ZMP

LOC792520

Ensembl ID:

ENSDARG00000074317

Human Orthologue:

FAM20C

Human Description:

family with sequence similarity 20, member C [Source:HGNC Symbol;Acc:22140]

Mouse Orthologue:

Fam20c

Mouse Description:

family with sequence similarity 20, member C Gene [Source:MGI Symbol;Acc:MGI:2136853]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38414	Nonsense	Mutation detected in F1 DNA	Not yet available
sa11878	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa38414

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
ENSDART00000113524	Nonsense	138	560	1	10

Genomic Location (Zv9):

Chromosome 3 (position 62557610)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	61660600
GRCz11	3	61896926

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGACAGCCGGCAGAGGCGCACTGATGTGCGGGTCTCCTCCGTGCTGCAGT[C/A]GCTGTTTGAACATCCGCTCTACCGGACCGTCCTGCCGGATCTAACCGAAG

Long Flanking Sequence:

TGGACAGATGCGCTCTTGAATATCTTTCCTCATCATCATCATCATCATATTGTGCTCTATTTAGCCTAAATATAATAAATAAACCATAATGATACTCTTTCGTAAATTCCGCGTGCTGATTTTAACGGTGTTCCTCATCGCCTGCACCATGCACATCATGATAGACCTGTTACCCAAGCTGGAGAAGCGCGCGGCGGGCTCGAGCTCCAGCGCTGGAGGGGGCAGCGGCTGCTCCTGCGCTCACACGCCGGGCGAGGAGCCTCGATCCTGGGGTAAACAGCGAGCCAGAGCCGCCGATCCCGGCTGGCCTAACAAGCACTCTCTGAGATTACTGCAGGATTTCAGCAATGAGCCCAACTCTAATTTGACGTCGCAGTCGCGGGAAAAGGTGACAGAGAGAGCCGGCTCTGAGAAGCAGGGCTCCGGGAAGAGGGGGCTGATGCGGGAGGCGGACAGCCGGCAGAGGCGCACTGATGTGCGGGTCTCCTCCGTGCTGCAGT[C/A]GCTGTTTGAACATCCGCTCTACCGGACCGTCCTGCCGGATCTAACCGAAGAGGACACCCTTTTCAACCTCAATGCGGAGATCAGACTGTACCCCAAAGCTGCCGGACAACAAGAATGGCAAGTGCCACTTTAAATCTGATCTTTCTCTTAGCATTGATTTACACCTAATTGAATGTAAAGTACATTATTCCTAAAATATAGGGTTGGGTGTTTTTGTGGAAGGTTGGTTTGGTTTAGGATCATTTTATATAATAAGACATAATTTAATATGAATTATTTATGTGCTGTCAAACAATCACATGCAAGATTAAAGTTTATACACTGTGCATTTTGCTTAAATATGCACAGAAACGCACTATATGAAGCACAAAAATATACACATGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGCTTTACATCTGATCTTTCTCTTAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11878

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113524	Nonsense	438	560	8	10

Genomic Location (Zv9):

Chromosome 3 (position 62621495)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	61724485
GRCz11	3	61960811

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCTCTCTCTCTGWTTTTGCACTGAACAGGCWACATGGACCGCCATCAYTA[C/A]GAAACTTTYGAGAAGTTTGGAAACGACACTTTCATCATTCATTTGGACAA

Long Flanking Sequence:

TGGAGCTATCAGGCCTTTAGGGTGGGGCTATCAGTCCTTTAGGGCAGAGCTGTCAGTCATTCAGGGCGGGGCTATCAGTCATTTAAAGAGGGGCTCTTAGTTCTCTGTGCCGGAGCTATCATTTATTTAGGGCAGAGCTGTTAGTCATTTAGGGAGGGGCTATCAGTTTTTTAAGGTGTAGCTTTGAGTTCTTTAGAGTAGAACTCTCAGTTCCTTAGGGTTGGGGCTATCAGTCTTTTAGGGTGGGGCTATGAATTCTTTAGGGGGAGGAGCTATCAGTCTTTTAGGGTAAAGCAATCAGTCCTGCAGGGCGGGGCTATCAGCGCAGAAAGTTCTGAACAATCTCCCGTTTATGCCAACTTTAAGAAAACAAAAATCATCAGCAATATTTTGTCAATCCACCAAGCTCCAGCGATTGTGTTTTACTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGTTTTTGCACTGAACAGGCAACATGGACCGCCATCATTA[C/A]GAAACTTTTGAGAAGTTTGGAAACGACACTTTCATCATTCATTTGGACAATGGCAGAGGGTGAGCTGTTTATATTAACATCTCTCTTCACCCCTCAGAGCTCCTCCTTTTACACTGACACCAGGTGAACAGAGTGTTCCTCTCTGAAGAGGCCTGAACATGTAGATGTGTAAGGTCAGATTTATACGCCGCCACGTCTCCGGCTGGGATATATGTGTGTGATAAAGCATTTTGATTACACCGTCATTCAGCTCGTTTGAAGCCGCAGCTTTTCATTCTCCACATTTGCGGCTGAAGTAGGCCAGTGTAGAGCCGCAGCTCCCTCGATGCCAGATTAATCCAGCACTTACATTCTTATTTAAATAAAGTGTGACCAGATAATGTGGTAACTTCCATTTCTGGCTGAACTTTCAGTACATTTAAGTGTGCGTTCAATGCAGTCAGTGTCATTTATTCCAATATAACGCAGTCGACTTGTGTTTATTTCAGCTTCGGAAAGCA

Associated Phenotype:

Not determined