ZMP
ift81
Ensembl ID:
ZFIN ID:
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 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| hu7911 | Nonsense | Available for shipment | Available now |
| sa31633 | Essential Splice Site | Available for shipment | Available now |
| sa14146 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu7911
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 |
|---|---|---|---|---|---|
| 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 |
| GRCz11 | 8 | 11642373 |
KASP Assay ID:
554-2408.1 (used for ordering genotyping assays)
KASP Sequence:
CACTAACGNNNNNNTAAYKYTTYAAGRWGAGCGAACAGCTYAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTASATTCGAC
Long Flanking Sequence:
ATCATTTTATCCAGTTAATTATATAGTGTATAGATTCCCTATATCATAATATATTATTAATTTTTTTAAACATCTTACGTTACTGATTATTGTTTAGTTTCAAAAAGAGTTAAAAGTCTTTTATGGGGACTTTTACTTTAAAAAGTAGGAAATCTCTTCACATTGTCCAACTTCCTGCTAGCAACCGGGCCTTGTGTGACAACGGTTTCTAGGCAGGATTTGTTGACGTGAGAGGGAACGTTATACGACGTTATTATACAAAAATTTATTATCGTTTTCATTCATCTAAAATCAAATATTAAACGACATTCTGTGCTTGCGCTACAAAAGCTATAATACGGTAAATAATTCGGCTGTTAGCTGCTAACGTGAGTTGGAAAAGTTATTTTGAACACATCGCAAGCTAACGGAAGTTAACGTTGTGAGAATATTTTTGTTAGCGGTAAAAGCCACTAACGTAATTCTTCAAGATGAGCGAACAGCTTAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGACTCTCTGGAGCCAATGCAGCTTCTGCAGACTTTAAGTGATGTTCTGGCTGAAATTGATCCAAAGGTAAGTTGAAGATCAAATTTAATATGACTAATAAAACCACAACCTATAGCAATACATATCTATAATAGTACATAGTATCAAAACGGTAAATAAAAGTAGGGCTTCACGTTATTTTATTTTTCTGCAGTTTCAGAAGATGGTTTAAATAGCTTTATTTGATTGTTTTTTTCTATGCAGTCTAACAGTATTCGGGTAACAGAAATTAAATAATCACAATGTAAAAAAATGCATTTCTTAACTTGCTTTGTTTTGTCTCGTTTTTAGTTACAAATATACAAACAATTTCTAAGACTAAGTAAAGATGCTGTTTAGTTTTAATCGTCCAAATAAAGTAAAAAATTAAAAAAAATTGTTTTAAGAGTTTTATCTTTTGTTTTAAGTGGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31633
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 |
|---|---|---|---|---|---|
| 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 |
| GRCz11 | 8 | 11644219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTCTGGGAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTG[T/C]AAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATT
Long Flanking Sequence:
AAAGGATAGTTCACACCATACTGAAAACTTCATTTACATCATTTACTTTATTTGTTCCAAGCTGGTTTGACTTTCTTCTGTTGAACCACTGACTTGCATAGTATTTGTTTATCCCAACTTTAGAAGTCAATAGTCACAATTTTTAAGTTTTCTGCAAAATATCTACTTTAATATTTAACAGAATAAAGAATTACAAAAAGTTTCAAAACCTCTTGAAGATGAGTAAATAGTGAGCAATTTTTCATTTTTGGGTGAACAAGGCCTTTAATATTCTTTCACAGTTTCCTTTGAAACCACATTTTATTTTTAGAGAGTACTGTATAGATCTTTATTTATGTAATGTGTTCACACTGATAGTTTTTGACACTTTTTCTTTTTTCTGAATCTTTTTTCAGCAAGCCATTGATATACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTGGGAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTG[T/C]AAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATTTATTCCAGTGATTTTAAAGATGATTTTTCAACTTCATTACTCCAGTCTTCATGATCCTTCAGAAATCACTCTGATATGAATTATTATTATTATTATTGTTATTATTATTATGAATGCTATATAATAAAAGCAATAATGACTGGAGTAATAATTTCATTTGAAACTACATTTAATAAGAAAGCAGTTATTTAGAATTGTGATAAATATTTTTAAAAAGTTTACATTTAATAAATGCTACTTTGATGAACAGAATGGTTTTTTTTTTAAAACATGGAGGAAAAAAAACAATATATATATATATATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTATTTTCTTCGTACTTCACACATCTAATCAGCTTTAAAATGTCGATTGAACAGAAGCAGTTTTCGTCAGGGTTTGGTGTCGGGCAGTAAGCCTGTGGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14146
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 |
|---|---|---|---|---|---|
| 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 |
| GRCz11 | 8 | 11648795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGGTGRTGCAGTACCTACARAAGGTGGCGTCTGAGCCTGCTATGGGC[C/T]AGGCAGAACTGAGGGAGCTKGAGGACAAGGTGAGCTTTTAAAGGGATAGT
Long Flanking Sequence:
AAGAGAGGAATCACTCGCTCATCAGAAACAGGAGCAGAAAAACCAGGTAGAGACCAAGAGTTTGCATGTTTGCAGGAAATCGAAGAGTTATTATCTATTTTCAAGTATCAAGTATCTGCTAGGCATTCCGATAACATAGATTGTGTTTCGTCTCTTCTGTAGCTCTTCCAGGCAGAGCAGAGACTGCAGAGATGTCAGATCCAGCTCAAAGACTTACAGCAGGCAGCAGCAGACGAAAAGCCAGAGAGTAAGTTAATTCGCCTAAGGAAACCTTTCCCTGAATGACTCATTACTTTGGTTAATAATAAGATGCCTTCAGTATTTTACTTTTTCGAAAGGTAACATGCATGTGTTCTTAAACCATAGGCCTTATGAAGAGACTTGAGGAGGACATTAAGTTCAACTCCTACATGGTGTCTGAGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTACAGAAGGTGGCGTCTGAGCCTGCTATGGGC[C/T]AGGCAGAACTGAGGGAGCTTGAGGACAAGGTGAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTCAAACTGGTTCTGTTTATACACCTACTCACATATCGTATAATCAACTAAATGAAACAAAGTAAGTATCTAAAGACTTTTTATTATAAGTTTTAGTCAAGAAGACATATTCTGTTAAAGGGATAGTTGACCCGAAAATTGAAAATAGTAGGAAATACTATTGAAGTCAATGCTTACAGGACTCCAGCTTTCTTCAAAGCTTGTTCTTTAGTGTTTAACAGAAGAAAGAAACTCAAAAAAGCTTTGGAACGATATGGGTGAGTAAATTATAACATAATTTTCAGTTTTGGGTGAACGGTCCCTTTAAGACGGAAGTTTGAACTTGAGTACTCTTCCAGTAAAAGTTTAAGATTGGTAGGATTTTTTTACCATGAAAGTTCAGTATAATCAGTAATATTGTGAAAAAAGCAGACATTCATTTT
Associated Phenotype:
Not determined