ZMP
si:dkey-27f16.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8A4R8]
Human Orthologue:
C6orf27
Human Description:
chromosome 6 open reading frame 27 [Source:HGNC Symbol;Acc:13939]
Mouse Orthologue:
D17H6S56E-3
Mouse Description:
DNA segment, Chr 17, human D6S56E 3 Gene [Source:MGI Symbol;Acc:MGI:1306798]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15280 | Nonsense | Available for shipment | Available now |
sa18346 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15280
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 |
---|---|---|---|---|---|
ENSDART00000101664 | Nonsense | 520 | 990 | 10 | 15 |
ENSDART00000138992 | None | None | 466 | None | 10 |
ENSDART00000146119 | None | None | 88 | None | 6 |
The following transcripts of ENSDARG00000069710 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 40716780)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39606189 |
GRCz11 | 1 | 40324262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTCAGGYGGTGAGAAGTCCAGCTATTGCAGAAAACTTTTCTWTTGTGT[T/A]GGATTCCTCTCTGTYTAATGTAACTGTGTACATCACAGGAGACTCTCCAT
Long Flanking Sequence:
GGCTTGTCGTGCATATCACCTTGTGATCAACTCACCTAAACTCTTCCATAAACCCAACCCATAATGTTTTTAATAGCAAACGTAAAAGAAAATTCCATCACGGCCACATAGTTTTACTTTGATTTTACATTGCTTTTATCTAAACCACTAGATTTACTGGAATTAGACACAAGTGCTTTGTATTTCAAGTACAACACTGTACAAAGTGAGAAATGAAGTAACTGACCATGGTAGAAAAGTTGTTGATATGGAGATAAACAAGTAATCCAATTTTCTGCTATGTATTTATTGTTGTGCTAGGACCCGCAAGAAAATAATCCTTTATTTCATTTCAAGTGTTCAAGTAAATCATATGCTGAAGTGCGCACGCTTTTACAAAAACGTAAGCAGAAGCATGTATTTCAATTGAGAGTGTGTTGAAGTCATCTCTATATTTCTTCAGGTGACCATTCTTCAGGTGGTGAGAAGTCCAGCTATTGCAGAAAACTTTTCTATTGTGT[T/A]GGATTCCTCTCTGTCTAATGTAACTGTGTACATCACAGGAGACTCTCCATTCTTTACTCTCTACAGCCCTACAGGTAAGCCTTATACATTTAGGAACGGTTTGTTTATGTGAGGGTTTTATTTTCTCCAACACAAAATCTGCTAATGCCGAAAACACTGTGTTTTGCCTGCTTTCAGGTGTGTCTCAGTCAGGTTCAGTGGCCAATGGTCTTCTGGGCAGCATTCTGACTGTAGGGAATCTAAAGCGAATTAAACTAAGCTCTGAAAACCAGAAAGGGGAATGGAGGATTAGCATTAATGCTACAAGTTTCTACAGCCTTAAAGTCACTGGTAAGAGTTGTTGTATTTATATTTTTATCAATTGAATTGCTATTGTTTAAGTTTTAAAATTGTTTTTATTGCAAAATGTGTGGATCAAGCTTTCCAGGGGGCATCTTGATGTCAAAAAGGCATCCATGTGACATCTAACACTGGGGTCAAAAACATAATTGATGTGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18346
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 |
---|---|---|---|---|---|
ENSDART00000101664 | Essential Splice Site | 624 | 990 | 12 | 15 |
ENSDART00000138992 | None | None | 466 | None | 10 |
ENSDART00000146119 | None | None | 88 | None | 6 |
The following transcripts of ENSDARG00000069710 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 40717704)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39607113 |
GRCz11 | 1 | 40325186 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGTCACAGAGTAGTGACTTTACACCAAAAGCCAATCGTCCTTTCATTG[G/A]TATGATATCGTCTTCAAATTGATATTTCTTGATTATTAATAKACATTTAC
Long Flanking Sequence:
CCAGGGGGCATCTTGATGTCAAAAAGGCATCCATGTGACATCTAACACTGGGGTCAAAAACATAATTGATGTGAAACGATGAAACAATGCATGATACAAATGTTTGATGTCTATTAAGGTAGTTCACGTGCATTGTAGGGATACAAAATCCCAGGTAGATTTCTAATTCGTCATCGAAGCTTTCCGATAATTTTTTCTTTCTTGTCCTATAATACTTTTGTGTCTGTCTTGGTGGGCAAAATGGCATCAATGTGTGGATGTCAAATGGATGTCAAAATTTTCACATCAAATCAGTTTGCATATTTAAATGTGTTGTTAATTAGTTTTTGACATCAACATGCTTGCTGGATTACAGAATCTGTAGCATATTGTAACAAAAACAGCTACTTACATATGTTTTATTGTGTATACAGCTGAGAGCTCAGTCAACTTTCTCTTCAACTTTGTGGAACAGTCACAGAGTAGTGACTTTACACCAAAAGCCAATCGTCCTTTCATTG[G/A]TATGATATCGTCTTCAAATTGATATTTCTTGATTATTAATAGACATTTACATACTGTAACAGTTCACATTTGGTGAATTCAATGCATCCATTCTGAACCTAGACACTAATTTCTTTCAAGATGAAGAATCTTGTGTATAAACATGAATATGTATACAGTGGTGTGAAAAAAAGTGTTTGCCCTCTTACCGAGCTCTTATTTTTTAAATGTTTATCACACTTTAATGTTTCACATCATCAAACACAATGAAACATTAGTCAAAGATAACATAAGTGAACACATCATGCAGTTAATCACACCTGAGCTAAAATTTTCCAGCCAAAACACAGCCTGATTACTGCCACCCCTGTTCACGATCAAGAAATCACTTAAATATAAAGTGAAAGAGAACAAAAAACATTTAAAAGCTAAACATCACGCAGAGATCCAAATTCAAAAACAAATAAGAAAGAAAATAATTGAGGAAATTCTAAGAATTATAACCGAAAAAAAGTTATAAA
Associated Phenotype:
Not determined