ZMP
ZNF335
Ensembl ID:
Description:
zinc finger protein 335 [Source:HGNC Symbol;Acc:15807]
Human Orthologue:
ZNF335
Human Description:
zinc finger protein 335 [Source:HGNC Symbol;Acc:15807]
Mouse Orthologue:
Zfp335
Mouse Description:
zinc finger protein 335 Gene [Source:MGI Symbol;Acc:MGI:2682313]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14003 | Nonsense | Available for shipment | Available now |
sa34400 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10622 | Nonsense | Available for shipment | Available now |
sa10609 | Nonsense | Available for shipment | Available now |
sa10510 | Nonsense | Available for shipment | Available now |
sa21289 | Essential Splice Site | Available for shipment | Available now |
sa27201 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14003
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112046 | Nonsense | 337 | 1348 | 7 | 33 |
Genomic Location (Zv9):
Chromosome 8 (position 25160931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 24286749 |
GRCz11 | 8 | 24307988 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTYCTATATTTGAATGCATTTTAATTGTACACACAGGTGACAGTGATTA[T/G]AAACCAGCTGATGAGGAGGCCAGATCCAGACTGGCTGTCAGTCACTTCAC
Long Flanking Sequence:
GCACTTTGTAGCCTCAAAGGCTCTTTAGATCCAAATTCATCTGTTGTAGTGACCTCCATTCAGTTCCCAATAGATTAAAACAAATTCCGCCTTATGTTTATTTTTCCAGAAGCCATCTCACTTACAAATACACCAAATCAGCTCTAAATAGTAAAAAAAACTTAATAAAAGGCACAACTGTTTTATGCTAACTTTTAAGATTCCATCAGCACTGATGCCTACAGGTATTTTTTAGGTTCTCGTTCTGGAGGTGCTGTCTCACATGCTGACGGTCCAGGCCAAAGGAAACGTGGACGGGGACGTCCTCGAAAATCTGAAAGCAAAGCTGGAGCAGTGGTTGTGGTCAAGAAGGAGGAGCAGCCTGAAGAGGAAGAAGATGACATTGTTGATGCAGGCGCTCTTGATGATCAAGGTCAGTGGAGTGCAGATTGCATTCTATATATTTCATCATTTCCTATATTTGAATGCATTTTAATTGTACACACAGGTGACAGTGATTA[T/G]AAACCAGCTGATGAGGAGGCCAGATCCAGACTGGCTGTCAGTCACTTCACTCCTCCTCCTTCCTGCTCTTCATCATCTCCTGCATCTACCTCACGGAAACGTCCTCGCAGGATGGTGGGGCCTCCTCGCAAATTTCTTCCAGATTCAGGTTAGGGTTAATCTACCTTTTGGGTCACAGAGGTATAATAAGTGAAGTTTTACAAACTAATTTTGAGAAGAGCGTGATATGATTGACCACAGCTAGTCCTTATCAGTAATCAATAGCTAGCCAATAGGATTATTCAAAATTTAACATAAATATCCAGCTTAATTTTACTTCCTATCTTCAATTAGTTGGTGGTCTATTCCTATTAGAACCGTCTTTATTAATCAAGGAATATTCCAAATGAATCGGATGGGGAGCTCTCGAAATCTACCTGATCTCGCATCCCTTTAAATGCTCATTATCCAGGCGGGAGCCTTAGGCTCATCTATATCTGAGCTCTGGGTTCTCTCCTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34400
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 |
---|---|---|---|---|---|
ENSDART00000112046 | Nonsense | 641 | 1348 | 14 | 33 |
Genomic Location (Zv9):
Chromosome 8 (position 25166205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 24292023 |
GRCz11 | 8 | 24313262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCTTCAAGAAGCGATACACCTTCAAAATGCATCTTCTCACACACATA[C/T]AAAACTGTGGCAACAGCCTGTAAGTAAGATGTCTGGACAAGTGTATACTT
Long Flanking Sequence:
GAAATAATAGTTTTTAAAAAATGTTTATTGACATGATATATTACTAATTCTGACCAGTCTGATGAGGGCAGTTTTTCATGCGACAACAGTCTTGTGTCAACCCTTCACAGGTTTCCAAAGTGTCTGAGTTTCCATGTCCCATCTGCAGTCGAGTATACCCCATGCAGAAACGCCTGACACAACACATGAAGACACACAGCACAGAGAAACCACACATGTGTGACAAGGTAAAGCTCAGTTTATAAGGCACATTTAATGCCTGTTATGTTATGGTTAGTTTAATGATGATTCAGTTTAGTTCAATACAATTGGTATTGTTGAAGGAAGTGATTATTTGTAGGGCAGCTCTAATTACCCCAACTAAACAACCCAAAGACAACACTGTCAGGAAATACTGTTTTTATTTACTATGGTAACACTAGTGTAAATGTGTTGCTTTACAGTGTGGGAAATCCTTCAAGAAGCGATACACCTTCAAAATGCATCTTCTCACACACATA[C/T]AAAACTGTGGCAACAGCCTGTAAGTAAGATGTCTGGACAAGTGTATACTTGTAAAAAAAAATTGTACTTGTCTGTTAAACAAACAGCCAAAGTATCTATTTCTTTGCTCTTTTGTCAGGTTTAAGTGTGAGTTCTGTGATTACACCTGTAATGACAAGAAGCACCTGCTCAATCATCAGCTGTCCCACACCAACGACAAACCTTTCAAATGTGAAGAGTGCAAGTATTCAACAAGCAAAGAAGACTTCCTGGTGTCCCACATCGCCATTAAACACACTGGTGAGTGGTGTAATTGTTAGGAATGTTTATACTTCAGGAAGGGCTGGGCGATTAATAGACAATTTTCATGCACATTTTGTCAGTAGAGCCGGTAAACGTCCAGCACATGCGTTCAAATGAAGCAGCATTCACTACACACTACACAGAGTCTTAGTACACTGATAACCTATGCAAAACTCTGAAAAAATGTAATCAGTCAAAAATGACACAGATATAATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10622
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 |
---|---|---|---|---|---|
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
Genomic Location (Zv9):
Chromosome 8 (position 25168215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 24294033 |
GRCz11 | 8 | 24315272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTTTTTTTTTTACCTAAAGGTAACAGTGGACCCTCTTACTCTC[C/T]AAACCATGGAGTCYATAGGGAACACATCTGTATCCCAAGATGCACTGRGC
Long Flanking Sequence:
ATCACTTTTAAATGTATGTTTCTGTATGTTTTAGATGGTAAAAATGGTACTTGTTTTCAAGAAAATACAATATAAAGTATATCATGCTTTTTCCATGGTCTGATTAATTCTTTATTCAGATTTTGATCAATAGTTTAATGCACAGGTAGTTCCAGTCAGTTTTGGTTACAGCTCTAAATAGTTTTGCTACCCTTAAACATTAGTAGTGATCATGGTAATCTAACGTGTTGTAATTGACAAATAAACCGCAAAAACAAATACTAGTTTTAACTTGTATATAACCTGGCAATTGTATGTGATATAATATAATATAATATAATAAGTGATATAAACAATGGCTTACTGTGTATTAAATGATTTTAAATGCACTTTATGGAGCCAAAGTACCACTAATCATTGCATTTTAACACATGGAAAACCATTGATTATTCTTTACTTATTTGTTATTGATTTTTTTTTTTTTTTTTTACCTAAAGGTAACAGTGGACCCTCTTACTCTC[C/T]AAACCATGGAGTCCATAGGGAACACATCTGTATCCCAAGATGCACTGGGCAACACTACCATCATTTACGAGCAAGGTCAGTAGAAAAGTTATCAGTAGATCAGTGATTATATCTAAAATATGTGTGTATTTTTTTAAATTCATCTACACATATTACACCATTCACATTGTGATAATAATATTCAGATTGCTCATTTAAATAAATGTTTACCTTCTCTAATAGCCCAGAACTCAGACCTCTCAGCACAGAATGCTCTAGATCTGCTGCTGAACATGAGCAATGCCAGAGAACTACAGGTATTGTGTGGCACATTGGTATTTTGTAATGAAATAAGTCATAATTCTATTGAAATATAAAATGCAGGGTTCCCATGCTTCTTGAAAGTACTTGAATTTCAGACATATGAATAACAAACCTGGAAATTACTTAAAAACAATCATAGGTCTTTGAAAGTGCTTGAATTTAAAGTTGATGATGTTATTTCAACAATTGCTGCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10609
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 |
---|---|---|---|---|---|
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
Genomic Location (Zv9):
Chromosome 8 (position 25168215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 24294033 |
GRCz11 | 8 | 24315272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTTTTTTTTTTACCTAAAGGTAACAGTGGACCCTCTTACTCTC[C/T]AAACCATGGAGTCYATAGGGAACACATCTGTATCCCAAGATGCACTGRGC
