ZMP
sb:cb986
Ensembl ID:
ZFIN IDs:
Description:
LOC572121 protein [Source:UniProtKB/TrEMBL;Acc:A5PL99]
Human Orthologue:
INCENP
Human Description:
inner centromere protein antigens 135/155kDa [Source:HGNC Symbol;Acc:6058]
Mouse Orthologue:
Incenp
Mouse Description:
inner centromere protein Gene [Source:MGI Symbol;Acc:MGI:1313288]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25220 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10414 | Nonsense | Available for shipment | Available now |
sa19355 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25220
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114610 | None | None | 331 | None | 7 |
ENSDART00000114694 | Nonsense | 18 | 324 | 2 | 9 |
ENSDART00000121440 | Splice Site | None | 759 | None | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 3563909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 3539071 |
GRCz11 | 25 | 3664640 |
KASP Assay ID:
554-7715.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTAGGAAACGGGACGAGCGTTTGAAACGGGTTGTAGAGGCTCGAGTG[A/T]AAAGCGAAAAGGAGAAGGAGCAGGAAAAGAAAAAGAAGATCGAAGAAAAG
Long Flanking Sequence:
GCGATTTTACGGCTGTTTCCTTTTTTTAGAGAGAGAGAAAGTAGTTTCATTTATCATGCACTTGTTTTTGATACATTTATGTTGAAGGACAGCTACATTACAAACAGCAGATTAGTTTTTTTTTTTTTTTTACTCCATATGGCCCTTTTTTTTAATCCCTATAATTTTTTTAACCCTTGACATTACAAATGCCAATTTAGATTTTTTTTTTTATCCCATATGACTCATTATTAGATTTTCTTTTTCCCAAATGACCTTTTTTAACCCATATGATTTTTAACCCATGACATTACAAAGGCAAATAAATTTTTTTAAATTTATTTTTATTTTACTCATAGTATTTTTTTAAACGCATGACATTACAAATGGCAAATTCGATTTATTTATTTTAACCCATATGACCTGTTCTTTAAGTGTGAATGCAAAAGTATACTCAAAAGTCGATTGTGAATTTTAGGAAACGGGACGAGCGTTTGAAACGGGTTGTAGAGGCTCGAGTG[A/T]AAAGCGAAAAGGAGAAGGAGCAGGAAAAGAAAAAGAAGATCGAAGAAAAGATGGCACAGCTGGAGAAGAAAAACGACCTGGTCAGTGCTGAAGATCTTTAGACTCAATGTAGACCCATGCACTCCACTTGATTTGGATTCTTCATAAAGCTCTTGTTTTTCTCTAAGCTGCGAGTGGAGCGGATGGCGGAGGAGAAAGCCAAGAGGAAGGTGGCCACTAAACGACAGGAAGAACTGGAGCTGCGCAGGAAACAGGAAGAGGCGGCGAGACAAAAGAAACAGCAGCAAGTTGTAAGTCAATCCTGCAATAAAAGGTGCTATTTGGACCTGGTGTTAACATGCGTTCAGATTCATGGTTCTGTTTGGTGTAATGCACGAGGACTGAATGAATTGCGTACGTGATCTAAAACAAGTGAATTTGAAGAAAGTAAATATGGAAAATCTTGACATTGCGATATTTTGTTTTGCTATCTAAGGGTGCTTTCACACCTGCCTTATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10414
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 |
---|---|---|---|---|---|
ENSDART00000114610 | None | None | 331 | None | 7 |
ENSDART00000114694 | Nonsense | 84 | 324 | 3 | 9 |
ENSDART00000121440 | Nonsense | 547 | 759 | 12 | 21 |
ENSDART00000114610 | None | None | 331 | None | 7 |
ENSDART00000114694 | Nonsense | 84 | 324 | 3 | 9 |
ENSDART00000121440 | Nonsense | 547 | 759 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 3563624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 3539356 |
GRCz11 | 25 | 3664925 |
KASP Assay ID:
554-6222.1 (used for ordering genotyping assays)
KASP Sequence:
TGGARMTGCGCAGGAAACAGGAAGAGGCGGYRAGACAAAAGAAACAGCAG[C/T]AAGTTGTAAGTCAATCCWGCAATAAAARGTGYTATTTGGACCTGGTGTTA
