ZMP
ikzf5
Ensembl ID:
ZFIN ID:
Description:
Zinc finger protein Pegasus [Source:UniProtKB/Swiss-Prot;Acc:Q6DBW0]
Human Orthologue:
IKZF5
Human Description:
IKAROS family zinc finger 5 (Pegasus) [Source:HGNC Symbol;Acc:14283]
Mouse Orthologue:
Ikzf5
Mouse Description:
IKAROS family zinc finger 5 Gene [Source:MGI Symbol;Acc:MGI:1914393]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23055 | Essential Splice Site | Available for shipment | Available now |
sa389 | Nonsense | Available for shipment | Available now |
sa42916 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23055
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079011 | Essential Splice Site | 103 | 419 | 4 | 4 |
ENSDART00000125335 | Essential Splice Site | 103 | 419 | 3 | 3 |
ENSDART00000136727 | None | None | 52 | None | 3 |
ENSDART00000141462 | Essential Splice Site | 103 | 168 | 3 | 3 |
ENSDART00000143832 | Essential Splice Site | 103 | 122 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 21650346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 21800495 |
GRCz11 | 17 | 21820331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTTTGTCAGCTTTACTATTTATAAACTCTTCTCCATCTCCTCTTCCA[G/T]GTGAAAAACCACACAGATGCCACCTGTGTCCTTTCGCCTCGGCCTACGAG
Long Flanking Sequence:
GATGGCTTTGAGAGGACATATGATGGAAAACTCAAGTGCCGCTACTGCAACTATGCCACCAGGGGGACTGCACGACTTATTGAACACATACGCATACACACAGGTAAATGATCTTTAACCTTAAAGGAATAGTTAACTCAAAAATACTAATTTACTCAACATTTACTCTCGAGTGTTTAAAAACTTTTATGCGTTTCATTATTCGGTCAAACACTAAAGAAGAGATTTTGAAGAAAGTTAAAAACATGTAACCATTGACTTCCTTGGTATTTGTTTTTTTCTACTATGGAAGTCAATTTGTTACAGGTTTCCAGCTTTCTTCAATATATGTTTTTAATATTCAACAGGATGTCAAACTGGTTTGTAACAAGTAAATGAAAAAGAATTTTCAGTTCTGGGGTGAACCAGCCCTTTTATTACACTCTGAGTGGTTTTAAAGACTGTATTTTGTCTGTTTGTCAGCTTTACTATTTATAAACTCTTCTCCATCTCCTCTTCCA[G/T]GTGAAAAACCACACAGATGCCACCTGTGTCCTTTCGCCTCGGCCTACGAGCGCCATCTAGAGGCTCACATGCGCTCTCACACAGGTGAGAAACCCTACAAGTGTGAGCTGTGCTCCTTCCGCTGTAGCGATCGCAGTAACCTTTCCCACCACCGTCGTCGTAGACATAAACTCCTCCCAATGAAGGGCGCCCGCTCTGCTCTTTCCCATCGGAAGATGCTCAGCGTCCTGCAGAAGAGAGGAAACTCTTTAGGTTATGGCCGCCGACTGCTCATCAACCTCAGCCCGCCATCCATGGTCTTGCAAAAGCCCAGCTCTGAGCAGCACCACCTGGGGGACTTCACTCACGACCTCCCTCCTCACGCTCACCTTCATCAGGAAGCTTATAACGGTCTAGGAAAGGATCCACAAGCAATCGGTGGAGCAATCGGAAGTGGTTCTAGAGAAGACCAGGATATGGCATTAGACAACCCACTGAACCAGCTTTCAACATTAGCCGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa389
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 |
---|---|---|---|---|---|
ENSDART00000079011 | Nonsense | 381 | 419 | 4 | 4 |
ENSDART00000125335 | Nonsense | 381 | 419 | 3 | 3 |
ENSDART00000136727 | None | None | 52 | None | 3 |
ENSDART00000141462 | None | None | 168 | None | 3 |
ENSDART00000143832 | None | None | 122 | None | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 21651182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 21801331 |
GRCz11 | 17 | 21821167 |
KASP Assay ID:
554-0251.1 (used for ordering genotyping assays)
