ZMP
si:dkeyp-53h3.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MED13
Human Description:
mediator complex subunit 13 [Source:HGNC Symbol;Acc:22474]
Mouse Orthologue:
Med13
Mouse Description:
mediator complex subunit 13 Gene [Source:MGI Symbol;Acc:MGI:3029632]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45410 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21755 | Essential Splice Site | Available for shipment | Available now |
sa41677 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1643 | Essential Splice Site | F2 line generated | Not yet available |
sa16900 | Nonsense | Available for shipment | Available now |
sa13843 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45410
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 |
---|---|---|---|---|---|
ENSDART00000088852 | Nonsense | 692 | 2157 | 10 | 30 |
ENSDART00000134491 | Nonsense | 692 | 2175 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 28732478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28164072 |
GRCz11 | 10 | 28050697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAAGACTGCTTAAGGTCTCAGATGAGCGGATCCAGATGTACCTGCAG[C/T]GACAGAACCAGCACCTGGCTGCAGCCATCACAGACGGCGACCACGAGCCA
Long Flanking Sequence:
ATAGACTAGCAGAGACCTCGAATATCAAGGTTTTGGAGGTGTCCAACTAATATCTGGATACCAAAGCCATATATACTTTATTTAATTTCTTAATTGATCTTCATCTTTATTTTTGTCTGCAAAATCATGATAATTATGATAATAGATCATGTAATCATGGAATATTGGTGTTTAAAAAAAAATAGACACATGGGGATAATACGACTACAATTATTAAGTTATCTTGAAGCTTGTAAAATATAACAAAAAAAAAATCCATATTCAGCTAATATAGTTTTTGTTGTCGTTAATATGTCCAGTTATTTTATCTTTAATCCGAAATGTGCCCCACTTGATTGGCCTGTGTGATATATTGATGTCTGGGCAGTATGGTTGCAAGTGTAGTTTAGTCAAAGTTTGCCCCTATAAATTATTATTTTTTTGTTGTCCTACCCAGGTCAATGGCAGCCTCCAAAAGACTGCTTAAGGTCTCAGATGAGCGGATCCAGATGTACCTGCAG[C/T]GACAGAACCAGCACCTGGCTGCAGCCATCACAGACGGCGACCACGAGCCAGAGGTCGACCCCTATGCCTTTGTCGACGGAGATGTCAAGTTCACGTTCTCGGATAAGAAAGACAAAGCTGGATTAGAGAGAGAACCAGGAAAGAAACACAAGGTAAGCACAACTTTTTGCTAAAGTTAACCATCTAGTCTAAAAGTGACCATTAAGTTTGACATTGGTAAGATTTTAGCTGTCATAGGATTTCTTTTTTAACTTTGGGGAAAAATACAGTAAAACACCAATTTTGTGAAACCTTATATAAACTGTTTGCTATATTAGTATAGTTAAATTTTTTTTTGTAAACAACCGTTTTAGTCCATTTGAAATCAATCCAAATTTGCAATGTTTACTTGGCTAGCTCAAAATGTTTTATTTTTTTTTTATAGGTGAACGATTATACAGTGTTTTGTTTTGTTAATCTTTAGTCAGAGTTGAGCATTTAAAGTGGTGGTCCATCAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21755
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 |
---|---|---|---|---|---|
ENSDART00000088852 | Essential Splice Site | 823 | 2157 | 14 | 30 |
ENSDART00000134491 | Essential Splice Site | 841 | 2175 | 14 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 28727542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28159136 |
