ZMP
cth1
Ensembl ID:
ZFIN ID:
Description:
cth1 [Source:RefSeq peptide;Acc:NP_571014]
Human Orthologue:
ZFP36
Human Description:
zinc finger protein 36, C3H type, homolog (mouse) [Source:HGNC Symbol;Acc:12862]
Mouse Orthologues:
Zfp36, Zfp36l3
Mouse Descriptions:
zinc finger protein 36 Gene [Source:MGI Symbol;Acc:MGI:99180]
zinc finger protein 36, C3H type-like 3 Gene [Source:MGI Symbol;Acc:MGI:3525151]
zinc finger protein 36, C3H type-like 3 Gene [Source:MGI Symbol;Acc:MGI:3525151]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20888 | Essential Splice Site | Available for shipment | Available now |
sa9814 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20888
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 |
---|---|---|---|---|---|
ENSDART00000079966 | Essential Splice Site | 40 | 256 | 1 | 3 |
ENSDART00000101601 | Essential Splice Site | 3 | 319 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 7 (position 19194080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17695463 |
GRCz11 | 7 | 17947436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGGTTTCTTCAGTTTTGTGCAGCAGTCTGAAAACGCAGTAATGTTTGAG[G/A]TAAGTTTGATCTTTCATTGTGTTTTAATTTGAACTACGTTAAGTTTTACG
Long Flanking Sequence:
CGCACAACCGGAGGTGTGACGCAGTAATTGATACAGGATGGGGCTGTGTGTATATTCTCAGCTCGCCCTTTGAAGTCTCCTAACAAGCTACTTGGCAAATGTTTATTCCAGGGGAATCGGCAAGAAATGCGGCGATCTCCAAATTTGATCAACTTGAAAACGCCCACCACAGACGCTTCAGACTGCCTCCAAATTAGATTGGCGGTCACCTGTGTTGAAAGTGATTGGGTGGTTCGCAGGTTGACGCGTCACAGCTGATTCGTGTTTTAAAGGGAACGCGGGAATGGACGCTGGTCGCTTTAAAACAGCAGCTCGAGCGGTTGGGCTATACGTAGGGCTTGCCAGGTATAAGGTGTAGTTCGCGTCTTTCATCTCGGATTGGGCAAAGGAGTATAAAGCGTGTGAAGAAATCTTTCCGGTGTAGTTGGGACGCTTTTGAAAGCTTAATATTCGGTTTCTTCAGTTTTGTGCAGCAGTCTGAAAACGCAGTAATGTTTGAG[G/A]TAAGTTTGATCTTTCATTGTGTTTTAATTTGAACTACGTTAAGTTTTACGTCAGGTTATCTTTGAGACATTACGACTAAACGCATGAAATATTTGCAGACCAACTGAACAATGATCTCTAGTTTGTTTTAGTTAAAGGCAGTTAACTGAACTCTTTAAAGTGCTTTCTATAGCTTTAAAGTGCTAAATTACATGAGATAGATCTGTATAGTTAGCTTAACCCTTTACTTAAAAAAAAAAAAAATTAAGTAAAAAAAAAAAAAGCATCTGTGACTCCCTAAAGACCCCTTTAGGCGATAACTCGTTGATATAGTCTACTATAGACTTTAATATTCCCAAAACATGGTAGATGACATGGTAGAAAACATTATTTGGCAATCGATGGCTACAAGTTCTCAGTATTTTCTTAACCTAAACCTGGTTGGAAAAAGTGGACCAGTGTTTACAATCTTTCCACATGGCAATTGTTCACAATAGTATTGTCTTTGAGGGGTATCTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9814
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 |
---|---|---|---|---|---|
ENSDART00000079966 | Nonsense | 115 | 256 | 2 | 3 |
ENSDART00000101601 | Nonsense | 78 | 319 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 7 (position 19195848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17697231 |
GRCz11 | 7 | 17949204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACYGAACTGTGCAGCCGTTATGCKGAGACGGGTACCTGCAAGTACGCC[G/T]AACGCTGCCAGTTTGCCCAYGGCCTCCATGATCTCCATGTGCCCTCCCGT
Long Flanking Sequence:
ATATTGGAGGCTTTTACCAAATAAGTGGATCCACTTGAATTTTCATTGTAAACCATTTAAATTTCATATGAAGTTTAGTTCTGACACTCTTAATCATTCTGCATAAATCCCAATTTAAAAAATAAATAGAGAAAAAAAAAAATGTTATCGCTGAAATGGCAAATGTCTGCAGATTCTGTCTGGGCCTAGTCATAAGATTTGTTACTAGGACTTGTATTCCAATAATCTGATCAAGCTTTGTCTTTTTAAGAGTCCTAAAATGCAGTCTTTTGTTCCAGACCAGTCAAGACGACCTGTTCCTGTTCCCCACTGAAGGCCTGAATGAGGCGTTCTTCCCCGAGGAGGGTTTAGGTGGTGGTGGTGGTGGTCTATCTCTAGCTGAGGCCTTGCTTCCCTTGGTCGAGTCTCCCTCTCCCCCAATGACCCCTTGGCTCTGCTCCACCCGCTACAAGACTGAACTGTGCAGCCGTTATGCGGAGACGGGTACCTGCAAGTACGCC[G/T]AACGCTGCCAGTTTGCCCATGGCCTCCATGATCTCCATGTGCCCTCCCGTCATCCCAAGTACAAAACGGAGCTGTGTCGTACCTACCACACTGCTGGCTACTGCGTTTATGGCACACGCTGTCTGTTTGTGCACAACCTTAAAGAGCAGAGGCCTATCCGTCCTCGGCGCAGGAACGTGCCATGCCGTACTTTCCGCGCATTTGGGGTTTGCCCGTTTGGCAACAGGTGCCACTTTCTCCATGTTGAGGGAGGCTCTGAATCAGATGGTGCTGAGGAAGAGCAAACCTGGCAACCTCCGTCACAATCCCAAGAGTGGAAGCCTCGTGGTGCCCTCTGCCGCACATTCAGTGCTTTCGGCTTCTGCCTCTATGGCACCCGCTGCCGGTTCCAGCATGGACTTCCCAACACCATCAAAGGTCACAATGCCAACCACACGTCCTGGCCTCAGCAGATGACCAACGGAGGGTCTATTTCGCCAATCTCTGACACCTGCACTTCA
Associated Phenotype:
Not determined