ZMP
si:dkey-201c1.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
LRDD
Human Description:
leucine-rich repeats and death domain containing [Source:HGNC Symbol;Acc:16491]
Mouse Orthologue:
Lrdd
Mouse Description:
leucine-rich and death domain containing Gene [Source:MGI Symbol;Acc:MGI:1889507]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1707 | Essential Splice Site | Available for shipment | Available now |
sa14411 | Essential Splice Site | Available for shipment | Available now |
sa44222 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1707
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 |
---|---|---|---|---|---|
ENSDART00000110105 | None | None | 752 | None | 17 |
ENSDART00000144907 | Essential Splice Site | 486 | 942 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 4743896)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 4397596 |
GRCz11 | 25 | 4524123 |
KASP Assay ID:
554-1653.1 (used for ordering genotyping assays)
KASP Sequence:
AAGAGGAAGTGACAAACACAGCTGCAGGCCTGGAGGACGTCCTGCACGGG[T/C]CAGCCAATCAGATCAATCACAGACAAACAACRTATTTCATATTGCTGCTT
Long Flanking Sequence:
TTGTAGTTAATCATTTATAAAAATTATAAATTAAAAAGTATGCATTTATAATTATAGTTAATGAACACCATTTATTACATAATTGTAATTTTAGTGTAGTAGTTTAGTCATAAGGTTTATGTTTTATAAACCATAAACAAAATAATTAATAAATATAAATGAATATACGCCGTAAAATATACAGTTAACTAATAATATAAAATATATGTAATAACTGAAATTATCTTGTTTTAATGATTTTAAATGATATTCATTTCAAAAAGAATAATTGTAATTAATAAACTTATTGAGCAATAAAAATAATAAATTCGAATACGTTTTTGTGTGTTTCCCCCTGTCACTCTTTTAGCTGGTTGGGGTGTGTATTCCCTATCGTAAAACACGGAAAGGTGACGTGGTGGTTCGCAGGTTTGATGGTCAGTCTTGGACGACACTGACCACCATGACCAGAAGAGGAAGTGACAAACACAGCTGCAGGCCTGGAGGACGTCCTGCACGGG[T/C]CAGCCAATCAGATCAATCACAGACAAACAACGTATTTCATATTGCTGCTTCTAGAATGCCTGATATTATCAGATATCAGCTATATGACAAAATGACCCAAAATATTGGCTTATTCTATATCATCAGTGGCCCAAATTTCCAAAATAATTTAAAATATCGGCTTATCAGATATCAGCTATTGGCCAAAATAATTTAAAATATCGGCCTATCAGATATCAGCTATTGGCCAAAATGGCTTAGAATTTCGGCTTATCAGATACTGTCATTGGTCAAAATTGCTTAAAATATCAGCTTATCAGCTATTGGCCAAAATAATTTAAAACATGGGCTTATCAGAAATCAGCTATTGGCCAAAATAATTTAAAATATCGGCTTATCAGATATCAGCTATTGGCCCCAATGGCTTAGAATTTCGGCTTATCAGCTACTGTCATTGGTCAACATTGCTTAAAATATCGGCATATCAGATATCAGCTATTGGCCAAAATAATTTAAAATAT
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:
sa14411
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 |
---|---|---|---|---|---|
ENSDART00000110105 | Essential Splice Site | 346 | 752 | 6 | 17 |
ENSDART00000144907 | Essential Splice Site | 544 | 942 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 4742115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 4395815 |
GRCz11 | 25 | 4522342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGTTTCCCTCCAAACTGTACAGCGGAGACGCGCACCGTCACACTGCAG[G/A]TCTGTACAATAATACAGAATTCTGAATTACATGATTCAATATTTGTGCTT
