ZMP
cep57l1
Ensembl ID:
ZFIN ID:
Description:
centrosomal protein 57-like 1 [Source:RefSeq peptide;Acc:NP_001003769]
Human Orthologue:
CEP57L1
Human Description:
centrosomal protein 57kDa-like 1 [Source:HGNC Symbol;Acc:21561]
Mouse Orthologue:
2410017P07Rik
Mouse Description:
RIKEN cDNA 2410017P07 gene Gene [Source:MGI Symbol;Acc:MGI:1915511]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12507 | Nonsense | Available for shipment | Available now |
sa8771 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8909 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23740 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12507
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 |
---|---|---|---|---|---|
ENSDART00000048537 | Nonsense | 17 | 494 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 32187208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32245448 |
GRCz11 | 20 | 32148327 |
KASP Assay ID:
2261-4549.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTTTTKTGAATTACAGAGTTTTAATCTAGACTCCCCATCTAAA[C/T]AGAGTTATGTTGGCAGTTTTTATCAGCCACCAGAGAAAATGYCAAGACCT
Long Flanking Sequence:
TTCAGTCGTTAGCTTTTTAAAGTTAGCTTATTTACACATTGCATCCTGAAAAGGCAGTTTTTGGTTCGTAACGTTTTTATGTAGCCTATCATGCAGCTTTCTTGGTGTTAAGTGACATAGCTATTTAATTGATGAACCATGAAATTTTCTAAGTTGACTATTTGCTACTGTTTATTCAGTAAGTTAGCGTGGCTAAAGGTTTTAGCTATTGTGCGTTAATTTACATTAAATGTGAACAGTGGCTCTTGTCTATCCATTTAGGCTAATTGTATTCTTTAACAAACTTTTTACTCTTAACTTTGTCACGGAAAGAATATGATTTATATATATGTTTAATTATTGTTTTGTTTTATACATGTTGTTATTATTATAGTTATTATTAATCGTACAACAGTATTATCATTGTCCTTCCTCCATGCATGCCATGTTGAATAATCTGTAAACTAACTTTTTTTTTTTTTTGTGAATTACAGAGTTTTAATCTAGACTCCCCATCTAAA[C/T]AGAGTTATGTTGGCAGTTTTTATCAGCCACCAGAGAAAATGTCAAGACCTTTGTATATGAACCCAGACACACATCCGCTCAACAGAAAGAGCTCAGGTTTGCAGGATATCAGCCCACAGCTTTATCAGACAGTTCCTGATGCTGGAAGCAGAGGTGATTTGAGTTTAAAAGTTGACCATACAACTATCTATATACAGTCAGATGTCTCAGTTTTGATTCACAAAGTTCTCACTTAGATTTAATTTCATTTTTTCTCAGTCACTTTGGTACATTTCCCAGATCAGAATTGAAAAAGTTTTAAAACTACCTGTTCAATCTTTAAATCATTGTGTCACTTGTTCACATCAAAAAAGCAATTTTCCTTTGAACAAGTTTTAAGTTTCCTACATTATCAGTTTCTTATATCACAATGATCAAAATGTATTTTTTGGTCTCTGTTGAATTGTCTCACCTCCCACGTTTAATCGTCTGTTCATGGCAAAAGTCTATACATGCAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8771
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 |
---|---|---|---|---|---|
ENSDART00000048537 | Nonsense | 145 | 494 | 4 | 11 |
ENSDART00000048537 | Nonsense | 145 | 494 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 32185614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32243854 |
GRCz11 | 20 | 32146733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTTTCTAAGCTTCACTCAGCAGAAAYGCGCTGCTCTCTCCTGGAAAAA[C/T]AGCTCAACTWCATGAAGAGAATGGTGGAGTGTGCAGAAAAAGACACARTT
Long Flanking Sequence:
GTGCTTTTTGTAAAGGTTTAATGTTCTTCGACAAACGCACTCGCTGGTTTGCAAATATTAAGAGTGATTTAAGAAATGTACCGAAGTGAATGAAGATAAACTCAGAGACCGTATACAATTTTTTTGTTTGTTTGTTTTCTAAGCAGCAGTGATTGCAGCCCTGAAAACACTGCAGGAGAAGATGCGGCGCTTGGAACTGGAGAGAGTTCATGCAGTAAAGAACGTCCATCACTTCTCTCAACCTACTCGACACCAGGAAGATGTTTCTGCATCAAAGGAGCAAGAGCACAACATGCGGGACAATGACTCAACACAGAGGAAAGGTAACCAAAAGTGTTGCACAGCAGTTACTGATAAATTCTCAAGTTTTTTGTAAAGTTCAATACTTTACAAAATGATCATAATATGTACTACTAGTACTAAGTAGAAAATGTCTTTTCATTTCAGTGCTGGTTTCTAAGCTTCACTCAGCAGAAACGCGCTGCTCTCTCCTGGAAAAA[C/T]AGCTCAACTACATGAAGAGAATGGTGGAGTGTGCAGAAAAAGACACAGTTACTCACACAGACAGAAAGGTTAGTGAAAGCATAAAGCTAGTAGAGATTTTGGATATTCAAGGAGTTTGAACAAATGTTGCAAATTCCCATTTACAACAAACTGTGCAGAAGCTCAAGAGTTTTTGAATCTTTCTTCAACTGTTATTGGTATTTAGGACTCTTTGCCTACGGAACACACACATGCAGACCCACAAATTCAGGCACAGCTCAATAAGCTTGAAAGACTGGAAAAGGAGTATCTCAGACTCACCAATACACAGTCTGTGGCTGAGGTATACATATAGAAGAGTCATGTGACTGTCGGGACCATATTATTTAATTTATCGTGTAATATTTGTGAAATATATTGATGTACAGAATTAATTTTCATTTGATGTCTTTCATCTACAGAGGAAGATTGAACTCTTAGAACAGAAACTTTTAGAGGAGGAGCATGAACGCAAACTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8909
