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 |
---|---|---|---|
sa35603 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12438 | Nonsense | Available for shipment | Available now |
sa35602 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17790 | Essential Splice Site | Available for shipment | Available now |
sa24948 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35603
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 |
---|---|---|---|---|---|
ENSDART00000083883 | Essential Splice Site | 129 | 1053 | 2 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 51408532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50119629 |
GRCz11 | 13 | 50432872 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGACAGCTCGGACTTTCCATTGTAGAAGACTGTCTGCGTGTGCCCAGG[T/C]AAAGATCAAATCAAGCATAAAATAAACAAAAATTAATAGATGAAAATAAA
Long Flanking Sequence:
CTCTATATAGTGGTTTTCGGTTTTGTTCTCATCCCTGCTCTTTACCAGGATCAGGCGCGGCGGGTAGAAAACGGGGCGGGGCAGGCAGCGGGGCATCAAATGCTGAATATAAGCGGGAGTGGTCGGGTTCGGGCTAAAACCTGGCGGGTGCGGGCGGGACTGGGATTCAAAATTTAGTCCAGCGCAGATCTCTACCTTATTGCGCCGGGTATATGATAGGTCCCTTATGTTTAAAAACAAATCTCTCTTTTAAACAGCACTTAGGAAGCATTTTCATTAAAATGAACAATATATTGCCTTTATTTCATGTAATCCTCTATGTTTCCATCTCGTCTCCAGAGCAGGTGGTGTCTCTGGATGCGCAGAACATTGTGGCGGTGTCGTGTGGAGAAGCTCATACTCTTGCTCTGAATGATAAAGGACAAGTGTTTGCGTGGGGTTTGGGATCAGATGGACAGCTCGGACTTTCCATTGTAGAAGACTGTCTGCGTGTGCCCAGG[T/C]AAAGATCAAATCAAGCATAAAATAAACAAAAATTAATAGATGAAAATAAATGGAGGAAAGCAAAACATGTGAGAAACGAATAATCAGCAGTCAAATATTAAGATTGGATCTATTTGCTCTATATATGAATTGCCAAATCAGTTGGAGCCCTGACTACAGTATGTATCCCTCTATAATTGGGTTCTGTACCAAAAAACACTGTGAATACTATACACTGCTCACAATTCATGATCTGCTCTTATTATTTTCTCTCCGCTTCCAGAACTGTCAAGAGCTTGTCAGAGGTTCACATTACCCAGGTGGCCTGTGGATACTGGCATTCCCTTGCTTTAGCCCGAGGTGTGCTGCTAAACATAATCCTAAACCAGATTCCTGCATCTAAAACTGCCTTCTTTACCCTAATTATCTGAAATGATGTATTCCTCCAGGAGGCGAGATATTCTCCTGGGGCCAGAATAAGTATGGTCAGCTGGGTCTGGGGCAGCAGGGAGCCTGTGTCT
Associated Phenotype:
Not determined
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:
sa35602
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083883 | Nonsense | 182 | 1053 | 4 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 51408023)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50119120 |
GRCz11 | 13 | 50432363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATGGTCAGCTGGGTCTGGGGCAGCAGGGAGCCTGTGTCTGCTCTCCA[C/T]AGGTCATCCAGTCTCTGCAGGGCATCCCGTTCGGGCAGATTTCCGCCGGT
Long Flanking Sequence:
