Busch Lab

ZMP

dzip1

Ensembl ID:
ENSDARG00000000943
ZFIN ID:
ZDB-GENE-040526-1
Description:
Zinc finger protein Dzip1 [Source:UniProtKB/Swiss-Prot;Acc:Q7T019]
Human Orthologue:
DZIP1
Human Description:
DAZ interacting protein 1 [Source:HGNC Symbol;Acc:20908]
Mouse Orthologues:
Dzip1, Gm7337
Mouse Descriptions:
DAZ interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1914311]
predicted gene 7337 Pseudogene [Source:MGI Symbol;Acc:MGI:3646689]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa8922 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa26672 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20624 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa8922
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049695 Splice Site, Nonsense 429 886 8 18
ENSDART00000083424 Splice Site, Nonsense 440 877 8 17
ENSDART00000125912 Splice Site, Nonsense 440 897 8 18
ENSDART00000136088 Splice Site, Nonsense 429 866 8 17
Genomic Location (Zv9):
Chromosome 6 (position 7182723)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7108739
GRCz11 6 7265908
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGCCACAGACTGCAGGAGCAGCAGCAGATCATTACCWCCCAAAACAAG[C/T]AGGTCAGTCTTGGATGCCAGCACAGGAAGAGGCTCCATTGTTCAGGATAT
Long Flanking Sequence:
AATATTTTACTTGATATTTTTTAAGACACTTCTATACAGCTAAAAGTGACATTTAAAGGCTTAACTAGGCTAATTAGGCAGCTTAGGGTAATTAGGCAAATCATTGTGTAATGATGATTTGTTCTGTAGACAGTGAGAAAATAATATAGCTTAAGAGAACTCATAATATTGACCTTAAAATGTGTTTTTAAAAATGTAAAACTGCTTTAATTCTAGCTGGAATAATACAAATAAGACTTTCTCCAGAAGAAAAAAATATTATAGGAAATACTGAAAATGTCCTTTTCATTTTTTGCTTAATATTTGAAAAAAAACTATTTGACTTCAACTATATGTCCACATAGTCACCAACACGTCTCTCTGTGCACCGTCAGCTTCAGGAGGAGCTGTGTAAAGTGAGCTCGGCCGTGTCTGAAGGAATGGAGGAATCGCGACGGCAGGTGCAGGAACTGAGCCACAGACTGCAGGAGCAGCAGCAGATCATTACCTCCCAAAACAAG[C/T]AGGTCAGTCTTGGATGCCAGCACAGGAAGAGGCTCCATTGTTCAGGATATCCTGTATTAGCGCAGCGGCACGAGCTGAAGGAGTGTACGGGTGTGAACACATCCGCACATTTTGAGCAATTATCATTACGCTGATTATGTTGTCAGCTTGTCGTTTATGCGGGTTGTATTTTAAGTTTGAAGCAACAGCTTAGATAATGTGTTGCCGACTGCAGATTTTTGTTGTTGTTGTAACCAATAACATATGGGTTTGTTTATGTGACAGATGAAACAGATCTCGTCAAAGCCGCCAACAATAACAGTACAGCGCGAAGGTTTGTGGATTTTACAGTTTTAGTCAAAAATATCATATAAACATCGTATCTGAGCAAAACTGTCCCCATAGTGTAATAAAAACAGACTTTTTTTAAAGTAATTGTGTTTTTGTTTCAGGGGTTTCCACCCCTTCTCCTGAAACTAAAGCGAAGGTGGTGGTCAGTGGTGAGTTCATTTATTTTTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26672
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049695 Essential Splice Site 445 886 9 18
ENSDART00000083424 Essential Splice Site 456 877 9 17
ENSDART00000125912 Essential Splice Site 456 897 9 18
ENSDART00000136088 Essential Splice Site 445 866 9 17
Genomic Location (Zv9):
Chromosome 6 (position 7183037)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7109053
GRCz11 6 7266222
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGAAACAGATCTCGTCAAAGCCGCCAACAATAACAGTACAGCGCGAAG[G/A]TTTGTGGATTTTACAGTTTTAGTCAAAAATATCATATAAACATCGTATCT