Long Flanking Sequence:
ATCACTTTTAAATGTATGTTTCTGTATGTTTTAGATGGTAAAAATGGTACTTGTTTTCAAGAAAATACAATATAAAGTATATCATGCTTTTTCCATGGTCTGATTAATTCTTTATTCAGATTTTGATCAATAGTTTAATGCACAGGTAGTTCCAGTCAGTTTTGGTTACAGCTCTAAATAGTTTTGCTACCCTTAAACATTAGTAGTGATCATGGTAATCTAACGTGTTGTAATTGACAAATAAACCGCAAAAACAAATACTAGTTTTAACTTGTATATAACCTGGCAATTGTATGTGATATAATATAATATAATATAATAAGTGATATAAACAATGGCTTACTGTGTATTAAATGATTTTAAATGCACTTTATGGAGCCAAAGTACCACTAATCATTGCATTTTAACACATGGAAAACCATTGATTATTCTTTACTTATTTGTTATTGATTTTTTTTTTTTTTTTTTACCTAAAGGTAACAGTGGACCCTCTTACTCTC[C/T]AAACCATGGAGTCCATAGGGAACACATCTGTATCCCAAGATGCACTGGGCAACACTACCATCATTTACGAGCAAGGTCAGTAGAAAAGTTATCAGTAGATCAGTGATTATATCTAAAATATGTGTGTATTTTTTTAAATTCATCTACACATATTACACCATTCACATTGTGATAATAATATTCAGATTGCTCATTTAAATAAATGTTTACCTTCTCTAATAGCCCAGAACTCAGACCTCTCAGCACAGAATGCTCTAGATCTGCTGCTGAACATGAGCAATGCCAGAGAACTACAGGTATTGTGTGGCACATTGGTATTTTGTAATGAAATAAGTCATAATTCTATTGAAATATAAAATGCAGGGTTCCCATGCTTCTTGAAAGTACTTGAATTTCAGACATATGAATAACAAACCTGGAAATTACTTAAAAACAATCATAGGTCTTTGAAAGTGCTTGAATTTAAAGTTGATGATGTTATTTCAACAATTGCTGCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10510
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 |
---|---|---|---|---|---|
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
ENSDART00000112046 | Nonsense | 782 | 1348 | 17 | 33 |
Genomic Location (Zv9):
Chromosome 8 (position 25168215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 24294033 |
GRCz11 | 8 | 24315272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTTTTTTTTTTACCTAAAGGTAACAGTGGACCCTCTTACTCTC[C/T]AAACCATGGAGTCYATAGGGAACACATCTGTATCCCAAGATGCACTGRGC
Long Flanking Sequence:
ATCACTTTTAAATGTATGTTTCTGTATGTTTTAGATGGTAAAAATGGTACTTGTTTTCAAGAAAATACAATATAAAGTATATCATGCTTTTTCCATGGTCTGATTAATTCTTTATTCAGATTTTGATCAATAGTTTAATGCACAGGTAGTTCCAGTCAGTTTTGGTTACAGCTCTAAATAGTTTTGCTACCCTTAAACATTAGTAGTGATCATGGTAATCTAACGTGTTGTAATTGACAAATAAACCGCAAAAACAAATACTAGTTTTAACTTGTATATAACCTGGCAATTGTATGTGATATAATATAATATAATATAATAAGTGATATAAACAATGGCTTACTGTGTATTAAATGATTTTAAATGCACTTTATGGAGCCAAAGTACCACTAATCATTGCATTTTAACACATGGAAAACCATTGATTATTCTTTACTTATTTGTTATTGATTTTTTTTTTTTTTTTTTACCTAAAGGTAACAGTGGACCCTCTTACTCTC[C/T]AAACCATGGAGTCCATAGGGAACACATCTGTATCCCAAGATGCACTGGGCAACACTACCATCATTTACGAGCAAGGTCAGTAGAAAAGTTATCAGTAGATCAGTGATTATATCTAAAATATGTGTGTATTTTTTTAAATTCATCTACACATATTACACCATTCACATTGTGATAATAATATTCAGATTGCTCATTTAAATAAATGTTTACCTTCTCTAATAGCCCAGAACTCAGACCTCTCAGCACAGAATGCTCTAGATCTGCTGCTGAACATGAGCAATGCCAGAGAACTACAGGTATTGTGTGGCACATTGGTATTTTGTAATGAAATAAGTCATAATTCTATTGAAATATAAAATGCAGGGTTCCCATGCTTCTTGAAAGTACTTGAATTTCAGACATATGAATAACAAACCTGGAAATTACTTAAAAACAATCATAGGTCTTTGAAAGTGCTTGAATTTAAAGTTGATGATGTTATTTCAACAATTGCTGCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21289
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112046 | Essential Splice Site | 879 | 1348 | 19 | 33 |
Genomic Location (Zv9):
