ZMP
ddhd1
Ensembl ID:
ZFIN ID:
Description:
phospholipase DDHD1 [Source:RefSeq peptide;Acc:NP_001025417]
Human Orthologue:
DDHD1
Human Description:
DDHD domain containing 1 [Source:HGNC Symbol;Acc:19714]
Mouse Orthologue:
Ddhd1
Mouse Description:
DDHD domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2150302]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa134 | Nonsense | Available for shipment | Available now |
sa43392 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8584 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12215 | Nonsense | Available for shipment | Available now |
sa6616 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa134
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 |
---|---|---|---|---|---|
ENSDART00000053841 | Nonsense | 294 | 859 | 2 | 13 |
ENSDART00000145439 | Nonsense | 294 | 644 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 9971762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 9803691 |
GRCz11 | 20 | 9790931 |
KASP Assay ID:
554-0085.1 (used for ordering genotyping assays)
KASP Sequence:
AGGACAGTGACCTTATTGAACTGGAGCACTTAGCCTGTTTCCGGGGCCAG[C/T]AGATGAAGGACACCTTTGACACGGAAGCAGTGGCCACCACAGTGGACAGC
Long Flanking Sequence:
GTACGTCACTGCGAAAAGGGGCGGGAAAATTATAGTAATTAGACATTAAAAAAGCATGCAATTGCTCCATATTTTAAATTTCTGTACAGAGCTTTGATCTTTTATTGGTCTCACGCTATCATGTGATTCGATTTCGCAGATCAGTAATCACCAAGCTTTAACTTTAAAATACAGCGACAAGGGAAACTTGTCGCATGAGCTTATGTTTACAGTTTGCCACATACGCATGCATATGAATGGAAGTCTATGTGGCGAAAAGTGCAAAAAGGGACTGTGACTTAACTGGTCCACCCTGATCCTTATATAGCATTGCCATTGTATGATGTTAGATATAGTCATACTTTAGAAATAGATAACAATTCAAACCACTCCGCTTTACAGAACAGGACCACATCCCAGTCATGAGAGGCCAGTGGTTCACAGACGGCACCTGGTTGCCCTTGGAGGAGGAGGACAGTGACCTTATTGAACTGGAGCACTTAGCCTGTTTCCGGGGCCAG[C/T]AGATGAAGGACACCTTTGACACGGAAGCAGTGGCCACCACAGTGGACAGCAAAGACGGTAACAGACCCTGCCATGACTAGTGTTTAGGGTTTAGGGTAAGCTTTGTGCTAGGGGTCAAGCACACAAAAAGAACGACTTAACATTGACGCTTAGTTCAGCTCACTCAGAGACAGTCGCTTAGTTAAATAAGCCACAAACCAGACTTCCTGTTTGTTTCATGTGACACAAGTCAAACACCGGTGGGACGTTTATTACTGATGGGGTATCAGCTGTCAGCTGTTTTTGCAAATGTTTAAAAAAGACCCTAATTGGAATGATCTAATCTATTCAGACATGAAGTTTACTTAACAGGAGGTAATTTGAAACAGACCTGTTTGACTTGTGCCCTTAATTCACTCAGCCATTCACAGTCTGAAACTGAGCCGGAGCCACGTGGACTGGCACAGTGTGGATGAAGTGTACCTTTACAGCGACGCCACCACCTCTAAGATTGCACGGAC
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:
sa43392
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053841 | Nonsense | 354 | 859 | 3 | 13 |
ENSDART00000145439 | Nonsense | 354 | 644 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 9972286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 9804215 |
GRCz11 | 20 | 9791455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCACCACCTCTAAGATTGCACGGACGGTCACTCAGAAGCTGGGATTCT[C/A]AAAAGGTTTGTTAAACATTTGATTAGTAAATACTCTCACGTGTTGCTAAT
Long Flanking Sequence:
GAAGCAGTGGCCACCACAGTGGACAGCAAAGACGGTAACAGACCCTGCCATGACTAGTGTTTAGGGTTTAGGGTAAGCTTTGTGCTAGGGGTCAAGCACACAAAAAGAACGACTTAACATTGACGCTTAGTTCAGCTCACTCAGAGACAGTCGCTTAGTTAAATAAGCCACAAACCAGACTTCCTGTTTGTTTCATGTGACACAAGTCAAACACCGGTGGGACGTTTATTACTGATGGGGTATCAGCTGTCAGCTGTTTTTGCAAATGTTTAAAAAAGACCCTAATTGGAATGATCTAATCTATTCAGACATGAAGTTTACTTAACAGGAGGTAATTTGAAACAGACCTGTTTGACTTGTGCCCTTAATTCACTCAGCCATTCACAGTCTGAAACTGAGCCGGAGCCACGTGGACTGGCACAGTGTGGATGAAGTGTACCTTTACAGCGACGCCACCACCTCTAAGATTGCACGGACGGTCACTCAGAAGCTGGGATTCT[C/A]AAAAGGTTTGTTAAACATTTGATTAGTAAATACTCTCACGTGTTGCTAATTAATAGAACACATCAAATCTAAAATAATGCAAATCACATATTTAATATACAAGTTCATGTTTGGATTTTACACATATAAAACTTGTTATTTCAAAAGATTACAAAAATTGAATTTCTTTTCTTTAAAGAGCCCCTATAATGGGTTTTTGAAATTGACCTTCCATGTAGTGTGTAACATAGCGCTAAGTGAAGTGAAATATCCAGCTAAGGCTTAAATCTGAAAGTGGACAGTTTTTAAAACTAATGTGGTTAAAATGAATCGTCTTGTTAGCGAGTTATTAGGCGTTTCGGAGTGACGTGGCTACGAAACATAAGCCCCGCCCAATTGTTGCTAGCATAAACCTGGGAAAATTTAAACCTGCGGCCCCGCCCACAAACACAGCAGCAAAGACAGATCCTGAAGTCTTGAGTCATGAAGATGCTTACCTGGATATTATTGGAAGTGTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8584
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053841 | Essential Splice Site | 356 | 859 | 3 | 13 |
ENSDART00000145439 | Essential Splice Site | 356 | 644 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 9972293)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 9804222 |
GRCz11 | 20 | 9791462 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTCTAAGATTGCACGGACGGTCACTCAGAAGCTGGGATTCTCRAAAGG[T/C]TTGTTAAACATTTGATTAGTAAATRCTYTCACGTGTTGCTAATTAATAGA
Long Flanking Sequence:
TGGCCACCACAGTGGACAGCAAAGACGGTAACAGACCCTGCCATGACTAGTGTTTAGGGTTTAGGGTAAGCTTTGTGCTAGGGGTCAAGCACACAAAAAGAACGACTTAACATTGACGCTTAGTTCAGCTCACTCAGAGACAGTCGCTTAGTTAAATAAGCCACAAACCAGACTTCCTGTTTGTTTCATGTGACACAAGTCAAACACCGGTGGGACGTTTATTACTGATGGGGTATCAGCTGTCAGCTGTTTTTGCAAATGTTTAAAAAAGACCCTAATTGGAATGATCTAATCTATTCAGACATGAAGTTTACTTAACAGGAGGTAATTTGAAACAGACCTGTTTGACTTGTGCCCTTAATTCACTCAGCCATTCACAGTCTGAAACTGAGCCGGAGCCACGTGGACTGGCACAGTGTGGATGAAGTGTACCTTTACAGCGACGCCACCACCTCTAAGATTGCACGGACGGTCACTCAGAAGCTGGGATTCTCAAAAGG[T/C]TTGTTAAACATTTGATTAGTAAATACTCTCACGTGTTGCTAATTAATAGAACACATCAAATCTAAAATAATGCAAATCACATATTTAATATACAAGTTCATGTTTGGATTTTACACATATAAAACTTGTTATTTCAAAAGATTACAAAAATTGAATTTCTTTTCTTTAAAGAGCCCCTATAATGGGTTTTTGAAATTGACCTTCCATGTAGTGTGTAACATAGCGCTAAGTGAAGTGAAATATCCAGCTAAGGCTTAAATCTGAAAGTGGACAGTTTTTAAAACTAATGTGGTTAAAATGAATCGTCTTGTTAGCGAGTTATTAGGCGTTTCGGAGTGACGTGGCTACGAAACATAAGCCCCGCCCAATTGTTGCTAGCATAAACCTGGGAAAATTTAAACCTGCGGCCCCGCCCACAAACACAGCAGCAAAGACAGATCCTGAAGTCTTGAGTCATGAAGATGCTTACCTGGATATTATTGGAAGTGTGAGGGGGGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12215
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 |
---|---|---|---|---|---|
ENSDART00000053841 | Nonsense | 666 | 859 | 11 | 13 |
ENSDART00000145439 | None | None | 644 | None | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 9985696)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 9817625 |
