ZMP
poc1b
Ensembl ID:
ZFIN ID:
Description:
POC1 centriolar protein homolog B [Source:UniProtKB/Swiss-Prot;Acc:A2CEH0]
Human Orthologue:
POC1B
Human Description:
POC1 centriolar protein homolog B (Chlamydomonas) [Source:HGNC Symbol;Acc:30836]
Mouse Orthologue:
Poc1b
Mouse Description:
POC1 centriolar protein homolog B (Chlamydomonas) Gene [Source:MGI Symbol;Acc:MGI:1918511]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11463 | Nonsense | Available for shipment | Available now |
sa44270 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32526 | Essential Splice Site | Available for shipment | Available now |
sa7529 | Missense | Mutation detected in F1 DNA | Not yet available |
sa30751 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11463
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004771 | Nonsense | 45 | 490 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 18921824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18338134 |
GRCz11 | 25 | 18434534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAAATAATTTTGCAGCTACTGGATCCTGTGATAAAAGCCTTATGATTT[G/A]GAACCTCGCTCCTAAAGCCCGGGCTTTCAGGTTTGTGGGTCACACAGATG
Long Flanking Sequence:
GTGTGTTGTTGACATTTTTAAAATTTTTATTTGTATGTCTATATTAAAATTATTTTATTTTGACATTTATTTTAGTTTACTTAGATTTAATTCAAGTCTAATATTTTGTATTTTTTGTCAGCTGAAATAGTTTAATTTGAACCATTTTAATTTTTTTAATTAAAATGGTACTTTATTATAGCTTTGATATTTTAGCTAACTTACAAAATATTTATTTATTTATTATCATTTGCTTTTTTTTTTTTTTTTTTTGCTTACACTTATAAGTTCTCTGTCTTATTCAGGAGGATCCCACCCTTGAGAGGCATTTTAAAGGTCATAAAGATGTAATTTCCTGCGCTGACTTCAACCCCAATAATAAACAGCTTGGTATGTGACATTTATCTTCATTATTTAAAATAACTCAGAATACAAAAAATATAATTTCACTCTAGCCCCAAAATAACCTCTTACAAATAATTTTGCAGCTACTGGATCCTGTGATAAAAGCCTTATGATTT[G/A]GAACCTCGCTCCTAAAGCCCGGGCTTTCAGGTTTGTGGGTCACACAGATGTCATTACAGGCGTTAATTTTGCTCCAAGCGGTTCATTGGTGGCATCTTCATCCAGAGATCAAACAGTTCGATTGTGGACACCCAGTATGTGAGTTCAGTTGGCACTTTATCAGTATTAATGTATTATTTTGTTATCTTTAACATTTCTAACCCAAAGTATTTTAGTTTTCTCATCCTTTGGCCATCCAAAATGCATGTGACCTTTCTTTTCCGTGTAATATAAAATAAGGTTTTTAGCTACAACATGGTCTTTTATGGTGATTCATAAAATACCAGTCAGTGGCTGCTGACATTAAGAATAATAATAATATAAATATATATATATTTTTTTTTTCCAAGTGTTGTTTAACGGAGCAAGAAATTTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTATTAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44270
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 |
---|---|---|---|---|---|
ENSDART00000004771 | Essential Splice Site | 187 | 490 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 18919654)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18335964 |
GRCz11 | 25 | 18432364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGATACATCCTCACATCAGTGCATCAACATTTTCACAGACTATGGAGG[G/T]TGAGAATTAAGTGTTTCTGGTCATTTTTGGAAATTTTTAAGTATCTATAT
Long Flanking Sequence:
CCCTGTATATGTTTCTCTTCACTCTCGAAGTCCATTGACTGAGGAAATTAAAAAGAAAATGATTTACATTTTTGGCTGAACTACTTTTTTTAATGTGTTATTTGTACATGTGCATTATAGAAAGGGTGAATCGACTGTGTTCAAAGCCCACACAGCAAGCGTTCGAAGCGTTCATTTCTCCAGAGATGGCCAAAGGCTGGTCACGGCCTCAGATGACAAGTCTGTGAAAGTATGGGGTGTTGAACGGAAAAAATTCCTCTACTCTCTCAACCGGCACACCAACTGGGTGCGCTGTGCGAGGTACGAGACTGCAGATTTAACACATCTAACCTTTCCGGTTTTGTCACATAAAGTGGGATTTCTCTCACTGTCACTTGGTCTGTCCCTGTTAGGTTTTCACCAGATGGTCGTCTCATTGCTTCCTGTGGTGACGACAGGACGGTTCGCCTCTGGGATACATCCTCACATCAGTGCATCAACATTTTCACAGACTATGGAGG[G/T]TGAGAATTAAGTGTTTCTGGTCATTTTTGGAAATTTTTAAGTATCTATATTACATTATTTCTAAATGAAATGTTAAATTTGGCTTTTTTGTCTTAATGTTTGGCTTATTTTCCAAAAAATATTATATATTTTAGCCCAAATGTAACAATACTGTCTTATTTAATTATTTGTTTACTGTCTAATATTGTCTGCTTAGGTCTGCCACATTTGTAGACTTCAACTCCAGTGGCACGTGCATTGCATCATCAGGTGCAGACAACACAATAAAAATCTGGGATATTCGTACAAACAAGTTAATACAACATTACAAAGGTACAATCTCAACTAAAATGGTTACACATTTTTGTAGTTGCATTAATTTGTAATAGACTTTAAATTTAATTAAGATTTTAACTTGTTTTTTCAGTCCATAATGCAGGAGTCAACTGCTTTTCCTTCCATCCCTCTGGAAACTATCTGATCAGTGGTTCGAGTGACAGTACAATTAAGATCTTGGACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32526
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004771 | Essential Splice Site | 369 | 490 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 18913555)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18329865 |
GRCz11 | 25 | 18426265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACTGACCCTCAGGTGGTTGAAGTGGGACGTGTTGTTTTCTCCACAACG[G/A]TAAGAATTCTCAACAATCTGGTTAATGAAATGATTTAGTCCAAGCACTAG
Long Flanking Sequence:
AAATTGGGGAAAAAAATAAACAAGCTGTCTTATAATTCAGGGGGGCAGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATCACTGTTGAAAACCTTTGGGCGTCTTCATATTTTTTGGTGAAAACTAATATAGTATTATTAAATATTTATTTGTTTTTTATTTATCAGGGACAGTTTAAAGAGTGAAACTACAAACCATCACAGGAACAAATACATTGATATCACAATTCAGGTTGACAAACAGGCCTGAATTCCCTCTCAGGATTCAGCACTCTGTATGTAGATCAATTCGATATGCTGCTGTCAGTGTGTTAGTTCTGTGTTAGTCTCATTGACGTCAGTTCTGTTGTCTGTTTTACTTTTTTTTCTTTTCTTAGATTAATCCTGTTGCTGATACACAGTCTACTGACCCTCAGGTGGTTGAAGTGGGACGTGTTGTTTTCTCCACAACG[G/A]TAAGAATTCTCAACAATCTGGTTAATGAAATGATTTAGTCCAAGCACTAGGGGGCAGTATAGACTGACTAATATTGATCCTTTGCTAAACAGTGTGCTGTAGCTGCAGTTTCTGCCAGGATTTAGTTTTTGTTTTTGCATACTGTGGTTTTGTTATTCAGTTAGTTTTTTTGTCATCTTCAAAGATCTGTCACTTTAATGGATATGGTTTAAAAATCTAAGAATGAAGTGAATGTCTGTCTTGTGGCCAAGACACCAAAATACTCTATAACTTTTTAAATCTCTGTGATAATATAATTTGTCAAGCGATTTCAAATATTTTTATGTTCAGTACCTTTAAATTCATGCATTTTTATTTCACTTTAGGAAATTCCAATTTGGATTGTGTAATCTATTTAATAAATGTATTAAATTATTTCACGTACAGTTAGCAAATTGTATTGAGTGTTTAAACAACATTTATAACATATATACAGTGCTCAGCATAATTGAATACACCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7529
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 > C
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004771 | Missense | 434 | 490 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 18856876)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18273186 |
GRCz11 | 25 | 18369586 |
KASP Assay ID:
