ZMP
ncapd2
Ensembl ID:
ZFIN ID:
Description:
condensin complex subunit 1 [Source:RefSeq peptide;Acc:NP_001155974]
Human Orthologue:
NCAPD2
Human Description:
non-SMC condensin I complex, subunit D2 [Source:HGNC Symbol;Acc:24305]
Mouse Orthologue:
Ncapd2
Mouse Description:
non-SMC condensin I complex, subunit D2 Gene [Source:MGI Symbol;Acc:MGI:1915548]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12163 | Essential Splice Site | Available for shipment | Available now |
sa19860 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12163
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027088 | None | None | 507 | None | 14 |
ENSDART00000098126 | Essential Splice Site | 553 | 1389 | 13 | 33 |
ENSDART00000113351 | Essential Splice Site | 530 | 1380 | 13 | 32 |
The following transcripts of ENSDARG00000005058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 44830325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 44915826 |
GRCz11 | 2 | 44768824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACWCYGCTGTCCAAATCGCTCAGTTTCTCMGAGAAAGCAAATACAAG[T/G]AMATGTCCATTAATTAACACKGATTCTCTTATCCCCTAATACTGGACACA
Long Flanking Sequence:
TTACAATTTAAAGTCTATTTTAATAAGCTGTTGTTTTAATTTCAAAACTTCACAATGATTGTCTCTGATTATACTGGCTAGTTTACTTACCCAGAAGTCAATTGAATCTGCTTTTGTTTTCTCAATGTTAAGCTGAGCAGTGTAGACCTGAAGAAACCCCTGGAAAAAGAGATGGCCAAATTAAAAGAGATGCGAGACGCTCAAGCAGAGCAAGTGCCTGGTATGCTGCTTTTGAAATTAATTATGCCTGATTCCATCAGTGATTTCTCAGTGTTCATCTGTATAATTTAAGCTTTGTATTTGTAGTTGCAGTCATAACAGCAACTGACCTGTGGGATGCGATGAAGCCTGAGGTGGAGCTGACTGTGAAGGCACTTCTGGAACCTGGCAGTGAGGAAGAGGATGATGAAGAGGAAGAAGAAGAAGCTGCAGAGGGAGATAGAAGTGACAGAGACACTGCTGTCCAAATCGCTCAGTTTCTCCGAGAAAGCAAATACAAG[T/G]AAATGTCCATTAATTAACACGGATTCTCTTATCCCCTAATACTGGACACAGGCATTTCATGTATGGTGTTTATTCCTCTGCAGGAAGGCAGTGGGTCTATGCATGCGAGCTCATTCACTGTTTCCAGAGTCCTCATTCTTTTCAGATTTGGCTGATTTAAATGCAGAATCCCTCATCAACACACTTGCAACACTTTTTAAAGGTATGCATGTCATTTTAAGAAGTTTTTTTTATTAAGCTATTTAAAGTCTTACTCGGGACAGAAAACTGTTCAGGGTCTCACCAGCCTAAATCAGGGTTCCTTGTTCAAATTATATGCGAGACATCCTTCTGTGACTCCTCTTAGGCCCAGAAGAGGAGACGCCTGAAGCAGTGTCCACTGATGCTCCTCCCACACCACAGAAGGAGAGTGAAGGCAGAGAGAGTGAACTGAAGAAGCAAGAGATGTTGGTTCAGTACTTGAAAGATACAGAGTGCTTTGCTCTTCAAGTGGAAAGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19860
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 |
---|---|---|---|---|---|
ENSDART00000027088 | None | None | 507 | None | 14 |
ENSDART00000098126 | Nonsense | 1269 | 1389 | 30 | 33 |
ENSDART00000113351 | Nonsense | 1260 | 1380 | 29 | 32 |
The following transcripts of ENSDARG00000005058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 44815249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 44900750 |
GRCz11 | 2 | 44753748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGCCTGGAGTCTATCAGCCCCTGCTGTCCATCGCTGCCAAACTCCGT[C/T]GAAGAGCCAAACCACAGTTTAAGGCATGTTATGAGCATTAATGAAGCTTA
Long Flanking Sequence:
CAAAACATCATTGAAATGACCATATGCGTGAGTTAGGGGGATGAAGCTGAGTTCAGCAATCTCAGATGCAAATGCAGCAGGAACTGGTTTTTCCCGCATTCCCCCCTGGTGGGTTGTGAAGTCACCAGTCTCTGTTTTCAGCTCATGTTTTGAATTGTCAAAGATATCAGAATATTTGCAATATTTCAATTCTTACACAGGCACTACACACCTACTCCACGAGTTTGGAAATACTGTGCGCACATGCTGTTTTTCACAAAATGCATAGGGAAATGTGCAGCAAATCTGTTCTGGATGAGGATGATCGCTCATGTGTATCCTGTCTTTTTCCTCTCTGCAGGACGGAGCGACAGTGGGCCGATCTAGCCGTGTCTTTGTCACTGCTGTCTGTGTGCGAGAGAGGTTTTAAGAAGCTGCAGGAGTGCTGGGACTGTTACAGTGATAAACTAGCTGAGCCTGGAGTCTATCAGCCCCTGCTGTCCATCGCTGCCAAACTCCGT[C/T]GAAGAGCCAAACCACAGTTTAAGGCATGTTATGAGCATTAATGAAGCTTATTTACTGTATACTGAGCCATTCTGAGACGCCAAAATCACTGATGTTTTTATGTGAGCAGCTCATTAAATGCCGTGTGCTGTGTATTCATACATAATTATAATATAGTCTTCGATAGGAGTGTACGAATAACAATCCGTGGTTCGGAACCCACATGCCCGCAGATTAAGAACTTTTTTTTTTTTTTTACTTATAGATTAATCCTAAATTTGTAATGATTGCTTTGATTTGCTGCATTCAAATCTGTTAGGTAGAGAGAGATCCAGTTTTTACACTTCAGTTATTTAATTGTTTGCAACAAACTGAAGTACTTGATAACAGTTTCCAGTTCAGATACTGTGATTACTGCTCCAAAATGTGTTTATTTCCCCCTTTGAACGCACAATATTATATTTTGAGAAGCTTTTAAAAATTTTGGAGCAGTAAACGTGAGGCTGAATAATTAAAATGAA
Associated Phenotype:
Not determined