ZMP
SBF2
Ensembl ID:
Description:
SET binding factor 2 [Source:HGNC Symbol;Acc:2135]
Human Orthologue:
SBF2
Human Description:
SET binding factor 2 [Source:HGNC Symbol;Acc:2135]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6088 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21129 | Essential Splice Site | Available for shipment | Available now |
sa45300 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2358 | Essential Splice Site | F2 line generated | Not yet available |
sa34231 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38653 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6088
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082664 | Essential Splice Site | 255 | 1898 | 7 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 68898740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 66776761 |
GRCz11 | 7 | 67000409 |
KASP Assay ID:
554-3858.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAGGCCTGCCGTGCCTTAGAGACCCTCATGTTTCCTCTTAAATACAGG[T/A]GAGTCAAGACTAGGGCTACTTTTGTCTTTTTCAAATATTCCCCNAAAGGA
Long Flanking Sequence:
CAATCGCCATCACTATTAAAAGGGGAAAAAAATCCAACATTTGCATAAATTATAGTGCTTTGCTGGTCTGCAATCGGTGTCAGTTGTCAAATATGTGCTTCTGTTAAACATAATAAACAATTAAACTTCAGAATAAATTAATGTTACACTAAAACCTATTTGTGTCAGTTTGTTACATTTTAAACTAACTAACAAGGTCTAATATGGGCTTTGTTATACATATATTGCAATATAATATATTTCAGTTCACTGTCATACATGTTATATTAACCTCAGTCATGTTTTAATAAATGGTTTATTCATTTGAAGTGAATGTTGCTGATGTTTCATAAGTATTTGTACAATTGTGTTGTTTTTCTCTTGCAGGAATCCAGAATGTTCTTAGTCTGTTTTGTGCAGTTCTGACGGAGCACAAGGTTTTGTTCCACTCTTCCAGCTATCAGAGACTAGGAGAGGCCTGCCGTGCCTTAGAGACCCTCATGTTTCCTCTTAAATACAGG[T/A]GAGTCAAGACTAGGGCTACTTTTGTCTTTTTCAAATATTCCCCAAAAGGATGTTTAACAGAGCAAAGAATTTTTCACAGTATTCCCTATAATATTTTTTTCTTCAGGAGAAAGTCCTATTTGTTTTATTTCAGCTAGAATAAAATAAATGTTTTTAAAAACATTTTAAGGTCAATGTTATTAGCCCTCTTAAGCAATATTTGTTTTGGTTGTCTACAGAACACACCACTATTTTACAATGATTTGCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTGAATACTAGTGTTGTATAAAAATAAATGAGTGAAAGGAAGAGAGAACCAAGTCCAGGAGACTCGAAACAAGCAGAATTCCTTTATTGAGACGTGTTGGTTAATCTGCAGTCATACAGCGTCTTTAAGGCCCCGTTTACACTAGTGCGTTTTAGTTTGAAAACGCATAAGTTTTGCTACGGTTACGCCATCCGTCCACACTACGCCGGAGTTCTCGAGCGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21129
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082664 | Essential Splice Site | 469 | 1898 | 13 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 68917621)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 66795642 |
