ZMP
HOMER2
Ensembl ID:
Description:
homer homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:17513]
Human Orthologue:
HOMER2
Human Description:
homer homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:17513]
Mouse Orthologue:
Homer2
Mouse Description:
homer homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1347354]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36549 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5905 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11712 | Nonsense | Available for shipment | Available now |
sa32179 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36549
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 |
---|---|---|---|---|---|
ENSDART00000082450 | None | None | 175 | None | 5 |
ENSDART00000124088 | Nonsense | 41 | 271 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 253 |
GRCz11 | 18 | 253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACACACACACACACACACACACAGCGCTGTGAGGATCTTCCTCTGCA[C/T]AGGGTTTATGGTTCATGTTGCCATGGAGATTTGGATCAGTCCCTCAGTGT
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAGAACTGGGTTCCCGCCAGTAAACAGGCCGTTACGGTCTCCTACTTCTACGACAGCGCACGCAACAGCTACCGCATCATCAGCGTAGACGGAACAAAGGTCAGACAGATACATGTGTACCTGTACGTGTGTGTGATAGAGTCAGAGTTAGGGTGATGCAAACAGCAGTCTTTCTCTCTCTCTCTCTCTCTCTCACACACACACACACACACACACACACACACACACAGCGCTGTGAGGATCTTCCTCTGCA[C/T]AGGGTTTATGGTTCATGTTGCCATGGAGATTTGGATCAGTCCCTCAGTGTGGAGGCGGCACTGATGATGTCACAGCGCAGACCTGCTGACACACACACACACACACACACACACACACACACACACACACACACACACACACACCTGCTGCTGTCACTCTTGGAAAGCACATGGATAAAGACGCATACACACAACCACACACATGCGCACACACACACACATTAGTGTGTTAGTAGCGGAGACACATTTACACACACCTGCTGCCATCATTCTGAAAACTCATGCTCAGAGTTTGAATGAACACACACACACACACTCACTCAGGTTGCACGGTTGACTGAATACACACACCGATTGCATGGCTGACTGAACACACACACACACACACACACACACACACACACACACACAAATGTTGAATTATTGACTGAACACATGCTTCTCTGATCAGCTCTGCGACTCACAGAATCACTTTATGCAGAAATAACACACACACACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5905
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082450 | None | None | 175 | None | 5 |
ENSDART00000124088 | Essential Splice Site | 78 | 271 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 841 |
GRCz11 | 18 | 841 |
KASP Assay ID:
554-3739.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTAATATTAGCGAGCTGCATGTSACTCATGTATTGAAGAGTGTTTACA[G/A]TTTTCATTGCGTACGCTGCGGCATCACGAGCGAGAGAAATGCAGCATGAA
Long Flanking Sequence:
GACACACACACACACACACACACACACACACACACACACACACACACACACACACACCTGCTGCTGTCACTCTTGGAAAGCACATGGATAAAGACGCATACACACAACCACACACATGCGCACACACACACACATTAGTGTGTTAGTAGCGGAGACACATTTACACACACCTGCTGCCATCATTCTGAAAACTCATGCTCAGAGTTTGAATGAACACACACACACACACTCACTCAGGTTGCACGGTTGACTGAATACACACACCGATTGCATGGCTGACTGAACACACACACACACACACACACACACACACACACACACACAAATGTTGAATTATTGACTGAACACATGCTTCTCTGATCAGCTCTGCGACTCACAGAATCACTTTATGCAGAAATAACACACACACACACACACACACACACACATTAGAGTGTAATGTATATTCATGTGTAATATTAGCGAGCTGCATGTCACTCATGTATTGAAGAGTGTTTACA[G/A]TTTTCATTGCGTACGCTGCGGCATCACGAGCGAGAGAAATGCAGCATGAACAATACAAGCATATCCATTAAACATTATCATTCCCTTTTCAGCTTAGTCCCTTTATTAAACCAGGGTCACCACAGCGGAATGAACCGCCAACATATCCAGCATATGTTTTACGTAGTGGATGCCCTTTCAGCTGCAACCCATGAGTGGGAAATAAACATTAACATGTTTTGAAAAAAATAAACAGAAATAAAAGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTATATATATATATATATATACACAAACACACACACACACACATACACCCATTAATAATGAAATGAATCTGTTTTCATTCCTCACACAGCGATGATTACAGCTCACATTTTGGAGAACTTGCGGAAATTGTGTGTAAAAATGTAATTGATATCAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGTGTGTGACTNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11712
