ZMP
si:ch211-281g13.5
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100148091 [Source:RefSeq peptide;Acc:NP_001139103]
Human Orthologues:
HERC5, HERC6
Human Descriptions:
hect domain and RLD 5 [Source:HGNC Symbol;Acc:24368]
hect domain and RLD 6 [Source:HGNC Symbol;Acc:26072]
hect domain and RLD 6 [Source:HGNC Symbol;Acc:26072]
Mouse Orthologue:
Herc6
Mouse Description:
hect domain and RLD 6 Gene [Source:MGI Symbol;Acc:MGI:1914388]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32762 | Essential Splice Site | Available for shipment | Available now |
sa25661 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32762
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113315 | Essential Splice Site | 324 | 992 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 1 (position 50035387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 48884568 |
GRCz11 | 1 | 49528988 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAACAGGTCAAGCAGTCTGTGCCGTTACCAGTGCTTCTGCCAACTGG[T/C]AATAGAAGTCATATTTTAGCAGTAGCTTTTATTTTCCTGAATGTTGTGTT
Long Flanking Sequence:
TCCATCTCATGTGGAGGAGAACACACTGCCACTCTGTCAAAGGTATTGTGGTTGATTTATGTAATACAACACAATGAGCACAGAATAAAGTAGTAAATGGTTGATATTTGTCAGGGAGGAACAGTGTTCACATTTGGATCAGGAGGTTTTGGTCAGCTTGGGCACAACTCACTTAAAGATGAACATCATCCACGACTGATTGCTGAACTGTGGGGATCTAAAGTGTCGCAGGTCACATGTGGGAGGTAAACTAGAGTGTTTTCAACACTTAAAACACTCTCAACCAACACATGGTGATTCTCTGAATGGTATAATTACATAATCCCAAATGCAAGTGTGTCCGGTTAAATATTTTTATTTCTAACATGAAGACATCACACGCTTGTATTTGAGGAATCGTCAAAGCTGATCTACTCATTTGGATGTGGGATGCAAGGGCAGCTGGGAAATGGAGAACAGGTCAAGCAGTCTGTGCCGTTACCAGTGCTTCTGCCAACTGG[T/C]AATAGAAGTCATATTTTAGCAGTAGCTTTTATTTTCCTGAATGTTGTGTTTGTTCTAAACCAGCTAAATATTTGATGCTCGCAGAATGTACTGAATTTACGATGGAAAAACTCATCACTGGAGAACACCACTCCTTTGCCTTGTTTTTCAAGGTAAGATGAACAGTCCTCATTTATAAATAGTTTGAGATTGATTGATGCTCTGCGTTAACTTTTACATTTTCTTTTGTAGAATCCTGGAAATGAGTCTGAAAAGCCTAAATCTGGTTCAAATGGAGGAATTTTGACACTAAATGACAGAATGATTGACCGCTGGGTGTCTGAAAGTGACCCATGGCCAACAGTAAAGAAGTGAGTTGTAAACTGTAGAACGACAATGTTGACATGATTTATAGTATATGATACTATGTGCATGTCCTAAATTATTTTGTAAATGCATCTAAAAGTGTGGTGGGACCTTAATACATTTGCCTTTCTTTTAATCTTACTAATTATTATAAT
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa18708
Status:
Allele not cryopreserved
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:
n/a
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113315 | Essential Splice Site | 347 | 992 | 9 | 24 |
Genomic Location (Zv9):
Chromosome 1 (position 50035157)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 48884338 |
GRCz11 | 1 | 49528758 |
KASP Assay ID:
2259-1071.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTTTGAGATTGATTGATGCTCTGCGTTAACTTTTACATTTTCTTTTGT[A/G]GAATCCTGGAAATGAGTCTGAAAAGCCTAAATCTGGTTCAAATGGAGGAA
