ZMP
ZNF513
Ensembl ID:
Description:
zinc finger protein 513 [Source:HGNC Symbol;Acc:26498]
Human Orthologue:
ZNF513
Human Description:
zinc finger protein 513 [Source:HGNC Symbol;Acc:26498]
Mouse Orthologue:
Zfp513
Mouse Description:
zinc finger protein 513 Gene [Source:MGI Symbol;Acc:MGI:2141255]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43410 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45692 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15908 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43410
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 |
---|---|---|---|---|---|
ENSDART00000023646 | Nonsense | 6 | 495 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 19496629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 19524886 |
GRCz11 | 20 | 19424469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGAGGTTGCACATATAAAAGGCTGTCTGGAAGATGCCAAGAAGAAAA[C/T]AGCAGAATCCACAACCTGTCAAATGTAAGCTGCTTTTTGAGTAATACTGA
Long Flanking Sequence:
CCGTGAGCAGTAGCGCTCCGTCAGACGCCGCGGTTTCTCCTCGACGGCTGCTGTTATTTGACGCGTTGGGCAGAAAGAGCAGGTATATTTCTGACATCTGCTGAGCTTGACAATATATAGCAGGAGTTCAGTGTTTAGATTTTTGCGTTAAATGTCGACTAAATAAACACGCAGGTAGGGCGAAATGAGTTCTGCAGTTCAGTACGTGTGCAACACAAAAACTGAGCTTTTTTCAGTCGCACTGAGTTTAAAATCCCCTTTATTCGCTGTAAATGACGCCAGTTTTATTTATTTTAAACAACAGTCTGAGATTAGCATGTTAGCCTGTACGTGCTGCGTGTGTTTGTAAAGGTTATATGGGCTGCGTTTATGTTTGTGTCAGTAATGTGTTATTTTAACGCTTATAAAGGCTACTTTGGAGAATGAGTTGATTGTTTCGCGAGGGAATCCAGAGGAGGTTGCACATATAAAAGGCTGTCTGGAAGATGCCAAGAAGAAAA[C/T]AGCAGAATCCACAACCTGTCAAATGTAAGCTGCTTTTTGAGTAATACTGACAGCAGAGCGATTCATTCTGTTTACTTGTGTTTTGATTAGGTTGTTATTTATATTTAGAGGGAAAATTATAGAAAATGGTCTTGTTTTATTATTAAAACAGTCATGTACTCCCTGAATTAATTCATCCAAGTCTGTCCGGTATCATTTGGATGTTAGCACTTGTGTGTCACAGTTTCAAGGACTATACATTAATAATGATGATAATAATAATAATAAACTAATTTTAAGCATAGTAAAGTATTCAATATAGACTACCGATCAAAGGTTTGGGGTCAGTTTGATTTTTAAATGTATTAAAATAAGCTTCTCCTGCTCACCAAGGCTAAATTTGTTTTTTATAAAAAATACTTAAAATGTTATGAAATGAAATGTTATTGCACTATAAAACAACTGTTCAAAGGTAGTTTATCATTTAATTTAATCATTTATTCCAGTGAATTTCAAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45692
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023646 | Essential Splice Site | 68 | 495 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 19500792)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 19529049 |
GRCz11 | 20 | 19428632 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAATGACCAAAAGATCATAGGCCTTGAAAAGTTCTCAGGTGAGATATG[C/A]AAGTTTACAATCTAAGCTTGTTATTGAAATGTTCCTGTCATCAATTACTT
Long Flanking Sequence:
CTTTTGATTTTAATGCAATAGCTGATGTTTACTAATGAGACATTAAAATGTTACTTACTGTATTTTATCATCATTTTGCTACTTAATTTGTTTAAACATTTGGTTTTTTCTAACATTTAAATGCAATAAAGAAATATACAAAGTAGCCTTTTTTGCAGCTTAGGTCAATATGATAATAGAGTATATCATGTAAATCACACTACATACTTGATACCAGACCGACAGATGCCTACTCATGGTTAAGCATTGTTAAATGTGAAACTAGGGTTAAATGTGAAAAGCAGTATGGAGATCTTCTTCTTTTCTACAACAGACACCATTGCTGAAGTATTTAACTATGACCCTTTGCTTTCAGTGGATTCTGAAGATGGTGTAGGCACTGTACGTCCAACAAACCTTACTTTTGAGAGCGATTTTCTCCTGGGACAAGAACTCGAGTTCTCAGATCCTGACAATGACCAAAAGATCATAGGCCTTGAAAAGTTCTCAGGTGAGATATG[C/A]AAGTTTACAATCTAAGCTTGTTATTGAAATGTTCCTGTCATCAATTACTTAATCTGTGTTTATGCCATGAAACTCGTCAGTTCTGATTTTGAAAACAGCACAGGTCTTCACAGTAATTGAAAAAAATAAAAAAAAATTAATCATGTATAAAAAGTTATGGACTGTTATTGTATGATGGCCATTATCAAATCCCAAAGATTCAAAACTTAGTTTGCTTAATTGCTGGAATTCATGAGGAGCCATACTCAGTAGGACATTACATTAAGGACACTAACTGCAGAAACTCACTTCGAATGTTCACATGATTATGCAAACGTGCTGCATTTCTTTCTGTTAGCAAGCAGTGTGATCTTTCATGTACAGATGGAAGAAGCCTGCTGCCTTGGAAAATTTCTTTGGTTTTGGCATTCTGACAGAACATAACATATCAAAATGGCAAATCAGGAAAAAATAGTGTGCCACTACTATTATATAAGGGTCATCAAGACAGTCATCACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15908
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 |
---|---|---|---|---|---|
ENSDART00000023646 | Nonsense | 121 | 495 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 19502271)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 19530528 |
GRCz11 | 20 | 19430111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAATGTGGAAGGCRTTGTGGACAGGAAGCTYTGCTCGGGCTTAGGCTTA[C/T]AAGCAGAGTCTAGAGGGGGAGGGAATGAGGGGACTGGTGAGGACGGTTCC
Long Flanking Sequence:
TTGTCTGTGTGATTGTCTTTAATAGTCAGTAACTATTAATACTAAGATAATAGTGTTAGTATATACTTCATTTATTATTACATATTTACATAATACAATTTCTCCTTTTTTTTAAGCAGTAAATTGCTGAAATTCTGTTGCATTTGAAAGTAGTTTCAGTTTGCTGAAAACATATCGATACATCTGCATAATGTAATGCTGTGGTCTGTACAGCTGACATCAGTCTGCCTGGCTTCCCCCTGGGAGACGAGGAGAACTCCCCCTTCAGTCGACTCAGTATGGAGAGTGACGCTGACGACCTCCGCGCAACCGAAAGCGAACGTGAAGAGAGGGTTTCTGAGTCTGCCTTTCCCTCTTACCTTTCTTGCAGGGGCTGTGGTCAGCTCCTGGAAGACCCCTTGGGACCCGGCATGGACTTAGTGGGGCCCTACTGCATGCGCTGCTGCAAAGGGAATGTGGAAGGCATTGTGGACAGGAAGCTTTGCTCGGGCTTAGGCTTA[C/T]AAGCAGAGTCTAGAGGGGGAGGGAATGAGGGGACTGGTGAGGACGGTTCCCTGAAGCTCCACTCATGCACGCTCTGTGGGTTCACATCACGCTACACTAATCATGTTAAAAGGCACATGAAGACGCACAACGGCGAAAAGCCGTACGGCTGTCCGCTGTGCTCCTACGCATCGGCACAACTAGTGAACCTGCAAAGGCACTTGCGCATACACACTGGGGAAAAGCCCTATAAGTGCAACACTTGCACATTTGCTTGTAGTTCCCTAGGGAACCTGAAGAGGCACCAGCGCATGCATGCAACCATAGGCCCGGGTCAGAGTGTCACTCAACCAGTCAGTGGCAATGGTTTAAACCACTCTACTGCAGCTCAGAAGGAAAAGGAAGCAGTTCCTGCTCCCACTGAAGGTAAGCAACATTCAGCTTTGTCTTCTTGATAGAAGTTTTTATAGAGCATTTCAGAGTTGTAATTCAACATCCTTCAGTTGCAGGCGCTGTTAGGT
Associated Phenotype:
Not determined