ZMP
si:ch211-152h14.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
CENPF
Human Description:
centromere protein F, 350/400kDa (mitosin) [Source:HGNC Symbol;Acc:1857]
Mouse Orthologue:
Cenpf
Mouse Description:
centromere protein F Gene [Source:MGI Symbol;Acc:MGI:1313302]
Alleles
There are 13 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12296 | Nonsense | Available for shipment | Available now |
| sa23122 | Essential Splice Site | Available for shipment | Available now |
| sa11610 | Nonsense | Available for shipment | Available now |
| sa10281 | Nonsense | Available for shipment | Available now |
| sa23121 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa12055 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12296
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 |
|---|---|---|---|---|---|
| ENSDART00000077444 | Nonsense | 256 | 1737 | 5 | 18 |
| ENSDART00000087589 | Nonsense | 256 | 2861 | 5 | 26 |
| ENSDART00000128418 | None | None | 953 | None | 13 |
| ENSDART00000135517 | None | None | 562 | None | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 32946069)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32787800 |
| GRCz11 | 17 | 32740311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCCTCTGGGATGCCGTGGTCTTATGATGACACACCAATAAAACCCCAY[C/T]AGCAGTTCACATCAGGCGCACCGAGTGACACAGTTGGATCACAGCAGATG
Long Flanking Sequence:
GCAACTCCTGCAACGCCTAATCACTGGCAACAGGGTAAGAGATTAATTTAATGAATAACAAACGACAATGCAAAACACATGCAACCAACTTCAATACTCAAATATTGCATTTTCAGACTCCAAAATCACAGACTTGCAGGAAAAGTACAATCGAGAGGTTGAGGAACGTAAAAAACTAGAGGCTGAAATCAAAGTAATGCATGTGAAAGTAAGTAAAACGCACAATTGTTTGGTAAAGAATATTGTAATTAACTAGTAGTTATTAAATTACTAATTAATAATAATGCAAATCTCTTTTGCATCACTTAAAGCTTCTAAACCAGTCTTCGGTGAGCCATAAGGACATTGCAAGACAGCAGACAGGGTCCTCAATATTTCCTTGGCAGCAAGATCAAAAAAGCAGTCATCAGTCTCTGCCTGTGATGGAGACACCCTCTAGGAGAAGAAATGGAGCCTCTGGGATGCCGTGGTCTTATGATGACACACCAATAAAACCCCAC[C/T]AGCAGTTCACATCAGGCGCACCGAGTGACACAGTTGGATCACAGCAGATGGAACAGCTTAAGAATATAAATCAAGGTTGTTCAGACCTTAGATGGGTTTATTTTATTATTACTGCATACATAAGAATAGGCTTTTGAATGCAGCATTACAATGAGGATTTTCTAGTGCCTCAAGGTAACACATCTTGTTGTTGTCTCTTTTGCTGCTCAGATCTGAGGTCAAAGGTTTCTGAGTTGGAGCTCCGTCTTCAGGCTCATGAAAAGGATATGAAGAATCAGATCAATAAGTTCAGTGAAATTCAAAGTCAACTCGAAATGGCAAAGAAAGATGTGGCAGAGAAGGACAAACTCCTGAACAAGTCCAGAGATGAACTTACCAAGGCTACGGGCCAGTATGAGCAGTCGGTTTCTAAGGTAATTCACCAGCATGGAACACGCCACACTTTGAGCTAGACTTTTTTGTAGGGATGAAAGAAATGGTAAGAGAATAGTGGGATGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23122
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 |
|---|---|---|---|---|---|
| ENSDART00000077444 | Essential Splice Site | 433 | 1737 | 8 | 18 |
| ENSDART00000087589 | Essential Splice Site | 433 | 2861 | 8 | 26 |
| ENSDART00000128418 | Essential Splice Site | 415 | 953 | 9 | 13 |
