ZMP
prc1b
Ensembl ID:
ZFIN ID:
Description:
protein regulator of cytokinesis 1 [Source:RefSeq peptide;Acc:NP_956528]
Human Orthologue:
PRC1
Human Description:
protein regulator of cytokinesis 1 [Source:HGNC Symbol;Acc:9341]
Mouse Orthologue:
Prc1
Mouse Description:
protein regulator of cytokinesis 1 Gene [Source:MGI Symbol;Acc:MGI:1858961]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38641 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7602 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38641
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 |
|---|---|---|---|---|---|
| ENSDART00000098824 | Nonsense | 169 | 605 | 5 | 14 |
| ENSDART00000134941 | Nonsense | 170 | 606 | 5 | 14 |
| ENSDART00000141926 | None | None | 86 | None | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 51821231)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50091467 |
| GRCz11 | 7 | 50364243 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAACTTAGGGTTCAGTTTGATTTACAGTTTGTTTATCTTTCCAGGAA[C/T]GAAGACATAAAGAATTTGTCACGTTGAAGAAGCAGATAATACTTTGCATG
Long Flanking Sequence:
TTTTTGTTAAAAGGTGGAGGGGGTACAAAACTTTAAGGAAGTGGCCGCATTGTAACTCTCTATGCAGGAAAAACCCTGCTATTTTGTTTTCATAGCGTCTCAATAAAAATAAAGAGGGGAAAAGCTTTCAAAGCATCTTTTTTTGACATTTAAAATCATTTTAGGAGGAGAAAAGTGGCACTATGCTTCAGCGGGAAAAAGAACTCCGGACCCATGTTGAAGTGATGTTAAAAGAGAAAAACCAGAGAATGCAAGCACTAAAAGCATTAACCGAGCAGGATCAGGATCTCTGTGACCTTCTCTGCTCGCAGCCGTTTTCTATCTCTCCTGGTTGTGTTCCATCCATGGAACAGCTGGAGAACTTTCATCAGCACATCTCCTGCCTCACTGCTGAGAAAGTATGACAATACTTCATTTTTATTTTTTACACAGTCTGACTAGATTTAAAAAAAAAAACTTAGGGTTCAGTTTGATTTACAGTTTGTTTATCTTTCCAGGAA[C/T]GAAGACATAAAGAATTTGTCACGTTGAAGAAGCAGATAATACTTTGCATGGATGATCTGGATCAATTGCCTGAGACTAGTTTTGAAAAGGATGTCGTTTGTGAAGATGAAGAGAGTTTTTGCCTGTCTAAAGAAAACATTGATTCACTCAAAGTCCTCCTTCAGCAGGTACAACAAACATAAAACAGTGACAAACTCTGGTAAAAGTTAAAGGAACACTCCACTTTTTTATAAGTCCCCAAGAAATAAACAGTTCAGTTTTACTACTTTTAAATCAATTCAGCCAATTTCCAGGTCTTGAGGAATCACTTTTAGCTTAGCTTAGCTTAGCTTCGCTTAAATCAAAGAATCTGATTAGACCATTAGCATCTTGCTCAAAAAGTGTTTTGATAAATTTCCTATTTAAATATACACTCTTCTGTAGTTACTTTGTTTACACAATGTTCCGATGCTAAAAGAAAAGTTGCTATTTTCTAAGTTGATGTGGCTAAAATGAGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7602
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 > C
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098824 | Missense | 385 | 605 | 9 | 14 |
| ENSDART00000134941 | Missense | 386 | 606 | 9 | 14 |
| ENSDART00000141926 | None | None | 86 | None | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 51819562)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 50089798 |
| GRCz11 | 7 | 50362574 |
KASP Assay ID:
554-4214.1 (used for ordering genotyping assays)
KASP Sequence:
AANAGGAAAGAGCCAAAGATCCATCCAGATTCACCAACAGAGGAGGAAACC[T/C]TCTAAAAGAGGAGAAACAAAGGGCTGATATTGTCAAAGGTCTMCCTAAGG
Long Flanking Sequence:
AGGTCAAACGTCTTGAGGAACTGAAGCTTAAAAACATGCAGAATGTTACAGAGACCCTTCGGAAGGAGATTGCAGTGTACTGGGAAAAGTGCTTTTACAGCGCTGACCAGCGACAAGCTTTTATGCCCTATTATGATGGTGAGTTTTTTTTTTTTTTCAATTATACTTTACTGATAGTTTACAGTTTAAAAGCTGTGTAAAATATAACGTTTGCCTTCTCTCTTAGATGATTTCAGTGAGGAACTCCTGAGCCTACATGATGCAGAAATTGTGCAGCTTAAACAGTACTATGAGGATCATAAAGAACTTTTTGAAGGTGTTCACAAGTGGGAGGAGAACTGGAGACTTTTCATAGAGCTCGAGGTAAGTTACATTGTCTGAACGTGATTATCAAATATTTTACCATGAGCTAATTTTCTGATAGGAAAGAGCCATGTTTCATGCTTTTTTAAAGGAAAGAGCCAAAGATCCATCCAGATTCACCAACAGAGGAGGAAACC[T/C]TCTAAAAGAGGAGAAACAAAGGGCTGATATTGTCAAAGGTCTCCCTAAGGTAATTATGAGAGATTTATGCTTATATACAGCGATAGTAAATATTTTAGCAGTCTAAAATAACAATAAAATAAATAAATACTGTGACAGTAAAAACTAGAAAGAGTTTTATTACGCTAAAAAAATTTTACATTTACAAAACTGACGATAATTGCCAAAATCACATCACAAATCACAATTACACAAATCACAGAATAAAACTAAACATTTATTTAGCAATTATAATATGACACTCCTTTTCAGTTAATATTTCTACACATTAATGCTTTTTAAAAGTAGCTAAACTAATGCATCCAGTTATTGTGGTCATATGGGTTTTTTGCAATATCATGCAATTTTTAAAAAAGCCTATTCCAGACATTAAAAGTGAATTTTATATTTTTGTTGTCCTAGTCATGAAATATCATGAATTTTTGTTTGTGATTTTACTTCCCATTTATCAAAATGTATTT
Associated Phenotype:
Not determined