ZMP
si:ch211-227c6.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate centrosomal protein 170kDa (CEP170) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
CEP170
Human Description:
centrosomal protein 170kDa [Source:HGNC Symbol;Acc:28920]
Mouse Orthologue:
Cep170
Mouse Description:
centrosomal protein 170 Gene [Source:MGI Symbol;Acc:MGI:1918348]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22243 | Essential Splice Site | Available for shipment | Available now |
sa22242 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22243
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 |
---|---|---|---|---|---|
ENSDART00000040704 | Essential Splice Site | 168 | 548 | 6 | 9 |
ENSDART00000108709 | Essential Splice Site | 168 | 388 | 6 | 13 |
ENSDART00000135989 | None | None | 697 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 10600444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10902773 |
GRCz11 | 13 | 11035248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCAGTCAAACCTGCGGAGCCTAACAAAGGAGACGACAAGATGCCAG[G/A]TAAAGAAACCGTATGATGATGTCAGGGTGTAAGATAATTATATTAATGGT
Long Flanking Sequence:
CTTTTGTTGTTGTTTTTTTTTTTGATCACACACTCCGCGACCCACTGAGAATGTTCCCGCGACCCACCAGTTGAGAAACACTGCTTTAAATGATCTTCTCTTATGTTCACAGAAGAATGAAACTCAAACCATTTTGGAACAACAAAGTAAACGATGATTGTTTTGGGATAAACTATGCTTTTAACAATATCCAAGTTCATCAGTTTAGAAACACTTTAGCCCTTGTATTACAAGAACTACGCTTGCTGCAGTTTATTTGTCTTCCCAAGGCTATGTTAGATGACAGTTTTCTGGCACTCACTGTATTCTTCTCCCTCCTTTCTGTCAGCATGAGAAGTTCACTAGCCAACTTCAACTGGGCAAGAAGCCCACCTGCGCGGAGCCCTTAAAATCCCCCAAGTCTTCCCCAGGCAAAGCCAAATTGAGCAAAGCTGCGGAGCCCATAGCTGAAGCAGCAGTCAAACCTGCGGAGCCTAACAAAGGAGACGACAAGATGCCAG[G/A]TAAAGAAACCGTATGATGATGTCAGGGTGTAAGATAATTATATTAATGGTTGACTCTTTCAAAACACTTTGTCGGTGATTGCAAACAAGGTTCATGTGTAAATGAGTAATACTGGACAAGCCAAGTCTGTGCCCCTTCTGACTCATCCATTGTCTCTTTTGTAGCTGAGCGAGGTGACTCAAATGATCACAGTGTATTTTTAATAAAGCACGGACTAGTAGTAGGTGTAAGTGACCTTCTATTATCTCATCTGATGGTCAAACACCAGGCCGGTGTCAGAAAATTAGCACTACACACATTATTGCAACACGTGACAGAGACATGACAGTTGTGAAAGCCCTCTGGCATAAGAGAGGATTGCCTCTCATTCTTTTCCTATTATGGAGAAAAAAAAAACACAAATGGAAAATGTATGTAAGGGAATTCCATTTAATTGAATGGATCTGAAATAGCTCAGCTTAAAAGTGCTGCATGTACGTTTGTAATTCTTCTAACTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22242
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 |
---|---|---|---|---|---|
ENSDART00000040704 | None | None | 548 | None | 9 |
ENSDART00000108709 | Nonsense | 348 | 388 | 12 | 13 |
ENSDART00000135989 | Nonsense | 661 | 697 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 10549337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10851666 |
GRCz11 | 13 | 10984141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCTGGATCTCAGAGCGGATGGGCACCTCTGCCCAGTAACGGAACCCCA[C/T]AACCACCACCACCAACAACCATAACCAACCCTAGCCCAGAAAAACCCAGT
Long Flanking Sequence:
ATCCATACACACTCATTAACACACATACACTACGGTCAATTTTAGCTTACCAGATTTCAGTTTTGGACTTGTGGGGTAAACCGGAGCACCCGGAGGAAACCCACGCAAACACGAGGAGAACATGCAAACTCCAGACAGAAATGCCAACTGACCCAGCTGAGGCTCGAACCAGTGACCTACAGCGCTACCCACTTTGCCACCGCGTCACCTATAGTGAATCATTTGAATGAAATAATGCTCCTTTAGTAATACAATGACATGTTGTCAGTTAATGCACTTTTGTGACCACGCCTAAATACATTGTCAAGATGTGTGTCAGGTACCTAATAAATTATCTAATGTATTTCTTCATTCCTGCAGTTATAAATGTCATGGTGGACCCTGATGGAACCCTTGACGCTCTAACCAGCCTTGGCTTGACCAGTCCAACTGCCCCCAAACCTAGAATCAGCCCTGGATCTCAGAGCGGATGGGCACCTCTGCCCAGTAACGGAACCCCA[C/T]AACCACCACCACCAACAACCATAACCAACCCTAGCCCAGAAAAACCCAGTGTAGGACTCAACTTCAGCCGCACACACCCCACCGGAGAGGAGAGTGCCATTGCTAGCAAATAAAAAAAAAAAACTTTTAGTAAACCGGACTAATAGAACTACATACTGTAACTTTTATGTGTATGTATAATGTGTCACGTGCCCTTCTGCAGGACTCTGTATGAGGTCTGTCTGTAGTTGTACTCTGTTAGTGTAACTTTTAGAATCACACACGTGAATCTGGACTGACTGCTCAGCGAAACACACACAAACAGCTGCATGTGACAGGACGCAAATGGCCAACCAAGCCGATTGAACTGCCAAACGAATCCCTCATGAACGGACTAAAACAACTCTCCAGTGCCTGTCTGCTCTCCTCTGAGCTTCGATAACACGGTTTACCAAACTGAATACAGAAAACTATGCGCAACTGTATTTTGAAATTTGTATTTAGATAACTGTCATTTTTGC
Associated Phenotype:
Not determined