Busch Lab

ZMP

ENSDARG00000076665

Ensembl ID:
ENSDARG00000076665
Human Orthologue:
ZBED1
Human Description:
zinc finger, BED-type containing 1 [Source:HGNC Symbol;Acc:447]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa13106 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa13106
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
ENSDART00000113139 Nonsense 369 630 5 5
Genomic Location (Zv9):
Chromosome 2 (position 14319591)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 14617635
GRCz11 2 14286225
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTCAGGTMCTGAAGGCAGACAAGGCAAGGCATTTGGYTCCATCCTGG[C/T]AAGATGTTGACGTGATGGAGTCTGTGAAAAAGGCACTGAGTCCACTRAGA
Long Flanking Sequence:
ATAACATTACACTGAATTAATTTTTTCGTGTGTGCCACCCCAAGATTTGATGTGGCCTCATTTGGCCACCCCTATGAAATTTTTCTGGGGGCGCCACTGGCACTGGTATGAGTAAATGTTTTGTAAATGAAATGTTTATATACATTTAAACATTTTATATACATTTTTACATTGTGTTGTGCATTAGGTTAAATCTAATTGATACATTGTTCTTTTTTTTTCTTTTTCTTTTTTTAGAAAAAAGTGCCAAAGACCCTCGTGTTGAACGTGCAACATCTGTTTGCAAGAAAGTTGTCAGCACATTCTCCTTCAGCTGGAAGAAAAAGAGGGAACCAAGTAATGCTCAAGCTGAGCTAAAGCTACCTTAACAGAAGCTCATCACTGAGTCCCCAACACGATGGGGTTCAAGTCTCAGCATGATTGAGCGAGTGCTTGACCAGAAAAAGGCGATTTCTCAGGTCCTGAAGGCAGACAAGGCAAGGCATTTGGTTCCATCCTGG[C/T]AAGATGTTGACGTGATGGAGTCTGTGAAAAAGGCACTGAGTCCACTGAGAGACTTTACAGATGCACTCTCAGGTGAGGACTATGTGAGTGTATCTTATGTCAAGCCAGTGCTTCACATGTTGAAAGTCAACATTTTGAGCCTGAATGATGAAGACACTGAACTAACAAAAACAATGAAGACAACCATTCTGAATTACCTCACTGACAAATATCAGGACCCCACCACTGATGACCTGCTGGATATGGCTTCGCTTTTTGATCCCAGATTCAAAACACAATTCATTGCCAAAGACAAGGTAGAGGGAATACAAACCAGAGCTGTGGCTGAGCTGGAGTCTTTGATGACCATACACATACAGTATCCAAAATCAGATCAGCAGTCTACATCTAATACCTCAGCCTCCACGTCACAAATCCTTGATGAGGATCAGACACCACCCAAGAAAGCAAAGAAAACACTTTCCAGCTTTTTAAAAGCCTTAGGTGTTGCAAGTGCATCT
Associated Phenotype:
Not determined