ZMP

sept7b

Ensembl ID:

ENSDARG00000019649

ZFIN ID:

ZDB-GENE-061103-265

Description:

septin-7 isoform 2 [Source:RefSeq peptide;Acc:NP_001119922]

Human Orthologues:

SEPT7, SEPT7L

Human Descriptions:

septin 7 [Source:HGNC Symbol;Acc:1717]
septin 7-like [Source:HGNC Symbol;Acc:30810]

Mouse Orthologue:

Sept7

Mouse Description:

septin 7 Gene [Source:MGI Symbol;Acc:MGI:1335094]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10940	Essential Splice Site	Available for shipment	Available now
sa44249	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10940

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000032825	Essential Splice Site	82	429	3	13
ENSDART00000137437	Essential Splice Site	81	428	3	13

Genomic Location (Zv9):

Chromosome 25 (position 13070715)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	12783744
GRCz11	25	12880249

KASP Assay ID:

2261-9459.1 (used for ordering genotyping assays)

KASP Sequence:

ATTCCAAAGACTACCCTGGACCATCTCAGAGGATCAAGAAGACTGTTCAG[G/A]TATGTCCCCTTTTGCCGACCTCTGACCCCTGATACCGATCCACTGGTCTT

Long Flanking Sequence:

AGAGAAGTACAGAGTTGGCTAGAGGGAATGGAGCAAGCAATGTTTTATTCTCTAAGAAGAAAAGAGCTTTCTCTCTCTCTCTCACGCTTCTTTTTTTTTGTCCAAAATGTTTTCCCAATATACCCATGAATCTACTGTCGTTCGATTGCTGTCCTCAAGAAGAAACTATTGAAGTTCTGGCAAGGGTCCATTGATTGGCTCAAAAACAACAAACTAATTGTGTGTGCCTGTGTGGGTGGATGGATGGCTGTGAGAAAGCTTGTGAGGATCTGTGGAGAATCTCATATTCATCACCTCCTTTTTTTTAAGCATGGGTGTCTGTGACATTTCGTTCTGGCACTTGTTAAGCATGGCCACTTAACTTTTTATCTTTTGCTTGCTTTCCTGTTTAAGGTGAGTCTGGACTGGGCAAATCAACGCTCATCAATTCCCTCTTCCTGACAGACCTGTATTCCAAAGACTACCCTGGACCATCTCAGAGGATCAAGAAGACTGTTCAG[G/A]TATGTCCCCTTTTGCCGACCTCTGACCCCTGATACCGATCCACTGGTCTTGCCTTTTATCTACCATTATCTTTACATTAGTATTGCACTCCCTTTCTTCCCTTACCTTTGACCCTTTATCTCCTGCCACCATTATCCTCCATTGCTCTGCAGCTATAGAGAAGCCATAAGGGAAGTTTTTGTGGTCTGATTCCTTGTCCTTTGGGACAAGATTGCCACTGGCAACCATTTCGTAATATTCAAAGTGGATCTTTTGGGTTGCAAGACTATCTGGATGGCACAGAATACAGATCTTTTTTTTTTCAGGTGTTTCACCATCCAATTTTTGTGTCTGAGAAGATCTTGTTGTCTAAAAATGGGACTTGAACTTGGGTCGTAGCCCTGCCCACAAAACTATTGGCTCTGGGAGTACTTATCTTATACAACTCATTAGACAAGCTGCATCACAATGAGAAAGGATGCCCTGCCTCAAAGCATTAATTGCACTCACACACGGAAGGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44249

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
ENSDART00000032825	Nonsense	296	429	10	13
ENSDART00000137437	Nonsense	295	428	10	13

Genomic Location (Zv9):

Chromosome 25 (position 13091666)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	12762793
GRCz11	25	12859298

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCAGGACTCACATGCAGGACCTGAAGGACGTGACCAATAATGTTCACTA[C/A]GAAAACTACCGCAGTAAGAAACTAGCAGCCGTCACCTGCAACGGGGTCGA

Long Flanking Sequence:

TCCAACATGTAAATATATTAGAATATCTATTGTGCATCCCTATTGAAAACAGATTACTACCTTTTATTTAGTTGAATAGAGATCCAGTTTCTTATTAAGTGTCTTATCATAACTGCATACATCATACCAGTTACCAAAATAATGCATTTTCATGTCAAACCCTTATTGATACACTTACCAATTTACTCCTTTGTATGTCATAGTTCTGCACATGTATATGCTTTCTTTCTTATGTGTTAAACATTGCAACATAGTCATTCTGATGATGCTAAATCATACTAAAATCTAAATTTTTTCCTGTTTCAGTGGAGAACGGTGAGCACTGTGACTTCACAGTCCTAAGGAATATGCTCATCAGGTGAGGAAAAAGCAGCATCATTTCCAACATCAACCTGTTAAATGATTAATAATCTTGTGAAAAAACCTGTGGTCTAATTATTGATTTGCTGTTCCAGGACTCACATGCAGGACCTGAAGGACGTGACCAATAATGTTCACTA[C/A]GAAAACTACCGCAGTAAGAAACTAGCAGCCGTCACCTGCAACGGGGTCGATGCCACCAAGAACAAAGGCCAGCTTACAAAGTACGAAAAAAACAGGTTGACGTCAACGTGTATGTGACTGAGAGCATGGATTTCTGGGGGATCAAACATAAAAGCTTTGTAGTGCATCATAGGACTGTAATATAGCTGTTCAAAATGTTTAAAAAGTACATTTTAATGATTAAAGGGAAAAGACTCTTTTTACAACTCCCCTAGAGTTAAATGGTTGAGTTTTACCATTTTCTGATCAATCAGCTGATCTTTGGGTCTGGCGGGAGCACTTTTAGCTTAGCATAAATCATTGAATCCGATTAGACTGTTAGCATCTTGCTCCAAAAAAAGCTTTGGATAATTCTCCTATGTAAAGGTTGATCTCAGAAGGCACAATTTTATTACGCAGTGCTTTTACCTAGCTGGGGAGTATTTTTAGGTGCTACGTAATACAATTGCTTCAGCTGCAGC

Associated Phenotype:

Not determined