GRCz11 | 10 | 28045761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGTCCTTTCACTAACATGTCATCTTTTTCTTTGCTTGTCCCTCCCTC[A/G]GGCACAGCCGATCTTCACCAGATGTTCCCTACGCCTCCGTCTTTAGAGCA
Long Flanking Sequence:
CATGTTGTAATGGAAATTTATTTTCTTCCAGAAATTGCTGCAATTTGAATGAAATCGTAGTCCTGATTTTTTGGCTAATTTGTGTGTTTCTCCATAGCCTGGAGCGCGGAGAGCTGTAAATGGAGCAGATGAGAAGTTTGGCAGCAAGGAGACAAAGCCAGCCACATTGGACCCTGTCTCCTGTATAAGTGAGCACAGTCTCGGTTTCTATAAATACACAGGTTTTGCTTCATCATTCAGACTCTGTATACTGCTCCCTGCTGGCCACTCTGACAACTTTTAAGTTGCATGCAGTGAAACAGACATCATGCACATATTTCTTTGAGTAAGAACTGCATGTTAGTATTCTACAGGGATAACGTTTTTATATGTAACACATCACATATTTTATCAATATATTTTTTCAGTATTAAACACAAATACTTATGGATATACTGCCATGCATCATTCCTCTGTCCTTTCACTAACATGTCATCTTTTTCTTTGCTTGTCCCTCCCTC[A/G]GGCACAGCCGATCTTCACCAGATGTTCCCTACGCCTCCGTCTTTAGAGCAGCACTTCATGGGTTACTCCCCCATGAACATGGGCAGTAAAGACGGCTGTATGGAGCCTGGCTCTGGCCTCAACGCTCTGGATGGCCCCACTGCTCTGGGTGGCCCATTTAAAATTGAGGTAGAGGAGAGCTTCTGCAGCCCCAAACCTTCTGAAATCAAGGTGAGATGCTACATTATACATGTCCTAAATTTGTGAAATTCAACAAGTTGTCCTCGTTTTAAATAAAAACTCGCAAAAGCATATTTTTTTCTATGATCTGTAGGCATTGAGTTGATATTTCATTGTGTGCATTTGTCAGTTTATATGCTGAGAATGGGCTTAATCTCTAGCAAATTAAATGTTTGTTTCTTTATCTTTTTTTTAGGACTTCTCATTTGTGTACAAGCCTGAGTTGTGTCAGCCATTTGTGGGGTGTTCAATGTTTGCCCCGCTGAAGTCATTGCCCAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41677
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 |
---|---|---|---|---|---|
ENSDART00000088852 | Essential Splice Site | 892 | 2157 | 14 | 30 |
ENSDART00000134491 | Essential Splice Site | 910 | 2175 | 14 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 28727330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28158924 |
GRCz11 | 10 | 28045549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGAGGTAGAGGAGAGCTTCTGCAGCCCCAAACCTTCTGAAATCAAGG[T/A]GAGATGCTACATTATACATGTCCTAAATTTGTGAAATTCAACAAGTTGTC
Long Flanking Sequence:
AATACACAGGTTTTGCTTCATCATTCAGACTCTGTATACTGCTCCCTGCTGGCCACTCTGACAACTTTTAAGTTGCATGCAGTGAAACAGACATCATGCACATATTTCTTTGAGTAAGAACTGCATGTTAGTATTCTACAGGGATAACGTTTTTATATGTAACACATCACATATTTTATCAATATATTTTTTCAGTATTAAACACAAATACTTATGGATATACTGCCATGCATCATTCCTCTGTCCTTTCACTAACATGTCATCTTTTTCTTTGCTTGTCCCTCCCTCAGGCACAGCCGATCTTCACCAGATGTTCCCTACGCCTCCGTCTTTAGAGCAGCACTTCATGGGTTACTCCCCCATGAACATGGGCAGTAAAGACGGCTGTATGGAGCCTGGCTCTGGCCTCAACGCTCTGGATGGCCCCACTGCTCTGGGTGGCCCATTTAAAATTGAGGTAGAGGAGAGCTTCTGCAGCCCCAAACCTTCTGAAATCAAGG[T/A]GAGATGCTACATTATACATGTCCTAAATTTGTGAAATTCAACAAGTTGTCCTCGTTTTAAATAAAAACTCGCAAAAGCATATTTTTTTCTATGATCTGTAGGCATTGAGTTGATATTTCATTGTGTGCATTTGTCAGTTTATATGCTGAGAATGGGCTTAATCTCTAGCAAATTAAATGTTTGTTTCTTTATCTTTTTTTTAGGACTTCTCATTTGTGTACAAGCCTGAGTTGTGTCAGCCATTTGTGGGGTGTTCAATGTTTGCCCCGCTGAAGTCATTGCCCAGTCAGTGCCTGCCCCCTATCAAACTGCCTGATGAGTGTGTTTACAGGCCCAGCTGGACAGTGGGAAAACTGGAGCTACTTAATTCTGTACCTGCTATGACCATTTTCAGCAAGGATGGGTGAGTTTTATATTTAGGGTAACACACAAATTCACTAAACCCCTGCCAAATAACTAATATAATATAGCCAGCAATCTGAAAAAAATTGCTTGCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1643
