Busch Lab

ZMP

NP_001177394.1

Ensembl ID:
ENSDARG00000090977
Description:
interferon-induced protein with tetratricopeptide repeats 5-like [Source:RefSeq peptide;Acc:NP_0011
Human Orthologues:
IFIT1, IFIT1B, IFIT2, IFIT3, IFIT5
Human Descriptions:
interferon-induced protein with tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:5407]
interferon-induced protein with tetratricopeptide repeats 1B [Source:HGNC Symbol;Acc:23442]
interferon-induced protein with tetratricopeptide repeats 2 [Source:HGNC Symbol;Acc:5409]
interferon-induced protein with tetratricopeptide repeats 3 [Source:HGNC Symbol;Acc:5411]
interferon-induced protein with tetratricopeptide repeats 5 [Source:HGNC Symbol;Acc:13328]
Mouse Orthologues:
2010002M12Rik, Gm14446, I830012O16Rik, Ifit1, Ifit2, Ifit3
Mouse Descriptions:
RIKEN cDNA 2010002M12 gene Gene [Source:MGI Symbol;Acc:MGI:2148249]
RIKEN cDNA I830012O16 gene Gene [Source:MGI Symbol;Acc:MGI:3698419]
interferon-induced protein with tetratricopeptide repeats 1 Gene [Source:MGI Symbol;Acc:MGI:99450]
interferon-induced protein with tetratricopeptide repeats 2 Gene [Source:MGI Symbol;Acc:MGI:99449]
interferon-induced protein with tetratricopeptide repeats 3 Gene [Source:MGI Symbol;Acc:MGI:1101055]
predicted gene 14446 Gene [Source:MGI Symbol;Acc:MGI:3650685]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa15526 Nonsense Available for shipment Available now
sa22070 Nonsense Available for shipment Available now
sa22069 Nonsense Available for shipment Available now
sa42002 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15526
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125902 Nonsense 134 446 2 3
Genomic Location (Zv9):
Chromosome 12 (position 18057111)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16868285
GRCz11 12 16990159
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATAAACTACCACATGGAGAAMTACACAGAGTGCGAAAGTTACCTGGTT[A/T]AGCTTCAGAAGATAMATGAAAGATTTGCAAYTGAGTCTTCAGCTGTTCCA
Long Flanking Sequence:
GTCATGGTGGGAAGCGTCATTTTCTTTCATGTAGTTTTTGCTTAAGAGTTTACATTAGCCTGCTGCTATTTCCAAGGCTATTTAACCTGAAGATGTTGCAATATTAGTCTAACTGAATCCTGAAGCTCTTTTTTTTCAATCCTTTTAGTTTAATTCAGGCCAGTTTAAAAAAGAAACTGGATCAGCTGGAGTGCCACTTCACATGGGACATTACAAAAGATCATCTAGACTTTACGAACCTCCTCAACAGACTTGAGGAACAAAACAAATTGGATTTAGGGAATGAGGAAGGAGCTGCACGAGCGCAGTGCTCAATGGGATATCTAAAATTCCTTCTCAACTGCAAAGAAGAAGCTCTTACTCACCTGTCGAGATCTGAGGCACTCATCAAAGAAAACTTTGCAGACAACAACGACAAGGCTCTTATTGTGACCTATGGAAATTTTGCCTGGATAAACTACCACATGGAGAACTACACAGAGTGCGAAAGTTACCTGGTT[A/T]AGCTTCAGAAGATACATGAAAGATTTGCAACTGAGTCTTCAGCTGTTCCAGAGGTGCTTGGGGAGAAAGGGTGGACTTATCTTAAATTCTCTCGTAAATATTATGACAAGGCAGTAGAAGTTTTTCAGAAAGCTGTGGAACTGGATCCAACAAATAGTGAGTGGAACGCAGGTTATGCCATCGCTCTGTATCGCACTGAGAATTTTAACCCACCACCTTGTACTGTGGAAACACCTGCAATAAAACAGCTGAGACAGGCCATTGACTTAAACCCAGATGATGATGTTCTGAGAGTTATTCTAGGAATTAAACTTTTGAATTGCTCCAAAGGTTTAATGAACGAGTCCGAGCAATTGGTTGAGAAAGCTTTGAATCAGTCTCCAGAACATCCACATGTCATTAGATATGTTGGAATGTTCCTCAGGGATCAGGGATCTGTTGACAGGTCCATTGAAATTCTGAAGAAAGCCCTTCAAAGATCACCAAAATCAGGCTTCATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22070
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
ENSDART00000125902 Nonsense 216 446 2 3
Genomic Location (Zv9):
Chromosome 12 (position 18056865)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16868039
GRCz11 12 16989913
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGAATTTTAACCCACCACCTTGTACTGTGGAAACACCTGCAATAAAA[C/T]AGCTGAGACAGGCCATTGACTTAAACCCAGATGATGATGTTCTGAGAGTT
Long Flanking Sequence:
ACAGACTTGAGGAACAAAACAAATTGGATTTAGGGAATGAGGAAGGAGCTGCACGAGCGCAGTGCTCAATGGGATATCTAAAATTCCTTCTCAACTGCAAAGAAGAAGCTCTTACTCACCTGTCGAGATCTGAGGCACTCATCAAAGAAAACTTTGCAGACAACAACGACAAGGCTCTTATTGTGACCTATGGAAATTTTGCCTGGATAAACTACCACATGGAGAACTACACAGAGTGCGAAAGTTACCTGGTTAAGCTTCAGAAGATACATGAAAGATTTGCAACTGAGTCTTCAGCTGTTCCAGAGGTGCTTGGGGAGAAAGGGTGGACTTATCTTAAATTCTCTCGTAAATATTATGACAAGGCAGTAGAAGTTTTTCAGAAAGCTGTGGAACTGGATCCAACAAATAGTGAGTGGAACGCAGGTTATGCCATCGCTCTGTATCGCACTGAGAATTTTAACCCACCACCTTGTACTGTGGAAACACCTGCAATAAAA[C/T]AGCTGAGACAGGCCATTGACTTAAACCCAGATGATGATGTTCTGAGAGTTATTCTAGGAATTAAACTTTTGAATTGCTCCAAAGGTTTAATGAACGAGTCCGAGCAATTGGTTGAGAAAGCTTTGAATCAGTCTCCAGAACATCCACATGTCATTAGATATGTTGGAATGTTCCTCAGGGATCAGGGATCTGTTGACAGGTCCATTGAAATTCTGAAGAAAGCCCTTCAAAGATCACCAAAATCAGGCTTCATATGTCATCAATTAGCAATGTGCTACAAGACCAAGAAAATAAACCTATGTAAAGAAAAACGGAGAAAAGTGGAGGTAGATGAGGCTCGCGATCAAAGCATATACTACTTAGAAGAGGCAACTTCCTTAATACCATCCTTTATCTCTGCAGTGTGTCAGCTCGGACTTCAGTATGGAGACCGACGTGATCTGCTTAAAGCAGAAGAGCAGTTTGACAAAGCATTTAAGTTAGTGAAAGAGAAAAACGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22069
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125902 Nonsense 237 446 2 3
Genomic Location (Zv9):
Chromosome 12 (position 18056802)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16867976
GRCz11 12 16989850
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTGACTTAAACCCAGATGATGATGTTCTGAGAGTTATTCTAGGAATT[A/T]AACTTTTGAATTGCTCCAAAGGTTTAATGAACGAGTCCGAGCAATTGGTT
Long Flanking Sequence:
GCTCAATGGGATATCTAAAATTCCTTCTCAACTGCAAAGAAGAAGCTCTTACTCACCTGTCGAGATCTGAGGCACTCATCAAAGAAAACTTTGCAGACAACAACGACAAGGCTCTTATTGTGACCTATGGAAATTTTGCCTGGATAAACTACCACATGGAGAACTACACAGAGTGCGAAAGTTACCTGGTTAAGCTTCAGAAGATACATGAAAGATTTGCAACTGAGTCTTCAGCTGTTCCAGAGGTGCTTGGGGAGAAAGGGTGGACTTATCTTAAATTCTCTCGTAAATATTATGACAAGGCAGTAGAAGTTTTTCAGAAAGCTGTGGAACTGGATCCAACAAATAGTGAGTGGAACGCAGGTTATGCCATCGCTCTGTATCGCACTGAGAATTTTAACCCACCACCTTGTACTGTGGAAACACCTGCAATAAAACAGCTGAGACAGGCCATTGACTTAAACCCAGATGATGATGTTCTGAGAGTTATTCTAGGAATT[A/T]AACTTTTGAATTGCTCCAAAGGTTTAATGAACGAGTCCGAGCAATTGGTTGAGAAAGCTTTGAATCAGTCTCCAGAACATCCACATGTCATTAGATATGTTGGAATGTTCCTCAGGGATCAGGGATCTGTTGACAGGTCCATTGAAATTCTGAAGAAAGCCCTTCAAAGATCACCAAAATCAGGCTTCATATGTCATCAATTAGCAATGTGCTACAAGACCAAGAAAATAAACCTATGTAAAGAAAAACGGAGAAAAGTGGAGGTAGATGAGGCTCGCGATCAAAGCATATACTACTTAGAAGAGGCAACTTCCTTAATACCATCCTTTATCTCTGCAGTGTGTCAGCTCGGACTTCAGTATGGAGACCGACGTGATCTGCTTAAAGCAGAAGAGCAGTTTGACAAAGCATTTAAGTTAGTGAAAGAGAAAAACGAGCATCTTCAATCTGTTCATTTGTCTTATGCTCAGTTCCAGCAGTACAGCAACAGACGTGAGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42002
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125902 Essential Splice Site 438 446 2 3
Genomic Location (Zv9):
Chromosome 12 (position 18056196)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16867370
GRCz11 12 16989244
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAATAGAAGTGCACAGAAACTGTGCAACATTGCCAAGAAAAATCTCAAG[T/C]TAAATCCAAATGATTGGAAAGCCAATGAAATACTGGGCTTAGTTTATAAC
Long Flanking Sequence:
TGTTCCTCAGGGATCAGGGATCTGTTGACAGGTCCATTGAAATTCTGAAGAAAGCCCTTCAAAGATCACCAAAATCAGGCTTCATATGTCATCAATTAGCAATGTGCTACAAGACCAAGAAAATAAACCTATGTAAAGAAAAACGGAGAAAAGTGGAGGTAGATGAGGCTCGCGATCAAAGCATATACTACTTAGAAGAGGCAACTTCCTTAATACCATCCTTTATCTCTGCAGTGTGTCAGCTCGGACTTCAGTATGGAGACCGACGTGATCTGCTTAAAGCAGAAGAGCAGTTTGACAAAGCATTTAAGTTAGTGAAAGAGAAAAACGAGCATCTTCAATCTGTTCATTTGTCTTATGCTCAGTTCCAGCAGTACAGCAACAGACGTGAGGATTTAGCAATCGAGCACTATGAGAAGTGTTTGACAATGAATCCACACACTCCTGATGGAAATAGAAGTGCACAGAAACTGTGCAACATTGCCAAGAAAAATCTCAAG[T/C]TAAATCCAAATGATTGGAAAGCCAATGAAATACTGGGCTTAGTTTATAACTTGAAAGGTGAAATGTTTGAAAGGTATGGGAACACTCCAGACAACGAAGATGATTCATTCCTCTGTAATCTTCTTGAGGTTATGTCTTTGTAATTTATAAAATATTATTGTAATATAGATAAATAAACACTAAAAATGCCCCATTTGCAAATTTATGATCTCAGAAAGCATGGAAGCAGTGGTGCAGTAGGTAGTGCTGTCGCCTCACAGCAAATAGGTCGTTGGTTCGAGCCTTGGCTGGGTCAGCTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCCGGGTGCTCTGGTTTCCCCCACAGTCCAAAGACATGCGGGTACAGGTGAATTGGGTAGTGTAAATTGTCCGTAATGTATAAGTGTGTAAGGATGTTTCCCATAGATTGGTTGCAGCAGGGCATCCGCTGCGTAAAACACATGCTGGATA
Associated Phenotype:
Not determined