ZMP
chtf18
Ensembl ID:
ZFIN ID:
Description:
CTF18, chromosome transmission fidelity factor 18 homolog [Source:RefSeq peptide;Acc:NP_001103572]
Human Orthologue:
CHTF18
Human Description:
CTF18, chromosome transmission fidelity factor 18 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:18
Mouse Orthologue:
Chtf18
Mouse Description:
CTF18, chromosome transmission fidelity factor 18 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Ac
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11678 | Nonsense | Available for shipment | Available now |
| sa18673 | Nonsense | Available for shipment | Available now |
| sa19429 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11678
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 |
|---|---|---|---|---|---|
| ENSDART00000092058 | Nonsense | 94 | 957 | 3 | 22 |
| ENSDART00000109177 | Nonsense | 94 | 348 | 3 | 17 |
| ENSDART00000092058 | Nonsense | 94 | 957 | 3 | 22 |
| ENSDART00000109177 | Nonsense | 94 | 348 | 3 | 17 |
The following transcripts of ENSDARG00000058480 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 8279172)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 8518977 |
| GRCz11 | 1 | 9203088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAGTATRAAGTTTGACTTCTCACAGCYCCTAAACCCAAGAAAAGGAGG[C/T]AAGATGTGGCGAAAAAGCTCCAGTTTGGCGTTGACCAAGATGATGACATC
Long Flanking Sequence:
AGCCAGTCACACAGCAGAAATGTGCAACAGTGAAAATCTAAAAGTTTTTTTGTGAAAACCACAAAAGTATTGGCCAACATAAATAGGTCATGTTATTTAATGGACCCTCTAATTTGTGGCTTCAGTTATTGTTGGTATACTCTTTTAAATCTGGAAGCATTAACAACTGATGTCAAAATATATATTGTTATTGTTTAATATAGAAAAAATTAATCAAGATTGCATTTTTGCCATATCACCCAGCCCTACTTTAAGCAAATTTAGAGTGTTATTTTTTTATTTAATGTTTAAAAAATTATTTTAATAATGTTAAAAAGTCAAATGATCATCATTTATTTGAATTTTTGTAACATTCTATTTGTCTTGAATTGTAAACATTCTTTAGTCTTAAAATGAAAAAGAATTCATTTCTTAACCTCAAAAATACCTACAAGCATTTGAAGAGGATTGTGTAGTATGAAGTTTGACTTCTCACAGCCCCTAAACCCAAGAAAAGGAGG[C/T]AAGATGTGGCGAAAAAGCTCCAGTTTGGCGTTGACCAAGATGATGACATCACTCCTCCATCTTCCCCAGAGGTTTACGACAGGGAAGTGAGAGACGGGTAAATATTTATGCACATTTATACCATATTTAAAATGTACCACTGAATGGAAGCGTTGGTTTTTGATCTTTTTTTTTTTTTTTCACAGGCCTAGATTTTCCCTAACCCTGAGTCCAGACAGACCAGCAGCAACAAAAATAACGACAAATGTTTTAGATATTAGTGGACTGGGAGCTTTACAGGAGTCACCGAAGCAGGTGACGGCAGCAAAACGTCATGCTCAGAAACGCCCACCTGCAATCGGAGATTACATCACAGTCACAGACTCTATGGGAAACAGGGTCTACCTTAACAAGAAAGAGGATGTGGAGAAGGTTTTATTCCATATTAACAACTTAACTTCACAGCTTACAGAAGTGCAATACGTAAAATATAATGGTTGATGTATTTATCATTTTTCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18673
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 |
|---|---|---|---|---|---|
| ENSDART00000092058 | Nonsense | 94 | 957 | 3 | 22 |
| ENSDART00000109177 | Nonsense | 94 | 348 | 3 | 17 |
| ENSDART00000092058 | Nonsense | 94 | 957 | 3 | 22 |
| ENSDART00000109177 | Nonsense | 94 | 348 | 3 | 17 |
The following transcripts of ENSDARG00000058480 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 8279172)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 8518977 |
