ZMP
depdc1a
Ensembl ID:
ZFIN ID:
Description:
DEP domain-containing protein 1A [Source:UniProtKB/Swiss-Prot;Acc:Q803Q4]
Human Orthologue:
DEPDC1
Human Description:
DEP domain containing 1 [Source:HGNC Symbol;Acc:22949]
Mouse Orthologue:
Depdc1a
Mouse Description:
DEP domain containing 1a Gene [Source:MGI Symbol;Acc:MGI:1923381]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21241 | Nonsense | Available for shipment | Available now |
| sa34360 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2458 | Essential Splice Site | F2 line generated | Not yet available |
| sa13687 | Nonsense | Available for shipment | Available now |
| sa41162 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16447 | Essential Splice Site | Available for shipment | Available now |
| sa18914 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21241
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 |
|---|---|---|---|---|---|
| ENSDART00000049676 | Nonsense | 57 | 800 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17243870)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16688758 |
| GRCz11 | 8 | 16724470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGAACTGCTTCACCGCATCCACCGCTGTGGACTGGTTACATGAACTCT[T/A]GAAAAACAACAGCAATTTTGGACCAGATGTCACCCGACAGCAGACAGTCC
Long Flanking Sequence:
TGAACAATATAGTGAGCATGTCAAAAGTTGTCACTGAATGAATGTGCGAATATCAAACCAACTTTACCTCACTTTAGCTCACTTGTAAGTAGTGTAAGTCATATGAAGTTAACTATATATGCTACTATTTATCTTCCAAGTGAACTATGTTTACAAATCATCATTTCTTTATGCTCATTGTGTGTATTTAATGACAATTATGAATATATTTTAACAACAAACTGTAACAATAGAACTTTACAGAATATTTTTTGTTATGCTGAATTATCAGTTTTTGTGTTTTGGACAATCTACCAACCAATTACTTAGTGATTATAGTTTATTATCTGAAGTGATAATAAATAAATGTATTGTGTGATATGATTTCTTTATTTTACAGTGGAATGAAGTGACCAAGCTTTTCCGAGCCGGGATGCCTTTGAAAAAGCACCGGCAGCACTTTAGAGTTTACACGAACTGCTTCACCGCATCCACCGCTGTGGACTGGTTACATGAACTCT[T/A]GAAAAACAACAGCAATTTTGGACCAGATGTCACCCGACAGCAGACAGTCCAGCTGCTGAAAAAGTTTTTGAAGAACCATGTTATTGAGGATGTGAAGGGTAGATGGGGCATGGAGGACCTGGAGGACAACAGCCAACTATACAGGTCTGATCAAATGGGTGTTTTATAAAGGTCTGAAAAAAATGCATACAGACATTAGACAATATTTTCTGGTTTAATATGTGTTTAAGGTTTCCATCAACATCTCCTCTGAAGCCTATTCCTAACCGTCCCACTGTTATGAGGAGAAAGAGCTTATCCATGATGGACAGGGAGAGTTTCTTCAAGTTCAGGGGCTCGAAGAAATTTGATAAAGAAACATTGGTAAATATTACTCGCTCTAAACATATTGTTATATTTGTAGTTCATCCAAAAATGAAACTGTGAGAAGACATTTACAACAGAACACTATAATTTTTGCTGAAACCCTGGTGTTTGCTGGTTTATAAAGTCAAAGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34360
