ZMP
med15
Ensembl ID:
ZFIN ID:
Description:
Mediator of RNA polymerase II transcription subunit 15 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVN7]
Human Orthologue:
MED15
Human Description:
mediator complex subunit 15 [Source:HGNC Symbol;Acc:14248]
Mouse Orthologues:
A230006K03Rik, AC129019.1, AL606965.1, Glrp1, Med15
Mouse Descriptions:
RIKEN cDNA A230006K03 gene Gene [Source:MGI Symbol;Acc:MGI:3644205]
glutamine repeat protein 1 Gene [Source:MGI Symbol;Acc:MGI:108038]
mediator complex subunit 15 Gene [Source:MGI Symbol;Acc:MGI:2137379]
glutamine repeat protein 1 Gene [Source:MGI Symbol;Acc:MGI:108038]
mediator complex subunit 15 Gene [Source:MGI Symbol;Acc:MGI:2137379]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17487 | Essential Splice Site | Available for shipment | Available now |
sa23898 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17487
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 |
---|---|---|---|---|---|
ENSDART00000021997 | None | 36 | 802 | 2 | 18 |
ENSDART00000139622 | Essential Splice Site | 23 | 48 | 2 | 6 |
ENSDART00000140129 | None | None | 138 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 17760327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 18908579 |
GRCz11 | 21 | 18945215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAATTACAGTGAGGAAGCCATGAGAAAAGCAGGAACTGGTCACACAAA[G/A]TCCAGTACTGAGATGGAGAGCCATGTTTTTACGAAAGCAAAGACCAGAGT
Long Flanking Sequence:
GCAAATGTAAAATACAAATACTGCCATTTAGAGTGTTTTTACTGTAATTAACTATCAAATCTAAATATCCAAATAAGTCACTTTCATTAAGTGTGATTTATAATTTTAATTGTAATAATAGAATAATTGTAACGTAATAATATAAAATTGTTGTCTAAAAAATAAATAAACCATGCCTGAAATCATGTCTGGTTTTGTGTTATTTCTATGCCAAACAAAATGCTCTAAACTACAAATATTGTAATTTGGGAAGAGATGCCATCAGTAGTTTACAGAATAAAAGTTATCAAATACATAACTATAAATCATACATCAAGACAAACTAATAATTTTCAAGCACTCGTGTAATCATTGTTTCTTAAATGATTAATCAGTGGCTGTAAATGATAGGTAACACTTTCTTTTTTTGGTCATGAATCAGTTGTGATTAAATATTCTGCTTCTGCTATATTAAATTACAGTGAGGAAGCCATGAGAAAAGCAGGAACTGGTCACACAAA[G/A]TCCAGTACTGAGATGGAGAGCCATGTTTTTACGAAAGCAAAGACCAGAGTGAGTATTTTTAAAATGTTTTTGTCAAAAAGAACTGTTGTGTTAGGGAGTGATAGATAGAAGTGCAATGAAAAAACAACAACTCATCTTTAATTTATGTTTTGGACACAGGAGGAGTATTTATCAATGGTTGCGAGGCTGATAATTCACTTTAGAGACATCCGTAAGTAACCAACACAGATTTCAATATAAATGTTTTTGCATTGTTGTGTTTGGATGCGATATTAAATAAATGGTCTTTTATTGTAGATAAAAAAGCACAAGGTGGGCCTGGTAAGTTAAATTTTAGTTAAAAATATAAGTACATTTCAAACTTTATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTATTTTCTGCTAAATTTCAAGGTGATCTTGTTAATTTTTAGATCCCATCAATGCCCTGCAGAATTTACCTGGAGGTGTTCCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23898
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 |
---|---|---|---|---|---|
ENSDART00000021997 | Essential Splice Site | 69 | 802 | 3 | 18 |
ENSDART00000139622 | Essential Splice Site | None | 48 | 3 | 6 |
ENSDART00000140129 | None | None | 138 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 17760115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 18908367 |
GRCz11 | 21 | 18945003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGTATTTATCAATGGTTGCGAGGCTGATAATTCACTTTAGAGACATCC[G/A]TAAGTAACCAACACAGATTTCAATATAAATGTTTTTGCATTGTTGTGTTT
Long Flanking Sequence:
AAACAAAATGCTCTAAACTACAAATATTGTAATTTGGGAAGAGATGCCATCAGTAGTTTACAGAATAAAAGTTATCAAATACATAACTATAAATCATACATCAAGACAAACTAATAATTTTCAAGCACTCGTGTAATCATTGTTTCTTAAATGATTAATCAGTGGCTGTAAATGATAGGTAACACTTTCTTTTTTTGGTCATGAATCAGTTGTGATTAAATATTCTGCTTCTGCTATATTAAATTACAGTGAGGAAGCCATGAGAAAAGCAGGAACTGGTCACACAAAGTCCAGTACTGAGATGGAGAGCCATGTTTTTACGAAAGCAAAGACCAGAGTGAGTATTTTTAAAATGTTTTTGTCAAAAAGAACTGTTGTGTTAGGGAGTGATAGATAGAAGTGCAATGAAAAAACAACAACTCATCTTTAATTTATGTTTTGGACACAGGAGGAGTATTTATCAATGGTTGCGAGGCTGATAATTCACTTTAGAGACATCC[G/A]TAAGTAACCAACACAGATTTCAATATAAATGTTTTTGCATTGTTGTGTTTGGATGCGATATTAAATAAATGGTCTTTTATTGTAGATAAAAAAGCACAAGGTGGGCCTGGTAAGTTAAATTTTAGTTAAAAATATAAGTACATTTCAAACTTTATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTATTTTCTGCTAAATTTCAAGGTGATCTTGTTAATTTTTAGATCCCATCAATGCCCTGCAGAATTTACCTGGAGGTGTTCCGGGGGTTATTGGACCACGTCCTCCTGGCGCACAGATGGGTGGAATGGGGCAAATGTCAATGGGTCCACATGCCATGCAGGGAGTAGCGGGAGGGCAGCAGGGTGGTAAGTTCAATCCGCTTGTTAAGTGGTGATGTGTTTGTGACGCATGTAATACTGTTTCCGGGTCCAAGCCGCCATTTACTTGAGTGGAGAAATCATTCGTTTATGATCACT
Associated Phenotype:
Not determined