ZMP
si:dkey-170m15.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RH17]
Human Orthologue:
C6orf103
Human Description:
chromosome 6 open reading frame 103 [Source:HGNC Symbol;Acc:21212]
Mouse Orthologue:
9130014G24Rik
Mouse Description:
RIKEN cDNA 9130014G24 gene Gene [Source:MGI Symbol;Acc:MGI:3605549]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37074 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37073 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10146 | Essential Splice Site | Available for shipment | Available now |
sa18046 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37074
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021575 | Essential Splice Site | 345 | 1471 | None | 35 |
ENSDART00000133556 | None | None | 225 | None | 6 |
ENSDART00000135492 | None | None | 716 | None | 17 |
ENSDART00000141636 | Essential Splice Site | 22 | 103 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 32022665)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32080905 |
GRCz11 | 20 | 31983784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCCCTTGCACCTAATGGAGAAAAGAACCTCAATGCTCACGAGGATGG[T/A]AAGCATATGAGTTTTAATCTGCAAGTCTGCACATAAACTACTGTTTAAAT
Long Flanking Sequence:
TCTTGATCATGTAACAGTCATGGCACTGATGGCCTGTTGTGAGATCAGAGATGGCCTTGGGAGATGAAGATCAAACACTGATAACAAAGTGCCTCTGTTTCTTCCTCTACACTGGAAGTTTGTGTGCTGTGTGAATTAGGAAAATATGGCTTGACAGATTACAGTGCCCTCTCCACTATTCACGCCTTTGTCTTTGAAACTCATGCCTTGATCTATTCGCTCATTCTCTCTTCCTATCATTGAAAATAGGCTGCGCTCTATTCATTTCATTATGTTTTAACTATTAAAGAGATGGAAGCCTGACAACAGGAAAAAAAAGTTACGTTTATGCATATAAAGTAGAAATGGCATCTCTTTCATGTTTATTTCCTAAGTCTTGTTTTTACAGATGTTCTTTTTTTCCGATTTAGCCACTGGTTCTGTTCCTCAGATAGTAGTGTGTGCCAGTTACCAGCCCTTGCACCTAATGGAGAAAAGAACCTCAATGCTCACGAGGATGG[T/A]AAGCATATGAGTTTTAATCTGCAAGTCTGCACATAAACTACTGTTTAAATGTTATGTATTTTTGATACATTAAATTGATCCCATGGCAATACAGACATTTATATGGTTACAAAAGATATATTTCAAACAAATGCTTTTAATTTGAATCTTTCTGTTCGTCAAATAACTATTAGCTAAAATGTGTGAAGGTTTCCATGTACAGTTTACATAAAATATCAAGCAGCAAAAACATTTGTTTTTAAGATTATTAATCATTTTAGAAGCATTTACTTAAGCACCAAAATGATCGCACACTAGAAAAGATTATGAAGGATCACATGACTCAAGCCTTAAACTTCAGATTTGCCATTACAGGGATAAATTATCTTTCAAAATATAATAAAATGGTAATCAGTTGTTTTGAATGTTACTTTATTACAGTTTTTGTGGTATTTATTAATTAAATAAATAAATGCATTATCATCATCAAAAATACTTTAAAGACTTAAATAAACAACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37073
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 |
---|---|---|---|---|---|
ENSDART00000021575 | Nonsense | 371 | 1471 | 10 | 35 |
ENSDART00000133556 | None | None | 225 | None | 6 |
ENSDART00000135492 | None | None | 716 | None | 17 |
ENSDART00000141636 | Nonsense | 48 | 103 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 32020582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32078822 |
GRCz11 | 20 | 31981701 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATGGGCTATCTCAGCTCTTCAGTCACCCAGTGCTTCTCACCTGCACT[C/T]GAGACTGTCCTCTAGTGGCCCCTCCTAAAACACCTCCACTGCCTCAATGG
Long Flanking Sequence:
ATACATGGTATTTTTTCCTACTTTGAAAATCAATGGCTACTGTTTACCAACATTTATCTAAATATCTTCTTTTGTGTCCCACAGAGTAAAAAACAGAACAAAAAAACGTACTCTTTAATATCATTGAATGCATGAGAATGAGGTCATGCAATATGCCACACAGCAGTATGGACTCTTGTTCGTTTGATTCATTAGTTATAAACCGTTATCACCACCCAGTTTGTATAATATAAACTCCTCCACCAAACACACTTACCTAAAGCTCATTAAAGGGAAAATCTGCCTCAAATGGTATACTCTCCCTTCTTCCATCTTAGTCTCAAGCAATATTTGGCTCCGTTTGGATTAGCGCTGGATGTCTAATCCGTTATTAAGTCTCTCTTCCCTAATCTATGATCATGGTGGGTGGTGTGTGTGTTCTCCAGGCTGATTCGTCTGAGAGTCTGAGGCAGTATGGGCTATCTCAGCTCTTCAGTCACCCAGTGCTTCTCACCTGCACT[C/T]GAGACTGTCCTCTAGTGGCCCCTCCTAAAACACCTCCACTGCCTCAATGGAAACTCATCCGGCCTCGCAAGCAGACTAACATTACTGATGAGCCCAAGGGTAAGATGTTTGGTTTTTATGTGTGAACATGTTTCAAATCCTTATGTAAATGTTGCTCTAAACTGATGTTTATGCACTTCAGAACCCCCTGTTCAGAAACCAGAGCAGTTCATTGAGGTTTCCAGCCCATTCATCAACTTCAAACTCATGACCATGAGTGCACATGATATGTAAGCTCTCTCTTTCTATCTCTCTTCATGTGTGTGTACTTCTTTATGGGGTTAGTAGAACACAACATGGTATGACCTACTGTAGGTGTTACTCTTGTGTATTTTTCTAATTTACAAAACTGAAAAAAAAAATTAAGTCAGTACACCAAAAACAAAAACATAATTATTATTTCCTTTCTAGTTTTCTTTTTCTTGTTCACTCAACTTTTGAAGACATCAGCTGCACTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10146
