ZMP

FCHO1

Ensembl ID:

ENSDARG00000015356

Description:

FCH domain only 1 [Source:HGNC Symbol;Acc:29002]

Human Orthologue:

FCHO1

Human Description:

FCH domain only 1 [Source:HGNC Symbol;Acc:29002]

Mouse Orthologue:

Fcho1

Mouse Description:

FCH domain only 1 Gene [Source:MGI Symbol;Acc:MGI:1921265]

Alleles

There are 6 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa2424	Essential Splice Site	Available for shipment	Available now
sa21259	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa2424

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029175	Essential Splice Site	65	895	3	32

Genomic Location (Zv9):

Chromosome 8 (position 20579254)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	20009151
GRCz11	8	20041236

KASP Assay ID:

554-2725.1 (used for ordering genotyping assays)

KASP Sequence:

AAGTCCATGAGCAAACTGGCCAAGATGGCCAGCAATGGAAGCCCTCTGGG[G/A]TGAGTGACATCATTACTGTTATCATGATCCCTGTTCCRTCCCATTCTGTT

Long Flanking Sequence:

TTTAACTTATCACAATCCAATAAGATGTTTTACAAGAGATAAGGCCAACAATACAGTCTAGTACTGGAAGAAAATGATAACATCCTTTTTCCTATCAGCAGAAACTCTGAAATCCGAACAACAAACTTGGTTGATAGAGAATGAATGCTTTTTTCACTGTTATCAATTGGTGGCTTTCACAAATGATTGCTTATATATTATGTATGAGTACATTTAGGTATAGACTGTGGGTGTTACTTTTTTATCCCCCAATACACTGTCTACCATTGCCAACATAAAACTTAGCAACTAGAACTGAAGAACTTTTTCCGAACCAGGAGCATTAATATTGGTTCTCCGTCAGTTTAGTGCAAAAGAGTTTTTTCTTTTGTGTAAGCAAACAATGTATCTGCTAATGCTCTTGTGCACTTGTGTTTGTATTTAAGGGCAGCCATTGAGGAGACTTACTCAAAGTCCATGAGCAAACTGGCCAAGATGGCCAGCAATGGAAGCCCTCTGGG[G/A]TGAGTGACATCATTACTGTTATCATGATCCCTGTTCCATCCCATTCTGTTCATATCTCACAATATCCTGCAATTCTGTATCATCCTGGTTTTCAAAGTTAACACTTCTTCACTATTCACTATCTTATAAAAAATATGACATTTTGTTCAAGCAGATACCCATGTAGAGTGGATATAGATTTTCAGGTATTATGGTTGACAATTACCGTCTAAGTACATGTCATCTAGAGAGATCTTATCTTATCTTTCTTTTCATTCATTCATTTTTCTTGTCGGCGTAGTCCCTTTATTATTCCGGGGTTGGCACAGCTGAATGAACCGCCAACTTATCCAGCACATTTTTACTCAGCGGATGCCCTTTCAGCTGGAACCCATTTCTGGGGAACACTTATTCACACACACTCATACACTACGGACAATTTAGCCTACCCAATTCACCTGTACTGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCAGATGAAACCCACGCGAACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa21259

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029175	Nonsense	486	895	18	32

Genomic Location (Zv9):

Chromosome 8 (position 20597174)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	20027071
GRCz11	8	20059156

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATCCTCTCTTGAGAATGTGGAGGATTCTGGACTGGATTCACCTTCTCAT[C/T]AGCCTCTTGGAGTTTCCCCTGATCCCACAGGATGGGCAGCCTGGCCGTCC

Long Flanking Sequence:

ATTTTTGTTGTTGATTATATTTAACTCATTTCATTTTATGTCTCAATTATTGTACATAAATAACAAATGAATAATTAAATAGGCCTAAATAATTATTTATTTAAAGGCATTACTAGTGAAACACAGAGAAACGGTCCGGCACATGGTCTAAAGAGCTCTTAAGCTGCATGTTAGTTGAACATATTGAAGTGGTGACATCTGTAGATGTACATAAAACCTAAAGATTAAATGTTGATTCCACAAATACAGGGAGAGACTCTGCAAGCTTTGAGAGCATTCATACACTCAAACAATATTCATACTATTACATTTTAATCATTTTGAATCTGATTAAAAAATAATATATATATATATGTTTTTTTCAAAGTTTTGATTAAAAAAAAAATCTACAGTATATCTTTCTTCTTAATCTTTCTTCATGTTTGACAGATGCAGCATTCTCATCAGATTCATCCTCTCTTGAGAATGTGGAGGATTCTGGACTGGATTCACCTTCTCAT[C/T]AGCCTCTTGGAGTTTCCCCTGATCCCACAGGATGGGCAGCCTGGCCGTCCTCTCAATCCCAGTCTAAAGACTCAATAAATTTGAGCCGATCCTCAGACCCATTCCTCGCTGCATTCCAAGACCCTTCACCCGGTCGCTCTCCCCTACCTCAGGACGACACCACCAACGTCTGGCCCTCCAATCTACGTTCTCCACGTGCTCCACCTGACGTCGAGCCCACCACTTTCAGCTTCCCAGCCTTCTCCCACAGCATAGCATCTTCAGAACTGGAGCCTTCTGTCTGGAGCTGTAAACACATTCCTCCAGAAGACCTTTTTCTTGCTGCTTTTGAACGATCCACCCCCAAGGACAACCTGCCTCCAACTGATGCCTGGGCTCCGCCTCCACCTCGGCCTAACAGGGAAGCCAGGACTGATCCCTTTTCCGTTCCTCTAAATGACACTAAAACCCTTCCTCCTCCATCCTCTTTGCGCAAGGAGCGGGACAGGAAAAGAGATCGT

Associated Phenotype:

Not determined