ZMP
si:ch73-210n19.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens MED1, mediator complex subunit 1 (MED1) [Source:UniProtKB/TrEMBL;
Human Orthologue:
MED1
Human Description:
mediator complex subunit 1 [Source:HGNC Symbol;Acc:9234]
Mouse Orthologue:
Med1
Mouse Description:
mediator complex subunit 1 Gene [Source:MGI Symbol;Acc:MGI:1100846]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41990 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45456 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15854 | Essential Splice Site, Missense | Available for shipment | Available now |
sa31866 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41990
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 |
---|---|---|---|---|---|
ENSDART00000111372 | None | None | 1377 | None | 15 |
ENSDART00000123701 | None | None | 1366 | None | 17 |
ENSDART00000145656 | Nonsense | 305 | 318 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 16155163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 15266128 |
GRCz11 | 12 | 15308435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACATGGGACGTACTGGTCAAGGAAGCTCGTGCATTGATACCATGGGA[C/T]AGGTTGGAGGTCAGCAGCAAGCAATGCAGCAGCAACATCAACAATCTCAG
Long Flanking Sequence:
ACAACCTACATTGCTAGTAAACGATTAGTTGTGAACTGTAACCATTGTTTTAAATAAAGTATGTTTATGACATTGATATTCCTACAAGGCCTACTTACTGGAAAGTTGTAAAATTTATGCTCCTAATAATGCCGTTTTAATGTTAACATGTAAGTTATGTGTTGCATCTATTTTCCTTTCCTAGATGCATGTCTATTCCGGTGACTATGCGTGCCATACGACGCAAGGCAGAGACCATTCAGGCAGACACACCAGCGTTGTCCCTTATAGCTGAAACAGTGGAAATTATGGTGAAGAAGAACTTGCCCCCAACTGGCAGCCCAGGTTACATGGGAATGGGTACAGGGCCAGATGGAAGTAACCCAATGGGTCTCCCTTTAAATAGTGGAAACAACAGTGTTGTGTGTGTAGGGGGGAATGGATCTTTCCAAGGTCCAATCACCTCAATGTTCAACATGGGACGTACTGGTCAAGGAAGCTCGTGCATTGATACCATGGGA[C/T]AGGTTGGAGGTCAGCAGCAAGCAATGCAGCAGCAACATCAACAATCTCAGAGCCATGGGTCAGATGACTTTAACAAAGTCACTCAGAATCCAATTCTAACCAGCCTTTTGCAAATAACAGGCAGTGTTGGGTCCAGTCCTACTCCCCAGCAACCTCAACCCCACCAAACACCTCCAACAACCACCTCACCAGCAAGCAACACCAAAAACCACCCTATGCTAATGAACCTACTGAAGGATAATCCATCACAGGATTTTGCTGCATTGTACAGCAGTAGCCCTCTAGAAAGACAGAACTCATCTGGGTCTCCACGGACTGACAACCAAGGCCAGCCTTGCTCTGGGACCAAGGGCAAAAAAAAGCGTCTGAGGGGCTCTGATAAAGGAGTAATGGGAGCAGCTGGGGGAATGAGTATGAAACAATCTCAGCAGCAAGTGGTAGACATGACACAACATCATCACCTCACAAGCCACTCTGAAGATGATTTCCACCGAGAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45456
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 |
---|---|---|---|---|---|
