ZMP
si:busm1-142b24.1
Ensembl ID:
ZFIN IDs:
Description:
kinetochore-associated protein KNL-2 homolog [Source:RefSeq peptide;Acc:NP_001006662]
Human Orthologue:
C14orf106
Human Description:
chromosome 14 open reading frame 106 [Source:HGNC Symbol;Acc:20190]
Mouse Orthologue:
C79407
Mouse Description:
expressed sequence C79407 Gene [Source:MGI Symbol;Acc:MGI:2145099]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42951 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12149 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42951
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062430 | Essential Splice Site | 502 | 1011 | 8 | 13 |
ENSDART00000113300 | Essential Splice Site | 531 | 857 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 28678863)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 28602790 |
GRCz11 | 17 | 28619753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGAACGTTACTGTCCATGAAGACTATTCAACCTCAGTACCATCCACGG[T/C]ACTCTTATTTGATTCAGCATTTCAAACTGTGTGTCTTTATCTATCGCTAT
Long Flanking Sequence:
AATCTTTGTTTTAGATCACAAAAAAGTCAAAAGGACAAAAGCAGTTCTGTGAAACCTTCTAAAGCCAGAAAAAACTCAACATCCAAACATTCTAAGGTTCAAGACATTACAACGTGTATGTATAAAATGTATCAACAGTGGCATTTTTATCTTTTTAAATGGGTTCACAAGTAAACCTTAAGGATTTGTTACTGAATTAATCAAAATGAATAGATTTATCTTATGTCTATTGCTGTAGAATTAAGAATTTTTGCTATTGAGATTCAGATATTTTTAAGATTATAAATTGTGGTTTGATAATGCTAATATACAGAATTTTGTTTGTGGTACAGCTCCTGTCACTCCCATTGATGGTGTTCAGCAGGACAGTGCAAAAGTGTCCCGCAGTGGCCGACTCATCAAACCACCACTGGAGTACTGGAAAGGAGGGAGGATTGTTATGGACTCTGAGATGAACGTTACTGTCCATGAAGACTATTCAACCTCAGTACCATCCACGG[T/C]ACTCTTATTTGATTCAGCATTTCAAACTGTGTGTCTTTATCTATCGCTATGGTGAATGTCGGCCATTTTTTAACTGAGGTGTTATTTTTGCCAGCCAAAGAAGCCGGCAACATCACAGATTGCAGAGGAAAAATCATTCAGACCCAAAACTGTGGAAAGAGGTGTGTATTGATTATCATAATTTTTATTATTACTTTTTTTTTTTTTTTCATTGCAATTTTCCATATTTATATGTTTTACTAAAGGGAGATGCATCACATCTAGCAGTGAAGATGAATTATCAGTGCCAAGAAGGAGAATCAAACAGGTTTCCAAACCCCAACAGAAGATACCCAGCAATCCACTTCCGGCTGAGAACACAGCACGGAGTAAACCTCCAAGATCTCAGAAAGGGCCCCTGGTAGTGACCACCATGTCTGATTCAATTCCTGCAGCAAAACAAAACGCTAGTAGACCTCAAAGAGCCTCTCTGAGAAAACAGCGTTCAGCAGAAAAGGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12149
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 |
---|---|---|---|---|---|
ENSDART00000062430 | Nonsense | 967 | 1011 | 12 | 13 |
ENSDART00000113300 | None | None | 857 | None | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 28680728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 28604655 |
GRCz11 | 17 | 28621618 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAAGATGACCATGATGACGTGTTTACCAGCTCGCCCATGCACAGTAAA[C/T]AAATCAAGGTGCTTTTGTRTGGACTGAGTTTGAGCACAACTTTAGACATT
Long Flanking Sequence:
AAAGTAGCAAGCAATTCTGAAAATGGTTTGAATGTATTAGATGCCATTTACAAATGTACACCAATCTCTGGACAGGGGTGTCAACTCATTACCCAAACACCAGAGCGGTTACTGGGCACATGTTGCATATGTTGTTGGCACCCGGTCTGCTGAAGAGTGTCATGAACAGTATAATGCCCATCAGAGGAAGAGCAAAATCCCCAGACAAAGACCATCAAAGAAACCAGCGGCAACTGAGGAGTCAAGTTAGTTTTTATACTTTATAGTTTCGAGAACTGTGAGTTTTAAAAAGTGTGGTAGAAATCCATGCTTTTGAAAATGACTACAATTTATCACCTCTTTTTTTTTTGTTTTCTATTTTGCTTATAGGCAAGGAAGTAGTTGAAATCACTGCTAAAGCTGGAACACTTAAAAGAAGACATCAGATGAGACATTTCTTGGAGCACATGCCCAAAGATGACCATGATGACGTGTTTACCAGCTCGCCCATGCACAGTAAA[C/T]AAATCAAGGTGCTTTTGTGTGGACTGAGTTTGAGCACAACTTTAGACATTTCAAGAATGTGCATTTAAAGTTAATATGAATGGGGGAAAGTGCAGTATAGTGGAATAAGTCCTGCCTTCTAAATAAAACGGCTAATATAGCACAATAGTGGGTTCTTCTCAATGTTAAAACTCCATTTGGGCTCTCTCTATATGGAAAATTATAATTATTAACAAGAACCAATAAACCTTTAAAAAATAGGTTCAGAGGTTTCATGTTTTTTATGCAACTCTTCTGATTGCATTAATTTGATAGATTTTTAAAAGGTCAAATCAATTTTAAGAGATACGTTTGTACAGTAAACACAACTTCAAAATAGATATCAGAGACATCAGAAAATTTACAGCAAAGTGCACAGACTTTCCTTTAAAAAGGGCATTTGTTTAGAGCCCCACGCTCTGAACTAAACAATATTTAGATGACTGCGACCAGCCCCCTGTCTGAATAACACCATGTTTTTT
Associated Phenotype:
Not determined