ZMP
NDC80_DANRE
Ensembl ID:
Description:
Kinetochore protein NDC80 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6DRJ7]
Human Orthologue:
NDC80
Human Description:
NDC80 homolog, kinetochore complex component (S. cerevisiae) [Source:HGNC Symbol;Acc:16909]
Mouse Orthologue:
Ndc80
Mouse Description:
NDC80 homolog, kinetochore complex component (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1914302
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22044 | Nonsense | Available for shipment | Available now |
sa14319 | Essential Splice Site | Available for shipment | Available now |
sa16762 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22044
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007335 | Nonsense | 156 | 632 | 5 | 17 |
ENSDART00000112640 | Nonsense | 156 | 608 | 5 | 18 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 11441918)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 10324989 |
GRCz11 | 12 | 10362832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGCCTACTGCCAAAGTGGAGGAAGAGATCCCAAGAATGCTCAAAGATT[T/A]GGGGTAATCAATATTATTTTATCACTACACCCTGTACAATTTACAGTAGT
Long Flanking Sequence:
TTAAAAATTGCTGAAATTACATATGTAAAATATTTTTTTTAGTGCTGTTAATAAGGGGAACCAACATTTTTCTTCTAACCATAACATACATATTTGCACAAACCTGTATGGGTCAGATTTCTTGTAAATAACGCAATAATTTATATCTATAGGAGGTTTATGGGGGTTCATTGGTGGATATTTATTACCAGAACAGTTAGATATTGCTCTATTTTCAAAGAAAAAAATAGTTTAGCTCATGATTTTTAAGAAACGTTAAGCTATAATCAAAAGTCAGAAATTGAATTGCCCAAAATTAATTACAGTGAATTTATTTTCCTATTGTTTCTAGTTCCTAGTGGACAGAGGCTTTCCAGGCAGCATCACAGTGAAGGCTCTCCAGTCTCCATCCACAAAAGAGTTTTTAAAGATTTACGAATTTATCTACAATTTTTTAGAACCATCCTTTCAAATGCCTACTGCCAAAGTGGAGGAAGAGATCCCAAGAATGCTCAAAGATT[T/A]GGGGTAATCAATATTATTTTATCACTACACCCTGTACAATTTACAGTAGTTCAAATAAAACTGATCTAATGCACACATTGGCCAGAGTTAACCACTTTGTAAATATTTTTTCATAGATACCCGTTTGCACTCTCAAAAAGCTCTATGTACTCCATTGGTGCTCCTCACACATGGCCTCTGGCTCTTGGAGCTCTCATCTGGCTCATGGATGCTGTCAAGGTAACTCTTCTTCAAACATTTATAAACTATATTAACTGAACTATTGCTGGTTTCCACATCATGTTGTAGCATAAAGAAGACCTCTTATTTTAACCAGAAATGGGCATTGTCACTTTACCTATAGCTCAGTGGTAGGGAACCTATGGCTCGTGTGCCACATGTGGCTGTTTGGCCAAAAATATGTGGCTCTCCAGCTGTCTCCTTTCAATAATATTTTACAGTTTACTAGAAATAAGTTTCCTGTTGGAAACACAATTACAATAGCCTTTTCATTGTCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14319
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 |
---|---|---|---|---|---|
ENSDART00000007335 | Essential Splice Site | 513 | 632 | 14 | 17 |
ENSDART00000112640 | Essential Splice Site | 489 | 608 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 12 (position 11433812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 10316883 |
GRCz11 | 12 | 10354726 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YAAGGAACAGATTCGCAAAGTCGACCAGCAGCTGGAGAATGCCATGCAGG[T/C]AAAATACACCTCCACRGGGCGTTTGGGTTTTAAATGTAATATTAAAAAAA