GRCz11 | 20 | 9804865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ANTTTTTTATCTATTTTTTTRTAGGTACAACACCACCAGCCCCACACCGTA[T/A]GACCAGATCCGTCCCACTCTACTGAATCCATCAAAGGAAAATGCGTCAGT
Long Flanking Sequence:
GCAAAAAATTAGTCTTTTTTCCAGTGTAATTTAGCAAATTGTAATCTGGCTTTTTTGTTGATTCTGGCTTGTTGATTTTCCCATGTTGTCACTACAGCAAGCAGTGTATTTGAGGTTTTCCTTAAATGCTATTCTACAGTTGTGCCTCCAATTACCTCAAATGTTGTCAAATGTTATCAGAAACTTCCAAAACCTTGGCACCATCATCTGAGCTTTTTCAGAGGCATAATTATTTTATTGTACGTAAACTTGACTTTCAAGAAAAGTTGTAGCAATTTCGCAAAAAATATCTCTCATTGTTCTGCTATTAAGCATAACAGAAACAAATTTGATAATCCTAACTTACCTAAAAAAGAATAAGTTTAGTCACATTAACATCTGACTTTTTCATGTTTATGTGTCTTTATACTATGTATGTAAACTTCTGGTTTAAGCTGAATGTGACCATTGATTTTTTATCTATTTTTTTGTAGGTACAACACCACCAGCCCCACACCGTA[T/A]GACCAGATCCGTCCCACTCTACTGAATCCATCAAAGGAAAATGCGTCAGTGTCGGATACGGAGAGTCTGCCAAGCCCCTGCACCTCTCCACCTCAGCCTCGCAGACACTACAGCGAGTCCATCACCAACCTGGGCAAGGCCAGCATAATGGGTAAGAGACTATTGAAGAAAAACCCCAGCAGGACATGTAGGGTGTTGTAGAACGTGATGGAGGATTATAGATAATGGCAGCCTGCCTACAATTACTGTGTATCTGGAGTTTATAGCTGTTTATTTGAGTGTGGAAAGCAATAAACAGAAACAGCTCAGCAAGGCATCAGATCAATAGAAAGTAATTAAGAAGTGTCACAGACACAAATTGAGATTTGGGAAAACCCTTACCAATAATAAATCTGTATCTTATCTATTGTTAGCAACAGTCAAGAGCAGAGGTGTGACACGCAGTGTTGGTTTTGCTTTTTTTTTTTTTTTTTGGAAATAAGACAGAACAGGATATTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6616
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053841 | Essential Splice Site | 800 | 859 | 13 | 13 |
ENSDART00000145439 | None | None | 644 | None | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 10004043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 9835972 |
GRCz11 | 20 | 9823212 |
KASP Assay ID:
554-4491.1 (used for ordering genotyping assays)
KASP Sequence:
GAMTATATTATCTCCAGGCCTCTATGTAATCTTTGTTGTTCCTGTGTTGC[A/G]GTGGAGCTGGAGAAGCGCATTGACTTTGAGCTGCGGGAGGGTCTGGTGGA
Long Flanking Sequence:
CGCAAAGTGGATTTTTCCATCCTTATATTAGCAAAAATGGATTCTGACACACCCTGAAAGCATTTGCACCCTACGCACTGCACTTTGCACATGGATTGTTAAAATAGAGCCCTTAGTTGCCAAGCTAAAAAAGTGGCTTTACATTTTATTACTCAATGTCCTACAACTTATTCCCTGCTTCAATAATGGTTGCCGCAGTGGAATGAACCACTAATCCCTCTGGTGTATGTTTTGTGATACGGATGCCCTTTCTTCCACAACCATAGTGGCCATAGTGTGTGTGGGTGTTGCCCAGCACTGAGGGAAAACAACCACACACACTACGGACAATTTTTAGTTCATCTAATCCAGCTTGGACTTGAACCAGTGGCATTTTAGCTGTGGGGCAACTGTGCTAACCACTTAGCTGATGTGCCACCTAAAGGCTCGTACACACCGGGATAAAATTATGACTATATTATCTCCAGGCCTCTATGTAATCTTTGTTGTTCCTGTGTTGC[A/G]GTGGAGCTGGAGAAGCGCATTGACTTTGAGCTGCGGGAGGGTCTGGTGGAGAGCCGCTACTGGTCAGCAGTAACGTCACACACGGCCTACTGGTGCTCGCACGACGTGGCTCTGTTTCTGCTGACGTTCTTGTACAGGCCAAACGAAGCCAATGACATGGCAGAGGACAATCTCGAATCCTAACACACACTCACAGACAAACTCTCACCCTCAATCACCCTCCTAATTTAGTTTAGCAGACCTCATTCACTGTGCATCAGAGATCCTGTCCTTGTCTTGTTTTTTCTTCATTCAGAAGCACATCCATCGAGGAGACTCACACTCTCCTCTACGTCCCCCAACTAGGACTGTTTGATGAAACGGTGTTAATGATCCTACTAGTAACTTCCGACCATTCACACGTTGACGTTTCCCAAAAGCAGCAAACTTTTCATATTGACCGATGTGTATGAACTTATTATGGTATGGCTCACTGAATTGGAGGAATTCAACTGAATTGC
Associated Phenotype:
Not determined