Busch Lab

ZMP

si:ch211-30i2.1

Ensembl ID:
ENSDARG00000008575
ZFIN IDs:
ZDB-GENE-070702-1, ZDB-GENE-070702-1, ZDB-GENE-070702-1, ZDB-GENE-070702-1, ZDB-GENE-081028-72
Description:
Novel protein similar to H.sapiens LYST, lysosomal trafficking regulator (LYST) [Source:UniProtKB/Tr
Human Orthologue:
LYST
Human Description:
lysosomal trafficking regulator [Source:HGNC Symbol;Acc:1968]
Mouse Orthologue:
Lyst
Mouse Description:
lysosomal trafficking regulator Gene [Source:MGI Symbol;Acc:MGI:107448]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa17821 Essential Splice Site Available for shipment Available now
sa14050 Nonsense Available for shipment Available now
sa14595 Nonsense Available for shipment Available now
sa4537 Essential Splice Site F2 line generated Not yet available

Mutation Details

Allele Name:
sa17821
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099439 Essential Splice Site 121 1862 4 17
ENSDART00000136165 Essential Splice Site 121 1216 5 8
ENSDART00000136516 None None 250 None 4
ENSDART00000143148 None None 522 None 9
ENSDART00000143262 None None 747 None 15
ENSDART00000148057 None None 431 None 9
Genomic Location (Zv9):
Chromosome 13 (position 50984077)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49695174
GRCz11 13 50008417
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGAAGAAWTCTGTTTAAATCCTGAATTAAYCTCTCAAACCTTTTACTC[A/C]GGAGTTGACCTGTCGGGAAGARCTGCTTAMGCTCTTATTGTCTCTGCTAC
Long Flanking Sequence:
GACACGGCCCTTTTCTCTGAACTCAGCACTGCTTAACTCTCTCTCGACACAACATCAATCGCCTGTGTGTTTGCATAGTGGTGGGTCAATATGGGTCCCCAGCCATTTTGCTAATTACCTCATGAGTATGCTGCCAGATCCTTGTTTACCTGAGGTCACACAGCACTGTGGCAGCAGCCCCCTGTATTTGCTTTTAATTCACACTTGTCAGAGTGCTTTCTCTTCTCCTTGTGAGGAATGCTCTCTCGCTCTGGGAGGAGACTCTGTATTTAGAGGCTCACTGTCGTAAGCCATTGCAAGAGGTCCTTCTTAATACAGTTTTGTCCTGTCATACTGTTGTCTGCAGTTCTTCCATCTTTTTCTGGATAGTAGCTCTACAAGAGATCTCTGTGAAGCAGACGTGAGAAAAGTAACTGCTTCTAGGAGACTTTGATTGGATTGCTTAGGCAGAGTGAAGAATTCTGTTTAAATCCTGAATTAACCTCTCAAACCTTTTACTC[A/C]GGAGTTGACCTGTCGGGAAGAACTGCTTACGCTCTTATTGTCTCTGCTACCTCTGGTCTGGAAGATTCCTGTTCAGGAGGAGAAAGCCCCAGGTAAGAGTCACGATAAAGAGCTTTAATAATGCATCGTATTAACAGCCTTGTTTTTGGCAGTGCACTAGACGTATACTGTAACCCACCTTGAAACTTGAATTAAGTAATTGTGTTAATATTAAATGAGATTCTGACATTGCATTCATTTTGAAAGATGATATACTTGTACACAATATGTTTTATAAAGCAAACGATGGAGGTAATCTTGCGAAGACTCTATGAATTGTTAAAAAGCTACGTGCATGAACAACAAGTGAAACCATGAGATGGCTTAAATTTTGAAACAGTACGATTGAAGGAAAATGGAAAGGATAAGAGTTCTCATCGAGCTTGAGGCCTGAGGTATTTAGAGCAGGCATGCTAATCTTTTCTAGCAGCTACTTTCCACATTGTTGAGTTATTAGCTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14050
