ZMP
im:7138144
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate LPS-responsive vesicle trafficking, beach and anchor containing
Human Orthologue:
LRBA
Human Description:
LPS-responsive vesicle trafficking, beach and anchor containing [Source:HGNC Symbol;Acc:1742]
Mouse Orthologue:
Lrba
Mouse Description:
LPS-responsive beige-like anchor Gene [Source:MGI Symbol;Acc:MGI:1933162]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39612 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32677 | Nonsense | Available for shipment | Available now |
sa780 | Nonsense | Available for shipment | Available now |
sa39611 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25575 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38265 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39612
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 |
---|---|---|---|---|---|
ENSDART00000025224 | Nonsense | 454 | 2861 | 10 | 56 |
ENSDART00000146960 | None | None | 1847 | None | 34 |
Genomic Location (Zv9):
Chromosome 1 (position 23035833)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 23570405 |
GRCz11 | 1 | 24261234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCCATTCACTCTATAGGAGGAGTCCAGGTCCTTTTCCCTCTGTTTGCA[C/T]AGCTGGATTTCCTCCAACACAGCGGTGACGAGCTGGACACCTCCGTCTGG
Long Flanking Sequence:
AATAGTCTGAGAAGCATTCGAATTGGTTAAAAGCAATGAATGAAAGACATTTTCAATTGATTCTTAATTATTTTCAGTTCATAAAAGCTTCTTAAGATCTGATGGCACCATCACATGCTAAACAGATGCAGTCGTTCCTCTTTGACAATGATTTTATGAAAATGCCATCTTGTGCCATCTGGGAGGGCACTCGTCTGATTAGAAGGACATTAAGAAGGACCTCACAGCTGTCCTTCTTCTTAATTACCCACCAACCCCTTCACACCATGCGTCAGTAGAGCTCAGATTTAGGAAATAACCTTCTCGTTCTGAAATAGTTGTTGCAGAATGACAGGAGGGTTTTATTATTATAGAGGAATATTTATAGAAATATCATTGATGGAGCAAATCTAACATCAAATCTTTCTATATCTCAGGATGTGAAGGCTGTGGTGACACATTCGGTTCAGAGTGCCATTCACTCTATAGGAGGAGTCCAGGTCCTTTTCCCTCTGTTTGCA[C/T]AGCTGGATTTCCTCCAACACAGCGGTGACGAGCTGGACACCTCCGTCTGGTGAGAACACATCAGCTTAGCATGAGGGCCTGAATGAAAATGTTTCTCAGTGGGGGGAAAAGACTGAGCTCTTCTCAGTTTTAGCTTGACCCGGAGAATCTGAGAATTTTGTTGATTTTTTTTTTTTTTTTTTCCCCTTTTAAAGTTGTTAAACCTGTTAGACACAATGACATGCTTATTAAAGATGTGTGGCCAGTGCTCACTGTTATTTAATGATATTTAATGTGTCGACATTGAATGAGAGCCAATACAAAGTTAAATATTTAACTTTAACCATATACTAATAAATGTGTTACCTGGAGTAGTATAAATGTATCAACCTGGGCCAATCTTAAATGATGTTCTTGTTCAACTAGCTTTTCAAACGACCTTTTTCATTAAATATCTTGTGCTTCATCTTATTACAACGTTAGATAGTGAAAATCCGCTTAGATTTGCTTGTTTACTCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32677
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025224 | Nonsense | 594 | 2861 | 13 | 56 |
ENSDART00000146960 | None | None | 1847 | None | 34 |
Genomic Location (Zv9):