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088852 | Essential Splice Site | 1320 | 2157 | 17 | 30 |
ENSDART00000134491 | Essential Splice Site | 1338 | 2175 | 17 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 28724297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28155891 |
GRCz11 | 10 | 28042516 |
KASP Assay ID:
554-1583.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCTYACATGGCAGCAGTTTCACAAAATGGCTGGAAGAGGTTCTTACGG[T/G]GAGTAACAAGCCACTCAAAACACTAAAAATGCCATCACAATTTTTGGAGG
Long Flanking Sequence:
CGAGGTGTTAGTGAAGAGCACGTGTTTGCATCATTGGGCCAAACGTAGCGGTGAGAGATTAGAGCATGTTTGTTCACACACAGTTTCTGTTTACAATACAAACTAACACATTCGTTAGGCTGATTATTACAGTCTTGATTAAATAAGGTGGAAGATATTTACACTATTACAGAAAAGAAGCCATGTCGGCCTTTGGTCAAAATTGACCCTGCTTAATTTTTGTTACACTTTCTTTTGGGTAAACATTGCTAAGTTCTGCTTGTTTTATCTGATGGTGAAAGTATCTATTCTTTATTTTGCTTGCTCACTCATTCTCTGTCTCTCTCTCTAGCGGTGGACGTGAGTGCGCTGTGCTCTCAGGACGTGTTGAGAGTTCTTCTCTCTCTCCAGCCTGTTCTTCAGGATGCTATTCAGAAGAAGAGGACTGTTCGCTCCTGGGGAGTTCAGGGGCCTCTCACATGGCAGCAGTTTCACAAAATGGCTGGAAGAGGTTCTTACGG[T/G]GAGTAACAAGCCACTCAAAACACTAAAAATGCCATCACAATTTTTGGAGGGGAAATGTTCATGACAAGGTTGTTAGTAGACTTTAAAATTGATGCCAGGGGATCCTTGACGCCACTCACCTCTCACTCTGTTCCTTTCCAGGCACTGACGAGTCTCCGGAGCCTCTGCCCATTCCTACCTTCCTGGTTGGGTACGAGTATGACTTTGTGGTGCTATCTCCCTTTGGCCTGCCGTATTGGGAGAAGCTACTACTGGATCCCTTTGGCTCTCAGAGAGATGTAGGATATCTGGTCCTCTGCCCGGACAGCGATTCTCTCCTCACTGGAGCCAAGAGTTTCTTTAGAGAGTTGACAGCGGTCTATGAGGTGAGAGAGTTCGTTCATCAATCATTACTTTAATGCTCACAGGAAATTCTCTCTCACGCTGTCAGACTAATTCATGCAGAAAAAAATTAAATATGTAAATGTGTAAGATTTCTAATTCATTAGTTTGTGGTCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16900
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 |
---|---|---|---|---|---|
ENSDART00000088852 | Nonsense | 1858 | 2157 | 24 | 30 |
ENSDART00000134491 | Nonsense | 1876 | 2175 | 24 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 28719440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28151034 |
GRCz11 | 10 | 28037659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGGAGAGTTGTGATTGGCCGGCTWGGACGGATAGGGCATGGAGAGTTG[C/T]GAGGTAATGGCTGTTTAAACGCTTTTACATTATACACAATACAGCTTGGC
Long Flanking Sequence:
