ZMP
si:ch73-277l12.1
Ensembl ID:
ZFIN ID:
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29316 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29315 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa16733 | Nonsense | Available for shipment | Available now |
sa14444 | Nonsense | Available for shipment | Available now |
sa36985 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29316
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104244 | Nonsense | 187 | 610 | 2 | 5 |
ENSDART00000130600 | Nonsense | 129 | 511 | 3 | 8 |
ENSDART00000134439 | Nonsense | 303 | 1197 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 10247800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 10073474 |
GRCz11 | 20 | 10060714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGTGTGAAATATGCTTGAAGGTATTTAGTGTCTTCTCTAATCTAAAA[C/T]GACATCGGTTTGTTCACTTAGCCTCCAAGCCTTACACTTGCACAATCTGC
Long Flanking Sequence:
GATTTAGCAGTGTACCTTGTAATCAAGCGTCAACTGCCCAAAGTGATGCCAATTCAACAGATGAACATAAATCAGTTGAAGTAGATTTAACCAAGACTTACTCAGATGTTGAAACTATTGGTTCAGAGAGTGGTTTAAAAATTATAAAGGGACCTCGGTGCCCTTTATGCTTAAAATGTTTTCAATCGCCATCAAAGCTTAAGCGTCACATTATGATACACACTGAGCAAAAGCCTTTCAAATGCTACGTGTGCTCCAAAACCTTCCATCTAAGATCTCATTTGAAAATTCACAAGTGTAAAGGTAAAATTAGACCCGAGTGCAATACTTTTTTGGGGAATGGGCTGGTAGAAGAGAACAGGGTAGAGGGTGAAGATCTCGGAACCAGGATGGCACCTGTGTCCAAATCATCAGATGTGCGTCCACTTTTACTCACAAAGAAAAATCGATATCAGTGTGAAATATGCTTGAAGGTATTTAGTGTCTTCTCTAATCTAAAA[C/T]GACATCGGTTTGTTCACTTAGCCTCCAAGCCTTACACTTGCACAATCTGCTGGAAGTCATTTAAGCAGGCCCGTTATCTCCATAAACACCTCAAGCAACATAAAGAAAAAAGGCACTTTCCTTCTAGGATGTGTGATGTCAAGAAGAAAAATGAAGGCAATTCTTCAACACCTGGAGCTTTTGATGGTTCAAATAACAGCAGGCTAAATGCCGGTGATGTGTCTCAAAATTTAAGCACTGTAGACAAGCAACATCTTGAAATGTTACAGTGTGACAACCATCTTAACCAAAATGCCCCTTTAATAAATTCCAGTGCTGACACCCTAAAGGAAGAGGTAATAGAAGAGCAAATTGCAGACGCCAACCCAACATATTTTAAGCACACAAGTAAAAATGTGAATCAGTGCAAAATCTGTCTGAAGAAATTTTCATATCCTTCTAGGCTCTCCAGGCACCTTTTGGTTCACACAGATGATAAACCATTTAAATGCAGCGAGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29315
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104244 | Missense | 301 | 610 | 3 | 5 |
ENSDART00000130600 | Essential Splice Site | 253 | 511 | None | 8 |
ENSDART00000134439 | Missense | 492 | 1197 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 10247233)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 10072907 |
GRCz11 | 20 | 10060147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCGTATCATTTGCGGAGGCACCAGAAGATCCACAAAAGAGAAAAAAAG[T/C]ATATTGCCAACAAAACAGGGCATCAATTACTCTATTCTTCTAATGTTACA
Long Flanking Sequence:
AGGCCCGTTATCTCCATAAACACCTCAAGCAACATAAAGAAAAAAGGCACTTTCCTTCTAGGATGTGTGATGTCAAGAAGAAAAATGAAGGCAATTCTTCAACACCTGGAGCTTTTGATGGTTCAAATAACAGCAGGCTAAATGCCGGTGATGTGTCTCAAAATTTAAGCACTGTAGACAAGCAACATCTTGAAATGTTACAGTGTGACAACCATCTTAACCAAAATGCCCCTTTAATAAATTCCAGTGCTGACACCCTAAAGGAAGAGGTAATAGAAGAGCAAATTGCAGACGCCAACCCAACATATTTTAAGCACACAAGTAAAAATGTGAATCAGTGCAAAATCTGTCTGAAGAAATTTTCATATCCTTCTAGGCTCTCCAGGCACCTTTTGGTTCACACAGATGATAAACCATTTAAATGCAGCGAGTGCTCGAAATCATTCCGGAATCCGTATCATTTGCGGAGGCACCAGAAGATCCACAAAAGAGAAAAAAAG[T/C]ATATTGCCAACAAAACAGGGCATCAATTACTCTATTCTTCTAATGTTACATCTACAAGTCTACTTAAAACCGACAGTGGGTATCAGTGTGATGTATGCTTAAAGACATTTAGTGTCCCCTCTAAACTAAGGCGACACCAAATTGTTCATTCAGGCACTAAGCCTTACACTTGCATGATCTGCAGAAAGTCATTTAGTCAGGCCTATTCCCTCACAAAACACATCAAGTTACATACAGGAAAAGTAAACAGTCCTTCCCTGTTGCATTGGCTGAGAGGGTCAAAATCATCAATAACTGGTGCTTTGCAGACAAATAATTGTGGACCAAATGATGCTAATGCGTCCCTGCCTAAGGAATTAGACTCTGTAGATGGCCAAACAAATGAAAAGCTTCAAGACCACAGCCAACTTGACCAAAATGTCTCCTTGACAGAGTCGTCAAATACTGTAAAGACTGAGAGTGAGGATGTTTTGAAGGATTCTGAAGAACCAACCGCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16733
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 |
---|---|---|---|---|---|
ENSDART00000104244 | Nonsense | 436 | 610 | 4 | 5 |
ENSDART00000130600 | Nonsense | 321 | 511 | 6 | 8 |
ENSDART00000134439 | Nonsense | 683 | 1197 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 10246658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 10072332 |
GRCz11 | 20 | 10059572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAGTAATGATGAGAATCAGTGCGTCATCTGTCTGAAGACCTTTCCATA[T/A]CMGTCTAAGCTCTCCAGACATCTTTTGACCCACACAGATTTCAAACCATT
Long Flanking Sequence:
AGTGGGTATCAGTGTGATGTATGCTTAAAGACATTTAGTGTCCCCTCTAAACTAAGGCGACACCAAATTGTTCATTCAGGCACTAAGCCTTACACTTGCATGATCTGCAGAAAGTCATTTAGTCAGGCCTATTCCCTCACAAAACACATCAAGTTACATACAGGAAAAGTAAACAGTCCTTCCCTGTTGCATTGGCTGAGAGGGTCAAAATCATCAATAACTGGTGCTTTGCAGACAAATAATTGTGGACCAAATGATGCTAATGCGTCCCTGCCTAAGGAATTAGACTCTGTAGATGGCCAAACAAATGAAAAGCTTCAAGACCACAGCCAACTTGACCAAAATGTCTCCTTGACAGAGTCGTCAAATACTGTAAAGACTGAGAGTGAGGATGTTTTGAAGGATTCTGAAGAACCAACCGCAAACTCCAGCCCAACAAATAGCTTGGACAAAAGTAATGATGAGAATCAGTGCGTCATCTGTCTGAAGACCTTTCCATA[T/A]CCGTCTAAGCTCTCCAGACATCTTTTGACCCACACAGATTTCAAACCATTTCAATGCACAGTGTGCTCGAAATCATTTCGAAATGAGTCCAATTTGCAAAGCCATGAGAAGTTCCACAAGAAAACTGGCAAAAAAAGAATATCTGCCTATTCCGGTCCTGTATATCAGTGTGAAATATGCTTGAAGAAGTTTAATTTCCCCTCCAGGCTAAAACGACATCTTAGCATTCATTCGGGTGCCAAGCCTTACAGTTGCATGATCTGCGGGAAGTCATTCAGACTGCCCGAATATCTTTCTGAACACCTCAAGATACACAAGGGAAAGAAGAGAAACCATTCTTCTCGGTTGCATGGAGTCCCTCAAAAGCAAGGGATGGACGACAAGGGATCAGACACCCAAACAGATGAAAATCAAAGCCAAAATTTATCTGATGTTTCATCAGATACTGAAACACAGACTCCAGGAAACTCCAGCCCAATGTACCCTGAGTCCAGAAGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14444
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104244 | None | None | 610 | None | 5 |
ENSDART00000130600 | None | None | 511 | None | 8 |
ENSDART00000134439 | Nonsense | 833 | 1197 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 10246210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 10071884 |