ENSDART00000111372 | None | 392 | 1377 | 9 | 15 |
ENSDART00000123701 | Essential Splice Site | 397 | 1366 | 10 | 17 |
ENSDART00000145656 | None | 315 | 318 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 16155195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 15266160 |
GRCz11 | 12 | 15308467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCATTGATACCATGGGACAGGTTGGAGGTCAGCAGCAAGCAATGCAGCA[G/A]CAACATCAACAATCTCAGAGCCATGGGTCAGATGACTTTAACAAAGTCAC
Long Flanking Sequence:
GAACTGTAACCATTGTTTTAAATAAAGTATGTTTATGACATTGATATTCCTACAAGGCCTACTTACTGGAAAGTTGTAAAATTTATGCTCCTAATAATGCCGTTTTAATGTTAACATGTAAGTTATGTGTTGCATCTATTTTCCTTTCCTAGATGCATGTCTATTCCGGTGACTATGCGTGCCATACGACGCAAGGCAGAGACCATTCAGGCAGACACACCAGCGTTGTCCCTTATAGCTGAAACAGTGGAAATTATGGTGAAGAAGAACTTGCCCCCAACTGGCAGCCCAGGTTACATGGGAATGGGTACAGGGCCAGATGGAAGTAACCCAATGGGTCTCCCTTTAAATAGTGGAAACAACAGTGTTGTGTGTGTAGGGGGGAATGGATCTTTCCAAGGTCCAATCACCTCAATGTTCAACATGGGACGTACTGGTCAAGGAAGCTCGTGCATTGATACCATGGGACAGGTTGGAGGTCAGCAGCAAGCAATGCAGCA[G/A]CAACATCAACAATCTCAGAGCCATGGGTCAGATGACTTTAACAAAGTCACTCAGAATCCAATTCTAACCAGCCTTTTGCAAATAACAGGCAGTGTTGGGTCCAGTCCTACTCCCCAGCAACCTCAACCCCACCAAACACCTCCAACAACCACCTCACCAGCAAGCAACACCAAAAACCACCCTATGCTAATGAACCTACTGAAGGATAATCCATCACAGGATTTTGCTGCATTGTACAGCAGTAGCCCTCTAGAAAGACAGAACTCATCTGGGTCTCCACGGACTGACAACCAAGGCCAGCCTTGCTCTGGGACCAAGGGCAAAAAAAAGCGTCTGAGGGGCTCTGATAAAGGAGTAATGGGAGCAGCTGGGGGAATGAGTATGAAACAATCTCAGCAGCAAGTGGTAGACATGACACAACATCATCACCTCACAAGCCACTCTGAAGATGATTTCCACCGAGAGCTTTTTTCTATGGATGTAGATGCCTCCCAAAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15854
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111372 | Missense | 581 | 1377 | 12 | 15 |
ENSDART00000123701 | Essential Splice Site | 584 | 1366 | None | 17 |
ENSDART00000145656 | None | None | 318 | None | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 16155950)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 15266915 |
GRCz11 | 12 | 15309222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGATATTAATGAYATTCTTTCTGATAYTCCTGATCAAGCCAACAAAG[G/A]AAGCAATATCGGTCATGGACAGCATCTTATGAYTAGTGAAGATGGAGGTT
Long Flanking Sequence:
AAGACAGAACTCATCTGGGTCTCCACGGACTGACAACCAAGGCCAGCCTTGCTCTGGGACCAAGGGCAAAAAAAAGCGTCTGAGGGGCTCTGATAAAGGAGTAATGGGAGCAGCTGGGGGAATGAGTATGAAACAATCTCAGCAGCAAGTGGTAGACATGACACAACATCATCACCTCACAAGCCACTCTGAAGATGATTTCCACCGAGAGCTTTTTTCTATGGATGTAGATGCCTCCCAAAACCCGATTTTTGATGTTAGTCTTCCAGGTGATGGACTTGACACTCCACACAGTATCACTCCAGCTCCAAGTCAGTGTGGAACACCACCTCCAGGTCCCGGAATGCAATACCACCCACAATGTCATGTCCAGCCTCAGATACAAGTCCAGTCACAATCACAAGGATCCATTCCTCGAATGGTCCGCCTCTCCAGCTCTGACAGTATTGGACCTGATATTAATGACATTCTTTCTGATATTCCTGATCAAGCCAACAAAG[G/A]AAGCAATATCGGTCATGGACAGCATCTTATGACTAGTGAAGATGGAGGTTCCTTGGGAACCCCAGTCCGGGACTCTTCCAGCTCTGGCCAGGGTAGTACAGTGTTTGAGGCAGACCTGTTTAATACAAATAGTAATGAAAATCCCTTTACTGATGCAGCAGATTTGATTGCAGAAGCTGCTACTGCAACAACACCCAATAGTGATACTTCCTCAACTAACTTCTTCCCAGACACAGACTTCAACCCAGAGCTTTTATCTGGGCAGGGAAGTTTTTCACAGACCTACTTTGAAGACAGCTCTCCCAGCCCTGATCCAGATCTTGAATTGGTTAAAAGTTTCAGTGGAGGAAGTCAGCAGAACACTCCTACAGGCACACCTCAGAATCCTGCCTCACATGGCCAAAATACTCCTGAGACTTCATTAAAAGACCCTTTTGAAATTGGTATTTTTGGTGGAAACGGTGGGGGAGGAAAACCATTAATGGCTCCAGCATCAGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31866
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 |
---|---|---|---|---|---|
ENSDART00000111372 | Nonsense | 1167 | 1377 | 14 | 15 |
ENSDART00000123701 | Nonsense | 1156 | 1366 | 16 | 17 |
ENSDART00000145656 | None | None | 318 | None | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 16157830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 15268795 |
GRCz11 | 12 | 15311102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACATCCTCAAAGCATTCTATGTCCTCCCAAGGAGGTGAGTTTTTGAGC[A/T]AACGAGACAAGATAGACAAAGATGGGAAATCCAAGATGTCTGGATCAGGG
Long Flanking Sequence:
AGCTGTCATCTCCCATGAAACAAGGCCAAGTACCTGGGACCCCACCCTCTTCTAAGGCTAAATCCCCTATTGGCTCAGGCAGTGGATCAGGGGGCAATAAGTGCTCTTCGGGTGGTGGAGTTGGATCAAAATCATTAAGCAGCAGTTCATCCAACAGCGCTTCTACATCCTGTGCTTCCTCCACTGGCTCCTCGTCATCTGGCTCTATGCCCTTTTCTTCAAATGGTCAGTCACAATATGGAAGCAGTGGTGGAAATTGCAGTGGTGGAGGGGGTGGTGGTGGCTGTGGAAACAACCCAAATGCAAAGGGTAAGTCCCCAAGCCGAAACAAAAAGCCATCTCTTACAGCTGTCATAGACAAACTCAAGAGTGTGGGAAGTGGGGGTAATGGTGGGGAGGAAATTGAAAGTTGTGGTGGTTCAAGTGGAGTAGGGCAGCAAAATACTGTTCCTACATCCTCAAAGCATTCTATGTCCTCCCAAGGAGGTGAGTTTTTGAGC[A/T]AACGAGACAAGATAGACAAAGATGGGAAATCCAAGATGTCTGGATCAGGGGGGAATTCAAGTGACAAAAAGATGATTGATGCCAAAAGTAACACAATGACTGGTACTGGTGTGGCAAAGATTATTATCAGCAAGCCAGAAGGAGGCTCTCCAAGCATTAAATCTAAAGTAACACTTCAGAAACCTGGGGAAGGTTCTGGTGATGGTGGCATTCGTTCCCAACACTCAGGCCACAAAGCATCACCTCTATTTAGTGGTTCTACACCAAAACATGACCGCAGCTCCCCAAGCCACAGCCGTTCTCCTGGGTGTACACCTATGAATCCAGACAGTGAGAGTGAGTCAGGTAGCAGTTCAGTTGCTGAAAAGTCACATCAGAATAGTCCTAGCTCTGATGATGACCAAACTATGAGATTACACCAACCAATTCAAGACTACATGAGCTCCATATCTATTAGCCAGAGTGAAAAACACAAAAAGCATAAAAAAGAGAAAAAGAAG
Associated Phenotype:
Not determined