ZMP
znf277
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 277 [Source:RefSeq peptide;Acc:NP_956724]
Human Orthologue:
ZNF277
Human Description:
zinc finger protein 277 [Source:HGNC Symbol;Acc:13070]
Mouse Orthologue:
Zfp277
Mouse Description:
zinc finger protein 277 Gene [Source:MGI Symbol;Acc:MGI:1890393]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30252 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa16599 | Essential Splice Site | Available for shipment | Available now |
| sa44302 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30252
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000121878 | Essential Splice Site | 99 | 457 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 22395455)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 21627331 |
| GRCz11 | 25 | 21724879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATAAACTGGTTATCGCTGATGTCAAACTCATTGCAGACTTTTCACAG[T/G]AAGGCTTGATGATTTTTAACCCACATGATGTAAGAAATAAAATACATAAA
Long Flanking Sequence:
ATTATATCCGTTAACAAGTTAAGGGGATACTGCTTTCAAAAAAAAACTAATCAATATTGCACTTTTTTTTTTTTCAAAAACCATTAGAATAAAACTTCACAATACACAAAGAATCCGATTTAATCACAGACAAATCACATGATTTTAAAAAATGTATGATTCCCCAGCATTAGTAAATACATCACAGTAAGGAGAGAAGTAAAATCACAACTTCCTTTTCTACTTTAACAGCGGATTTACATTTTTGGTGGGACTGTCCATTTTAAATGTGTTTTCCCTCATCATTAGGTAAACAGGATTGTATACTAGAGCCACTTTGTTTTCCTGAGAACTTCAGCGATGGGGTTTGTCTCGCCTCCTCCAGCGATGGATGTCCAATGACCTGCGCTCTGTGTCCTGACTTGTTTCCTGCTTCTGAAAAAGACCAACTTCTCAAGCACATGGTGTTGGAGCATAAACTGGTTATCGCTGATGTCAAACTCATTGCAGACTTTTCACAG[T/G]AAGGCTTGATGATTTTTAACCCACATGATGTAAGAAATAAAATACATAAACATTATAAATAAAACAAAAATGATTTGTTGCAGGTACATGCTGTACTGGAAGAAACGGTTTACAGAACAGCCCATCACAGACTATTGCAGTGTTATCAAGACCAATTCTGAAGGTCCTGTTGGTAAGACATTTGAGTCAAACAGTTTTAAACGTTAGTTAGTTGGTGTGTTTTTGCTCTTTGAAGCACGCGTGTTTTAAATAGGTCTCAACACAAACAACTAAAGAAACAAGCTGCAAATTGTTCACAACACTTGCAAATATGCACATAACGCAACAGAAATGTTTCTAGGGAACCCAAAACCATGACAGAACGTGCTGCGCACACATCATGAATGTTTACAAACCAGTAATTCATCTATAGGTTTGCAAAAATTGCAATTTCCCCAAAATTTATATATATATATATATTTTTTTTTTAAGTAAAATTACCTGTGCCTAACATGGCAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16599
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000121878 | Essential Splice Site | 291 | 457 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 22409572)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 21641448 |
| GRCz11 | 25 | 21738996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAAKTGCAGTCTGAAGACGACCGAGAGATGCTTGAAGAYGAAGATGAG[T/C]AAGACCTTTATATTTTWAATGTTCGTTTTCAGATNAATGTAATAAATATSG
Long Flanking Sequence:
GAAAGATCACATGAGGAAAAAGCAGCATCGCCGAATAAATGCCAGAAACCACGACTACGATCGATTCTACGTCATCAACTACCTGGTCTGTCCGTGCATCATTTTGAAGCATGAATCTATTATGTGTCAAAATATTATGTATTATTAGAATTTGTGTAATTTTATTTATGTATTTATTTTTATGTATGTATTATAAAAGTGTAATTATTCATTAATTATATTATATTTGTTTGTTTATTTATTTTATTTTATTAATAATATTATTTATTTATACTTTCATTTATTAAATTTTGCTTAAGAACTACCAAACAATATGTTTTAATGTATTATTATTATGATAATAAAGTCTCTTGTTCTATGATTGGGTTCTGATTCTAAAAAAAAAAAAAGATTTTTTTGTTAACGTTATTGTGTTGTTTTTCGTAATACAGGAGTTGGGAAAGACATGGGAGGAAGTGCAGTCTGAAGACGACCGAGAGATGCTTGAAGATGAAGATGAG[T/C]AAGACCTTTATATTTTAAATGTTCGTTTTCAGATAATGTAATAAATATCGATCATATTTTTCATTGTGCCCTGCAGTGATTGGTCTGATTGGCAGGCTCATCCGGTGTGCGCCGTGTGTTTGTTTTGTGATCAGCAAGCAGAGACCATGGACAAAATTTACACACACATGCAGGTACGTTTATTTGTTTTAAATTAATTTTAATATGTCAGTGCATGTTAAAATATATGTATATATATTTTACAATTATTTTCCATACTTTTTAACGTATCACTTAATTTTGTGGTATCCTTCCTGCACACGTTTCATGTACAGTACTTGCCATAGTAATACCAGTAAATTCTGCAAATTTACGTGCAACTAACCATTCATCTAACCTGCATTAAACCCTAACCATATTTGGTAATTAATTAATATTACTCATGAATAGTTAAAATGTGTGTAACTCCTTTTACATCAGCAGCAATAGTTATGTTTACATCCACATATTTTTATCAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44302
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000121878 | Essential Splice Site | 396 | 457 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 22414151)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 21646027 |
| GRCz11 | 25 | 21743575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGTTCTTATACAATAAAAATGTAAAGTGTTATTCACGTTTTGTTTTTC[A/T]GATACTACTTTCCTACATATGAGAACGATGCTCTTCTTACAGCTCTGTCG
Long Flanking Sequence:
AAACTGATCTGAGCTCGCAGCGCGTGTTGTGAAGGACAGATCAATCGATCCTCGAAATCATGATCAGCAGTGCAACGATTGGCTGACGGCACAGCAGCGTAATAACATCATCTGATTAATATTTAGTTATCCGTGTGAGCTAAATTACATAAAATTAGCAATAAACGGTGTGTTAAATATGACAAGCAATAACTTTCCACGTTTGTTGTGAGCTGCAGGCTTTACATCTTCATGTGTCGAGTATTCATCAAATATTTGTATTTGTATTCATTGCATATAATTGTAGTTAGTTCTACATTTAGAGAAGATTTTCTTTATTGCTATTATTATTATTATTATTATTGTTATTATTATATATTCCAAATATAATCGTTTGTGTTAACCTGAACCAAGGAATAAATTTTTAGGTGTACTTTCCCTTTTAATTGGCTTAGGATTTCAGAATGAGAACCGGTTCTTATACAATAAAAATGTAAAGTGTTATTCACGTTTTGTTTTTC[A/T]GATACTACTTTCCTACATATGAGAACGATGCTCTTCTTACAGCTCTGTCGGACGGCGAGAGCGAATCAGAGGGTACAAATCACAGCTCTGAAGTTCCTGTTATAGCTGAAGATATCTCAAACCTCAAGGTGTTAAGACAGACCAGTGTGCTTAATAAACTTCTCAAAGACAGAGGAGCCACCAACTGAAGCTCAGAGACTTGCAGAGGTTCACTGACGTTAGAATTGCTTTCAGTGTAAAAACATGAATATGTTAAGATTAATGATGTGATTTTCACTCTGTTGAACTGGTGCCAGTGCTCACATTATGAAAATCATCTCAAATAAACCTTGTATTTCAAGAGTTCACACTTAGCTGATGATTGATTATAAGCAAGCTTGGCATGCTGTCCTGGGAGAGAGCCCTGAGCTCAAAGGTTCTTGAGCCCTGGGCTCCCTCCCGTTTGGAGGAAGAGAGGGGAGCCTTGAGCTCAGGTAGATCTCGACAACTCCCCCTTGATA
Associated Phenotype:
Not determined