Chromosome 8 (position 25169317)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 24295135 |
GRCz11 | 8 | 24316374 |
KASP Assay ID:
2260-0579.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCAAAAGATTGTAACCTTCCATGTGTCGGAGAACGGGGACACTTTGG[T/A]GCAGGAGGCGTTTGAGACTGCAACAGGGGCTGTGGAGCAAGAGGAGACTG
Long Flanking Sequence:
TGAATTCCACTAATTGTATTAAAGTTCTTTAAAGTTGTTTAAAACAGTCAACATTTTTTAAAATGACACGTTCAAAACATCATCATCATGACATTTTAATGAATGTTAAGTGTAAGTGAAATGTTAAGTACAGATAGGACTTTCATAGCAATATATTTGCTGAGGTGTGGATTGCAAAGATCCTTGATTTAAAATTATTAGTGATTTAAAAGTCTTTGAATTTGGTGTCCATCAAAGAGTGGGAACACTAAGAAATGATCTAAATGACATTATTAGGCCATTTGTAAAAAAAAAAAAAAAAAAGTAAGATTTTATAAATTATTATTTTTCCATAGCGGATAATCGGTTTATTTACTCTACTCAGGTGGCGGTGCTGAAAACAGATGGCAAAGCTCTGGAGACGGGGTCATGGTCTGGATCTGGCTCTGGGAGTGAAGGCTCATCCTTACAGCCTCAAAAGATTGTAACCTTCCATGTGTCGGAGAACGGGGACACTTTGG[T/A]GCAGGAGGCGTTTGAGACTGCAACAGGGGCTGTGGAGCAAGAGGAGACTGCTGTGGCACAGGAAGTGGAACAGGAAGTGGCACAGATTGGCATTGGTGCATATGAAGGCACTGATTTCAGTGTGGTGGAGCAGACCTCTGAGGAGACAACACACAGGTACTACTACTGAATGTCAAAAACAGACAATAGGTGCATTTTCCATTACAAATGTGTGTAAAACTGCGATATTGTGTTGATTAAATATTATTGTGAAGTGTTATGAGACAAACTCATTCTCAGGAAAAATCATTCCAACAATCATACAATGACACAAATGTGTGTTTTTTTCCTGGAAAGTTATAGTGTGTGATTTCACAGAGAACCTGAGGATTCAGAATATCAAGATGAACACAAAAACTGTGAAAGTTGTGAAACAAAAGTTGTGCAAATGCATCTTGTAAAATCTTTTTTTTATACTAATAAGAGATCCATATCTTTAAAAAAAAAGGACTTTTTGTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27201
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 |
---|---|---|---|---|---|
ENSDART00000112046 | Nonsense | 1151 | 1348 | 27 | 33 |
Genomic Location (Zv9):
Chromosome 8 (position 25171894)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 24297712 |
GRCz11 | 8 | 24318951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTTCACACTCAGGAGCCGTCTCCCCGTAAAGCTCGCTCCGTCCCCTCA[C/T]AGCAGACCATCATCATCAACAGCGATGAAGAAGCTTTAGCCACACTGCAG
Long Flanking Sequence:
CATGGCCTTGCATGCATATTTGAGACCTCATAAATGCACCAGCTGCAGTTTTGCCTCTAAAAACAAGAAAGACCTGCGACGCCACATGATGACACACACCAACGAGAAGCCTTACTCCTGCCAGGTGTGCGGCCAAAGGTGAGCAACTGAGAAAGAATCATTCAAATAAATAAGCAAATATTAGAATTTGTGCTCTTTACAATATTAATACAAACAGATCCATAAAAGCTTTTTTAACTTGAAAAAGCAGTAATTTTGCTGGCAATTTACACACCCTCAGGCCATCTAAGATGTGGGGAATTTTTTTAAAGAAGATGTTTAGCTGAAACCGTAATAAATTGCCAGTGTAAAAGGCTAAACAACACAGAAACACGTTGTCCCTTATATTAAAACTCTCATGAATTAATTTTAGGTTTAACCGTAACGGCCATCTGAAGTTCCACATGGAGAGGCTTCACACTCAGGAGCCGTCTCCCCGTAAAGCTCGCTCCGTCCCCTCA[C/T]AGCAGACCATCATCATCAACAGCGATGAAGAAGCTTTAGCCACACTGCAGAGTAAGTGCTGGAATGAATATAATTGAGTGGAGGAACTATGACGTCAATTTGTATGTAAAAACCTGGAATCAAGTTCCAGTTCCCTTGTCCCAAAGTCAATGGGTTTCTTAAATAGGATTTTGATTAAATCGCTTAAATAAGCTTCGAGGCTACCACAAACTCAAGATACTTTTATGTTTTGTTTAATGACATAAAGCACATCAGATACATCCCACTTTTTATTTATTTTTTTTATTTAATCGGTTATGCTTCTCTTAAAAGACAGTTGCTAATTGGAACAACAGGCAATGTCGTAGACATTATTTATCATTGACCTGAACTGGTCTGCAATGCAGCCCACTTTAAATTTACAGCTTTTGTTGGACATTTGGATTTGTCTGTTTTTTTGATTCATAAATAGTGTTTTATATAGGTTGTCGTATTTTTTTCTTATTGGGCCTTCTTATTGT
Associated Phenotype:
Not determined