Chromosome 1 (position 23030732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 23565303 |
GRCz11 | 1 | 24256132 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAATGCCATCCGCAGAGTTGGGACCGTACTGCAGGTCATGCACACGCTC[A/T]AGTATTTCTACTGGGTTGTAAACCCACTGGACCGCAGCGGAATCACACCC
Long Flanking Sequence:
GTGTTGTGCTGTGATGCAGCAAAATCTTAAAACTTTGAAAAAACCTGCACTGATTCAGTTTTTATTTTACACATTTGTTTGACGATTTTATTAATATTTGCTCTGATGTTTGTGTTTTCTTCTCAGTCTTCCAAAGTACATGTGACACGACCTGTGCTGGACATCGTCCTTGCCTTCGCCCGTTACCTTAGCAACCTTCCTACTGGTGTTATGCTCTTGAAACAGCTGTGTGACCACATCCTCTTCAACCCTACCATCTGGATTCATGCCCCTGCGAAGGTCTCTTACACATTTATACAGAATGCTGAGTAGTTTATTAGTTTACCAGTTCTTTGTTTTCTCCAAGTGATCCTTTTCAAGGCTGATTTGAACAGTTTTGCTGCCCCCAACAGGTACAGCTGGTTCTCTACACCTACCTGGCCACAGAGTTCATCAGCACTGTCACCATTTACAATGCCATCCGCAGAGTTGGGACCGTACTGCAGGTCATGCACACGCTC[A/T]AGTATTTCTACTGGGTTGTAAACCCACTGGACCGCAGCGGAATCACACCCAAGGGTCTCGGTAAGAGACTAAACCAACTTCTCAACACATGGTCACTATTCTGCAAGAAGAATGGCTCAAAATCCCTCTGGCCAATGTACAGGACTTGTGTCTGTCATTCCCAAGACAAATGGAGGCTGCATTGGCTGAAAAAAGAGTCCCTATACCATAATAATGAATAATTGTGGGCTAAAACCAGGCGTTTCAGTTTAATTGCTCAACCCTTTATTTTTGTACTGTATGTATGCATGTATGTATGTATGTATGTATGCATGCATTTATGTATGTATGTTTGTATGTATGATTTTTTTTCTTTCATTTATTCATTTATGCAATGCTATTTTTTATGTTTATTGTTATAATAGAGTGGAAGAACTATGACGTCACCTTGTAGGCCAATCGGCTGCTAATATAAAACTGGTTCCCTTGTTAAAATCCCTATAGGATGAATTAAGATTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa780
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025224 | Nonsense | 971 | 2861 | 22 | 56 |
ENSDART00000146960 | Nonsense | 358 | 1847 | 9 | 34 |
Genomic Location (Zv9):
Chromosome 1 (position 23002535)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 23537511 |
GRCz11 | 1 | 24228340 |
KASP Assay ID:
554-0685.1 (used for ordering genotyping assays)
KASP Sequence:
TTATTGAGCTACGTGTAGAGGAGCAGGACAACGATCAGACTGCAGACAAT[G/T]AGGAGATGCAGACCCAGATCCCTGTCACAGTGTCCAACATTCTGGTCAGA
Long Flanking Sequence:
GCATTATGGACTTGGCTTTGTTTACTGCAGCAAGTTGACATGACAACCGTTTAAAACCATTCCTGAGCGCTGCGTTTCGCGTTTCAAGTGCAGAGATGCAGGAATGTCTCCCAAATCCGTGCATGTGGTGCAAAATTTTGCGGTAAAAAATGGTCGCACATAACTATTTTTTGTACTCGCACAAATGCACCCAAATATATTTAATATAAGTCCCATTTTTTCCTTCTTTATAATTAACATTTCTTTCAAAACATTTGTGGTTGTTTTAACAGGTCACCTTTGAGCAACACAAGGAGAATCTGGCCCGAATGTTTCTTGAGTACCAGCGAATGGGATCTGAGGGAGGATCTGAAAGCAGGATCCGAACGATCTCTGGAGTCAGCCAAGATTCTCAGTTCCTTGCCTCGGCCAACGGGGAACTGCATACAGAAGAGAAGGCTCCATCTACTGTTATTGAGCTACGTGTAGAGGAGCAGGACAACGATCAGACTGCAGACAAT[G/T]AGGAGATGCAGACCCAGATCCCTGTCACAGTGTCCAACATTCTGGTCAGAGATGAGGAAGAGAGGCAGACAGACACTGTTGCCACCTCACTGGAGATGCAGGACAGGGATAAGGATGAACAGTACGCTGTAAAAGAACCAAAAAAAGATAATGAAATAAAACATATGGATGACAATCATAAAACAGGGGATGAAGACCGTGAACAAATGGAAAATGTTAAGACTGAAGGTAGAGTTGAAGAGGAGAGCAGTAATCTGAGTATAAAAGACGATACCGACAGCCCACAGACTGAAACTGACAAGAATGCCAAAGATGCAACTGAAGCTGTGAAGATGTCAGATGAAGGTAAAACAAGTAATGCGGAAAATGAGCAAAACGTTCAGGTAGAAGATGAAAAGAAAGATCTTGGAGATTCTACTCTTGAAGCTGTTAAGGAAGATTCCACTCAAAAGTCTTCTGAGGTTTTAGTCCATGAGGAAACCAGCACGACTGGGGCCTCT
