ZMP
supt6h
Ensembl ID:
ZFIN ID:
Description:
Transcription elongation factor SPT6 [Source:UniProtKB/Swiss-Prot;Acc:Q8UVK2]
Human Orthologue:
SUPT6H
Human Description:
suppressor of Ty 6 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:11470]
Mouse Orthologue:
Supt6h
Mouse Description:
suppressor of Ty 6 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:107726]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23947 | Essential Splice Site | Available for shipment | Available now |
sa16076 | Nonsense | Available for shipment | Available now |
sa16191 | Nonsense | Available for shipment | Available now |
sa37322 | Nonsense | Available for shipment | Available now |
sa37323 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23947
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028007 | Essential Splice Site | 488 | 1726 | 13 | 37 |
Genomic Location (Zv9):
Chromosome 21 (position 25429039)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25998857 |
GRCz11 | 21 | 26035552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGTTTATTAATGCATTACACCAAAACCTTTTGTGTGTTTTTATTTCC[A/T]GGGGAAGAAGCAGAAGTGGAGGAGGAAGAGGAAGAAGAGGAGCAAAAGGG
Long Flanking Sequence:
TTTGTGGTTTTCATTTAAAAATTGACAAATTATTTATGCTGTCCTATTCAGTGGACCCAGCTGAAGACCAGAAAGCAGAACTTGACACGTCTTTTCCAGAGAATGCAGTCTTATCAGTTTGAGCAGATCTCGGCTGACCCTGACAAGCCTTTAGCTGACTCTACTCGTCCCCTAGACACTGCTGACATGGAGAGGTATAACTGTTTAAACATGTGCTCCTAAATTTGACTCTTTGTCCACAGTGCTCACTTCTTTATTGCTTTGACAGACTGAAAGACGTTCAGTCTATTGATGAGCTGGGTGATGTCTACAATCACTTCCTGCTCTACTATGGCAGAGACATTCCTAAGATGCAGAATGCAGCAAAGGGTGGCAAAAAGAAACTAAAGAAGATCAAGGAAGTTTCAGAGGAAGATGGTATAGCAGAATTTTACTAGGACGAGTGAATTCTAATGTTTATTAATGCATTACACCAAAACCTTTTGTGTGTTTTTATTTCC[A/T]GGGGAAGAAGCAGAAGTGGAGGAGGAAGAGGAAGAAGAGGAGCAAAAGGGTCCAGATCTGAAACAAGCCTCACGCAGAGATATGTACAGCATCTGCCAGAGTGCAGGCCTTGGTGTGTATATCTTGCACATTTAAATAAGACTCGGTTATAATAAAAGAAGAAAAAAATGGAACCTATTATATAAATATAATGTCACATGATATAATAAAAAAATGAAAAGGTAATTTTATTACATTAATAATTTTTTCTTTTATAAATAAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTATATATATAAATTTATAAATATTATAGTGTCATTTTTAAAAGTTATGAATTCATGCACACACTTTTACTAATTGTTAATGGCTTATGGTAACCTTTATTTTATTTTTTAAGATGGTCTTGCCAAGAAGTTTGGTCTGACCCCAGAACAGTTTGGTGAAAACTTGCGAGACAGTTATCAGAGGCATGAAACCGAGCAGTTTCCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16076
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 |
---|---|---|---|---|---|
ENSDART00000028007 | Nonsense | 600 | 1726 | 15 | 37 |
ENSDART00000028007 | Nonsense | 600 | 1726 | 15 | 37 |
Genomic Location (Zv9):
Chromosome 21 (position 25429748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25999566 |
GRCz11 | 21 | 26036261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTGGCCATGCAGATTGCCCGCGAGCCTCTGGTCAGACACGTGCTCAGA[C/T]AAACCTTCCAGGAGAGGGCCAAGATTAACATCAAGCCAACTAAGAAGGGC
Long Flanking Sequence:
AAAAAATGAAAAGGTAATTTTATTACATTAATAATTTTTTCTTTTATAAATAAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTATATATATAAATTTATAAATATTATAGTGTCATTTTTAAAAGTTATGAATTCATGCACACACTTTTACTAATTGTTAATGGCTTATGGTAACCTTTATTTTATTTTTTAAGATGGTCTTGCCAAGAAGTTTGGTCTGACCCCAGAACAGTTTGGTGAAAACTTGCGAGACAGTTATCAGAGGCATGAAACCGAGCAGTTTCCTGCAGAGCCTTTGGAGCTGGCCAAGGACTATGTTTGCAGGTAATGGATCAGTTGGAATTCTCTTTTTTTTTTTTTTTTGCCCTGTAGTCTTTTTATAAATCAATGTTTTTTTTCTAGCCAATTTAACACCCCAGAGGCTGTCCTGGAAGGCGCTCGCTACATGGTGGCCATGCAGATTGCCCGCGAGCCTCTGGTCAGACACGTGCTCAGA[C/T]AAACCTTCCAGGAGAGGGCCAAGATTAACATCAAGCCAACTAAGAAGGGCAAGAAGGTTGGTTCTTGGATTTGTTTAGGATTAACAGACCAAATTCTAAATGTTTGAAGTAGGGGTGTGCAAAATATGTTGGCTATAGTATTATGTTTTATTGATATGCAATCATCATTTGTGTAATAAAGCCTATTAGAATGACAATATGATTTATAATAATGATATTGTCAATCTAACAGGCTTTGTCATACAAATGATAATATTGCTTAAATATCAATTATCTACTAATATGTTACTGAATGTTAATTAAAGGGTATCTGTGGGGTCTTAAAATGTCTTAAATCTAAATTTTCATGTCGGCTTAATCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCACCAACTTATTCAGCATGTTTTTTGGCAGCGGATGCCCTTTCAGCCATTTATTTTCAGGGAAATAAATCTAAATTTTAGGTCTTATACAGTTTTAAATCTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16191
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 |
---|---|---|---|---|---|
ENSDART00000028007 | Nonsense | 600 | 1726 | 15 | 37 |
ENSDART00000028007 | Nonsense | 600 | 1726 | 15 | 37 |
Genomic Location (Zv9):
Chromosome 21 (position 25429748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25999566 |
GRCz11 | 21 | 26036261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTGGCCATGCAGATTGCCCGCGAGCCTCTGGTCAGACACGTGCTCAGA[C/T]AAACCTTCCAGGAGAGGGCCAAGATTAACATCAAGCCAACTAAGAAGGGC
Long Flanking Sequence:
AAAAAATGAAAAGGTAATTTTATTACATTAATAATTTTTTCTTTTATAAATAAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTATATATATAAATTTATAAATATTATAGTGTCATTTTTAAAAGTTATGAATTCATGCACACACTTTTACTAATTGTTAATGGCTTATGGTAACCTTTATTTTATTTTTTAAGATGGTCTTGCCAAGAAGTTTGGTCTGACCCCAGAACAGTTTGGTGAAAACTTGCGAGACAGTTATCAGAGGCATGAAACCGAGCAGTTTCCTGCAGAGCCTTTGGAGCTGGCCAAGGACTATGTTTGCAGGTAATGGATCAGTTGGAATTCTCTTTTTTTTTTTTTTTTGCCCTGTAGTCTTTTTATAAATCAATGTTTTTTTTCTAGCCAATTTAACACCCCAGAGGCTGTCCTGGAAGGCGCTCGCTACATGGTGGCCATGCAGATTGCCCGCGAGCCTCTGGTCAGACACGTGCTCAGA[C/T]AAACCTTCCAGGAGAGGGCCAAGATTAACATCAAGCCAACTAAGAAGGGCAAGAAGGTTGGTTCTTGGATTTGTTTAGGATTAACAGACCAAATTCTAAATGTTTGAAGTAGGGGTGTGCAAAATATGTTGGCTATAGTATTATGTTTTATTGATATGCAATCATCATTTGTGTAATAAAGCCTATTAGAATGACAATATGATTTATAATAATGATATTGTCAATCTAACAGGCTTTGTCATACAAATGATAATATTGCTTAAATATCAATTATCTACTAATATGTTACTGAATGTTAATTAAAGGGTATCTGTGGGGTCTTAAAATGTCTTAAATCTAAATTTTCATGTCGGCTTAATCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCACCAACTTATTCAGCATGTTTTTTGGCAGCGGATGCCCTTTCAGCCATTTATTTTCAGGGAAATAAATCTAAATTTTAGGTCTTATACAGTTTTAAATCTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37322
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 |
---|---|---|---|---|---|
ENSDART00000028007 | Nonsense | 632 | 1726 | 16 | 37 |
Genomic Location (Zv9):