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099439 Nonsense 332 1862 5 17
ENSDART00000136165 Nonsense 332 1216 6 8
ENSDART00000136516 None None 250 None 4
ENSDART00000143148 None None 522 None 9
ENSDART00000143262 None None 747 None 15
ENSDART00000148057 None None 431 None 9
Genomic Location (Zv9):
Chromosome 13 (position 50982884)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49693981
GRCz11 13 50007224
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTGAAAAGGTCTGCAAATTTGACAKGACCATCAATCATAACCCAGGCT[T/A]GGCGGTCAGCGTTGTTCCCACCCTCACAGAGATACTCACTGACTTTGGTG
Long Flanking Sequence:
GGGAAGGACCATCTCTCAAAAGGCGGGGCAGGATCCATGTGATGTGCAGAACTCTACGAAGCGTTTATCTGGCTCCTGGAAGTCACGTCGCTCACGTAGGACAGCTCAGCGGTACTCTGTAAGGGATGCACGCAAATCTCAGCTTTCCACGTCAGACTCTGAAGCCAACTCGGACGATAAAACCACAAACACTGGGAGCAAACATCGCAGATTCCATAGTACGGCCATTCATGTTAGTTGCCAGCTTCACCAGTCCAACAACTCCTCGCAACCAGCACCGCAACATCCCACTCTTGATGCAATGGGCACTTTTGAGCCATCACAACCTCACCTGAGACTTTTTGGATCTCACACAATGGATCCTAACATGCTATCAGACCCCACCACTCTCTCCATCTTCAACCGCATGGAGAACTCGCCTTTTGATCTCTGCCATGTTCTTCTGTCCCTTCTTGAAAAGGTCTGCAAATTTGACATGACCATCAATCATAACCCAGGCT[T/A]GGCGGTCAGCGTTGTTCCCACCCTCACAGAGATACTCACTGACTTTGGTGACTGCTGTGGTCCCAGTGGTGGAGGGGGAGGTGGGATTGATGAGTTAGCTGGAGGCTGGACTGAGGAGCCAATTGCACTTGTTCAAAGGATGCTTTTACGCACAATTTTGCACTTGATGTTTGTTGATGTTGGTCAAAATGAGACACTGCCTGATAATCTACGCCGAAGCTTGACTGACCTCCTTAGAGCAACTTTAAAGATTCGTACCTGTTTAGAAAGACAAGCGGACCCTTTTGCTCCAAGGCCAAAGAAGACTCTGCAGGAGATTCAAGAAGATTTTTCCTTCTCAAGGTACCGCCACCGGGCCTTGCTACTGCCAGAACTCTTACAGGGTGTCTTACAGCTACTGCTGGGCTGCTTGCAGGCCTCTGCTCCAAACCCTTTCTTTTTCAGTCAGTCGCTTGAGTTAGTTCATGAATTTGTGCAACACCGTGGCTTGGAGCTCTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14595
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099439 Nonsense 1539 1862 12 17
ENSDART00000136165 None None 1216 None 8
ENSDART00000136516 None None 250 None 4
ENSDART00000143148 None None 522 None 9
ENSDART00000143262 None None 747 None 15
ENSDART00000148057 None None 431 None 9
Genomic Location (Zv9):
Chromosome 13 (position 50955757)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49666854
GRCz11 13 49980097
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGATTCAGCGCATCGCTGTGGGTGCGGGCTGGGAAAGATGAAGACGKA[C/T]GATCTAAGAAGGGTGAGAAGAACRTTAWTAGCTTTATGTACTTACYCGGG
Long Flanking Sequence:
TGCGCAATAAAAATACACATTACATTCAAACCAAACCATCCACTTGAATACTGATATATGTCATGTAACACATTCTGCAGTGTTGAAAGCGTTAAGTATTTTCTTCACTGAATGCCTGATTATGTGTTTGTTTGGATCATTTGCAGGAGATCTTGCTACGAGGCGTGCTTCAGATCGTGGAGGCAAACACAGACACAGAACCGCTATACTTCATGTCCTTTCCCATGATCCCTGGCTCTGGGGGTCCTGGCCTGAGCCCCTCCCCTGGGACAAGGCCTCATGGGGCGACTGCTGGTAAGGGTGGTGTAAACACTATTCTGAGGGGTAAACTACCGCTCGGCCGTGGTGAAGCAGACATGAGCCGACCTGGTCACCTGCGCTCCTCGCCCTGGCATGCTGCACCCTTCCACCTGCCCTTGGTGGGACAGAACTGCTGGCCTCATATGGCTAGTGGATTCAGCGCATCGCTGTGGGTGCGGGCTGGGAAAGATGAAGACGGA[C/T]GATCTAAGAAGGGTGAGAAGAACATTATTAGCTTTATGTACTTACCCGGGCTGTGCCATTAATCTAGGATGTGTGCAGAGTCATTCTTACTTTAATTTTCCTTTGGCTTAGTCTCTTTATTTAATCAGGAGTCGCCACAGCGGAATGAATCGCCAACTTATCCAACATATGTTTTACACAATAGATGCCCTTCCAGCTGCAACCCAGGATTGGGAAGCATCCATACACACTCACTTATACACTACGACCAATTTAGTTAATCAATCCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACATGGGGAGAACATGCAAACTCCACACAGAAAACGCCAACTGACCCAGCCAGGACTCAAACTAGCCACCATCTTGCTGAGGTGACAGTGCTAACCACTGAGCCACTGCGTCACGCTAAATAATATTGTAATTAATTTCCAGCAGTTTGCATTTGTTCCTCTCTGCAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa4537
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099439 None None 1862 None 17
ENSDART00000136165 None None 1216 None 8
ENSDART00000136516 Essential Splice Site 62 250 2 4
ENSDART00000143148 None None 522 None 9
ENSDART00000143262 None None 747 None 15
ENSDART00000148057 None None 431 None 9
Genomic Location (Zv9):
Chromosome 13 (position 50917146)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 49628243
GRCz11 13 49941486
KASP Assay ID:
554-3548.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTCTCTCGGTCATGCTTGGATACACAAACCTGTCCATRTATTCCCGTA[G/A]CTCCTGGACGCCTACTTCAGCCGCGCTCAGAAAGAGCAGAAGGAGAARTT
Long Flanking Sequence:
AACGGATCCGCAGCTCAATTTGGATCTGAATTTTCCGCATACGGAGATGATCGGAACTCAACGCAGCTCCCGGACTGCTCTCCATTGGAAAGAATGACTTCCGCTTGTCGTTTGTCGTGTGCAGTGGAAAGGAGGCTTTAGAAGGAATGCCAACCAATAAAATCTAAGAATATGGTGTTAGCTACAGTATATTCTGTTTCAGCTGTAAATGCTCAGCTTAAAGTCTTCTGCTTCTTGCTGACGTTTTTACTTCACTATTTCATTTCAAAGGCATTATAGTGTGAGATTTTTAAAAACATGAATATGACACAAAGGAGAGTGTGGTAAAATGAAGATTGATTACTGACAGTCTCTGTCTGCGTATCTCATCTGATATGATGAACCCCTGCTTTGACTAATAATCCCCTTTATATGCTGCTCTGATCCATTGATATTAGCTTTATTTTAATGTCTTCTCTCGGTCATGCTTGGATACACAAACCTGTCCATGTATTCCCGTA[G/A]CTCCTGGACGCCTACTTCAGCCGCGCTCAGAAAGAGCAGAAGGAGAAGTTCCTGAAGAACCACGGCTTCTCACTGCTGGCCAATCAGCTGTACCAGCACCAGGGTTCACAGGGGCTGCTGGAGTGCTTCCTGGAGATGCTGTTCGGACGACCGGTCGGTCTCGAGGAAGAGTGAGTATGAAAACTAGGGATGCACTGTATTTTCACCGTATACATATAAAGTAGACCAATGTAATAAGAAAATATCAGTTTGCAACATTAACAAGCCATTTTTAACGTCTGAAAATCAATGAAAGTGTAAGTCTGGAGCCAAAAAGATTCTAATGGCTGTCAATAAGGTCAATAAATTAGCTTGAGTATATGTATGTCATTGAGTGACGAGCAGTATTTTCTATTCCCTCAGTCTGGATCTGGAGGATATGGAGAACATCTCTCCATTCAGGAAGCGCTGTATCATCCCAGTGCTGGGTCTGCTGGAGAACTCTCTGTATGAGAACTCAC
Associated Phenotype:
Not determined