AATCAAGCATAAAATAAACAAAAATTAATAGATGAAAATAAATGGAGGAAAGCAAAACATGTGAGAAACGAATAATCAGCAGTCAAATATTAAGATTGGATCTATTTGCTCTATATATGAATTGCCAAATCAGTTGGAGCCCTGACTACAGTATGTATCCCTCTATAATTGGGTTCTGTACCAAAAAACACTGTGAATACTATACACTGCTCACAATTCATGATCTGCTCTTATTATTTTCTCTCCGCTTCCAGAACTGTCAAGAGCTTGTCAGAGGTTCACATTACCCAGGTGGCCTGTGGATACTGGCATTCCCTTGCTTTAGCCCGAGGTGTGCTGCTAAACATAATCCTAAACCAGATTCCTGCATCTAAAACTGCCTTCTTTACCCTAATTATCTGAAATGATGTATTCCTCCAGGAGGCGAGATATTCTCCTGGGGCCAGAATAAGTATGGTCAGCTGGGTCTGGGGCAGCAGGGAGCCTGTGTCTGCTCTCCA[C/T]AGGTCATCCAGTCTCTGCAGGGCATCCCGTTCGGGCAGATTTCCGCCGGTGGAGCTCACAGCTTTGGCCTCACGCTCTCTGGGGCCATTTTCGGATGGGGGCGGAACAAGTTCGGCCAGCTGGGCCTCGGAGACAATGATGGTAAAACAAACACCTTCAGTTTTCTCTGCTCGAGTCACCTTTACTTACAGCAGGGGAAATAAGTATTGAACACGTCATGTTTTTTTCCTGGGAATAATGTCTCTAAAGGTGCTGCTGACATGAATCAGATTTTGGTAGAAATACAAACAATACAAACATGAAAATTGAAATGAGTCGTGTGTAAAAACAGCGGAATTACACAAGGAGAAAGAGCTGAACTACTGAAACATTATTAATACTTTATATAAAGGCTGTTTTTAATGATGGCAGCTTAAAGACACCTCTCATATGGAGGATGAGGCCTCATGCATTGCTCAGGTGTGAGTTTCTCAAAGACTTAAACAGAGTGTCAAAATCCT
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
Mutation Details
Allele Name:
sa24948
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083883 | Nonsense | 639 | 1053 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 13 (position 51381773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50092870 |
GRCz11 | 13 | 50406113 |
KASP Assay ID:
554-7323.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTAGACGAGCTGATCGACATCAGGAATGATTATGCGACCTGGTTTCAG[C/T]AGCAGATGTTCTCTGTGGTTGGTTTATGATCATAACAAACACCCACACCG
Long Flanking Sequence:
TTATATTAATGAACAATATACGGTTAAAGTTTAAATTATTCGCCCTCCTGTGAATTTAGATTCTATTTCAAATATTTCCCAAATGCTGTTTAACAGATTCAGGAAATGTTTCACAGTATTTCCTCTAACATGTTTTCTTCTGTAGAAAGTTTTTTTTTTTTTTCGGCTAGAATAAAAGCAGTTTTTAATTGTTTTAAACCTATTTAAGGTTAATATTATTAGCCCCCTTAAGCAATATTAGTTTTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCTGAATTATACTAATGCTGAGAGATGGAACCTGATAATTCTGCAGTGATCATTTTCTGATATCGTCTTTATAATCCCGTTGCAGGTCAATGAGCGTGCCGGACAGATCATCCAGTATGATAAATTCTACATCCATGAGCTAGACGAGCTGATCGACATCAGGAATGATTATGCGACCTGGTTTCAG[C/T]AGCAGATGTTCTCTGTGGTTGGTTTATGATCATAACAAACACCCACACCGACACGGTTAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCTGAGGTCACGCCAAGCCTTCTTGGTGTGAAGCCACAGTGCTGACCACTGAGCCACCGTAGGAACACCTTGAAACCGGTTATCTCACCATGTATGCTTCCAAACATTAATATAAGTAAATAAATCTCTGTTTTTCGCAGGTCATGGACTCTCAGGTCACCCTCTGCAAATACCCGTTTGTGTTTGACGCTCAGGCGAAGACGGCTCTGCTGCAGACTGATGCTGTGATCCAGATGCAGGTCAGACTGATGCGTTTCAGTCAGAGATTCAGCCTCATGTTTCTCTGCTATAGTCTTCTGACAGAGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGCGTGTGCAGATGGCG
Associated Phenotype:
Not determined