ZMP

LOC100330676

Ensembl ID:

ENSDARG00000037183

Human Orthologue:

FAM46A

Human Description:

family with sequence similarity 46, member A [Source:HGNC Symbol;Acc:18345]

Mouse Orthologue:

Fam46a

Mouse Description:

family with sequence similarity 46, member A Gene [Source:MGI Symbol;Acc:MGI:2670964]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa16593	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa16593

Status:

Available for shipment
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Availability:

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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000054071	Nonsense	272	404	2	2

Genomic Location (Zv9):

Chromosome 16 (position 5860243)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	5086167
GRCz11	16	4913569

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGAAATACTGCCATCTGCTGGTCAGGGGTTTCCGCGCCGCCTCCGAGTCT[G/T]AAATGAAGTCTCTYCAGCGCTACATGTGCTCCCGCTTCTTCATCGAYTTC

Long Flanking Sequence:

CTGTATATATATATATATATATATATATTATGGAAACCTACGGTTAACCTGTTGAGTTGATTACAGCTATTTGTTTTACAGTAATGTCACAAGGATTAACAGTCTCTTGTCTTGCATTGCAGGAGGCGTATGTTCAGAAGATGGTGAAGGTGTGCAATGATTCGGACCGCTGGAGTCTCATTTCCCTCTCCAATAACCGGGGCAAAAACGTTGAGCTGAAGTTTGTGGACTCGCTACGCCGACAATTCGAATTCAGTGTCGACTCCTTCCAGATTAAACTAGACTCTCTGCTCCTTTTCTACGAGTGCTCCGAGAACCCGATGGCCAAAACATTCCACCCTACCATCATCGGCGAGAGCGTGTACGGAGATTTCGCCGCCGCGTTGGACCACCTGCGCAACAAAATAATCTGCACCAGGAATCCTGAGGAAATCCGAGGCGGAGGCCTGCTGAAATACTGCCATCTGCTGGTCAGGGGTTTCCGCGCCGCCTCCGAGTCT[G/T]AAATGAAGTCTCTCCAGCGCTACATGTGCTCCCGCTTCTTCATCGACTTCTCGGACATCAGCGAACAGCAGCGCAAGCTTGAGTCGTACCTCCAGAACCACTTTGTAGGCTTGGAGGATCGCAAGTACGACTATCTGACGACTCTTCATAGTGTGGTGAACGAAAGTACGGTGTGTCTGATGGGACACGAGCGGCGGCAGACGCTAGGACTCATCGCCATGCTAGCAGTGCGTGTGCTAGCCGAACAGAACGTCATTCCCAACGTGGCTAACGTCACATGCTATTATCAGCCGGCTCCGTACGTAGCTGATGGCAATTTTAGCAATTATTACATCGCTCAAGTTCAGCCGGTGTTCACATGCCATCAGCAGAGCTACTCCACGTGGCTACCGTGCAACTGAGAGAGAGAAATCTGCTGAATCACGGCTGTTGTTGTAACACTTTTCGCAACTGTCTCACTTCCCCAGTGTGCTTGGGTTGGTGTGCGCAGATAAGTGCTG

Associated Phenotype:

Not determined