ZMP
ikzf1
Ensembl ID:
ZFIN ID:
Description:
DNA-binding protein Ikaros [Source:RefSeq peptide;Acc:NP_571061]
Human Orthologue:
IKZF1
Human Description:
IKAROS family zinc finger 1 (Ikaros) [Source:HGNC Symbol;Acc:13176]
Mouse Orthologue:
Ikzf1
Mouse Description:
IKAROS family zinc finger 1 Gene [Source:MGI Symbol;Acc:MGI:1342540]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31915 | Essential Splice Site | Available for shipment | Available now |
sa11269 | Nonsense | Available for shipment | Available now |
sa22256 | Nonsense | Available for shipment | Available now |
sa22255 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31915
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 |
---|---|---|---|---|---|
ENSDART00000016430 | Essential Splice Site | None | 537 | None | 9 |
ENSDART00000042377 | Essential Splice Site | None | 294 | None | 4 |
ENSDART00000046079 | Essential Splice Site | None | 392 | None | 6 |
ENSDART00000050481 | Essential Splice Site | None | 434 | None | 7 |
ENSDART00000079724 | Essential Splice Site | None | 526 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 15948378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 15863411 |
GRCz11 | 13 | 15994403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGGGACAGCTGGAAGAGCTTCATACTGCAAACTCAAGGAATAGCAGG[T/A]AAATCACTCTCGCAGGCTGTTCCAAGTCACAAATTTCAAACATTTAGTAT
Long Flanking Sequence:
TAATAAACAAGGCCCTATGTATTTCACATTTTGGTTTCTCATTTAAACAGGCATCATTTCACTTTTCATTTAAGGAAGGTGTTCCTCCCATAACACTAAAACAGGTGACATGAGATAAAGAACCCCCCGTTCTTTTAAGAGAAATAAATAAATAAGAAATGATCAGTGCACTGTCCTAACCCGCCTCATCCCATCTCATGCATGGCTGCCAGTGATGGTCTACTGGGTGTCAGCTTTTATTGGCACGATACAAAGCGAAGTGCCAAGCTCTGCTGCCTCGATTCCCCGAGCAGATTCGGTCTCTGGAATAAAAGCTTGCAAAATGTCTCGCACGAGCACAGAGACATAGCAATGCTGGGCTGGAAGGAGGAAGTGCAGTGGAGAGGGGAGGGACCGCGCGCGGAGTTCCAGACTGCAGCCGCGGCGCTGAAAACTTGTGCGCATGGAGCGGCAGGGGACAGCTGGAAGAGCTTCATACTGCAAACTCAAGGAATAGCAGG[T/A]AAATCACTCTCGCAGGCTGTTCCAAGTCACAAATTTCAAACATTTAGTATAGGGAAGTTAAGGAAAGTTTTCAGTTCTTTTAAGTGCGGGCGAGAAAAATTGGCGTAGTGGAAATATTTTGTCCTGAACTCTAGCAGGTGCAAGCGCTTCAATCCACTTGACATGGCAAAAGGCGCGTTTGTTGAGCGCGTAAGCTTGAATACTTTGGCTTCAGGCGAGGGATTCTTTATTAGAGGTTTTAGGTAAAGGTCATATGTTTTCCTATCTTTTCCTTTGTTTTTGGTTTCATCTTTTTTTTCCAATTTTCCATACGGAAAAAGTTTCCCGATGTCCCAAATGTGGAGTCGGGTGAAATTTTCCCAGTCATTTAACTGATAATAAAATTAAAATACACACAATTTAATCGCGAATTGTGTTCCTTGTGAATATCCTGTATAATTGAACTTTTAAACGCACTTTCATTCTTTCGATACGCACCTGTTGCTCAGCATGGAAATGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11269
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 |
---|---|---|---|---|---|
