ZMP

cyth4b

Ensembl ID:

ENSDARG00000039932

ZFIN ID:

ZDB-GENE-080219-45

Description:

cytohesin 4 [Source:RefSeq peptide;Acc:NP_001108375]

Human Orthologue:

CYTH4

Human Description:

cytohesin 4 [Source:HGNC Symbol;Acc:9505]

Mouse Orthologue:

Cyth4

Mouse Description:

cytohesin 4 Gene [Source:MGI Symbol;Acc:MGI:2441702]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38532	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

This allele has been removed from public view.

Allele Name:

sa3604

Status:

Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

n/a

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000028022	Essential Splice Site	53	394	3	13

Genomic Location (Zv9):

Chromosome 6 (position 605235)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	373641
GRCz11	6	396348

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTGAGAATGTGATGGCTGATATTCAGGACTTCAAGTCGGCAGAAGACAAG[T/C]GAGTCCAGCATCTCCTGGGGTGTTGTTGGTGTTGTTAGTGTTGTTTGTAA

Long Flanking Sequence:

GTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTAAGTGTGTGTATGTGTGTTTTTGGGTCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTTTGTTAAACGTGTGTTTTTGGGTCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTTAAACGTGTGTTTTTTGGTCAGTGTCTGTGTGTGTGTGTGTTTGTTTGTTTGTTAAGTGTGTGTATGTGTGTTTTTGGGTCAGTGTGTGTGTATGTGTGTGTGTCTGTGTGTGTGTGTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGTCATCTGATGTGTCCTGCTGTTTTCCAGAAACTGAAGAGTCAGATTGAGAATGTGATGGCTGATATTCAGGACTTCAAGTCGGCAGAAGACAAG[T/C]GAGTCCAGCATCTCCTGGGGTGTTGTTGGTGTTGTTAGTGTTGTTTGTAATATTATCTGTGTTGTGTCTCTCTGTAACTCCGGCTCAGGTGTAAAGGGTTGTTGTTGTTGTTGTTGTTGCAGTAAGACACTGGAGAGAGAAAAACGCTTCAGCAGTGGAAAGAAGAAATTCAACATGGACCCTAAAAAGGTGAGAGGGTGAAGAGGATGATGATGAGGATGATCAAGATGATGATGATGATGAAGAAGATGTTTTCCACTGTGGGGTGACGATTGGAGCGTCTGTCTCTCTGTCTCTCCTTTATTGATCTGAGACCCCCATGTTAAACAGAGGTCGGAGCCAGCTGGAGGTCTTATTTATTGAAAGTCTTGTGCTTGACACAGAGTCCAGTGTTGTGCTTTATGAACGTCTACACCCACCTCAACCCTAAACCCAACCTCACACTCACCTGATGTGTCTTATTAACATCTGCTCCACCCACTCCACCTAAACCCAGCCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38532

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000028022	Essential Splice Site	293	394	11	13

Genomic Location (Zv9):

Chromosome 6 (position 593115)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	385761
GRCz11	6	408468

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTAAATGTAGGTGTGTTTGTGGATCAGGGTTGATGACGGTGTGTGTGTTC[A/G]GGATAAAGAGCCACGCGGGATCATTCCTCTGGAGAATCTGTGTGTCAGAG

Long Flanking Sequence:

CTTAAAAGCTACTTAACACATGACTTTTTACAGCAAAATTGCAATGTTACTTTTAAAAGACTACTATTGAGTTTTTAGCACTGTTTTATTTTTGTTAGTTTGTTTTGTATTTAATATAAAATTAAAATTAATTTCAGAAACTGTTGTTTTATATTGTTGAAAGCAAGCAAGCACACAAATGAACACAAACTTAATTAATTATTTTATTTTATAAATAATTAGAGCAACATTTTAAAGCATTACTTTTAAAAGACCACTACTACTGTTAAGTTTCTTTTGTTTTTTTTATGTAATGTATAAAATGTAAGCTATCAGCATTAATCCTGTATTGTTGTCACCTGCAGGCGGTCGTGTGAAGACGTGGAAGCGCCGCTGGTTCATCCTGACTGATAACTGCCTGTATTATTTTGAATACACCACGGTAAGAGTGATGTTTATTAATATTAATGATTAAATGTAGGTGTGTTTGTGGATCAGGGTTGATGACGGTGTGTGTGTTC[A/G]GGATAAAGAGCCACGCGGGATCATTCCTCTGGAGAATCTGTGTGTCAGAGAAGTCATCTTTCAACGCAAACCGGTGAGAACACATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTATCTATCATCTGTCTGTCTTTACATTTTTCCATCCATCCATAGACTAGACTGTGGGTTTGGTTAACATTAGTAATAGTTGACCTTTGACCTCTGACCTTTGACCTATGCAGTACTGTCTGGAGCTCTACAACCCCAACAGTCGAGGGCAGAAGATCAAAGCCTGTAAGACGGAGACAGACGGACGCGTGGTGGAGGGAAAACACCAGTCATACACCATCAGCGCATCTACAGCGGAGGAGAGAGACCAGTGGATAGA

Associated Phenotype:

Not determined