ZMP
hectd3
Ensembl ID:
ZFIN ID:
Description:
HECT domain containing 3 [Source:RefSeq peptide;Acc:NP_001070627]
Human Orthologue:
HECTD3
Human Description:
HECT domain containing 3 [Source:HGNC Symbol;Acc:26117]
Mouse Orthologue:
Hectd3
Mouse Description:
HECT domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1923858]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19769 | Essential Splice Site | Available for shipment | Available now |
sa19770 | Essential Splice Site | Available for shipment | Available now |
sa11205 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19769
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056795 | Essential Splice Site | 287 | 854 | 5 | 21 |
ENSDART00000144837 | Essential Splice Site | 287 | 854 | 5 | 21 |
The following transcripts of ENSDARG00000038905 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 26631425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26827621 |
GRCz11 | 2 | 26483255 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGACAGCACTGGATCCGTCTGCACATGAGGAGAGGCACTGTGGTCAA[G/A]TAAGGACGACTGGTCTGCTAGCGACTGTAATTAAAAAGGACTTTTTCCAC
Long Flanking Sequence:
ACCGTTTAACCTAATATACGTCAGAAATTTTGTTCTTAATAGTCTTACAAAAAAGTCCTACATTTTACTTTGTGAAACCTGCAGAAACCCTGAAATAAATAAATAAATGTCATATCACTGATGTGCATATTTGGTCCTCAAGGTATGTGCCTCCGACATGGACGTTTGAATGTGACGAGGACCTCGTGCACTACTTCTATGACCACATTGGAAAGGAGGATGAAAATCTTGGCAGTGTGAAGCAATGTGTGACCAGTATTGACGTGTCTTCTAGTTCGGTATGTGATGGCACAGTATCATTCTGCATTACACTGAATAGCAGAGAGCTGCAAACATATCAGATGTTTTCGACTAGTAAGGGAGTTGCTCTGCTTGAAGGAGGACCCTAGTGGTGGAGCAAGCTGTCTGACAGATGGAGACACGGAGACGTACTGGGAGAGCGATGGCATGCAGGGACAGCACTGGATCCGTCTGCACATGAGGAGAGGCACTGTGGTCAA[G/A]TAAGGACGACTGGTCTGCTAGCGACTGTAATTAAAAAGGACTTTTTCCACACTGTACTTAAATCCAGTTGGTTCTAGATAATTTCACAAGTTATGAAATCAGGTCAGTCTGTTCAAACTTTTGTTTTAATGATTTAATGGTTAGTGGACTAGCTCAAAAACAAACTCTTGAGTGTTCTTGAATAAAATACTTTTTACCTTTTAAATATTACACACTAGTAGGTAATCAATAAGTGTGTAGGAAAAATGTACAAAAATAAATATCTGATTTTTCACTGAACATATTAAAACTAGCCTATTAAATCAGCTTATTGTCTTTTTCCACAAATAAATGAAGTGAAATTTATGACTTTTTTCAGGTTTCAAACCTTGTCTTTTTGTTCACATCAGATTTGTTGTTTGCGTGCGTGCGTGTGTTTGTGTGTGTGTGCGTGCATGCGTGTGTTTCTGTGTGTGTGTGTGTGCGCGTGTGCGCGTGTGTGCGTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19770
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056795 | Essential Splice Site | 408 | 854 | 9 | 21 |
ENSDART00000144837 | Essential Splice Site | 408 | 854 | 9 | 21 |
The following transcripts of ENSDARG00000038905 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 26634874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26831070 |
GRCz11 | 2 | 26486704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTTTTAGTGGCACTCAGTGTTTTTTTTTTATGTGTGTGCATGTCTGT[A/C]GGTTCATCACACTTCTGGACAGTCTATTGCCTCATATGGTGCCTGCATGG