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049676 | Nonsense | 191 | 800 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17241566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16686454 |
| GRCz11 | 8 | 16722166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAAATGTCATATTGTTGTTGAATTTGATTGTCATTTGAATGTTCAGTT[T/A]GCAGAAGTTGGTGGGATCTGCTTCTCTGGAAGGCGTTTTGGATCCAGCCA
Long Flanking Sequence:
ATGGTAAGAATTAATAATTGAATTCAATGTTTATTATCACTCCTAATAAAAACAGAAACACTTTGATTAACACCCCTTTTGTTATGTCATCAGAGGGGGAAAGCCCCACACATTAGAGACGATCTCTCCCTCATTAGCATAAACAGCCCTGAGTGAGAAGCAGCCATCTGTTATTAGAGTTTTCACCTGCTGAAGATAATGTCAGCGACTAAGAAGGTTAAAATGTGGAGCTTCAGGATGCACAAATAAACTCTCAAGTCTCCGTAGACGACCTTCTTCTGAGAAATTTTCAGTTTTTCGCAGAGATAACGTTAGTCTTTAATGTCTAGAAATCTTTGCTGATGGCTTGTTTTGCATTTTTGTTTCTGAAAATTGTGCAATGGAGTAAAATTGTAAAGAATTCCTTTAGAAAATGATTACACATTAGTTGCATATTTTAATTAGTAATTTAGTAAATGTCATATTGTTGTTGAATTTGATTGTCATTTGAATGTTCAGTT[T/A]GCAGAAGTTGGTGGGATCTGCTTCTCTGGAAGGCGTTTTGGATCCAGCCAAGGTCAATCCTCAGTTCATTGTGTATAATATGACCAAAGTCAATAAACATGGAGTCGTTTCATTGGAGGATAAAACAGGTAGGCCAGATGTGTGTCATCTCTGTGTAAAAACATAGTGGTGATAGTCATATTTTCACATCGTGAATAATATCTTATTTTTCTCCCTCCGTAGAAGATTTACCGCACTGGGTATTGTCTGCTATGAAATGTCTAGCAAACTGTAAGTTTTATATTACAAAAATTAAAAACTGTATTTTGTAAACATGTCAACTTTGGGTTTTGGAAGTTCAGGTGCTTTTATAAGATACTAAATAAGATATTACTTAAAAGGTTTTATTTGGACAATCAAGATCATTATGAAGTTAATATTTCTTGCTTTTAATCTTTAATAATGCTACACATAAACAATGATATTATTTTGGTGATGTTTTTGTATCTGAAGCCTTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2458
Status:
F2 line generated
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049676 | Essential Splice Site | 296 | 800 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17240757)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16685645 |
| GRCz11 | 8 | 16721357 |
KASP Assay ID:
554-3331.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCCACTGCTCACTTATCAGTATTACGAACTCTTTGTCAACATCCTGGG[T/A]ATGTATGAAACATGTTTTGGATTTTGCATGTCTGTSATCAGGTTATGCTG
Long Flanking Sequence:
