ZMP
si:ch211-169p10.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S599]
Human Orthologue:
CCDC120
Human Description:
coiled-coil domain containing 120 [Source:HGNC Symbol;Acc:28910]
Mouse Orthologue:
Ccdc120
Mouse Description:
coiled-coil domain containing 120 Gene [Source:MGI Symbol;Acc:MGI:1859619]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41120 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21197 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41120
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022469 | Essential Splice Site | 94 | 601 | 3 | 9 |
| ENSDART00000137920 | Essential Splice Site | 94 | 601 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 8565545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 7982127 |
| GRCz11 | 8 | 8020712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGGCTGGTCTTTCCCGCAGCAGCTCCAAACATAACACGAAAAATGAG[G/A]TGTGCAGACTTGTTTGAAGAATAAGAGTGGACACTGATTTAATATTGCTA
Long Flanking Sequence:
TGTCACAGCTATCAGCCAATCAGATTCGAGAACCAGACAGAACTGTTATATAAATATATATATTTATAGATGTATTTATGTATGTATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGAGAATAAATGTAAATATTTTTTTTTATTCTGGTGTTTTGCTTGAAATAGAAATCAATTCTCCAATAATCATTTTACATAAAAGAGCAAATTTATTACAAAAATATATGTAATATATGTACAAAAGTGACAAAAGTGAAGGGTACCAACAATTTTGTCCAGGCCTGTATTTTATGAACTTTTCACAGTCTATTTGTTAATTTGTGCATTTAATTGTAATTTTTCCCAGGAGTTGACAGGTGAAGTTCCTCATGAATATCCTCTGGAAAGCGGAGAGAAAGCTCCTCATGTGAGACGCAGGGCTGGTCTTTCCCGCAGCAGCTCCAAACATAACACGAAAAATGAG[G/A]TGTGCAGACTTGTTTGAAGAATAAGAGTGGACACTGATTTAATATTGCTATGTGATGGATAAATATCATGAATTGCTCGATGTTTGTGTTCAGGAAGAGGACGGCTCTCAGCGCAAGACAAAGAAAACCCTGTTCAGCGGCGCCCTCCGCAGGCACACCGATGCAGAACAGCATCCACAGCACAGCAAACGCACGGTTCATAGAGGATGCCACACAGGTAAGCTTGTAGATTACACACATCATAATAATACACAACATTTGTGCATGTTTCAACCATTATTTTCAAGTGTTACCAACAAATTATTTGTGATTTATTTGATCAAGTCTCTTACATATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAGAGTAAAGCCTCAGAAAATAAATAAGTTATATATTAAAAAAGCAACACATGTTAAAATCTTTAATATTTCTACAAATGTAAATATATAGAGATAAAACAAGTATTTACATAATTTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21197
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 |
|---|---|---|---|---|---|
| ENSDART00000022469 | Nonsense | 120 | 601 | 4 | 9 |
| ENSDART00000137920 | Nonsense | 120 | 601 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 8565714)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 7982296 |
| GRCz11 | 8 | 8020881 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGAAAACCCTGTTCAGCGGCGCCCTCCGCAGGCACACCGATGCAGAA[C/T]AGCATCCACAGCACAGCAAACGCACGGTTCATAGAGGATGCCACACAGGT
Long Flanking Sequence:
ATATTTTTTTTTATTCTGGTGTTTTGCTTGAAATAGAAATCAATTCTCCAATAATCATTTTACATAAAAGAGCAAATTTATTACAAAAATATATGTAATATATGTACAAAAGTGACAAAAGTGAAGGGTACCAACAATTTTGTCCAGGCCTGTATTTTATGAACTTTTCACAGTCTATTTGTTAATTTGTGCATTTAATTGTAATTTTTCCCAGGAGTTGACAGGTGAAGTTCCTCATGAATATCCTCTGGAAAGCGGAGAGAAAGCTCCTCATGTGAGACGCAGGGCTGGTCTTTCCCGCAGCAGCTCCAAACATAACACGAAAAATGAGGTGTGCAGACTTGTTTGAAGAATAAGAGTGGACACTGATTTAATATTGCTATGTGATGGATAAATATCATGAATTGCTCGATGTTTGTGTTCAGGAAGAGGACGGCTCTCAGCGCAAGACAAAGAAAACCCTGTTCAGCGGCGCCCTCCGCAGGCACACCGATGCAGAA[C/T]AGCATCCACAGCACAGCAAACGCACGGTTCATAGAGGATGCCACACAGGTAAGCTTGTAGATTACACACATCATAATAATACACAACATTTGTGCATGTTTCAACCATTATTTTCAAGTGTTACCAACAAATTATTTGTGATTTATTTGATCAAGTCTCTTACATATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAGAGTAAAGCCTCAGAAAATAAATAAGTTATATATTAAAAAAGCAACACATGTTAAAATCTTTAATATTTCTACAAATGTAAATATATAGAGATAAAACAAGTATTTACATAATTTTAATTATATAAATAGAATAAATATAAATATAAATAAATATTTACATAATTATATAGACATATAAAAATATTTTACAAAAAAATTGAAATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined