ZMP
zgc:174928
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC792701 [Source:RefSeq peptide;Acc:NP_001107099]
Human Orthologue:
ZNF473
Human Description:
zinc finger protein 473 [Source:HGNC Symbol;Acc:23239]
Mouse Orthologue:
Zfp473
Mouse Description:
zinc finger protein 473 Gene [Source:MGI Symbol;Acc:MGI:2442697]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25708 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19631 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25708
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073833 | None | None | 524 | None | 4 |
ENSDART00000073836 | Nonsense | 329 | 491 | 7 | 7 |
ENSDART00000073862 | Nonsense | 173 | 346 | 2 | 2 |
ENSDART00000127718 | Nonsense | 487 | 650 | 3 | 3 |
ENSDART00000127941 | None | None | 174 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 59172527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 57882179 |
GRCz11 | 1 | 58617861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATCCTACATGAAGAACCACATCCGCATTCACACCAACGAGAGGCCGTA[C/A]CAGTGCAGCGAGTGCGGAAAAACCTTCAAAACAAACAACTCTCTAAACTC
Long Flanking Sequence:
CTTTCAGGTGACAACACTGGATCGTCTGATGAAGAAGCGCCGTTAACTTTGAAAGGTAAGCCGAAGGTCAAGAAGAGTTTCTCCTGCACCTCCTGTGGAAAAGCATTCGCCTGTCAAAGTTATTTATTGATTCATGAAAGAAAACACTCAGAACCGAAGGTCTTCATCTGCTGGAGATGTCGTAAGTGCTTTCCAACATTACAGGAGAGAAAACTTCACCTGAAAGAGCATCTGGCAGAAAAGGAGTTCCACTGTGAACAGTGCGGGAAGAACTTTTTATTGTCTAATCAGCTAAAAGTTCACATGAAGACGCACAGCGGTGACCAGCGTGTCCAGTGTGACGTATGCAACAAATCATTCAGCACCAAAGCAAACCTGGAGGTTCATAAGAGAATCCACACGGGCGAGCGGCCGTATAAATGCCCTCACTGCAAGAAGAGCTTTAATTACAAATCCTACATGAAGAACCACATCCGCATTCACACCAACGAGAGGCCGTA[C/A]CAGTGCAGCGAGTGCGGAAAAACCTTCAAAACAAACAACTCTCTAAACTCTCATCTAAAATTCCACTCTGAGGAAAAACCGCATCAGTGCAAATACTGCGACAAGCGATTCCGCATGAAAGCAAATCTGAATGTCCATGAGAGGATTCACACCGGAGAGAAGCCGTACCTGTGCGCCGAATGCGGGAAGAGGGTTAAAACTTCTACTGAGCTGGTTTGTCACCAAAGAATCCACACTGGAGAAAAACCGTACCTGTGCAACATATGTGGGCGGAGTTTCAGTAAACCAACCATCTTAATAAACCACATGAGGACTCACACTGGAGAAAGACCCTATAAATGTTCACACTGCGACAAGACGTTTGCACGATCTGACGTGCTGAAGACCCACGAGAGGGTTCATACCGGAGAGAAACCGTACCGCTGCTCCATCTGCGAAGAGAGGTTTGCGTATTTAGGAAGTTTTCAGAGCCACCAGAAGAAACATGGAGCAGAACTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19631
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 |
---|---|---|---|---|---|
ENSDART00000073833 | None | None | 524 | None | 4 |
ENSDART00000073836 | Nonsense | 452 | 491 | 7 | 7 |
ENSDART00000073862 | Nonsense | 296 | 346 | 2 | 2 |
ENSDART00000127718 | Nonsense | 610 | 650 | 3 | 3 |
ENSDART00000127941 | None | None | 174 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 59172160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 57882546 |
GRCz11 | 1 | 58618228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTGGAGAAAGACCCTATAAATGTTCACACTGCGACAAGACGTTTGCA[C/T]GATCTGACGTGCTGAAGACCCACGAGAGGGTTCATACCGGAGAGAAACCG
Long Flanking Sequence:
AAGCAAACCTGGAGGTTCATAAGAGAATCCACACGGGCGAGCGGCCGTATAAATGCCCTCACTGCAAGAAGAGCTTTAATTACAAATCCTACATGAAGAACCACATCCGCATTCACACCAACGAGAGGCCGTACCAGTGCAGCGAGTGCGGAAAAACCTTCAAAACAAACAACTCTCTAAACTCTCATCTAAAATTCCACTCTGAGGAAAAACCGCATCAGTGCAAATACTGCGACAAGCGATTCCGCATGAAAGCAAATCTGAATGTCCATGAGAGGATTCACACCGGAGAGAAGCCGTACCTGTGCGCCGAATGCGGGAAGAGGGTTAAAACTTCTACTGAGCTGGTTTGTCACCAAAGAATCCACACTGGAGAAAAACCGTACCTGTGCAACATATGTGGGCGGAGTTTCAGTAAACCAACCATCTTAATAAACCACATGAGGACTCACACTGGAGAAAGACCCTATAAATGTTCACACTGCGACAAGACGTTTGCA[C/T]GATCTGACGTGCTGAAGACCCACGAGAGGGTTCATACCGGAGAGAAACCGTACCGCTGCTCCATCTGCGAAGAGAGGTTTGCGTATTTAGGAAGTTTTCAGAGCCACCAGAAGAAACATGGAGCAGAACTAGTGGATGCGCAGATCAGCGCATGATGGAGAATTGACGACTGAGTGTTTCTGACAGCGTTTCTTCATCCTAGTCCTCAATCTCCACTGCTCTGCGTATTTTGATATTTGGAAAAGAAGTTAAAATTGTGCACTGCTAGCTATTGACTTCCATAGTACGTTGTCATCAAAACAGTGCTGATGTGAAAGATGCTGCAAAACGCATAAGCGTAATGGTCATGTCCATTAACTGCGTGTCTACCTAGAGAAACAATGAAAAAGTAGCTCACTAGAATGGACAAACCTGTTCTTTGCGATATTATATTACCATATTAAAATACACCTTTAAAAATAAAATTTATAAATCAAAAACTAAGTGTCATAAATTAAACA
Associated Phenotype:
Not determined