Busch Lab

ZMP

si:ch211-197g15.7

Ensembl ID:
ENSDARG00000071355
ZFIN ID:
ZDB-GENE-030131-4763
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]
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]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa13424 Nonsense Available for shipment Available now
sa25179 Nonsense Mutation detected in F1 DNA Not yet available
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa25179
Status:
Mutation detected in F1 DNA
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
ENSDART00000105453 Nonsense 330 491 5 8
Genomic Location (Zv9):
Chromosome 22 (position 17701408)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 17452343
GRCz11 22 17477321
KASP Assay ID:
554-7759.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGCAATCAGGAGCAGGACTGGACATTGAGGACATCAGCAGCATTCTT[C/T]AAGGACACATACCAGACCGCTACAAAGTAAGAGCATAAGTTCATTTTTAG
Long Flanking Sequence:
ACTACCTACTGCGCCACTGCCTCACGAGTATGTTTATAGTTTATGGTTATTTTTTGATATGGTAATTTGTAATAATAAACTTTTTTGTAGACGAAAAGCAGAGCTCATGGGGTTAATCAGAAGTCATAAACCCCTGATTTCATCTGCGAGTCGGGTCAGAATCCTAATGATTGGTCCTGTTGGTGCTGGAAAATCCAGTTTCTTCAACTCCATCAACTCCATCTTTACTGGTCATGTGACCAGCAAAGCCATGTCAGGATCTGCAGGCACCAGTCTAACTGTACAGGTCAGTTCATATGATCAACAGGACTATGGGACATGCTTTGGTTTGTAATATTAAACAATTATTTCACAATTATTCCTATTGTTGGCAGTTTCGCACTTACCCAATAAATGACGGTCGTGAAGGAAAGCCATTGCCATTTGTGTTGTGTGACACCATGGGCCTCGAGGAGCAATCAGGAGCAGGACTGGACATTGAGGACATCAGCAGCATTCTT[C/T]AAGGACACATACCAGACCGCTACAAAGTAAGAGCATAAGTTCATTTTTAGGGGCTTGGAAATGTATATTTGTTTGTAAAGTTTGGTAATCTTTTGTTTAATCTATTCTTAATTCAGTTCAACCCTGCAGCACCATTTCAACCTGATGAGCAAAAGTCCTCCAGACCTGCGTCTCTACAGGAGAAGATCCACTGTGTGGTGTACGTGATCGACGCCACCAAAATCTCCCTCATGTCTGAGAAACTAGAGGAAAAACTGTCTGCCATACGCAGAAAAGTCAACTCACTGGGTGAGCAAGCATATTTATGCTACTTTTGTGACTAATATGTAGGTTATACACAAAGCTACTTGACAGAGATGTACTTTAAAATGTATCGCGATGATTTCAGGCATTGCACAGATTGTCTTGATGACAAAAGTTGATGAAGCTTGTCCTCTAGTGGATGAAGACCTTGAAAATGTTTATCTTAGTTCCTACATCAAGACGAAAGTAAGACAATC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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