Busch Lab

ZMP

setd1ba

Ensembl ID:
ENSDARG00000060847
ZFIN ID:
ZDB-GENE-050309-289
Description:
Histone-lysine N-methyltransferase SETD1B-A [Source:UniProtKB/Swiss-Prot;Acc:Q1LY77]
Human Orthologue:
SETD1B
Human Description:
SET domain containing 1B [Source:HGNC Symbol;Acc:29187]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa12989 Nonsense Available for shipment Available now
sa13004 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12989
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086165 Nonsense 22 1844 1 19
ENSDART00000086165 Nonsense 22 1844 1 19
Genomic Location (Zv9):
Chromosome 10 (position 43352037)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 42158532
GRCz11 10 41986912
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAGATAGTGGTGTATTGTAAGAGACAGAAACCCCAGACTAGAGGCACA[C/T]AATATGTGTTGGCTCGCAAAAAGGAGGCAGTATCTTTAAAATCATGTAAT
Long Flanking Sequence:
CACAATAAGCTACACGGAAAAGCTTTATTATACACATTTATATGTTTTGTTTATATAAGGTCACTTAAGTTCTTTTTAAAGACGTATATTTATATACACCACCTAAAACATATTTATAAATAAATGTTTGAACGAATGCAAATCTGCGTTTCATTTTTAAAACACATTATGTGCGCGTTCGGCGCGTGTCCCAATTCAGTTTTAACAACCTTCCCCAGCGTTGCTCCTCCATGTCCATCTTGTATTTAACGTTCATGTAAATCTATCGCGCAGATTCAACGCGGACCCAACCTTCGTGTTTCTGCTGGAAATGCAAGATATTCCACCTTTCTTTTCATTTCTCACATGTAACTCAATTTGTTTGATTTATCGACGCTCGTATAAAAATTCTGCGTTTTCTCAACGCTTCAGAATAATAATTTGAAAGCGCGTGTCGAATGTGCTGGAAGGTTGAGATAGTGGTGTATTGTAAGAGACAGAAACCCCAGACTAGAGGCACA[C/T]AATATGTGTTGGCTCGCAAAAAGGAGGCAGTATCTTTAAAATCATGTAATGTGATCGGCGAATCGTTCAAGATCAAGCCGTTTTATATAAAACTACTCGATCGGGCACAACATGTCCAGACCTGGAGAAAGAAATAAGCTAAATGAAGATCACGGTAGAAGACAGAGTTCAAGTAAGCTCTCTTTTTTTCCTTCCTCTGTAATGTCTGTTTCGGGCACCGCTTCAAACCCCCCATTTTCTACAATGTAGTGTTTGTGTGCAAATAAACTGCTTGCGATGTCAGTATCATGAGGAGTACTTTATGTTTTTGTCATCTCTTCGCTAGGTTTGGCGAACGGAATGGACAACAGCCATCCTATCTGCAGTTCGGGAGAGAAACGAAGTCATCATTGGAGAAGTTACAAGTTGATTATTGACCCAGCGTTGAAAAAGGGTTCGCACAAAGTGTACCGCTACGATGGACATCAATTCAGCTCGCCGGTGAGAGGAACCAGCCGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13004
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086165 Nonsense 22 1844 1 19
ENSDART00000086165 Nonsense 22 1844 1 19
Genomic Location (Zv9):
Chromosome 10 (position 43352037)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 42158532
GRCz11 10 41986912
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAGATAGTGGTGTATTGTAAGAGACAGAAACCCCAGACTAGAGGCACA[C/T]AATATGTGTTGGCTCGCAAAAAGGAGGCAGTATCTTTAAAATCATGTAAT
Long Flanking Sequence:
CACAATAAGCTACACGGAAAAGCTTTATTATACACATTTATATGTTTTGTTTATATAAGGTCACTTAAGTTCTTTTTAAAGACGTATATTTATATACACCACCTAAAACATATTTATAAATAAATGTTTGAACGAATGCAAATCTGCGTTTCATTTTTAAAACACATTATGTGCGCGTTCGGCGCGTGTCCCAATTCAGTTTTAACAACCTTCCCCAGCGTTGCTCCTCCATGTCCATCTTGTATTTAACGTTCATGTAAATCTATCGCGCAGATTCAACGCGGACCCAACCTTCGTGTTTCTGCTGGAAATGCAAGATATTCCACCTTTCTTTTCATTTCTCACATGTAACTCAATTTGTTTGATTTATCGACGCTCGTATAAAAATTCTGCGTTTTCTCAACGCTTCAGAATAATAATTTGAAAGCGCGTGTCGAATGTGCTGGAAGGTTGAGATAGTGGTGTATTGTAAGAGACAGAAACCCCAGACTAGAGGCACA[C/T]AATATGTGTTGGCTCGCAAAAAGGAGGCAGTATCTTTAAAATCATGTAATGTGATCGGCGAATCGTTCAAGATCAAGCCGTTTTATATAAAACTACTCGATCGGGCACAACATGTCCAGACCTGGAGAAAGAAATAAGCTAAATGAAGATCACGGTAGAAGACAGAGTTCAAGTAAGCTCTCTTTTTTTCCTTCCTCTGTAATGTCTGTTTCGGGCACCGCTTCAAACCCCCCATTTTCTACAATGTAGTGTTTGTGTGCAAATAAACTGCTTGCGATGTCAGTATCATGAGGAGTACTTTATGTTTTTGTCATCTCTTCGCTAGGTTTGGCGAACGGAATGGACAACAGCCATCCTATCTGCAGTTCGGGAGAGAAACGAAGTCATCATTGGAGAAGTTACAAGTTGATTATTGACCCAGCGTTGAAAAAGGGTTCGCACAAAGTGTACCGCTACGATGGACATCAATTCAGCTCGCCGGTGAGAGGAACCAGCCGTTA
Associated Phenotype:
Not determined