Busch Lab

ZMP

setd6

Ensembl ID:
ENSDARG00000043986
ZFIN ID:
ZDB-GENE-030131-1067
Description:
SET domain-containing protein 6 [Source:UniProtKB/Swiss-Prot;Acc:Q803K4]
Human Orthologue:
SETD6
Human Description:
SET domain containing 6 [Source:HGNC Symbol;Acc:26116]
Mouse Orthologue:
Setd6
Mouse Description:
SET domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:1913333]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa1825 Essential Splice Site Available for shipment Available now
sa38042 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa1825
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064573 Essential Splice Site 9 460 1 9

The following transcripts of ENSDARG00000043986 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 17713698)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 17260539
GRCz11 25 17356939
KASP Assay ID:
554-1817.1 (used for ordering genotyping assays)
KASP Sequence:
GACGGGTTTGCGTTTTAAAGAAATGGCGACGGAAGCAAAAAGACCAAAGG[T/C]AAGTTANNNNNGATTTTTTCTTAAGTTGTCAGTATAGTGACAGTTCACAAGTTAT
Long Flanking Sequence:
TATAACTATAGTTGTGTTACTACAGCATCTATATAATCCCAACAACAGATTAATTTAAGTACTGAAGTAGGCTATGGTAAAAAAAAACAAAAAAAAAAAACATGTGGAACGTGCTACAAACACTAAGGACTGATAGATTGACTTTCTTGTCGAAAATGTACCGATAGCTCGATTTGTACGTTGATTTTAAAGTCTAAAACCTTAATATTAAGTAAAACATCGCGGATTGTATCTATTCATTTTGATTAGTTTTTCTGCGGTTATCTCATGCAAGCATAGTAGAGGGCGCTCGTGCACAGTACTGTGTTTGTTTTTACACACACTGGAAGAAGAAGAAGTGACCAGCGCTGCTTATCACATGGAGGCATTATAGGAAAATATATTATTATATTTTTATGTTGTTTTTCCGTGCAGTCGTCACTATAACAATATAGACTTTTATCACTCACCGACGGGTTTGCGTTTTAAAGAAATGGCGACGGAAGCAAAAAGACCAAAGG[T/C]AAGTTAGATTTTTTCTTAAGTTGTCAGTATAGTGACAGTTCACAAGTTATTAATATATACTTGATATTGGGACACAGATGTTTTAGAGTTTCTATGTTTATTATAATGTGTGCCTTTAGACAGGTGATGAAAAGAGTGTGCTGGAGCCCCTGAACAACTTCTTGCTGTGGTGTGAAAGTGTGCAGCTCACTCTCAGCGATAAGGTAAGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTTGATAATTATTATAATTAAATTAAATACACAAATAATATAATGTGTGTATATTTGATATACATATCATAATGTTGTGTGCATGTATGATGTTATGCATGTGTTAATGTTATGTCGATTCTTGGGACGTTATACCTAATATTTATTCAGATTTACATTATATTATAAAATATTATTTTTTCATATTGTTTCGTATATTAAAATGAATTAAATAAACAAAATTAAATTTATAATAAAATATTGCTAGTAAAACGCTGTAATAGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38042
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064573 Essential Splice Site 133 460 None 9

The following transcripts of ENSDARG00000043986 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 17712129)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 17258970
GRCz11 25 17355370
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGTCTCTTTGGCCAGATTTTAGGACTCTGGATCAACCCATGTTCTGG[T/C]GAGACCTTTCAGATATCCTTCACGGATCCTACTGATTATTATGGTCATCA
Long Flanking Sequence:
CTGAGGCAATATTAATCTCTGGGATTGTGAACCCACTTTAAGTATAAAATGCTTGATTATACAAGCTCTTGTCAAGATGATAAACTTAAGATATTTACTCACCATAGTCTACTTTAATTTCTATAGGTGTACTTAAGTAAAGAGGGTACAGCAGCAGAATATGGTATGCTTGCCAAAGAGGACATTGAAGAGGGACACGTCCTGTTCACCATTCCCAGAGATGCTCTTCTGCATCAGGGCACTACCAAAGTCAAAAAAGTGCTGGAAGAAGGTATGGAAACTTTCAGATGTATTCAAAAAACACCTTCTGTAGCAGTTTTGTAGCCTCCATATCTTGAATTCAAGTGTGTTTTCTAGGAAAGAAGTGTTTGGAGAGTGCGTCAGGCTGGGTACCTCTTCTTCTGAGTCTCATGTATGAGTACACCTCTTCAACATCCCACTGGAAACCATATTTGTCTCTTTGGCCAGATTTTAGGACTCTGGATCAACCCATGTTCTGG[T/C]GAGACCTTTCAGATATCCTTCACGGATCCTACTGATTATTATGGTCATCATGTTTAAGTTGAACCAGGCGCTAAAACATGTTAGAAATGTGTTAGCAAAACATGTAAGCCATTTGTTGAACATGCTCAAAACATGTTAATACTGAAACGTTCAATTCTTAGTCATGATATTTGCGTTTTAATAGGAATTCCAGCAATATGGTGAAATATGTTAGCCATATGCTAAAACATGAATGAAATGTGTTGCTATATCTTACTAAAACATGTACATAAATCTACAGGGTGGGCCATTTGTACGGATACACCTTAATAAAATGGGAATGGTTGGTGATATTAACGTCCTGTTTGTGGCATATTAGTATATGTGAGGGGGCTTGTAAATAACTCATGAAAGAATAAAGTTACGTTAAAACCAAGCACACCATTGTTTTTCTTGTGAAATTTCCAGTAAGTTTTTTTAAGGTGTATCCATAAATGGCCCACCCTGTAGATTTTAACAAA
Associated Phenotype:
Not determined