ZMP

sept6

Ensembl ID:

ENSDARG00000010721

ZFIN ID:

ZDB-GENE-030131-1414

Description:

septin-6 [Source:RefSeq peptide;Acc:NP_997791]

Human Orthologue:

SEPT6

Human Description:

septin 6 [Source:HGNC Symbol;Acc:15848]

Mouse Orthologue:

Sept6

Mouse Description:

septin 6 Gene [Source:MGI Symbol;Acc:MGI:1888939]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35719	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa35718	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35719

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000018750	Essential Splice Site	49	427	2	11
ENSDART00000136442	None	None	163	None	5
ENSDART00000137997	Essential Splice Site	54	432	2	11

The following transcripts of ENSDARG00000010721 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 14 (position 34300595)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	32985295
GRCz11	14	33325609

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCAACAAGTCCGTCAACCATGGTTTCTGCTTCAATATCCTCTGTGTGGG[T/C]GAGTGTGTCATGTGGGAGCTCCTTTTTACTTGGGGCAAAACTAAGCATTT

Long Flanking Sequence:

GTGCTGGAGTGGAATACAGATCAAAATTTGACATTTGTGTTTAGTTATTGACAACCGTTTTGCTACACAAGTATCTTACAGGTTACTTGATAAGGGAAACATTGGTCTGCAACTGCAGATGGTTTACGTGTTTGTTTGCCTGATTGTGGTTTCAAGAGTTGAGATCAGACAGGAAAGAGGAAGTGCACAGAGGAGAAACTAGAGATCTGTACTACAGTATTACAAATTGTACTGGGTTTGTTTTTAAATATTTTTTGTATTCTTATAAATGCATACAAAGACTTTTTTTGCATTGCTACCAATGAGAAACTGTTCAAAGAATCGATTTTTTTAAAAGTTGTCTTGCTTGTTTCATTTATATGCTTTGCTTTTCTTGTATTTTAGGGAGAGGGTGCACGTGCTGTCCCACTCTCTGGTCATGTTGGCTTTGACAGCATGCCGGACCAGCTGGTCAACAAGTCCGTCAACCATGGTTTCTGCTTCAATATCCTCTGTGTGGG[T/C]GAGTGTGTCATGTGGGAGCTCCTTTTTACTTGGGGCAAAACTAAGCATTTGCTTCAGTCTATGTCACACCACTCCACTGCGTACACATACTGATTTTGTCCTGTGACCCACTTACTAAATACTGGTGCACTGATGGAGAGCAGTTGCAGGAACTTGGGATTTAATTTCATACTATCAGTTAAGTGATAGTATGAACGAAAATCATCATTAAAAAAGATTATTGCAAGTTAGTTTTTTGAGAATGCTGGTTTGCAATAAAATGCATCATTTAGGGAAAATTACAGAAGCCGAAAAAGGTTAAACATGATATGAGTTAAATCACATACGCAAATAGAAAAACCCTAACGAATTGAGAAAACATCTTCAACGCACACACAAATTCTTACAGCACATGCAAATACAGAAACAAGCTGCAAGTAGGGTACAACAGTCAGGGTATCTTCTGTCTATTCCATATCCATTTTAAATTTTTGTGCACAACTTCTTGCACACCCTCAAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35718

Status:

Mutation detected in F1 DNA
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
ENSDART00000018750	Nonsense	56	427	3	11
ENSDART00000136442	None	None	163	None	5
ENSDART00000137997	Nonsense	61	432	3	11

The following transcripts of ENSDARG00000010721 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 14 (position 34294611)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	32979311
GRCz11	14	33319625

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTAGATAAGCTGATGTGTTTTTGTTACAGGGGAGACGGGTTTGGGAAAGT[C/A]AACCCTCATGGACACCCTGTTTAACACCAAATTTGAGGGCGAACCTACAC

Long Flanking Sequence:

CAGGGTATTAGATTACTTGTATCGTGATATGCAATTTTTGTAATATTGCTCAGCCCTAGCCTGTAGTGAAAGCATGAAAGAGGCTTGCGGGAATGGGATTTGCAGCCCGAGTTTGAGAAAACGGCAAATGTGAGCCATCCATATAATTAACATTCTGGTGGTGTTGCATGATGTCCATTTCTGCTGCGCTTGTGGTTGTCAGGAGTGCAAGAATAGGACCTTCAGGCAGACCGAGCCAGGACTGCTGCACGGCTTTTAGACTTGCACACAGATTAAATGGGCTAAAGTGTTTGCATCAGCTGAAAGGAGAATTTTTTTTATATTGAAGCTGACAAAAATATGTATGCTATAATTTAACAAACTATATTTAGAATATCCTATACATGGCATAATCTGAGGATTGTGGATGTAAAAGTTGGTATCTTGAAGATTGTAGAAAATTTGTGTGTGGTAGATAAGCTGATGTGTTTTTGTTACAGGGGAGACGGGTTTGGGAAAGT[C/A]AACCCTCATGGACACCCTGTTTAACACCAAATTTGAGGGCGAACCTACACAGCACAATCAGCCTGGAGTGCAGCTCAAATCCAACACTTATGAGCTGCAGGAGAGTAATGTCCGACTCAAGCTCACTGTGGTCAACACTGTAGGATTTGGAGACCAGATCAACAAAGAGGACAGGTAAGATACATATTTGCCCCCATTTGCAGTACATTGTTTTACATGTGGTCAGATGTGCTGTGTTATACCAAAGCACATGGATTAAGTTGACATCCTCGCATCTTTCTTTCACTTGCTTTTTTGTGCTCATTTTAAGCATGTAACACATTGATTGATTCAGTTTTTTCACATTGAGTACTTATGCTCTCAATGAGTACGATTACATGGACACCAATAATCAGATATTAATAGCTTAAGACAGTACTCTGATTAAGAGTCTACCATGTACACAGTGATTTTTGATAAATTAATCTGATTTAAGAATCATAATGAAACTAAACAAATCA

Associated Phenotype:

Not determined