ZMP
si:ch1073-376g14.1
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa30689 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11375 | Nonsense | Available for shipment | Available now |
sa28674 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10089 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30689
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127080 | Essential Splice Site | 39 | 1271 | 2 | 4 |
ENSDART00000133696 | None | 1 | 89 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 30186045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 28023183 |
GRCz11 | 16 | 27957806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATGCATAACCAACAGTCTCTTTCTCTCTCTTTCTCTCTCTCTGTTTT[A/C]GGACTACGCTAAGAAAGAGAAAGCCATTGCAAAAGCCCTGGGGGATTTGA
Long Flanking Sequence:
CAAGAACAAGACTGTGTTTCTTTCTCATGTGTTAAAATGACTTGTACGTAAGTAGTTAAGTACAGTTATATTATGGCTAATTATTACCATGATCACAATGAAGGTTGTCATTTCTCACAGACTAATATCACAACCCTGTTGTCATAGCAACAAAGCAATGCTAAAATTCAAGCATCTTCTTAAAAATGCTGTTGTTGCTATGCTAGTAATTATGGCAAAATATATTTTAAAAAACACATGATAAAAAAAAAAAAAAAATCTGTAATGGTTTGGTTTCATCACGTTCTTCTTGATAGAATGAGACAATCTGTAAAAAATAAAAATACCTGATTGATATTTATGTGATGTTTATAGCCGTTTCCCTTCTTTTGTGGTTTTAAATAATCAGGGAAATCAATTTGTATTCTTAAAAAAAGGACTGTGTGATTGTCAAGTGTCGTTATAAGCAACTACATGCATAACCAACAGTCTCTTTCTCTCTCTTTCTCTCTCTCTGTTTT[A/C]GGACTACGCTAAGAAAGAGAAAGCCATTGCAAAAGCCCTGGGGGATTTGAAGGCTAACTTCTATTGTGAACTGTGTGACAAGCAGTACCATAAATATCAGGAGTTTGACAACCACATCAACTCCTATGACCACGCACATAAACAGGTAAACTTATAACATGGGTAGGCAGGAAAGCAAAGAAATGAAAGAATAGTTGAAGCATTAATTTACAAGTCAATACTAATAAGCAGTTTGTCTGTATACATAATGTTATGCATAGAAATTATTGTGTGCTTGATCGGGCAAACACACTGCTTGACCATTGTTTGCTTTTTGTTTTCCCAAATGGTCTTACATCATGCGGACAGCTGTTGACAAACCGAATATTTGCACACTTTGCTTATTATCCTGAAATTCTAACAGCATTCAGGGACACTGAATAAAGCACATGAGGTGTACCTGAGGTGATCATTGTCAGTTTTCTGTTGTTCAGCTGCAAGAAATAGAAGCTGTTTCTATT
Associated Phenotype:
Not determined
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa28674
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127080 | Nonsense | 868 | 1271 | 4 | 4 |
ENSDART00000133696 | None | None | 89 | None | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 30231228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 28068366 |
GRCz11 | 16 | 28002989 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCCAGTTCCTCTAGTAGCACTAGCATCTCTGATCTTAGTGGGGATTG[G/A]TCATCTAATTGCCAAATTAAACCATCACCTACGAGACAGAGCCAGAAACA
Long Flanking Sequence:
AACTATCTATACCCTTTGAGAAAGGAGCACAGTCAGCCCAGGTCTTACTTTAGAGGTTCCTCAAACAATGTTCCTCACTACAGTTGTAGTCCATGTAGAGATTTTGAAGATACAGGAGAAAGTTGGGATTACGCAGACTCGTACATCTACAATAAGCAAAGAAATTCAACTATTTGTAATGGCCCAGATCAGCATGAGAGGTACGGCATAAGAAGGCACAAACCATTTTTTGAGAACCATAAACATAGAGAGCACAGAATTCAACATGCAGGCAGACAGTTTTTTTACAGAGTCTTTGACAGCCCCGAACCTCAGGAAGATGACAGGGACTGGTGGTACAATGACAGACTTAGTCCTGTAGGTAGGAGGCATCAGGAAAGAGAAGAATTTCAGTGGTCAAGTCCAGAAAGAAGTGAAGACAGGTGGTATAACAAGCCAGTGCCCATTCGTAGCCCCAGTTCCTCTAGTAGCACTAGCATCTCTGATCTTAGTGGGGATTG[G/A]TCATCTAATTGCCAAATTAAACCATCACCTACGAGACAGAGCCAGAAACATTCTGAATTGCCTTCTGAGAGATTGGTCAAGACCAAATCCTCCCTTTCTCCTCTTAGAAAGAGAAGCCATTTACCACCATTAGCCACAAGTAACCATTGCACACAGTCTAATTCCTTAAACATAGGTGTAGTGAAGGAAGATGTTACACACAAGATTAACACAATCGCAGCAGATCCATTGGTTGAGAAGGATTCTAAATTAAAGAAAGGACATTTTCTCTCACTTCCACTAATTGGCAAATTACCATCTATTAAGAATGGGGCAAGAAAAAGAGGGATTAATAAAGATGCAGGTGCCAGTATTAGTAGCCTGGTTCAAACAACCTCAACTCCCCTATCAAATCCACAAGTTATGCCTCACATCGGCATCAAGAATCCAGAATGCTTGCAAGACAGAAATGGCCAAAATCCCAGTGAGGCCCATACTTGTCTTGAAACTACCAATGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42736
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000127080 | Nonsense | 945 | 1271 | 4 | 4 |
ENSDART00000133696 | None | None | 89 | None | 2 |
Genomic Location (Zv9):
Chromosome 16 (position 30231458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 28068596 |
GRCz11 | 16 | 28003219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGAAGGAAGATGTTACACACAAGATTAACACAATCGCAGCAGATCCAT[T/A]GGTTGAGAAGGATTCTAAATTAAAGAAAGGACATTTTCTCTCACTTCCAC
Long Flanking Sequence:
TGAGAACCATAAACATAGAGAGCACAGAATTCAACATGCAGGCAGACAGTTTTTTTACAGAGTCTTTGACAGCCCCGAACCTCAGGAAGATGACAGGGACTGGTGGTACAATGACAGACTTAGTCCTGTAGGTAGGAGGCATCAGGAAAGAGAAGAATTTCAGTGGTCAAGTCCAGAAAGAAGTGAAGACAGGTGGTATAACAAGCCAGTGCCCATTCGTAGCCCCAGTTCCTCTAGTAGCACTAGCATCTCTGATCTTAGTGGGGATTGGTCATCTAATTGCCAAATTAAACCATCACCTACGAGACAGAGCCAGAAACATTCTGAATTGCCTTCTGAGAGATTGGTCAAGACCAAATCCTCCCTTTCTCCTCTTAGAAAGAGAAGCCATTTACCACCATTAGCCACAAGTAACCATTGCACACAGTCTAATTCCTTAAACATAGGTGTAGTGAAGGAAGATGTTACACACAAGATTAACACAATCGCAGCAGATCCAT[T/A]GGTTGAGAAGGATTCTAAATTAAAGAAAGGACATTTTCTCTCACTTCCACTAATTGGCAAATTACCATCTATTAAGAATGGGGCAAGAAAAAGAGGGATTAATAAAGATGCAGGTGCCAGTATTAGTAGCCTGGTTCAAACAACCTCAACTCCCCTATCAAATCCACAAGTTATGCCTCACATCGGCATCAAGAATCCAGAATGCTTGCAAGACAGAAATGGCCAAAATCCCAGTGAGGCCCATACTTGTCTTGAAACTACCAATGAAAATAGATCGAAAGAATTCTGTGCTACTTTAGCTTCGGATTCAAACAATATTCAGAAGCATACTGTCAGAGGCCAAGCAGACCATCCAGAAATTGCAGGGATTCACTGTTCAAAACGTACCACTCCTCCCCTTTCTGAACAGCCAATCACCTTCACTGATGATGAAATTGAGAAGTACAGATTGCTTCAACTCCAGGCCCAGCAGCACATGCAGCAGCAGCACCTTCAAGAGC
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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