Long Flanking Sequence:
CTATTTGACTTCAACTATATGTCCACATAGTCACCAACACGTCTCTCTGTGCACCGTCAGCTTCAGGAGGAGCTGTGTAAAGTGAGCTCGGCCGTGTCTGAAGGAATGGAGGAATCGCGACGGCAGGTGCAGGAACTGAGCCACAGACTGCAGGAGCAGCAGCAGATCATTACCTCCCAAAACAAGCAGGTCAGTCTTGGATGCCAGCACAGGAAGAGGCTCCATTGTTCAGGATATCCTGTATTAGCGCAGCGGCACGAGCTGAAGGAGTGTACGGGTGTGAACACATCCGCACATTTTGAGCAATTATCATTACGCTGATTATGTTGTCAGCTTGTCGTTTATGCGGGTTGTATTTTAAGTTTGAAGCAACAGCTTAGATAATGTGTTGCCGACTGCAGATTTTTGTTGTTGTTGTAACCAATAACATATGGGTTTGTTTATGTGACAGATGAAACAGATCTCGTCAAAGCCGCCAACAATAACAGTACAGCGCGAAG[G/A]TTTGTGGATTTTACAGTTTTAGTCAAAAATATCATATAAACATCGTATCTGAGCAAAACTGTCCCCATAGTGTAATAAAAACAGACTTTTTTTAAAGTAATTGTGTTTTTGTTTCAGGGGTTTCCACCCCTTCTCCTGAAACTAAAGCGAAGGTGGTGGTCAGTGGTGAGTTCATTTATTTTTGTGTTTTATTCCTTATTGTAGGATGTTGGGTAAAATATCATAGGTCCAGTTAAAGTTAAAATTATTCGCCCTCCTTTTAATTAATTTATTTTTTCATTTTAAGATATTTCACAAATTATGTTTAAGAGAGCAAGGAATTTTTCCACAGTATTTCCTATAATATTTTTTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGTTTTAATTAATTTTTTTAACCATTTTAAAGTCAATATTATTAGCCCCTTAATCTAGTTATTTTTTATTGTCTACAGAACAAAGCATCATTATACAATGACTTTCCTATTTACACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20624
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
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049695 Nonsense 593 886 13 18
ENSDART00000083424 Nonsense 584 877 12 17
ENSDART00000125912 Nonsense 604 897 13 18
ENSDART00000136088 Nonsense 573 866 12 17
Genomic Location (Zv9):
Chromosome 6 (position 7189851)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7115867
GRCz11 6 7273036
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTGAAGGAGAGGAACACAGAGCAGCCTGTCAAACCCAAACTACATGAA[C/T]AAGGTCAGGATCTTTGATTTCACACACAGTATCAAAGCTGAGATATTTTT
Long Flanking Sequence:
ACGGGATTTTGTTGAAACATATTTTCCTCACGCTTGCATATATATTTTTTTGCTTGTTAGTTTGATTAGTGTTGATTTCAAATCTTATAAATATGTTTGTAGTAACGGTGCTCAAAATTGTTGGGTGCGACTAAATTTTGCCTCATGCGCCTAAATTTTTAAAGTTCGGAGCACCTCTCCTACCAAGCAAAAAGGTTAATTTCGAGCCCTGTAATATAATGGTAGGGGAAACTCTGAAGGGGGTACATGACCAACCGAATGAACAAAAACATGATGTGAACAAAAAGAGTAACCTCAGTTTCTGTTGTGCTGTTCAGGGAGTCAGTGGTCTGTCTAAAAACCTCTATAAGAGCAGCATGACCCAGATTATCAGCGATCGGCGGAAAAAACTGGAGGAGGATCCTGTTTATCGAAGGGCACTGAAGGAGATCAGCCATAAACTGGAGCAGAGGGTGAAGGAGAGGAACACAGAGCAGCCTGTCAAACCCAAACTACATGAA[C/T]AAGGTCAGGATCTTTGATTTCACACACAGTATCAAAGCTGAGATATTTTTATTTGGTTCTTCTTAACAGGTTTATCTGTTACTAAAACAAATAGAGTAAACATTGCATTTAATTTTCTCTCCACCTGTACAATGTAAAAACATATATTTAATGTACACAATAAGTACATTGTATTAATTAATTTCAGTGTAATTACATGTTAGTTAAGGACAATTAATATAAAGGAGGATATTATTGGCTGTTTTTTATGTGTTTTTTTTTTTTTTGGATGTACTTGATGTCAGTTTTTTGACGTTTTGACATTAAGGTGACTGCTGGGTTGCTTTTTATTTTTACAGTAAAGCTGATGTCTTGTTTTCTTACAGTGGTTCAGTCCAGACCCAGATCCAGCAGTTTTCCATCGACAGTAACTCGAGTGATGTCTGGCCCTGCTTCTAAACAGCAAAGAACCCCTCAGCCTGTCCCACGCAGCAGATCCAACGTCCCACACAAGACCTCCA
Associated Phenotype:
Not determined