ifit2

Ensembl ID:
ENSDARG00000043584
ZFIN ID:
ZDB-GENE-030131-1055
Description:
Ifit2 protein [Source:UniProtKB/TrEMBL;Acc:Q5U3W8]
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:
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]
RIKEN cDNA 2010002M12 gene Gene [Source:MGI Symbol;Acc:MGI:2148249]
RIKEN cDNA I830012O16 gene Gene [Source:MGI Symbol;Acc:MGI:3698419]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa4711 Nonsense Mutation detected in F1 DNA During 2014
sa13361 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa4711
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2014.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064003 Nonsense 211 449 2 2
Genomic Location:
Chromosome 17 (position 23438255)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TTGCCATATCTATGAGCAAAGCATGTTTATGGTATAAATGCACTCCAGAG[C/T]AGAAAGCKGAGATTTTAGAGAAGGTGAAAACGGCAGCAGAGATCAACCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13361
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > G
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064003 Nonsense 313 449 2 2
Genomic Location:
Chromosome 17 (position 23437947)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TCAAKCAAAGTGTTGAAATGCCTGGCAGACACCTACAAATGGAAGGTTTA[C/G]AAAATGAATGAAGACACAGAGGAAAGGRTGATTCTGGCTAGGAAAACCAT
Associated Phenotype:
Not determined

Register

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* quick link - http://q.sanger.ac.uk/ojsp3nzf