ZMP
ncapg2
Ensembl ID:
ZFIN IDs:
Description:
condensin-2 complex subunit G2 [Source:RefSeq peptide;Acc:NP_001082961]
Human Orthologue:
NCAPG2
Human Description:
non-SMC condensin II complex, subunit G2 [Source:HGNC Symbol;Acc:21904]
Mouse Orthologue:
Ncapg2
Mouse Description:
non-SMC condensin II complex, subunit G2 Gene [Source:MGI Symbol;Acc:MGI:1923294]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16326 | Essential Splice Site | Available for shipment | Available now |
| sa10405 | Essential Splice Site | Available for shipment | Available now |
| sa2364 | Nonsense | Available for shipment | Available now |
| sa12675 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16326
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 |
|---|---|---|---|---|---|
| ENSDART00000084090 | Essential Splice Site | 128 | 1140 | 3 | 26 |
| ENSDART00000084093 | None | None | 322 | None | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41600431)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39936688 |
| GRCz11 | 7 | 40207705 |
KASP Assay ID:
2259-9278.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAAKGACAATTATACCACTCTTCTCAAATGTGCCCAGATGCTGAATGG[T/G]ATGGACTTTTATTGTCACTCTTCATCTAGACATTTCTGNTTTTTTGTGAG
Long Flanking Sequence:
ACCAAATGAAAAACAAATGAGAAAACGTTTTGAAGGGGGCGGGACATGTCAGATACTAGAGAGCATTTGATTGGCCAGAAGATTTGATGAGAAACTGAGGTGATGTCAAAATAATCATTGATCCATTTAGGCTAAGGTGACATACTGGAAGTTTTGGATGCTTTTAATGAGGTTTTTATCTTCTAAATGGAAATGCTTTCACTGTTTTGAAGCACACTAGCATGTATATATCCTTACAACTAGCAAACTGATACTTTAACATCTAAAAAAACGCTTTTATTTAACTTTATTTGACAATTTTTAGTTTTTAAACTTTAATTACATTTTTTGATTTCTTTAATGCATAGGAGAATGATTGAAGGCGTTGTTCTTGTTTACTTTCAGATACAAACCATGGCTGTAATAGAGGGCGTCACTATTGTTTCTACAGTCTCTGTAGACGCTTTGCAGGAAAAGGACAATTATACCACTCTTCTCAAATGTGCCCAGATGCTGAATGG[T/G]ATGGACTTTTATTGTCACTCTTCATCTAGACATTTCTGTTTTTTTGTGAGAGAGAGCACATGACAGAATATTCAACAAAGGACTAGTTCACCTAAAAATGTAATGTTTGTTGTTGCTCACTTATCCTCATTTTGTTCCAAACTTCTTTGAACACGACTGAAGGTGTTTGTAATTAAGCGTGTGGGTTTTTTGTCTCTCCATTGACAACCTACTGTACGCAACTAATGTTCTCCAGGCCCAGATAGGCAGTAAAAACTTGATTAAAGTAGTCCATGTTACTCCGGTGGCTAAACTGCAATTTTATGAAGCAACTGGGAATGCTGTTTGTGCACAAAGACAAAGAAGAACATTCATATTGAACAATTGTGTTTTTATTACCTTTCTGGGCTGAGAATGGCTATTGTGTAGGCTGTCAATGGAGGGAGAGAACCTTCACAAATTTCTTTAAAATTAATATATTCATTGAACAAAAGTCTTAGAGGTTTGGAACAACATGCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10405
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 |
|---|---|---|---|---|---|
