ZMP

CYTH3 (1 of 3)

Ensembl ID:

ENSDARG00000005159

Description:

cytohesin 3 [Source:HGNC Symbol;Acc:9504]

Human Orthologue:

CYTH3

Human Description:

cytohesin 3 [Source:HGNC Symbol;Acc:9504]

Mouse Orthologue:

Cyth3

Mouse Description:

cytohesin 3 Gene [Source:MGI Symbol;Acc:MGI:1335107]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10350	Essential Splice Site	Available for shipment	Available now
sa8572	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10350

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
ENSDART00000050576	Essential Splice Site	148	401	6	14

Genomic Location (Zv9):

Chromosome 3 (position 56853551)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	56374641
GRCz11	3	56442077

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTTGTGGAGCTCCACGAATTTGCCGACCTCAACCTCGTTCAGGCTCTGAG[G/A]TGGGAAAACTGTTCATTTCCTCCAAAAATGCTTGAATTTATTACATTTAC

Long Flanking Sequence:

TAAAGGCGAAGGCTTGAACAAAACTGTTATCGGGGATTACCTAGGGGAACGGTAAACATTAGCTTCAGTGTTTTTACTCTGCTTTATTCAATGTATGTCCATCGCACTGTGAGATGTTCGCCTGATTCTTCACAAAACTCCTCCGGAAATTGACTGTCTGGGTTAGAGATGGTAATATGTGTGTGTGTCTGTGTGTCTGTGTGTGTGTGTGTGCCGCTGGAGGAAGTGCAGTTCCTCTCGGGATGTGACTTGTCAAAACAACAGGATTGCGTGAAGCATTGCTGCACACACAAACAGCTGAAGCAGCTCACGAAAAGCCGCCCAACATCCTGAAAGATCTTAAAATCCTACAAGCGATCGATCCTTTTGTGCCAAAAAAGTAACCGTTGCTTCTGTGTGTGGTGCTTGTTTCCTCGTAGGGATGAATTCAACATCAAAGTGCTCCAGGCTTTTGTGGAGCTCCACGAATTTGCCGACCTCAACCTCGTTCAGGCTCTGAG[G/A]TGGGAAAACTGTTCATTTCCTCCAAAAATGCTTGAATTTATTACATTTACATTTATTTGAATCTATTATATACAAAAAAGAGTTGGATTGTTTATGGTTTAAAGGGGAATCTTATGTTTATTACATTAGAAATATTGTTTTAATGAGCAGTATTTTTTGCACTGTCATTTTTTTATTTTGTATGACCATGAAACATTTCCAATATTAATCTCATATGCTATTATTTGAAGTTTTTAATAATAAAATATAAAATATATTATGCAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTAGAGCTGTGAACCTACACTAGTCTCACGGTTCGGTTCGGTTACGATTATCATGCCATCGATTCCGTTCATTTGGATATTTTGGTGCGTCACGGTGCATTGACGATGCTTTTATATTTTCTTCACAGCAGCAGCTCTTGTATTAAAATGTATGAATATATTTATATTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8572

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050576	Nonsense	284	401	10	14

Genomic Location (Zv9):

Chromosome 3 (position 56828394)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	56349484
GRCz11	3	56416920

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTTTGATTTGCTTTGCAGGTGGACGGGTAAAAACTTGGAAGAGGCGATG[G/A]TTTATTCTCACCGACAACTGCTTGTACTATTTTGAGTACACAACGGTAAG

Long Flanking Sequence:

GTAAGGGAGGTGTCGTGGATGCCGCCCTCTCTATACTGCCGCCCTAGGCGGCCGCCTAGGTCGCCTCTATGGACGCGCCGGCCCTGCTTAGGAGCAGTATCAGCAGATATTAAGCAGACAGTCTACTAATACACAAATGGACCTTCAAAGTAAAGTGTTACCTAAAAAGCACACATTTTAAAAACTACTTGGTATAAACAATTCCTGAGAAAACTACACTTTACAATTTGGTTGTCTAGAGAGTTATCTGTGGAGGAACAGAAGGCAATATAACGTTACAACTTCTGTGATCGTGGAGACTGAAATAAATGAGTGTACAGCAGAAGATTGTTGATGCTGCTGCTGAAATGAGAAACAAATGAGAGCCTTTATTGTTGCGTTGGCTCAGAAACTGGGTCACTGGCCTTCTTTCTGTTTCTGTTTGAAGGCGCTCTGAAGATTCTCTCTTTCTGTTTGATTTGCTTTGCAGGTGGACGGGTAAAAACTTGGAAGAGGCGATG[G/A]TTTATTCTCACCGACAACTGCTTGTACTATTTTGAGTACACAACGGTAAGTAGACAATTCCTCATTATTATTGTGTTGTTACAGTATCTCATTCATGATCATGAAGGGATCAGTGTACCCAAAACCTTTTATGTATTTACTCATTCTCAAGTAGTGCCTTAATATACAATTTTTCGAAACTGATTGCCATTGACATCAATAGTAAGTACTCTGGAAGATAATGTTTGCCGGTTTCTGGCATATCTTCCTTTGTGTTGGACAAAATTAATAATCTCAAAGATGTCTGGAGCAAGTGGAGGATGAATAAATGATGACAGAATTTCCATTTTTGAGTGAACTGTCCCTTTAAATCAGTGGTCACCAAACTTGTTCCTGGAGGGCCAGTGTCCTGCAGGTTTTAGCTCCAACCCTAATCAAACACACCTGAACAAGCTAGTTAAGGTCTTACTAGGTATACTTGAAACATCCAGGCAGGTGTGTTGAGGCATGTTGGAGCTAAA

Associated Phenotype:

Not determined