ZMP
si:dkey-72l14.3
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC562480 [Source:RefSeq peptide;Acc:NP_001038450]
Human Orthologue:
HYAL3
Human Description:
hyaluronoglucosaminidase 3 [Source:HGNC Symbol;Acc:5322]
Mouse Orthologue:
Hyal3
Mouse Description:
hyaluronoglucosaminidase 3 Gene [Source:MGI Symbol;Acc:MGI:1330288]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6100 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21305 | Nonsense | Available for shipment | Available now |
| sa7138 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6100
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 |
|---|---|---|---|---|---|
| ENSDART00000086601 | Essential Splice Site | 171 | 505 | 1 | 4 |
| ENSDART00000135456 | Essential Splice Site | 171 | 505 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 26830360)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25958278 |
| GRCz11 | 8 | 25977417 |
KASP Assay ID:
554-3726.1 (used for ordering genotyping assays)
KASP Sequence:
GAGRATTTTTTCCAGATTGGAGTGTAGAGGAAGTGGAGAAATGGTCTCAG[G/A]TGATGACATTTNAATAAAGTATAGAAACTAAAGCTGTATACAAAATCAYY
Long Flanking Sequence:
AGCGCATGTTCATCCTCCCCTCCCTTTCTCTTACATTCCTTTATCTCTGTTTCTTCATTCCTGCACGTTTCTGTGGTCCTTCCCGGGCCCCTCTCCTTGCGGGCCAGCCCTTCCTGGTGCTTTGGGGGGTTCCAGATAAAGACTGTTTGGGCCGGCCAAACCCAGCTGCATTTGGGATGGAGTGGGAAGGTCGTGTGGCAATATTTTATGAAGACACGCTCGGACTTTATCCATATTTCACTGTGCAGGATCGTCCTGTCAACGGAGGCCTACCACAACACACCAGCCTTGACCTTCACCTCCAGAGGGTGGAGGGGGACCTGACTGTCTCATTACCCCAGGCAGGAGCACCTGGGCTGGGGATTCTGCGCTGGCAGGAGTGGGCACCTCAGTGGAACAGGAACAGAGAAAATAAAGCAAAGTACCTTGTTGAGTCGAGAGCTCTTCTCCGAGGATTTTTTCCAGATTGGAGTGTAGAGGAAGTGGAGAAATGGTCTCAG[G/A]TGATGACATTTTAATAAAGTATAGAAACTAAAGCTGTATACAAAATCACTCCTTATACACTCATTCACTATTCCCTACAGCAGTCCACAAATGTAGTCCATTAGATGATTGAATAAAAACGAAGGAACACTCAGCGAGCGGTCTAATAGTATGAAACAAAGTATTTTGATTTGTCATGTATACAAATGTTACTTTATGTTGTACACTCATTATTGTAGGGCATTGTGGGATTGATTGAGCGCACTTCAGAATGTCCACTATGGTTTCAGACACCACTACAAATAGCTGCTCCCTGAAATAGTGCACTATTTAATAGTATAGGGGCAATACTGCCTATCATACAGCCTATCATTCTGCATTCAACTGTATTAACCAATTATATTATGTGATTTCACGTTAGGTTGACTTTGAGGCAGCAGCACAGTCCATAATGATGGAAACCCTGCGGGAGGTGAAGAGGCTCCGCCCACAGAGATTATGGGGCATGGCTCCATATCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21305
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086601 | Nonsense | 312 | 505 | 3 | 4 |
| ENSDART00000135456 | Nonsense | 312 | 505 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 26827859)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25955777 |
| GRCz11 | 8 | 25974916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGTATGTACTGTATGATTTACAGGCTGACCTGGTGAATACAATTGGA[G/T]AGAGTGCTGCTATGGGAGCATCTGGAGTCATTATATGGGAAAAATCATTA
