ZMP
ZNF580
Ensembl ID:
Description:
zinc finger protein 580 [Source:HGNC Symbol;Acc:29473]
Human Orthologues:
ZNF524, ZNF580, ZNF581
Human Descriptions:
zinc finger protein 524 [Source:HGNC Symbol;Acc:28322]
zinc finger protein 580 [Source:HGNC Symbol;Acc:29473]
zinc finger protein 581 [Source:HGNC Symbol;Acc:25017]
zinc finger protein 580 [Source:HGNC Symbol;Acc:29473]
zinc finger protein 581 [Source:HGNC Symbol;Acc:25017]
Mouse Orthologues:
Zfp524, Zfp580
Mouse Descriptions:
zinc finger protein 524 Gene [Source:MGI Symbol;Acc:MGI:1916740]
zinc finger protein 580 Gene [Source:MGI Symbol;Acc:MGI:1916242]
zinc finger protein 580 Gene [Source:MGI Symbol;Acc:MGI:1916242]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12449 | Nonsense | Available for shipment | Available now |
sa12651 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12449
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 |
---|---|---|---|---|---|
ENSDART00000110785 | Nonsense | 153 | 886 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 16 (position 15310546)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13669005 |
GRCz11 | 16 | 13559125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAACATTGTTAACACCTCAANNNATGATTTTCTAGAGGTTAAGGTTCAA[C/T]GACAATCTGTTCTGAATAAAGATTTTCATAATGACAAGCTAGTGTCATCT
Long Flanking Sequence:
TACTGAATAATGATTTCTCTACTGCTGAATGTACTGAGGTTGCTATGCGAAAACAACAAACATTGGACAGCTTAGGTGGGATCATTTCACAAAATAAATGGACTGATCTTACTGCAACCAAAGATTGTCAAATGTCTGTGGGTCAAGAAGGCGAGTCATCAGGTGAGGGGCTTTCATTGAAGAATGAACATAAGGACAAGGTGCCCCCAGATGGGTTTCCTGTCCCATCACAAGATCAAACAGAAAATGTAAAGGATTACAGCAAGCAGAATTCACCAAAATATACATCAATCTCAGACCAGATGAGTCCTCTTGAAAACCAGACGCCTAAAAATAAATGTGTCGCTTCTGAGGAAAAGACAAGAAGTCTACCAACAAACATGCAGCTGATACCCAAGATGAAGTCTGATAATGCTAAGACAGACATTTGTGAAGTAACAACCAAAGCTACAAACATTGTTAACACCTCAACAAATGATTTTCTAGAGGTTAAGGTTCAA[C/T]GACAATCTGTTCTGAATAAAGATTTTCATAATGACAAGCTAGTGTCATCTGATGGATGCAACCTTTTTGAGAAAAAGACGCAGGTCGTTGATGTGGCACATGCAAGAGGGAGTAAACCTGGCATTGACATGAATGCAAACATAGAAAATTTAGAACATACTAAAGAATGCACCGAAGATGATAAAACACAAACTTTGGGTAGCGTAGGAGAGAATAGACTTTTTCTCAGAACAAACTTGGCAATGACAAGTGCAGGAAAATCTCTGGGACAGTATGATCAAGACGAGGTATTAGATTTAAGTCTACCAAAAAAGAAAGATCGCAATAATGAGAGGCAGTGTGAATGGGTTGTAGACCCTGAATTTGAAGGTTCACTTCACATGGAAGTTGACGAAATTGAAGATGAACCCCAACATGATGAAGTGGAGCAGGAGGATGATATTGGATATTGCTGGATGCCTTCAGTAAGTGATGCTCACGCATATCTCCCACAGCCTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12651
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 |
---|---|---|---|---|---|
ENSDART00000110785 | Nonsense | 756 | 886 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 16 (position 15308737)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13667196 |
GRCz11 | 16 | 13557316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTTGAGCGCCATTCCATCACACACTCCCAAAGCAAACCCCATGTGTGT[C/T]AACTCTGTGGCAAGGCATTCAAAAGATCAAGCCATCTTGAGCGACACAAA
Long Flanking Sequence:
TTCCTGCTAGCCCTACCTCATCAACTGCTTCCTCTAGCACTTCAACAGTGACCTCTACAAGTCCAGCCAAGCAATTCAGCACTGATGCCTGCTCTGACACACCAGTGCCCACTTCCTTTCGGGAGGCTCTTCTCAGATTGGCTGTGTCTGTGGAAAAAAAACAGGAAAACCAGACTGAGGCTCAATCGGTCACTTCACCTTCCTCATGTTCAGAAGCAACCAAGCCGGATTCCTCTGCCACAGTCCAGGAAATTAAAAACCAGGAGGTAAACTGTGACGGTGAAACTGAATCTACCTGTGTGGACCAAGCAGACTCACTAGATACCACCTCTTCCACCTCTCCCCTTTGTCCTGTATCACCCACCAATCCTTCAAAGAGCCAAGACTCTTTAGGGCCACGTCGCATTCTTTACTGTCAGTATTGTCCTCGGATCTTCTACTATCTCTCGGACCTTGAGCGCCATTCCATCACACACTCCCAAAGCAAACCCCATGTGTGT[C/T]AACTCTGTGGCAAGGCATTCAAAAGATCAAGCCATCTTGAGCGACACAAACACATCCATACAGGACAGAGAAACTTTGTGTGTCAGCTTTGCCCAAGGCGTTTTCGTGAATCAGGGGAGCTAATGAGACACCAGAGAGTACACACCGGTGAAAAACCCTTTCAATGCTTAATATGCCATATGCGTTTTGCAGAGCGCAACACACTGCGACGTCACACAAAGCGCAAGCACCAAGGCCAGCAGCTGGAAGCAGTGGACATGAAGGAGAAGCTAGAAAGTGGAGGGATTTCCCTCGCTGGTGTGCAAGCAGAGGCAGAGGAGAATGCAGAGTGGTACAGTTCAACAGTTCCTGAAATGGAGTCCGACAGTGACACAGGGGGAGAAGGAACTACATGAGGATATAAACAATTAGGTCACCTTTTTTTTTTTTTACAAAACGGTTAGATATAAGAATAGTTGTATATATATTTAATTTATTCTGTATTGATATAACAATTCCTT
Associated Phenotype:
Not determined