ZMP
huwe1
Ensembl ID:
ZFIN ID:
Human Orthologue:
HUWE1
Human Description:
HECT, UBA and WWE domain containing 1 [Source:HGNC Symbol;Acc:30892]
Mouse Orthologue:
Huwe1
Mouse Description:
HECT, UBA and WWE domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1926884]
Alleles
There are 16 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa618 | Essential Splice Site | Available for shipment | Available now |
sa37739 | Nonsense | Available for shipment | Available now |
sa15608 | Essential Splice Site | Available for shipment | Available now |
sa24357 | Nonsense | Available for shipment | Available now |
sa17915 | Essential Splice Site | Available for shipment | Available now |
sa24358 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa618
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 |
---|---|---|---|---|---|
ENSDART00000006657 | Essential Splice Site | 231 | 4569 | 7 | 80 |
ENSDART00000146990 | Essential Splice Site | 235 | 4474 | 7 | 79 |
Genomic Location (Zv9):
Chromosome 23 (position 28740634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28571201 |
GRCz11 | 23 | 28497742 |
KASP Assay ID:
554-0528.1 (used for ordering genotyping assays)
KASP Sequence:
GTCAAGCAGTAATACGCTACACTACATTCATATCGAACAACTTGATAAGG[T/C]GAGTTTCTGGGGTTTACATTTGCTGTCCTTGTGGAACAGTTAATGGAAGT
Long Flanking Sequence:
GTCACATGACTGCATTTTGGTTTTTTTAACTGGTTCAGACTAAAACAATCAGTGTGGTGTGAAAATGTCCCAAAAATGGCAGAAAAATGCTACAATGTGTCATTTATTCCCCTTTTTCTGGACCAAATGAACCGAACCACAGATGTGAAAGCCCGCTTAAACTTCATCTTGCAAGTGTTTCTTTTTTCTGAGTCGTCTGTTTTTTTGTTTTGCGCAGAAATATCCACCGAGTGCCACCACATTGCACTTTGAGTTCTATGCAGAGCCCAGCTCTGAGGTCAAAGTGGAAAAGAAGGTATGCACTGAGTCGCGCTTCCCTTTATATTGCCATTCTCTTTTTACAATGTTTTTGTTTCTTTTTTTTGTTAAGCTGAACAATTCATTTTTTTTGTTCTGTCTTGTTGTCGTGTAGACGCTTTCAACCATTTTTTTGTACCTTTTATGTCAACAGTCAAGCAGTAATACGCTACACTACATTCATATCGAACAACTTGATAAGG[T/C]GAGTTTCTGGGGTTTACATTTGCTGTCCTTGTGGAACAGTTAATGGAAGTGCATAGACGCTTAATAGCTATTGATTGCACTTGAATCTAATTTCTGCTCCTCCCCGGTGCACCCTCAGATTTCTGAAAGCCCCTCTGAGATCATGGAGTCTCTAACGGCTATGTACAACATACCTAAAGACAAGCAAATATTGCTTTTTACACACATTCGCCTGGCTCACGGCTTCTCCAACCACAAGAGGAGACTGCAGGCTGTTCAAGCCAGGCTGCATGCCATCTCCATACTCGGTGAGTGACCCCTCTGGTGCTGACCAAAATAAGAATCGGTATTTATTTTCATGAAATGGCACTAGGTTCTCGCTTTCTGTCTGGTGAGGTTGATGTAATGTGTGGTTATATTTTTTGTGCAGTGTACTCCAACGCCCTCCAGGAGTCAGCCAATAGCATACTCTATAATGGGCTTATAGAGGAGCTAGTGGATGTACTTCAGATCACAGACAA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa37739
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 |
---|---|---|---|---|---|
ENSDART00000006657 | Nonsense | 423 | 4569 | 12 | 80 |
ENSDART00000146990 | Nonsense | 426 | 4474 | 12 | 79 |
