ZMP
cenpi
Ensembl ID:
ZFIN ID:
Description:
Cenpi protein [Source:UniProtKB/TrEMBL;Acc:Q08C73]
Human Orthologue:
CENPI
Human Description:
centromere protein I [Source:HGNC Symbol;Acc:3968]
Mouse Orthologue:
Cenpi
Mouse Description:
centromere protein I Gene [Source:MGI Symbol;Acc:MGI:2147897]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42432 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1693 | Essential Splice Site | Available for shipment | Available now |
sa35744 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13382 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42432
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074438 | Nonsense | 83 | 759 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 42747264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 40904369 |
GRCz11 | 14 | 41271623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTTAAATCTTATAAGTTGTGTCTGCTTGTGTTTTTGCATGTTTTAGTT[A/T]AAGCTGGCACAACAGTCAGAGGCAATGATGAGCTGGAGAGGAGTATTTTG
Long Flanking Sequence:
TGGCGTTTGGTTTGAATGGGTTGTTGCAGCGAGTTAGCGACCGAAGCGAAAACGAGAGACGACAACAAATAATATTATGTAGCCACAAAATGGCTGGTTTATCTAACCTTACGGGGTTAGTCTCCGAGCCGTCCGGAGAAGCAGAGTCGTCCGTCTCCTCCGTGAGCAACAGAAGTTTGCGTTTGGCAGAAAAAGAGAAGAAAAAAGGCGAGGCGGATCCCTTTACTGCAGCGGCGAAGTATCTGTCTCAATGTAAGTGCTGCCAAAACACATCAGAAATACTTTACATGTCTTTTTAAAAGCATAACTATTCAATATTGTGTCAAATATCCCATTATTTGTTAACTATTAGTTGTTTTTAGTAAACTAGTTAGTGGCTTCGTGGTGTTAGGTCTTTTGTTTGTGTTGACGGGGTCGCTTCATCATGTGCTGTATCCACATGTAGCGTTAACGTTAAATCTTATAAGTTGTGTCTGCTTGTGTTTTTGCATGTTTTAGTT[A/T]AAGCTGGCACAACAGTCAGAGGCAATGATGAGCTGGAGAGGAGTATTTTGGTGGTGGAGACGGTGGCTGTCAGTAAGGGTCTTCCCCCTGAGGTCATCACAGTGCTGCTGGATTTGGCCTTGAGTCTCAATGCAGGTAACGTTAACTTAACTTTATATATTCAGGGGATGGTTGGCTTTACTAGATGTATTTGTTTCTGCTAGGATTCAGGTTATTAAAGATTTGTTTTGATCTGAAAATAGCAAAGTAGAATAGAAAGTAGCAAATTTGGGCATCATGTTCAGGCCAAAAACGACAAGATACCAAAGTAGATGTTGGGTGTTCTTGTTTGCATTCATTTTGTGTAGGTTTTGCCATTCAGGATATTCACAAGTGTCATTTAATTAGATGGAACAACATGTGTCCTTCTTCTCTATTGTAAACAAACCATATTAAATCATATGTTTGCATCAGTCTGACAGAAGGCTTGCACTCCAGACTGTGGTGAATGCACTCAGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1693
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074438 | Essential Splice Site | 204 | 759 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 42744253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 40901358 |
GRCz11 | 14 | 41268612 |
KASP Assay ID:
554-1639.1 (used for ordering genotyping assays)
KASP Sequence:
TTTGTGAATTGTTTTTCACCTTAATTTAAAATRTAMAATTTTTTTCTTGC[A/G]GTGCCCTTTTATTTGCCACTTGTTATATCTTTTAACCACACGGGAACATG
Long Flanking Sequence:
ACAGCCTTAGACTTCAAGTTCCTCTGTTTTACTTTTAAAGAAGCAAACCAACAAATCACTGAAAAGGTTAAAATGGATTCTATATAGGCCATATAAAATGCCACCATCAGAGTCCTATCAATTTTAAAATTTGTTTTAACCGTGCATATAAAAAAAAAAGACAACCAAAGAATAGAAGTTTCTTATCTGTTTTTTCTCTTTTTATCTGTTAATTTGCATGTATGTCACAGTAGGGAAGAAAATATCTGTTTTTTTTAAAACATTTGTTAACTTGTTTTCTTTTAAGGTTCTATTTCTCCGCTGGGTACTCACTGTTTTTGACCTGATTGACTGCAAAGATGACTTAAGATCCATTTATGGCTTCATTTTCAGCTTTGTGACAGAAGAAACTCTGGTTAGGATTGTCTTGCAAATGCTCATTTTAATTCAATGTGTTTATCTTGATATCGTTTTGTGAATTGTTTTTCACCTTAATTTAAAATGTACAATTTTTTTCTTGC[A/G]GTGCCCTTTTATTTGCCACTTGTTATATCTTTTAACCACACGGGAACATGGTGAGTTGTTAATTATGTGGTTAATTAATTTTTAAATGTATGCGAACGCTGCAGTATTACAGGATGTTATTCTGTTGTTCTTCTGCTTGTTTTCCCCTACTCAGTTCACCCGTACAGAGTCCGGAAACTGTTGGATATTCAGGCAAAAATGGTAATGAAAAAAAAATAAACACCTCAGTATCCTTTATTATAAATACATACTTATTGCAGTGGTGAAGAATGTTTGTTTTGACCAGAAATATTTCATATAACTCTGATTTTTCCTTTTTAGGGCAGACAACCATTTCTCACACAACTTCTAGCCCTCTACAAAGTGTTTCGCCCAGACTTAGTGACACTCTCTCTTCCGTCAAGAGCAAGGGTTAGTGTATTCAATACTGTTTTCTCTAGCAGAACTTTTTTTTCTGCAGGTTTTTCAGGCTCTTATACTGCAATTGTTTTTTTTCCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35744