CCCCAACGAAAGACAAGCAAACGGAGCTGGGTGAGACTTTCGGAGAGGCGTCTCAGAAGTATAACGTCCTTTTTGTTGGCTACTGCCTGTCGCATGATCAAAGGTGGCTGTTGGCAACTTGCACGGACCTGTACGGAGAGCTGCTGGAAACTTGTATCATCAGCGTAGATGTACCCAACAGGTGAACTACAACTTTCTGCATTTTCAGACATTAACTAGGATTAATTATTCACTCCACACACTTCAGGAAAAGTGTCAGGTTTACAACCGTTATTACAACTATAATTGTGACAAGTGAACGTGTAAAACTTCATCTCAGTGGTTTTGACAGTTTTTTTTTTTTTTTTTTTTGTGGTCTCAGAGCAAGAAGGAAAAAGGGATCTGCACGGAAGATGGGTCTGCAGAAGCTTTGGGAGTGGTGTTTGGGTTTGGTTCAAATGACATCGTTGCCATGGAGAGTTGTGATTGGCCGGCTTGGACGGATAGGGCATGGAGAGTTG[C/T]GAGGTAATGGCTGTTTAAACGCTTTTACATTATACACAATACAGCTTGGCTTTGAGTTGCTAATTCCTCTTTTATAGTGGTTGCTGCTTGGATTTATTAATGTTTATAAAATTAAGATGTAGTTTTATTAAGAATTCATTAAGTGGCGTCCTTCCAGCCAACACACCTATCAGCATCCTGGACCAGAATGAATCAGTTTTATAATGCATATTTAAATTCACAAGATTTATTAACACTGCAGTGCAAACATGGGGAGTTTTGCCCGCAGGGAATTAATTTATAGTTTTTCTCTTCCTCTTTCTCAGACTGGAGTATTTTACTGAGCAGACGGAATCTGCAGTCGGTGTCTCGGAGGCTGAAGGAGAACTGTAAGCTGTGCGGGATCTCAGCATCTGACACTCCCAGCATTCTTAGCGCCTGCCTGGTTGCCATGGAACCCCAGGGCTCATTTGTCATCATGCCAGGTAGAATCACACTTCCTGTTTCTCTCCGTATGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13843
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 |
---|---|---|---|---|---|
ENSDART00000088852 | Nonsense | 2117 | 2157 | 30 | 30 |
ENSDART00000134491 | Nonsense | 2135 | 2175 | 30 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 28712986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28144580 |
GRCz11 | 10 | 28031205 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATTAATAAGCATTAATATTTAACTGTTTCTSTTTTGTAGATTTGTGT[T/A]GGAGCAGTAYAATGCCCTTTCCTGGCTGACCTGTGACCCTGCGACCCAGG
Long Flanking Sequence:
TTACTTTGTCATTTAAAAAAAGGAACATTACGTTGAAAAAGTATATGACAAATTAAAATATTTGGCTAGAAATAACTTGTATCAAATGACATTAGGAAAAGCAAGAACAAACGAGCCATTAGAAAAAATCCTTAGTGTTTAGCGCTGTATAAGTCTAAAACTTCATTCAAAATGGACTTAAAGTCTTAAATTTGACTTGTTGAAACCTGCAGAAACCCTGAATCTGTACCAATTAAGACAGAATTTGAAAGAAATGGGAGCTATTGAAAAATAACAACAACAGAAAAAGCTTACAATTATTGGATGAGAGGAGTGGTATATAACGCTTAATCACATTTTATTCCCACATTAAGACAGCAGATTAGAGGATTTTAGCATTAAGCTCCCCACGTTTATCAATAGATTAATACTGTAGTACTGTAGTTTGAATATGTGTACCATTACACCTTCCAGATTAATAAGCATTAATATTTAACTGTTTCTCTTTTGTAGATTTGTGT[T/A]GGAGCAGTACAATGCCCTTTCCTGGCTGACCTGTGACCCTGCGACCCAGGACCGCCGCTCTTGCCTGCCCATCCATTTTGTGGTGCTCAATCAAATGTACAACTTCATCATGACCATGTTGTAACACTCACTGAGCAGAACTGAGAGCAGGACCTTATCAGGGAACAGAAACGAGGAGAGTGAAGAAGAAAAGGCGGATCTAAAAACAATCCAACGGAAAACTACAGTGCTGGACTTTATAAGTGCGCGAGATACGATCTGGGTAGGCAGTCACTACACCTCAGACCCAGCACTGTGGAGGAGGATCAGGCGTCTGGTGTTCATAACACTCACTCGAAGACAACGAGAGGCCTTGAAGGAGGATGCAGAGGCCAAAGAAGGAAGATGGAAGTGCTGACTGCTGGTGTTCGACATCCCAGGTTCAACGGATGCTACAAGCAATGGTAGCGCGTGGTTCCTCGGTTAGCACGGATTCAGCCAGTTCTTTAATCAACGTGTAT
Associated Phenotype:
Not determined