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 |
---|---|---|---|---|---|
ENSDART00000048537 | Nonsense | 145 | 494 | 4 | 11 |
ENSDART00000048537 | Nonsense | 145 | 494 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 32185614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32243854 |
GRCz11 | 20 | 32146733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTTTCTAAGCTTCACTCAGCAGAAAYGCGCTGCTCTCTCCTGGAAAAA[C/T]AGCTCAACTWCATGAAGAGAATGGTGGAGTGTGCAGAAAAAGACACARTT
Long Flanking Sequence:
GTGCTTTTTGTAAAGGTTTAATGTTCTTCGACAAACGCACTCGCTGGTTTGCAAATATTAAGAGTGATTTAAGAAATGTACCGAAGTGAATGAAGATAAACTCAGAGACCGTATACAATTTTTTTGTTTGTTTGTTTTCTAAGCAGCAGTGATTGCAGCCCTGAAAACACTGCAGGAGAAGATGCGGCGCTTGGAACTGGAGAGAGTTCATGCAGTAAAGAACGTCCATCACTTCTCTCAACCTACTCGACACCAGGAAGATGTTTCTGCATCAAAGGAGCAAGAGCACAACATGCGGGACAATGACTCAACACAGAGGAAAGGTAACCAAAAGTGTTGCACAGCAGTTACTGATAAATTCTCAAGTTTTTTGTAAAGTTCAATACTTTACAAAATGATCATAATATGTACTACTAGTACTAAGTAGAAAATGTCTTTTCATTTCAGTGCTGGTTTCTAAGCTTCACTCAGCAGAAACGCGCTGCTCTCTCCTGGAAAAA[C/T]AGCTCAACTACATGAAGAGAATGGTGGAGTGTGCAGAAAAAGACACAGTTACTCACACAGACAGAAAGGTTAGTGAAAGCATAAAGCTAGTAGAGATTTTGGATATTCAAGGAGTTTGAACAAATGTTGCAAATTCCCATTTACAACAAACTGTGCAGAAGCTCAAGAGTTTTTGAATCTTTCTTCAACTGTTATTGGTATTTAGGACTCTTTGCCTACGGAACACACACATGCAGACCCACAAATTCAGGCACAGCTCAATAAGCTTGAAAGACTGGAAAAGGAGTATCTCAGACTCACCAATACACAGTCTGTGGCTGAGGTATACATATAGAAGAGTCATGTGACTGTCGGGACCATATTATTTAATTTATCGTGTAATATTTGTGAAATATATTGATGTACAGAATTAATTTTCATTTGATGTCTTTCATCTACAGAGGAAGATTGAACTCTTAGAACAGAAACTTTTAGAGGAGGAGCATGAACGCAAACTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23740
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 |
---|---|---|---|---|---|
ENSDART00000048537 | Nonsense | 195 | 494 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 32185325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32243565 |
GRCz11 | 20 | 32146444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAAATTCAGGCACAGCTCAATAAGCTTGAAAGACTGGAAAAGGAGTA[T/A]CTCAGACTCACCAATACACAGTCTGTGGCTGAGGTATACATATAGAAGAG
Long Flanking Sequence:
AACATGCGGGACAATGACTCAACACAGAGGAAAGGTAACCAAAAGTGTTGCACAGCAGTTACTGATAAATTCTCAAGTTTTTTGTAAAGTTCAATACTTTACAAAATGATCATAATATGTACTACTAGTACTAAGTAGAAAATGTCTTTTCATTTCAGTGCTGGTTTCTAAGCTTCACTCAGCAGAAACGCGCTGCTCTCTCCTGGAAAAACAGCTCAACTACATGAAGAGAATGGTGGAGTGTGCAGAAAAAGACACAGTTACTCACACAGACAGAAAGGTTAGTGAAAGCATAAAGCTAGTAGAGATTTTGGATATTCAAGGAGTTTGAACAAATGTTGCAAATTCCCATTTACAACAAACTGTGCAGAAGCTCAAGAGTTTTTGAATCTTTCTTCAACTGTTATTGGTATTTAGGACTCTTTGCCTACGGAACACACACATGCAGACCCACAAATTCAGGCACAGCTCAATAAGCTTGAAAGACTGGAAAAGGAGTA[T/A]CTCAGACTCACCAATACACAGTCTGTGGCTGAGGTATACATATAGAAGAGTCATGTGACTGTCGGGACCATATTATTTAATTTATCGTGTAATATTTGTGAAATATATTGATGTACAGAATTAATTTTCATTTGATGTCTTTCATCTACAGAGGAAGATTGAACTCTTAGAACAGAAACTTTTAGAGGAGGAGCATGAACGCAAACTTGTGCAGGAAAAAGCAGAGGAGGTAAAATATATATTTTTTTCATGAAATTAATTATTAGAAATCTTTTATTAAAAAGTGGTTTACAAAATTGATGCAGTTATGTCATTAATTTTTTTTTTTCCTGCCATCAGTTGCAGCGAGAGCTTGAAAATAATATTCTGTCCCTTTCTGCTGCGACTCAACCTAAAGGCAAGAAAAAGAGGAGAGACAAGGCCTCATGCAAGGTACGACTTTGTATGCAGAAATGCATAGTGAGCACTAGGTGGCAGTATGTTTACAGAACAATATTACA
Associated Phenotype:
Not determined