Long Flanking Sequence:
GACATTACAAAGGCAAATAAATTTTTTTAAATTTATTTTTATTTTACTCATAGTATTTTTTTAAACGCATGACATTACAAATGGCAAATTCGATTTATTTATTTTAACCCATATGACCTGTTCTTTAAGTGTGAATGCAAAAGTATACTCAAAAGTCGATTGTGAATTTTAGGAAACGGGACGAGCGTTTGAAACGGGTTGTAGAGGCTCGAGTGAAAAGCGAAAAGGAGAAGGAGCAGGAAAAGAAAAAGAAGATCGAAGAAAAGATGGCACAGCTGGAGAAGAAAAACGACCTGGTCAGTGCTGAAGATCTTTAGACTCAATGTAGACCCATGCACTCCACTTGATTTGGATTCTTCATAAAGCTCTTGTTTTTCTCTAAGCTGCGAGTGGAGCGGATGGCGGAGGAGAAAGCCAAGAGGAAGGTGGCCACTAAACGACAGGAAGAACTGGAGCTGCGCAGGAAACAGGAAGAGGCGGCGAGACAAAAGAAACAGCAG[C/T]AAGTTGTAAGTCAATCCTGCAATAAAAGGTGCTATTTGGACCTGGTGTTAACATGCGTTCAGATTCATGGTTCTGTTTGGTGTAATGCACGAGGACTGAATGAATTGCGTACGTGATCTAAAACAAGTGAATTTGAAGAAAGTAAATATGGAAAATCTTGACATTGCGATATTTTGTTTTGCTATCTAAGGGTGCTTTCACACCTGCCTTATTCAGTTCGATTGAATCACACTAGAGTTCATTTCCCCTTTTGGTACGGTTCGTTTGGGCAGGTGAGAATGCAGCAATCGTACTCTAGTGCGCACCAAAAGCGGACCAAATAAGCGTACCGAGACCTGCTTGAAGAGGTGGTCTCGGTGTGCTTTCAAACGAACCCTGGAGCGGTTCGTTTGTGGTGAGAATATGATCCGTACTAAAACGGTCGAACCGCAAAAAGTACTGCGCCTTTTAGACCAATTCAGCTGCCGTAGGCCGATGCGCTGTGCATTATGGGATATAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19355
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 |
---|---|---|---|---|---|
ENSDART00000114610 | None | None | 331 | None | 7 |
ENSDART00000114694 | Nonsense | 84 | 324 | 3 | 9 |
ENSDART00000121440 | Nonsense | 547 | 759 | 12 | 21 |
ENSDART00000114610 | None | None | 331 | None | 7 |
ENSDART00000114694 | Nonsense | 84 | 324 | 3 | 9 |
ENSDART00000121440 | Nonsense | 547 | 759 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 3563624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 3539356 |
GRCz11 | 25 | 3664925 |
KASP Assay ID:
554-6222.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCTGCGCAGGAAACAGGAAGAGGCGGCGAGACAAAAGAAACAGCAG[C/T]AAGTTGTAAGTCAATCCTGCAATAAAAGGTGCTATTTGGACCTGGTGTTA
Long Flanking Sequence:
GACATTACAAAGGCAAATAAATTTTTTTAAATTTATTTTTATTTTACTCATAGTATTTTTTTAAACGCATGACATTACAAATGGCAAATTCGATTTATTTATTTTAACCCATATGACCTGTTCTTTAAGTGTGAATGCAAAAGTATACTCAAAAGTCGATTGTGAATTTTAGGAAACGGGACGAGCGTTTGAAACGGGTTGTAGAGGCTCGAGTGAAAAGCGAAAAGGAGAAGGAGCAGGAAAAGAAAAAGAAGATCGAAGAAAAGATGGCACAGCTGGAGAAGAAAAACGACCTGGTCAGTGCTGAAGATCTTTAGACTCAATGTAGACCCATGCACTCCACTTGATTTGGATTCTTCATAAAGCTCTTGTTTTTCTCTAAGCTGCGAGTGGAGCGGATGGCGGAGGAGAAAGCCAAGAGGAAGGTGGCCACTAAACGACAGGAAGAACTGGAGCTGCGCAGGAAACAGGAAGAGGCGGCGAGACAAAAGAAACAGCAG[C/T]AAGTTGTAAGTCAATCCTGCAATAAAAGGTGCTATTTGGACCTGGTGTTAACATGCGTTCAGATTCATGGTTCTGTTTGGTGTAATGCACGAGGACTGAATGAATTGCGTACGTGATCTAAAACAAGTGAATTTGAAGAAAGTAAATATGGAAAATCTTGACATTGCGATATTTTGTTTTGCTATCTAAGGGTGCTTTCACACCTGCCTTATTCAGTTCGATTGAATCACACTAGAGTTCATTTCCCCTTTTGGTACGGTTCGTTTGGGCAGGTGAGAATGCAGCAATCGTACTCTAGTGCGCACCAAAAGCGGACCAAATAAGCGTACCGAGACCTGCTTGAAGAGGTGGTCTCGGTGTGCTTTCAAACGAACCCTGGAGCGGTTCGTTTGTGGTGAGAATATGATCCGTACTAAAACGGTCGAACCGCAAAAAGTACTGCGCCTTTTAGACCAATTCAGCTGCCGTAGGCCGATGCGCTGTGCATTATGGGATATAGA
Associated Phenotype:
Not determined