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082450 | None | None | 175 | None | 5 |
ENSDART00000124088 | Nonsense | 87 | 271 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 868 |
GRCz11 | 18 | 868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGTATTGAAGAGWKTTTACARTTTTCATTGCGTACGCTGCGGCATCA[C/T]GAGCGAGAGAAATGCAGCATRAACAATACAAGCATWTYCATTAAACATTA
Long Flanking Sequence:
ACACACACACACACACACACACACACACACCTGCTGCTGTCACTCTTGGAAAGCACATGGATAAAGACGCATACACACAACCACACACATGCGCACACACACACACATTAGTGTGTTAGTAGCGGAGACACATTTACACACACCTGCTGCCATCATTCTGAAAACTCATGCTCAGAGTTTGAATGAACACACACACACACACTCACTCAGGTTGCACGGTTGACTGAATACACACACCGATTGCATGGCTGACTGAACACACACACACACACACACACACACACACACACACACACAAATGTTGAATTATTGACTGAACACATGCTTCTCTGATCAGCTCTGCGACTCACAGAATCACTTTATGCAGAAATAACACACACACACACACACACACACACACATTAGAGTGTAATGTATATTCATGTGTAATATTAGCGAGCTGCATGTCACTCATGTATTGAAGAGTGTTTACAGTTTTCATTGCGTACGCTGCGGCATCA[C/T]GAGCGAGAGAAATGCAGCATGAACAATACAAGCATATCCATTAAACATTATCATTCCCTTTTCAGCTTAGTCCCTTTATTAAACCAGGGTCACCACAGCGGAATGAACCGCCAACATATCCAGCATATGTTTTACGTAGTGGATGCCCTTTCAGCTGCAACCCATGAGTGGGAAATAAACATTAACATGTTTTGAAAAAAATAAACAGAAATAAAAGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTATATATATATATATATATACACAAACACACACACACACACATACACCCATTAATAATGAAATGAATCTGTTTTCATTCCTCACACAGCGATGATTACAGCTCACATTTTGGAGAACTTGCGGAAATTGTGTGTAAAAATGTAATTGATATCAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGTGTGTGACTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32179
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082450 | Essential Splice Site | 86 | 175 | 2 | 5 |
ENSDART00000124088 | None | None | 271 | None | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 2013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2013 |
GRCz11 | 18 | 2013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACGGTCCGAATTCAAGAGTTGGAAGCAGATCTGCAGGACAAACAACAG[G/T]TGACACACACACACACGCACACACACACACACTTTCTCTCTGTGCTCCCG
Long Flanking Sequence:
TGAACACCTTTCAGAATGTAGAGGAGATCTTATTCTAAAAGCAGCTCAATAAACGTGTTTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGCGCGCGCAGTAAGAAGTGTGAGTCGGAGCTGCAGGCGCTGAGGGACAGTAGCGCCCGTCTGCAGGAGGCGCTGCAGGAGGCAGAGAGCTCCGCGGAGAGCTGGAAGACTCAGGCCACGCGGAGCCTGGAGGAGAACAACCAGCTGCGCAGCAAGGTGAGGAGCACACCTGTCTGACCTCTGACCCCTGACCCCTGACCAGACACACCACAACCATTCCAGACACTTTAGTACATGAGCTGACCTAACCTGTGGAGAGTTCTCATCTGTGTTTGTGTGTGTGTGTGTGTGTGTAGATCGCAGAGCTGGAGCTTCAGTGTAAGGAGCTGAGTGTGGAGAGAGAGAGGAACGCTCAGCTCACGGTCCGAATTCAAGAGTTGGAAGCAGATCTGCAGGACAAACAACAG[G/T]TGACACACACACACACGCACACACACACACACTTTCTCTCTGTGCTCCCGCTGAAAGTGTGTGTGTGATGGTGTTTTGCAGGAGCTGGAGAATCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATACACACACACACACACACACACACACACACACACACACACACACACATATACACACACACACACACACACACACACACACATACACACACACACACATATACACACACACACACACACACACACACACACACACACACACACACACACATACACACACATATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTCGAGGTGTGTGGGGGAGGAGATCAGTGTTATTCAGTGTGTGTGAAGCCGCTTTTCAAGCATTGCACACACACTCATGA
Associated Phenotype:
Not determined