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:
sa39611
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025224 | Essential Splice Site | 1984 | 2861 | 37 | 56 |
ENSDART00000146960 | Essential Splice Site | 1369 | 1847 | 24 | 34 |
Genomic Location (Zv9):
Chromosome 1 (position 22866717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 23401693 |
GRCz11 | 1 | 24092522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTACTTCTCTTTCTCCATCTCTCTCTTTCTTTCGCTCTTCCTCTCGGC[A/T]GCAGACCGCGGGAGTTCTGGCGCCTGGACTACTGGGAGGATGACCTGAGG
Long Flanking Sequence:
TTTTTTATTTTTTTTTTATTAAAAGCTGCTTTTATTCTAGCCAAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAAAATATATTATCAGACATACTGTGAAAGTTTCCTTGCTCTGTTAAACATAATTTGGGAAACATTTAAAAAAAAGAAAAAAAAATTAAATGGGGGGTTTAATAATTCTGATTTCAACTGTGCAAAAAAAATTATAATAATAATATATTTCACACTTTGACCCACATTGATTTATTTTTTATTTTTATTTTATTGATTAAAATTTATTTTATTGATTTAAAAATAAAATCCAATTTTAGCTATTCTCCAGTTTGTGCAGTTTCAGTTGCAGAAGGTTGCAGCAAAACAAGGCTTGTATTATGCCGGTACTGTGCTGCGTCTCACTGCATTGGCTAATTGCTAACATATGTGCCTGCCTCTCTCTCTCCCTCTCTCTCTACTTCTCTTTCTCCATCTCTCTCTTTCTTTCGCTCTTCCTCTCGGC[A/T]GCAGACCGCGGGAGTTCTGGCGCCTGGACTACTGGGAGGATGACCTGAGGAGACGTCGGCGCTTCATCAGGAACCCGTTTGGGTCCACACACTCTGAGGCCACGCTCAAGGCTGCAGCTGAGCATGGTGGGTAATACATAGTCACACAGTATCATGCGCTTACACACACACACACACACACACATACGCAGCCTATTCTGTTACGCTTGTAACCCATGATAACAGGTAACAGTCTGTGTAAAGCATTTATAGTTTTTAGAAGACAAACAAAAGGCATTACAGTCTCTCACAGAGGATTTTGTCTCGGATAGTATTATGGCAGCAATTTTAGGCTAATTTGTTTATTTACTACGAGCAGTTCCTAGCATTAGCTCGGATTTTTAAGTATGGCTAATTGTTAAATTGTCACTGTGTTCCTTCCTTCTCATGCATGTCAGCTGCTGGTATTAAAGGTAAGTGAAACTGTGAAGTTAATTGGAAAGCTAGCAGCAGTGGCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25575
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 |
---|---|---|---|---|---|
ENSDART00000025224 | Nonsense | 2213 | 2861 | 42 | 56 |
ENSDART00000146960 | Nonsense | 1598 | 1847 | 29 | 34 |
Genomic Location (Zv9):
Chromosome 1 (position 22820162)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 23355138 |
GRCz11 | 1 | 24045967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCCAGCCCGAAACAGCTCTACAAGGCCTCCAACATGACACAGCGCTGG[C/T]AAAGACGAGAAATCTCAAATTTTGAATACCTCATGTTCCTTAACACCATC
Long Flanking Sequence:
ACATACTGTGTGTGATAATGAAAGGATCACATTAATGTTAGGCCTGTTAATAATCTGTTCAAAGAATAATTATAGTGAAAGCAGTGACCGCTGCTGCTTACAAAAAGACATTTAACATAATAATACAATTCTGGAGCTCTTGAAAGCAGCATTTAGGTTCCCTAAATGATCAGCACATTCTCTTCAACATCTGTTAGATGAGCCTATTCTTATCTTGCTACAATTTGTGGTGTGCAGAAATATCTTGTAAAGATTTTCCACTACTTGTGCCATGTGTTTATATATTTTTTATTTCCATCTTATGAAATACACTAATGCTTTAGTTTTATTTCTTATATTTGTATTTGCATGTTATATTTTAAATGAACTGAGCAGCACAGATGTATACATTTTTAGTTGCTCTTTGAAGTTGTTAATGTGATTTATCTTTTTCCCACAGACGGATTTCTCTGGCCAGCCCGAAACAGCTCTACAAGGCCTCCAACATGACACAGCGCTGG[C/T]AAAGACGAGAAATCTCAAATTTTGAATACCTCATGTTCCTTAACACCATCTCTGGTAAAAAACAAAAAAAAACAAACAAACAAACAAACAAACTGTCATATCCAAACGCTAACTGATGTTCTCCAAACAGCAAACAAGCTGAATGTACTAATTATAATACAGCTAAGAACAAATGCTATTTCTAAGTTTAGGAAAGTTTTTATGCATATATGACTAGCTAAACATTTTAGCTTTTATTTTTTCATTAAAAGTATTAGTTGCCTTATGCTTCCAGTAATGAGACTAGGGATGTCCCGATCAGGTTCTTTAGCCTTCGAGTCAGAATCATTTGATTTTAAGTATCTACCGATACCAAAACCTGATCAAATTCTTCTATAATACATAAAAAAGAATAAAGAAGAGTGAAGATCCAGGATGTTTCTTATTTTTGATTTAATTGACCCTATTTTAACATTCAACAACTCTGTTAACAAACAGAGCACATCTGTGAGGTAGCTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38265
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 |
---|---|---|---|---|---|
ENSDART00000025224 | Nonsense | 2240 | 2861 | 43 | 56 |
ENSDART00000146960 | Nonsense | 1625 | 1847 | 30 | 34 |
Genomic Location (Zv9):
Chromosome 1 (position 22818642)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 23353618 |
GRCz11 | 1 | 24044447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGACTCTGCTTGTGTTTCAGGCCGTACATTTAACGATCTGAACCAGTA[T/A]CCTGTGTTCCCCTGGGTAATCACCAACTACGACAGCGAAGAGCTCGACCT
Long Flanking Sequence:
CGAAACAAGATCATGAATATTGACCTAAAAAATTTGGAAAAGTCATGGAATTTTAGTAGTAAAAATGTGTATGTGGCCTTGTGAAAATAGTGACTAGTGATTCACAAAAACAGTCATAAATGTATTTTTAATAAGCTTTTAATTGGTGTATACTTTGTTAGAATAGAACATTGTTTGACCAATATGCATCTATTTGAAAATCTGAAATCTGAGGGTTCAAAAATAAAAACAAAAATACTGAGAAAACGTCTGAATGAATTTCTTAGCAATGCACATTAATGCGTTTTGATATATTTAGAGTAGGATATATACACAATATTTTCACTGAACTTTATTAAATATTCTAATGATTTTTGGACATAAAAGAAACTCAATAATTTGACCCACACAATGTATTTTTTATCCATTGCCAAAAATATACCAAGGCAACATAAAATGTGTGTTTGAATTCCTGACTCTGCTTGTGTTTCAGGCCGTACATTTAACGATCTGAACCAGTA[T/A]CCTGTGTTCCCCTGGGTAATCACCAACTACGACAGCGAAGAGCTCGACCTCACCCTGCCCAGCAACTACAGAGATCTGTCCAAGGTAAACACATGACCACACACACAAACACTCCGCATCTACTCTCAAAGACTGAAGGACATGTCTGGAGTGAAGTTTCCAACACACAAATACATAGGAGTGTTAGTGTGAAATCAACGTCCGGCAGCTTTAACGATGAGTCTGAGTCTGATAGACAGATGTAGCTGTCTAGCAAGGGAGGGAATGATCGCAGCTCTAGACTCATTGCAGAGAGACTGACCGTACTTGTAGTACAACGCTCGCGGCCCTGTGCACGTCACCTCATGCCAGGCACCCTCAACCGCAGACAAGTCAGATAATGGGCCCATGTCTGTCCTCCACCCTTCTCCCCCTCAATCAAGCCCTCAGAAGCCCCTGCATCCCGCCTCTCGCCTCCTCCCCCATTCCCGTTAGCCAGCCAGCCTCCCTAAGGAGCTAAT
Associated Phenotype:
Not determined