ZMP
si:dkeyp-11g8.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RG85]
Human Orthologue:
C1orf25
Human Description:
chromosome 1 open reading frame 25 [Source:HGNC Symbol;Acc:16782]
Mouse Orthologue:
1190005F20Rik
Mouse Description:
RIKEN cDNA 1190005F20 gene Gene [Source:MGI Symbol;Acc:MGI:1916185]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15727 | Nonsense | Available for shipment | Available now |
sa37096 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3081 | Nonsense | F2 line generated | Not yet available |
sa23758 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15727
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 |
---|---|---|---|---|---|
ENSDART00000061637 | Nonsense | 94 | 691 | 4 | 16 |
ENSDART00000139648 | Nonsense | 92 | 213 | 4 | 7 |
ENSDART00000146924 | Nonsense | 92 | 691 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 34414941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 34487454 |
GRCz11 | 20 | 34390333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TSAACCTATTYACTCATTTTGACAGCTGGGAGAAAATCTTGTCCATTGTG[T/A]CCAGAAGARAAGTTTAAGGCCTGTTACAGTCATAAGCTTAGACGGCACCT
Long Flanking Sequence:
AAGCCGAAAAGAACATGAATGAATGAATTCATGATCATTTGAATCGGTAAGCAAAACTGGAACATCTGATTATGTTTCATAATGCAATATTTGTGGATTTGTTGTTTATCTCAACAGACATTGTGATTGACAGTAGTGCGATTCTGACAGAATCTAAGGAAACTGAGCAAATTTCCACTTGTGAAGCCTCGACTAATTCAGTGAAAATAGAGGACAAAAATGAAAACACAACCTCCAGTGCTGTGTCAGGTAAATATTACACTCCCCTATTGTGTCTCAGCATGGTTAATTCCCTGAAATGAATCATCGCTGTCTGTTTCAGAGAGACATGTGTCTATCCAGACCACACTGGAAGGGCTTGAGATGCTTGTGGATTTAAATGGAGGTATAGACAGAAGTATCACTTTATTCTGTCTGTTTGCTAAAACCATCAGCTATACCACTTGGATCTCAACCTATTTACTCATTTTGACAGCTGGGAGAAAATCTTGTCCATTGTG[T/A]CCAGAAGAGAAGTTTAAGGCCTGTTACAGTCATAAGCTTAGACGGCACCTGCAGAACTTGCACTGGAAAGTTTATGTGGAATTTGAAGGTAAAAAGTCTTGTTGGTTCTTTCTGACCAAAAAAAAAGAATTTGAAAGTTATTCATCATCTAATACATGTCATAATGTTGCTTCAGTGAAATATATTTCTTTCTCCTTCTACAGGCCAAAGAATGTGTATCTGTCATCTGCCTTGCAGGCAACTCAAGTCAAGCTTAGGCTCTGACCAGGTAAGGCTTTGAAGTGTTTCTCCCCATGTGCCTGCTTGGACTATGATTAAATTCAGGTTATACTCAAGGTTATATAATAAACATTAGTGTCATGATTAGCCATGTCAAGCCATGGTCAAGAAGATATTCTCAAGTTTTAACTAAATATCAGAATGTGAAATGGTGATTCTAGTGACTTTAAGCATGGCTTGAATGGTTATTGGTGCTGGTGGGAGTATTTCAGAAACCGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37096
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 |
---|---|---|---|---|---|
ENSDART00000061637 | Nonsense | 465 | 691 | 11 | 16 |
ENSDART00000139648 | None | None | 213 | None | 7 |
ENSDART00000146924 | Nonsense | 463 | 691 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 34420236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 34492749 |
GRCz11 | 20 | 34395628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCCAGGCAGATGAGTCTGCTAAAAAACTGCGGCAGCTGTTGCACTGC[C/T]AATGGTGTGAAGAAAGGGTGTTCCTCAAGCCAGGAAGTATGGTGGAAGGT
Long Flanking Sequence:
TTTATTCAACAGTTTTTTTCTCCTCAGTGTCAGTATATTTTGGAAATGAACATGTGCACAATATACTGACACTGAGTAGAAGAAACTGTTTTCATTTTTGTTTTACATCTGCACAAAAACATTCTCATAGTTTGCTAATATTCCGAAGGGCATCTGTTTTGAGTTTTTTTTTTTTTTTGTATAAGTCGGGACCATTGCTATCTGTGGAGGATAAGAGAGCTCTCTGATTTCACCCAAAATATCAAAAAAAAATTCTCTAATGAGAAGTCTGGTGAGTTTGGAATTACATAAAGGTGATTAATTAATAACTGAATTAATATTTTTGCGTGAACTAACACTTTAATGCATGTATATGCAGGGCAGCTGCCCGATGCAACAAAGGGATTGAGGTGCTGTTAGCTGTGGCTCTTGAGCACTTTGTCCTCGTGGTGGTGCGAGTTCTCCGAGGGCCCACCCAGGCAGATGAGTCTGCTAAAAAACTGCGGCAGCTGTTGCACTGC[C/T]AATGGTGTGAAGAAAGGGTGTTCCTCAAGCCAGGAAGTATGGTGGAAGGTGAGAAGTCAATTTGGCAAATAAGCAGCTGCATCTTTATTGAGTCCCAATAGCCTAAATTGCCAGTACTGGCAAAGCTTATGGGTTGATTTGAATGGAGATGTACTTGTAATATGGATACCTGCCAAATTCAAATACAGTTAAAGTCACAATTATTAGCCCACCTGTGATTTATTTATATTTTATTATATGTTTATTTATTTATTTTTCAGGTATTTCCCAAACAATGTTTAACAGAGCAAAGAATTTTTACACAGCATTTTCTTTAATATTAATACTTGACTGAAAATTGAATTCCCTTGCTTTAAGAACACTGTGGTCACAATGTACACAGTCTTTATGGTTACTTCCCATAGACTTTTATAAGCACCTTTATACTGTACAAACTGTATATTCTATCACTCTACCCAAAAACCCAACCCTGAAATGAAACAATATGCATTTATACATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3081
Status:
F2 line generated
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061637 | Nonsense | 466 | 691 | 11 | 16 |
ENSDART00000139648 | None | None | 213 | None | 7 |
ENSDART00000146924 | Nonsense | 464 | 691 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 34420241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 34492754 |
GRCz11 | 20 | 34395633 |
KASP Assay ID:
554-3197.1 (used for ordering genotyping assays)
KASP Sequence:
CAGGCAGATGAGTCTGCTAAAAAACTGCGGCAGCTGTTGCACTGCCAATG[G/A]TGTGAAGAAAGGGTGTTCCTCAAGCCAGGAAGTATGGTGGAAGGTRAGAA
Long Flanking Sequence:
TCAACAGTTTTTTTCTCCTCAGTGTCAGTATATTTTGGAAATGAACATGTGCACAATATACTGACACTGAGTAGAAGAAACTGTTTTCATTTTTGTTTTACATCTGCACAAAAACATTCTCATAGTTTGCTAATATTCCGAAGGGCATCTGTTTTGAGTTTTTTTTTTTTTTTGTATAAGTCGGGACCATTGCTATCTGTGGAGGATAAGAGAGCTCTCTGATTTCACCCAAAATATCAAAAAAAAATTCTCTAATGAGAAGTCTGGTGAGTTTGGAATTACATAAAGGTGATTAATTAATAACTGAATTAATATTTTTGCGTGAACTAACACTTTAATGCATGTATATGCAGGGCAGCTGCCCGATGCAACAAAGGGATTGAGGTGCTGTTAGCTGTGGCTCTTGAGCACTTTGTCCTCGTGGTGGTGCGAGTTCTCCGAGGGCCCACCCAGGCAGATGAGTCTGCTAAAAAACTGCGGCAGCTGTTGCACTGCCAATG[G/A]TGTGAAGAAAGGGTGTTCCTCAAGCCAGGAAGTATGGTGGAAGGTGAGAAGTCAATTTGGCAAATAAGCAGCTGCATCTTTATTGAGTCCCAATAGCCTAAATTGCCAGTACTGGCAAAGCTTATGGGTTGATTTGAATGGAGATGTACTTGTAATATGGATACCTGCCAAATTCAAATACAGTTAAAGTCACAATTATTAGCCCACCTGTGATTTATTTATATTTTATTATATGTTTATTTATTTATTTTTCAGGTATTTCCCAAACAATGTTTAACAGAGCAAAGAATTTTTACACAGCATTTTCTTTAATATTAATACTTGACTGAAAATTGAATTCCCTTGCTTTAAGAACACTGTGGTCACAATGTACACAGTCTTTATGGTTACTTCCCATAGACTTTTATAAGCACCTTTATACTGTACAAACTGTATATTCTATCACTCTACCCAAAAACCCAACCCTGAAATGAAACAATATGCATTTATACATTTTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23758
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061637 | Essential Splice Site | 628 | 691 | 15 | 16 |
ENSDART00000139648 | None | None | 213 | None | 7 |
ENSDART00000146924 | Essential Splice Site | 628 | 691 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 34423344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 34495857 |
GRCz11 | 20 | 34398736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTACTACAGCATCCATCGGCACAGCATTCGCGGCATGAACATGCCCAA[G/A]TACGTCAGTGCAAAACCTTTACATAAACAGTCATGCATTGCCATCCTGTG
Long Flanking Sequence:
TTCAAACGTTCATTGCATGTCAGCATTTGTCTTCTGATGCGCAAGTCGTTTATTAAATAAAGAAAAGATTCACGCAGCCTCTTCTACTGCAGTAAATTCCATTTTTACTGTTGATATTTGGCGCTAGTTCATCTAGAAGTGACAATTTTGTTTGTAGTAGGATGGAAACGCTGCTTTATTTGCACGTCTTTTATGCAATATTTTAGTTTTGTGCTTAAATTGAATTAGCATATTTAGATGGAAACATAGCTATTATCACCTTATTTGACGTGCATAATGTTGTTTTTATTTCTATAAAAGTGGACACACAAACTAAACGCATCAAATATAATAAACGAAAGTTTAAATATGTTGAACCATTTGTATTCAGGGAAAAGAAAGACCACAGGAGACGACGGTGGGAATGTGCTGAAAAAAGTCAAACCGGACACCTCTTTGGAGCATCCAGCGTTCTACTACAGCATCCATCGGCACAGCATTCGCGGCATGAACATGCCCAA[G/A]TACGTCAGTGCAAAACCTTTACATAAACAGTCATGCATTGCCATCCTGTGATATAATTGTCTTTTCCTCTCTAAGGTTGAATAAGTTCCTGCAGTATCTGACAGAGGCTGGGTTCAGAGTGAGCCGTACACACTTCGATCCAACCGGCGTGCGAACTGATGCCACCCTGGCTCAGTTTAAAGAAGTGCTAACAAAATATAGTGTGCCCACTTACTCGTCCGCTCCTCAGAGCAGTGCTATCAGCTCAGACCGACGACAAACTCTCTGATTTCAGATGCGAATGTAACCAAACCAGAATTTATATTTTGTCTAGAAGATCTTGGAAAGCAAAGAGGTCACTAACTCTTTCTTTGGCTTTTTAATTGCTGATTTATCGATGTTTATTGCAGATTTAACAGCAAGAGAATTTCATGAAAAGAAAACAGATTCATTTGAATGAAAATTGTTGTTTTATTTTTTGTTTATTGTGGATTGCACTGAGGCTTTGATCCATAATGGCT
Associated Phenotype:
Not determined