Busch Lab

ZMP

LOC100002134

Ensembl ID:
ENSDARG00000054584
Human Orthologues:
SLC30A10, SLC30A2, SLC30A3, SLC30A4, SLC30A8
Human Descriptions:
solute carrier family 30 (zinc transporter), member 2 [Source:HGNC Symbol;Acc:11013]
solute carrier family 30 (zinc transporter), member 3 [Source:HGNC Symbol;Acc:11014]
solute carrier family 30 (zinc transporter), member 4 [Source:HGNC Symbol;Acc:11015]
solute carrier family 30 (zinc transporter), member 8 [Source:HGNC Symbol;Acc:20303]
solute carrier family 30, member 10 [Source:HGNC Symbol;Acc:25355]
Mouse Orthologues:
Slc30a10, Slc30a2, Slc30a3, Slc30a4, Slc30a8
Mouse Descriptions:
solute carrier family 30 (zinc transporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:106637]
solute carrier family 30 (zinc transporter), member 3 Gene [Source:MGI Symbol;Acc:MGI:1345280]
solute carrier family 30 (zinc transporter), member 4 Gene [Source:MGI Symbol;Acc:MGI:1345282]
solute carrier family 30 (zinc transporter), member 8 Gene [Source:MGI Symbol;Acc:MGI:2442682]
solute carrier family 30, member 10 Gene [Source:MGI Symbol;Acc:MGI:2685058]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa6536 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6536
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076803 Essential Splice Site 228 462 3 3
Genomic Location (Zv9):
Chromosome 18 (position 47801370)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 48956151
GRCz11 18 48950938
KASP Assay ID:
554-4789.1 (used for ordering genotyping assays)
KASP Sequence:
AAKTTCTGCGTGAACTAACCCCCCTTTATTGTRCTTATTTGTWACCTGCC[A/T]GCACCTCAGTGTGTTYCCCAAGTCTCYATCTTCMGAGWGCATCATCTGGG
Long Flanking Sequence:
ATTTTCTGTAAACCCTAGAGATGGTTGTGCGTGAAAATCCCAGTAGATCAGCAGTTTCTAAAATACTCAGACCAGCCCGTCTGGCACGTTTAAAGTCACTTAAATCCTTAAATTCTTCCCCATTCTGATGCTCGCTTTGAACTGCAGCAGATCGTCTTCACCATGTCTACATGCCTAAATGCATTGAGTTGTTGCCATGTGATTGGCTGATTAGATATTTGCGTTAACGAGCAGTTAGACAGGTGTACCTAATAAAGTGGCCGGTGAGTGCATTTATAAATTTTTATGTTTTGCATTTCAAAAATATAATTTATTGTGTTGAATATAGGGAGGGAGGGTGAACTATCCCTTAATAACAGAATTGTAAAAAAAAAAAAAGTGTGTGAACTATCCCTTAATAACAATTTTAATTTCTAGTTGAACTATCCTTAATATGCATTACAGAATTTTAATTTCTGCGTGAACTAACCCCCCTTTATTGTGCTTATTTGTAACCTGCC[A/T]GCACCTCAGTGTGTTTCCCAAGTCTCTATCTTCAGAGAGCATCATCTGGGTCTCCTCAGTATAGTCCAGGATCTCCTGTGTTCAGTCCTGGTTCTGTCTAATGGTCTGGTTCTGCTGCTGTCCCGAGCTCACTGTCACCGGCCTCACTCAGACTGTCACCTGCTGGTTTACCTGGATGCTGTTTTCTCCACGGTTTGTGTGGTATTTTTACTTTCCGCCGCCCTGCCGAGGTTACACAGATACGGGCTGCTGGTTCTCCAGGCGGCGCCTCTGCATCTTTCTGTCCGCCAGGTGCGACTCTGTCTCGGTCAAGTTCCCGGAGTATTATCGGTCCACGAACTTCACATTTGGCAGCTCTCAGATTCCCTCATTATCGCATCTCTGCATGTTCACTGTCCCGCCGGGATGAGCGCAGCAGAGTGCGAGGAACTTATAGCAAATATCAAAGCAGTGTTTTACTCTTTCGGCGTCAATCATTGCACGGTCCAACCTGAGTTTCT
Associated Phenotype:
Not determined