ZMP
zgc:85644
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein C1orf93 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6NV24]
Human Orthologue:
C1orf93
Human Description:
chromosome 1 open reading frame 93 [Source:HGNC Symbol;Acc:28390]
Mouse Orthologue:
2810405K02Rik
Mouse Description:
RIKEN cDNA 2810405K02 gene Gene [Source:MGI Symbol;Acc:MGI:1913719]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13891 | Nonsense | Available for shipment | Available now |
| sa21971 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13891
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000047412 | Nonsense | 92 | 201 | 3 | 8 |
| ENSDART00000112140 | Nonsense | 92 | 201 | 3 | 7 |
| ENSDART00000147264 | Nonsense | 92 | 201 | 3 | 7 |
The following transcripts of ENSDARG00000029795 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 42118366)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 40378147 |
| GRCz11 | 11 | 40642292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTCATCTTCCTGATTCTGTGAATCTTTAACCTTTNGTTTTAGACATCTA[C/A]ATTGAWGAGATGAAACAGTGTTACAAAGATTTAGGCTTTAAAAGGTAATG
Long Flanking Sequence:
TATAGTTTGACCTACAGTAATCTCTGAGATGGTTAAACATAGGATGCTGTAGGTTAGATTAGAATACACTAAATATCCCTCAAAACACTAAAGACTTAAATATGTTTTATTTCTAGTACTAGGTTGCAGCTGGAAGGGTATCCGCTGTGTAAAACGTGCTGGAAGAGTTGGTGGTTTATTACGCTGTGGCGACCCCTGATTAATAAAGGGACTAAGCCAAAGGAAAATGAATGAATGAATGAATCTTTTCACTAATGATCACTAGGGCCTGAGTAAGAGAATGACTGCAATTCTTTGTATTCTTTCTTTTGAAATGGCTGATAACCTCAGGTAAGCTCATTGTGTTGGTCTGAGTTTATTAGTGACTAGATTCCCACCTTTTACTCTAAATTTATGACCCGTTACTATGCCTACCATGTGTTTACCTTGGGTTTGCCACTGATAAAAAAGGTGTCATCTTCCTGATTCTGTGAATCTTTAACCTTTGTTTTAGACATCTA[C/A]ATTGATGAGATGAAACAGTGTTACAAAGATTTAGGCTTTAAAAGGTAATGTAAACCTATTCAAGAGAATTTTTTGCCTATGATTTTTTTAAAGTCCATGTGAAATCAAAATTCAGCATGTTTATTTTGCACATAGCACATAGTTTTATTTATTAGGTGAACAATTAATCCGTGCAAGTTAATCCACTGAAAAAAAGGTTGTTTTGGTAATCTTCAGTCAAATCTGAGCATCTCATTTTGTGTTTGGATTGGCTTCTTCTCTGATGATCTCAACTTGACTGCTTCAGCCGCAGTATTTATAACCACTCCCCCTTATCATTAGTTTGCTATGAGGGAATGAAGCACAAAAAGAAAGCCCCACCCCCTACTCAATATTTTGTTTCAGTTTGAAGTACATAAGCATACCAATATAAAAATCTTATAAATTTCCAGTTCACATGGACTTTAAACCTTCAACAACAACAAAAAAGTTAAAGTGCAATCAAGGACCATAATGCTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21971
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 |
|---|---|---|---|---|---|
| ENSDART00000047412 | None | None | 201 | None | 8 |
| ENSDART00000112140 | Nonsense | 194 | 201 | 7 | 7 |
| ENSDART00000147264 | None | None | 201 | None | 7 |
The following transcripts of ENSDARG00000029795 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 42112740)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 40372521 |
| GRCz11 | 11 | 40636666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTCAGTAGTTACAGATTTTCAACATTTTTCAAAATATCTTCTTTTGTG[T/A]TCAACAGTTGTGTGTGACAAGTAAAGGTTGAGTAATTGAAGGCAGATTTT
Long Flanking Sequence:
AGGTATAGATTATGTGCTTTATTCAGTGTTAAATGCTTCTCAATGTTAGTTTAAATGTCATTTTACATGACATTTACTGTTATACTACTGAAAGCTTGAAAATATATATAGATTGAAAATATAATAGGTTTGAAAATGAAATCAGTGCCAACCAACATCAGTCATTCAGAAGCCTATTAATAATGTTAAATAGGTTAATTATTTATTAATTAGATTAAAAGCCTTGTGATTTAGTTGGGAGTGCAATGGCTGGTATTTACAGTAAATGTTTGTCATGTTGTGTTTGGTGCAGACAGACAAATTACTTGTTGTTGGATTCTTGTTGCATGTTGTTAGTACACATTGTCAAGTAATTCCAAGCATTTATGAGTTTCTTTATTCTGCTGAAGATATTCTGAAGAGTTTTGTAAAAACCTTTGAGACCCATAGTAGGAAAAACTAATACTATGGAAGTCAGTAGTTACAGATTTTCAACATTTTTCAAAATATCTTCTTTTGTG[T/A]TCAACAGTTGTGTGTGACAAGTAAAGGTTGAGTAATTGAAGGCAGATTTTACGTTTACTACTTAATGCATTAATATAGTGTTAAACTTGAATACACTGAATGCTGCTAATGCAGTCAGAATTTACTCTCCCTATTTTAAGTTTCTTATATTTGGACACAATGTTTTTGTGCTAATGTTGGACTTTATGTTCATGTGATCTATTAAATGCCAAGTAAAACGAAGCACAATAACTGACTAGAAAGTTAAAGACTGGTACTATATGACAATAATCATTACTATATTTCGTTTTAATTTTTCATTCATTCATTTTCCTTCGGCTTAGTCTCTGATTTATCAGAGGTCGCCACAGCGGAATGAACCGCCAACTATTCAGGCATATGTTTTACACAGCGGATGCCCTTCTAGCAGCAACCTAGTACTGAGAAACACACTCTGACGTATACTCGTACACCGGCCAATTTAGTTTACTCAGTTCACCTATAGTGCATGCCTTTGGACT
Associated Phenotype:
Not determined