Busch Lab

ZMP

ZNF580

Ensembl ID:
ENSDARG00000078220
Description:
zinc finger protein 580 [Source:HGNC Symbol;Acc:29473]
Human Orthologues:
ZNF524, ZNF580, ZNF581
Human Descriptions:
zinc finger protein 524 [Source:HGNC Symbol;Acc:28322]
zinc finger protein 580 [Source:HGNC Symbol;Acc:29473]
zinc finger protein 581 [Source:HGNC Symbol;Acc:25017]
Mouse Orthologues:
Zfp524, Zfp580
Mouse Descriptions:
zinc finger protein 524 Gene [Source:MGI Symbol;Acc:MGI:1916740]
zinc finger protein 580 Gene [Source:MGI Symbol;Acc:MGI:1916242]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa12449 Nonsense Available for shipment Available now
sa28605 Nonsense Mutation detected in F1 DNA Not yet available
sa12651 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12449
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
ENSDART00000110785 Nonsense 153 886 1 1
Genomic Location (Zv9):
Chromosome 16 (position 15310546)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13669005
GRCz11 16 13559125
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAACATTGTTAACACCTCAANNNATGATTTTCTAGAGGTTAAGGTTCAA[C/T]GACAATCTGTTCTGAATAAAGATTTTCATAATGACAAGCTAGTGTCATCT
Long Flanking Sequence:
TACTGAATAATGATTTCTCTACTGCTGAATGTACTGAGGTTGCTATGCGAAAACAACAAACATTGGACAGCTTAGGTGGGATCATTTCACAAAATAAATGGACTGATCTTACTGCAACCAAAGATTGTCAAATGTCTGTGGGTCAAGAAGGCGAGTCATCAGGTGAGGGGCTTTCATTGAAGAATGAACATAAGGACAAGGTGCCCCCAGATGGGTTTCCTGTCCCATCACAAGATCAAACAGAAAATGTAAAGGATTACAGCAAGCAGAATTCACCAAAATATACATCAATCTCAGACCAGATGAGTCCTCTTGAAAACCAGACGCCTAAAAATAAATGTGTCGCTTCTGAGGAAAAGACAAGAAGTCTACCAACAAACATGCAGCTGATACCCAAGATGAAGTCTGATAATGCTAAGACAGACATTTGTGAAGTAACAACCAAAGCTACAAACATTGTTAACACCTCAACAAATGATTTTCTAGAGGTTAAGGTTCAA[C/T]GACAATCTGTTCTGAATAAAGATTTTCATAATGACAAGCTAGTGTCATCTGATGGATGCAACCTTTTTGAGAAAAAGACGCAGGTCGTTGATGTGGCACATGCAAGAGGGAGTAAACCTGGCATTGACATGAATGCAAACATAGAAAATTTAGAACATACTAAAGAATGCACCGAAGATGATAAAACACAAACTTTGGGTAGCGTAGGAGAGAATAGACTTTTTCTCAGAACAAACTTGGCAATGACAAGTGCAGGAAAATCTCTGGGACAGTATGATCAAGACGAGGTATTAGATTTAAGTCTACCAAAAAAGAAAGATCGCAATAATGAGAGGCAGTGTGAATGGGTTGTAGACCCTGAATTTGAAGGTTCACTTCACATGGAAGTTGACGAAATTGAAGATGAACCCCAACATGATGAAGTGGAGCAGGAGGATGATATTGGATATTGCTGGATGCCTTCAGTAAGTGATGCTCACGCATATCTCCCACAGCCTTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28605
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
ENSDART00000110785 Nonsense 556 886 1 1
Genomic Location (Zv9):
Chromosome 16 (position 15309336)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13667795
GRCz11 16 13557915
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCGCCTCTTCCACTGTTGCACTTCCCTTAGCCACGTGTCCCCTTGATT[T/A]GGGATCTACATTAATTTCACATCCGTCACTTCTCAGCCTCAGCACGGTTT
