ZMP
si:ch211-198d18.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC561983 [Source:RefSeq peptide;Acc:NP_001124071]
Human Orthologue:
USP6NL
Human Description:
USP6 N-terminal like [Source:HGNC Symbol;Acc:16858]
Mouse Orthologue:
Usp6nl
Mouse Description:
USP6 N-terminal like Gene [Source:MGI Symbol;Acc:MGI:2138893]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16612 | Essential Splice Site | Available for shipment | Available now |
| sa20282 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16612
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000038627 | Essential Splice Site | 25 | 405 | None | 13 |
| ENSDART00000100391 | None | None | 747 | None | 14 |
| ENSDART00000123199 | Essential Splice Site | 26 | 827 | None | 14 |
| ENSDART00000143571 | Essential Splice Site | 43 | 423 | None | 14 |
Genomic Location (Zv9):
Chromosome 4 (position 22750244)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 24093579 |
| GRCz11 | 4 | 23814554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGAAGTTGGAACAGGAGCGAGCTGAGATACTCGYMAAATATGATAAGG[T/G]GAGAGAAGACAGCTKATRTTCATTTATGAGCWAACACCCYTCCAAAACWC
Long Flanking Sequence:
TTCATATTTGTCAAATCAAGAATGCATTCAATTGATGTTTTTTAGTACTCTGCCTCCAATTGTGCACATTTTTACAATAACTAAAGAACACATCCACATTATTCGCTGTACATCATGTAGACATGCACTTTATAGAGACCCTATTGATTCTGGATCTTTCCTATAAAAGCAGCCTCAGAATGTTTGCTTTAGCCGCGAATGACGCAGTTTGCCCTTGAGGGCCACAGACTGGCTCAGACCTATTTGAACAGCCACTTGTTGCTATGCTCGAGCAGATAGAAAAGAGAAAATGTGTGCGTGTGTCCATGTGGGGACAAAAGTCCACCATTCTTGTATCTTAATTTCTGAAAGCCAGGCTTATTAGAGAGGATTCGCACAGTGGATGGTGAAAATTGCAGCTAATTGGTGTCTGTTTCTCTTTCCAGCGTCTGATTCTGAGCAAGATGCTGCAGTGAAGTTGGAACAGGAGCGAGCTGAGATACTCGCCAAATATGATAAGG[T/G]GAGAGAAGACAGCTGATATTCATTTATGAGCTAACACCCTTCCAAAACTCTTGGATCTAATACATTTTCCCATCCAATCAGATTTGTCATAATTCACAAGCCGCAAATGTCACAATTAATGTTCTTGCTTTCATCTCAATTATTCTCTATTCTAATCAGAGCAGGGTAAAAATCTGGTGTCAAATCTGCTGCTTAATCAATATGTTGAAAACAGGACCAGTGGCTAAACCAGGGGTTCTCAAAGTCTCAATTCAAAGATACAATAGTGATGATTTTGTGGTAATGAATATGAAGTTAGCTTTGGCTTTGTCATCTTTCTAAGAGTATTGTGCCTTGGCGTTTAAAAGGTCTCGTTATTTTCCGCTATAAAGTCTCTCATGTGTGTCCGGTTTGTAAATTGATAGGCTAAATAGAGTGTAATCTGAGCTCTCATTAGGGGGCTGTAATTCCGTAACGTGTGTGTTAATTGGATTGTGATAAGCTCTCCTACACTGGGATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20282
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000038627 | Nonsense | 286 | 405 | 11 | 13 |
| ENSDART00000100391 | Nonsense | 209 | 747 | 12 | 14 |
| ENSDART00000123199 | Nonsense | 289 | 827 | 12 | 14 |
| ENSDART00000143571 | Nonsense | 304 | 423 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 4 (position 22716736)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 24060071 |
| GRCz11 | 4 | 23781046 |
KASP Assay ID:
2259-4954.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTGAATAGACTCCATTCACGCTGACACTGAGAATATGGGACATTTA[T/A]ATTCTGGAAGGAGAGCGAGTCCTGACTGCAATGTCTTACACCATCCTGAA
Long Flanking Sequence:
TATACATATCGTTTTTGTAGTTTTGAAGCCAACTCCAAATAGGATAGAGCGTGCATCCACACCTCTATAGGCTTTTGGAATATTTTTTTTACATTTGACACCCTTACAGCCTTACTAACACCCTTTATGTAAGCTCAGGTTTTATTTATGGTGATAAATATGGTTATAGTCTGTTATTTAGAAACAATGCTTTGTTTGATTTTTGCCTTGCCCGTACAGTAACTGTTCTTTGCTGCCCTCTGCAGGATAACCAGGAGGTCTACACCAGCTTATACACTATGAAGTGGTTCTTTCAGTGTTTCTTGGACCGGGTATGAACACTTAATACACAGTTTTAGTAAATCTAAGCATATTATTTTTATTACTGTTGTTGTTGTTGTTATCATTATTGTATATCATGATGTTCTATTATTGCTTTGTACAATATGTAGTGTTATTGATTTATGTGCGTGTTTTGAATAGACTCCATTCACGCTGACACTGAGAATATGGGACATTTA[T/A]ATTCTGGAAGGAGAGCGAGTCCTGACTGCAATGTCTTACACCATCCTGAAACTTCACAAAAGTAATGAGTGTGTGTGTGTGTGTTGTGTTTGTTTGGTTTTATAGGCAACATTATTCCCAGATGTAAGCTAAATCTCCTCAAAATATGTTTAAACACTATTTAAATGTATATTATTTTTAAATAGAAGAAACTGATTTGTCTGTGCAAAATAGACTGTAATAATTATAATTAGCTATAATCATTGAGTGATTCTTAAAGGGATAGTTCACCCAAAACTATTAAAACATCCTCATCATTTACTCACACTCTTTAACAAGCGTTAAAACTCATATAAAAAAAAACACAAAACAAGTTAAACACAAAACAAGACATTCTGAAGAATGTTTGGAAAACATATTAGGAACTAAAAAATACTATGGAAGTCGATGCCTGCTTTTTCCAACATTGCCCAGATTGTTTGTGTTTGACAGAAGAAAGAAGCTTAAACAGTTTTGGAACA
Associated Phenotype:
Not determined