ZMP
her6
Ensembl ID:
ZFIN ID:
Description:
transcription factor HES-1 [Source:RefSeq peptide;Acc:NP_571154]
Human Orthologues:
HES1, HES4
Human Descriptions:
hairy and enhancer of split 1, (Drosophila) [Source:HGNC Symbol;Acc:5192]
hairy and enhancer of split 4 (Drosophila) [Source:HGNC Symbol;Acc:24149]
hairy and enhancer of split 4 (Drosophila) [Source:HGNC Symbol;Acc:24149]
Mouse Orthologue:
Hes1
Mouse Description:
hairy and enhancer of split 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:104853]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38559 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20748 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38559
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023613 | Essential Splice Site | 36 | 270 | 1 | 4 |
ENSDART00000114279 | Essential Splice Site | 99 | 331 | 2 | 7 |
The following transcripts of ENSDARG00000006514 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 36331007)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36574541 |
GRCz11 | 6 | 36552435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGAACACTACACCTGATAAACCCAAAACGGCTTCGGAACACAGAAAG[G/A]TTGGTATTGATATTAAGCTACGAACTATAGTGCTTCAAGAAGTGATTAGA
Long Flanking Sequence:
GCCACCCGCTCAAACGCTAAACAACCAATGGAGGGGCGCCGACCACGAGCCATCCTCCCCTCGGGCCGCGTGTCCCGCGCGCTGATTGGTAGAAAGTTACTGTGGGAAAGAAAGTTTGGGAAGTTTCACACGAGCCGTTCGCGTGCAGCCGGAGATATAAATAAGACCAACACGACGCTGAGGCAGGCAGTTGCTACGACCGCTGGCGAACGGTGAAATCAGAGACTGTGACATCATTGCCGCACCAGTTGAACTCGGGACACTTCGTGCGGATATCCATTCATAACTGGAACTGTATCAGCGTACTTGACAGCGTTTACTCCACTAGAAGCAGCTGTGCGGGAGGATTTCTTTTTATAAACAAGATCACGAAAGGATACTTCCCAGAGAAGATGCCTGCCGATATCATGGAAAAAAACTCCTCTTCTCCGGTCGCCGCGACTCCGGCGAGCATGAACACTACACCTGATAAACCCAAAACGGCTTCGGAACACAGAAAG[G/A]TTGGTATTGATATTAAGCTACGAACTATAGTGCTTCAAGAAGTGATTAGACAGATTGACTCATTTTGTTTTTATTTTGCATTTTAGTCTTCTAAACCCATTATGGAGAAAAGAAGAAGAGCGAGAATCAACGAAAGCTTGGGTCAGCTGAAAACGTTAATCTTGGATGCTCTGAAAAAAGATGTAAGTACCGAAAGTCCGACTGAGTCTTTCAGTTAGGCTATATCTGGCTGGAATATTAATGCATTTCTTTATATAGCCGCATATCTAAATCAGTCTCTTTCTTCACTCTCAGAGCTCCAGACACTCTAAACTTGAGAAAGCCGACATCCTGGAGATGACAGTGAAACATCTCAGAAACATGCAGCGCGCACAAATGACCGGTAAGTCGCCAGAGTTAAAACCTTTCAGAAAATGCACCTTGCATTCTCTTTATGTAACTAATGCAATAAAATAAAGACGTTTAAGGAGCTAAAATAATTTAAGTTGAACTTAATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20748
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023613 | Essential Splice Site | 68 | 270 | 2 | 4 |
ENSDART00000114279 | Essential Splice Site | 131 | 331 | 3 | 7 |
The following transcripts of ENSDARG00000006514 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 36330824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36574358 |
GRCz11 | 6 | 36552252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCTTGGGTCAGCTGAAAACGTTAATCTTGGATGCTCTGAAAAAAGAT[G/A]TAAGTACCGAAAGTCCGACTGAGTCTTTCAGTTAGGCTATATCTGGCTGG
Long Flanking Sequence:
CAGGCAGTTGCTACGACCGCTGGCGAACGGTGAAATCAGAGACTGTGACATCATTGCCGCACCAGTTGAACTCGGGACACTTCGTGCGGATATCCATTCATAACTGGAACTGTATCAGCGTACTTGACAGCGTTTACTCCACTAGAAGCAGCTGTGCGGGAGGATTTCTTTTTATAAACAAGATCACGAAAGGATACTTCCCAGAGAAGATGCCTGCCGATATCATGGAAAAAAACTCCTCTTCTCCGGTCGCCGCGACTCCGGCGAGCATGAACACTACACCTGATAAACCCAAAACGGCTTCGGAACACAGAAAGGTTGGTATTGATATTAAGCTACGAACTATAGTGCTTCAAGAAGTGATTAGACAGATTGACTCATTTTGTTTTTATTTTGCATTTTAGTCTTCTAAACCCATTATGGAGAAAAGAAGAAGAGCGAGAATCAACGAAAGCTTGGGTCAGCTGAAAACGTTAATCTTGGATGCTCTGAAAAAAGAT[G/A]TAAGTACCGAAAGTCCGACTGAGTCTTTCAGTTAGGCTATATCTGGCTGGAATATTAATGCATTTCTTTATATAGCCGCATATCTAAATCAGTCTCTTTCTTCACTCTCAGAGCTCCAGACACTCTAAACTTGAGAAAGCCGACATCCTGGAGATGACAGTGAAACATCTCAGAAACATGCAGCGCGCACAAATGACCGGTAAGTCGCCAGAGTTAAAACCTTTCAGAAAATGCACCTTGCATTCTCTTTATGTAACTAATGCAATAAAATAAAGACGTTTAAGGAGCTAAAATAATTTAAGTTGAACTTAATCTATTTTCTCGTTTACCCAACAGCTGCCCTAAACACAGATCCCACCGTTCTTGGGAAGTACCGAGCTGGATTCAGTGAATGCATGAACGAGGTTACCCGGTTCCTGTCCACATGTGAAGGGGTTAACACCGAGGTCAGGACTAGGCTGCTAGGTCACCTAGCCAGCTGCATGACACAGATCAACGCC
Associated Phenotype:
Not determined