ZMP
spen
Ensembl ID:
ZFIN ID:
Description:
Si:ch211-125c5.1 protein [Source:UniProtKB/TrEMBL;Acc:Q58EE7]
Human Orthologue:
SPEN
Human Description:
spen homolog, transcriptional regulator (Drosophila) [Source:HGNC Symbol;Acc:17575]
Mouse Orthologue:
Spen
Mouse Description:
SPEN homolog, transcriptional regulator (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1891706]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24332 | Nonsense | Available for shipment | Available now |
sa17259 | Nonsense | Available for shipment | Available now |
sa24331 | Nonsense | Available for shipment | Available now |
sa24330 | Nonsense | Available for shipment | Available now |
sa14508 | Nonsense | Available for shipment | Available now |
sa24329 | Nonsense | Available for shipment | Available now |
sa37703 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24332
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 |
---|---|---|---|---|---|
ENSDART00000109248 | Nonsense | 658 | 3476 | 10 | 15 |
The following transcripts of ENSDARG00000074245 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24739070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24525190 |
GRCz11 | 23 | 24451731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTCTACCGTTCAATGCAGGGATCTGGACAAGACATAAGAGATTTCTA[T/A]GAAATCATATCTGAACGAAGGTGAGATTTTATATTTTAATATTTATTTTA
Long Flanking Sequence:
ACATGTGTATGGTTGGATGGCTTGTCCTCCAGTATTACTGAACAGTATCTCACGAGGCACTTTTGTCGTTATGGACATGTAGTAAAGGTACTCTTTCTGTGCATGATTTACATTTTTTTAAACTCAAGTTCTATTTAACTTTAGTAGAACAAAAGGATTGCTATTTGTATTCTCTAAAATAAAAAAAAAATTAAAAAACATACTTTTCTTTAGGTTGTCTTTGACCGGCTGAAAGGAATGGCCCTCATCTTATATAATAATATAGAGTATGCGCAGGCTGCTGTCAAGGAAACAAAGGGTTGGAAAATTGGAGGAAATAAAATAAAGGTCTGTAATATAATTTGTATTGTACTAATGCACTTTAGAGTTACTAGACTTAACATTTGTTTGTCTAACACTGTTAATTAAACGTGTTTGTAGGTTGACTTTGCTAACCAGGAAAGTCAGATGGCTTTCTACCGTTCAATGCAGGGATCTGGACAAGACATAAGAGATTTCTA[T/A]GAAATCATATCTGAACGAAGGTGAGATTTTATATTTTAATATTTATTTTATTGTTTAGAATCCCTGCTGTTTTGAATAATTTCATATAATTTGTCTTTTTTTTTCAGAGATGAGCGCCGGACGCCATATCACGAGTTCACAGCTGAACGTGCATACTATGAAAATGTGCGTACCCCAACTTCTTACACAGAGGATCCACGTCGAAAATATCCTGCCAGAAGTCGAGAGTTTTTTTCAGAATGGGATCCCTACCAGGGAGATTACTATGACCCACGATATTATGATGACTCCCGTGAATACAGGGATTTTAGAGACCCATATGAGCAGGACATTAGAAAGTACAGCTACTTGCAAAGAGAACGTGAAAGGGAAAGAGAGAGGTTTGAAACAGATCGTGAGCGAGACCATGGTCGACGAACAATTGAACACCAACAAAGCCCAACCCATTCACGTCGTCCTGCTAGTCCAACTGCTTCTCCATCCCTTTCTGAACGTCCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17259
