ZMP

LOC100333552

Ensembl ID:

ENSDARG00000079559

Human Orthologue:

FAM196A

Human Description:

family with sequence similarity 196, member A [Source:HGNC Symbol;Acc:33859]

Mouse Orthologue:

Fam196a

Mouse Description:

family with sequence similarity 196, member A Gene [Source:MGI Symbol;Acc:MGI:3605068]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9680	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa9680

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115373	Nonsense	60	483	1	3

Genomic Location (Zv9):

Chromosome 12 (position 44827110)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	45342719
GRCz11	12	44611094

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACAAAGCCCTTCAGGTGCGTTTCAAGGACATCTGTGAGGCACAGAATGAA[C/T]AGGCAGCTGCTGCCCGGGGAGGAAAGCCGGTCTACAAAGTGGCRTACCGC

Long Flanking Sequence:

GGCGTAGTGTAAACGGATGGCGTAACCGTAGCAAAACTTATGCGTTTTAAAACTAAAACGCACTAGTGTAAACAGGGCCTTAGAGAAACTTGTTCATGCTTTTATCAGCATTAGAATGGATTACTGTAATGGACTCCACAATGGCCTTCCCAAAAAGACAGACAGTTGCGGCTCATCCAGAACGCTGCGGCCCGGATTCCACTTACTAGCATTGTGTATGAAATTTGCTTTATAAATAAACTTGCCTTGTCTTGTCATTTGAATAATACCATGCGCCATTTCATCAAGAAATAACATCCTAATTGTTTGTGTTTGCAGGAACCATGGTGAGCAAGGACGCTGGAAAATGCATGCTCACCAACTCTGAGTCAGACTCGGAGGCGACGGCGGTCTCTATGGCCCTGGAGGTCAAAGGCTCATCGGATGAAAACCGGCATGTTAGAAAGCGGAACAAAGCCCTTCAGGTGCGTTTCAAGGACATCTGTGAGGCACAGAATGAA[C/T]AGGCAGCTGCTGCCCGGGGAGGAAAGCCGGTCTACAAAGTGGCATACCGCAAGTACATGACTGTCCCGGCTCGCAGATCAATCCCCAATGTCACCAAAAGCACTGGAGTGCAAACTTCACCAGATCTGAGGAAGCGCTACCAGACTTTTCCATTTGAGCGTAAGAAAGGACACACGGTCAAGCATGCTGCTGCGGTGGAGAGCTGCAAGGACCAGGATGACGGTTTTGTTATTGATGTCAAGAGGGCAAAGGCAACCGAAGCAGGTAGAGAATGTGTGCCCTCTCATAATGTGAGAAAAACTAGGGCATTAATGCACACTAACCAATGTGTTGCAACTATTGAACAGCATCCGCAACGCAGAGACTGTCCGGAAAGAGCGGACGGATGCTCAGACGCTTTGGTTCTTCCCTGCTCCACAGAAAGAACCACAGCGGACAATTCGGACTATCAGATCTGTAGCGTGAGAAGTAAACACAGTAAGGGCTTCCAGAGAAACTCT

Associated Phenotype:

Not determined