ZMP
si:ch211-197g15.7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate interferon-induced protein 44 (IFI44) [Source:UniProtKB/TrEMBL;A
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13424 | Nonsense | Available for shipment | Available now |
sa13418 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13424
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 |
---|---|---|---|---|---|
ENSDART00000105453 | Nonsense | 223 | 491 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 17701817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17452752 |
GRCz11 | 22 | 17477730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGGTTATTTTTTGATATGGTAATTTGTAATAATAAACTTTTTTGTAGA[C/T]GAAAAGCAGAGCTCATGGGGTTAATCAGAAGTCATAAACCCCTGATTTCA
Long Flanking Sequence:
TACTAGATCCCCAAGTGAGTGTTGAAGAGAAACCATGGCGGAAAGTTCTGTGGACGGCTGAGTATGTTTCATCATTCATTCATTTTATTTTCAGCTAAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGAATGAACTGCCAACTTATGCAGCACATTTTGCGCAGCGGATGCCCTTCCAGCCGCAATCCATCTCTGGGAAACATCCACACTCTCATTCACACTCATACACTATGGACAATTTAGCTTACCTAATTCACCTATACCGCATGTCTTTAGACTTGTGGGGGAAACCGGAGCACCCGGAGGAACCCACACGAACACAGGGAGAACATGCAAACTCCACAGAGAAACGCCAACTGACCCAGCTGAGGCTCGAACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCCTCACGAGTATGTTTATAGTTTATGGTTATTTTTTGATATGGTAATTTGTAATAATAAACTTTTTTGTAGA[C/T]GAAAAGCAGAGCTCATGGGGTTAATCAGAAGTCATAAACCCCTGATTTCATCTGCGAGTCGGGTCAGAATCCTAATGATTGGTCCTGTTGGTGCTGGAAAATCCAGTTTCTTCAACTCCATCAACTCCATCTTTACTGGTCATGTGACCAGCAAAGCCATGTCAGGATCTGCAGGCACCAGTCTAACTGTACAGGTCAGTTCATATGATCAACAGGACTATGGGACATGCTTTGGTTTGTAATATTAAACAATTATTTCACAATTATTCCTATTGTTGGCAGTTTCGCACTTACCCAATAAATGACGGTCGTGAAGGAAAGCCATTGCCATTTGTGTTGTGTGACACCATGGGCCTCGAGGAGCAATCAGGAGCAGGACTGGACATTGAGGACATCAGCAGCATTCTTCAAGGACACATACCAGACCGCTACAAAGTAAGAGCATAAGTTCATTTTTAGGGGCTTGGAAATGTATATTTGTTTGTAAAGTTTGGTAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13418
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105453 | Essential Splice Site | 338 | 491 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 17701380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17452315 |
GRCz11 | 22 | 17477293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGGACATCAGCAGCATTCTTCAAGGACACATACCAGACCGCTACAAAG[T/C]AAGAGCATAAGTTCATTTTTAGGGGCTTGGAAATGTATATTTGTTTGTAA
Long Flanking Sequence:
TATGTTTATAGTTTATGGTTATTTTTTGATATGGTAATTTGTAATAATAAACTTTTTTGTAGACGAAAAGCAGAGCTCATGGGGTTAATCAGAAGTCATAAACCCCTGATTTCATCTGCGAGTCGGGTCAGAATCCTAATGATTGGTCCTGTTGGTGCTGGAAAATCCAGTTTCTTCAACTCCATCAACTCCATCTTTACTGGTCATGTGACCAGCAAAGCCATGTCAGGATCTGCAGGCACCAGTCTAACTGTACAGGTCAGTTCATATGATCAACAGGACTATGGGACATGCTTTGGTTTGTAATATTAAACAATTATTTCACAATTATTCCTATTGTTGGCAGTTTCGCACTTACCCAATAAATGACGGTCGTGAAGGAAAGCCATTGCCATTTGTGTTGTGTGACACCATGGGCCTCGAGGAGCAATCAGGAGCAGGACTGGACATTGAGGACATCAGCAGCATTCTTCAAGGACACATACCAGACCGCTACAAAG[T/C]AAGAGCATAAGTTCATTTTTAGGGGCTTGGAAATGTATATTTGTTTGTAAAGTTTGGTAATCTTTTGTTTAATCTATTCTTAATTCAGTTCAACCCTGCAGCACCATTTCAACCTGATGAGCAAAAGTCCTCCAGACCTGCGTCTCTACAGGAGAAGATCCACTGTGTGGTGTACGTGATCGACGCCACCAAAATCTCCCTCATGTCTGAGAAACTAGAGGAAAAACTGTCTGCCATACGCAGAAAAGTCAACTCACTGGGTGAGCAAGCATATTTATGCTACTTTTGTGACTAATATGTAGGTTATACACAAAGCTACTTGACAGAGATGTACTTTAAAATGTATCGCGATGATTTCAGGCATTGCACAGATTGTCTTGATGACAAAAGTTGATGAAGCTTGTCCTCTAGTGGATGAAGACCTTGAAAATGTTTATCTTAGTTCCTACATCAAGACGAAAGTAAGACAATCTGATCATATGAACTCTCCAATCAGCACT
Associated Phenotype:
Not determined