ZMP
zgc:163136
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100073325 [Source:RefSeq peptide;Acc:NP_001092233]
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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1203 | Nonsense | F2 line generated | Not yet available |
| sa6605 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1203
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000113072 | Nonsense | 674 | 997 | 18 | 25 |
| ENSDART00000145960 | Nonsense | 671 | 994 | 18 | 25 |
Genomic Location (Zv9):
Chromosome 1 (position 50041737)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 48890918 |
| GRCz11 | 1 | 49535338 |
KASP Assay ID:
554-1112.1 (used for ordering genotyping assays)
KASP Sequence:
AACTTGTTGCACATAAACAGGGAATCAGTGCTGACGGACACCCTTCAGTA[T/G]CTTAGACCATTTACCTACTCGTTTATGCATCCATTGCAGGTAAAACAGAG
Long Flanking Sequence:
AAAGGAAAACCAAAATATCACTGAAATCTTTTTTTCTATGCCAAAAGCTGGACGCCACTTCTGCAGAAGTGCTTTGGATGGCATCGCGGCTTCCAATCAATGAAGAATTGCACAATAGGATGAAACTGGAAGATTACTACTTTGTGAGTATTAAAGGTATCTTGCATGATATGCATAATGAGCTTTGTTTAAGAAATCTAAAAATGCTTTCATGCATCTTTACTTTCAGAAAACAGCTGAAATATTGGTCAAGTTCCCTTTTGTGTCTGACTTTTTAACTAAAAAGAGCATGTTTATTGTAAGTCAACTTACTGTATTTGGACAGAAATACATATTTCATTCCTCTGGACAACTATCCTTTAAAAGATAACATAATTGTACTCTTTTTAGCTCTTGCAGGAGCAATGCATACGGAGCTTACTAGACCTACTGGTGGTACATTTGAATGGCAACTTGTTGCACATAAACAGGGAATCAGTGCTGACGGACACCCTTCAGTA[T/G]CTTAGACCATTTACCTACTCGTTTATGCATCCATTGCAGGTAAAACAGAGAAATGAAATCAGAGTTGAAATGTCTGAAATGGATTTTTACCTTAATGAAATTGTCTCCTGTGCAGGTGGCGTTCATCGGGGAGGATGAAATAGATGAAAAGGTTATATCAGCCGAATTCTTCTCCCTTATCTCCAAGTCTTTTATTGAATGGGATAAAAAGATTCTGGAAGTTCATGAGAGTTCACTGGTTTGGTTCAATCCTCATGTATGTTTGACAACATTTATTCGTTTTGCCCAGTGTGACATTTCTCATGTATTGATGTGAATGATGCTGATGTCTTTTAGCATACACAGGACCATAGGGATTTCTACTATCTTGGAGTGATCTGTGGAATGGCGCTCTACAACAGACATCACATCAACATTGACTTTCCACTGGCCTTATTCAAGAAACTCCTCCAGCAGAAGCCCAGTCTGGATGATCTGGAGGAGCTCTCACCTGTGGAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6605
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 |
|---|---|---|---|---|---|
| ENSDART00000113072 | Essential Splice Site | 812 | 997 | 21 | 25 |
| ENSDART00000145960 | Essential Splice Site | 809 | 994 | 21 | 25 |
Genomic Location (Zv9):
Chromosome 1 (position 50041082)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 48890263 |
| GRCz11 | 1 | 49534683 |
KASP Assay ID:
554-4496.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGGAGGACGAGGANNNAGTAGTGGATTTGCAACATTTGGATTTCASGG[T/C]AATATAGTTTCTATGCAGGCCCGGATTGGATTATCAGGAGAACCGGGAGA
Long Flanking Sequence:
ATATCAGCCGAATTCTTCTCCCTTATCTCCAAGTCTTTTATTGAATGGGATAAAAAGATTCTGGAAGTTCATGAGAGTTCACTGGTTTGGTTCAATCCTCATGTATGTTTGACAACATTTATTCGTTTTGCCCAGTGTGACATTTCTCATGTATTGATGTGAATGATGCTGATGTCTTTTAGCATACACAGGACCATAGGGATTTCTACTATCTTGGAGTGATCTGTGGAATGGCGCTCTACAACAGACATCACATCAACATTGACTTTCCACTGGCCTTATTCAAGAAACTCCTCCAGCAGAAGCCCAGTCTGGATGATCTGGAGGAGCTCTCACCTGTGGAGGCCAGGTAAACACCTGACGTTTTTACCATTTCTCGAATGGTTTCAGAGTAGATCATATTTTAATTGTACTTTTATAAATTCTCATTAGAAGTCTGAAAAACCTTCTTGAGGAGGACGAGGAGGAAGTAGTGGATTTGCAACATTTGGATTTCACGG[T/C]AATATAGTTTCTATGCAGGCCCGGATTGGATTATCAGGAGAACCGGGAGAATTCCCGGAGGGCCGGTCTGTTTTTTTTGGCCGCGAGGGCCGGTGTCCCTAGCTGCTTGCACTCTCAGCAGTTGCACTTTTTTCATTTATTTGTTTATTTGACCATAACCTCACTCTTTTTATTCATTAATTTGCTGCAGCTCCGCTCTTTTTATTTATTTTCTCGCAGCCCCGTGAGCAAAATGTAGCCCGCAGGTTAATGATGATCATCATTAACCTGCGGGCTGCACCCCATTTCACCACTAACAGCTTCACCTTAGTGAATATTAATTAATATTAATGAATATTACACCTGCTCAATGAAAATCAGATGATTCACTACATTAATAAATCTGACATAACTTGATCAGAAATCTAAAAAGGGGAGAAAAAGAGTAGACATCAATAGCAGCAGATAACAGTGCAGTGCTTACCTGAGCCATCGTGGTCTAGTGGTTAGCACGTTACGTT
Associated Phenotype:
Not determined