Busch Lab

ZMP

si:ch1073-376g14.1

Ensembl ID:
ENSDARG00000086290
ZFIN ID:
ZDB-GENE-100922-265
Human Orthologue:
ZNF804B
Human Description:
zinc finger protein 804B [Source:HGNC Symbol;Acc:21958]
Mouse Orthologue:
AC112662.1
Mouse Description:
zinc finger protein 804B [Source:RefSeq peptide;Acc:NP_001156695]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa11375 Nonsense Available for shipment Available now
sa10089 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11375
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
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Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127080 Nonsense 110 1271 3 4
ENSDART00000133696 Nonsense 72 89 2 2
Genomic Location (Zv9):
Chromosome 16 (position 30227041)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 28064179
GRCz11 16 27998802
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGAGAATTTGCACGGAATGTTTCCTCCAAGTCTTGGAAAGATGAAAAA[A/T]AGCARAAACGWGCTCTGAAACGACTGCATCAGCTTGCACAACTCAAACAG
Long Flanking Sequence:
GTCTACAGAACAAATTCTGGCACAGCTGACACTTTTATTGTTTTGTGATTGTATTTAGGCTTTGCTGATTTTCTGTTTACTTTGTTTCGATTTTTTTTCTCCTCTGCCCTAAAGGGATATTGTGATAAATAGACAGGCATCCATCGGTGAGGTTTATGCCTTTTCAAAGGAGCCTTTTATGTGGAAAACTGATGGACTGCACAGGCTCTGTTAGCAGAAGAATTAGAAAGAGGTGTTTTTTTTTTCTTAAAGGGATTATTTTTTTTAATTGTTTTCTCTCAATTGTACGCTAGGTTAGACCTTGATTCTTTTGTTTCTTTTTTTTCTCCTGATGTAAAATTCATTAGGTTCTTTATATAGCCAAACAATTGTTCTTTTTATGGGAGACTTTAGATTTTTAGAACTTCTCATCTGTTAATTTTGTCTTACAGAGGCTGAAAGAGTTAAAGCAGAGAGAATTTGCACGGAATGTTTCCTCCAAGTCTTGGAAAGATGAAAAA[A/T]AGCAGAAACGAGCTCTGAAACGACTGCATCAGCTTGCACAACTCAAACAGCAAAGAGACAGGTAAATCATTGTGCACTTTTAATTCTGTGTGTGGTAAGTAGCCGCGTTTCCACTATCGCGCCTAAAGCGAGCGAGCCAGGGCGAGCCAAGGCCAGTGGGGTTTCCACTGTCACTTCCGGGGCCTGATCGGGCCAAAGCGGGGCTTTCTTGGGGCCAGCGGCCGGCCTTTTTCGGCCCGCCGAATACCTTGGGAGGGCCAGCTGGGGCTTCGGGGCGGAGTGAAAGGAGAGGCGGGCAGTTTTCTGATCGCACATGAGTACATGCGCCAAACAAATAAAGAAATAAGGGAAATAAAACATCTAGCCTTATAGTCTGGGGTCTTTTTGCGTATGATCACCCTTATGTTTCCCTTTTAAATGTAAGGCTGCTGCATAAAATAATAAAATAGTTTTAATTTATAGTGACGTTCTTTGCTGCGTCCTCCTTTATGTTTCAATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10089
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127080 Nonsense 1160 1271 4 4
ENSDART00000133696 None None 89 None 2
Genomic Location (Zv9):
Chromosome 16 (position 30232103)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 28069241
GRCz11 16 28003864
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCTCTCCAACCTCCTCTATCATTCCTCACCSWTCCCCTGTTACCCTCT[T/G]ACCTACCATTCATCACTCYCTTTCTCTGCCCCATTTTGCCCCTTCGATCC
Long Flanking Sequence:
CTCAACTCCCCTATCAAATCCACAAGTTATGCCTCACATCGGCATCAAGAATCCAGAATGCTTGCAAGACAGAAATGGCCAAAATCCCAGTGAGGCCCATACTTGTCTTGAAACTACCAATGAAAATAGATCGAAAGAATTCTGTGCTACTTTAGCTTCGGATTCAAACAATATTCAGAAGCATACTGTCAGAGGCCAAGCAGACCATCCAGAAATTGCAGGGATTCACTGTTCAAAACGTACCACTCCTCCCCTTTCTGAACAGCCAATCACCTTCACTGATGATGAAATTGAGAAGTACAGATTGCTTCAACTCCAGGCCCAGCAGCACATGCAGCAGCAGCACCTTCAAGAGCAAGCATCTGAGGAGATGACTTTACCAATCCCAGCTCCAAAGCCACTCAACCAGACTGCACTTTCAGCCTGTATGCCATACAGCATACTTCAGCCATCCTCTCCAACCTCCTCTATCATTCCTCACCCATCCCCTGTTACCCTCT[T/G]ACCTACCATTCATCACTCTCTTTCTCTGCCCCATTTTGCCCCTTCGATCCCTGCTGCCTTTTTTCCTGCGCCCCCTGCAACTGTGTTGGCAGCTCAGCCACTCCAACTGATCCCAGCCTCATCCCTCCATCCAGTTCACCCTCACCATCATGTTTCTGGGTTGACTCTCCACCCCCTGCCTCCCACTTCTCTGCTCCCTGCAATGCTTAGTCCAATGCCCATGGCTGCTGCCGCTGCTGCAGCCGTCGCTGCTGCCAGTACCCTGCAGATCCACCCCCTACTACACCCTCTGTTCCACAGCCAGGACCTTCAGCGGCACCCTGGACCAACCAGTTAGTTCTGGTCAGAATTATAAGGAAATTTTGAATAAACAAAAAGATTATAGTTCTGACATTTTTTTTTTTTTTTACAAAATTACTGCAAATGTGCTGTGAACTTTTGAGATGTTTAGGTTCTCTCTGCCAAAGGTCCTGTTCAGCCGTGATTTATTTTTGTTTTAT
Associated Phenotype:
Not determined