ZMP

LOC564932

Ensembl ID:

ENSDARG00000075803

Human Orthologue:

SLC41A2

Human Description:

solute carrier family 41, member 2 [Source:HGNC Symbol;Acc:31045]

Mouse Orthologue:

Slc41a2

Mouse Description:

solute carrier family 41, member 2 Gene [Source:MGI Symbol;Acc:MGI:2442940]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa16306	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa16306

Status:

Available for shipment
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Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109702	Nonsense	90	494	1	10

Genomic Location (Zv9):

Chromosome 25 (position 29643534)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	28333628
GRCz11	25	28776830

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

KCCACACAATATCCWGGAGATGCCCAGTGAGTCAATCAGGGCCATGGTTT[T/A]ACAGATTTTGTTTCCATTCCTGCTTGCGGGTTTTGGAACGGTGCTGGCTG

Long Flanking Sequence:

CGATGCAAATATTCAGCAGTCAGATTTTTCTTTTTAATCTTTAAATTTTTATATTCTGACTTATGTTTTTCAGATGAAACAAGCAACCATCAAATCATCTTACATTGGTCCGTAATTACATTTTTATTCTGAATATCCAACAGTGAGATTCATTATACAACATATCTATACATGGTCCACCACTCATCAATTCAAACTCCAAGACTGTGTAAAAAATATTTGGCATGGTGTGATGGCGATGGAATCAGTCATTGAAGTGAATCAGGGAGAGGGTCAGCTGACATCGTCTCTCCTGTCCTCCAGTGAAAACAGCCATCAGCTTTCTCCAGAGACCGGAGATCTTGACAGGGCATCTAGTTTGACTCGTGTCTGCAGTAGGGAGCCTTCAGAGTCTGATCCTCTGCTTTCCACTGCTTTTTACGGGGCAACAGTGAACATATCACAAGATGAGCCACACAATATCCAGGAGATGCCCAGTGAGTCAATCAGGGCCATGGTTT[T/A]ACAGATTTTGTTTCCATTCCTGCTTGCGGGTTTTGGAACGGTGCTGGCTGGGATGTTGCTGGACGTAGTGCAGGTAAATGTATGGGGGATGAAGATTTTGGGGGCTGGATTTGAAATATAATTGTAAATACTTGTTTTTTGTTTTGGTCAATCAGCACTGGGATGTTTTCCGTAACGTGACTGAGATCTTCATTCTTGTCCCACCTCTGCTGGGCCTAAAGGGAAACCTGGAGATGACGCTGGCTTCAAGACTTTCCACTGCTGTAAGATTATATTTTATCTTAAAGAGATAGTTCACCAAAAGAAACTGAGATTATAGTTTATTTATTCATGTCTTGCAAGGTTATTTTCAAAGTTTAAAAAATGAAACAGCTCTTTAAATTGCCAAGAATGGACTTTATTGCTGCAAGAAAGTGTCTGAAGGCTGGTGTCTTAGGCCATGTCCACACCCTGCAAGCACAGGACATCAACATGATGTCTGATTGACGTTGTACTCCAAT

Associated Phenotype:

Not determined