ZMP
ncapg
Ensembl ID:
ZFIN ID:
Description:
Si:dkeyp-26a9.1 protein [Source:UniProtKB/TrEMBL;Acc:Q58EG5]
Human Orthologue:
NCAPG
Human Description:
non-SMC condensin I complex, subunit G [Source:HGNC Symbol;Acc:24304]
Mouse Orthologue:
Ncapg
Mouse Description:
non-SMC condensin I complex, subunit G Gene [Source:MGI Symbol;Acc:MGI:1930197]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32673 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32674 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39609 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19499 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32673
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102609 | Nonsense | 190 | 1003 | 4 | 21 |
| ENSDART00000133659 | Nonsense | 190 | 1003 | 5 | 22 |
| ENSDART00000142879 | None | None | 178 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 22335805)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22870972 |
| GRCz11 | 1 | 23561711 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATAAATAAATAAATTTAATTCTGTTTGTGTATAGCTTATGTTCTGCTTT[T/A]GGAAAATGACTCAAACCCTGAGGTTCGTCGTGCTGTGCTGTCCTGCATTG
Long Flanking Sequence:
TTTTTGAACTTTTTGTTCAATTTCCTTTTGGAGGTAATGTCACTAAACTGCATAATGTCATTAAAATGCAAAATGTTTGTCTACCTAACGTTTCCTTTTTATCTTCATATATTTCTCTCTCAGTCTCATGGTGCAAACAGCCATGCCGTGCGATTTCGAGTTTGTCAGCTGGTGAATAAATTGCTGGGCAGTCTGAGTGAAAACGCTCAGATCGACGATGATCTGTGTGATAGGATCCATGAGGCCATGCTGGTCAGAGTCACAGACAAATACCCTAATGTCAGAATTCAGGCAGCACTGGCCATGGCCAGACTCCAGGACCCCACTAATTCGGATTGCCCAACTATTAAAGGTACTCAGAAATGTCTTACTAGAGCTCTTTCAAAAGGATATTGAGGTGCATCTTTCCCTGGCTAACATTTCAATACAATTGATTTATGAATTAAGTAATATAAATAAATAAATTTAATTCTGTTTGTGTATAGCTTATGTTCTGCTTT[T/A]GGAAAATGACTCAAACCCTGAGGTTCGTCGTGCTGTGCTGTCCTGCATTGCACCTTCCGCCGTCACACTTCCTAAAATCTATAAGCGCACAAGGGACGTCAAGGAGAAAGTCAGGAAACTTGCTTATGAGGTAATTTTATTTGACAGAGTAATAAGTAAGGAAAGTTAACAAATAATAATTATCATTCATAATCAAAAACGCACATTGTCTAAATTAGAATCTAACTGACCCTAAATGTTTAAACATTAGTATGCATTACATACCGTAAGTTTATACATTTCCCACAGGTACTTGCAGAGAAAGTGCATATTCGAGCTTTGACAATTGCTCAGAGAGTAAGTCTGTTACATGAAGGCCTCAGTGACTCTTCAGGTAAGAAAATGGATTGTTAATTAAGCTGTCAATATATATATACAACTGTATGAAATTTCCATAACATGTTTGCAGACAAGTCAGTAAATCATGTTTTTCTCTCAGATTCAGTGAAGGAGGTTGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32674
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102609 | Essential Splice Site | 377 | 1003 | 8 | 21 |
