ZMP
si:dkey-106l3.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
DEPDC5
Human Description:
DEP domain containing 5 [Source:HGNC Symbol;Acc:18423]
Mouse Orthologue:
Depdc5
Mouse Description:
DEP domain containing 5 Gene [Source:MGI Symbol;Acc:MGI:2141101]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1323 | Essential Splice Site | Available for shipment | Available now |
sa41618 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21700 | Nonsense | Available for shipment | Available now |
sa41619 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9750 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1323
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 |
---|---|---|---|---|---|
ENSDART00000111088 | Essential Splice Site | 121 | 1604 | 5 | 44 |
ENSDART00000131751 | None | None | 266 | None | 7 |
ENSDART00000134059 | Essential Splice Site | 125 | 1568 | 5 | 41 |
ENSDART00000138777 | None | None | 149 | None | 5 |
The following transcripts of ENSDARG00000078105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16931419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17261667 |
GRCz11 | 10 | 17219631 |
KASP Assay ID:
554-1237.1 (used for ordering genotyping assays)
KASP Sequence:
AGATCAGTATATTGGGCGAGGAGACATGTGGCGACTAAAGAAGAGCTTAG[T/C]GAGTAGATAAAGTAGAAATCTGCATCTTTGTTCATTTTTTGTTGACTAAC
Long Flanking Sequence:
GTATGTTTTATTAAAAGTACCTAATTAAAAGCACATTGCGACTACTGACATTTAATAATCCCCATTAATATCATAATAATTATATCATATATTTAAACGACAGATTCAGTTAATGATTTTGTCTCTTTATAAAACCTTCTTTGCCCAAAACTAAAACAAACAACAAACAAAAATCTATCGTAAACTTTCAGTTTAAACCATTTTGGTCTTTCCTAAGAATAATGTCTTTTATCCACTGACAGAAACTATCAGTGTCGATCAGACTGTGGCTCAGGCTTTCAAGCTGCGTGCCTACCAAGACGTCATCATCAATATTGTGGATCCAAAGGTATTTCATACTGAAATATTAAATTATTAAATGGTTGGAGACAATATTTACCACCTAATGTCTTAATGCTCTATTGAAATTGAAAAGGAGGTGACTTTGGATCTGGTGGAGCTCACCTTTAAAGATCAGTATATTGGGCGAGGAGACATGTGGCGACTAAAGAAGAGCTTAG[T/C]GAGTAGATAAAGTAGAAATCTGCATCTTTGTTCATTTTTTGTTGACTAACATTGATCCTGATGTCTCTGTTTTGTTGTTTCAGGTGAGCACATGTGCATATGTGACACAGAAAGTAGAGTTTGCAGGAATCAGGTAACAACATCTACTAAGAAATAAATACTGTCTGGAATACTGGATTATGATTGGTTAATTTAAGTATTCTAATGTTAGAAGTATTGATATAATGACTTTTTATTATGTCAAATGTAACATGCACTACTGTTCAAAAGTTTGGGGCAGTAAGATTCTTTTAAAAAAATTAAGGATGTAAAATATATAGATGTATATATATTCCTAACTCATTAAATTTATCATATGTGACAGTAAAAATATTTATGACATGATTAATGATTTCTATTCATTTACGAGTCCTGTATTAAAAATGATTGAGCATCAGATTGACATATTATGCTAATTTCTGAAGGGTCATGTGACACTAATTTTAGTTGCTGATGATTCT
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:
sa41618
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111088 | Nonsense | 476 | 1604 | 19 | 44 |
ENSDART00000131751 | None | None | 266 | None | 7 |
ENSDART00000134059 | Nonsense | 480 | 1568 | 19 | 41 |
ENSDART00000138777 | None | None | 149 | None | 5 |
The following transcripts of ENSDARG00000078105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16941371)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17251715 |
GRCz11 | 10 | 17209679 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATGCGTATGATTCTCAGGTCTTCAGGCTTCCTGGGCCCTCCAGAGCT[C/T]AGAGGTCCACCAACTTTAGGTACATTAGACAAATGAAAAACATAGATTCA
Long Flanking Sequence:
