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 |
---|---|---|---|
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:
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