| ENSDART00000084090 | Essential Splice Site | 442 | 1140 | 10 | 26 |
| ENSDART00000084093 | None | None | 322 | None | 9 |
| ENSDART00000084090 | Essential Splice Site | 442 | 1140 | 10 | 26 |
| ENSDART00000084093 | None | None | 322 | None | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41605470)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39941781 |
| GRCz11 | 7 | 40212798 |
KASP Assay ID:
554-6147.1 (used for ordering genotyping assays)
KASP Sequence:
GCTGGCTAATGACACCAGCTCTCCAGATGTCCGCTGCTCTGTCTTCATGG[T/C]AAAGCCCCTGGCTGACTGTCTGTCACTNNNTGACAAAGTGCTGCTTGCTA
Long Flanking Sequence:
TTTTGTTCTCTGTAGGCTTTGCTAAGGTAACTCTGTAAAAGCCACCAATGTCTCCCTTTGCATTGAACTTTGAGCGTCTTAAATTTAGAGATGTTGTTTATGTTCACACAGCTACATTACACATCAACTAAACTTTAAAATTTGATATCATAGTGGACCACCCCTTTAAAAAATATTAAGTTGGAATAATGCAAGATGATGACTTTAACAAAGGCATATGCCACTGAATAACAAGCTTGAATTCAAGAGCAGTCAGAAAAGACATCAGCATGTTGTACTGCTGTGAGACTTGTCTGTGTCTGTGTGTGTGTGTCTGTAGGCTCTTCTTGATGACCCTCAGCCCCTGGTGCGCTCCTCTGCAGTGCTGGGTGTGTGTTCAGTGCTGGCTCGCTGCTGGGAGGTCATTCCATCTGCTGTCATCACTGACCTGCTGGAGAAGCTCATCCTGCAGCTGGCTAATGACACCAGCTCTCCAGATGTCCGCTGCTCTGTCTTCATGG[T/C]AAAGCCCCTGGCTGACTGTCTGTCACTGAGTGACAAAGTGCTGCTTGCTATCTTTTCAGTTTTTGTAGTTTGTAGAATCCAATTTAAAGCCATCTACAGCAGGGGAAGGACAATGTCTTCTGCTCAGTGATTTCAGCATGAGTTGAGCTCCACACTAAAAAGCTTTTTAGGGGGAATGGAATGTACCCAATCATTAATTTATAGTTCAGAGGTTAGCACTGCTTAAAAAATCATCTTAGCCTAAAAGACTTGAAATTAATATGTTCACACTTCATTTGAACTTTTGTGCTCATAATGACTAGGAACATAATTACAGTTTTAAATATCCTGTCAAATGGCATTTTTTTTGCTTGACTAAGCCTTTGTTATACCCTGTTTGTTTGCTCTGCAGTGTATTTCTATAATTTTGGATAACAGTTTAAGTCATCCACTCATGGAAAAACTGTTGCCTGCATTGAAGAGCAGTCTCCATGACAGCTCTGAAAAGGTGCGTGTTGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2364
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 |
|---|---|---|---|---|---|
| ENSDART00000084090 | Nonsense | 448 | 1140 | 11 | 26 |
| ENSDART00000084093 | None | None | 322 | None | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41605878)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39942187 |
| GRCz11 | 7 | 40213204 |
KASP Assay ID:
554-2876.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCTTTGTTATACCCTGTTTGTTTGCTCTGCAGTGTATKTCTATAATTT[T/A]GGATAACAGTTTAAGTCATCCACTCATGGAAAAACTGTTGCCTGCATTGA
Long Flanking Sequence:
ATCTGCTGTCATCACTGACCTGCTGGAGAAGCTCATCCTGCAGCTGGCTAATGACACCAGCTCTCCAGATGTCCGCTGCTCTGTCTTCATGGTAAAGCCCCTGGCTGACTGTCTGTCACTGAGTGACAAAGTGCTGCTTGCTATCTTTTCAGTTTTTGTAGTTTGTAGAATCCAATTTAAAGCCATCTACAGCAGGGGAAGGACAATGTCTTCTGCTCAGTGATTTCAGCATGAGTTGAGCTCCACACTAAAAAGCTTTTTAGGGGGAATGGAATGTACCCAATCATTAATTTATAGTTCAGAGGTTAGCACTGCTTAAAAAATCATCTTAGCCTAAAAGACTTGAAATTAATATGTTCACACTTCATTTGAACTTTTGTGCTCATAATGACTAGGAACATAATTACAGTTTTAAATATCCTGTCAAATGGCATTTTTTTTGCTTGACTAAGCCTTTGTTATACCCTGTTTGTTTGCTCTGCAGTGTATTTCTATAATTT[T/A]GGATAACAGTTTAAGTCATCCACTCATGGAAAAACTGTTGCCTGCATTGAAGAGCAGTCTCCATGACAGCTCTGAAAAGGTGCGTGTTGCCTTTGTGGGCATGCTCCTCAAGATCAAGGCTGCTCGGGCTGCCAAGGTAAGAGTTTAAATCACACTTTGTTTTAATTAATTATTTATGGCACTGTATTTTTTTTTTCATCAAATGTTTGCCCACATACTTATTCCTATATTTTCCCAATTTGTCATGTTCCAGTTTTGGAAAGTTTGCTCCCTGGAGCATCTTCTGGCTCGATTGGAGATGGACTCTGCTCCTGTGTCCAAACGCATTGTCAATTTGCTGTTTAACTCGTTCTTTCCAGTCAACCAACCAGAGACTGTCTGGTGTGAACGATGTGTCACCTTGATTCAGACAAACCCTGGAGCGGCTCGCAAGTTTTACCAGCATGCTTATCTGTACACGGCTCCTGCTAATATAGGTGAGGGTGCCTTAGATAAGCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12675
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 |
|---|---|---|---|---|---|
| ENSDART00000084090 | Essential Splice Site | 657 | 1140 | 14 | 26 |
| ENSDART00000084093 | None | None | 322 | None | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 41608253)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39944563 |
| GRCz11 | 7 | 40215580 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTGCAAAGTTTGGATCTTCTCTGCCCCARTACCTTAAAATCTTTCAGG[T/C]AAGAGGCACGTTCAAGCGATGAAACCAAAGGACAATTTAAAGATCAAAAT
Long Flanking Sequence:
CTAGAGGGCCTCAGTAAATTTAAAGGTGAGCACAAAACATTGTTTAATGTTTTTTAAAATACAAAAAACTTTTTTTTTTAAATAAGCTAATATAAGATAAAAACTACTTATTTAACTGTCCGTCATCAACATTTTTAGCATTTTCTTAATGTACTGGAAAGTATGAATATATGAATAACTAATACAAAAAAAACATAAAATCTGTAGTAGTAAATGCGCACACACATATATGTATGTAATCTGTTGAGCAATAATGTAAAACTGTAAACAATACATATTTATATATATAAATGAAAATGCCTATGTTTGCTATTATTGACACTAGCTGCTGGAAGATGTTCTCTCAGTTCAGGACACCTCCTCCATGGCCAGCCTGCTGGAGATCCTCGTCATTCTGTGGAAGAGTGTTCAGAAATCTCTAATGGCTAATCAAGAGGCCTTTAAGTACACCACTGCAAAGTTTGGATCTTCTCTGCCCCAATACCTTAAAATCTTTCAGG[T/C]AAGAGGCACGTTCAAGCGATGAAACCAAAGGACAATTTAAAGATCAAAATGGCACACTATAATCACATCTTCAAAGCTGATGCAACATGGGTGCAACATGACGCATTTGTGTGTGTGTTTGTGCATGTGCGCAGGAGGAGCGATGCAAAGCACCTCTCATTCTTCTAGCATCTTTACTTCCTGCCTCTGCTCTTCCAGCTCTGAGGTTAGTACACTTATTACACTATAGGAACTTCCCCTTAAAAAAATCCCTAAATGCCCCATTTTAGAAGAATAATGCAGCCAACAATGAAAACACTCTTTCTTGACATAAGGTGAATTGTCTAAATAGTAAAAAATATTAACAAGTGTACCAGCAAAGGACAGTTTTAAAAAGAACAGCACTTCTAAATATATGTTTTTCTGATGATTATCTAGCACAGTCCACGTGCTTCAGTCAGTCGTCTCCCCAGAACAGCAGGTTGGCTCAAAAGCGAATTGCCAATTCTAATTTCCATTTG
Associated Phenotype:
Not determined