ATAACATGAATTTCAGTCAGAAACAGGGGCTTGGTATAATAATGTATAATAATAAATGTGATTTTTACAGCTTTTACACATCAAAGAGTCAAAACTCTTGCAGCTGTTTTACACCTCGGATCAAGCTGGCTGGAAAGAAGGTTAGAAATGTCACACTTTCACTGAACAACAGCTTGTGACTTTGTTATTGTTATTATGAGAAGGTATTCATGCCTGTAAAACTGCTAATGAAGCAGCTGTCTCTTTGATTCATTTTCACTTTAAGGTTCATGCTGAGAAAGCCAAAAACAGCAAAGAACATTGTAAGTCATTGTCGCTATTAGTTTTTTGGAATTGATAGTTGTTGTATGTTTGCAGCGTTCTGATTTGATGTGGATTTATTTGTTTTTTTTTTCTTAGCTCTTGGCGCTCCCAAAGATGCTGAGAACAGCCTTCCCATCCAGGTGGATTATGATGCGTATGATTCTCAGGTCTTCAGGCTTCCTGGGCCCTCCAGAGCT[C/T]AGAGGTCCACCAACTTTAGGTACATTAGACAAATGAAAAACATAGATTCAAAGCTTAGAAGGTACTTAAAAACAAACAGGTCCTTGAAAATGCTTGTATTCAATCTGAAGTTAAATTGCTGTCAAAAACCAAGAAAAAGCAATGAGAAATTCTTGATTTTAAAATGTTACTTGTTAATTTTGTACAATGACTATGACAAATAATGCACATTTTAACAATATTTCAGAAACTGCATGCATTTTAATATTACCTTTATAGTATTCAGCAAATTTTATTCAAATATTTTTTTCAAATGAGACATTCAAAACATTATTATCTCTCATTTTATTGTAAATATTAAGTGTAAGTGAACTGTGAAGGACAGTAAGGATTTTCACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACTGGTGGTAGGCGTGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21700
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111088 | Nonsense | 922 | 1604 | 28 | 44 |
ENSDART00000131751 | None | None | 266 | None | 7 |
ENSDART00000134059 | Nonsense | 909 | 1568 | 28 | 41 |
ENSDART00000138777 | None | None | 149 | None | 5 |
The following transcripts of ENSDARG00000078105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16958874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17234212 |
GRCz11 | 10 | 17192176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGAGCGGCTGGAGGAGTACAAGTGGAACTATTTAGACCAGTACATCTG[C/A]TCTGCCGGATCAGAGGACTTCAGGTAAGTAGTGTTATTCAGTTCACACCA
Long Flanking Sequence:
AGCAGTCCCCTGTATTCCAGAGGTACATCACCTGCTGGAGGCCCTTAGATATGAACACTAGCTGCATTTTGTCTTCCTGTTATGAACTATGCTTCAATATAATGCAGGTGAAAGAATTAAAGGTGTGCTTTTCAGGGCTGGTGTCTCGCCGTAAACCAGAAGAAGAAGAGAGTCTTTACTGGCTCAGTATGGGCAGAACTTTTCATAAAGTCTGTCTTAAAGATAAGATCATCACAGTCACCCGCTACCTCCCAAAGTCAGTTGATGTTTTTATTCATTCAGATTCAGATCATGTCATTTGCTCTTCTATACATGAATTGTGTGTGTGTGCATTTTTATTTTTGGTTCATCTTTAGGTATCCATATGAATCAACACAGATTCAGTACAGCTACAATCTGTGCCCTCCACATGCAGATGCCCACTTCATGCCATTCTGGGTAGAGTTCAGCCACGAGCGGCTGGAGGAGTACAAGTGGAACTATTTAGACCAGTACATCTG[C/A]TCTGCCGGATCAGAGGACTTCAGGTAAGTAGTGTTATTCAGTTCACACCATGGCACTGACACAAAACCTATACAGGTCCACAATAGGGTTGGGTACCATACCAATATTCTTAGACTGAATCACATTTTTTTTCACTTTATCTCAAAAAACATCTACAAACACACAAACTCCAAAAAACAATGTAGTGTACATGCCAAACCGGTGTGTGGTGTTGTAATTATCCTACAGAGATGCTCAAAAATGGAGAAGAAGAATTGAAGCATGCACATATGCACACATTACTCACTATTACCTACATTAGTCCACTAATATAGTCTTCTTGAAGGGGTGAATAAATTCAGTGAGGGAATTCGTGCACTGAAAAGAATACCGTTTTCTTTGTGTTTTGCTGCTTGACGAATCTTTCAGATTAATTAGATTTTCATCTTCTTGGTCAGACCCTGTAATAGTTATTCAACACTTAGTGAGCTGTCTATTAGTAATGAAACAAAGACTTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41619
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111088 | Nonsense | 1315 | 1604 | 39 | 44 |
ENSDART00000131751 | Nonsense | 70 | 266 | 2 | 7 |
ENSDART00000134059 | Nonsense | 1279 | 1568 | 36 | 41 |
ENSDART00000138777 | None | None | 149 | None | 5 |
The following transcripts of ENSDARG00000078105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16974539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17218547 |
