ZMP

MED16

Ensembl ID:

ENSDARG00000040779

Description:

mediator complex subunit 16 [Source:HGNC Symbol;Acc:17556]

Human Orthologue:

MED16

Human Description:

mediator complex subunit 16 [Source:HGNC Symbol;Acc:17556]

Mouse Orthologue:

Med16

Mouse Description:

mediator complex subunit 16 Gene [Source:MGI Symbol;Acc:MGI:2158394]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14925	Essential Splice Site	Available for shipment	Available now
sa38833	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14925

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059752	Essential Splice Site	154	847	3	14

Genomic Location (Zv9):

Chromosome 11 (position 14349383)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	14050679
GRCz11	11	14108338

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACTTTCATGGTTACACAATGGAGTCAAACTCGCCCTGCATGTTGAAAAGG[T/C]AYAGTATGTGAATTYCCTTMCCTGCCACTGTTACTTTTGGCTTGCTTGGT

Long Flanking Sequence:

GCCCTCCGTCCGCTGAAAACGCACATCACGTGACCACACACAAACACACACATACAGACAGAAACAGACAGACATTCACAGACGCAAGTGGTGCTCACTTCAGAGCCACACACTGTCATGCGCTCCTCTGAGTTCCAGAGACAGAGAGTCGTGCATGTTTGACAGTTTATCAAGGGTGTACCACTGGATTGCGTCTCATTATAGTTGTTAAACTTGATATTCAGACATACCGTCATATGCCATCGTCCATCGCGATGGTTTACATTAGACATTGTATGATGCCAAATTGGTCGACATTGCTCAACCCTACCTCTTGTGTGGTTTGCTAGGTTCGAGGTTGTTGTCTGCTGATGGTGATGGTCAGATCAAGTGTTGGGGCATGACAGAGCACCTGGTGAACAGCTGGGAGTGCGCACAGAGCAGCTCAGTGGACGGAGACCCTATTGTAGCACTTTCATGGTTACACAATGGAGTCAAACTCGCCCTGCATGTTGAAAAGG[T/C]ACAGTATGTGAATTCCCTTACCTGCCACTGTTACTTTTGGCTTGCTTGGTTAGGGCCGGCGAAGCTGATCTTCAGTCTATTGTCCTGCAACTACAGTTTGACATTCTTATTGAACTGGGCTGCATTTCCCAAAAGCTTAGTTAGCCTACAGTATGTAGATTCTAAAAATAATTGTACGATTGATCTTAATGTTATGGTCTGTGTCCCAAAAGCATCGTAACTTAATAGATCTGGAAAGTCATCAATGATCTATGAGTGCATTAAAATAATTGTTAAAGCTTTATGGCAATTTCAGACTGTATGATTTTCAAAATCTTCTGGTTGCCATTGTTTTCAAACTAGTGATGAGAAGTTTGGATCTTTTCCGGGAACTGGATCTTGATGAAGATGAAAAGCTGTGTGCTTGAAACGTTACACACTTTATGTCAGCCTTTTTTAATTTAATAAATTTTCTTGTTTTTGCGCTTTGGTGTTGCCACCTTTTTGAATATATATGTTGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38833

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059752	Nonsense	804	847	13	14

Genomic Location (Zv9):

Chromosome 11 (position 14384024)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	14085320
GRCz11	11	14142979

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGCGATGTTTACATCTGGGCATCTCTCCAACCGAGGATAGCAAAGCTTG[C/A]ACAAGGTATCACATTAGAATTATTCCTCTAATTAATTTAAAGTAATTCAT

Long Flanking Sequence:

TTGTGCGTCAGCGATGGTTACAGGCAAGGGCTATGTAACCACATGCAGGCTGCACCACAGTATACATTTCCTAACTATAAGAATCCTTTGCATCTGTGATACACAAGGAAGGCACCTAACCCCTGATTGCTCCCAGGGTGGTGTAAGCAATAGCTGGCCACTGCTCTGGTTGTGTGCTCAGAGTTTGTTTGTGTGCTCTCACTACTCACCCATAATGTGTGTGTGCACTTGGATGGGTCAAAATCAAGGATCTATTACGAGCATGAGTAAAACCATTCTTGTCTTGTCAGTATTCACTTGCTTGTGCACTTGTGCAAGTCCTTTAATTAAGGCAGTACTATTTGGGACAGTGAAAATTGTTTTTGAAAGTCTAATTGTTGCTAGTGGTTAATTCAGTGTTGGTTTTGGTGGTCTATTCACAGAAGTCCAGCGTCACAGAGAGTGGATCACCTGCGATGTTTACATCTGGGCATCTCTCCAACCGAGGATAGCAAAGCTTG[C/A]ACAAGGTATCACATTAGAATTATTCCTCTAATTAATTTAAAGTAATTCATGAATAAATATATTTTTACATGCTCCATTTTTTTAATGTCTGTGATGATTCCTCTGCAAATATGCATGCATGTGATGTCAACATAGTAATATTTTATATATTTTTCATCCTGAGTTATTGTATGCGCAACAAAAAATATCACTGCTGAATACAGTTGGTTCTAAGAATAGTAAGTTATACTGGAACTGTTATAATTAAATGACACTTGTACAGAGAGACTGCCTTGAAAACTCTATATTTAGCACAGCAGCACTAGCCAATGAGGTCTTGTCTCTCGGAACTGTTTAGGTGCGGCTGTGTCACCATGTTAAGATCTCCAAATAAAACAAATGCCACGAGACAATGGGAGCAGCGTTGGATCAAGAACTGTCTGTGTGGAGGTCTCTGGAGAAGAATCCCCTCCACATTAAGCTAAAGACCACACCATTTGGAAATGTTAAAGCAGCATGGG

Associated Phenotype:

Not determined