49082038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46935433 |
GRCz11 | 8 | 46925899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCTCAATCACCTAAAAACTCTTATTCTCCCACTGGTCGGCAAAGATG[T/G]AAGTATCTTAACTTTGTTTCTTTGGCAATACATACAATACTAATAAATCC
Long Flanking Sequence:
TCAACAGATGGCAACTTATGGGACAGCCAGATCAAATCTTTTCTCCTCGGCGTCAAACTAAACGCGACACAATAGATCGGAGACCCTCCCTCCACGCCAAAGGGGACTATAAAAGACCTCTCTCTTCCATCCTGACCACAAAACTCTCAAACTCCTCTCTCAAGAGCACAACTAGAGAAATCAACCGATTAAATCATGACTCCAAACATTATTACCGAAGCTCATCCCCACTCATTCGGCTCTCGAATGACTGTAGCTCAGAGAAAAGAGGCACATGAACTGAGAAAGGTGAGGGCGATTTTCAGTTCTTTTAATGAACACACCTGAATCATTTAATGGTTCTTATAAAATCCTAAAACACACACTCATACTGACCCACTTCTTTCTTCCTCTTTTTCCCCAGACTCTCAAGCCATTGATGGAAAAGAGAAGGCGGGCTCGCATTAACGACAGCCTCAATCACCTAAAAACTCTTATTCTCCCACTGGTCGGCAAAGATG[T/G]AAGTATCTTAACTTTGTTTCTTTGGCAATACATACAATACTAATAAATCCAAGTTTATGTCAGTGTCTGAACAATATGCTAATCTTTGAAATCACTTTAATTCGTAGGCTTCACGTTATTCAAAGCTCGAGAAAGCCGACATTCTTGAAATGACCGTCCGGTTCCTGAGAGATCTTCCTTCCTCATCAGCTAAAGGTGAGTTAGCTATCAAATTTGCCCTTTTCCACATTTTTATCGTTTGTTTATGGTCTGCATTTTTTCAAAACGAATACTTTATTAATTGTCTCCCTTTTTCTCCTTAAAGGTCAAACAGACAGCTATAAAGAGGGCTATAAAGCCTGCTTGCAGCGCATATCTACGATGCTCCCGCAGTCAAACCTGGAAACAGAAGCCCATCAGCGCGTCAGCGAGTTCATCCACACTGTTAGACATTTCAAAGGGTTTTTACAGTAACTTACTGGCAACACTGTTGCCAGTAAGTTACTGTATTTTAGATTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7157
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111075 | Nonsense | 98 | 195 | 4 | 5 |
ENSDART00000143321 | Nonsense | 98 | 150 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 49081717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46935112 |
GRCz11 | 8 | 46925578 |
KASP Assay ID:
554-4545.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTTATTAATTKTCTCCCTTTTTCTCCTTAAAGGTCAAACAGACAGCTA[T/G]AAAGAGGGCTATAAAGCCTGCTTGCAGCGCATATCTACGATGCTCCCGCA
Long Flanking Sequence:
ACCTGAATCATTTAATGGTTCTTATAAAATCCTAAAACACACACTCATACTGACCCACTTCTTTCTTCCTCTTTTTCCCCAGACTCTCAAGCCATTGATGGAAAAGAGAAGGCGGGCTCGCATTAACGACAGCCTCAATCACCTAAAAACTCTTATTCTCCCACTGGTCGGCAAAGATGTAAGTATCTTAACTTTGTTTCTTTGGCAATACATACAATACTAATAAATCCAAGTTTATGTCAGTGTCTGAACAATATGCTAATCTTTGAAATCACTTTAATTCGTAGGCTTCACGTTATTCAAAGCTCGAGAAAGCCGACATTCTTGAAATGACCGTCCGGTTCCTGAGAGATCTTCCTTCCTCATCAGCTAAAGGTGAGTTAGCTATCAAATTTGCCCTTTTCCACATTTTTATCGTTTGTTTATGGTCTGCATTTTTTCAAAACGAATACTTTATTAATTGTCTCCCTTTTTCTCCTTAAAGGTCAAACAGACAGCTA[T/G]AAAGAGGGCTATAAAGCCTGCTTGCAGCGCATATCTACGATGCTCCCGCAGTCAAACCTGGAAACAGAAGCCCATCAGCGCGTCAGCGAGTTCATCCACACTGTTAGACATTTCAAAGGGTTTTTACAGTAACTTACTGGCAACACTGTTGCCAGTAAGTTACTGTATTTTAGATTTACAGTATACAACTGTAAATCCGTTTACAGCATGTTACTGTAGTGTCTGAAAATGGTTAACTACTGTAAAAACCTAAGTTAACAGTTAGCTACTGTAAACCTTTTAATTTTGTCCTAAATATTTTATAATATAATTTTATTAATATTATTTTAATACTATAGACCTAAAAAAGACACAATTACAAAATATTAACAAAATAAACACTCTTTATTTAAAACATTGGAGATGCTTAAAACAAGCTTAAAAATGTGTAAAAACATTACATTTCAATCATTCAAAATATTTTATTTTAAGAAAAAAAAACATTGAAAATGACAAAGCAC
Associated Phenotype:
Not determined