ZMP
zgc:113026
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 281-like [Source:RefSeq peptide;Acc:NP_001012505]
Human Orthologue:
ZNF281
Human Description:
zinc finger protein 281 [Source:HGNC Symbol;Acc:13075]
Mouse Orthologue:
Zfp281
Mouse Description:
zinc finger protein 281 Gene [Source:MGI Symbol;Acc:MGI:3029290]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30958 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8722 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17826 | Essential Splice Site | Available for shipment | Available now |
sa10191 | Nonsense | Available for shipment | Available now |
sa10475 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30958
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 |
---|---|---|---|---|---|
ENSDART00000052127 | Nonsense | 15 | 809 | 2 | 7 |
ENSDART00000123020 | Nonsense | 32 | 826 | 1 | 6 |
ENSDART00000141898 | Nonsense | 32 | 826 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 17161229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 16040939 |
GRCz11 | 12 | 16089749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGAGGCATGGACCCCAACTATACCCCAAGCATGATCATGTTCAGCCATT[T/A]ACCTCCAGTGACCAGCTTCACGCGCTTAACTTCACAGACCTCTATGGCAG
Long Flanking Sequence:
TTTTTAAATAATTAATTTACAGTGTTGTAATTGGTTGCACGAATCTCTTAAAATTATAATTCACCTCAAAAAGAAAATTATATCACCATTTGCTCACCGTTGTTCCAATCCAAACCTGTTTTAGTTTTTTCTGTTCAGCTCAAAGGAAGATATGTTTGAAGGACATAAATTTGAAGAAAACTGGAAAACAAATACCAAGGACATCAATGTTTACATGTTTTCAACTTTCTTTAGAATATCTTATTTAGATGAAAATAATCTCATGAAGGTTTGTAAACCCTTGAGGATGAGTAAATGGCAAATAAATGTTTGGATGAACTGTTTTATTGATAAGCAATCACATCTTTTATTGTTTTTTTTCATAGGATATTTTGCCAATGAACTTTAGCCTGTTGAAGATCCAAGCATGAGTATCATCCAGGACAAGCTAGGAAATGAGTTTTTACGGAACGGAGGCATGGACCCCAACTATACCCCAAGCATGATCATGTTCAGCCATT[T/A]ACCTCCAGTGACCAGCTTCACGCGCTTAACTTCACAGACCTCTATGGCAGATTTGCCCCAGGAGATGATCCTGAAGAAGGAGCGTGACTCTCCTGAACATGGTGGTGGCTTTCTCCACAGTATGGGTATTAAACAGGAGAAGCTCAATGAGTTGGACTACCACCTCCCAATGTATACAACAGGAATTGGGACAGCAGGAGGAAAAAATACTGATATGTTGGACATGTCACTTGGCAACCACCAAAATATGCTTTTGCATGACCTAAGCCTTAGCAACGTAAGTGAACATGAAGGATGGATGAGTTATCATTGAATGTTGTTCTCAGTATTGTAATGTCATTGCTGGGTTTTTATTATTATTTTTTATTATTAAAGCCATTTTTCTGTGCTTCATTAGCAGTTCTCTGGAAGACTGGGGAAAGACCCAAAGGAAACTGGGCCTAGAAAAGGAAGGAGAGCAAATGGAGAAGGACTAGAGGGGAAAGCCAGAAGGAAACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8722
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052127 | Nonsense | 24 | 809 | 2 | 7 |
ENSDART00000123020 | Nonsense | 41 | 826 | 1 | 6 |
ENSDART00000141898 | Nonsense | 41 | 826 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 17161256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 16040966 |
GRCz11 | 12 | 16089776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCATGATCATGTTCAGCCATTTACCTCCAGTGACCAGCTTCRCGCGCT[T/G]AACTTCACAGACCTCTATGGCAGATTTGCCCCAGGAGATGATCCTGAAGA
Long Flanking Sequence:
TAATTGGTTGCACGAATCTCTTAAAATTATAATTCACCTCAAAAAGAAAATTATATCACCATTTGCTCACCGTTGTTCCAATCCAAACCTGTTTTAGTTTTTTCTGTTCAGCTCAAAGGAAGATATGTTTGAAGGACATAAATTTGAAGAAAACTGGAAAACAAATACCAAGGACATCAATGTTTACATGTTTTCAACTTTCTTTAGAATATCTTATTTAGATGAAAATAATCTCATGAAGGTTTGTAAACCCTTGAGGATGAGTAAATGGCAAATAAATGTTTGGATGAACTGTTTTATTGATAAGCAATCACATCTTTTATTGTTTTTTTTCATAGGATATTTTGCCAATGAACTTTAGCCTGTTGAAGATCCAAGCATGAGTATCATCCAGGACAAGCTAGGAAATGAGTTTTTACGGAACGGAGGCATGGACCCCAACTATACCCCAAGCATGATCATGTTCAGCCATTTACCTCCAGTGACCAGCTTCACGCGCT[T/G]AACTTCACAGACCTCTATGGCAGATTTGCCCCAGGAGATGATCCTGAAGAAGGAGCGTGACTCTCCTGAACATGGTGGTGGCTTTCTCCACAGTATGGGTATTAAACAGGAGAAGCTCAATGAGTTGGACTACCACCTCCCAATGTATACAACAGGAATTGGGACAGCAGGAGGAAAAAATACTGATATGTTGGACATGTCACTTGGCAACCACCAAAATATGCTTTTGCATGACCTAAGCCTTAGCAACGTAAGTGAACATGAAGGATGGATGAGTTATCATTGAATGTTGTTCTCAGTATTGTAATGTCATTGCTGGGTTTTTATTATTATTTTTTATTATTAAAGCCATTTTTCTGTGCTTCATTAGCAGTTCTCTGGAAGACTGGGGAAAGACCCAAAGGAAACTGGGCCTAGAAAAGGAAGGAGAGCAAATGGAGAAGGACTAGAGGGGAAAGCCAGAAGGAAACAAGGCGACTCGGGAAAGGTGTGTTTACCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17826
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052127 | Essential Splice Site | 107 | 809 | 2 | 7 |
ENSDART00000123020 | Essential Splice Site | 124 | 826 | 1 | 6 |
ENSDART00000141898 | Essential Splice Site | 124 | 826 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 17161507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 16041217 |
GRCz11 | 12 | 16090027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTTGGCAACCACCAAAATATGCTTTTGCATGACCTAAGCCTTAGCAAC[G/A]TAAGTGAACATGAAGGATGGATGAGTTATCATTGAATGTTGTYCTCAGTA
Long Flanking Sequence:
CCTTGAGGATGAGTAAATGGCAAATAAATGTTTGGATGAACTGTTTTATTGATAAGCAATCACATCTTTTATTGTTTTTTTTCATAGGATATTTTGCCAATGAACTTTAGCCTGTTGAAGATCCAAGCATGAGTATCATCCAGGACAAGCTAGGAAATGAGTTTTTACGGAACGGAGGCATGGACCCCAACTATACCCCAAGCATGATCATGTTCAGCCATTTACCTCCAGTGACCAGCTTCACGCGCTTAACTTCACAGACCTCTATGGCAGATTTGCCCCAGGAGATGATCCTGAAGAAGGAGCGTGACTCTCCTGAACATGGTGGTGGCTTTCTCCACAGTATGGGTATTAAACAGGAGAAGCTCAATGAGTTGGACTACCACCTCCCAATGTATACAACAGGAATTGGGACAGCAGGAGGAAAAAATACTGATATGTTGGACATGTCACTTGGCAACCACCAAAATATGCTTTTGCATGACCTAAGCCTTAGCAAC[G/A]TAAGTGAACATGAAGGATGGATGAGTTATCATTGAATGTTGTTCTCAGTATTGTAATGTCATTGCTGGGTTTTTATTATTATTTTTTATTATTAAAGCCATTTTTCTGTGCTTCATTAGCAGTTCTCTGGAAGACTGGGGAAAGACCCAAAGGAAACTGGGCCTAGAAAAGGAAGGAGAGCAAATGGAGAAGGACTAGAGGGGAAAGCCAGAAGGAAACAAGGCGACTCGGGAAAGGTGTGTTTACCTTTTTTATTTAATTTGAATTACGTTTTTTTTTTCCAGATTAAATAAAAATGTAAATAAATTGTCCTGCAAAGTTTTTGAAAACAATCATGCATACAAAAAAGTGGTTTAAGTAAATTTATTTTCCCCTAAAATATTATTCCTTCTGGTTTGCTATTAGGTTAATATTTTGTGGCCTATGACAACTAGCTTGCTTTATGTTTGTTATGTACATTCACGCATTATGTTAAATAATTCCATTGTAAATTTCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10191
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052127 | Nonsense | 197 | 809 | 5 | 7 |
ENSDART00000123020 | Nonsense | 214 | 826 | 4 | 6 |
ENSDART00000141898 | Nonsense | 214 | 826 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 17165256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 16044966 |
