Busch Lab

ZMP

zgc:77346

Ensembl ID:
ENSDARG00000009257
ZFIN ID:
ZDB-GENE-040426-2307
Description:
protein zer-1 homolog [Source:RefSeq peptide;Acc:NP_998066]
Human Orthologue:
ZER1
Human Description:
zer-1 homolog (C. elegans) [Source:HGNC Symbol;Acc:30960]
Mouse Orthologue:
Zer1
Mouse Description:
zer-1 homolog (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2442511]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa8461 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa37191 Nonsense Mutation detected in F1 DNA Not yet available
sa43556 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa29482 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa8461
Status:
Mutation detected in F1 DNA
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
ENSDART00000085341 Essential Splice Site 56 774 2 14
Genomic Location (Zv9):
Chromosome 21 (position 6260)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 157342
GRCz11 21 103440
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTGCGTGCGAATGCTCTGCTTCAGTGAGTGACTCTCTGCTGTACTGTGC[A/T]GGTATATGGATCTGRTGCACACAGACAGTGAGTTTGAGCCGCAGGACGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37191
Status:
Mutation detected in F1 DNA
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
ENSDART00000085341 Nonsense 57 774 2 14
Genomic Location (Zv9):
Chromosome 21 (position 6265)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 157347
GRCz11 21 103445
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGAATGCTCTGCTTCAGTGAGTGACTCTCTGCTGTACTGTGCAGGTA[T/A]ATGGATCTGGTGCACACAGACAGTGAGTTTGAGCCGCAGGACGGCTTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43556
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085341 Essential Splice Site 461 774 6 14
Genomic Location (Zv9):
Chromosome 21 (position 11553)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 162635
GRCz11 21 108733
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCATACAGGTGGTGCTCAACGGCATGGAGCATTACCAGGAGGTCACGG[T/A]GAGAAAACACACACACACTTAAATACATGCGCACATTTATGTGTTAAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29482
Status:
Mutation detected in F1 DNA
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
ENSDART00000085341 Essential Splice Site 533 774 7 14
Genomic Location (Zv9):
Chromosome 21 (position 11905)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 162987
GRCz11 21 109085
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGACAACGACCACAAGGAGGCGGTGGGGAAGATGGGCTTCGTCAAGG[T/C]GATGCACACACACACACACACACACACACACACACACACAAACACACACG
Associated Phenotype:
Not determined