ZMP
sept4a
Ensembl ID:
ZFIN ID:
Description:
septin 4a [Source:RefSeq peptide;Acc:NP_001032456]
Human Orthologue:
SEPT4
Human Description:
septin 4 [Source:HGNC Symbol;Acc:9165]
Mouse Orthologue:
Sept4
Mouse Description:
septin 4 Gene [Source:MGI Symbol;Acc:MGI:1270156]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13158 | Nonsense | Available for shipment | Available now |
sa37365 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14138 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13158
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 |
---|---|---|---|---|---|
ENSDART00000006971 | Nonsense | 116 | 476 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 38368708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 39488787 |
GRCz11 | 21 | 39533845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTTAWAATGATGTCATCKTTCTTTCTTTTAGGATCAGGATAAGGAGTA[T/A]GTTGGCTTTGCAACGCTGCCYAACCAAGTGCACAGGAAATCWGTGAAAAA
Long Flanking Sequence:
ACAGGAATAAAGCCAATACTCTCTAGGAGTGTAATAGCCCAGTGGAACGGCATTATGTTGTCATGTCATAAATCACTTAAATCAGATGTGCAAGTCATTTTCATTAAAATAATGGGTCAAACTTTACAATAGTTTATTAGTTAATGTTAATTAATGCATTTACTAACATGAACAAACAATGAACAATACATTTACTACTGTATTTGTTCATGTTACTGTAGTTAATGTTAGTAATGAAAATACAGTAGTTCATTGTTAGTTCATGTTAACTAATGGTGCATTAACTAATGTTAACAAGCATGTACTTGAATGTTAATAATGCATTAGTAAATGTTCAATTATTAATAATAAATACTGTACATCTGTTGTTCATGATTAGTTCATGCTAGTAAATGCATTAACTAATGAACCTTATTGTAAAGTGTTACCAAATAATGTTATCTAAAAAACATTTTATAATGATGTCATCTTTCTTTCTTTTAGGATCAGGATAAGGAGTA[T/A]GTTGGCTTTGCAACGCTGCCCAACCAAGTGCACAGGAAATCTGTGAAAAAAGGTTTTGCCTTTACTCTTATGGTGGCAGGTGAAATTATATAAATTTTTATTATTATATATTTATATGATTTTTCTATTTTATGAAATCCTGATATAAAACTTTGTCAATCCTTCCAGGAGAGTCCGGTTTAGGGAAATCCACACTGGTCAACAGTCTCTTTCTCACAGACCTTTATAAAGACCGGAAGATGCCGAATGCTGAGGGTAAGAACCAGGGTTATTGTTGATAATCAAAATATTAATATGAATAAAAAACTAAAATAATAAATAAAATAAAATATTAATCTATATTAGGCACTAAAATCCTAATAAAACTGTGCAAACATTTTTCTGAAAATCAAACCATTAAAATGAACAAAAACAAAATCACAAAAAAAAGTACAAAAACACCAAAACTACTAGTTAAATTAACAGAAATGATCAGTCTGAAGTCTGAACAAAACTATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37365
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006971 | Essential Splice Site | 258 | 476 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 38362382)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 39482461 |
GRCz11 | 21 | 39527519 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACATAAATTTGTGAACATGACATTGCCTTTTCCCCTCTTTTTTTTCC[A/T]GTCTCAGACCAATTGATGTGGAGTTCATGAAGATTCTCCATGAGAAAGTC
Long Flanking Sequence:
TGCATTTATTTTCTGTTTTATTTTGAAATTTGTAGTTCCCTTTTATCATATTACTGACTGATACTTCTCACAGTTGTTTGTTGACAATGAAGCTGATTCAGGGGTTTGGTGTCATTTTGTTTTTTTAACGCAGTGAGTTTTAACTCTAGGATTCACTCCGAGTAATTAGATATTTGCTTTAAGCAGTTAAACAGTTGTACCTAAAGTGGCCTGTGTTTATAGATATTTTATGCCACATATACTCAGATTTCGTTTTTTAGCTTGTCAATAAAGTGGAAAACGTAATTTTTCAACGAGAGTGTCAGAGTAATGTAACATCAGCTCATATTGTTGAAACAACATAGACAATGCATTTTAGCCTTGACTAACTGCTGTAGTCAATTTATAAACTGATGCATTGTACTGCAACCATAATCTAGAGATGAATTCAGTTTAACATAAATATTGAGTTTCACATAAATTTGTGAACATGACATTGCCTTTTCCCCTCTTTTTTTTCC[A/T]GTCTCAGACCAATTGATGTGGAGTTCATGAAGATTCTCCATGAGAAAGTCAACATAGTGCCTGTGCTGGCCAAAACCGACAGTCTAACTCCAGAGGAAGTCAGAAAAATGAAAATGAAGGTGCAATTTATAATAATAATAATAATATTAATAATTCTAATAATAATAATCACCATATACATAAAATGATTGTTGGTTTGTTTTCTCTCCAGATTCGAGAGGAGATCGAGAGATTTGACATTATGATCTACCAGTTCCCTGAGTGTGAATCAGATGAGGAAGACGAGTTCAAACTCCAGCAGCAGGAACTGAAGGTGAGCACATTTACACACCACTGACTCACTGACTAACACTGATTTGGTTCTAATCTGGATTTGCTTTGTTACAGGATAGCGTTCCCTTTGCGGTAATTGGCAGTAATGTTCAAGTTGAAAGCCAGGGCAGGCGGTTCAGAGGCCGGCAGTATCCCTGGGGTTTGGTGGAAGGTACAGTACTTAGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14138
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 |
---|---|---|---|---|---|
ENSDART00000006971 | Nonsense | 465 | 476 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 38347501)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 39467580 |
GRCz11 | 21 | 39512638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTTTACAGTTGCGTCGAATGCAGGAGGTTCTGGAAAGGATTCARGAA[C/T]AGATGCGTCAAGGACATGAAGATTTACCCATTAATTRAARTGTATTTAGG
Long Flanking Sequence:
CTGTTTCTGAAAGAGAGGTAACTTTAACTCTGAGTCAGTTACTGTGGTAACTTACTCTGTGAACTTAAACTGGTAAGGAGCAGGTTTTATTCTCTAAACTCAGAGTTTCTGTCAGTCTTCTCCCCTTTTTTTTAAAGACGAAGTGATTATTTCTTGCCTTAGCCTTATGTTTCCACCCAACTATTTTAATGCTCATTTTGGAGATGTGCATAAAAACGATTCATGGAAACGTCATGATGCACAAATTGAAAATGCGCATAAAAAACACACGCATAACCGAGTAGAATGAACTTTTATTCGATAGAAAATATGTGCATAAACTACGATGGACAAAAATATTACTAAACAAATTACAGTATGAACTACTTACAAGTTTAACCTCAGAGTTGGTTGAACCTTCTTACTGAAACAGGCCCCTGATCATTTAATGTTGTTTTTGTTTGTTTGTTTTTTCTTTACAGTTGCGTCGAATGCAGGAGGTTCTGGAAAGGATTCAGGAA[C/T]AGATGCGTCAAGGACATGAAGATTTACCCATTAATTGAAATGTATTTAGGATGAGATTTCACAAGCTTAACATGGAGGAAACTGAAGTGAATGTATGCTTTTAGCTTTCAGAATCTTTAGAGCTTTGGCTGACAACAGAACCTTTAATGTAAATATGAACAACTGTTGTGGTACATGAGAAATAAGACCAGTACAACTTGACTTGTAAATGTCATAAGATTTATTATGAATCGTCATTGTTTTTGTTTTGTTTTTTTGTAGTAATCTAGCATATTTTTAATAAGTTTATTACTATTTCAGTTAAACATGGTGGACAATTTGAATCTTAATGCAGCCCAAAATGTACAGGCGATATATAACTTAAACTTTCTCCATAGGGAAAATGCACAGTTTGTCATATATTTATATATAATATCAATGTAGAATGAGGTCTAACGGTCCCGCCCACATCATACAGTATGATACATGGTCCCAAAAAATGAAAAAGAGGGAGGGAATAA
Associated Phenotype:
Not determined