ENSDART00000016430 | Nonsense | 179 | 537 | 6 | 9 |
ENSDART00000042377 | None | None | 294 | None | 4 |
ENSDART00000046079 | Nonsense | 76 | 392 | 4 | 6 |
ENSDART00000050481 | Nonsense | 76 | 434 | 4 | 7 |
ENSDART00000079724 | Nonsense | 168 | 526 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 15919958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 15834991 |
GRCz11 | 13 | 15965983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGTGCAATCAATGTGGTGCTTCATTCACTCAGAAGGGTAACCTGCTC[C/T]GACACATCAAACTTCACTCTGGCGAGAAACCTTTCAAATGTCACCTGTGC
Long Flanking Sequence:
AGAACATTTTTACAACCTAAAGATACATTTTTTTTACATGAAACCGTCAATAAAACGAATTTCTAAGAATGATGCTAACAAAATCTCTAAATCCCTTAAAGGGATAGTTCACATACAATTGAAAATTATGTTGTCATTTACTGATGTTCTGGCCCTGTTAAACATAAAAGAAGATATTTTGAAGAAAGAACTGTAACTACTGACTTCCATAGAATTTTTTTTTTCAAATATAGAAGTCAACGGTGACAGGTTTTCACCTTTCATCAAATCTTCTTTTGTGTTCAACAGAATAAAGAAACTCATAAAGGTTTGGAAACACTTGAGTATACAGAGAGTAAATTTTCATTTTTTGGGTGAACTATCCCTGTAATTATCAAACATCCTTTACCTATTTATGTGGAGTGCATAAGTAATGTGTTATCGTTATTTGTCACATAGGTGAAAGGCCATTCCAGTGCAATCAATGTGGTGCTTCATTCACTCAGAAGGGTAACCTGCTC[C/T]GACACATCAAACTTCACTCTGGCGAGAAACCTTTCAAATGTCACCTGTGCAACTATGCTTGCCGCCGCAGAGACGCTCTCACTGGACATCTGCGCACTCATTCGGGTAACTCATGATGGAATATTTTGAAACTCTTTATTGTATTAAAACAACAACTAAATGATGTGGTCTGACTGAGCAGATTTTGTTTCTATTTCGACCTGTCAGTTGGAAAGCCCCATAAGTGTGCATATTGCGGACGCAGTTACAAGCAGCGGAGCTCACTGGAGGAACATAAGGAGAGATGTCACAACTACTTGCAGTGCATGGGCCTTCAGAACAGCATTTATACAGGTCTGTGAATGAATGATATTTCTATGTGTTGGTTTAAATCCGTGGTGTCCAAACTCGGTCCTGAAGGGCCGGTGTCCTGGAGAGTTTAGCTCCAACCCTAATCAAACACACCTGAAACAGATAATCAAGCTCTTACTAGATATATGAGAAACTTCCTGGCAGGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22256
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 |
---|---|---|---|---|---|
ENSDART00000016430 | Nonsense | 294 | 537 | 8 | 9 |
ENSDART00000042377 | None | None | 294 | None | 4 |
ENSDART00000046079 | None | None | 392 | None | 6 |
ENSDART00000050481 | Nonsense | 191 | 434 | 6 | 7 |
ENSDART00000079724 | Nonsense | 283 | 526 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 15916302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 15831335 |
GRCz11 | 13 | 15962327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTAGACAGGATAGCTAACAATGTAGCTAAGCGTAAGAGCTCTATGCCA[C/T]AGAGGTTTGTGGGTAAGAGTTGAAGTTTGCTTTCATTGTGCAGCAATATA
Long Flanking Sequence:
TAAATGGCATCTTCACCATCAAATTAGCAGCAATTGTCTTTTTTGGGTGAACTATCCCTGTATCTGTTGTATAAAAGTAGATATACAACTTCCACCAACAATGCAATGGCAGTTCTCTATCAGGTGACAGATAACCCTATATCAAATAACCCATAGCTACAGTATAAGCCTTTAAAGACTCAAAGCTTAAGAAAACAATTCTCAAGATGAGGAGAAAACTATAGGGACAAAACTAAAGTAAGAGACAGAAAACCATATAGCAATGTGTGCAACATCATATTGCATGAAACATCCTTCCTCATAGTTAGCACCATGCCAGAAGATGAGTTTAGGTTAGATACAGCAATCTAAAACTTATGCGTGGTTTCTTTGTCTTGCTTTCCATAGTGAAGGAAGAGAACAGCCAGAATGAGCAGAGGGAGGACATGCCTGCATCTGAGAGGGCCTTGGTGCTAGACAGGATAGCTAACAATGTAGCTAAGCGTAAGAGCTCTATGCCA[C/T]AGAGGTTTGTGGGTAAGAGTTGAAGTTTGCTTTCATTGTGCAGCAATATATTATAGATGTTAGATAATCCAGCGATCACTGTTTAATATGCATTTACAGTATGTATCTGACTTAAAGAAATACTTAATAATGATAGGAAGCTACATCATTTCTTTTTCTTGGATGAGTTTACTTTAAAAAGCAAAAAGATGATCATTATGGCTTGCGATAGGAATTTCACGTTGCTAGTTTCTTACAAGATTATTAAATTTCTATTGCTTATTTAACAGCTACAGTATAGCTGGTGAACCATTCCAAAAATGTAAAAAGAGGCTTTTAAAATGTGCTTTGCATAAACAAACATCAATATTTTAAGATTTTTATTTATTTTTTTCACTAAAAGGTTCTTTGGGTTACTAATAATGGTTCTCATACGTAATGAGTGTAAGCCCATTGCTGTTTTTTACATGCATGTTTTACTTGAGAGTACCTTAGAAATTAAAAGATAAATATGAGGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22255
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 |
---|---|---|---|---|---|
ENSDART00000016430 | Nonsense | 330 | 537 | 9 | 9 |
ENSDART00000042377 | Nonsense | 87 | 294 | 4 | 4 |
ENSDART00000046079 | Nonsense | 185 | 392 | 6 | 6 |
ENSDART00000050481 | Nonsense | 227 | 434 | 7 | 7 |
ENSDART00000079724 | Nonsense | 319 | 526 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 15913086)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 15828119 |
GRCz11 | 13 | 15959111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATGCAGCCCCATGTGATTGATCAGGCCATCAACAGTGCAATTAGCTA[T/A]CTGGGTGCAGAGTCCTTGCGGCCTCTGGTTCAGACCTCTCCTGGGTCCGC
Long Flanking Sequence:
TTACTTCAATTTAAATGGAGAATGTTTACAGTGCTCATATAGGTTAGTTTTTCAACTCAAAATTTTTGTAGCAATCAGTTTCCTTAAACGGTTTGAGTTCCCTTAACTTATTGGGTTTTACAGCACTCAGTTGGTTTGAGTTGGTTTGAATCTCGTCATTTATTGCTCTTTACTGTGCTCAAATTGCTTTGTTTACTCAAATGGATTAAGTTCACAGTACTCATTAGGATTAGTTTTTGAACTTAAATGATTTGTTGCAATCGGTTTCCTCAAATGGTTAGAGTTACCTGAACTTATTGGGTTTTACAGTGCATTAGAAATGCATTTTCTTGTGATAGGTAAATTCCTTTTTAAATCAAAATTAATTAGTTAAATCCTTTGCTCTCTCACATTTTTTCCTCAGGAGAGAATCGTCTGTCAGAGCTATCTTTCGAGAGTGGCTCAGGTGAGCTGATGCAGCCCCATGTGATTGATCAGGCCATCAACAGTGCAATTAGCTA[T/A]CTGGGTGCAGAGTCCTTGCGGCCTCTGGTTCAGACCTCTCCTGGGTCCGCCGACATGGTGGTCAGCCCTCTATACAACCTGCACAAGTCACAAACAGCTGAAGGCAATGGTGTTTCTGCTAAAGACAGCGCCGCAGAGCACCTTCTCCTACTCTCTAAGTCCAAATCCGCCTCTGTTGACAAAGACGGTTCCCCCAGTCCCAGCGGGCAGGATTCCACTGACACTGAGAGCAACAACGAGGAGCGTTCGGCCGGGGTAAGCGGAACAGCAGCCACAGGTGGTCTCATCTACCTGACCAACCACATGGCTCCAGGTATGAGAAATGGAGGCCTGCCAGGGGTAAAGGAAGAACAACACCGGCAGTTTGAGGCTTTGCGAGCAGCAGGAATGGATTTGAGTATAGCGTCATCAGAAGGATTTAAGGTGCTAAGTGGAGATGGAGAAGAATTGAGGGCGTACCGCTGTATCCACTGCAGAGTTTTGTTCCTGGATCATGTCAT
Associated Phenotype:
Not determined