ZMP

sept4a

Ensembl ID:

ENSDARG00000010385

ZFIN ID:

ZDB-GENE-051120-87

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
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.

Availability:

Order Allele From ZIRC
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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:

sa14138

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

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