GRCz11 | 7 | 67019290 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAACTCCAGAAGCGCTTGAGGGAGCTGTCCGAGCAGCTTTACAAAAAC[G/A]TAAGCACATGACGCTGATTCTCATGTCCCTTCCGTCAGGTGTTTGAGAAC
Long Flanking Sequence:
TCTGTTAAACATTATTTGGAAAATATTTAAAAAAGAAAAAAAAAATCAAAGGGGGGCTAATAATTCTGACCTGTATGTGTAAGAATTTTATAATTTGTGCTATTAAAAAATTCTGACGACATCTAAATGAAATTAGTGAGCATGCACTGTATCGCCTGGTCCAGTAAACAACTGTAATCGGATCGAATAATTGTTAGAGCAAATATTTACTCCCCTACTAAGTAACATCATTCCACAGGAGGAAGATAATACATGCGTGACTCAGTGGAGCTGAGCGAAATTCCAGCTATTGTTCAGGGCAATGCTAAATCAATTACAGGTGGAAAGTCTGATTTCTTGTGCACAGTGTTACCACAGATTCATCACTTTCTTCATCAAATGGCTTTGTTTCTGTTCTGTAGCTGGTGGCCTTAGACGTCGACTGCTTTAAGGATGAAGACGAGAACCTGGTCAAACTCCAGAAGCGCTTGAGGGAGCTGTCCGAGCAGCTTTACAAAAAC[G/A]TAAGCACATGACGCTGATTCTCATGTCCCTTCCGTCAGGTGTTTGAGAACTTCATTGGCCTCCACTGACCATTTATAAGCTTGTTGATGCGAGAAGTGTTATTGTAACACCGCTGCTAGCTAAAGTGTCAAAACAGCTCATTTGTTTCAATGGGAGCGAAAGACAGTGTGCTCATATTTAATAATGTGGGCATCAAGGAGATTGAAAATGAGCCCACCCCAAATGTTCTCATTGGTTGAGGTCTGTGATGATGTCTATTCCTCGCCAGTGTTCAGCACTCAATCACTTGTGACCTCTTTGTGTGTGTTCAGAGCCAAGCAGTGGATTTTTAAAGTAATATAAAATCTGTGTTAACTTGCATTGAAATAAGTGTTGGCATTAATTAATTGTGTTAAATCAGTTGCATAATTGCGTTAATGCAACAATAACATGTTAATATGCTCAGATCTAATATTTATGTATAATATCTTTGCATGTAATACCTATTCTGTATAAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45300
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082664 | Essential Splice Site | 574 | 1898 | 15 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 68922102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 66800123 |
GRCz11 | 7 | 67023771 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGTGCATCGGCTTCATCTTCGACAACAAGACTCTGGAGACCGAAAAGG[T/G]GATGCAATAATTCCTGTGATGAAGATTAAACTTGCACATCTGGGGAAAAA
Long Flanking Sequence:
GCTCTTAAAGGGAATGGGAGATGAGACTCTAATTGGTTTATTCTCAAAACACACCTATAACTCATTAAGAAAATAAGCTCAACCCTTTTAGAACATGTGCCATGGCGCAAAACAGATTTTCCCGTCCTTAAATTAGCAAAACTGCGTTCTGACACGCCCTGAAAGCATTTGCGCCCTGCGTATTGCGCTCTGCGCATGGACTGTCAAAATAGAGCCCGTTATCTGAGAATTAAATTAAAAAAAAACAGGAAGCGCATTTTTAGGAAGGACAAACTTTTTTTTTTGTGCTTATCATGGTTAAAAGCTTTATAGGCTCTCTGCTTAAAAGCACAGTTAAAAAAGCCACTAAGCTTCTTTAATAAGTTTTCATTTCTTATCTTTTCTTGCAGTATCTATCATGGGCAAGGCCAGCTCGGTTTTCAACAGCGCCCGTAGACTAGAGGTGGTCCGGACGTGCATCGGCTTCATCTTCGACAACAAGACTCTGGAGACCGAAAAGG[T/G]GATGCAATAATTCCTGTGATGAAGATTAAACTTGCACATCTGGGGAAAAAAAAGACAGCATGCAGATTAGCCGGCATTAGCGATGGCATTCACAGCACGATAAGCAAAGCTCTCCAGCTGCAAGTCGTACAGACGTAGGAGGAAAGGGGTGAACAAACAGTCTCACATATTCTTCTAATTTCCCTGCGCTTATCGCTAATGCTAATATTATTCTAACATTAACCGTGACTAGTGTTTGTCTAAGCTAAGGCATCTTAACATTTTTTTAGGCTAAATAACTTTGTGCAAATTACCTGATATTTCCTGACCAGCAGTGTGGTGGAAAGAGGACGAAAATAAAATCCTATTCAAGTAACAGTATCATTGCTTGCCAAAACATGGAGGGCATGTAGAGTAAAAGTATGAGTAAAATGTGTTTTTTTTTGTCTTGTTTCTAGTTCAAATATCTAAAAATTCCTAAATCAAGATTAATTTTCCAGAAAAGCAAGAAATATTCACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2358
