Busch Lab

ZMP

ENSDARG00000088331

Ensembl ID:
ENSDARG00000088331
Human Orthologues:
ZFP62, ZNF268, ZNF585A, ZNF585B, ZNF624
Human Descriptions:
zinc finger protein 268 [Source:HGNC Symbol;Acc:13061]
zinc finger protein 585A [Source:HGNC Symbol;Acc:26305]
zinc finger protein 585B [Source:HGNC Symbol;Acc:30948]
zinc finger protein 62 homolog (mouse) [Source:HGNC Symbol;Acc:23241]
zinc finger protein 624 [Source:HGNC Symbol;Acc:29254]
Mouse Orthologues:
5430403G16Rik, Gm13212, Gm14124, Gm14295, Zfp26, Zfp27, Zfp619, Zfp62, Zfp658, Zfp788, Zfp808, Zfp873
Mouse Descriptions:
RIKEN cDNA 5430403G16 gene Gene [Source:MGI Symbol;Acc:MGI:1924450]
predicted gene 13212 Gene [Source:MGI Symbol;Acc:MGI:3651014]
predicted gene 14124 Gene [Source:MGI Symbol;Acc:MGI:3652002]
predicted gene 14295 Gene [Source:MGI Symbol;Acc:MGI:3709624]
zinc finger protein 26 Gene [Source:MGI Symbol;Acc:MGI:99173]
zinc finger protein 27 Gene [Source:MGI Symbol;Acc:MGI:99174]
zinc finger protein 619 Gene [Source:MGI Symbol;Acc:MGI:1917477]
zinc finger protein 62 Gene [Source:MGI Symbol;Acc:MGI:99662]
zinc finger protein 658 Gene [Source:MGI Symbol;Acc:MGI:2652821]
zinc finger protein 788 Gene [Source:MGI Symbol;Acc:MGI:1914857]
zinc finger protein 80 Gene [Source:MGI Symbol;Acc:MGI:3704127]
zinc finger protein 873 Gene [Source:MGI Symbol;Acc:MGI:3040689]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa31366 Nonsense Available for shipment Available now
sa26177 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa31366
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127302 Nonsense 315 1005 2 4
Genomic Location (Zv9):
Chromosome 3 (position 61975022)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 61133547
GRCz11 3 61366135
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACATGAGGATCCACACTGGAGAGAGACCATTCACATGTACTCAGTGT[G/T]AGAAGAGTTTCCAATACACATCAAACTTGAATAAACACATGATGATCCAC
Long Flanking Sequence:
ACATTTATGTGCATCAAAGTTAATGTTTTTGTAGCCAGTGTTTACAGAGTCTTTACACTTCAAATTTTCATCCTACTTTTTATTTTTTATTGACTTACTAAAAAAGGAACTTTGTTTCAGACCCATTTGGAGAGAATAAGGAGAGTGAAGAGGAGGAACGTCATGTTGAAGCTGAGAAAAACCCTAATTTACAGACTTCTGGTGTTTTAAAAAGGAGAGACAAGAATCGTTTGACCTGCACTCAGTGTGGAAAGAGCTTTAGAACCAAAAAGAGTCTTAAGCTTCACATGAGGATCCACACCAGAAAGAAACCATTCAAGTGTACTCAGTGTGGAAAGAGTTTCCAATACTCATCAAGCCTTAATTTACACATGAGGATCCACACCGGAGAGAGACCATTCACATGCACTCAGTGTGGAAAGAGTTTCAAACACTCATCACACCTTAATCAACACATGAGGATCCACACTGGAGAGAGACCATTCACATGTACTCAGTGT[G/T]AGAAGAGTTTCCAATACACATCAAACTTGAATAAACACATGATGATCCACACTGGAGAGAGACCATTCACCTGTACTCAGTGTGGTAAGAGTTTCAGAGAGACTTCACAACTTAATAAACACATGATGATCCACACTGACGAGAAACCATTCACCTGTACTAAGTGTGGGAAAAGTTTCAAACACGAATTGAGCGTTATTAAACACATGATGATTCACACTGGAGCGAAACCTTTCATATGTTCTCAGTGTGGGAAGAGTTTCAGGCTATCATCATCCCTTAATCAGCACATGAGGGTCCACACCGGAGAGAAACCATTCACATGTCCTCAGTGTGGGAAGAGTTTCAGATACGTATCAAACTTTACTAAACACAAGATGATCCACACTGGAGAGAAACCATACGCATGTTCTCAGTGTGGGAAGAGTTTTAGCCACTCATCACACCGCAATAGACACATGAGGACCCACACTGGAGAGAAACCACACACATGTACTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26177
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127302 Nonsense 322 1005 2 4
Genomic Location (Zv9):
Chromosome 3 (position 61975000)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 61133525
GRCz11 3 61366113
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAGACCATTCACATGTACTCAGTGTGAGAAGAGTTTCCAATACACAT[C/A]AAACTTGAATAAACACATGATGATCCACACTGGAGAGAGACCATTCACCT
Long Flanking Sequence:
ATGTTTTTGTAGCCAGTGTTTACAGAGTCTTTACACTTCAAATTTTCATCCTACTTTTTATTTTTTATTGACTTACTAAAAAAGGAACTTTGTTTCAGACCCATTTGGAGAGAATAAGGAGAGTGAAGAGGAGGAACGTCATGTTGAAGCTGAGAAAAACCCTAATTTACAGACTTCTGGTGTTTTAAAAAGGAGAGACAAGAATCGTTTGACCTGCACTCAGTGTGGAAAGAGCTTTAGAACCAAAAAGAGTCTTAAGCTTCACATGAGGATCCACACCAGAAAGAAACCATTCAAGTGTACTCAGTGTGGAAAGAGTTTCCAATACTCATCAAGCCTTAATTTACACATGAGGATCCACACCGGAGAGAGACCATTCACATGCACTCAGTGTGGAAAGAGTTTCAAACACTCATCACACCTTAATCAACACATGAGGATCCACACTGGAGAGAGACCATTCACATGTACTCAGTGTGAGAAGAGTTTCCAATACACAT[C/A]AAACTTGAATAAACACATGATGATCCACACTGGAGAGAGACCATTCACCTGTACTCAGTGTGGTAAGAGTTTCAGAGAGACTTCACAACTTAATAAACACATGATGATCCACACTGACGAGAAACCATTCACCTGTACTAAGTGTGGGAAAAGTTTCAAACACGAATTGAGCGTTATTAAACACATGATGATTCACACTGGAGCGAAACCTTTCATATGTTCTCAGTGTGGGAAGAGTTTCAGGCTATCATCATCCCTTAATCAGCACATGAGGGTCCACACCGGAGAGAAACCATTCACATGTCCTCAGTGTGGGAAGAGTTTCAGATACGTATCAAACTTTACTAAACACAAGATGATCCACACTGGAGAGAAACCATACGCATGTTCTCAGTGTGGGAAGAGTTTTAGCCACTCATCACACCGCAATAGACACATGAGGACCCACACTGGAGAGAAACCACACACATGTACTCAGTGTGGGACGAGTTTCTCTGAAC
Associated Phenotype:
Not determined