KASP Sequence:
CTCCATCACTGCCCACATTGTCACATATATTTCCCAGATAACATCCTCTA[T/A]ACCATTCACATGGGCTGCCATGGCTATGAGAACCCTTTTCAGTGTAACAT
Long Flanking Sequence:
GACTTCACTCACGACCTCCCTCCTCACGCTCACCTTCATCAGGAAGCTTATAACGGTCTAGGAAAGGATCCACAAGCAATCGGTGGAGCAATCGGAAGTGGTTCTAGAGAAGACCAGGATATGGCATTAGACAACCCACTGAACCAGCTTTCAACATTAGCCGGACAGTTAGCCAGCATCCCATCTGAAGCTGAAGGTGCGCCTGTGTCTCCCGGAGCTGAATCGCTACCTGATGAAAAACCTACATTCCTCGTCCAGCAGCCTGTAACAGCGCCCGCTGCGGTTTCGGTCAACACAGCTCAAGCTTCTTCTCCCATCACCCCAGAGCCCAGACCAGCTGCACACAGCGGCTGCAGTCCAGGTGTGGGACCCTGCAGCGAGAGGACCAGCACTCCGAGCGGAACCAACAGCCAGCCAGGGACGCCCACTCCAGTACAGGACCCCCAGATGCTCCATCACTGCCCACATTGTCACATATATTTCCCAGATAACATCCTCTA[T/A]ACCATTCACATGGGCTGCCATGGCTATGAGAACCCTTTTCAGTGTAACATATGCGGGCACAGGTGCAGAAACAGTTATGACTTTGCCTGTCACTTCGCAAGAGGGCAGCACAAATAAGGACACACACTAGGGTTTTACCGGCCTCCTCTTTGCCCTGTTTTACATAATAATGCGATTTTAGTATCAGGAACATTCCAAAGACAAATTCGGGTGAGCCTGCGTTGTTCTTATTTTATTTGAACTCTTATTGGCATGTTATTTGTCTTTGTAAAGGTTGTAAATGGTGTCCTCCTCACATTAAAAACTATCAATATAGATTATCCGACTTTTGCAGTCATGCAGATTTTTTGCCTCAACTCTCTTTTATAAGTGCCAGAGTTTGATAATCAGTGCCTACAGTTATTTTCTGAAAGTTAACACTTCAAATTTTGTATTTTCTTTTGCTTTTTTACATTTGGACTTCTGAATGACTGTAAATGTTCTCATGTTTTAGTCGTGAC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa42916
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079011 | Nonsense | 411 | 419 | 4 | 4 |
ENSDART00000125335 | Nonsense | 411 | 419 | 3 | 3 |
ENSDART00000136727 | None | None | 52 | None | 3 |
ENSDART00000141462 | None | None | 168 | None | 3 |
ENSDART00000143832 | None | None | 122 | None | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 21651272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 21801421 |
GRCz11 | 17 | 21821257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGTAACATATGCGGGCACAGGTGCAGAAACAGTTATGACTTTGCCTG[T/A]CACTTCGCAAGAGGGCAGCACAAATAAGGACACACACTAGGGTTTTACCG
Long Flanking Sequence:
ATCGGAAGTGGTTCTAGAGAAGACCAGGATATGGCATTAGACAACCCACTGAACCAGCTTTCAACATTAGCCGGACAGTTAGCCAGCATCCCATCTGAAGCTGAAGGTGCGCCTGTGTCTCCCGGAGCTGAATCGCTACCTGATGAAAAACCTACATTCCTCGTCCAGCAGCCTGTAACAGCGCCCGCTGCGGTTTCGGTCAACACAGCTCAAGCTTCTTCTCCCATCACCCCAGAGCCCAGACCAGCTGCACACAGCGGCTGCAGTCCAGGTGTGGGACCCTGCAGCGAGAGGACCAGCACTCCGAGCGGAACCAACAGCCAGCCAGGGACGCCCACTCCAGTACAGGACCCCCAGATGCTCCATCACTGCCCACATTGTCACATATATTTCCCAGATAACATCCTCTATACCATTCACATGGGCTGCCATGGCTATGAGAACCCTTTTCAGTGTAACATATGCGGGCACAGGTGCAGAAACAGTTATGACTTTGCCTG[T/A]CACTTCGCAAGAGGGCAGCACAAATAAGGACACACACTAGGGTTTTACCGGCCTCCTCTTTGCCCTGTTTTACATAATAATGCGATTTTAGTATCAGGAACATTCCAAAGACAAATTCGGGTGAGCCTGCGTTGTTCTTATTTTATTTGAACTCTTATTGGCATGTTATTTGTCTTTGTAAAGGTTGTAAATGGTGTCCTCCTCACATTAAAAACTATCAATATAGATTATCCGACTTTTGCAGTCATGCAGATTTTTTGCCTCAACTCTCTTTTATAAGTGCCAGAGTTTGATAATCAGTGCCTACAGTTATTTTCTGAAAGTTAACACTTCAAATTTTGTATTTTCTTTTGCTTTTTTACATTTGGACTTCTGAATGACTGTAAATGTTCTCATGTTTTAGTCGTGACATGACCTTCGCCACATTTAACACTTTTCCTCTTCTCTAATTACGGATTAAATTATTATTTGCTTTGTGCCTCATTATTTAAACTTAACTT
Associated Phenotype:
Not determined