ZMP
cstf3
Ensembl ID:
ZFIN IDs:
Description:
cleavage stimulation factor subunit 3 isoform 2 [Source:RefSeq peptide;Acc:NP_999884]
Human Orthologue:
CSTF3
Human Description:
cleavage stimulation factor, 3' pre-RNA, subunit 3, 77kDa [Source:HGNC Symbol;Acc:2485]
Mouse Orthologue:
Cstf3
Mouse Description:
cleavage stimulation factor, 3' pre-RNA, subunit 3 Gene [Source:MGI Symbol;Acc:MGI:1351825]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16190 | Nonsense | Available for shipment | Available now |
sa16073 | Nonsense | Available for shipment | Available now |
sa32217 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16190
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025423 | Nonsense | 30 | 716 | 2 | 21 |
ENSDART00000052437 | Nonsense | 30 | 715 | 2 | 22 |
ENSDART00000025423 | Nonsense | 30 | 716 | 2 | 21 |
ENSDART00000052437 | Nonsense | 30 | 715 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 18 (position 44173627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45762682 |
GRCz11 | 18 | 45759508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTCCGGAGAAGGTWAAGAAAGCAGAGAAGAAGTTGGAAGAAAATCCATA[T/G]GACCTCGACGCTTGGAGCATACTGATTCGTGAAGCACAGGTTTAGTGACA
Long Flanking Sequence:
CTGTAATGTTTACCATAGTACTTTAAATAATCAGTCTGAAATCACATGCAAGTATGACTTGAAAGCAACATTAGCACTGTTTAATTGACTGAGCATTACTTATTTCGATAGTCATTGGCTATATAAACCTAATGATCTATTCAGAATTAGCTGTAAATACTTTCCTAACATGATATAAATAAGGAGAAGGTCTGAATGTGTGGATGTAAAACCAACTTTACCTCAACTGTGACTCAATATCAGATTTTCCTCATTCTGAATCATATTTTATTATCTTAGACTCACCCAACGTGTAGCATCATCTTTCATTTAAGCAGAAATTATCTGCAGGATTTAAGCATTGAGTTATGGTTGTCTAAAATAAAGATATTAAGCATGTAACATCCATAATTCAGAGTCTGTTTTTCATTCATGTGCCTTTTTCCCACTCCTCAACAGGCGGCAGAGTACATTCCGGAGAAGGTTAAGAAAGCAGAGAAGAAGTTGGAAGAAAATCCATA[T/G]GACCTCGACGCTTGGAGCATACTGATTCGTGAAGCACAGGTTTAGTGACACAGGATTGCATTCCTTTTTACCTGGGGTTCCATGTTTTGGGAGGGAACGGGAGGGTCGCGGATTTGTAAATCATGTAACAATCTAGTCTTTTGGGACGTACGTTCTGATTCTGTATGTAAATGAATTTCACTTCTTTTAGAATCAACCCATAGACAAAGCAAGGAAGACATATGAGCGACTTGTCGCCCAGTTTCCCAGTTCGGGCAGATTCTGGAAGCTATACATTGAAGCTGAGGTTATATTTCATTTTAATTTAAAAACATCTGTGCATGACGAAGCTTTCTCCACATTTTGATCGACAATGTGATATTCACACAACAGCAATAATCAGGGCATCAAGGGAAACTCTTATAGCTTGTATCATTTAGGGGTCATTTTTTTCTATTTTCTAAGTTTTATGAGGTGATATTGTTGCATGTTTCATCTGCAACAGCATTAAAACACTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16073
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025423 | Nonsense | 30 | 716 | 2 | 21 |
ENSDART00000052437 | Nonsense | 30 | 715 | 2 | 22 |
ENSDART00000025423 | Nonsense | 30 | 716 | 2 | 21 |
ENSDART00000052437 | Nonsense | 30 | 715 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 18 (position 44173627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45762682 |