Long Flanking Sequence:
GGTCACATGTGGGAGGTAAACTAGAGTGTTTTCAACACTTAAAACACTCTCAACCAACACATGGTGATTCTCTGAATGGTATAATTACATAATCCCAAATGCAAGTGTGTCCGGTTAAATATTTTTATTTCTAACATGAAGACATCACACGCTTGTATTTGAGGAATCGTCAAAGCTGATCTACTCATTTGGATGTGGGATGCAAGGGCAGCTGGGAAATGGAGAACAGGTCAAGCAGTCTGTGCCGTTACCAGTGCTTCTGCCAACTGGTAATAGAAGTCATATTTTAGCAGTAGCTTTTATTTTCCTGAATGTTGTGTTTGTTCTAAACCAGCTAAATATTTGATGCTCGCAGAATGTACTGAATTTACGATGGAAAAACTCATCACTGGAGAACACCACTCCTTTGCCTTGTTTTTCAAGGTAAGATGAACAGTCCTCATTTATAAATAGTTTGAGATTGATTGATGCTCTGCGTTAACTTTTACATTTTCTTTTGT[A/G]GAATCCTGGAAATGAGTCTGAAAAGCCTAAATCTGGTTCAAATGGAGGAATTTTGACACTAAATGACAGAATGATTGACCGCTGGGTGTCTGAAAGTGACCCATGGCCAACAGTAAAGAAGTGAGTTGTAAACTGTAGAACGACAATGTTGACATGATTTATAGTATATGATACTATGTGCATGTCCTAAATTATTTTGTAAATGCATCTAAAAGTGTGGTGGGACCTTAATACATTTGCCTTTCTTTTAATCTTACTAATTATTATAATTGAATTATGCAATTACTATTTTCTCCATCAAGTATTAATCTTAATCTTTAGTATAAGAAGAATCTTGCTTCCATTTTTTTTAGAAGTATAGTAATGTAGTAATGAAATTGAGCTATGTATTATGCTGAAGTAATGCATATGAATATTAAAAATGTGTTATTCTATAATTTACAGTGAAATAAACACAGTGTTCTCCTCCGCTGCCTCACTGAATGGAAGTTTTCTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25661
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 |
---|---|---|---|---|---|
ENSDART00000113315 | Essential Splice Site | 406 | 992 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 1 (position 50034652)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 48883833 |
GRCz11 | 1 | 49528253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTGTTCTCCTCCGCTGCCTCACTGAATGGAAGTTTTCTCAAAACAAG[G/A]TAAAATTAGGTAGTCTTGTCTAGTAATCTAGACCTTTTTTAAATCAGTCT
Long Flanking Sequence:
CCTGGAAATGAGTCTGAAAAGCCTAAATCTGGTTCAAATGGAGGAATTTTGACACTAAATGACAGAATGATTGACCGCTGGGTGTCTGAAAGTGACCCATGGCCAACAGTAAAGAAGTGAGTTGTAAACTGTAGAACGACAATGTTGACATGATTTATAGTATATGATACTATGTGCATGTCCTAAATTATTTTGTAAATGCATCTAAAAGTGTGGTGGGACCTTAATACATTTGCCTTTCTTTTAATCTTACTAATTATTATAATTGAATTATGCAATTACTATTTTCTCCATCAAGTATTAATCTTAATCTTTAGTATAAGAAGAATCTTGCTTCCATTTTTTTTAGAAGTATAGTAATGTAGTAATGAAATTGAGCTATGTATTATGCTGAAGTAATGCATATGAATATTAAAAATGTGTTATTCTATAATTTACAGTGAAATAAACACAGTGTTCTCCTCCGCTGCCTCACTGAATGGAAGTTTTCTCAAAACAAG[G/A]TAAAATTAGGTAGTCTTGTCTAGTAATCTAGACCTTTTTTAAATCAGTCTCATATTTATAAAAATGTGTCTCTGTAGTCGCGATGAACATTATCAGACGTCTGTGGAGCATTGTGGCCTGGATTTTGATCTGGTTAAAACATCCTTTGCAAAGTTATTCGCAAGTAAAAGTCTGATTTCAGAGGTAATGATGATCTAACATTGACATGTTCCTTGCATCTGAACCAAATAGCTGCAGTGAATGTTTATTTTGTACCTCAGGTGGTGAAGGTGGTTCAGCAGACGCTGCTGCCATCTCTGAATCCAAACCCAACTGGTGTGGAAGCTCTGAGACTTTATCTTCTCCTCCCTGAGCTCATCAATGGTCTCAAGAAACAAAGAACCAAACTCATTGAAGCTCTGGCCTCCAAAATCCTTGAGCTGAATTCTGCAGCTCGCAAGGTGCTAGGTAAAGCTGGAAGACATTTACAACACTCAGGTCTGTGGCCATGTTGGATTTGT
Associated Phenotype:
Not determined