Long Flanking Sequence:
TGAAGATAAGCCCTCTTCATTTGCTGGCGCACAGGATATTGCAGACTCTAGACTGCAGACACAACCTAATTCACTGTGTCCAAATATGTCTCTTGGCCTTGTCTCTGAGGAAGCCTCACAAGTTACCTCAAACCAGGAGACTACAGCTTCTTCCAGTTCTGTAACTCGTGCAAAACCCACAATCATACCTGCTGTGTCTAACTTGGCATCAGTTCCCATTCAGATCGTGGCCAATACTACAGGGTCAAATACTCCCATTCTTCTCCTTCCTCCATCTCAGCTTCAGTCACTTTCCTCACCAGCCTCTAAGGCTAACCCAGGACTAATTACCCTTTCTTTACCAGTTTCTCTCAGTCAGAACACTCAGTCCTCCCCCATGTTCTTAGTTTTGTCATCTCCTCAGGTGTCTTCAACTCCGGGTTTGTCCTTGCCTGGGCAATCATCTCAAATTTCCGCCTCTTCCACTGTTGCACTTCCCTTAGCCACGTGTCCCCTTGATT[T/A]GGGATCTACATTAATTTCACATCCGTCACTTCTCAGCCTCAGCACGGTTTCCTCTGCCACAGCTAAAGACATCTCAGGATCCAATAACCCCTCTAATCTTCCTGCTAGCCCTACCTCATCAACTGCTTCCTCTAGCACTTCAACAGTGACCTCTACAAGTCCAGCCAAGCAATTCAGCACTGATGCCTGCTCTGACACACCAGTGCCCACTTCCTTTCGGGAGGCTCTTCTCAGATTGGCTGTGTCTGTGGAAAAAAAACAGGAAAACCAGACTGAGGCTCAATCGGTCACTTCACCTTCCTCATGTTCAGAAGCAACCAAGCCGGATTCCTCTGCCACAGTCCAGGAAATTAAAAACCAGGAGGTAAACTGTGACGGTGAAACTGAATCTACCTGTGTGGACCAAGCAGACTCACTAGATACCACCTCTTCCACCTCTCCCCTTTGTCCTGTATCACCCACCAATCCTTCAAAGAGCCAAGACTCTTTAGGGCCACGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12651
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
ENSDART00000110785 Nonsense 756 886 1 1
Genomic Location (Zv9):
Chromosome 16 (position 15308737)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13667196
GRCz11 16 13557316
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTTGAGCGCCATTCCATCACACACTCCCAAAGCAAACCCCATGTGTGT[C/T]AACTCTGTGGCAAGGCATTCAAAAGATCAAGCCATCTTGAGCGACACAAA
Long Flanking Sequence:
TTCCTGCTAGCCCTACCTCATCAACTGCTTCCTCTAGCACTTCAACAGTGACCTCTACAAGTCCAGCCAAGCAATTCAGCACTGATGCCTGCTCTGACACACCAGTGCCCACTTCCTTTCGGGAGGCTCTTCTCAGATTGGCTGTGTCTGTGGAAAAAAAACAGGAAAACCAGACTGAGGCTCAATCGGTCACTTCACCTTCCTCATGTTCAGAAGCAACCAAGCCGGATTCCTCTGCCACAGTCCAGGAAATTAAAAACCAGGAGGTAAACTGTGACGGTGAAACTGAATCTACCTGTGTGGACCAAGCAGACTCACTAGATACCACCTCTTCCACCTCTCCCCTTTGTCCTGTATCACCCACCAATCCTTCAAAGAGCCAAGACTCTTTAGGGCCACGTCGCATTCTTTACTGTCAGTATTGTCCTCGGATCTTCTACTATCTCTCGGACCTTGAGCGCCATTCCATCACACACTCCCAAAGCAAACCCCATGTGTGT[C/T]AACTCTGTGGCAAGGCATTCAAAAGATCAAGCCATCTTGAGCGACACAAACACATCCATACAGGACAGAGAAACTTTGTGTGTCAGCTTTGCCCAAGGCGTTTTCGTGAATCAGGGGAGCTAATGAGACACCAGAGAGTACACACCGGTGAAAAACCCTTTCAATGCTTAATATGCCATATGCGTTTTGCAGAGCGCAACACACTGCGACGTCACACAAAGCGCAAGCACCAAGGCCAGCAGCTGGAAGCAGTGGACATGAAGGAGAAGCTAGAAAGTGGAGGGATTTCCCTCGCTGGTGTGCAAGCAGAGGCAGAGGAGAATGCAGAGTGGTACAGTTCAACAGTTCCTGAAATGGAGTCCGACAGTGACACAGGGGGAGAAGGAACTACATGAGGATATAAACAATTAGGTCACCTTTTTTTTTTTTTACAAAACGGTTAGATATAAGAATAGTTGTATATATATTTAATTTATTCTGTATTGATATAACAATTCCTT
Associated Phenotype:
Not determined