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109248 | Nonsense | 672 | 3476 | 11 | 15 |
The following transcripts of ENSDARG00000074245 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24738941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24525061 |
GRCz11 | 23 | 24451602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTCATATAATTTGTCTTTTTTTTTNCAGAGATGAGCGCCGGACGCCATA[T/G]CAYGAGTTCACAGCTGAACGTGCATACTATGAAAATGTGCGTACCCCAAC
Long Flanking Sequence:
TCTATTTAACTTTAGTAGAACAAAAGGATTGCTATTTGTATTCTCTAAAATAAAAAAAAAATTAAAAAACATACTTTTCTTTAGGTTGTCTTTGACCGGCTGAAAGGAATGGCCCTCATCTTATATAATAATATAGAGTATGCGCAGGCTGCTGTCAAGGAAACAAAGGGTTGGAAAATTGGAGGAAATAAAATAAAGGTCTGTAATATAATTTGTATTGTACTAATGCACTTTAGAGTTACTAGACTTAACATTTGTTTGTCTAACACTGTTAATTAAACGTGTTTGTAGGTTGACTTTGCTAACCAGGAAAGTCAGATGGCTTTCTACCGTTCAATGCAGGGATCTGGACAAGACATAAGAGATTTCTATGAAATCATATCTGAACGAAGGTGAGATTTTATATTTTAATATTTATTTTATTGTTTAGAATCCCTGCTGTTTTGAATAATTTCATATAATTTGTCTTTTTTTTTCAGAGATGAGCGCCGGACGCCATA[T/G]CACGAGTTCACAGCTGAACGTGCATACTATGAAAATGTGCGTACCCCAACTTCTTACACAGAGGATCCACGTCGAAAATATCCTGCCAGAAGTCGAGAGTTTTTTTCAGAATGGGATCCCTACCAGGGAGATTACTATGACCCACGATATTATGATGACTCCCGTGAATACAGGGATTTTAGAGACCCATATGAGCAGGACATTAGAAAGTACAGCTACTTGCAAAGAGAACGTGAAAGGGAAAGAGAGAGGTTTGAAACAGATCGTGAGCGAGACCATGGTCGACGAACAATTGAACACCAACAAAGCCCAACCCATTCACGTCGTCCTGCTAGTCCAACTGCTTCTCCATCCCTTTCTGAACGTCCTCCCAGTGACTCTGAACATCACGTTTACAGTCGCTCATCTGAGCGAAGTGGTAGCTGCAGCTCACTTTCTCCACCACGCTTTGAGAAGCCAGACAAAATTCGTTTGGAGAGGCACAATAGGAATGATAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24331
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 |
---|---|---|---|---|---|
ENSDART00000109248 | Nonsense | 721 | 3476 | 11 | 15 |
The following transcripts of ENSDARG00000074245 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24738796)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24524916 |
GRCz11 | 23 | 24451457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGTTTTTTTCAGAATGGGATCCCTACCAGGGAGATTACTATGACCCA[C/T]GATATTATGATGACTCCCGTGAATACAGGGATTTTAGAGACCCATATGAG
Long Flanking Sequence:
AGGCTGCTGTCAAGGAAACAAAGGGTTGGAAAATTGGAGGAAATAAAATAAAGGTCTGTAATATAATTTGTATTGTACTAATGCACTTTAGAGTTACTAGACTTAACATTTGTTTGTCTAACACTGTTAATTAAACGTGTTTGTAGGTTGACTTTGCTAACCAGGAAAGTCAGATGGCTTTCTACCGTTCAATGCAGGGATCTGGACAAGACATAAGAGATTTCTATGAAATCATATCTGAACGAAGGTGAGATTTTATATTTTAATATTTATTTTATTGTTTAGAATCCCTGCTGTTTTGAATAATTTCATATAATTTGTCTTTTTTTTTCAGAGATGAGCGCCGGACGCCATATCACGAGTTCACAGCTGAACGTGCATACTATGAAAATGTGCGTACCCCAACTTCTTACACAGAGGATCCACGTCGAAAATATCCTGCCAGAAGTCGAGAGTTTTTTTCAGAATGGGATCCCTACCAGGGAGATTACTATGACCCA[C/T]GATATTATGATGACTCCCGTGAATACAGGGATTTTAGAGACCCATATGAGCAGGACATTAGAAAGTACAGCTACTTGCAAAGAGAACGTGAAAGGGAAAGAGAGAGGTTTGAAACAGATCGTGAGCGAGACCATGGTCGACGAACAATTGAACACCAACAAAGCCCAACCCATTCACGTCGTCCTGCTAGTCCAACTGCTTCTCCATCCCTTTCTGAACGTCCTCCCAGTGACTCTGAACATCACGTTTACAGTCGCTCATCTGAGCGAAGTGGTAGCTGCAGCTCACTTTCTCCACCACGCTTTGAGAAGCCAGACAAAATTCGTTTGGAGAGGCACAATAGGAATGATAAATTGGAGAAAGAAAAATCACTTTTTGAGACAGAGCGTGGAAATGGTGGGGAAAAAGAAAGGCGAGCAGGACGTAAGGAAAAAGGAGAAAAGGACAGGACTGAGAGACAGAAGTTGAAGAAGTTAAAACTTGCATCTCCCACTGTTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24330
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 |
---|---|---|---|---|---|
ENSDART00000109248 | Nonsense | 1153 | 3476 | 11 | 15 |
The following transcripts of ENSDARG00000074245 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24737500)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24523620 |
GRCz11 | 23 | 24450161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCATTAGATAGCCTTGATCAAAAGATAGGTGCTTTTGGAGCTAACAGA[C/T]AACCAAGTTTCAGTCTTGCAGTCTCCGACGATGGAAGTGTAGATATGGAT
Long Flanking Sequence:
CTAGAGATTTCTTTAAGCATGGAAAACATCTCAAGGAGAAAGGCCTGGCAAGCCAAGTTGAGGTAGTGGATAAAGAGGAAAAAGTGAAAAACAAAAAATATTTCAAATCTGATCTTGCATTTGAATCCAGCTCTTCTGTGGATGCTGACCGCAAGGCTGCACGAAAGAGACGCTTTGAAGAAACATCGGCTAAGGCTGATAATTTAAGGAGAGTAAGTCAGGAGGAGGATGAAGGGAAATTAAGGAGAATTATTGATGAACCTTTGCTGAAAGACACTGATTATGATAAAAAGTTGCTTCGGAAAGAAGCACACAAGAGAGAGCGAAAAATTAAACCAGAGAGGATGGTTACTGTTAGTACTACAATAGAAGAGTTAGACAATGTAATGCCAGTAGGCCCCAGTTTAGACCTTCAGGCTCGACTTGGGGAACCAGCTGAAGATGCAATAGATCCATTAGATAGCCTTGATCAAAAGATAGGTGCTTTTGGAGCTAACAGA[C/T]AACCAAGTTTCAGTCTTGCAGTCTCCGACGATGGAAGTGTAGATATGGATTTTTCAAGAGAGCAAGAGCAGCAGCATTTAACTAGCTACCACACATTATCCTCAAGGCAAGAAAGAGTTTCTGAAAGTAAGGAAAGTTTGCTCTCAGACATTGATCATTCGCAGAGTTGCAGAAAACAAATGGAGCAAAATCGCCGCTTACAGCAGCAAATGCTGGAGTGTGATAAATCAGATAAAACTGAAAGCACACCAAGCACTGATGCGGAGGAATTTGAGCATCGAAGTATTGTGCATGAGGTTGTAAAACCATTACAAGATGTAACGGGAAGTTCTCCGACCAGCAAGCAAAAAAAATTGGGAGGATTCGAATTTGATTTTGGCAAAAGAGAGCAAAATTATGAAATGTTTCGACTGAGAAATGATGAACCTGAAAGAGGACTTGCTTCACATCCAGGGACACCCCTTGCTGAGGAGGAGAGAAATGCATCACAATTGTTGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14508
