ZMP
zgc:101028
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein C9orf25 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6DC60]
Human Orthologue:
C9orf25
Human Description:
chromosome 9 open reading frame 25 [Source:HGNC Symbol;Acc:19920]
Mouse Orthologue:
2310028H24Rik
Mouse Description:
RIKEN cDNA 2310028H24 gene Gene [Source:MGI Symbol;Acc:MGI:1919151]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16139 | Essential Splice Site | Available for shipment | Available now |
sa32337 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16139
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024616 | Essential Splice Site | 20 | 186 | None | 6 |
ENSDART00000135623 | Essential Splice Site | 20 | 64 | None | 4 |
ENSDART00000144866 | Essential Splice Site | 20 | 185 | None | 6 |
The following transcripts of ENSDARG00000016396 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 11324569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13025934 |
GRCz11 | 21 | 13122922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTGACAGATTTCAAGTGCCACCAGTGAATCCAGAGAWGAAGCTGCTGG[T/C]AAGTGTCACTTTCACTACATGRWTAGAGAATAACACTATGTACTTTTACA
Long Flanking Sequence:
CTTACTACAGTAATACCTGTCAATTATTACAATTATTCTAATTACATACAATGACATTAAACCAAACTCCAAACTTAAAACACGTACGATGCCAGATAACATTACTCATATTACTCAAAAGTTAAACTAGATTATAACAAGGGCAAACTAAATAAATTAATGTGCAAAGTTTTACATTTTCTTCTTATTACAGTAGACGTTCTGCCTCATTAATTATTCATCAGCTTGTCAGCATGGGCGGGGTTCCGGACCCGGAAGTCAGATGTTGCTGTTGAGTCACCCCTGACTGGTAGCAGCCAGATAGCGGAAAACAACTAGAGATGATGCTGGAAAGCACGGCATCTTTGAACCGATCCAGAGAGTGAATAAATGCGTTTGTCCATACGGATACCGCCTTGAGCATTTGTGGTTCGCTCTTCGAGACTGACGTTGTATCAAAATGATGGAGGAAATTGACAGATTTCAAGTGCCACCAGTGAATCCAGAGATGAAGCTGCTGG[T/C]AAGTGTCACTTTCACTACATGATTAGAGAATAACACTATGTACTTTTACAGGACAAGGGAAATGACAGTGTGTGTATGAAGACAGTAATTCTTGTCTGGCCCACTAACGCAGGGTACATTACCAAAAGGATCCGTGGGGATGTTTAGACTGTTAAACCGACATATGCAACTCTCTAGATGAATGATTCCCTGTTGTTTTGGTGCTGACATTGACTCAGTCGTGCTTCGAGAATGTTCGTGAGTAAAACATGTGCAAAATAACCCTGCCTTAATGAGACAAAACAAAAATGCCCAAATTATAAGCTATATTTGTAATGCTGTTTACTGTGTGTAATTAGGGGTGACTGATACGTGAATGTGTTGATGTAGTGAATCGGATCTTTTAATTGATTCGGTCCAAGCGGTTCATTTACTATTTTCGATTGTAATTGAATCACTATGAAAATACAGTTCTTGCTCCAGATGCATCTGTTTCCGATTGATAATATAATGAGCTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32337
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024616 | Essential Splice Site | 116 | 186 | None | 6 |
ENSDART00000135623 | Essential Splice Site | None | 64 | None | 4 |
ENSDART00000144866 | Essential Splice Site | 115 | 185 | None | 6 |
The following transcripts of ENSDARG00000016396 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 11300773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13002138 |
GRCz11 | 21 | 13099126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGACCAGAGTCCAGATGAGAAGCCGCTTGTAGCACTGGACACAGACAGG[T/C]AAAACACTCATCAGACATTAAACCTTCACTCATTCTGTCATTCTTTCTCT
Long Flanking Sequence:
CAACAAATGTTTTATTATTTCTGTAGTTTTCTTCATAATAAAATAATGTTTTTTTAACAATGTTAAACTTGTTATAAAAAAAGAAACATTATGTTCAAAAAAGTCTATACAACTAACGTTTTCTTGTTTTCACACATTAAAATATGTGGTTAGGAAATTACTACATTTGTTTTTTCGAATTCCATTGGTCCAACCAGGCCATTACAAAAAATTAGTAACCCTTAGTGTTTAGCCTCGTATAAGTCTAAAATCTCTTTCATATTGGATTTGAAAGGGTCTTTAAAAGTCTTAAACTTGATTTGGTGAAACCTGCAGAAACCCGGATACATTACCGTCCATCAGAGAACAACAGCAGAGATAATGAACATATGTAAATATAAATCAAAATTTTACTGATTTTCTTCTACTCCTATTCCAGGTTGGTTGTCCCTAATAAAGGCTATTCATCCTTAGACCAGAGTCCAGATGAGAAGCCGCTTGTAGCACTGGACACAGACAGG[T/C]AAAACACTCATCAGACATTAAACCTTCACTCATTCTGTCATTCTTTCTCTAGAAATCTGTTATGAACATTACAGAATATTTCATTTAAATTGACAGATTAATATGCAACAAGCAACCAGATGGGAATAAATCCTCCAATTAAAGCTTGCGCCGCTTTTCTAACAGATGCAATGCCAGCCATCTCCATGTAAAAAAAAAGACCTGACAGACCTGACATTTAAACAAAATACCAGCTAATTTTAATAGCTCTAAAGCTGGTGCCCTCTGACAAGCGTGAAAAACTGTCAAAGGGAAAAAAAGATTTCAAGTGAATGTGCTTTCTTGATCGCAACGCTCTGGCTAAATGAATAAACATTTGCTGTTGCATATAATGTATATATGTTGGCAAAAGCTGAAAAGTCTCACTTCAGACATTACAAAAATTTTCTCATCCATCACAGCAAAGACCATTAACTATATACAGAATTGTCCAAAATGCTGTTTTTTTGTATATATATATA
Associated Phenotype:
Not determined