ift81

Ensembl ID:
ENSDARG00000007444
ZFIN ID:
ZDB-GENE-040714-3
Description:
intraflagellar transport protein 81 homolog [Source:RefSeq peptide;Acc:NP_001002313]
Human Orthologue:
IFT81
Human Description:
intraflagellar transport 81 homolog (Chlamydomonas) [Source:HGNC Symbol;Acc:14313]
Mouse Orthologue:
Ift81
Mouse Description:
intraflagellar transport 81 homolog (Chlamydomonas) Gene [Source:MGI Symbol;Acc:MGI:1098597]

Alleles

There are 7 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa7332 Nonsense Mutation detected in F1 DNA During 2016
hu7911 Nonsense Available for shipment Available now
sa41136 Nonsense Mutation detected in F1 DNA During 2016
sa31633 Essential Splice Site Available for shipment Available now
sa38673 Nonsense Mutation detected in F1 DNA During 2016
sa14146 Nonsense Available for shipment Available now
sa34331 Essential Splice Site Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa7332
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 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Nonsense 11 675 1 18
ENSDART00000004288 Nonsense 11 675 1 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12159905)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11604668
KASP Assay ID:
554-2408.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CACTAACGNNNNNNTAATTCTTCAARATGAGCGAACAGCTYAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
hu7911
Current 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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Nonsense 11 675 1 18
ENSDART00000004288 Nonsense 11 675 1 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12159905)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11604668
KASP Assay ID:
554-2408.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CACTAACGNNNNNNTAAYKYTTYAAGRWGAGCGAACAGCTYAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTASATTCGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41136
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 2016.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Nonsense 70 675 2 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12161709)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11606472
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTG[G/T]GAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTGTAAGACAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31633
Current 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:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Essential Splice Site 83 675 2 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12161751)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11606514
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CTCTTCTGGGAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTG[T/C]AAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38673
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 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Nonsense 296 675 8 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12166297)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11611060
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTA[C/T]AGAAGGTGGCGTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14146
Current 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
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Nonsense 306 675 8 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12166327)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11611090
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GAAAGGTGRTGCAGTACCTACARAAGGTGGCGTCTGAGCCTGCTATGGGC[C/T]AGGCAGAACTGAGGGAGCTKGAGGACAAGGTGAGCTTTTAAAGGGATAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34331
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 2016.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Essential Splice Site 315 675 None 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12166358)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11611121
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTTGAGGACAAGG[T/C]GAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTC
Associated Phenotype:
Not determined

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