ZMP
zgc:153654
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC565601 [Source:RefSeq peptide;Acc:NP_001070637]
Human Orthologues:
IFI44, IFI44L
Human Descriptions:
interferon-induced protein 44 [Source:HGNC Symbol;Acc:16938]
interferon-induced protein 44-like [Source:HGNC Symbol;Acc:17817]
interferon-induced protein 44-like [Source:HGNC Symbol;Acc:17817]
Mouse Orthologues:
H28, Ifi44
Mouse Descriptions:
histocompatibility 28 Gene [Source:MGI Symbol;Acc:MGI:95975]
interferon-induced protein 44 Gene [Source:MGI Symbol;Acc:MGI:2443016]
interferon-induced protein 44 Gene [Source:MGI Symbol;Acc:MGI:2443016]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15481 | Nonsense | Available for shipment | Available now |
sa16411 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15481
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084876 | Nonsense | 190 | 445 | 4 | 8 |
ENSDART00000114157 | Nonsense | 190 | 283 | 4 | 9 |
ENSDART00000123695 | Nonsense | 190 | 445 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 36637977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36934687 |
GRCz11 | 2 | 36917144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTAATGTCTTAGGAAAAAGAAGGCACTCTTGAGCTCCATCTCCAGCTGG[A/T]AGCCTTCTGTGAGCTCAATTAAACAGGCTCGGATTCTKTTGSTGGGTCCC
Long Flanking Sequence:
TAGTACTCTGCTACATAGATCATTTACAGGGAACTTCAGATCATCCAAGATGCAGGTGACCTTTTCTTAAATAAACATTAAAAGAAGATTTTAGCTGAAATATTGGTTCTTAATGATTTATGCAATGCAAGTAAAAAACTACTGATACTTTCTGTAGAAGAAATACCTAGGACTGCTTGTGATAAATTAAAGGTCTCAAGAATGAAATGATCAGTCTGTACAAATAACTGAACATTATTACCTTTAAACCACAGTCTTCGAAAATGGTCTTCAACATGTTCACTATAGTCATGAGTGTTGTGTAACAACATAAATCAAACACTGAGAATCTGCAAAAGTCAATCTTACTTATTCAGCAAAAAAATACTTTAAAAATTCACATTTCAGGAGTGAGGGTAAGTTCATTTTTGAATTATTTGTCATATAAGAAATTTGACCACTATTATAATTGTTAATGTCTTAGGAAAAAGAAGGCACTCTTGAGCTCCATCTCCAGCTGG[A/T]AGCCTTCTGTGAGCTCAATTAAACAGGCTCGGATTCTGTTGCTGGGTCCCATTGGTGCTGGAAAATCAAGCTTCTTCAACTCCATCAACTCTGTATTCAAGGGTTACGTGAGCATGCAGGCCAACACTGGCACTGCCGAAACCAGTTTGACTACTCAGGTAGAACTGAATTAATATTATTCCACCTCTGTTTTAGTTAAATATTGGGAGACTTACGGCATAGTGAAACAAGTTTTTTTTTATGCCGCATAGTTCCGTACCTACTACACAAAGCCAGGCAGCAGTGTCAGCCATGTTCCCTTCACTCTGTGTGACACAATGGGTCTGGAGGAGGGTCTGAACTGTGGTTTGGATGTGGATGATTTTGCCAGTATTTTGAAGGGTCACATTCAAGACCGCTACCAGGTGAGACCTTTAGATAAAATGTAAACATTTAAGGTTTCAGGTCAGATAGATATTTTAGTTACAGGGGTTTACATTTTTTAATTCTCTCTAATGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16411
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 |
---|---|---|---|---|---|
ENSDART00000084876 | Nonsense | 405 | 445 | 8 | 8 |
ENSDART00000114157 | None | None | 283 | 9 | 9 |
ENSDART00000123695 | Nonsense | 405 | 445 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 36636142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36932852 |
GRCz11 | 2 | 36915309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCACTCAGCTTGGAGTTTCTCTGTCTGCTGTGGTTCCAGTGAAAAATTA[T/A]TGCCAAGAACTGGAAATAGACCCTCAAACCGACATACTGCTCCTGAATGG
Long Flanking Sequence:
GGATTTACACAATATGGGTGTTGTTTGATGGGAGGATAGTTACCTACATTTATGTCATGTGTGATCATAGAGGTTTTGCCAGGGACATCAGAGAAAAGCATGGGGTATTTGTTAAACAGTTGGGCAAGACATTCCTTTTCATATCTTCTATAGTATAGTCAAATCTGAGACGTCATAGAATTTCACAATGGAGAATGGCTGTATGTTCTTTAGGTATTCCTCAGCTAGTTCTGCTGACCAAGGTGGATGAAGCCTGTCCCTTAGTGGCAGAAGACCTGAAAAATGTCTACCGGAGTCACTACATCAACCAAATGGTATACAAATAAATGCATTTCACATAATATAATTTATACAGCAGTCATTATGCTTTACACTGTTTGTCCACATAATATTTCTGAGTATTTCTGATGTACTGTATATTTTTTGGTGATACTGTAGATGCAAGAGGTTAGCACTCAGCTTGGAGTTTCTCTGTCTGCTGTGGTTCCAGTGAAAAATTA[T/A]TGCCAAGAACTGGAAATAGACCCTCAAACCGACATACTGCTCCTGAATGGACTTATTCAGATGCTTAGAGCTGCCGAAGGTTTTTTTGATGATTGTTACAATCCAGAGGAGAAGTCTGAGTAGTGTCAACTTGTTAAGTCATTCCTTTCTACATTTATTCATTAAGCAGATGCTTTTATCAACAGCAACTTAGCACTAAAGTAGTTTAACTCAGGTCTATTTTTAGCTAGATGCTTCATTGCTGGATGGGTAAAAATATAACCATTGTAATAGAAAGTGATATAAAAGTATTGCAAGGGTTAGGGTTATGTAGGATGATCCCTGCTGCATTTGTTTTTGCTTCTTTTGGTCTGAAGATGCAAGTTGTTTATTAAGTATTCCCTTACAACTATTGCCCTCTAGGGGTGACAGTAGGCCATTTTGCAATACAGGTAGATGCTGTGTACAGTTTGAACATTGTACGTAAAATCAAAATGAGCCGACAAGTTTGACGTTTAACA
Associated Phenotype:
Not determined