GRCz11 | 12 | 16093776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATTTGCTTTTTATTGTACAGGTGAGAGGCCTTTCAGGTGCAGTCAGTG[T/A]AAWATGAGCTTCATACAGAAGTATCTACTGCAACGGCACGAGAAAATCCA
Long Flanking Sequence:
TTGTCGAATGGTTACCATATTCTGACAATAAGGAGTTTAATACCACAGTTGTCAGATTTGTGAATGTTTTACTCAGAATTGTAAGCAAAATTCTATTTTTAAACATGCAAGAAAAAAAGATTTGAAATGATATTAAGATTATATTGATTTAAAAGTAAAATTTTTTTTAGGGAGGAACTATTGCTTGGCCCTAAATTTAGTTTTAATATTATTATTATTTTTTTGTCTAATCTCTGTTTTTAGACACTTATGCTGGATGGGGATGCTGGCCCCCTCTCTCCCAGCTCTAAACCGCACATATGCGAGCACTGCAGTGCAGCCTTCCGCAGTTCCTATCATTTGCGCAGACATGTGCTTATTCATACAGGTGAGCGTGCATATAACTGGCAGCAGAGTCATACTTAAGCTGCGTTCAAACCGTATTGCTGTTTACTAACATTGTTGAAAAATGGATTTGCTTTTTATTGTACAGGTGAGAGGCCTTTCAGGTGCAGTCAGTG[T/A]AATATGAGCTTCATACAGAAGTATCTACTGCAACGGCACGAGAAAATCCACAGCGGTAAGCCTGTTTACTCTTGTCTTATACTTGTCACTAGCAAAAATTTAAATGGTGCTAATGTATATACGTACACATTTTACTTTTACCAGGGGAGAAACCATTTAGCTGTGACCAGTGCAACATGCGCTTTATTCAGAAGTACCACATGGAGAGACACAAAAGGACACACAGTGGAGAAAAGCCATATAAATGTGACACATGTCTACAGGTAATAGACGATTCTTATTTGCTTTTTTGGTAGGCATGGGCCCTTATAAGTTTCTGATGGTATGATAACCTTGGATAAAAATATCACGGTATTAGGGCTGGGTGGTATATTGAGTACTGGGGATATATCGATATGATTCACCTACATGATGCGGTATTATCCAAAATTGTTTATATCGATATGGTTTGAGGCCTCACGTGCGCATTCTGCGCGAAACTGACCAAGGAAGCACGCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10475
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052127 | Nonsense | 754 | 809 | 7 | 7 |
ENSDART00000123020 | Nonsense | 771 | 826 | 6 | 6 |
ENSDART00000141898 | Nonsense | 771 | 826 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 17171696)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 16051406 |
GRCz11 | 12 | 16100216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATAGAGAATTTCGCCCAAGCCTTCGGCTCACAGTTCAAGTCTGGTCGG[C/T]GAACTCCGCTAGGTTACGGCGGCGACCCACGAGTAGGTGTTGTTGAGGTT
Long Flanking Sequence:
TGTCTTCAAGCAGTAGCCCTGCAAGCTCACTCTACACCACCTCTCCATTAGAGTGTGGATTTGTACAGCCTGTTTCTTCCCCTCTTGCTCCATCCTCCTCAACTTCCCTAAGCAAGTCTCATTTTGGAATGCTGGTAGGTTCTCCATCACCATCTCATGCCTCGCCATCCTCCCAGCAAGCTTTTCATCTCAGCAGTCTGGAGCCAACTCCTCACCAGCAGCTTACCCCATCTCAAGAGCTCACTGACCAGCTGGAGAAGCAGCACTCGCCACCGTATTCTCTCACAAGTCAAGAGCTGACAAATGGTGGCCAGAAAGACCAGCAGACCAAGAATGGCAGCTCTTCAGCCAATGGAAGCAACAATGGCAATGTCCCCAGCGGGGGCTCATCTAATGGCTCGGTCTATTCTGACCTCACTGCTCTAGAGCCATCTAAGGAGGTCACCTATCAGATAGAGAATTTCGCCCAAGCCTTCGGCTCACAGTTCAAGTCTGGTCGG[C/T]GAACTCCGCTAGGTTACGGCGGCGACCCACGAGTAGGTGTTGTTGAGGTTGACCACAGGATACAGCGGACTCCCGTGTCTGAATTCTCAGGGTATACTAGTCTGTTAGCAGATGTCAACGAGCCCGCTAGCTCAGGATCCAAAACTCCCACAAGCCAAAGCTACAGGTAAAGGTTAAGGGACTCACCTGACCCTGTTCTGTGGGACGTGGACTGTCTCCCAATGCTTCCCACTCCTTGCTGAGTAGAACTTTAATTATTACACTGCCATTAAATGTCGATAGTAGACATTACCAGGGAAGGTCTACAAGACCTCAAATGCAATTTTTCATGTTCTTCTTTTTAATGTGTTTTAGACATTTTGTTTTATGAGTGTAGTGTATGTAAGAATAGATTTTAAACAGAAATTTCCAGCAAAATTAGATGCTAGTGAAGGACTTTTTAAAGAAACCTTGTATGTCTTAGCATTCATAGTCCAATTGTAAGAGTAAGTTAATAATTA
Associated Phenotype:
Not determined