Busch Lab

ZMP

LOC561535

Ensembl ID:
ENSDARG00000080021
Human Orthologue:
ZMAT3
Human Description:
zinc finger, matrin-type 3 [Source:HGNC Symbol;Acc:29983]
Mouse Orthologue:
Zmat3
Mouse Description:
zinc finger matrin type 3 Gene [Source:MGI Symbol;Acc:MGI:1195270]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa9729 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9729
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109833 Nonsense 136 361 2 6
Genomic Location (Zv9):
Chromosome 11 (position 35366316)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 34266690
GRCz11 11 34528789
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTGTGGCYGCTGACCAGGAAGCCACTCTGGAAGAGCTTTGCAAACCTT[T/A]GTACTGTAAGCTTTGCAATGTCACTCTCAACTCTGCCCAACAGGCTCAGG
Long Flanking Sequence:
AAAAATGTTCCCCATGCAGATTTTACATGTAATCAAGTTGATCACAGTTTTCTTTGCCCTGAAAATGAAAACCGTGATTGGTTTGAAAGTGACTTCAGTTTGAGTGCTGCTTCATAAATGTCTGTGCTATCAACAGCAGATTACACTGCAATTTCAGTAGTGTTATGGCACTTCTTCAATCTGATTCTAAATTCTGTCATTTGGCTTTCCAGGTCCAGACCCGATTCTGAAGCCCCCTATTAGTTTGATGTGTCAGCAGCCACCTCAGCCCTTCCAGGCCATGACCCCGACTCAGAACCTCAGACCTCCACCAGTGATGATGCCTGACCCCTTGCCATTCCCACACTGCACTCCACCCATAAAGCCACCTCCTCATCTCCAGTTGCCACCCAACCCACCCTTGCCACCACCTCCTGTCATCAGCCCAAAGCCCCCCGAGGAAGATGCTCAGGCTGTGGCCGCTGACCAGGAAGCCACTCTGGAAGAGCTTTGCAAACCTT[T/A]GTACTGTAAGCTTTGCAATGTCACTCTCAACTCTGCCCAACAGGCTCAGGCACATTATCAGGTAATCTAAAACCCATGAGGGATGAAAATGAATCAGTAAATTCATTCACAATCTGACTTTAACAAATGCAGTTTTGCATTGCACAATTGTCTGATGATAGTAAGCCTTGATTGTTTAGCTGCATGCTCTCACAATCATGAGTTCATACTTTCAGTTTTGGTTTCTTTCAGCGAGTTGTTTTTCTTGAGGTCCTGGTCTTTGCTGCGATGAAGCACGCAATCTATCCTTTGTTTTGTCTACAGGGGAAAAACCACAGTAAGAAGCTGCGCAATTTTTATGCCGGTAGCCAACAGCCTCCTCCCATTACAATTCCAGAAGTAGTAGAGCCTGTTTCCCAGCAACCCTCAGCCACTACACCCACAGATTCTGCTAATGCGACTGCCAACCAGGTGCTTATGACTCTGAACTGCTGCATTTCTGTCTAAACAAGTATGTTTTT
Associated Phenotype:
Not determined