554-4386.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTCCAGCAGAGCGCTCTGGTATTCCATCAAGCCTTACTAGCACTCTGG[A/C]GAACATTGTRCAGCAGCTGGACATCCTGACCCAGGTGAATTTATTTTAGG
Long Flanking Sequence:
GGCGCTCTCTCCCGGGACAGCATGCCAAACACGCTTTATAATTAATCATCGGCAAGGGCAAACTCTTGAATCGATTATTTCAATGAAAAAAGCACTTATGACAATTTACAAAGCATCTTCTTTTCTGTTCTACAAACGAAAGTAAGTTATATGGCTTTGTCAATGAGTTACAACAACTAAGTAATAAGAACAAATTAAAATGTTATTGCCTTTCCTTCAAATTGCTGAAAAAAATGATGCACATTTTTTGTCTCGATAGTGAATTAATCATCACAGAATTTTCTGTTTTGGTTTCCTTATTCCCCAGGATGCAAGAAACTATGATGGTGCATCAAGCAGCAGAGCTCAGTTCACCTCAGGAATGGACTCAGGTCCATTTCGGACTCATACACAAGCCAGAGAAGAAGAGGATGAAAACCAAGAGGAAAGATTTGCTGGCGGCATGACAGCATCTCCAGCAGAGCGCTCTGGTATTCCATCAAGCCTTACTAGCACTCTGG[A/C]GAACATTGTACAGCAGCTGGACATCCTGACCCAGGTGAATTTATTTTAGGTCATCTTAATCTGTTGAATAGTCCTGCTTTAGTGTACTAAGAAAAACAGAAAGCATGTTTTTCTAGTCACTACTATAAGCTACTTTAGCGAAAGTTGGCCTTTTTTTTTTTTTTGTGAGTTTTTTCATTGATCAGATCACAAGTACTCGAGGGAAAGGTTTATAGGTGAATGCATGCATCTATGGGCTTTTTCTGTCCTTTCAGTGGAATACTGAGAATAAGCTTGTGCACTTTACATATGATTATGAAAGTAGATAACAGCATGTAGAACAGCAGCTTTCATTTCTGCTCTGAAAGCCACAAAAATGCAGAACTGGTTTTTATTAGAATCAAGACTGATAATAGGACATTGTGTTTTGCACATTTTGGCCTTCAAGTCACACAAAGTTGACAGTTTAAACCCTGTCTGGTTAGTGCACTTTATCAAAAATTCAATTTCATTTTTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30751
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 |
---|---|---|---|---|---|
ENSDART00000004771 | Nonsense | 477 | 490 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 25 (position 18855167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18271477 |
GRCz11 | 25 | 18367877 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGAGGACCTGCCTGGACAATCAGGTCCTGCTTATGCAACAAAACCAA[C/T]AATTAGACCGATCTGACGAGGAATCCGAGGGACCCCCGTTGTGATGGATA
Long Flanking Sequence:
TAATCAATTTTGGTTGCATCAGCAAGTGATCAAAACTGAACAAGCTCAAATTATTGTAAATAATATTTACAAACTTTATTTGGAATTCCCCCCTTGTGTTTGAACCAACAACAAAAAGGTAAGTACTAGAATAGAATCAATTTACTATATAAGCGTTTACACCATAGAAGCAATCCAGATTGACCCATTCATCCATTGTCCATTTGTGATCAAATTGACAAAAAAAAAATACCATGTGCAAATGTAGCAAGTTTTCTGCATGCAGAATATAGTAATTTTAATAGGAATCCACATGATCTGGATTTCCCCACACATTTCTTTGTTACAATATTAACAATATACAATGGATTCTTTCTTACTTACAAAAGCACATCTTACCACACCTAAACTCTTGGTTCTCATCTCAGACCGTTGCTGTCCTCGAGGAGCGTCTTACCCTGACCGAAGACAAACTGAGGACCTGCCTGGACAATCAGGTCCTGCTTATGCAACAAAACCAA[C/T]AATTAGACCGATCTGACGAGGAATCCGAGGGACCCCCGTTGTGATGGATACCCAACCCTGGTGGCCCTCAACCCAATGGTAACTTCCTCTAGCCCGCAGAGGGGGACACACCAAACTTTTTTTTTTCATTTTAGCTTAAAGACATCCAGCTGTGTCATTTCAAATGAGGACATTGTACTTAACAATGCAAAAAAAGGACACAAGATGAAAAGACAAAAAGCAGGATGAAGGAAGGACAGGAGGGGGGATTAGAGGAGCAGTCTCACCCCAATAAAGTCATGTTGATAAGACATCTGCAGCTAAAACAACAACCCGCTCATGTTTTTTAAGTGGCAAAGACTGTCATGGTCCAGACTTCTAGAATAGTCAAACACATTTTTACTTGGTCTAAGTTTATGTCCTCTAAATCACATATATTACTTAGCTATAGGCCCTTATGAATGGATTCTAGCCGGAGTCTCTGTTGTGATTGCATGAATGGTTTGTGGATGTGTATGTAG
Associated Phenotype:
Not determined