GRCz11 | 10 | 17176511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTATGGAGGAACGTCGACCATGTGACTTACCTGCCTTTCTGCTGCCTT[G/A]GTTGCCCAGCCGGCCAGCCTCGTATGCAAGTAGGCATAGCTCCTTCAGCC
Long Flanking Sequence:
TACATCAAAGTAGAAAAGTCTACCAGAAATCAGCATCACCTTAACACAGCAACCCCCAGGCATTTAGTCGATGTCAGTGTTAAACATCTCTCCACTAGTTCTTATTTCTCTGAGCATAAACAGTTCTTCTGCATGGGTAGCATTTTATTTTATGTTGCCTTTTTATGTTGAATCGCTGAATGCCTCCACATTTGTAAGTCGCATTGGACAAAGTGTCTGCTAAATGACTAAATGTAAGTTAACCGGTCTTCAGGCAGCAGGTCGAGCTTCACTGTTTAATTTCCTTTACTTAGCATGACTGTACCTTGGTATTTCTACCCTCCATGAAAACAGACCTCTATTCCCTGCAGCCCCGCTGACTCAGCTTCCCCCAGCTGGAGCGAATGTATGGTCAGCTGCAGCTTTGGAAGACTTCGCTCTTTTCCAGAGGAAGTGGTTCGAGGTGGCCTTTGTTATGGAGGAACGTCGACCATGTGACTTACCTGCCTTTCTGCTGCCTT[G/A]GTTGCCCAGCCGGCCAGCCTCGTATGCAAGTAGGCATAGCTCCTTCAGCCGCAGCTTCGGAGGACGCAGCCAAGCTGCTGCACTGCTAGGTACACACAGCCGGCTCTGACCCCATAAAAGTCATGCTCCACACCGTAAGGCAGCATGACACTCCTTACCCCTGCAGTGGTACCCCTCTGGAAGACTAGTAGATGAGTTACACAAAGTCAGATCATTTCCTCTCTTACTAAAGCATTCAGAGATTAACCTTTCCATCTAGTCACCCAACAACAGTGCACAATTGGAAATTTCTATGACTCAACTAACATATAAAGTATGCAATAACATCACTCTATACAACACCATATTCTTCTCTAAGGGTGCTTTCACACTTGGTTTAATTGCCTGGACCATACCCAAGTTCGATTGTCCCCCCCTTTGCCACCTTCTAAGTTGGTTTGTGTTCACCCTTTTTTTTTTCTTTCTGAACCCCGGTACGCTTGCGTCATCGAGCTGCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9750
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 |
---|---|---|---|---|---|
ENSDART00000111088 | Essential Splice Site | 1459 | 1604 | None | 44 |
ENSDART00000131751 | Essential Splice Site | 194 | 266 | None | 7 |
ENSDART00000134059 | Essential Splice Site | 1423 | 1568 | None | 41 |
ENSDART00000138777 | None | None | 149 | None | 5 |
The following transcripts of ENSDARG00000078105 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 16976898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17216188 |
GRCz11 | 10 | 17174152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAAATATCCAGTGCCTGCTAAAGGAGGGCTCTGATAACCTTTTTGAGGG[T/C]GAGGACACAAGAAGTAATTGTGCAGTTGTTGTAGTCCAAGGGACAGATTC
Long Flanking Sequence:
CTCTGTCTTTTTCGCTGTGTTTTCACCCCTCCCCTCTCAGCCGCCACAGTTCCAGAGCAGAAAACAGTCACCTTGGATGTCGATGTGAACAATCGTAGTGATCGGACAGAATGGTGCAGCTGCTATTACCATGGCAACTTCTCCCTTAATGCTGCCTTTGAAATCAAGCTGCACTGGATGGCCGTCACTGCAGCCGTGCTCTTTGAAATGGTGAGCGTGGGATGAACATATTACCATTTAGAGATAATATTAGGAGGTGCTTGCATTGTTATGCATTGTTGCACAGTAAGTACATGGGTACAGTTCTTATGCATTCTTGTGTTTTAGGTGCAAGGCTGGCACAGGAAGGCAGCATCTTGCGGATTCCTGCTTGTCCCTGTGTTGGAGGTGCCCTTTGCTTTGTCGTCATACCTATATGGCGACCCACTCCGTGCTCAGTTGTTTATTCCCCTAAATATCCAGTGCCTGCTAAAGGAGGGCTCTGATAACCTTTTTGAGGG[T/C]GAGGACACAAGAAGTAATTGTGCAGTTGTTGTAGTCCAAGGGACAGATTCACTTGCAGCAATTTAACCTATTGTTTTTTTTCTTTAAAGCATTGTTTGACTTTCCTTTTCTGATCCTAGTTTATGGGAGAAGAATATTTAAATGCAGTATGATTTACAAGAGATTTGCCAGATTCAGTTTACTGGCATTTTTTTAAATTATTTAATGCCCAAAAAAGCATGTCTGAAAACATGCACATTTCTCAGATTATTGTGAGCTAAGTTTTACATTAGTATATTTATTAGATCAGGGGTTCCCAACCTTTTCAACCCGTGACACCTAAAATAGCAATGCCAGTGACTTGCAACCCCAAATTTCTCAGAGGTGGTTATAAATATACAAAAGTTGCGCACACATCAATAGGCCAATAAAAACATGAACATAGTGCTAACACAAAACATGTGCAACAGTCTAACAACCATTTCAATTTCATAGTCAATTACTAATTTGCTTAATTTAAT
Associated Phenotype:
Not determined