Busch Lab

ZMP

hectd1

Ensembl ID:
ENSDARG00000054213
ZFIN ID:
ZDB-GENE-030616-153
Description:
E3 ubiquitin-protein ligase HECTD1 [Source:RefSeq peptide;Acc:NP_001002504]
Human Orthologue:
HECTD1
Human Description:
HECT domain containing 1 [Source:HGNC Symbol;Acc:20157]
Mouse Orthologue:
Hectd1
Mouse Description:
HECT domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2384768]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa36435 Essential Splice Site Available for shipment Available now
sa17678 Essential Splice Site Available for shipment Available now
sa18554 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa36435
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076340 Essential Splice Site None 163 None 5
ENSDART00000076344 Essential Splice Site None 2576 None 42

The following transcripts of ENSDARG00000054213 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 28729598)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 28653525
GRCz11 17 28670488
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAATTCTGTCCACCCTGTGTGTGTTTTCTCGTCGTTCGGCGATAAACGG[T/A]GAGTGTTTGTGTGTGTCGGCAGAGGGTTTGTGTCTCTGCTTCAGAGGCGC
Long Flanking Sequence:
AAATGTCTTAAAATCTCTTAAATATGTCTCTTTTGTTATTATTCATCGATAAAACGGATAATGCATTCAAGTAGTTTTGGGATTTACGTTAACCAAATATAGCTTGCTTCGTATATTAGACAGCGAGCGTCTTTGTTCACTTTGTACAATTTCGCAATATAGGTGAATGAATGTCTGATCTGTTTTTTTGTCGACCTCGATGAAGGCGAGGTGTTTTAGCACCCCCTGTCGCTGAGCCGCATCGCTGCGTGTTTCTGACCGCTGCTGCTGCTGCTGCCGCGGAGCCTCGTGATATGCGGAGCCTCGACTAGTTCTCTCGTCTGCTCTCCATTTCACTCGATATTTCACCCGTCGCCTTCCCGTTCACTTTGACCTCTACCTTACGACCAACAGAAGCGGGGAATGAAGCAATATTCACATCTCTCCGACTGATACAACTTCATTCCGAGACGAATTCTGTCCACCCTGTGTGTGTTTTCTCGTCGTTCGGCGATAAACGG[T/A]GAGTGTTTGTGTGTGTCGGCAGAGGGTTTGTGTCTCTGCTTCAGAGGCGCGTTGAGGCCTCGGGCTTTCACTCAAATTTAGCTCGCGGATTTAGTGGTAAACAGGAGGCCGCTGATGTGTGTCTTTGTTTTATGGGTTTTCAACGTTAAAATGTTTTCAGATCTATTTTATGTATGGATGGAAAACATATTCCTTCGTTATTCAAATAAAGTAAACGAAGTTTGGGATTAATTAGGTCTCCCGAAGTGAAGCTAACAGGACGCATTTTAGCTAACGTAATCCCAGCTAGCCAAGTGTCGCTTTCACAGCCGTTTATTAGTGGTTTTACTCTTTTAGTGGGAAAAACATATAGTCAAATACAATTGTTAACGAGAAATTAAACGTTTGTAGAGTCTGTCATGGCGTTTAAGCTAACATAAGCTGTTTGAGCTCCAGAAAGAGGCCATCAGGACCAGATTGGACGTGAATATATTATTATTTCTTTGCTTAACTTGTTTCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17678
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076340 None None 163 None 5
ENSDART00000076344 Essential Splice Site 958 2576 18 42