Long Flanking Sequence:
GTTTTATTTACACCGTAAACTTTATCTGGCAGTTTATTCATTAAACATTTTTATTGCCATTTATATAACATTTTTACCTTCTGTGTGGGTTTTATATTAGCACACTTATAACCAAAATATAGGCAGATAAATAGAAGTCGATTTTATAATTTAATGTTTTATATTGAGCCGATAACAAAAGCTTTACGAATAAGCAGTTGTCATCTGCTGATACTGAAATTGGCGCTATGTTGTGAATCACTTAATAAAAGGCGTCTTGATCATACAATTGTTTTATTTACCGCTTTTGCAGTTAGTCCCAGCCTGTTTAATTAGGTAAATTTAAGATTCAGGTAGGCTGTGCACTAGATTTTGCATGTACCTATAAAGGTGAGCTCATCTATGTACAACTGCATCTGTCTATTAGGTGAAGTCCAACATCTTTGATAAGGAGAACGACATTAAGCAGCTTAAGGAACAGATTCGCAAAGTCGACCAGCAGCTGGAGAATGCCATGCAGG[T/C]AAAATACACCTCCACGGGGCGTTTGGGTTTTAAATGTAATATTAAAAAAATATGCTTGGATAATAAATAGTGCATGGAAATTGAAGTCATTCAGGTAACACTTTATTTTGATGGTCCATTTGAGTATTAGTAGACTGTCTGCTTAATATCTGTTAATACTGCTCCTTCAACAGACATTTAACTGACTATAAGAAACTTTGCTTGTACATATTAACTTACACTAACCCAAAACCCAACCTAACTGTCTACTTATAATTTAGTGAGAATTAGCTGCAATGTAACTTAAATTCAACAAATGGACCATTAAAATAAAGTGTGACCATCCTTCATTTTCAGAAACGATACATATTAAATAGTTGTTTTGTGCATGCGATTGATCTTATTCTGCTGTTTGTAGGAAATGGCGCTGGAGGATGACAAGTGGGCAGCTGAATTGGACTCTGCCGAAACTCATAAGAAGCTTTTTGAAAAGAATGTAATGCAGGGGATTGAGGAAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16762
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007335 | Nonsense | 632 | 632 | 17 | 17 |
ENSDART00000112640 | Nonsense | 608 | 608 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 12 (position 11432576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 10315647 |
GRCz11 | 12 | 10353490 |
KASP Assay ID:
2260-5040.1 (used for ordering genotyping assays)
KASP Sequence:
TAACCAGCTCACAGATCTGGWGGAAAACTTCATWAAGAAAGCCAACAGCT[T/A]GTAATGCTTRACTKTCCTGTTTTGTAAATACTKTTAYTATTAGACKAATT
Long Flanking Sequence:
TTACCTTGACTTGACATGTGCTGCAGAGTTTGCAAAAAGTCTTTTAAAAAGTGTAAGATTTCAAAACCATTTTAGGCCTTAGTCTTAAAAGTGGCATAGAGTGCATTGACAACAAAGATTACAAAACAAGATAATTTGAAGAATGTTGTCATTGACGTCTACGGTAGCTGTTTTTTTCAACATTTCTTTTCAGTCTTCTTTTGTGTTCAACATAAACTCAAACTGGTTTGAAACGAGTAAAATTTGAATAAATGTGTCTTTAAATTACACTCCATCCATTACACATGACCCTATTCTTTACCATTACCGAGTATTTTACTTGTCTACTTGATAAGTCAATTATCATCCTTTTAACCAAAATGTTTTGTTTGTCTTCTAGAAACACTGTGATGAGCAGTTGAAAAGGTTTGACAAGCTGAAGGATATCGTCCGTGAGGATGAGGCTGACATTAACCAGCTCACAGATCTGGTGGAAAACTTCATTAAGAAAGCCAACAGCT[T/A]GTAATGCTTAACTGTCCTGTTTTGTAAATACTTTTACTATTAGACTAATTTACTGATTCTAGCACCACAGAAACGTCTTTAAATACAGAATCAAATGTTTTGTATTTATCCTGTATTTACATCATTTTAATAAATGTGTTTTCATTTCTAAATGTGACGTCTATTGTTCATGTTTGATTTCATTGTTTACAGATTCTTAAGGTATATTATTTTCATATTCAGTATATTGGTTTTGTTCGATTTAATTAGTCTGTAAATAAAACCTTCTTTTGACTCGTAAATTTGCCTGTTTTAATATTATTTGTGAAATTTAGACCTGGTGTTAGCACTACATTCTTTGATAATTTAACCTATTGACTAGAAAGAATAACAAGGTTTAATAAAAAATGCAAATAAACGGCTGCTTTCTAAAGATATCTGGAGTAATTATGTTTTAGTTAGATCCAAGTAGCGTTTTTCTCATGACATGCCTTTTTTCTGGGAAAAATACGAAAATCAAT
Associated Phenotype:
Not determined