Chromosome 21 (position 25431538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26001356 |
GRCz11 | 21 | 26038051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTCCAGGATGTGGATGAGGCGCACTTTGCCTATTCTTTCAAGTACT[T/A]GAAGAACAAGCCTGTGAAAGAGCTCAGTGGAGATCAGTTCTTGAAGATGT
Long Flanking Sequence:
TTAAAGAATCGGCTATTTTAAACAAATCTATTAAATTAAGGGTTCAGCTAAGCTCATTTAGAAAGCCACCACCTACTGAGGATTTTGGTGGTATGTTCAAAACACTCCTAGCAAAAATACAAATGTTTTCAGTATTGCACACCTTAGAAGGCAATAAATGTATTCAACCTGTATTTTATTAACTGTTGTTTTTGTTTATCCTCTAACTTTTGCTTAACCGTATTCATCAAGGAAAGGGTATAAGCAGAATATCAACCTTTGCAGCATAATCCCAAGTCTGTTGTGTTAGAGCTTTAGCTAGAATATTCAGTTGTTGCCTGTAGGTGCGAGATGTAGCCATTGTTTTTGCTGTGCAACAATATTAGCATAGTGAATTGCTATTCAAACCCAAAGTGAACTGATGTGCTCCATTGTTTGCTCTTTACTAAGTTTGTCTGCTATTGCCTGTCATGTTTTCCAGGATGTGGATGAGGCGCACTTTGCCTATTCTTTCAAGTACT[T/A]GAAGAACAAGCCTGTGAAAGAGCTCAGTGGAGATCAGTTCTTGAAGATGTGTCTGGCTGAGGAGGAAGGCCTTCTCGCCATAGACATCTGCATTGACCTTGTTGGAGTCAAAGGGTATAGTTGTATTTTTAGCTTTAGAGGAAACCTGAATTTAGTGTCAAGAAATGTTTATGGTCCGTTTCCACTGAGTGGTACAGTATGGGTCACCTTTATCAGACTTGCGTTTCCACTGCCTAAAGGGTACCAATGGTGGACGTGATGTACGACAGAAAGTCTCAGTTGACGTCATTCTCGCTAGGACTGCTCGATTATGGGGGAAAATCATAATCACGATTATTTTGGTCATAATTGTAATCACGATTATTCAAAACGATTATCAGTTGAAGTCAAAAATATTCGTCCTCCAGTGAATTTATTTTTATATATAAATATTTCCCAAATGATGTTTAACAGGGGGATTTTTTTTACAGTATTTCCTATAAATTTTTTTCTTCTGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37323
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028007 | Nonsense | 1115 | 1726 | 26 | 37 |
Genomic Location (Zv9):
Chromosome 21 (position 25443045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26012863 |
GRCz11 | 21 | 26049558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTTTTCTATCTTTTTTAGGGTTATGGTAATAAGGGAATTACACTGTA[T/G]GACATCCGAGCAGAGCTCAGCTGTAGATATAAAGACCTGAGAGCTCCATA
Long Flanking Sequence:
TTCAAAACAAGATATTCTGAAGAATGGTGGAGAAAAAGCAGCTGTATACATTCATACAGTAGTAGAAACACAAAGTACTATGGATATCAGTGGCTGATTATTTGTCGAATATTTTTCAGTATATCTGTAGATACAAGTTCAGGATGATGTAAATGATGGATGAACTAAATAGTTTGGTGAACTATTCCTTTTACATGAGTTTATTGTGACTTACTTGTATTTTTTTTTATTTTTTTATTGAGACTATTTCCTTTTTTTTATTTATTTTTTTTAAGTGGAAACCTTACCGAAGACATTTATATATGTATTTAGCATCACCTACTTGTGATCTGATGGACAGAAATGCATCTTAATGCCAGCTGTAAACAGGGCCAGTGTTTCATAGTATACCCTCATTGTTTAATGTTAGCAGGCTTCAAACGTAACTGATTTGAACACGTACTTAACTAGACATTTTTCTATCTTTTTTAGGGTTATGGTAATAAGGGAATTACACTGTA[T/G]GACATCCGAGCAGAGCTCAGCTGTAGATATAAAGACCTGAGAGCTCCATACAGACCTCCCAACACAGAGGAAGTCTTTAACATGCTCACCAAGGAGACACCTGAGACTTTCTATATTGGTAAACCACTACTTGATTGCTTTTAGAAATGATAAAAGATCGTAATGATCCATGCTCTGTGATATTTATGGTGATATTTTTGTATTTTTAATATATAATGTAAATCTTTGTGCATCTACAGGTAAACTGATCACCTGTGTAGTAACTAACATCGCACACAGACGACCACAAGGTGAGAGTTATGACCAGGCCATCCGTAATGATGAGACTGGACTCTGGCAGTGTCCTTTTTGCCAGCAGGACAACTTCCCTGAGCTCAGTGAGGTGGGAAGCTTTTCTGATATCTTTTTAAAGGAATGAGACTGTTCATTTTAGCTTTTGCACATCAGTGAATGCTGTTACCATGGTGTTGTGTATTTCTCAGGTGTGGAATCACTTTGAC
Associated Phenotype:
Not determined