ZMP
ktn1
Ensembl ID:
ZFIN ID:
Description:
kinectin [Source:RefSeq peptide;Acc:NP_956375]
Human Orthologue:
KTN1
Human Description:
kinectin 1 (kinesin receptor) [Source:HGNC Symbol;Acc:6467]
Mouse Orthologue:
Ktn1
Mouse Description:
kinectin 1 Gene [Source:MGI Symbol;Acc:MGI:109153]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36502 | Nonsense | Available for shipment | Available now |
sa32174 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36502
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 |
---|---|---|---|---|---|
ENSDART00000017376 | Nonsense | 383 | 1189 | 6 | 37 |
ENSDART00000041447 | Nonsense | 383 | 1234 | 6 | 35 |
ENSDART00000086149 | Nonsense | 383 | 1233 | 6 | 37 |
ENSDART00000121550 | Nonsense | 383 | 1262 | 6 | 36 |
ENSDART00000122996 | Nonsense | 334 | 1343 | 7 | 41 |
Genomic Location (Zv9):
Chromosome 17 (position 44001701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43841379 |
GRCz11 | 17 | 43955144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACTGCTTTTGTTTCTTAGTCTACGGCTAAATTTGAGCCTACCCCCCAG[C/T]AGCTGGCAGAGAAAGATCGTCTCCTGAACACATTACAGGAGGAGGCGTCC
Long Flanking Sequence:
GCAGGTCTACATTTATAATAAATGATAAAAGTCTTCTTCTCTTCACTGTCTTCAAAGAAAATTTTCACTAAGCCATTGAACTTACCTCAATGCATAATGGTATGTATGTCATCCTATCTTAGATTTGGCCTAAAGAGGTATTATTATTAGACAAAACTTATGATCTTCATAAAGTATTGCCCATTAATGGTTTTGAAAGTGTGAATTTTTTTTCTTGATTTGTGTTCTGTTTATTTTCCCACAGAGAACTCTGAGGTGAAACTTAAGGAGCTTCTGGCCAGTATTGGTGGACTCGTGCTGTCAGATTCAGATGTGGTCAGTCTTGTTTCACTGCTTCGAGAAAAGAGTCCCAATGCTCTGGACAACTGGTATAAGGTAATAGGATAGAGTTCACTTTTATTATTTTGTTATGCATTTTTGAAGTAAAAGTGAAAGTTTGAGTTGATTTTTCCACTGCTTTTGTTTCTTAGTCTACGGCTAAATTTGAGCCTACCCCCCAG[C/T]AGCTGGCAGAGAAAGATCGTCTCCTGAACACATTACAGGAGGAGGCGTCCATCGCCAAGGGCAAAGTCAAACAGTTAAGCCAGGTTAGTAATTTACCTCCATACAAGTTTCCTGATGTGAATTTAGATATGTTTCCTTGAAAGGGGTACAATTTAAGATTTAAGGTGTTCTTCACCCCCATAAAAGACTATTTGCTGTTAATTTACTCAAGCTCAGGCCATCCAAGATATAGAAGACTTTCTTTTTAAGTAGAGCATTATAGAAGATATGAAGCTAATTATGTCGTCTTCGGTGATTCATACAACTCAAGTCAGTGTCAAAATCGGTCTGTGCAAGAAACATTTTGTACAATGAGAAATTTAGAACATTGGACTCTTGGAGGAAAAATTTTTCACTATTTATTGCTTACATTTAGGTTTAATTGTTGTTTTTGTTACTAGCAAATAACCAAATAACACAAAGCAGGGTTGTAAAGACCTCAGTTAGGTAAGTTACCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32174
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 |
---|---|---|---|---|---|
ENSDART00000017376 | Nonsense | 651 | 1189 | 12 | 37 |
ENSDART00000041447 | Nonsense | 651 | 1234 | 12 | 35 |
ENSDART00000086149 | Nonsense | 650 | 1233 | 14 | 37 |
ENSDART00000121550 | Nonsense | 651 | 1262 | 12 | 36 |
ENSDART00000122996 | Nonsense | 602 | 1343 | 13 | 41 |
Genomic Location (Zv9):
Chromosome 17 (position 44008642)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43848320 |
GRCz11 | 17 | 43962085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTAAATGAAAACAAAACGCTCAAGGTTCAGATTGATAATCTTCAGACT[C/T]AACTCAACACTCAGGTATGTGTGTGGGCTGGTAGATGCGGGTGAATTTGC
Long Flanking Sequence:
CTCGCAAAGGTTTTATGCTGTTGTTCATTTTTGCGCATAAATCTGGTTTGCATCCTTGGATGTAAACAGCGCTATTGACAGGAGCCATTGAGCAAAAGTGCCCTCAGAAGTGTAGCACCACCGCTTAACCTTTTTTTCACTGTCTATTCCAGAGCTGCAGAATCAGATAATGGTAGCGGAGAGCGAGATGGCCAGTAAGAACAAGGAGATCCAGAGTCTCCACAGCAGCCTGAAGGACACGCTGATGTTCAAGGATCAGGAGCAGCAGAAGGTGTTGCAGCTAGAACAGCAGGTTCGGCAGCTGTTAGAGGCCTCGCAGCGCTCCATGCAGCCTGATGACCAGCTGCAGGAGAAAGTCCAGGTGCCTCCTCTAGACACTATATACTACAGAAGCCAATTCAATAGTTATATCAATGCTAATAGTCACATTATGTCACTCTTTACAGGATCTTCTAAATGAAAACAAAACGCTCAAGGTTCAGATTGATAATCTTCAGACT[C/T]AACTCAACACTCAGGTATGTGTGTGGGCTGGTAGATGCGGGTGAATTTGCCTCTGTTTGTTGGTGGACATTAATTTGAGTATTTTTGTCCTTTCTTTTAGGCTACGACAGTATCACATTTTGAGGAGCTCCAAAAACTGTAAGTCATCAGCACAAAGCATTCTTGTTTTAGCATTTTTTTTCAGTGTGAAACACTAAGGCCTGTTTCATACTGCATATATAGTTGCCGGTTAGATATTAATGATCAAACTGATCATGCGTAACAGAGGAATTGCTCCACGAAATGTTGAAAATGTGAATTTGTTTGGTGTTAAGTGCTGAAACCAAGGGTTATCACGGTACCAAAGTTTCTGTATTCTTTAGCAGTGAAAATACACAGTTCTTGGTACCAATTTCTACAAATAATAAAAAAACCACACTAATTAAACAACCCAATTTTTATATTAAGTAAAACTGCTGTCAAACTATCAATTATGGAAGAGGGAGCACTTCACAGAAATT
Associated Phenotype:
Not determined