The following transcripts of ENSDARG00000054213 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 28744148)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 28668075
GRCz11 17 28685038
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATAAATGTGTTCAAGACTGCATTCACTGAAAATGAAGATGACGAAAGG[T/C]AAACTGTATATTATGTTCCACTTGAACGGTTTGTGTTTTTGTTGGGCTCT
Long Flanking Sequence:
ATTGCCACTCAGCTGGAGTCTGCTTGGGAGCTACATACTAACAGACAGGTAGAATTATGCTAAATGTGCAAATTTGAAATGCAAATATATGTTCTCTCATTTTACCCCATGTTGTTGAGGTCGAAAAAACAAAAAAATTTTCCCGTGTTTTTTCTTTTTTATCAGTGCATTGAAGGTGAAAACACATGGCGAGACCTCATGAAAACAGCACTAGAGAATTTAATAGTAGTTCTCAAGGATGAGAACACCATTTCTCCTTATGAAATGTGCAGCAGTGGCCTCGTACAAGCGCTTTTTACTGTCCTCAGCAATGTGAGTCACACACACAAATTAGTTTTGTCAGTTGTAAACATGTTGTCAGCTTTTATTCTCATTGCTCATTACCTTCTTACTATTTTTCTCAGAGTGTGGAACTTGACATAAAACATGATTGTAAGCCTCTGATGGAAAGAATAAATGTGTTCAAGACTGCATTCACTGAAAATGAAGATGACGAAAGG[T/C]AAACTGTATATTATGTTCCACTTGAACGGTTTGTGTTTTTGTTGGGCTCTTCTTAGAAGTCTACATCTTAACCAGCAGTTTATTTGTATGGTTAGGATGAAATGAGAGAATTTGTTTGTAGTCTGTTTGTCTTATGTCAATGCCTCTCTCTCTCTCACCTCCAGCCGACCCGCAGTTGCCTTAATCCGCAAACTGATAGCAGTGCTGGAATCAATAGAGCGGCTACCTTTGCACTTATATGATACCCCAGGCTCAACATATAATTTACAGGTCAGTCTCCATCTTTGCAGATGTATTTTTAGTTTAGAACATTTTTAAATGGTGACCTCTTTCATTATGAATAGTATAGTTTCACTGAATGGTTTTCCTGTTGTATTAGATACTGACAAGGAGGTTACGCTTCCGCCTGGAACGTGCTCCAGGTGAAACAGCCCTGATTGATCGAACTGGAAGAATGTTGAAGATGGAGCCGCTGGCCACTGTTGAGTCACTTGAGCAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18554
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076340 None None 163 None 5
ENSDART00000076344 Essential Splice Site 993 2576 19 42

The following transcripts of ENSDARG00000054213 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 28744419)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 28668346
GRCz11 17 28685309
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTACCTTTGCAYTTRTATGATACCCCAGGCTCAACAWATAATTTACAG[G/T]TCAGTCTYCATCTTTGCAGATGTATTTTTAGTTTAGAACWTTTTTAAATG
Long Flanking Sequence:
GCAGTGGCCTCGTACAAGCGCTTTTTACTGTCCTCAGCAATGTGAGTCACACACACAAATTAGTTTTGTCAGTTGTAAACATGTTGTCAGCTTTTATTCTCATTGCTCATTACCTTCTTACTATTTTTCTCAGAGTGTGGAACTTGACATAAAACATGATTGTAAGCCTCTGATGGAAAGAATAAATGTGTTCAAGACTGCATTCACTGAAAATGAAGATGACGAAAGGTAAACTGTATATTATGTTCCACTTGAACGGTTTGTGTTTTTGTTGGGCTCTTCTTAGAAGTCTACATCTTAACCAGCAGTTTATTTGTATGGTTAGGATGAAATGAGAGAATTTGTTTGTAGTCTGTTTGTCTTATGTCAATGCCTCTCTCTCTCTCACCTCCAGCCGACCCGCAGTTGCCTTAATCCGCAAACTGATAGCAGTGCTGGAATCAATAGAGCGGCTACCTTTGCACTTATATGATACCCCAGGCTCAACATATAATTTACAG[G/T]TCAGTCTCCATCTTTGCAGATGTATTTTTAGTTTAGAACATTTTTAAATGGTGACCTCTTTCATTATGAATAGTATAGTTTCACTGAATGGTTTTCCTGTTGTATTAGATACTGACAAGGAGGTTACGCTTCCGCCTGGAACGTGCTCCAGGTGAAACAGCCCTGATTGATCGAACTGGAAGAATGTTGAAGATGGAGCCGCTGGCCACTGTTGAGTCACTTGAGCAGTATCTGCTCAAGATGGTAGGATGTTGTCTCTTTTTTCCTATTATTCTATATTGACTCATTTGTATTCTTACAGGCCTCTTAGAAAAAGTAACTTTTGTCTCATCCTTCCCCAGGTGGCCAAGCAGTGGTATGACTTTGACCGGTCCTCATTCATCTTCGTTAGGAAGCTCAGAGAGGGCCAGAACTTCACCTTCAGGCACCAGCATGACTTTGATGAGAATGGAATTGTGTATTGGATTGGTACCAATGCAAAGTGAGCAGCTTTGTGCTTT
Associated Phenotype:
Not determined