ZMP
sap130b
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate Sin3A-associated protein, 130kDa (SAP130) [Source:UniProtKB/TrEM
Human Orthologue:
SAP130
Human Description:
Sin3A-associated protein, 130kDa [Source:HGNC Symbol;Acc:29813]
Mouse Orthologue:
Sap130
Mouse Description:
Sin3A associated protein Gene [Source:MGI Symbol;Acc:MGI:1919782]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31276 | Nonsense | Available for shipment | Available now |
sa31275 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31276
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 |
---|---|---|---|---|---|
ENSDART00000065266 | Nonsense | 822 | 1051 | 17 | 21 |
ENSDART00000143412 | Nonsense | 814 | 1043 | 17 | 21 |
The following transcripts of ENSDARG00000079352 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 22401492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23288197 |
GRCz11 | 2 | 22943848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCTCATTCCTCTCAGTGGCCTTAGGGCCAAACAGTGGTGCACAGATGT[T/A]GACAGTGCCTCCTACAGACCTCACGCTTGGAGCTTCACCCAGAAAGAAGC
Long Flanking Sequence:
CATCAGTAACACCACCTTCCCTACCTGCACCTGCTCTTTCAGCCTTGCCTGCAGCCATGACTGTTACTCAGCCAATCCCCTCAATGACCAATGTAGTGGCTCAACCCATTCAGCCAGCAGCCAATAATACTTCAGTATGTACAATCAACTCCAATCTTCCAGAGTTGAATATTAAGCAGGAGCCGGAACCAATGGATAGTTCAAAACCAGGTGGGATCTTTTGCATTTGATGTCAAGCCTATCGTGAAAATTATAATTCAGAACAATTTATAAACACACAGAAATTAAATCTTGCAATCAGTAGCTTAGGCAGCATTTAATTGTTTGCTTGTATTGGGTCTTAAAACCAAACAAGATAATGAAGAGAAATATAATCTTTCAGAAGCGCATAAATCTGCAACTCAAAGTATGAACCAGCTCCTCTTTTAACTGATGAAGTGTATTTTTTTATACCTCATTCCTCTCAGTGGCCTTAGGGCCAAACAGTGGTGCACAGATGT[T/A]GACAGTGCCTCCTACAGACCTCACGCTTGGAGCTTCACCCAGAAAGAAGCCCCGCAAACAACAGCACATCATCTCCACAGAGGAGAGCGAGATGATGGAGACCAACAGTACAGATGAGGAGAAGTTTCCTCCCAAACCCCTCAGCCAACGGGCTGAGAAACGCAAGTCCCCTCCTAAAGAATACATCGGTAAGATTCATCATTATAAAGCTGCATTCAACAGTGATTAACTTTATTTACTGGAAAATAAGTTGATTATGGGTCGCTAGGTCAAAATTGCATTCTTGTGAATAAAAAAGCAAGTAGGTAGTTTGCATTGATTTGCACAAGTCACATTTTATACTATTATTCAAAATGATTATGTAAAATAGGCTTTATTAAGATGTTTTAGTTCCAATCACTACACTACAAATATTTTATTTCAATGGTGTTCAGAACAGAAAATAAATAATTCAAGGGTGCTAAAGGTTCTTTCTCATTTCTCACCAATTCAGATTAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31275
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065266 | Essential Splice Site | 884 | 1051 | 17 | 21 |
ENSDART00000143412 | Essential Splice Site | 876 | 1043 | 17 | 21 |
The following transcripts of ENSDARG00000079352 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 22401303)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23288008 |
GRCz11 | 2 | 22943659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCAGCCAACGGGCTGAGAAACGCAAGTCCCCTCCTAAAGAATACATCG[G/T]TAAGATTCATCATTATAAAGCTGCATTCAACAGTGATTAACTTTATTTAC
Long Flanking Sequence:
CAATGGATAGTTCAAAACCAGGTGGGATCTTTTGCATTTGATGTCAAGCCTATCGTGAAAATTATAATTCAGAACAATTTATAAACACACAGAAATTAAATCTTGCAATCAGTAGCTTAGGCAGCATTTAATTGTTTGCTTGTATTGGGTCTTAAAACCAAACAAGATAATGAAGAGAAATATAATCTTTCAGAAGCGCATAAATCTGCAACTCAAAGTATGAACCAGCTCCTCTTTTAACTGATGAAGTGTATTTTTTTATACCTCATTCCTCTCAGTGGCCTTAGGGCCAAACAGTGGTGCACAGATGTTGACAGTGCCTCCTACAGACCTCACGCTTGGAGCTTCACCCAGAAAGAAGCCCCGCAAACAACAGCACATCATCTCCACAGAGGAGAGCGAGATGATGGAGACCAACAGTACAGATGAGGAGAAGTTTCCTCCCAAACCCCTCAGCCAACGGGCTGAGAAACGCAAGTCCCCTCCTAAAGAATACATCG[G/T]TAAGATTCATCATTATAAAGCTGCATTCAACAGTGATTAACTTTATTTACTGGAAAATAAGTTGATTATGGGTCGCTAGGTCAAAATTGCATTCTTGTGAATAAAAAAGCAAGTAGGTAGTTTGCATTGATTTGCACAAGTCACATTTTATACTATTATTCAAAATGATTATGTAAAATAGGCTTTATTAAGATGTTTTAGTTCCAATCACTACACTACAAATATTTTATTTCAATGGTGTTCAGAACAGAAAATAAATAATTCAAGGGTGCTAAAGGTTCTTTCTCATTTCTCACCAATTCAGATTAGCCATGTGCAGGTATAAGTTTCTGACGGTATGATAACCTTGGATAAAAATATCATGGTATTGTGATTACTGCTCTAAAATAAGCTCTTTTTAAATTGTCTGGGTAAAAAAATTGAACATTGAACCATTGAACAAAATACATTTTCTTTTATGAAACATTTATAATATTTTGGACCAATAAACATGTCTGGCT
Associated Phenotype:
Not determined