Long Flanking Sequence:
GCAATTGAATAAATAGGAAAATGCCCATGAATCAAAAGCTTTGAGCAAGTGTCAATAGATTCACACTGATGAACTTTTAAAGGTGTGACAATATATGAATTTAGACTTTTTTCAACTCTAATGAGGAAACAGATTTTAAAAGGAGATGTGCCATGTTTGACATGATTCGGACTAAAAACACAAATTAGGATAGTTGTGTTGTTGATTTGAATTATATCTATAAACAAAACTGACCGTTTTGAAAGTCTTATTTCTTTCCTCATTTAATATAAGTTATAAATATATATTTATATATATTAGTTGTAAATGTAGGACTGTAAATAGTTCATGTCTTATCATGATACCTGCTTAGTGGAACAACGAACATTAAAAGACATTGGTGAACAACTAATATTAAAACAGACATTGGTGAACAGCTAATTTTAAGAGTCATTGGTGTTTCTTCTATAAATATGTATGTACTGTATGATTTACAGGCTGACCTGGTGAATACAATTGGA[G/T]AGAGTGCTGCTATGGGAGCATCTGGAGTCATTATATGGGAAAAATCATTAGCAGTTAAAACACAGGTAATCGTTTAGTTTACACTTAATGTTTGACTTTTTTTATTGATCAGAAATGGCTCGAAACATGTTAAGAAAGATTTCTATCTCACATAAATAATGTCCTGAAATAAATGTTCTTGCACATAAAATGAAGCATCACAACTATTTTTACCATTCCCAGCAAACAATTTTGTTTAAGAGAAGTCTAATAGACATCTAAACGTAGACAGCTTGGATAAAACAAGGCTAAACTTGATTTTAAATCTCTACTAAATCTAATAGACCTCAAAGAATAGGCAAAAAAATCTGTCAAACAGACAGACTTTATATGTATAGTCATTCATTTCTGTTTATTTGATGACTAGTCTAGTTTTGGACTATTCTTAGACCTCTATTAGATTTTCACAGACAGCCCAAGTTTAGCCTTGTTTTAGCGAAGATGACTATGTTTAGACGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7138
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086601 | Nonsense | 378 | 505 | 4 | 4 |
| ENSDART00000135456 | Nonsense | 378 | 505 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 26826958)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25954876 |
| GRCz11 | 8 | 25974015 |
KASP Assay ID:
554-4924.1 (used for ordering genotyping assays)
KASP Sequence:
GYGGGGTCTCTCTGTGYCAAGGCCGYGGACGATGTGTGCGCAAGAAACCC[G/T]AGGACCCCACATACCTGCATCTTCCCTCAGCTCACTTTATGCTGATCCCA
Long Flanking Sequence:
GACTAGTCTAGTTTTGGACTATTCTTAGACCTCTATTAGATTTTCACAGACAGCCCAAGTTTAGCCTTGTTTTAGCGAAGATGACTATGTTTAGACGTCTATTAGACATTTATTAGACATCTTTTTAAAAACAAAAAAATGCTTGCTGGGGCACAGATCCCAAGACTAAATTATATTTTAAAATCAAGCCATTTTAAAGTTAATAAAGATGTTTTGACTGGATTTTGCATCAGATAAGTTCAACAATGCTGAGGCAATGAAATGAAGCGCTTCTTTCAAAAATGTTTAGCCTATAAATTGTACTGACGCCAAAACTTTCAAATCGTTGGTTGATTTTGCTGTATAATTTCCTCCTGTGTCTCCTGCAGAAATCCTGCTCAGAGTTTGGCTCATATGTTCGTCAGGTTCTCGGCCCTTACTCGGTCAATGTGACCACAGCAGCACGTCTCTGCGGGGTCTCTCTGTGCCAAGGCCGCGGACGATGTGTGCGCAAGAAACCC[G/T]AGGACCCCACATACCTGCATCTTCCCTCAGCTCACTTTATGCTGATCCCAAATGGGGCAGAAGGTGTGCGGGCCACCGGCGAGCTTCCCACAGCTTACATTGACCTCTGGAAGAAGGACTTCCGGTGCCAGTGGTTCGAGGCGCTGGAGGGTGCAGCAGCAGATCAAGAATCAGGAGCAGTGCTGGAAAACAGAAGGAAAGCAACATCAGCGACAACAACAACAGTAAAGCCAGTGGTTGGCTCGAGCCAGAGTCAGAGTACAGTGGGTGCAGTGGTACCAGTGGCAGCAGTGCCTACCAAACAGCCAGTGGAAGGTGGAAGCTCAGCCCTTAAAACTCCCGTCGTCCTCCTCTTTTCGCTGGCTCTCTTCAGCTTCGTTGTGTAGGGAGATAAAGTATGACGGGACATTTGGGAACTCCAGTTGGCCTTGATTTTGAAGGAATATCTTCAAGAGAGTTTTGTGAATTGGTGTCTTACATGGGTTTCAACTAACTTAAAA
Associated Phenotype:
Not determined