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021575 | Essential Splice Site | 1192 | 1471 | None | 35 |
ENSDART00000133556 | None | None | 225 | None | 6 |
ENSDART00000135492 | Essential Splice Site | 680 | 716 | None | 17 |
ENSDART00000141636 | None | None | 103 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 31975018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32033258 |
GRCz11 | 20 | 31936137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGTATTTTGTGAATTTGTATAATTTTGATTGTTCTGTTTGACATTGAC[A/G]GTGTTTGGAGATATTYTGGATGGCACATCTATGCCTGTGGGTACAGACCA
Long Flanking Sequence:
TTTACATATCTACTGTCTAAGCCTCAAGAAATTCTGTTTAATATATTTGAAAGTTTTCAAGTATTATTTCTCCAACTACGTTATAATGTTTAGACGAAAGTATAATTTTTTTTTAAACACATCATCCTATATGTGCCAATGCTGTCAAATAACTCTTCAAGCAACCTAGAAACACTTTAAAGGTTTGAAGTAATATTTTTGTGTCACTACATTGTATATTTAATAAATAATAAATAATTAATACATTTCTACTTCCAAAATAGATTGTTCTGCTCCAAATCCTTGATACTAGCAAATACTGTCAAATTATTAAACTAATTTTTTTTCCAGGCTAGAAACACTTTGAATGTTTGAAGAACTGTGTTATTTTTGTCAGGCCATTGCTGTCAACTCACTTAACGTTTTATCAATTTGAAAATTACTTTTGCCCTAATTTAAGTGTCAATCAGTTGAGTATTTTGTGAATTTGTATAATTTTGATTGTTCTGTTTGACATTGAC[A/G]GTGTTTGGAGATATTCTGGATGGCACATCTATGCCTGTGGGTACAGACCAACAAAACAGAGAGGGTCAGAAATCTACTCCCAAATCAACCCACAAGGCCAAGGAAAAAGAAAAGGACAAAGACAAATTAGCATTAAAGTCGAGCTCCATTATGGACCTGGTCAGTACAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCGTGTGTGCATATATTGTAATGCCATTATCAATCCCACTATATATTTAAATCATTCGCACTGAGATAAAAAGCTTTTCTTTTTAAAGCTTTGAATGGATTAGGATATATAACATGTTTAAAATGATACATTTGCAGGTTAAGGTCTGATATAGTGTCTCTTTGTTAGAAATGTAAGAAAGTGCTATACTTTACGTTTGTAAATCTTAATAGGATGAGTTAGAAGAATATATTACCATTCAAAAAATATGGGACAATTTTGATTTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18046
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021575 | Nonsense | 1211 | 1471 | 30 | 35 |
ENSDART00000133556 | None | None | 225 | None | 6 |
ENSDART00000135492 | Nonsense | 699 | 716 | 17 | 17 |
ENSDART00000141636 | None | None | 103 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 31974960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 32033200 |
GRCz11 | 20 | 31936079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGATATTYTGGATGGCACATCTATGCCTGTGGGTACAGACCAACAAAAC[A/T]GAGAGGGYCAKAAATCTACTCCCAAATCAACCCACAAGGCCAAGGAAAAA
Long Flanking Sequence:
AAGTATTATTTCTCCAACTACGTTATAATGTTTAGACGAAAGTATAATTTTTTTTTAAACACATCATCCTATATGTGCCAATGCTGTCAAATAACTCTTCAAGCAACCTAGAAACACTTTAAAGGTTTGAAGTAATATTTTTGTGTCACTACATTGTATATTTAATAAATAATAAATAATTAATACATTTCTACTTCCAAAATAGATTGTTCTGCTCCAAATCCTTGATACTAGCAAATACTGTCAAATTATTAAACTAATTTTTTTTCCAGGCTAGAAACACTTTGAATGTTTGAAGAACTGTGTTATTTTTGTCAGGCCATTGCTGTCAACTCACTTAACGTTTTATCAATTTGAAAATTACTTTTGCCCTAATTTAAGTGTCAATCAGTTGAGTATTTTGTGAATTTGTATAATTTTGATTGTTCTGTTTGACATTGACAGTGTTTGGAGATATTCTGGATGGCACATCTATGCCTGTGGGTACAGACCAACAAAAC[A/T]GAGAGGGTCAGAAATCTACTCCCAAATCAACCCACAAGGCCAAGGAAAAAGAAAAGGACAAAGACAAATTAGCATTAAAGTCGAGCTCCATTATGGACCTGGTCAGTACAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCGTGTGTGCATATATTGTAATGCCATTATCAATCCCACTATATATTTAAATCATTCGCACTGAGATAAAAAGCTTTTCTTTTTAAAGCTTTGAATGGATTAGGATATATAACATGTTTAAAATGATACATTTGCAGGTTAAGGTCTGATATAGTGTCTCTTTGTTAGAAATGTAAGAAAGTGCTATACTTTACGTTTGTAAATCTTAATAGGATGAGTTAGAAGAATATATTACCATTCAAAAAATATGGGACAATTTTGATTTTATTTTTTCAGAAATTCATCTTTTTATTCAGCATGGATCCATTTATCTGATATAAAGTGATGG
Associated Phenotype:
Not determined