| GRCz11 | 1 | 9203088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAGTATRAAGTTTGACTTCTCACAGCYCCTAAACCCAAGAAAAGGAGG[C/T]AAGATGTGGCGAAAAAGCTCCAGTTTGGCGTTGACCAAGATGATGACATC
Long Flanking Sequence:
AGCCAGTCACACAGCAGAAATGTGCAACAGTGAAAATCTAAAAGTTTTTTTGTGAAAACCACAAAAGTATTGGCCAACATAAATAGGTCATGTTATTTAATGGACCCTCTAATTTGTGGCTTCAGTTATTGTTGGTATACTCTTTTAAATCTGGAAGCATTAACAACTGATGTCAAAATATATATTGTTATTGTTTAATATAGAAAAAATTAATCAAGATTGCATTTTTGCCATATCACCCAGCCCTACTTTAAGCAAATTTAGAGTGTTATTTTTTTATTTAATGTTTAAAAAATTATTTTAATAATGTTAAAAAGTCAAATGATCATCATTTATTTGAATTTTTGTAACATTCTATTTGTCTTGAATTGTAAACATTCTTTAGTCTTAAAATGAAAAAGAATTCATTTCTTAACCTCAAAAATACCTACAAGCATTTGAAGAGGATTGTGTAGTATGAAGTTTGACTTCTCACAGCCCCTAAACCCAAGAAAAGGAGG[C/T]AAGATGTGGCGAAAAAGCTCCAGTTTGGCGTTGACCAAGATGATGACATCACTCCTCCATCTTCCCCAGAGGTTTACGACAGGGAAGTGAGAGACGGGTAAATATTTATGCACATTTATACCATATTTAAAATGTACCACTGAATGGAAGCGTTGGTTTTTGATCTTTTTTTTTTTTTTTCACAGGCCTAGATTTTCCCTAACCCTGAGTCCAGACAGACCAGCAGCAACAAAAATAACGACAAATGTTTTAGATATTAGTGGACTGGGAGCTTTACAGGAGTCACCGAAGCAGGTGACGGCAGCAAAACGTCATGCTCAGAAACGCCCACCTGCAATCGGAGATTACATCACAGTCACAGACTCTATGGGAAACAGGGTCTACCTTAACAAGAAAGAGGATGTGGAGAAGGTTTTATTCCATATTAACAACTTAACTTCACAGCTTACAGAAGTGCAATACGTAAAATATAATGGTTGATGTATTTATCATTTTTCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19429
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 |
|---|---|---|---|---|---|
| ENSDART00000092058 | Nonsense | 337 | 957 | 8 | 22 |
| ENSDART00000109177 | Nonsense | 337 | 348 | 8 | 17 |
The following transcripts of ENSDARG00000058480 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 8282665)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 8522470 |
| GRCz11 | 1 | 9206581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGTCCGGTCCCTGTAGAGGCCAGATCAAATTTTACAAACGCTCAAAAT[C/T]AAAACCAGGCCCAACGTTTCAAAACCAAGTCTCAAATGACAGAAGAGATA
Long Flanking Sequence:
ACTATGATAAAGTAAATTCATTTATGTGTGTTCTGCAAAGTCCTTAACAAAAATCCATCCTAGACCTGGCTTCCAAAAGCAAGAAAGCATGACAATATCTAAATCTGTGTTTTATCTTCTGCTTTGACTGAGGCACAACTAATTTACTATGGAGTTAAATAGTTTGAATATAATGAGTTAAAAAACATAAACTTTATTATTGATATACCATACTAGTTTCCTTGTGTGTTGGAAACTGTGCTTTATTTGCAAATATTTTATGTTAGATTAGAATTTTTACTTTAAATGGAGTCATAGATGTGCTGTTTATTCAAACCCGTTCTGGTTAATTAGTATCCATCAGTTTTGTTATTATTTACATTGTCTCTGTATTCCTGTAGTTTACTAATCGCTGTCTGCTGAAATGGCTGAAGCTCTGGGACACTGTGGTCTTCGGGCGAGAGAGGAAAAGCCGTCCGGTCCCTGTAGAGGCCAGATCAAATTTTACAAACGCTCAAAAT[C/T]AAAACCAGGCCCAACGTTTCAAAACCAAGTCTCAAATGACAGAAGAGATACTAGAGGCTGAGCTAGACCAGTACAAAAGACCGAAATTTAAGGTGAGTGCAATTGCGCAATTACAATATTGTTAAATTTGTTTTTTATTATTCGATTTTTAAAATATAAATATATATATATATTTTTTTTTTATTTTGTAATATTTTTATTTATTCATTTAATATTTGTGTCTGCTTCCCCTGTATTTTTTGAGAAAAAAATTAATAATAAATTAAAAAAAAATAATCTATATATATATATATATATAATTTTTTAAAAATATTTTAAAGATTATTTTTTAAAAATAAAATAAAAAAATAAAAATAGAGTTAATCATTTCTGATGTAAATTGTTTTTGTATTGTCTAAAATAATATAATTATCTGAAACCATTGTACCTTTTTATCTTTTTATTTTGTGCAAAAAAATATTTTTATTGTTTATTTAGGAAGTAATAGCATCACTTTCAGT
Associated Phenotype:
Not determined