ZMP
ZNF462
Ensembl ID:
Description:
zinc finger protein 462 [Source:HGNC Symbol;Acc:21684]
Human Orthologue:
ZNF462
Human Description:
zinc finger protein 462 [Source:HGNC Symbol;Acc:21684]
Mouse Orthologue:
Zfp462
Mouse Description:
zinc finger protein 462 Gene [Source:MGI Symbol;Acc:MGI:107690]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9742 | Nonsense | Available for shipment | Available now |
sa18187 | Nonsense | Available for shipment | Available now |
hu7881 | Nonsense | Available for shipment | Available now |
sa10748 | Nonsense | Available for shipment | Available now |
sa17083 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9742
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 |
---|---|---|---|---|---|
ENSDART00000092579 | Nonsense | 17 | 2502 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 537801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 396014 |
GRCz11 | 21 | 345565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGATGGAAGGGCTGCAGTGCGATGGCTGTGATTTTCGTGCAGAGTCGTAT[G/T]AGGAGCTGAAGGCTCACATCCGGGACATCCACACTGCCTTCCTGCAGCCC
Long Flanking Sequence:
TCCTTTAGGGGGCGTAGCTATCAGTCCTTTAGGGGCGGTGCACTCAGTCCTATGGGGTGGAGCTATCAGACCTGAAGGTTGGTGCTATCAGACCTTTAGGGCGGAGCTTTCAGTCCTGTAGGCTGGTCTTATCAGTCTTTTAGGGTGGAGCTATCTGGACTGTAGTATGGTGCAATCAGTCCTTTAGGGCGGGCTATAAGGGCGTGTCTCATTTCTGCTCTGTTTGATCTGTTTGTCAATTTTTCTCGATTTCTGATACATTTTTTTCTAATTTCCAAATCTTTTTCAAGTGGACGTACGTTACAATAGAGGAAAAAAGAACAATCTTAACTTCTATTTTGTGCTGACGTTTCATTAAGACTTTAGACATTAGTATTCACTTTATACTTGTACTCATCCAGCGGTCTCTCTCTCTCTCCAGGTTTCCCTGATTCTCCAGGGAGTGTTGAGCGATGGAAGGGCTGCAGTGCGATGGCTGTGATTTTCGTGCAGAGTCGTAT[G/T]AGGAGCTGAAGGCTCACATCCGGGACATCCACACTGCCTTCCTGCAGCCCGCAGAGGTGCAAGACGGAGACGGAGACGAGACCCCGAAACGCTCCAGATCCACATCACTGAGCCAAACTGAGGATGAGGAGGACTCCACCAACCAGGAGAGAGACCCACTGAAGGAGGAAACAGGTTACCACTATGTTTATTAAAGTCAGGGTTACAATTACTGGGGGGTGGGGGTTGGTTATGGTTTGACTACCCTATATATTGCTTTATCCCCTTTTAAAGACGTTGAAATTAGATGTGGGGTGGGGTGGGGGGGTGTCTGGAAAATAGTGTGCACTGATCTGTATCTGCAATAATAATAATATGTTAATAATATTATAAGATGCCTTTCATTGCATGTTGCAGCATCGTCTGTTGTTAGGACACAGTTTTAACACTCTGAAAGTACAGAAACTACATCAGAAGAAAGTCATGTTGCACTTCATTCTTGTGTGAAATTGAAGCACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18187
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 |
---|---|---|---|---|---|
ENSDART00000092579 | Nonsense | 987 | 2502 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 541066)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 399279 |
GRCz11 | 21 | 348830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAYTATCAAAAGAAGCAYCCCGAGCAAAAGGCCTCATACTTCCGCATA[C/T]AGAAGACCATGCGGGTCATTWCTGTCGAGCGAGCACAGATGGCCAGCAAT
Long Flanking Sequence:
ACTTTAATGATCTGCACCAGCACTATATGACCCATCATCCAGAAGCAAGCAACGTCTTAAACTTTAACCAGCCAGATCTTGTGTATATGTGTCGTTTTTGTTCCTACACAAGTCCAAATGTGCGTAGCCTGATGCCCCATTATCAAAGGATGCACCCTTCGGTGAAGATCAACAATGCTATGATCTTCTCAAGCTATATGGTCGATCAGCCTCATAAGGGTGCGACTGAGTCGCAAACACTGAGAGAAATCTTGAATTCTGGCCCAAAGAGTTTTAGCTCCACCTCATCTGGGTCCAGATCGTCATCCAGCCCTGCTCTCAAAAGCATTTCCAAAACGCCAGAAGCAAATGCAGAGGTTGAAACACTTCGAGAAAGCCTGGGGGGCAATGTGGTGGTGTATGACTGTGATGTCTGTTCGTTCTCAAGTCCCAACATGCACTCAGTACTGGTCCATTATCAAAAGAAGCATCCCGAGCAAAAGGCCTCATACTTCCGCATA[C/T]AGAAGACCATGCGGGTCATTTCTGTCGAGCGAGCACAGATGGCCAGCAATTCAACCTACAGCCTGACCAGCACTCCTAAGTCTTCAAACCCCATCCTGCCTGTGCCTCTGGATGAGGATGTTTACTACTGCAAACACTGTGTCTACAACAACCGCTCTGTCGTGGGCGTTCTGGTCCACTACCAAAAGAGACATCCGGAGATTAAAGTAACAGCAAAGTACATAAAACAGGCACCTCCAACCCCTGGACTGCTGAAACTCATGGATGAGCTACAAATCGCCCCGCCTAAACAATTTCTGAAGCAGTTTAGCAACAACGGCATTGAAGGGTCTGGTAATTCCAACACTAAAGGAGCATCCGACAAGGGGGAACCAGAAATGCTGTTTTTCTGTCAGCACTGCGACTACGGGAACCGCACTGTGAAGGGGGTGTTGATTCACTACCAGAAGAAACATAGAGACGTGAAGGCCAATGCAGACCTCGTTCGTAGACACACCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7881
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 |
---|---|---|---|---|---|
ENSDART00000092579 | Nonsense | 1293 | 2502 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 541986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 400199 |
GRCz11 | 21 | 349750 |
KASP Assay ID:
554-2385.1 (used for ordering genotyping assays)
KASP Sequence:
TTAGTAATGTCCCAAATGGAGCATGCCTCAAAGGCGCAATCTCTACACTG[A/T]TAATGCTTTGYTTCAGAATTCCCAGCTTGCCTGCTTGTGGAAGAATYAGG
Long Flanking Sequence:
GTGAAGGGGGTGTTGATTCACTACCAGAAGAAACATAGAGACGTGAAGGCCAATGCAGACCTCGTTCGTAGACACACCGCTGTGGTCCAGAGTCAGAGAGAGCGAGCGCAGATGATCCAATCGGGAAGTTCTACATCCACTTCTACTGTAGCTACTGAAGCTGAAAAATCCAGGTCGTTGCGATCTTTGAAGTGTAGACACTGTCCATACACTTCTCCTTATGTGTATGCCTTGAAGAAGCATCTAAAGAAGGATCATCCTACTGTGAAGGCCACAGCTATGACTATCTTACACTGGGCTTATCAGGACGGCGTGCTGGAGGCTGGTTATCACTGTGAGTGGTGCATCTATTCCCACGCTGAACCAAGTGGGCTGCTCATGCATTACCAAAGACGCCACCCTGAGCACAATGTGGACTACACGTACATGGCCAGCAAGCTGTGGGCTGGTCCTGATTCTTCCACAAGCAGGCAAGCTGGGAATTCTGAAACAAAGCATTA[T/A]CAGTGTAGAGATTGCGCCTTTGAGGCATGCTCCATTTGGGACATTACTAACCATTATCAAGCAGTGCACCCTTGGGCCATCAAAGGTGACGAGTCTGTTCTCATCGACATTATCAAAGGAAACAAAGCACCAGATAAGCAGCTCCCACAACAAACCAAAGCACATGCTTCGATGTCCAGTCCGTTCAATAGTCACCATCAGGAAGATGTTGCAGTTGAAATGAATCGGCCACCTCTAGATCGGCAGCCAAATCTATCTCTGTCTGCCACCTCGTCGATCTCAAACAACCCTTACCAGTGCACCGTCTGCTTGTCTGAGTACAATAGTCTTCATGGACTTCTGACCCACTACGGCAAGAAACACCCAGGCATGAAAGTGAAAGCTGCTGACTTTGCTCAGGAAGCGGACATCAACCCTAGCTCGGTTTACAAGTGCAGACATTGTCCGTATGTGAACTCCCGAATACACGGGGTTCTCACACACTATCAAAAACGCCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10748
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 |
---|---|---|---|---|---|
ENSDART00000092579 | Nonsense | 1534 | 2502 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 542707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 400920 |
