ZMP

si:dkey-263h23.7

Ensembl ID:

ENSDARG00000063682

ZFIN ID:

ZDB-GENE-060503-633

Description:

Novel protein similar to vertebrate formin homology 2 domain containing 3 (FHOD3) [Source:UniProtKB/

Human Orthologue:

FHOD3

Human Description:

formin homology 2 domain containing 3 [Source:HGNC Symbol;Acc:26178]

Mouse Orthologue:

Fhod3

Mouse Description:

formin homology 2 domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1925847]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23403	Nonsense	Available for shipment	Available now
sa9923	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa23403

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

Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000093281	Nonsense	303	1407	9	25
ENSDART00000146050	Nonsense	309	1323	9	24

Genomic Location (Zv9):

Chromosome 19 (position 719466)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	740953
GRCz11	19	740762

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGGTGGATGTTCTTGAGGAGCAGGGCATGGAGAGCGTTTCTCAGCGGTA[T/G]CTGGGCCGCAAGGGCACCGATCTGGACCTGCTGGAGCAGCTCAACATATA

Long Flanking Sequence:

AACACTGATTCTGATTCATTCACACTGATTCTGATTCATTTACAACCACACACTGATTCTGATTCATTCACACTGATTCTAATTCTGATTCATTTACAACCAAACACTGATTCTGATTCATTCACACTGGTTCTGATTCTGATTCATTTACAACCACACACTGATTCTGATTCATTTACAACCACACACTGATTTTGATTCATTCACACTGGTTCTGATTCTGATTCATTTACAACCACACACTCTTTCTGATTCATTCACACTGGTTCTGATTCGTTAACAATCACACTATGTCTGATTCAATCACACTGGTTCTGATTCTGATTCATTTACAACCACACACTCTTTCTGATTCACACTCTCAAAGTGGTTCAGATTCTGATTCTCTCTCTCTCTCTCTCTCTGGGTCAGACGTTGGCGGCTCTGCCTGATCAGGACTCGTTTTATGATATGGTGGATGTTCTTGAGGAGCAGGGCATGGAGAGCGTTTCTCAGCGGTA[T/G]CTGGGCCGCAAGGGCACCGATCTGGACCTGCTGGAGCAGCTCAACATATATGAGGTCTGACCATCTCAATCAGTGACTCCTTCATGTGGGTTTGGACTAATTGACTGATTCCAGGGTGTGTGTGGGGTCTTAAAAATATTAAAAGTTGATGAGTCAATTCAGAGAAATTGAAAAGGCCCTTAAAAAGTACTCCTGAGACACTGTTGTTTATTAATATAGATCATAAAAACACAAACATGAAAGTAAACATTCTAAAAGGGATTGAGTTTGGCTGTCTGATTCCTGTATATACCCTGATCCTCTTCCTCTGTCCTGCAGGCGACGCTCCGTCATGAGGATGGAGATGAAGACGGTTTGCCTCCATCCTGCGGTCGGCGGGACAGACGGAGGTCCAGTGTGGGTGGAGAGAGGCGGGGCTTGGAAAGACGCCGCAGCCGCAGGCATTCATTGGGCAGACCAGGCCACGCCTCCCCGCTCAGTCCCGCCTCCCCACACCGCAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9923

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000093281	Nonsense	1085	1407	20	25
ENSDART00000146050	Nonsense	1001	1323	19	24

Genomic Location (Zv9):

Chromosome 19 (position 740242)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	761729
GRCz11	19	761538

KASP Assay ID:

2261-2726.1 (used for ordering genotyping assays)

KASP Sequence:

AAGTGTAGCTGATGCTGGTGTGTGCAGGCYAAGGGCTTCGATCTGAACTA[T/A]CTGGAGAAGGTTCCGGAGGTGAAGGACACGGTGCACAAACAGTCTCTGCT

Long Flanking Sequence:

ATATACTTAATCTGACAATTTAACTGAAAAAAACAGGAAGTGCATTTTCAGATTTCCATGAAAGATTAGAAAGGCAAACTAATGCTTTTGCTCTTAATGACACGCACAGATGAAGTGATCAGCACACAGCTAACAATGAGAGAAAACTAAATCAGTATGAGGAGATCTGAGCCCATGCAGACTTCACATGGAGCATTCCACTATGTAAGAGTCTACAGTAAAGCATTCAGAAATGGAACAGTCTAAACTGATGCAGTGTGTTCGGTCTGACAGGAAGTGGCCGAGCCTCTACAGGACCTGAAGGAGGGCATGGATCAGCTGGAGAAAAACAAAACACTGAGATACATTCTGTCCACTCTGCTGGCCATCGGGAACTTCCTGAACGGCTCAAACGTGAGACTCCACACACACACACACACACACACACACACACACTCATGTGATGACAGTAAGTGTAGCTGATGCTGGTGTGTGCAGGCCAAGGGCTTCGATCTGAACTA[T/A]CTGGAGAAGGTTCCGGAGGTGAAGGACACGGTGCACAAACAGTCTCTGCTGCATCACGTCTGCAGCGCCGTGCTGGAGAACTGCAGCGACACCACTGACCTGTACTCTGAGATTGGCGCCATCACACGCTCGGCCAAGGTACAACAAACACACACACACACACACACACACTCATGCATAGACTGTGAGTGACTCTGTGGTTGTGGTGTGCAGGTGGATTTCGAGCAGCTGCAGGAGAACCTGACTCTGATGGAGCGGCGCTGCAAAGCATCATGGGACCACCTGAAGGTGATCGCCAAGCACGAGATGAAGCCGGTGCTGAAGCAGAAGATGTCGGACTTCCTGAAGGAGTGCGCAGAGAGGATCATCATCCTGAAGATCGTGCACCGCCGCATCATGAACAGGTGATGAGCAGACCATACTCTGACTGCTAATATTACCCACCATATCATTAGAACTACAAACCCTGGGTGAAAAGTGTAAACAACTACAAACATGGC

Associated Phenotype:

Not determined