TAAACATGTCAACTTTGGGTTTTGGAAGTTCAGGTGCTTTTATAAGATACTAAATAAGATATTACTTAAAAGGTTTTATTTGGACAATCAAGATCATTATGAAGTTAATATTTCTTGCTTTTAATCTTTAATAATGCTACACATAAACAATGATATTATTTTGGTGATGTTTTTGTATCTGAAGCCTTCACATACAGAGATATGGCCTCGAACATTTGTCCACTCTGTTAAGTTTGCATTCCTGTACAGTATTACATATTACAACAGCCAGATAGAGACCATGCATATATTGTCTTTTGTCATTTTTCCGTGTATAAAACTCAAAATAATAAATTTTTTAATATTATGTATTATTTTTCAGGGCCAAAGTATGACTCAGACCAGCCGACTTACCTAGGATTTGAGCGGGATGTGTTTAAAACGGTCTCAGACTACTTCTACAGTCTTCCTCAGCCACTGCTCACTTATCAGTATTACGAACTCTTTGTCAACATCCTGGG[T/A]ATGTATGAAACATGTTTTGGATTTTGCATGTCTGTGATCAGGTTATGCTGTAATTAACTGGTTACATATACACCACTGTTCAAAAAGTTTGGTGTTCAGGATTATCTAAGGTATTTTTTTAAGGTAAGATTTATCTATTTAACTTTAAAGATCAACACTGAAATGCTTCTCCTTTTGATTTTTTTATTATTATTTATAAAAAATTCTGATTTAACTTAACAAAAATATTAAGAAGCAAAAGTATGTTTTGCAAACTCCAAATAATAGACGGATTTGCCAATACAGCAATAATTATTTTTAAATATGTGTGGTCATGGACCACAAAAGCAGTTTTATGTTGTTCAGAAATGTTAGCAAAAGCCAAAAATACAGTGTATGGGTAAAAATTAACAATTTTGTTTCATTCTACAAAGCATTAGCATATTAAGTAAAGTTCATGCTCCATGTAGATATTTTGTCAATTGCCTTATGAATAAATCAAAACTTGATAATTTTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13687
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 |
|---|---|---|---|---|---|
| ENSDART00000049676 | Nonsense | 344 | 800 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17238403)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16683291 |
| GRCz11 | 8 | 16719003 |
KASP Assay ID:
2260-0354.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGAACCCAGCCAACCTGTTCAGGTCCACCGAATGYCTWCTGCTCAGCY[T/G]AATAAGAAARGAGGCCATCGATGAAGCCGATTCGCCCATGAAGGAAGTTT
Long Flanking Sequence:
AATATATATTTAAGATTTACACAAACATTTGAAAAGTTGTGTATATATTTAATATAATGTACCCATGTTAATGTTTTTTGAGATTTTAGGCTTGTGTTTTGTTTTTTTACACACTCATCCTTTGTCCTTTCTGGGGAAAGTCCTACTAAAAGGGTCATCAAAATCATTTGGCTGTGGGTCTCAATTTACAAAATGTTAATAAGAACAAACTATGGAGATGCGTGTCTACTGACTGCACTGCTTTTGTGGTGTCAGACGATGTTCAAAACTAACCCTGTCTGCTCTGTTTTACATGTCTCACTTCGTTGCCTGCCTCTTTGTTGTTTTATGTTCTGTTGTCTGGTCCTTTTTGCTAGTTATGTGTGGCTACATCACGACTCCTAAATCCCAACCTGGAAAGCGTAAAAACCAGGAGGAGCCAAACTGCCCACAGCCTGCCAAAAACCCATATGTGAACCCAGCCAACCTGTTCAGGTCCACCGAATGCCTACTGCTCAGCT[T/G]AATAAGAAAAGAGGCCATCGATGAAGCCGATTCGCCCATGAAGGAAGTTTTCAGTTCAAAAACAGAGACCAAGTTAGAAACCCGTAGAGTTTTTAGAGGTAGAAGGGTCAGCGATGGAGACAGGCTGGATGGTAGCTATCTAGATGTTTCTCAGGCCCACAAAACAGATGTCCCATATGGCAGGCTTCGTCCCAGAAGTTGTTCACTGGAGGGAAACATTAATAACTGTGCCAAAAACAGACTTTTTAGGTCGTCTGAAAGCCTCGAGTCCTGTAGCAGTGATAAATCAAACCCTGAAACTGATTCTCCATTAGAACCAAACCTCCAGAGTTCCTTGGTATCCATAAACACTTCCGGCAGCAGCGTGAGCTCCCAACTTTCAGCAGATCTGCGGCGAAACAACTCGAGACCTGCCAGAGCCCGGCCCAGAAGCATTGGTAACTTGTTTGATATAGAGGAGAATAGAGAAATGTCTGCTAGCAGCTTTAGTGTTCATGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41162