| ENSDART00000135517 | None | None | 562 | None | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 32944490)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32786221 |
| GRCz11 | 17 | 32738732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCAAGCCAAAAAAGACCACAATGTTTTGCAATCAGAAATGGATAAGG[T/C]AATTTAATGTGGCATTTCTTTCTTTCTTTCTAGTTTCAAACATTATACAT
Long Flanking Sequence:
TAAGTGTCCAAATATATTTGGAATCTATTTAATTGTTTTGATTGTGTGTTGTGCAGTCATTTGATTAATGGGAAATAAGTTGAACTAATCACAGTTTGCCTGTAGTATTTAATCTTTGGTTGATTTGGCTCCTCAGTGTTCAGCCTTCGAGATTAAGCTGAAGCAGGTAACCGAAGAAATGAACTGTCAGAGACATAATGCCGAAAGCATGCATCGATCTCTGGAGCAGAAAATCAAGGATCAGGAGAGAGAGAGTCAAAAGGTATTGTGTCTTTACCATCATACATAACATTAAATATTTGTTTTAGACACCTGAATGTCTATCGGATTAATATTGAAAATATATATTTGTCTTAAAACTTTAATCCAGGAACTTGCACAGCTTCAAAGCTCCTATCAAGCTCTTGATCAACAGTTCACCCAGGTGAAAAATAAAACCAGCATGGAGATCCAGCAAGCCAAAAAAGACCACAATGTTTTGCAATCAGAAATGGATAAGG[T/C]AATTTAATGTGGCATTTCTTTCTTTCTTTCTAGTTTCAAACATTATACATATTTGGATTAAATCAACTTAATAGAATTGTGTTGATTTCAAAGGTGACTGCTCTAAAGAATCGACTAGAGAAAGAACTGGAGGAGCTAAAACAGAAACTTCTCAGGTCTGAGCAGGCCTTACAAGCCAGTCAAGTAAAGGAGGCAGAGACTAAGAAGAAGTTTGAAGTAAGTTAGTTTGTGTATCTGTTAAAGATGAGACATTTGTTTCTTGATTTCAAGCTTCTGCTACATCATGCCTGTTATAATAGAACTGATAGAATATACAGATTGTTTTGACCGCATATAAATCTGATGTTTCTTCTTTTTTTAGGAAATGCAGAGAGAGAAAAACACTCTTAATTGTCAGTTAGACCAAGGGATGAAGAGGGTCAAACAACTTGAAGATGAAAAGCAAAATACTGAGCAAATTCTTGCCAAAAACCGCATGATGGTGGATGATTTAAAAGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11610
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077444 | Nonsense | 899 | 1737 | 12 | 18 |
| ENSDART00000087589 | Nonsense | 994 | 2861 | 11 | 26 |
| ENSDART00000128418 | None | None | 953 | None | 13 |
| ENSDART00000135517 | None | None | 562 | None | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 32942472)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32784203 |
| GRCz11 | 17 | 32736714 |
KASP Assay ID:
2261-1277.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAAAAACTGCATGATGCTGWTTGCCAAGAGAATGCAAATCATCTTAAA[G/T]AGATTTCCATARTGACAGAAGCACTTGCTGAAAAAGATGCCATGGCAGAA
Long Flanking Sequence:
TACTTGCGAAGTTTACCCTCTTGGAATCAGACCTAAGATGTCAAAAAGATTTAAATGCAGAAATCCAAGGAAAGTATGATGAGCTTTCTAAAATCAAAGAAGACCTAGTAGAAAAAGTTTCTTCATTGGAAAAGAGAGAAAAGGATCTTATTAATGAAGTTGAAAGTCTATTACAAAAGAATAAATCCTTATGTTCTCTCGAAGAACAGTTTAATTGCCTTGTTGCTGAAGCAGAAGAAACCAGAAGTTCCCTAGAAAAGGTAAAGGAGCTACAAGTTCAGACCACCACTGAGCTGGAAAATCAGAAGACAATAGCGGAGAATCTTGCAATAGATCTTGAAGAAGAAAAAAAGAAGGCATTAAGCATCAAGCAGGAAAACACACAACTAAAAGTCAAACAAGAAGAAATTGAAAATAAAGCAAATGATCTTTTTGAGAAATATGAAAGCCTGCAAAAACTGCATGATGCTGTTTGCCAAGAGAATGCAAATCATCTTAAA[G/T]AGATTTCCATAGTGACAGAAGCACTTGCTGAAAAAGATGCCATGGCAGAAAGGATTGCTTTAATAAAAACTGAACTTGAGACCTCAAATAATTTGTCGGCCACACTGAAGAATTCATTAGAAAATCTTCAGACACAGTTTGACTCTTCTGTAGAGCTAATTTCGAGTCTGGAAAAAAAATTGCATGACATGTCTGATGAAAAATCTTTATTAGAGATCAGTATCAAGGAGCTCACTGAGAGGCATAATAAGGAATCTGAAGTTTATGTCTCTGAATTGGAAACACATATTAAAAAACACAAGAGTTTAGAGGAGCACATCAGTGTTCTTGAGACAGAATTGCAGAACAAAAGTCTGGAAACAAAAACTGCTTCAGAGAAACTGGAGGTGACCACTCAAGAAATGATCAAGCTTAAGCAAGATTTTAGCCTCTCTGAAAACAAACTCAGTGTGGTCACTGATTCTAATAAGAAAGTAGCAAAGGAGCTTGAAGACATGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10281