Long Flanking Sequence:
GTGAAAATAGCTATTGAAATAAACCTGAAGTGAAAACTTAAATATAACAGCAATACAGTCAAAGCATTTTGTACTACTACAGCAAGTCGGGCTCAAAATGTTTTAGTTTACACATGTATTTAGCATCATCCACTTTTAATTATATTAAAACTCTTAACATCAGACGTAATTGAGGCATTTGCCGTCATCTGAAAGAGAAAGCATGATTAGTAATCTTTATTCATAATATATATTTTTGTTTTAGATGAGGGAATCGACGTACGGATCAGGGGTCTAAAGATCAAATCGTCCTGCGAACGTGACTTGGGCCTGAATGCAGATGTGTTCCAATCTCCCAATCTAGTGCGCTATCCGAGATTGGAGGGCACACCACCTGATGTCCTCTACCGACGTGCACTGGTAATTCAAAGGTAACAACCGGCAACATGTCAATTTCTAAGGGCTTTATTTGAGCTTTTAGTGGCACTCAGTGTTTTTTTTTTATGTGTGTGCATGTCTGT[A/C]GGTTCATCACACTTCTGGACAGTCTATTGCCTCATATGGTGCCTGCATGGGACTACAGTCTGGGAACATTCAACCAGATCAAAGTTAGTACTCTTGTCTTGAGCAAATTTGTCCTATGCCATTCTTTATACTTTCAGTAAGTAGTTTGTGTTCACTGTTCATGTCTATATGTAATCCTCCATCATTCATGTCAGTTTCTTTAATTATTATTATTATTATTATTATTATTGGTGAACTTACTGCCTCATTTAATTTCTTAATAGAATATAATCAGGGTAGCTGCTGGTCTTTAAAAGGTCTTAAAATGCCTTAAAAAGCCTCAAATTCAGATTTGATAGGTGTTACCTAAAAAAAAGTCTTCAGTCTGATGGAACCAATAATTTTTTTACGATCATTGAACAGATATAAGAAGTTTTTTCCTTTGGTAGTAATTGTGTTATTGGGAACTAAGGTAGCAGATCAAAGCACATTTAAATAAAAATGTATTCACACAACTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11205
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056795 | Nonsense | 494 | 854 | 10 | 21 |
ENSDART00000144837 | Nonsense | 494 | 854 | 10 | 21 |
The following transcripts of ENSDARG00000038905 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 26636437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26832633 |
GRCz11 | 2 | 26488267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGCACCGGGACAATCCCACTCTRGATGTCACATGCAAAAATGCWGTTT[T/G]AACTCAGGTAGTCCACAAAATATGTACAGTAGATTTGTGNNNTTTTTTTAATA
Long Flanking Sequence:
AGCCAGTGAATGATGTTGATGCCATGTTTGCAACATTTTAGGGTAACACTTTATTTTGATGGTCCATTTGAGTATTAGTAGAAACTTTGCAAGTACATGTCGACTTACATTAACCCTAACCCCAACCCAACAGTCTACTTAGAATCTAATGAGAATTAGTTGGCATGTATATGCAATATCAATTAAATTCAACAAACAGACCATCAAAATAAAGTGATACCCATTTCAATGATTATTTACAATCTAGTATTGCAACATGATACTGTACATGTCAGGAATTGAGATTAATGTTTGATTTTGTTTCTTTGATCTCTGTGCTGGTTAGAGCATAAAGCAGTTCCTGCTGTTGTCCAAGCGTCGCTCTGCTCTCATCACCCAGTGCCTGAAGGACTCCGAGACCAGTAAGCCTAACTTCATGCCCCGCCTTTACATCAACCGTCGCCTTGCCATGGAGCACCGGGACAATCCCACTCTGGATGTCACATGCAAAAATGCTGTTT[T/G]AACTCAGGTAGTCCACAAAATATGTACAGTAGATTTGTGTTTTTTTAATATTTCCCTAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTGTGTCTGATAATATTTTTTCTTCTGGAGAAAGTTTTATTTGTTTTATTAAGGTTAGAATAAAAGCAGTTTTTTTTTTTTAAACCCATTTTAAGGTCAAAATTATTAGCCGCTTATTTAATTATCAGCTATATTTTTTCGATAGTGTACAGAATAAACCATCATTATACAATAACTTGCCTAATTACCCCAACCTGCCTAGTTAACCTAATTAACCTGGTCAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAATGTCTTGGAAAATATCTAGCCAAATATTATTTACTGTCGTCATGGCAAAGATAAAATAAATCAATTATTAGAGATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAAATCTTCTCTCCGTTAAACAGAAATTGGAGAAAAATAAA
Associated Phenotype:
Not determined