Genomic Location (Zv9):
Chromosome 23 (position 28743691)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28574258 |
GRCz11 | 23 | 28500799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTAACCTATGCCACTTTCACATCAGGTGATCAAGTTCCTAGGGGACGAG[C/T]AGGACCAGATTACCTTTGTGACGCGGGCAGTGAGAGTTGTGGATCTCATC
Long Flanking Sequence:
CAGATTTTATTGATGAACCGTCAAAACAATTGTTGCAGGACATTAAGGCTGCTTCTTTGCGGACGTTGACATCAATAGTCCACCTGGAACGCACCCCCAAGCTCTCCAACATCATCGACTGCACAGGAACAGCCTCCTATCATGGATTTCTGCCTGTGCTTGTTCGCAACTGCATACAGGCAATGATCGGTAAGGAGATGTAAACTTTCAGCTAAGATTTCTCAACTTCAGATTCTGTATTTTTGACATTTGTTCCTGTTTTAGACCCACTGATGGAGCCGTACCCCCACCAGTTTGCCACAGCCCTCTTCTCCTTCCTCTACCACTTGGCTAGCTATGACGCAGGTGGAGAGGCCTTGGTGTCTTGTGGTATGATGGAGGCATTGCTAAAGGTTTGTAAATTGCTGCTTCCTTATTTGTTCAGCATTTAATGAGAAAGTTTTATGTGTTGTTAACCTATGCCACTTTCACATCAGGTGATCAAGTTCCTAGGGGACGAG[C/T]AGGACCAGATTACCTTTGTGACGCGGGCAGTGAGAGTTGTGGATCTCATCACCAATCTGGACATGGCCGCTTTTCAGTCCCACGGCGGCCTCTCAATCTTTATCTGCAGACTGGAGGTATTGAAACTCGTTCAGCCCCTTGTTCCTGCATAGACCATTCAGCTTTTTGCATTCTGCCCTTTTGTTGACGGAATGTGACCCCATTGTTTTTTTGTGCAGCATGAGGTTGACCTCTCCAGAAAAGAGTGCCCTTTTGTAATCAAACCAAAGATCCAGAGGCCCAGCACAGCCACTGAGACAGAGGACATGGATACAGATATGGACAGTTAGTAGTATCATCTTATTAGTGGTACCTTGCTTAGTTTATTCTTATTTAAATCTGTGTTTTGTATGCACAGACTGTGTAATCTTCACACTGGGGTTTTGTTAATGGTAATACAAGGATTATATTTTTTGCTTTTGTAAAGTCACCTTATGGAAGAGGCTCACTTCATTCCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15608
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 |
---|---|---|---|---|---|
ENSDART00000006657 | Essential Splice Site | 533 | 4569 | 14 | 80 |
ENSDART00000146990 | Essential Splice Site | 536 | 4474 | 14 | 79 |
Genomic Location (Zv9):
Chromosome 23 (position 28746954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28577521 |
GRCz11 | 23 | 28504062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACCGATTCGCGAGCACARAGCAATGCATCCAGCACCCCAAGAGCAGG[T/C]AAAAAYACTNCCAARTACTCTAACTCACAWGTCAGTGGGTGTGYAGTTTAG
Long Flanking Sequence:
CTAATTTGGTGATTGCTTTAGATGTTCGGGCTGCAGTAAACCAGTCATCTCGTTGCTAATGGTTTTTGCTTAAAAGAAATTTAAACGGACAAAGAATAACATAACATAAAATAAATTTTAATACTGAATCATGTCTTGCCTACTTGCTCAATCACTGCTGTAAAAACTTCTATAAAATATAAGGAAAGCTTGTCAATACCCAGTCTTAAAATGAATATGTATAGAATGTCGGAGGCTTCAAAAAAAAAGATGGCAGTAAACAGTAAAATTAGTCTGTATGACATAATCCAGTTCTAAATCCATATGATTGAAGTAAAGAATTAGGGATTGTTGCTTTTCTATTTTAATGTCTGTTTTTGATGAAATTATTAAAACATGATTGTTAATGTAGTGTCCGAGGTTGCCATGGAGAGCAGTCCTGGACCATCCACTTCTTCTGGCTCCAGAGCAGAGACCGATTCGCGAGCACAAAGCAATGCATCCAGCACCCCAAGAGCAGG[T/C]AAAAATACTCCAAGTACTCTAACTCACAAGTCAGTGGGTGTGCAGTTTAGGAAATCTGGGCCATTTGTTAACATTTGTTTTTTGTTTTTGTTTTTCCTAACAGGAGTGCAGTGCATCCCTCAAAGGGCCGCTCTGTTGAAATCCATGTTAAACTTTTTGAAAAAAGCCATTCAGGACCCTGCTTTCTCTGATGGCATTCGCCATGGTATGAAACTCGTCGTATTTAATGATGATATAATTTTTACGTGATTTCTTAATAGTGTTTTTATTTGCTTTATTTGCCTCTGCGCTCTCTTTATAGTAATGGATGGGTCCCTTCCTACCTCTCTGAAACACATTATCAGTAATGCAGAGTATTATGGACCATCACTGTTTCTCCTGGGTAAGCACATTGAGGCCAGTATTTTTGCTGCCGTTGAAATATTAGCTAAGTTCCTCGTGGATATGGCTTCAAGGTCACCTCTACAAAAGAGTAGTCACTAAAGCAATATGGTTAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24357