Long Flanking Sequence:
AATTTAAAATATCAGCTTATCAGATATCGTAATTAGCCACAATGGCTTAAAATTTTGGTTTATCAGATATTACCGGATATCATCATTGGCGAAAATTAGTTAAAAAAATATTGGCTTATTGGATATTGTCATTGCCCAAAATGGCTTAAAACATCGGCATATCAGATATTGTCGTTGGCCAAAATTAGTTTTAAAATATAGCCTTATTAAATATCTACTATTGGCCACAAAGGCCTAAAATATCAGGTTATCATATATCGGCATCGCTAGTACTGTCAATCCTTTAACATCACCCTGACACATGAATGTTATGATGTGTGTTGTAGCTGGCCTGCTGCAGTGTGTCTCAGTTCTCCTGGTTTGTGGCCGTGTGTTGTCCATTCCTGGACAGTTGCAGTGTGTCTCCAGAGGGGGCGCTGCTTGTCTCTCAATGCGACCCGGGGATCAAACTCAGTTTCCCTCCAAACTGTACAGCGGAGACGCGCACCGTCACACTGCAG[G/A]TCTGTACAATAATACAGAATTCTGAATTACATGATTCAATATTTGTGCTTATAGTCCTATTTTTAATACGAGAAATTATAAATAATATTATTATATTAATAATAAATGAACCAGAGTGAATATTATTTAAAAATAATAATATTAATTATAGTTTCCCATATTATACTGATACTGTACTTTTGTTATTTATACTATAAGGTATAGTTAATACAGTTAACAACTAAGTTGATTAATAAAATCTCATTAATAAAACATTTAAACAATACAGCTATGGTTTTTGTTTTAGATAACAATAGTAATCTGAGTAATGCTAAGAATTTAAAAATAAAATAGTAATAATTGTTTGCTAGCAGCTACTGTTCCAATCTCGAATCTTTCAGCTTTTGTTAAGTTAACTTGATCCATTTGTGAGTGTGTTTTCTCCCTCAGGTTCTGCAGGTGGCTCTGTCTGAGGTGCAGGATCTGGCTGGAGACCCTCATGCCAGTGCTGGTCCACTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44222
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 |
---|---|---|---|---|---|
ENSDART00000110105 | Nonsense | 431 | 752 | 9 | 17 |
ENSDART00000144907 | Nonsense | 629 | 942 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 4739327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 4393027 |
GRCz11 | 25 | 4519554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGGACAGACGTCACCGCTCAAGTGTCCCTGTACGTCACACACATCTA[C/A]GCCGTCTTCTTCATCACACACTTCTCATGGTGAGCAACTGCAAACACACA
Long Flanking Sequence:
ATTGTAACAGTAAGTTACAGTTTGAAGCGAGTTCTTCACTTTCAAACATTTAGTCTTGAATCTGTCTTTTATTTTTACAAAATTTATAGTTTATAGTTTAATGTTATAGTATAAAATTCAAGTATACTGTTGTGCTGTATATATATTTATACTGGCATTTAAAAAATTTAAAAATTAAGTAAACGTAATAATTAATATTAAAATTTTTGAATGATAGAAAATCACAGAACATTTGTTTGGTGGAAAACTGCTATGTTTACATACTGCTAAACTATTGTACTGTGTAAAGTACTACTGCTTACTGTAGATGAAAGTTTTAGGTTCACACATTTATATATAAATATATATAAATATATCTAAATATATATATATATATGTGTGTGTGTGTGTTCAGGACACATGTTGGACCTGTCCCGTCTGCACCTGATGCATGGCGACCCCACGGCCCACACCTGGACAGACGTCACCGCTCAAGTGTCCCTGTACGTCACACACATCTA[C/A]GCCGTCTTCTTCATCACACACTTCTCATGGTGAGCAACTGCAAACACACACACACACACACACAATCTAATGTGAACCCATACAGTCTGACATATGTGTGTTTGTTTGTGTATGTATGATATTTGCGTATGTATGATATTTGTGTGTGTGTGTTCAGGTACTGGTTGTGGTACACCACTCACAGGTGTGTTAGCGGAGTGGTCAGAAAGATGTATCGCCGATTGAAACAGTTTCGGGTTCGATTCCTGGCGCTACAGAGGAAAAACGACCCAGAGCAGATTCTGCTGCAGTGCCTGCCATCTGACAAGGTGTGTGAGAGAGAAAACCTCCATCATTCTCAATAAGGGTGTGATATAGACAAAAAATGAGGTCCCACTTTATACTGATCCCAGTTGTAAGAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTGGAAAAGTGGCAGAAGGTGGATTTTTCTGATGAATCATCTGTTGAGCTGCATCCCAATCATCAC
Associated Phenotype:
Not determined