Busch Lab

ZMP

si:dkey-157l19.2

Ensembl ID:
ENSDARG00000060340
ZFIN ID:
ZDB-GENE-090313-190
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8A570]
Human Orthologue:
KIAA1522
Human Description:
KIAA1522 [Source:HGNC Symbol;Acc:29301]
Mouse Orthologue:
C77080
Mouse Description:
expressed sequence C77080 Gene [Source:MGI Symbol;Acc:MGI:2140651]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa5864 Nonsense Mutation detected in F1 DNA Not yet available
sa11087 Nonsense Available for shipment Available now
sa42253 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa14517 Nonsense Available for shipment Available now
sa38961 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa5864
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000084929 None None 1390 None 7
ENSDART00000133565 Nonsense 14 221 1 5
Genomic Location (Zv9):
Chromosome 13 (position 36436143)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 35908712
GRCz11 13 36034544
KASP Assay ID:
554-3664.1 (used for ordering genotyping assays)
KASP Sequence:
AAGCACTATTCCAGACTCACTGCTCTCTGAGGGACGACTTTGTCCGAAAA[C/T]AGTTTTGTGGAAATGCCTCACCTGAACTTTCCAGACCAGACTCACATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11087
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
ENSDART00000084929 Nonsense 123 1390 2 7
ENSDART00000133565 Nonsense 177 221 3 5
Genomic Location (Zv9):
Chromosome 13 (position 36397229)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 35869798
GRCz11 13 35995630
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAAATATGTGTTGGACCTCCACACAGAAGCCCAGCAGGGCCTGAAACTG[C/T]AACAGCAAGAGGGTAGGAAGACTTYAAAATCAGTCTGCTTTTGTAAAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42253
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
ENSDART00000084929 Essential Splice Site 189 1390 5 7
ENSDART00000133565 None None 221 None 5
Genomic Location (Zv9):
Chromosome 13 (position 36396658)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 35869227
GRCz11 13 35995059
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTTCAAATATACAATGCCAAAGAAAAAATTCTCATTTCCTTTCTCC[A/T]GCCTCAACATTCAGGCCTCTGAAACCAGATAAGTCTGCAGAGAAGCCCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14517
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
ENSDART00000084929 Nonsense 276 1390 6 7
ENSDART00000133565 None None 221 None 5
Genomic Location (Zv9):
Chromosome 13 (position 36396304)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 35868873
GRCz11 13 35994705
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTAGCAGCTCTGAAMAAGAAAGCTTACAAGACTATCCACAGAGAGGA[C/T]AGAACCTGCACATACTTTTGGAAAACAACACAGAGGTCCCCATGCTGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38961
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000084929 Nonsense 1123 1390 7 7
ENSDART00000133565 None None 221 None 5
Genomic Location (Zv9):
Chromosome 13 (position 36393667)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 35866236
GRCz11 13 35992068
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTAACTGAATCAGAGCCTCAATCAAACCACATTGACCAAACAAGAGTA[G/T]AGCCAACATGCTCATCACCTACTGAACCAAGTACCGCTTCAGCTCCTACT
Associated Phenotype:
Not determined