ZMP
si:ch211-112m17.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human chromosome 6 open reading frame 204 (C6orf204) [Source:UniProtKB/TrEM
Human Orthologue:
C6orf204
Human Description:
chromosome 6 open reading frame 204 [Source:HGNC Symbol;Acc:21638]
Mouse Orthologue:
Gm9766
Mouse Description:
predicted gene 9766 Gene [Source:MGI Symbol;Acc:MGI:3642684]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23786 | Nonsense | Available for shipment | Available now |
| sa23787 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23786
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 |
|---|---|---|---|---|---|
| ENSDART00000061141 | Nonsense | 173 | 781 | 3 | 13 |
| ENSDART00000146349 | None | None | 433 | None | 10 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 41938891)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42010050 |
| GRCz11 | 20 | 41907160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCACCTCTCGACATCCCCCTGGACATGAAGGATCCCCGTCCCGTGCGT[C/T]GATGGTCCTCCCTCACCCGCCTCACCGCCCAAGAAAAGCCCTCTCCAACA
Long Flanking Sequence:
TACATTCATTACAGTTGAAGAATAACATCCAAACACTTTCTCTTTTTTTATTTTAGAATTGGTTTTAATTAAATAAATCTGTCATCGTCAGCCCGTATAAGAATATTTTAAAAACAATTGCTTGGAACTCTCCAATATTTATTTATTTATTTTTTTTTATGATTGGTGAAATCATAATTTGACTTTTTACACTTTTAAATGTATTATTATTATTGTTATAAAGAATAATAATAATTTTACTCATTACAGTCCAAGAGTAAAAACTTTTTAAAAAATAGTAAAAACTTTTCTCTCTTCCAGATCACTCCAGCTCTAGCGGGACGTTGTCCTTCCTCCCTCTGCGTCCCCACGGCCCGATCCCGACGGCCCACGTCATGCCCTCTCCATCCAACTCCAAACTCAGCGCTCCCTCTGCACCCAGCAGCCCCTGGAGCAGCAGCTGCCAGCTTCCCTCACCTCTCGACATCCCCCTGGACATGAAGGATCCCCGTCCCGTGCGT[C/T]GATGGTCCTCCCTCACCCGCCTCACCGCCCAAGAAAAGCCCTCTCCAACAAACCGTCCTTCCCACCGCACGGACCCACATGGATCCCTAGATCGAGGTGTGCTTTACGGATACCGGCACGACCCTCAATACTCTGATGGATTTATTTCTGAAAACTTGCTTAAACTTTCGACCAATAAGTATGACCTGGGTAGCAGCAACACTTTAGGTAAATCGGACTCATGTTGTTCATCTCCCCTGAAGCCGAGTACACTAGACCTCAGTTTTAGTGCCTTACCAGAGAGTAAGACGCCACCTGTGGGACTGGCAACGACGGGACAGAGAGGGTCGTCTTCACTCAGGCAGCAGGCGGTCGGTGGGTCACCCATCCAGCCAGCGGTCAGGACTCAGATGTGGCTGAGTGAGCAGATGGAGTACCGGCCGGGACCTGACGGGTGTGGATCATGGCAGCAGGAGCAGCAGCAGCAGAGGGAGAGACTCAGACAAGACTCTGAACAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23787
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 |
|---|---|---|---|---|---|
| ENSDART00000061141 | Nonsense | 248 | 781 | 3 | 13 |
| ENSDART00000146349 | None | None | 433 | None | 10 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 41939118)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42010277 |
| GRCz11 | 20 | 41907387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTATGACCTGGGTAGCAGCAACACTTTAGGTAAATCGGACTCATGTTG[T/A]TCATCTCCCCTGAAGCCGAGTACACTAGACCTCAGTTTTAGTGCCTTACC
Long Flanking Sequence:
ATAATAATTTTACTCATTACAGTCCAAGAGTAAAAACTTTTTAAAAAATAGTAAAAACTTTTCTCTCTTCCAGATCACTCCAGCTCTAGCGGGACGTTGTCCTTCCTCCCTCTGCGTCCCCACGGCCCGATCCCGACGGCCCACGTCATGCCCTCTCCATCCAACTCCAAACTCAGCGCTCCCTCTGCACCCAGCAGCCCCTGGAGCAGCAGCTGCCAGCTTCCCTCACCTCTCGACATCCCCCTGGACATGAAGGATCCCCGTCCCGTGCGTCGATGGTCCTCCCTCACCCGCCTCACCGCCCAAGAAAAGCCCTCTCCAACAAACCGTCCTTCCCACCGCACGGACCCACATGGATCCCTAGATCGAGGTGTGCTTTACGGATACCGGCACGACCCTCAATACTCTGATGGATTTATTTCTGAAAACTTGCTTAAACTTTCGACCAATAAGTATGACCTGGGTAGCAGCAACACTTTAGGTAAATCGGACTCATGTTG[T/A]TCATCTCCCCTGAAGCCGAGTACACTAGACCTCAGTTTTAGTGCCTTACCAGAGAGTAAGACGCCACCTGTGGGACTGGCAACGACGGGACAGAGAGGGTCGTCTTCACTCAGGCAGCAGGCGGTCGGTGGGTCACCCATCCAGCCAGCGGTCAGGACTCAGATGTGGCTGAGTGAGCAGATGGAGTACCGGCCGGGACCTGACGGGTGTGGATCATGGCAGCAGGAGCAGCAGCAGCAGAGGGAGAGACTCAGACAAGACTCTGAACAGGTCAGATTTGTTGTTGTTTTTTATGTAGGGGATACTGACGTATGATGGGTGCTACTGGAGGATTTATTTAATTTTATTTTATATTTTATTTTATTTTATTTATTTATTTATTTATTTGTTTGTTTGTTTTAGTTTAGTTTACCCATTACAAATTTGACATAATTAAATCATTTTATATTAGAATTTATTTTATTATTATTTATTATTTTAATTAAGTATTATTTATTTGT
Associated Phenotype:
Not determined