ZMP
LOC100000685
Ensembl ID:
Human Orthologues:
SLC22A4, SLC22A5
Human Descriptions:
solute carrier family 22 (organic cation/carnitine transporter), member 5 [Source:HGNC Symbol;Acc:10
solute carrier family 22 (organic cation/ergothioneine transporter), member 4 [Source:HGNC Symbol;Ac
solute carrier family 22 (organic cation/ergothioneine transporter), member 4 [Source:HGNC Symbol;Ac
Mouse Orthologues:
Slc22a21, Slc22a4, Slc22a5
Mouse Descriptions:
solute carrier family 22 (organic cation transporter), member 21 Gene [Source:MGI Symbol;Acc:MGI:192
solute carrier family 22 (organic cation transporter), member 4 Gene [Source:MGI Symbol;Acc:MGI:1353
solute carrier family 22 (organic cation transporter), member 5 Gene [Source:MGI Symbol;Acc:MGI:1329
solute carrier family 22 (organic cation transporter), member 4 Gene [Source:MGI Symbol;Acc:MGI:1353
solute carrier family 22 (organic cation transporter), member 5 Gene [Source:MGI Symbol;Acc:MGI:1329
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12067 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12067
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099284 | Nonsense | 485 | 549 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 44311062)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 45637378 |
GRCz11 | 21 | 45670306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACTGAAGGTGTTGTTGACTGATGRATTCTGCTCTTCAGGCACGTTTAAC[A/T]GACACCTGCCGTATGTGCTGATGGGCAGCCTGACCATCACCGCCTCACTG
Long Flanking Sequence:
TATGTGACACTACAGTTGCTATGGTAACACAACTACTATAGTAATTGATCTGCTGTGGTGATTCTACAGTTGCTATGGAAACACAACCACTATAGTAACATAACCAAATGAGCCAATACTGTAGTTTTCCACAGCTACAGTGTATATTACACTACAACACACCACTGTTTACTACAGTAAACTGAAAGTATACTACAGTAGTTGAGTTTATCAGTTCACTATAGTATGCAGCAGCAGTTGTAGCTACTTAATACACTTGTAACTTGTAATATAAGCGTTAGAGTATCTACTATAAATGACTGTAGTAAGTTTTCATATGAACTCTTTTCAGCTGTAGGTGTAGCTGTAATCAGACAGGGTTACTCTCCTGTGTCGATACTCAGAGCTGTAAATGAGTGATGGTGTGTCCTCACTGCTCCTGCACACACAGTCTCTCAGCTCTTCTTAAAGGACTGAAGGTGTTGTTGACTGATGGATTCTGCTCTTCAGGCACGTTTAAC[A/T]GACACCTGCCGTATGTGCTGATGGGCAGCCTGACCATCACCGCCTCACTGGCCAACCTCTTTCTGCCCGAGACCTTTGGAAAAGTGCTGCCCGAGAACCTGGAGCAGATGCAGAAGAGCAGAAGGTGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATGCTCACTCTCGCAAACATAAACAAACACACTCTTGCTCGCATGCATGCACCAACACAAACACACACTTGCTCTTTTGTCTCTGTTTTGTTGAGTTGATTATAGTTTAGCCTGTATTATAACGTTGTTAAGCTCATTAATATTCACAACAACCTCTCCAAACACGGTCAAAAGCAACCGCATCACATTAGAGCCGTTTCCTGCGCTCATATATGCACATGTGAAACTGTTTCTGAACTGACCTGAGAGAGACACACACACCTACCACACTGAGATCAGAGAAACACACCGACTCAATGGCAGCTTTCA
Associated Phenotype:
Not determined