| ENSDART00000133659 | Essential Splice Site | 377 | 1003 | 9 | 22 |
| ENSDART00000142879 | None | None | 178 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 22336984)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22872151 |
| GRCz11 | 1 | 23562890 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATGGATAATAAACTAATATTCAGCTTAACAAGAGCCTTTTTGTTTCA[G/T]TTTTCTAAAGAGCATTACTCAGCTGTCTGAGGCGCAAAGAGCTGATATGA
Long Flanking Sequence:
GTTGCTTTAATCAAAACACTGAAACCAGGATATTTCAGTCACTGCAGCAGAATTCAGTCCACCAATATAATTTTTTTTTTTTTTGTAGACAAAACCTATAAAAAAATGCTTTTTTAAACTGATTATTTACAAGTTTATTTTAAAATGTTAAACTAGCTACACATGCTGTTGTTACTATTATCATTATCATTCTTATTCTTTATTATATTGAGTTGGTGCCAGTATATTTGTCTTATGCAGGTTTAATTCTGTCTCTGTACAGGAAACTGATTCCTGTCAACTCCCTCACATGTGAAAATGTGTTGTACTGGAGAGCACTGTGTGAATTTGTCAAGAGTAAGGGAAATGAGGGTGAAGAATTACTGGAGCAGTTACTCCCCGAGGCAGCAATCTATGCTGAGTATCTATACAGGTGAATGTGCCCTACGCTTGTGTTTACTGTCTTGCTTTTAAATGGATAATAAACTAATATTCAGCTTAACAAGAGCCTTTTTGTTTCA[G/T]TTTTCTAAAGAGCATTACTCAGCTGTCTGAGGCGCAAAGAGCTGATATGACACAGCTTGAGATGGTGATGACCCAAGAGTTTGTTGGGCAGCAGTTGATTCTGCTTGTTGGATGTCTGGACACTTCCGAGGAAGGCGGCAGGTCTGATTTATCAATATATCTGAGGCTGGTTGCATAAACTGGAGACATTTAGCTGTGATAATTCAGCAGAGGCTTTTTTTGAGCAGAGTTGCAGTTATCTAAATTTAGTTGCATGAATCTGTAATGTAGAGGTGCAAGTGGACGTAAATCTTTTGTTGCTCATTGTAGAAAAAATGTTTTTGTTCAACATTCAATTCTTTAGGGTTTGATCATTTTATTTTCTGAAGACAATATTGATATTTAATTAATTGCATCTAAAGGTAAAATGTTTTAACCTTCTCAACTACTGTTTAGGAAGCGCATGGTAGCAGTGCTGCAGGAGATACTTGTGATGCCCAACACACCTGTTTCTCTGATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39609
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102609 | Nonsense | 432 | 1003 | 9 | 21 |
| ENSDART00000133659 | Nonsense | 432 | 1003 | 10 | 22 |
| ENSDART00000142879 | None | None | 178 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 22337442)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22872609 |
| GRCz11 | 1 | 23563348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTAACCTTCTCAACTACTGTTTAGGAAGCGCATGGTAGCAGTGCTG[C/T]AGGAGATACTTGTGATGCCCAACACACCTGTTTCTCTGATTGGTCTGCTA
Long Flanking Sequence:
TAATAAACTAATATTCAGCTTAACAAGAGCCTTTTTGTTTCAGTTTTCTAAAGAGCATTACTCAGCTGTCTGAGGCGCAAAGAGCTGATATGACACAGCTTGAGATGGTGATGACCCAAGAGTTTGTTGGGCAGCAGTTGATTCTGCTTGTTGGATGTCTGGACACTTCCGAGGAAGGCGGCAGGTCTGATTTATCAATATATCTGAGGCTGGTTGCATAAACTGGAGACATTTAGCTGTGATAATTCAGCAGAGGCTTTTTTTGAGCAGAGTTGCAGTTATCTAAATTTAGTTGCATGAATCTGTAATGTAGAGGTGCAAGTGGACGTAAATCTTTTGTTGCTCATTGTAGAAAAAATGTTTTTGTTCAACATTCAATTCTTTAGGGTTTGATCATTTTATTTTCTGAAGACAATATTGATATTTAATTAATTGCATCTAAAGGTAAAATGTTTTAACCTTCTCAACTACTGTTTAGGAAGCGCATGGTAGCAGTGCTG[C/T]AGGAGATACTTGTGATGCCCAACACACCTGTTTCTCTGATTGGTCTGCTAGTGGAGAAACTTGTCAACATTTTGCGAGATGATGCCCAGAAAATTCAGATGGTGAGTCCTTGTTGAACAACATATTACTTCTGAAAAATCTTCTGTTTGTGAAAGAATGAGGTTTAATCAGTATATTTCTTTGAGATTGACCATGTAGTTTTTCTTGAATGTGCCGACATATTCAAAATTGACCCTAATTGGGTGCTAAAAAGCTGAATAAATAGTTTTTCATGCTTAAAATAAGTTTAATCATTGGCTGACAAATAAATGTAATTGGTTGACTGTGCTATATTTTCTTCAGGTTGCTGAAATAATCTCTGATGTGAGGGAGCCTATTTTCCCCATCTCTGAGCCAGTGGATGAGAATGAGAAACGCAGAAAACAAGTCAGAGTGAGTTATATTTATAAATCACTGGTGCCTAATGTCATAAATCGATTGCATTCATCTTGATTTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19499
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 |
|---|---|---|---|---|---|
| ENSDART00000102609 | Nonsense | 762 | 1003 | 15 | 21 |
| ENSDART00000133659 | Nonsense | 762 | 1003 | 16 | 22 |
| ENSDART00000142879 | None | None | 178 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 22340887)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22876054 |
| GRCz11 | 1 | 23566793 |
KASP Assay ID:
2259-0565.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGTAACCGAGGATGACCAAAGACTGCGCCATTGTCTGGGAGTTTTCT[T/A]ACAACTGTATGCTCGAGCAAGCAGGTATGCATCTGGTCAGGTACTTTTGA
Long Flanking Sequence:
ATTAAAATGTTCTATCGCGATTTATAAATTGATATTTACTGTTCAATGAATGTGTATCTATTTTTGGATGTATCATTCAACACTTGTATGCCCAGCTTTACATAGGTGTATGCTTTATTGAGAAAGATGTCCTTGTGAGCATGTTAACTCTACACTACAAATTGCTGTGAAGATTATTAAAATAACTGTTATGGCTTTCTAATGTTACAACGAGTCAGTGTAGAGCTTTATTTTACAATTCATTAATATGGAAAGTCCTGTAGCCGATTGGCTAGCATTTTGACAATTTGCCCTAAATGTTCTGCAAATGCTGCATTAAATGATATTAACTGATATTTTTCAGGTCTGCGAGCTTCGCACAGAGACAGCAGAGGGTCTGGCCAAGCTGATGTATTGTGGAAGAATCTTAAGCCCAAAGCTGTTGTCCCGCCTGGTGTTACTGTGGTACAATCCTGTAACCGAGGATGACCAAAGACTGCGCCATTGTCTGGGAGTTTTCT[T/A]ACAACTGTATGCTCGAGCAAGCAGGTATGCATCTGGTCAGGTACTTTTGAACAGAAATATGATGGCAAATTCAAATGCCAAAATGAATTGAGTGCACTGGTAATGTTTACTTGCTAGGTCAAGTGAACTGCGAGAAGATAACAGACCTACACACGCGGAAACTGGCGGCCGTTCGTGTATTATATAAAAATGGACTTTTAATTATTTAACATTCATTTAATCTATCTAAAAAATGTTATTTTGTAAGTGACGTTTAAAGTAGTGGTTCTAGATTTCATCAGTGTGTGTGTGTGTGTCCCACAAAAGATGAAATCTTAGAACCACCCCTGTAAACAGATTAAAATCAAAAATTGTTTACGTGTTGTATTTTATATACTTTAAGTCTCATTGATTCAATGACTTTCTTCATAAAGACTTCATGTTTCAATAATTTTTAAAGAATATTATAGTGACAGACATTTAGATGGGTGTTTGTCGACACCTATTGGCACAAAAATGTA
Associated Phenotype:
Not determined