ZMP
herc4
Ensembl ID:
Human Orthologue:
HERC4
Human Description:
hect domain and RLD 4 [Source:HGNC Symbol;Acc:24521]
Mouse Orthologue:
Herc4
Mouse Description:
hect domain and RLD 4 Gene [Source:MGI Symbol;Acc:MGI:1914595]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12438 | Nonsense | Available for shipment | Available now |
sa17790 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12438
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083883 | Nonsense | 163 | 1053 | 4 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 51408080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50119177 |
GRCz11 | 13 | 50432420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTATCTGAAATGATGTATTCCTCCAGGAGGCGAGMTATTCTCCTGGGGC[C/T]AGAATAAGTATGGTCAGCTGGGTCTGGGGCAGCAGGGAGCCTGTGTCTGC
Long Flanking Sequence:
GGACAGCTCGGACTTTCCATTGTAGAAGACTGTCTGCGTGTGCCCAGGTAAAGATCAAATCAAGCATAAAATAAACAAAAATTAATAGATGAAAATAAATGGAGGAAAGCAAAACATGTGAGAAACGAATAATCAGCAGTCAAATATTAAGATTGGATCTATTTGCTCTATATATGAATTGCCAAATCAGTTGGAGCCCTGACTACAGTATGTATCCCTCTATAATTGGGTTCTGTACCAAAAAACACTGTGAATACTATACACTGCTCACAATTCATGATCTGCTCTTATTATTTTCTCTCCGCTTCCAGAACTGTCAAGAGCTTGTCAGAGGTTCACATTACCCAGGTGGCCTGTGGATACTGGCATTCCCTTGCTTTAGCCCGAGGTGTGCTGCTAAACATAATCCTAAACCAGATTCCTGCATCTAAAACTGCCTTCTTTACCCTAATTATCTGAAATGATGTATTCCTCCAGGAGGCGAGATATTCTCCTGGGGC[C/T]AGAATAAGTATGGTCAGCTGGGTCTGGGGCAGCAGGGAGCCTGTGTCTGCTCTCCACAGGTCATCCAGTCTCTGCAGGGCATCCCGTTCGGGCAGATTTCCGCCGGTGGAGCTCACAGCTTTGGCCTCACGCTCTCTGGGGCCATTTTCGGATGGGGGCGGAACAAGTTCGGCCAGCTGGGCCTCGGAGACAATGATGGTAAAACAAACACCTTCAGTTTTCTCTGCTCGAGTCACCTTTACTTACAGCAGGGGAAATAAGTATTGAACACGTCATGTTTTTTTCCTGGGAATAATGTCTCTAAAGGTGCTGCTGACATGAATCAGATTTTGGTAGAAATACAAACAATACAAACATGAAAATTGAAATGAGTCGTGTGTAAAAACAGCGGAATTACACAAGGAGAAAGAGCTGAACTACTGAAACATTATTAATACTTTATATAAAGGCTGTTTTTAATGATGGCAGCTTAAAGACACCTCTCATATGGAGGATGAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17790
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083883 | Essential Splice Site | 605 | 1053 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 51381877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50092974 |
GRCz11 | 13 | 50406217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATAATTCTGCAGTGATCATTTTCTGATATCGTCTTTATAATCCMGTTGC[A/T]GGWCAATGAGCGTGCCGGACAGATCAWCCAGWATGATAAATTCTWCATCC
Long Flanking Sequence:
TGTTCATTTGATTTTTAAAAGGTTCTGGTTTTCTTTTTATTAATGCATTGATGTTGATTTTAGTGATTAACTTCAGTATATACAAGCTTTTCATAATAACGAAATTATATTAATGAACAATATACGGTTAAAGTTTAAATTATTCGCCCTCCTGTGAATTTAGATTCTATTTCAAATATTTCCCAAATGCTGTTTAACAGATTCAGGAAATGTTTCACAGTATTTCCTCTAACATGTTTTCTTCTGTAGAAAGTTTTTTTTTTTTTTCGGCTAGAATAAAAGCAGTTTTTAATTGTTTTAAACCTATTTAAGGTTAATATTATTAGCCCCCTTAAGCAATATTAGTTTTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCTGAATTATACTAATGCTGAGAGATGGAACCTGATAATTCTGCAGTGATCATTTTCTGATATCGTCTTTATAATCCCGTTGC[A/T]GGTCAATGAGCGTGCCGGACAGATCATCCAGTATGATAAATTCTACATCCATGAGCTAGACGAGCTGATCGACATCAGGAATGATTATGCGACCTGGTTTCAGCAGCAGATGTTCTCTGTGGTTGGTTTATGATCATAACAAACACCCACACCGACACGGTTAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCTGAGGTCACGCCAAGCCTTCTTGGTGTGAAGCCACAGTGCTGACCACTGAGCCACCGTAGGAACACCTTGAAACCGGTTATCTCACCATGTATGCTTCCAAACATTAATATAAGTAAATAAATCTCTGTTTTTCGCAGGTCATGGACTCTCAGGTCACCCTCTGCAAATACCCGTTTGTGTTTGACGCTCAGGCGAAGACGGCTCTGCTGCAGACTGATGCTGTGATCCAGATGCAGGTCAGACTGATGCGTTTCAGTCAGAGATTCAGCCTCATGTTTCTCTGCTATAGTCTTCTG
Associated Phenotype:
Not determined