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074438 | Nonsense | 489 | 759 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 42733390)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 40890495 |
GRCz11 | 14 | 41257749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATCTGAATGTGCCTTTTCACATTGTCGTCCTCATAGTGTAGTGTCATC[G/T]AGTGTCTGAATAGCATGCTGGTGAAGTGGCTGACATGGCACTCAGTTAGT
Long Flanking Sequence:
AAAAGTGCTGTCTTAGTTTCTGTAAATAATAATGGGCAGTTTTGTCATTATAACTAATGCCAGAAATGACAAATTGTCTAAAAATTGGTGGGCTTTTATCCATCGGAGCAAAAAAAAAATCCTTTTGCAAAAATCTCTAACATTGTTTTCTTTGTCTTCAGACATGAACAAGCTTCTCTTTGAGCCGCTGAAGCAGCTTTATTTTACCTCGACAGTATTTTTCAAGGTTTGTATGTTCTTGTTCTGTTTTTAATGCACTTTCTCTCGGTTTGTGTGAAGCACAGGCATTACTGCAAGAGCCAGATTATGTCAATGAATGCTAAAGCAGTTCGGAGATAAGTGAATTACTCTTTCCACGCTAAGCGGTGGCATCTTCACACTTTACTGTTGTTTGAGTGGTGTTATTTAAGCTTGCAGCAGTTGCAAGCAGGTTCAGATTTTTTTGCACCATTATCTGAATGTGCCTTTTCACATTGTCGTCCTCATAGTGTAGTGTCATC[G/T]AGTGTCTGAATAGCATGCTGGTGAAGTGGCTGACATGGCACTCAGTTAGTGCATCAGAGGGCAGTTTGGATATCAGTCTTAACAGCAACAGCACCATGTGAGTATCCCACAATTATTCAAATGTTTGAAATCTAAATATATTATGGTTTCAACCAACTATAAGTCAAAAAATAAATAAACAAACAAAAGTTTCATTGGCATGTCACATTTTTTCAATTTAATTAGACACAATGTAAGGTGCCTACTGGCAGTAATAAGACTTGCTAACACTTTATAATAAGGTTTCATAAGTTAGTTATGTATTTACTAGCATGAACTAATAATGAACAAAACATTTATTTATCATAGTTTAACATTTACTGAATGCATTATTAAAATCTAAACACTAATAAATCCATAAACACTGTTATAAATCTATTGTTGTTTGTTCATGTTAGTAAATGCATAAACAAATACAACCTTATTGTAAAATGTCACTCAAGACTTGCGCATATTTATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13382
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 |
---|---|---|---|---|---|
ENSDART00000074438 | Essential Splice Site | 566 | 759 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 42730479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 40887584 |
GRCz11 | 14 | 41254838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACTGCCACGTTCTTCTGCTCAACCAGACACTCGCCTTCTATGAGACGG[T/C]ACACTCCGCTATGATTAACTTAATTAACATKATGTTCTTGGCAGGGTGAC
Long Flanking Sequence:
CGTGTATTGCTTCTCTCTCACTGCTGATTTGGTTATTTTTTTATTACATTACCGAAGTGCACAGCTGAAGGAGAAATTATGATCAAGGGCAAAACCCTGTTTGACTGCACCGGTGTGCCATGCATCAATGCGATACGCCCATTATTCCCTTTTTCACTCTGGGTCTGCGCTGTGCGAATTGTGTGGGTGCCAAACATAGCACAAAGACACATCTGGTGTATACTAGGAGTGATTTAAAGCTGATTTATTGTTCACCTTAGGAGAAATATAGTACACCCTACAAGGGAAAACTCACTTTTCACATGCTATTTTGTGTGTATGCCTTCAAAAAGAATAAATAATCCCCTATTTTTATTTTTCTAGGACTATGACCTTGTCTGGCTTCATGGACTCCGTTATGGAGCTTGTGCGCTTTGTGGGACTGCTGGCGTCTGAGGGACTCCGTCTGGAGAACTGCCACGTTCTTCTGCTCAACCAGACACTCGCCTTCTATGAGACGG[T/C]ACACTCCGCTATGATTAACTTAATTAACATGATGTTCTTGGCAGGGTGACATCAGCTGAAGTTCCTGCCTGAGATTTGTGTGTTGATTTTTCAATCGTAGATTTAGCACAACAAGCAGCGATGATGTTGATATCTTTTAGGGATGCACAATGTATATTTCATCATCGATATCGCAGTGTGCAAATCTGTATAGTCATATTGCAAGATCTGTAATTTGAGATTATTATTATTATCCATGAAACACAGTTCAGAACATGTAATTTTTTGGGGGTGATATTGCAAAAAAAAAAAAAAATCACGATATCATGTTTCATATAATTCAATATCGATAATTATTGAATACATTTTACCTGTGCATTTAGGAATGTTAGGATTTAACCACTTTATTTTAATTTACCAACATACCAACTACTAAGGCAATTAATTTTAATAGTCAAAAACAAATATTTCAACAAAATATCTCATATCTTAAAGAGACTTAAACTTGATAAATAAAAAGT
Associated Phenotype:
Not determined