GRCz11 | 21 | 350471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAATACCATAATCAGCCTGCTGCASACATGTTTAAAGCAAGTAAYATA[C/T]AGTCGCCRACTGGAAGGGATGATTTAGTGGCCGAATGCAGCACTAGCAGT
Long Flanking Sequence:
TGAATCGGCCACCTCTAGATCGGCAGCCAAATCTATCTCTGTCTGCCACCTCGTCGATCTCAAACAACCCTTACCAGTGCACCGTCTGCTTGTCTGAGTACAATAGTCTTCATGGACTTCTGACCCACTACGGCAAGAAACACCCAGGCATGAAAGTGAAAGCTGCTGACTTTGCTCAGGAAGCGGACATCAACCCTAGCTCGGTTTACAAGTGCAGACATTGTCCGTATGTGAACTCCCGAATACACGGGGTTCTCACACACTATCAAAAACGCCATCCATCAATTAAAGTCACCGCTGAAGACTTTGTTGATGATGTTGAGCAAGTAAACGAGGTGTCGAGTGAGAACGAAGAGCGATCTAAAACCCAGAGGCAAGGCTACGGCGCATACCGCTGCAAGATGTGTCCTTACACACATGGCACTTTAGAAAAACTCAAAATACACTATGAGAAATACCATAATCAGCCTGCTGCACACATGTTTAAAGCAAGTAACATA[C/T]AGTCGCCAACTGGAAGGGATGATTTAGTGGCCGAATGCAGCACTAGCAGTCAACCCGAAGTTCCGGAGGTGTGTGACTATAACGTACCAATTTCCGAAGTCGCAAAAAGCGATAAGCATGCAGTGTTTAAATGTCAGCTGTGCAAATACTTCTGCTCCACCAGGAAGGGCATTGCCCGCCACTACCGTATCAAGCATAATAATGTCCGAGCACAGCCAGAAGGGAAGAATAACGTCTTTAAATGCGCTCTCTGCTCTTACACCAACCCCATCCGCAAAGGCCTCGCGGCACACTACCAAAAACGCCACGACATTGATGCATACTACACACATTGCTTGGCAGCTTCCAAGACTGTGACTGAGAAACCAAATAAAGTGATGTTGCCCCTGGCGTCAGAAGCCGATTCTTCGGGGATGAGCGAGGAGTTACGGCAAGCGGTGGACCGAAGGAAATGTTCGCTTTGCTCCTTCCAGGCTTTCAGCAGGAAGAGTATAGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17083
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 |
---|---|---|---|---|---|
ENSDART00000092579 | Nonsense | 1833 | 2502 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 543604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 401817 |
GRCz11 | 21 | 351368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACTCTTCCAGAACTCWGCATCCATCTCACGAACCACAACGAGGACTTT[C/T]AGAAAAAAGCCATGCGGATGGAAAGGAGAAAACAGCTTCAGAGCAAGCAG
Long Flanking Sequence:
AAGCCGATTCTTCGGGGATGAGCGAGGAGTTACGGCAAGCGGTGGACCGAAGGAAATGTTCGCTTTGCTCCTTCCAGGCTTTCAGCAGGAAGAGTATAGTTTCTCATTACATAAAGCGCCACCCAGGAGTCTTTCCAAAAAAGCAGGCCGCCAGCAAACTGGGCCGATACTTCACTATGATCTACCCCAAGGACGCGGAAGAATCTCCTATAGTGGAGAACGTGGAGATAGTTGAAGTGAAGGATGAGGTGGAGCCTGAAGGAGAGGTCGACTGGCTGCCCTTTAAATGTCTGAAATGCTTCAAACTCTCGTTTAATGCGGAGGAGCTGCTGGTGATGCATTACAACGACTGTCACGACAAGGAACTGAAGCGGGATTTCGTCACCGTCCCGAGCCCTGTAGAAGATGGCACTGAGCTCTACCAATGCACACACTGTGAAATCAAGTTCCTGACTCTTCCAGAACTCAGCATCCATCTCACGAACCACAACGAGGACTTT[C/T]AGAAAAAAGCCATGCGGATGGAAAGGAGAAAACAGCTTCAGAGCAAGCAGAAGACGGTCGAGCCGCCGGAAGCCAAACCAGAGATTAAGGTGAGCTTGAACACAGAGTTGGTATATTAGGTTATTTGTAGAATTACTTGTAGATTACTACAACTATTTGTAGAAGTCATGATAAGTGCTGCCAAATGATTTCCAGTGTGCACCTTGGTGTCAAAACAACACCAGAATCCAACTAAAATAATCAATTTGATGTCCAAACTTTGAAGTCCATTTGACAGATATAGATGCCCTTTTGATCACCAAAATAAAGACAAAAAGTAAAATAATATATGGAATATTTTATAATCATCTGAAAGCTTCAGTTGCAAACTACAAATCTATATGTATCTGTATAGATCAGGGGTGCCCAGATTTGTTCCAGGAGAGCCGGTGTCCTGCAAAGTGTAGTTCTAACCCCAATCAGACACAACTGGGATAGCTATTCAAGCTCTTACTAGGCTT
Associated Phenotype:
Not determined