GRCz11 | 18 | 45759508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTCCGGAGAAGGTWAAGAAAGCAGAGAAGAAGTTGGAAGAAAATCCATA[T/G]GACCTCGACGCTTGGAGCATACTGATTCGTGAAGCACAGGTTTAGTGACA
Long Flanking Sequence:
CTGTAATGTTTACCATAGTACTTTAAATAATCAGTCTGAAATCACATGCAAGTATGACTTGAAAGCAACATTAGCACTGTTTAATTGACTGAGCATTACTTATTTCGATAGTCATTGGCTATATAAACCTAATGATCTATTCAGAATTAGCTGTAAATACTTTCCTAACATGATATAAATAAGGAGAAGGTCTGAATGTGTGGATGTAAAACCAACTTTACCTCAACTGTGACTCAATATCAGATTTTCCTCATTCTGAATCATATTTTATTATCTTAGACTCACCCAACGTGTAGCATCATCTTTCATTTAAGCAGAAATTATCTGCAGGATTTAAGCATTGAGTTATGGTTGTCTAAAATAAAGATATTAAGCATGTAACATCCATAATTCAGAGTCTGTTTTTCATTCATGTGCCTTTTTCCCACTCCTCAACAGGCGGCAGAGTACATTCCGGAGAAGGTTAAGAAAGCAGAGAAGAAGTTGGAAGAAAATCCATA[T/G]GACCTCGACGCTTGGAGCATACTGATTCGTGAAGCACAGGTTTAGTGACACAGGATTGCATTCCTTTTTACCTGGGGTTCCATGTTTTGGGAGGGAACGGGAGGGTCGCGGATTTGTAAATCATGTAACAATCTAGTCTTTTGGGACGTACGTTCTGATTCTGTATGTAAATGAATTTCACTTCTTTTAGAATCAACCCATAGACAAAGCAAGGAAGACATATGAGCGACTTGTCGCCCAGTTTCCCAGTTCGGGCAGATTCTGGAAGCTATACATTGAAGCTGAGGTTATATTTCATTTTAATTTAAAAACATCTGTGCATGACGAAGCTTTCTCCACATTTTGATCGACAATGTGATATTCACACAACAGCAATAATCAGGGCATCAAGGGAAACTCTTATAGCTTGTATCATTTAGGGGTCATTTTTTTCTATTTTCTAAGTTTTATGAGGTGATATTGTTGCATGTTTCATCTGCAACAGCATTAAAACACTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32217
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025423 | Nonsense | 77 | 716 | 4 | 21 |
ENSDART00000052437 | Nonsense | 77 | 715 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 18 (position 44168090)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45757145 |
GRCz11 | 18 | 45753971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACGAAAACGTGGTTTAATAATGTTGGTTTTCAAATGTGTCCACAGATC[A/T]AGGCTAAAAACTATGACAAGGTTGAAAAGGTAAGCATTTGTTGTCGTATG
Long Flanking Sequence:
ACTTTAATGCAGGTGGCTTTGAAAAAAGAAATTGTAGATTGGGGTGTCCAAACTTGGTCCTAGAGGGCTGGTGACCTGGAAAGTTTAATTCCAACCCTAATCAAACATACCTGGACCAGCTAATCAAGCTCCTACTAGACATACTAGAAACTTCCTGCCAGATGTGTTGAAGCAAGCTGGAGCTAAGCTCTGCAGAACATCGGCCCTCCAGGACTGAGTTTGGACACCCCTGCTCTAGATGCATCATGTAACTTTTTCCAAAGGCTTGCACTCCAAAAAGCAGCATTTCAACTAAAACAATACAAAACAATCAGCTAAGTAGTTTTGTCTATCATTTGCACACATAAAATGGATTAAATTGAATAAAGGTTGAGATGAAAATGAAATGCAGGGTTGTGTGAATGTCACATTGTTGACCTCAAAGTGTGTGGAGCCACTCAATTTCACTTCATACGAAAACGTGGTTTAATAATGTTGGTTTTCAAATGTGTCCACAGATC[A/T]AGGCTAAAAACTATGACAAGGTTGAAAAGGTAAGCATTTGTTGTCGTATGGCAGCCACGTGTTTAATTTATGGATCGTGTGAAATTGCTGTGACTTGTGACAGACTCATGAACCATAAAATCTGGGCTTTATCTAGGTCACCACTTTAGGTCCTCAGAGTAAACAAAGATGGTGTTAAGGGATTAAACGACGCCTGCTTCGCTAGAAACACCCTGTTTACTCTTCTCAGTCCATCAACGGTCAATATGATATTAAAATATGAGAGGGAAAAAAATATATTTCAGGATGGGGATACATCCGAGTTTGAGATCACAGTTCAAAGACAAAACATCGTTCTGGTTGTGTAGATCTAGGGTTCCCAAGTACTTTATTTTCAGACATGAATCCAAGGCCTGGAAAGTACTTAAAAACAAACATTGGTCCTCGAAAGTGCTTGAATTGAAAGTTTATCTTGTTTTTTTCAACAATTGTACTTTTAAACGGTTGCTTAAAATGGTCAA
Associated Phenotype:
Not determined