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109248 | Nonsense | 1395 | 3476 | 11 | 15 |
The following transcripts of ENSDARG00000074245 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24736774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24522894 |
GRCz11 | 23 | 24449435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTGAGAGAAATGAGCTTTCCCACAAGCATTGTTAAACGGGAAAGTATC[A/T]GAAAACGTCCTGAACGCGAATTAGAACCTGGAGAGGTTCAGTCAGACTCT
Long Flanking Sequence:
AATCAGATAAAACTGAAAGCACACCAAGCACTGATGCGGAGGAATTTGAGCATCGAAGTATTGTGCATGAGGTTGTAAAACCATTACAAGATGTAACGGGAAGTTCTCCGACCAGCAAGCAAAAAAAATTGGGAGGATTCGAATTTGATTTTGGCAAAAGAGAGCAAAATTATGAAATGTTTCGACTGAGAAATGATGAACCTGAAAGAGGACTTGCTTCACATCCAGGGACACCCCTTGCTGAGGAGGAGAGAAATGCATCACAATTGTTGGACAAAGACCCAGATTTACCAGTGACAATGGATAAAAATAGCTCGCATTTAGATGTTTCAAAATACAATACTAGCAATGCAGTGCATCAAGGGCTTTCACCACATGCAGAGATACTAAAAGTGAAACCATCAGTTACTAAAGAGGAGTTCAGTTGGGAGAGCAATATTAGGCAGGGCACATTGAGAGAAATGAGCTTTCCCACAAGCATTGTTAAACGGGAAAGTATC[A/T]GAAAACGTCCTGAACGCGAATTAGAACCTGGAGAGGTTCAGTCAGACTCTGATGAAGATGAAAGCAGACACTATTCATTAAAGCCAATTTCTTTCAAAAGAGAGCATGAAGAGCGGCTTTCAGATGTAAAGTATTCTGAGTCTCTTGAAAAGAATAAGTTCTATGAATTTGCATTGGATAAGACGATAACACCAGACACAAAAGCTTTGCTTGAGCGTGCTAAGTCACTGTCTTCATCTAGAGAAGAAAATTGGTTTTTCCTTAATCATGACTCAAAATTCAAAAGTTTACAGAATAACATCGACAAGGAAAAGTCTGAACCTACTCCAAGACCTATTCCTTCATGGTACTTGAAGAAAAAGAAAAGTCGCTCTGACTCTGATGGAAAACTTGATGAAAAAAAGCAAGATGCTAAGCCTGATGAACAAGAAAGACAAGATCTCCTAGCTTCACGATTTCTTCATAGCTCAATCTTTGAACAGGATTCACGTCGGCTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24329
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 |
---|---|---|---|---|---|
ENSDART00000109248 | Nonsense | 1449 | 3476 | 11 | 15 |
The following transcripts of ENSDARG00000074245 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24736610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24522730 |
GRCz11 | 23 | 24449271 |
KASP Assay ID:
2261-7744.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCTTTCAGATGTAAAGTATTCTGAGTCTCTTGAAAAGAATAAGTTCTA[T/A]GAATTTGCATTGGATAAGACGATAACACCAGACACAAAAGCTTTGCTTGA
Long Flanking Sequence:
CAAAATTATGAAATGTTTCGACTGAGAAATGATGAACCTGAAAGAGGACTTGCTTCACATCCAGGGACACCCCTTGCTGAGGAGGAGAGAAATGCATCACAATTGTTGGACAAAGACCCAGATTTACCAGTGACAATGGATAAAAATAGCTCGCATTTAGATGTTTCAAAATACAATACTAGCAATGCAGTGCATCAAGGGCTTTCACCACATGCAGAGATACTAAAAGTGAAACCATCAGTTACTAAAGAGGAGTTCAGTTGGGAGAGCAATATTAGGCAGGGCACATTGAGAGAAATGAGCTTTCCCACAAGCATTGTTAAACGGGAAAGTATCAGAAAACGTCCTGAACGCGAATTAGAACCTGGAGAGGTTCAGTCAGACTCTGATGAAGATGAAAGCAGACACTATTCATTAAAGCCAATTTCTTTCAAAAGAGAGCATGAAGAGCGGCTTTCAGATGTAAAGTATTCTGAGTCTCTTGAAAAGAATAAGTTCTA[T/A]GAATTTGCATTGGATAAGACGATAACACCAGACACAAAAGCTTTGCTTGAGCGTGCTAAGTCACTGTCTTCATCTAGAGAAGAAAATTGGTTTTTCCTTAATCATGACTCAAAATTCAAAAGTTTACAGAATAACATCGACAAGGAAAAGTCTGAACCTACTCCAAGACCTATTCCTTCATGGTACTTGAAGAAAAAGAAAAGTCGCTCTGACTCTGATGGAAAACTTGATGAAAAAAAGCAAGATGCTAAGCCTGATGAACAAGAAAGACAAGATCTCCTAGCTTCACGATTTCTTCATAGCTCAATCTTTGAACAGGATTCACGTCGGCTTCAACACCTTGAACGGAAAAATACTGACCCTGACGTTAGAATTGGCAGAGATAGTGTTACAAGTAATTCTCAAGGTGAACAACCTGGAACAGGAGGATCAGACTTGACTCAAGAACCAAGAGTACTTTTTCATAGCCGCTTTTTGGAACTTCAGCAAAGAGACAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37703
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 |
---|---|---|---|---|---|
ENSDART00000109248 | Nonsense | 2606 | 3476 | 11 | 15 |
The following transcripts of ENSDARG00000074245 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24733141)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24519261 |
GRCz11 | 23 | 24445802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATAGACCTAGCCCTATAGCTCAGCTTGTACCCCGTACAACACCACCG[C/T]AGCCCCCTCCTCTACAACAATGTGAGACTCCACAGATCTTAAAGGAGAAA
Long Flanking Sequence:
CTGAACCTCAAGAATCTGCCTTCCATTCTGGAAATAACAGTCCTTCTTATTTGAGGACACAACAGTCATCTCCTGAGCGAGGAGCATCTGCCCTTACTTCACCTACAACACGCCTAAATTCACCTGCATCCTCTAACATTCCTCCTGAATGGAATACCAGGACAGAGGAGAAAGTAATGCTACCTAAACCACAAGGTAATGTGGCTTTGTCTATCCCAGGAGCTGGGGGACCCCCAGCAAATCCTCCCATGCCTCCTGACACAAAAGCCTCTGATATTAATGCAAGTTCTAGTACACTGCGAAAAATTTTAATGGAACCAAAGTATGTTTCTGCTTCAAATAGCAATTCAGTGACAAGTATGCAGTTTACTACCACATTAGCAGATCCACGGATGTCTGATAATGAAAATTCAGTTGAGGCTGTGCTGCCTTTAAAAACCTCTCTACCTGAAGATAGACCTAGCCCTATAGCTCAGCTTGTACCCCGTACAACACCACCG[C/T]AGCCCCCTCCTCTACAACAATGTGAGACTCCACAGATCTTAAAGGAGAAACTAGCTATAACTTCCACTGCCACTTCAGTCATTAGTCGGATCCCTATGCCCTTTGATTTTGAGGACACTCCTCGCATCTCTTTAAGTAATCGTAACTCTGGAATGTCTTTGCCAAAGCAGAAATATCGTACTGGCTTGAATGAAAATAATAGATATCATGGACATAATACTTCTGAGGATGGTGGAAGTGTTGGGCGCCCAGTTGTTGAAGGCACACATTGTAACACGGGGTCTAGTACTGGTTTGAGGGTCAACACATCTGAGGGTGTGGTAGTATTAAGTTATTCTGGACAAAAGACAGAGGGACCACAGCGGATCATTGCAAAAATTAGCCAAATCCCTCCAGCCAGTGCAGTTGACATTGAATTTCAGCAGTCTATAACAAAATCTCAGATTAAACAAGAACCTTCATCTCACCCCTCTACCCCAAAAGGATCACAGACACCTACA
Associated Phenotype:
Not determined