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 |
---|---|---|---|---|---|
ENSDART00000006657 | Nonsense | 957 | 4569 | 24 | 80 |
ENSDART00000146990 | Nonsense | 960 | 4474 | 24 | 79 |
Genomic Location (Zv9):
Chromosome 23 (position 28753635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28584202 |
GRCz11 | 23 | 28510743 |
KASP Assay ID:
2261-7913.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATCTCTTGCTCCTCCTTTCAGAGCGAGATTCGTGCTATCTCTGTGAAT[C/T]AATGGGGATCTCAACTGGGTCTTAGTGTTTTGAACAAACTGAGTCAGCTG
Long Flanking Sequence:
TTCCACTGAATGCCCTCATGTGTCAGTTAATTTTTCTGTATTTAGTGTTTTGATTATTTTGTTTGCTCATTGTGTCCTAGACTTTATCTCATGAGCCAAAAGTCCTCCAGGAGGGTCTGTGTCAGTTGGACAGCATACTCTCTGCTCTGGAGCCACTTCACCGGCCCATTGAGGTTCCTGGAGGCTCTGTTCTGCTCAGAGAGCTGGCTAACGCAGGCCATGTCACAGACGCCACACTGTCTGCACGCGCCACCCCACTGCTGCATGCCCTCACAGCGGCACATGCGTACATCCTCATGTTCGTTCATACCTGCAGAGTCGGACAGGTACGCAAATAGGCAGCTGTTTGGAGCTCCTTCATTTAATAATTTATTTGAATAAAATTCTGAAAGTCAACAAAGTTTTGGGAATTGTAGCTTTTTAATGGAAAGACTTATGGTGGAGCTAACAGCATCTCTTGCTCCTCCTTTCAGAGCGAGATTCGTGCTATCTCTGTGAAT[C/T]AATGGGGATCTCAACTGGGTCTTAGTGTTTTGAACAAACTGAGTCAGCTGTATTGCTCTCTGGTGTGGGAGAGCACTGTGCTACTGTCCCTCTGTACACCAAACAGGTAAGGACTGCTCTCATCACAGCTGAGCCCCAAGTACACAGTAGGCTGATAACAGGTGGTCAGCCAGGGCACATTACTGTTTTCAAATGATTGAAACATGAATGATTTGGAAATTTGACAGTAGTTGTGTGTGACCTTTTTTAAAAAATAAGTGATTTGTCTTTTATTTTGCAGTTTGCCTCCTGGCTGTGAGTTTGGTCAGGCTGACATGCAGAAACTTGTGCCTAAAGAGGATAAACCTTCTAGTAGCACTGCAGCTACAGGACGGAGAACTGGTAAAATACTGCAATTTACTCTATTGTACCAGTTCATGCTTCATCCAAGTTCATGATTAAGCTCATTATTTTTTCTGCCTCCTTATTTAATATGATTTAATATATACACTTTGTTTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17915
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 |
---|---|---|---|---|---|
ENSDART00000006657 | Essential Splice Site | 1437 | 4569 | 31 | 80 |
ENSDART00000146990 | Essential Splice Site | 1404 | 4474 | 31 | 79 |
Genomic Location (Zv9):
Chromosome 23 (position 28758134)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28588701 |
GRCz11 | 23 | 28515242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGTACCTGCTCACACACCCTCCACCACTGCTCAGCGCGGCTGTCAGAG[T/G]AAGACCCTAAYCAACACAGACAAAACCCTCWGTCTTTCTCCCATACACTC
Long Flanking Sequence:
TCAGGAACAGCCGGAGTAGTTGGAGAAGCAGTGGCTGCAGGTGCCAATGGAAACACTGCTGGAGGCTCTACAGAGGAGGCCAGCAACTCTACTACAGCACGCAGAGAGCCACAGGTCAACCAAGCTCAGCTCACACAGGTATGTCACTTCCTGTTATTAGATATTCCTGCTGCATTTAAATTTGACTTTTAAAATTCTTTTTCAAGGATTTCAAGAATTTCAAGCATTAATATTATAGTAGTATTTTTGGGCTTTGATCATTTAATTTCTTACCATAAAAAGGCCCTGTTAAGTGTATTAATATGTAATATTTGTGAACTAAGTCTTTAATATTTGAAAAAAGAGCTAATCAACCAAATCTCTACCTCTTTCACAGCTAATGGACATGGGCTTCTCCAGAGAGCACGCAATGGAGGCTTTGCTGAACACCAGCACTATGGAACAGGCCACTGAGTACCTGCTCACACACCCTCCACCACTGCTCAGCGCGGCTGTCAGAG[T/G]AAGACCCTAACCAACACAGACAAAACCCTCTGTCTTTCTCCCATACACTCATACTCACAAATACACACACACACATACATGCAGACAGGATGCACACACAAGGCATAAGCTAGTGTAGTCACTCTGAGCTTTGTTTCTGTAGGAGTTCACCATGTCTGAAGAAGACCAGATGATGCGGGCCATTGCCATGTCTCTAGGTCAAGAAGTTAGCATGGAGCAGCGCTCAGACTCACCTGAGGTGGGCACTCACACACACACACACATTATATAAAAATAGGAATAATTGAGCAGCACAGCATAGGTCACCTCACATGTCTGCTTCTCATCTTCTTCAGAAAACTTTCTCTGCCTTTAAACAGACACTCAAATCTAACCCATTCCTTTTTGTCTGCAGGAAGCAGCTCGCAGGCGTGAGGAGGAGGAGAGGAGAGCGAGGGAGCGGGTAGAGGAGGAAGAAGCTCGTTGTCTGGAGCGCTTTCTGGAAGCAGAGCCTCTTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24358
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 |
---|---|---|---|---|---|
ENSDART00000006657 | Essential Splice Site | 4472 | 4569 | 78 | 80 |
ENSDART00000146990 | Essential Splice Site | 4396 | 4474 | 77 | 79 |
Genomic Location (Zv9):
Chromosome 23 (position 28807193)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28637760 |
GRCz11 | 23 | 28564301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCAAGGCCAATACTGAATACCATAAATATCAGTCCAGTTCTATTCAGG[T/C]GTGTACACACACAATAGGATGACATGAAATAAAATATTTGATTGTTTATT
Long Flanking Sequence:
ACACAAAAATATAAATTACTTATTAAATATGAATTACAATATGAGTTTCCTTCTAACATTTTCATATTAAGAGATTTGTGATAATCTCCTCCTCATGTTATATTCACAGGTCCAAGAGTTTGGCGTGTGTGAAGTGAGAGATCTGAAGGCCAACGGTGCCAACATTCTTGTCACAGAAGAGAATAAGAAGGAATATGTGCATCTGGTCTGCCAGATGAAGATGACAGGTGAGTGCACACTCCAATAAACGTCACTGCTCCAGAGGAAGGGGAAGCTTAAAGAGTATGTCAGGAAGCTGAAACATCTATGTTTCTCAGGTGCAATCCGTAAACAGCTGGCTGCCTTCCTGGAGGGCTTTTATGAGATCATCCCCAAGAGACTGATCTCCATCTTCACTGAGCAAGAGCTGGAGCTGCTCATCTCCGGCCTGCCCACCATTGACATCGACGACCTCAAGGCCAATACTGAATACCATAAATATCAGTCCAGTTCTATTCAGG[T/C]GTGTACACACACAATAGGATGACATGAAATAAAATATTTGATTGTTTATTTTTTAATTACTGTTGTCTTCATCTTGGCACATCATTCTGAAGGTTTTATGACCTTTGCTTCAATAGTAGTGAAAGAAATTCCACGTTATCAGGCATGGAAAAGGATAGGGTTGATAGCTTTTGTATGCCAACTCAGAAGTAGGGCTGGGCGATTTGGCCTAAAATTAAAATCTCGATTAGTTGAACATTTTAACTCTTACGATTAGTGAACGATAATTTTATTTATTTATTTATTTATTTATTTAATGTTTTTGCCCTCTTAGTTCACTGACAGGTTTAATACAGTGAATATGTTCACATATTACAAGTGAGAGATTTCTGAATGAAGGGTGCATTATTTGGTTATTTGCGTGTCGTTGTGACGTGTAGTTACATTTTTTATGTGTGCAGGTATGCGAAGGCTGTGGCAGACTGTATGCGTACACTTGGCAGAAGTACAATATCAGAATT
Associated Phenotype:
Not determined