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 |
|---|---|---|---|---|---|
| ENSDART00000077444 | Nonsense | 1038 | 1737 | 14 | 18 |
| ENSDART00000087589 | Nonsense | 1256 | 2861 | 12 | 26 |
| ENSDART00000128418 | None | None | 953 | None | 13 |
| ENSDART00000135517 | None | None | 562 | None | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 32941670)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32783401 |
| GRCz11 | 17 | 32735912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCACAAGTAGAGGAGCTGCAAGGCAACGTTAGCATTCTTGAAGCAAAAT[T/A]AAGTGAGAGTGAGGCCCAGAGGTCCAACCTAGAATCAAAGCTTGAATCTG
Long Flanking Sequence:
GAGTTTAGAGGAGCACATCAGTGTTCTTGAGACAGAATTGCAGAACAAAAGTCTGGAAACAAAAACTGCTTCAGAGAAACTGGAGGTGACCACTCAAGAAATGATCAAGCTTAAGCAAGATTTTAGCCTCTCTGAAAACAAACTCAGTGTGGTCACTGATTCTAATAAGAAAGTAGCAAAGGAGCTTGAAGACATGAAGCAAAATGTGTTTCTGCAAGAGCAGGAGATGGAAGGTCTCAGGTTAGCTCTGTCTGATTTGAAAAACCAAGAAGCAGCAAAGTCCTGTGAGATTGAAACTTTGAAAGAAAAACTTCAGAAGGCTCAGTCTGAGCATGCTAAAACGTCAGAGACATTGAATGAAAAAAACATCAACATGAGTAAAATCAAAGTACAGCTTGAAATGCTGCAGATGGATCTAGAAGATAATGAAAACTGCATTAATGCATTTGATGCACAAGTAGAGGAGCTGCAAGGCAACGTTAGCATTCTTGAAGCAAAAT[T/A]AAGTGAGAGTGAGGCCCAGAGGTCCAACCTAGAATCAAAGCTTGAATCTGTCAAAGAAGACTATGTGAAGAGTTCACTTGAGGTGTCACAGCTATCTGCTTGTTTGGAGGAATCCCAGAAGGAACAACAGTCTCGTTCTGTATTAGTTGCTGAGTTGGAGTCTCTCCGTGTAATCCATGAACAACTAAAAGTTTCTCTTGAGCAAGAGAATTGTAAGCAAGCAAACCTTGAAGCAATGTACACCAATCTTATGGACCAGAAATTAAAGTTGGAATCTGAAATCCAGGAATTAAAAGCAGATACTCAAGGTTCTCAGAAGCAAATTGATCAATTAAAGCAGGCAAATGATAGGCTGGCATCTCAGATTGCAGAACAGCAAATTCACATAGAACAGCTTCAATCTGAGAAGAACCTTGCAGACACACTCAACAAAGAGCAAACTTCAGGTGGGAATGATCAAGATATTTGTGAAATGCCGTTTGCCAACACATCTCTTCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23121
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:
G > A
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077444 | Essential Splice Site | 1039 | 1737 | 15 | 18 |
| ENSDART00000087589 | Missense | 1305 | 2861 | 12 | 26 |
| ENSDART00000128418 | None | None | 953 | None | 13 |
| ENSDART00000135517 | None | None | 562 | None | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 32941524)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32783255 |
| GRCz11 | 17 | 32735766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTTGTTTGGAGGAATCCCAGAAGGAACAACAGTCTCGTTCTGTATTA[G/A]TTGCTGAGTTGGAGTCTCTCCGTGTAATCCATGAACAACTAAAAGTTTCT
Long Flanking Sequence:
GTGTGGTCACTGATTCTAATAAGAAAGTAGCAAAGGAGCTTGAAGACATGAAGCAAAATGTGTTTCTGCAAGAGCAGGAGATGGAAGGTCTCAGGTTAGCTCTGTCTGATTTGAAAAACCAAGAAGCAGCAAAGTCCTGTGAGATTGAAACTTTGAAAGAAAAACTTCAGAAGGCTCAGTCTGAGCATGCTAAAACGTCAGAGACATTGAATGAAAAAAACATCAACATGAGTAAAATCAAAGTACAGCTTGAAATGCTGCAGATGGATCTAGAAGATAATGAAAACTGCATTAATGCATTTGATGCACAAGTAGAGGAGCTGCAAGGCAACGTTAGCATTCTTGAAGCAAAATTAAGTGAGAGTGAGGCCCAGAGGTCCAACCTAGAATCAAAGCTTGAATCTGTCAAAGAAGACTATGTGAAGAGTTCACTTGAGGTGTCACAGCTATCTGCTTGTTTGGAGGAATCCCAGAAGGAACAACAGTCTCGTTCTGTATTA[G/A]TTGCTGAGTTGGAGTCTCTCCGTGTAATCCATGAACAACTAAAAGTTTCTCTTGAGCAAGAGAATTGTAAGCAAGCAAACCTTGAAGCAATGTACACCAATCTTATGGACCAGAAATTAAAGTTGGAATCTGAAATCCAGGAATTAAAAGCAGATACTCAAGGTTCTCAGAAGCAAATTGATCAATTAAAGCAGGCAAATGATAGGCTGGCATCTCAGATTGCAGAACAGCAAATTCACATAGAACAGCTTCAATCTGAGAAGAACCTTGCAGACACACTCAACAAAGAGCAAACTTCAGGTGGGAATGATCAAGATATTTGTGAAATGCCGTTTGCCAACACATCTCTTCTGCCCTTTGAAGAAGATACTGCTATTCTGGGTATGTCATCTCCTAAAGGGAAGCATGATTCACAAGAAGAGCCCAAAACACCATTGTCTGCAGAAGAGGATTACAAAGACTTTGCTCTACAAGAGCAGATGCAAAATAAATCCAGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12055
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 |
|---|---|---|---|---|---|
| ENSDART00000077444 | None | None | 1737 | None | 18 |
| ENSDART00000087589 | Nonsense | 2381 | 2861 | 17 | 26 |
| ENSDART00000128418 | None | None | 953 | None | 13 |
| ENSDART00000135517 | Nonsense | 132 | 562 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 32936917)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32778648 |
| GRCz11 | 17 | 32731159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAGATTAATCAGAATCTTTTGACTTGTCAGCTGCAGGAGTCTCAAAAA[C/T]AAATTGAAGARTATAAGGTAAGAATATTCTTCACCATATTTTACTCTGGC
Long Flanking Sequence:
CAACAGGAGCTTAGCGAAGAAAACACACAACTCCGATCACAAATAGCTGAACTGCAGGCACTCTCTTTAATTCGAGAGGAGCAAGATGAGGAATTGCAAAAGGACAAGGTTGAGTTACAGTCTACTATTGCACAGCTGGAAGAGAAGACACAGATGCAGTCTACCAAGATGGAGGTCATGCAGAATAGTATATCTTCTCTTGAGATTAATATTCAACAGCTGGAGGGTCAACTTGATGCTATGAAGCTGATGAACGTTGAACTTACGGGAAAGGTATTATTTTTTTCCCCATCACCTTTAATGGTTTTTAATTTCTCCCCTCACATTCACGTCACATATATTGATTGATATTTGTTAATTTTCAGTTAAATTCGCTACAAGAGAGCAGTTTGCATCTTGAGACACAACATAAGCAAGAGCTATGTGAGGCAAAGGAAATACAGAATGCTTTGGAGATTAATCAGAATCTTTTGACTTGTCAGCTGCAGGAGTCTCAAAAA[C/T]AAATTGAAGAGTATAAGGTAAGAATATTCTTCACCATATTTTACTCTGGCCTCGTGGATGTTCAGTCTATGCTAAAACTACATTTTCTTTGCACCTTTTAGTTCAGCCTGGAAGCACTGGCAGCTGAGAAAGATGGCCTACAGAAAAGTATATCTGTTATTCAGGAAAGTCATGATGTTCAGTTGAAGGAAAATAACATGAGACATGAGGAGAACCTGAAACGCACACAGCAGCAGGTGGGCTGATGCAACATTGCAACAATGTGCCTTTTTCTGTGCATTCTGTCAAGAGGAGGTCTTATTTTAGAAGATTGCATAATAGTGGGAGATCAGTTTAATATTATAGAAATGTGTATACAGTGCTCAGCATAATTGAGTACTCCCTTTTTTGAAAATGAATATTTGTATCCATTTCTCAGTGAATATAGGCAATGTATTTCGGTGAATTTAAACAAAACCGTTTTATTAAACTGATATGTTTATAAAATAAAAAATTTGTCA
Associated Phenotype:
Not determined