GRCz11 | 20 | 10059124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACAGATGAAAATCAAAGCCAAAATTTATCTGATGTTTCATCAGATACT[G/T]AAACACAGACTCCAGGAAACTCCAGCCCAATGTACCCTGAGTCCAGAAGT
Long Flanking Sequence:
ACAAAAGTAATGATGAGAATCAGTGCGTCATCTGTCTGAAGACCTTTCCATATCCGTCTAAGCTCTCCAGACATCTTTTGACCCACACAGATTTCAAACCATTTCAATGCACAGTGTGCTCGAAATCATTTCGAAATGAGTCCAATTTGCAAAGCCATGAGAAGTTCCACAAGAAAACTGGCAAAAAAAGAATATCTGCCTATTCCGGTCCTGTATATCAGTGTGAAATATGCTTGAAGAAGTTTAATTTCCCCTCCAGGCTAAAACGACATCTTAGCATTCATTCGGGTGCCAAGCCTTACAGTTGCATGATCTGCGGGAAGTCATTCAGACTGCCCGAATATCTTTCTGAACACCTCAAGATACACAAGGGAAAGAAGAGAAACCATTCTTCTCGGTTGCATGGAGTCCCTCAAAAGCAAGGGATGGACGACAAGGGATCAGACACCCAAACAGATGAAAATCAAAGCCAAAATTTATCTGATGTTTCATCAGATACT[G/T]AAACACAGACTCCAGGAAACTCCAGCCCAATGTACCCTGAGTCCAGAAGTGGGGGTGTGAATCAGTGTGTCATCTGTCTAAAGATATTTCCTAATCATCCTTTGCTTTTCAAACATCTTTTGGGCCACGCAGATTTCACACCATTAAAGTGCAATGTGTGCTTGAAATCATTTCGATATCTGTGTAATTTGGAGAGCCACAAGAAGATGCACCACAAAGCGGCTAAGGAGAAAATTGCAGGCAATTCACAACAGGACTGTGCAGATTCTGGAAAAGCTGTCGCATCTAAAGACCAAGATCTGAAAATGCCATCGTCTCAAGATGGAGCTACAGTTCACCAAGATCCAAACATGCTTGCAGATAATGCATCTCAGAAAATGAGTGGTAACTGCAGTGATTCAGGTGGATTGACCTCAAATGGTACTCGTTTTCTAGGAAATGTTGTGCCCAATTCCGAGGTCATTACTCAGTCTAGCAAGAAAACTGTTTTGGGTTTGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36985
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104244 | None | None | 610 | None | 5 |
ENSDART00000130600 | None | None | 511 | None | 8 |
ENSDART00000134439 | Nonsense | 931 | 1197 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 10245916)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 10071590 |
GRCz11 | 20 | 10058830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCACAACAGGACTGTGCAGATTCTGGAAAAGCTGTCGCATCTAAAGAC[C/T]AAGATCTGAAAATGCCATCGTCTCAAGATGGAGCTACAGTTCACCAAGAT
Long Flanking Sequence:
AGCCTTACAGTTGCATGATCTGCGGGAAGTCATTCAGACTGCCCGAATATCTTTCTGAACACCTCAAGATACACAAGGGAAAGAAGAGAAACCATTCTTCTCGGTTGCATGGAGTCCCTCAAAAGCAAGGGATGGACGACAAGGGATCAGACACCCAAACAGATGAAAATCAAAGCCAAAATTTATCTGATGTTTCATCAGATACTGAAACACAGACTCCAGGAAACTCCAGCCCAATGTACCCTGAGTCCAGAAGTGGGGGTGTGAATCAGTGTGTCATCTGTCTAAAGATATTTCCTAATCATCCTTTGCTTTTCAAACATCTTTTGGGCCACGCAGATTTCACACCATTAAAGTGCAATGTGTGCTTGAAATCATTTCGATATCTGTGTAATTTGGAGAGCCACAAGAAGATGCACCACAAAGCGGCTAAGGAGAAAATTGCAGGCAATTCACAACAGGACTGTGCAGATTCTGGAAAAGCTGTCGCATCTAAAGAC[C/T]AAGATCTGAAAATGCCATCGTCTCAAGATGGAGCTACAGTTCACCAAGATCCAAACATGCTTGCAGATAATGCATCTCAGAAAATGAGTGGTAACTGCAGTGATTCAGGTGGATTGACCTCAAATGGTACTCGTTTTCTAGGAAATGTTGTGCCCAATTCCGAGGTCATTACTCAGTCTAGCAAGAAAACTGTTTTGGGTTTGACGCATAACACTGACATCTCTGTGCCTGCTGAGAAAAAGGCATTTGACATTGTGCCTTTTGGCAGAGTGAGCGACTTTCCACCCAAAACTGATTCATCTCTCCAGCCTTGTGCCTCCAATTCAAGAACCGAGCAAACCTGGGCACATCACACTGGTAATATTAAAGAAGAAGTTTCCTTTGTGGATTCTGACACTATTAAACATGTCCCAGAGTCTTCCGTTCCCCCTGTAAGTCTGCACACTCAGAAACCAGACAATTCCAACTTGAGTAATGCTGATGTTAGGGGGCAGTTGAAC
Associated Phenotype:
Not determined