Status:
F2 line generated
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082664 | Essential Splice Site | 648 | 1898 | 18 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 68977578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 66855599 |
GRCz11 | 7 | 67079247 |
KASP Assay ID:
554-2789.1 (used for ordering genotyping assays)
KASP Sequence:
TATTTTAGCAGACTGCCTTGTGCTGCCCGCTGATCCATCTTTTTGCTTGC[A/T]GAAACTGGCAGSTGGAGTGGATCAGTTCGCCTACACCTGCATCCAGGAGC
Long Flanking Sequence:
GGATAGTAATCTAATCGGAGGTGTGAGCCGTACAGACCAATAGAAGGTGAGAAAGACGTCATGCGTCTTTAAAACTCTGTATCCACATGTGCAAATACTAAAAAAAAAAACAGCCTTTATATTTTCAACAGATGGCCTTCAGAGCCAGCTCTCGGGTGATCTGGTTTGCTTCGAAGAGCACAAAATAACACCAGAGCCATGTTTTCAAAGTCTTGCCTCGCAGTCTCTCTCCATATGAGGCCTACTGTATGTGTTGAGAGCATTACGGGCTCTAAAAATGACTGATTGCTCCTAAAAACCTTTGGCAACAACGTACTGCTTTCCTGTTTTTACCATGCTTTTTAATGGACTCCTTTACAAGCGTAGTACAGGCCAGTTGGTTTCATGAGCGGTGAGAACCTCGGCTCGGCTGATTTGAGCTGTTATATAGACAGTAGCGGGCTCTGTGTTTATTTTAGCAGACTGCCTTGTGCTGCCCGCTGATCCATCTTTTTGCTTGC[A/T]GAAACTGGCAGCTGGAGTGGATCAGTTCGCCTACACCTGCATCCAGGAGCATCCCATCTGGACCAATCAGCAGTTCTGGGAGGCCACTTTCTACTCGGAGGTGCAAAACCAGATCAGAGCGCTTTACCTCACTGCCCCTGAGGACAAGCCACTCATCACTGCCAAGATCAAGGTAAAGGCTTAAAGTGGAAGTTAAACAGGCAGTCAAGTTTACATTATTTTGTGAATTGATCATTTTGCTTGAATAAAAACATTGATAACAAACTGTATAAATGTAACCATTTTAAAGCAAAAGGCATGTTTTACTGTAGCTTTTAGAGCTCTGTGCTAACATCTTGGAATATCGCTGTGTCTGAGATCACAGGGTTGGTTCCATTCCCTGAGGCAAACAGATACAGTAGAAGTAATGGACCGACCATGGAGACTGAAAGGCCTAATTTTATCTATTGTGTTAGTTTGTAGACATGGGGCTAGTGCAAACACAAGTATCAACTTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34231
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082664 | Nonsense | 757 | 1898 | 19 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 68980275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 66858296 |
GRCz11 | 7 | 67081944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTGGTGAAGAGTGAGGAGAGCACAGTGTTCAGTCAGGCCATCCACTA[C/A]GCCAGCCTGATGGTTTACCTGCTCGTCCCATTGGACACCAGCAAAAACAA
Long Flanking Sequence:
CTCTCAGTAATGATTTAAATCACACTGAACTGAGCTAAACTGAACTGAACTTAAACACTAAAAACTGAACTACACTGTTCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTAAATACATATTTTTAAGTCAGTATAAAAAGCGGTGGGTTTTGACAGAATTGCAAACAAACCATAATAAGCACCAATTCTGACAGCTTTTTCTGTTAAACAACCCCTTCCCCCACCCCCCATCACCAAAAAAAAACAAAAAAAACAGGGATGTCATTTAACCCTAGTTTCTCTTGTCTTTATCAGGAACCGAGTAGATTGTCCACAGCAGCGGGTCAATCCGAACGGACCGCCATGGATCTCGCAGCAGAGCAGTTGCGTGCTTGGCCCGGCCTGAGCAAAGAGAAGCAACATGAGCTGGTGAAGAGTGAGGAGAGCACAGTGTTCAGTCAGGCCATCCACTA[C/A]GCCAGCCTGATGGTTTACCTGCTCGTCCCATTGGACACCAGCAAAAACAAGCTCCTGCGCTCCAATCCTGCGGCCGACTGGGAGAGCGGGAGCAACAGCATCCTCACAAACAGGCAAGGCTAACATTAACATTCTGATCTATGCCATTCCATATATATACAGTTTAAGTCAGAATGATTAGCCCTCCTGTATTATTAGTGCCCCCTGTATAATGTTTCCCCAATATCTGTTTAACAGAGAGATTTTTTTACCACGTTTCTAAACATAATAGTTTTAGTAACTGATTTCTAATAACTGAATTCATTTATCTTTGTCATAATGACAGCACATAATTTTACTAGATATTCAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGCAAGTTACAGTAATCAGACAAATCGTTGTATAACAATGGTTTGTTCTGTAGACAGTGGACCCAATCTTTTTATTACCATGGACAGGTCAATGCTTGACAATTTTACCGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38653
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 |
---|---|---|---|---|---|
ENSDART00000082664 | Essential Splice Site | 1294 | 1898 | 30 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 69034456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 66912477 |
GRCz11 | 7 | 67136125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCCTGTTTCTCCGTGCCATCAACAACTCCTGCACCTCTAATCTACCA[G/A]TACTCGGGTACAGGGATAAACTTTTCACTCACTCAAACCAAAAAGCTTCA
Long Flanking Sequence:
TTATTATTTTCATTGTCCGGCAGCTAAAACATTTCACAAAATGTGTTAAATCAGCTGCACAAAGCAATTGACATGCTGAAAAGCCTATACATTTACTTGATATAAAGATTTGGCATTTATCGATTCGTGATTATTATCGATATCGTCTGATATGAAAAAAAAATATTGTGATCATTTTTGTTTGCCATATCGCTCAGCCCTAGTTCCAGCCTTTAAAGAAAAGATCTGATGCATGGATTAAAAAGACATATTAAAATACTAATTGTGAATGGAAATGTTTCCCCCTCATCTCCAATCAGCCAAAAACGCTGAATCTTTAATTCCAGGTGTAAAGCAGCCGTCTCACTGGTCTCATCGAGCTAATAACTGTTCTGTCTGTCTTCAGAAAGGGGGTGTTTGCTGCATGTGTTTGAATTTTGTTATATGTTGTTTTGTTTTGTTTTGTTTTTTATTTCCTGTTTCTCCGTGCCATCAACAACTCCTGCACCTCTAATCTACCA[G/A]TACTCGGGTACAGGGATAAACTTTTCACTCACTCAAACCAAAAAGCTTCAGCTAAGGGAAGAATTCACAATCAAGGTATCGTTTCTGTTTACTCATTCACACTAACCTGATCCATACTTGACTGACCTTTTCTCTGCATCTCTTTGACCTCCATCCATATAACCACAAGCGAGCTTACCAGCAGCTTTATTCTGCTCTACGTCAGATTTTTGTAGTAATTTTTGTAGTTCATATACACTGAAAATAAAAAGATTCATTAGATTTACTAAAAAGAAGATTAAGGTAAGTGTTTGCAAACAATTTATATGTGCAAACTAATTAAGCTGAACATTACCTAAATTAATTTGTTTAAATTCAGCTTATACGCTGTACATTTACCGGCCACTTTATTAGGTACATCTTACCGGGTTGGACCCACTTTTGCTTTCAGGACTTTGTGGCATAGATTCCATGTTCGATATATTACAGCACTTTGTTCTCCTAAAGTTATTTTTGTAATC
Associated Phenotype:
Not determined