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049676 | Nonsense | 535 | 800 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17237830)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16682718 |
| GRCz11 | 8 | 16718430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGACTCCACATCCAGTGTTGGCTTCAGAGGTCTCGGTTTGTCCAGTT[T/A]GCATGGAAGTTGCGTGGATGTTAGAACAGGTCCAAGCTTTAGCAGACGCT
Long Flanking Sequence:
GTTAGAAACCCGTAGAGTTTTTAGAGGTAGAAGGGTCAGCGATGGAGACAGGCTGGATGGTAGCTATCTAGATGTTTCTCAGGCCCACAAAACAGATGTCCCATATGGCAGGCTTCGTCCCAGAAGTTGTTCACTGGAGGGAAACATTAATAACTGTGCCAAAAACAGACTTTTTAGGTCGTCTGAAAGCCTCGAGTCCTGTAGCAGTGATAAATCAAACCCTGAAACTGATTCTCCATTAGAACCAAACCTCCAGAGTTCCTTGGTATCCATAAACACTTCCGGCAGCAGCGTGAGCTCCCAACTTTCAGCAGATCTGCGGCGAAACAACTCGAGACCTGCCAGAGCCCGGCCCAGAAGCATTGGTAACTTGTTTGATATAGAGGAGAATAGAGAAATGTCTGCTAGCAGCTTTAGTGTTCATGCACCCGTGGCTGAAATTACTATGAGACCTGACTCCACATCCAGTGTTGGCTTCAGAGGTCTCGGTTTGTCCAGTT[T/A]GCATGGAAGTTGCGTGGATGTTAGAACAGGTCCAAGCTTTAGCAGACGCTGTCAGAGCTCTCTGGACCTGAGCAAACCTGCACCCGCTCGGCCTCCTTCAGCCCTGTTAACACACCAGCCTGAGCAAAGTAAGAGCATGTGAAAAACACACGTGAGGATGTGCTTGTCTATTTGTGCTTTAGCATGTGTATGTTGTGCTTGTCAGACTAACATCTAGGATTCTTGAAAGCGATAGTTCATGCAAAAATAAAATTATTGTACAGACCCTCATGTTATTCCAAATCCACATGATTGGCTTGCCTGTGTAGAACACAGAAGAGATACTTTTATTATTTTAAATATATCCTTTCAGATTAGGAATAACATTACAATTTTTATTTTGGTGTGAACTATCATTTTAACGCTAACTCATTCTATGGCACACTTTGAATACTAATACATACTTTTTGTCACATTATCTAACATTATCATTATCTAACCCCCCCACCCCAAACCCCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16447
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 |
|---|---|---|---|---|---|
| ENSDART00000049676 | Essential Splice Site | 635 | 800 | 9 | 12 |
| ENSDART00000049676 | Essential Splice Site | 635 | 800 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17235304)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16680192 |
| GRCz11 | 8 | 16715904 |
KASP Assay ID:
2260-0353.1 (used for ordering genotyping assays)
KASP Sequence:
GAACGTGGACATGCCACGGTTACAYGACGTCATCGGAACACGCACTCTGG[T/C]CAGGAGKAGTTCAATRGATGCAGCTGATTTGTTATATTTAWAACCATAAT
Long Flanking Sequence:
GTCATCCTATATAAAATCATCATATATATATATATATATATGTATGTATATATGTATGTATGTATGTATGTGTGTGTGTGTGTGTTTTATATATATATATATATATATATATATATATATATGTATATGTGTATAATATAGATATATAGATAGAGATGTGTGTGTGTATATATATGCGTGTATATATATGTGTGTGTGGATTCATATGTGTGTATATGTATTGATAATTCATATTGTTCATGTGTTGTTTGTAGTCTCTTGTATTTCTAGTTGTAGTATTTTCGCAGTTTTGTGCTGTGGTTTATTTCGCCCACATGATGTTCCAGGTTTATTACAGCCGTCACTGGAGCAGGTGGCCGTCGAGGCTCTTCAGCTCTGCACGTTACTCTTGCCTCCCGTCAGCCGCCGCAAACTCCAGCTGCTCTTGCGGATGATCTCACGCATGAGCCAGAACGTGGACATGCCACGGTTACACGACGTCATCGGAACACGCACTCTGG[T/C]CAGGAGGAGTTCAATGGATGCAGCTGATTTGTTATATTTATAACCATAATCTCACTCGCATTAAAGCAAATGCTGACTTGTTGAATGTCCTGTTGTGCACATTCACGCATGTCGTACACATTACAACTACATTTGTGTTTCTGTGTGCAGTTGGTGCAGACGTTCTCCAGGTGTGTGTTGAGCTGTGAGGAGGTGGACGATCTGGATGAGCTCTTGGCTACGAGGCTGTTGTCTTTTCTCATGGATCACCATCAGGAAGTCCTGCAGGTGCCTGTCTATCTGCGCAATGCTGTGGAAGATCACATCAACTATCTCAAGTCACTGGTGAGTCTACAAGGACCACACAGAAAGGAAAGGATTTACTTACAATTATGAATTTATACAGCTCTAAATAACTCAAAAGTGTTTAAAACTTAAACAATACAGTTTTGAAAGCTTCTCTTCTCATCAAGAATGCATGTATAACTTTATGGACGTTTTTGTCTATATTTATGGTCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18914
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 |
|---|---|---|---|---|---|
| ENSDART00000049676 | Essential Splice Site | 635 | 800 | 9 | 12 |
| ENSDART00000049676 | Essential Splice Site | 635 | 800 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 17235304)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 16680192 |
| GRCz11 | 8 | 16715904 |
KASP Assay ID:
2260-0353.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACGTGGACATGCCACGGTTACACGACGTCATCGGAACACGCACTCTGG[T/C]CAGGAGGAGTTCAATGGATGCAGCTGATTTGTTATATTTATAACCATAAT
Long Flanking Sequence:
GTCATCCTATATAAAATCATCATATATATATATATATATATGTATGTATATATGTATGTATGTATGTATGTGTGTGTGTGTGTGTTTTATATATATATATATATATATATATATATATATATGTATATGTGTATAATATAGATATATAGATAGAGATGTGTGTGTGTATATATATGCGTGTATATATATGTGTGTGTGGATTCATATGTGTGTATATGTATTGATAATTCATATTGTTCATGTGTTGTTTGTAGTCTCTTGTATTTCTAGTTGTAGTATTTTCGCAGTTTTGTGCTGTGGTTTATTTCGCCCACATGATGTTCCAGGTTTATTACAGCCGTCACTGGAGCAGGTGGCCGTCGAGGCTCTTCAGCTCTGCACGTTACTCTTGCCTCCCGTCAGCCGCCGCAAACTCCAGCTGCTCTTGCGGATGATCTCACGCATGAGCCAGAACGTGGACATGCCACGGTTACACGACGTCATCGGAACACGCACTCTGG[T/C]CAGGAGGAGTTCAATGGATGCAGCTGATTTGTTATATTTATAACCATAATCTCACTCGCATTAAAGCAAATGCTGACTTGTTGAATGTCCTGTTGTGCACATTCACGCATGTCGTACACATTACAACTACATTTGTGTTTCTGTGTGCAGTTGGTGCAGACGTTCTCCAGGTGTGTGTTGAGCTGTGAGGAGGTGGACGATCTGGATGAGCTCTTGGCTACGAGGCTGTTGTCTTTTCTCATGGATCACCATCAGGAAGTCCTGCAGGTGCCTGTCTATCTGCGCAATGCTGTGGAAGATCACATCAACTATCTCAAGTCACTGGTGAGTCTACAAGGACCACACAGAAAGGAAAGGATTTACTTACAATTATGAATTTATACAGCTCTAAATAACTCAAAAGTGTTTAAAACTTAAACAATACAGTTTTGAAAGCTTCTCTTCTCATCAAGAATGCATGTATAACTTTATGGACGTTTTTGTCTATATTTATGGTCCAT
Associated Phenotype:
Not determined