ZMP
si:ch211-57h10.1
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein C4orf22 homolog [Source:UniProtKB/Swiss-Prot;Acc:A2AVJ0]
Human Orthologue:
C4orf22
Human Description:
chromosome 4 open reading frame 22 [Source:HGNC Symbol;Acc:28554]
Mouse Orthologue:
1700007G11Rik
Mouse Description:
RIKEN cDNA 1700007G11 gene Gene [Source:MGI Symbol;Acc:MGI:1916571]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44613 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20494 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44613
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097872 | Nonsense | 77 | 239 | 2 | 6 |
| ENSDART00000131245 | Nonsense | 77 | 257 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 41171609)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 38965501 |
| GRCz11 | 5 | 39565654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACAAGAAAAGCAGCTGCCGAGGCCTCCAGGCTTGCTTCAGGAAGCCAA[C/T]AGAAGTAAGGTTTTTGTGTAGTGACCATGAAAAGGGGACAGATTTCAAAC
Long Flanking Sequence:
AACCCAATGCCCTATAACCACATGTTAGCAGCTCCTCCTTTTGTGGGCATAAGGCATCTCGCTAAATCATATGGAAATGATACAATCCAGGTTTAACTAGGCTGCAGTGACATGTGGCAAAAAATCCTTGATTCTGGCAGCCACGAAACTGTCAGCACAGCTCAAGTCATGTCCTTTTGTCATATAAATAGCATGTATACTAAAATTGGATTGATATAAATAGCACTTGAGCTCAAAACTAGCACAAATGTGTTGTACATACACTAGCCTGTTTGTTTAAAAATGCCATGCCAGGGTAGATTGTCGAATGCCATGATTTTTTTTTTTTCATATTGTACAGCCACCTCTAGCTCAGCAGATCTGTGTTATTGCTCCTCCAGGATCAGGAACTGGCCCGCCAGCTGGTGGAGCTGGGCCTCAAGGATAGCAGTTTGGAGAGGGAGGAATTTGAGACAAGAAAAGCAGCTGCCGAGGCCTCCAGGCTTGCTTCAGGAAGCCAA[C/T]AGAAGTAAGGTTTTTGTGTAGTGACCATGAAAAGGGGACAGATTTCAAACCAGTATGTGACCTTGAGAACATGTATTTTCCAGTTAACGTGTCAGGCTTCCTTCGTGAAACGTGAGCAGAGTGAATTTCTGTGTATATCGTTTGTTAAACCACTCTGACGTACATCGTCACATTCAATTTAATGTCACAATCTACGTGCGAAGGGTTTTACGAACAATTCATTCTGCTCCTGTTGGATGAATGAGGTCCATTGACTTTGGAGAATGAATATATTATTGACACAGACTCATTGTAAATATCAAAGACATCAAATGACGTTAAGATGGTAACTTATGTTGGATTATAGGATCTAAAACTCCAAGGACACAACAGCCTCTTTCTAGATAGATCTTGGCTGAAAGCAGCATGGACTTTCTGCTGACGCGAATGCTTTTTATAGACGCACCTGACAGCTCAAGTGTATCTTAAATGCAGATCTTTCGTCCCTTCACTGTAAGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20494
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097872 | Essential Splice Site | 156 | 239 | 5 | 6 |
| ENSDART00000131245 | Essential Splice Site | 156 | 258 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 41266566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39060458 |
| GRCz11 | 5 | 39660611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAATCTCTAAACAATTAGAAATGTATTAACCTCAACCTTTTCTTTCA[G/T]CTTCTACAACTGGAGGACGCAGAAGTCCAAACACAATAACAGCTCAAACT
Long Flanking Sequence:
ATTAAAATTAAAGATGTATTGTTTCTTTATTATAATTGAAAATGTTCTCCAGCCATATTAATTCCTTTTAGCTATTTAATATTTTTGAGAGAAAAATGCACCATAAATATAATTTTTTGAATGTCAAGAGCATGACTGCACTTCTGCCTTGTAGCAGTTGTCAATAACAATACATAGAACAAGAATGGAGGAGCAAAACAATTTCCATTTGTCCAAAACACTGAATAGACTGAATGTCTTATACACAGTTTAACACCTGGCTTTTCTAAGTGCACATTTGATCAAACTAGAAACTTTAAATGAAATCATTTTCTTAAGAATAGCAAACAAAGCACATCCTCATTTTTTTTCAGGTGAGCATTTTTACATTATAGTCTTAAGTTTATTTTATTCCCCCAAGTGGTTCAATCATACTGCAGTGTTTTTCAGTCTAAACCTTTAAGGCATGCATTTTAATCTCTAAACAATTAGAAATGTATTAACCTCAACCTTTTCTTTCA[G/T]CTTCTACAACTGGAGGACGCAGAAGTCCAAACACAATAACAGCTCAAACTATGAGGTAATCACGGAGAATCCAAGCGGTCTGCTCTTCAAGTGCAAGAACGACAGGAAAATCTTGAATGTTGACCCAGAGGTGAGCAGCTTTGATAGGAGGGGTAAACAGAGTGCTGACCTCTCTCTCAGTTCTTATTTACCATCCACAAGTAAACCAACACCTGCACTATGTTTAACAGAGTATTTGTGTAATGAATCAGTCAAGCCTGATTAAGGATTAGAAAGGCCATTGTATTTTCTCTGTATTACTATTAGATACAGTTTTTTAATCCATTGATTACAGGGTTATTTCACCCCAAAATGTACATTCCATCATCATTTCCCACCCTTGTGTTGTTCTAAAACACAAAGTTTTTTTCTGTCTTTGCAAATATATATTTTTAAATCAAATTTGTGAGGTTTCTGTCGCCATTGCATTTTTTTTTCACTTAAAACTTGGATGCATAGAA
Associated Phenotype:
Not determined