ZMP
slc47a1
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 47, member 1 [Source:RefSeq peptide;Acc:NP_001014332]
Human Orthologues:
SLC47A1, SLC47A2
Human Descriptions:
solute carrier family 47, member 1 [Source:HGNC Symbol;Acc:25588]
solute carrier family 47, member 2 [Source:HGNC Symbol;Acc:26439]
solute carrier family 47, member 2 [Source:HGNC Symbol;Acc:26439]
Mouse Orthologues:
Slc47a1, Slc47a2
Mouse Descriptions:
solute carrier family 47, member 1 Gene [Source:MGI Symbol;Acc:MGI:1914723]
solute carrier family 47, member 2 Gene [Source:MGI Symbol;Acc:MGI:3588190]
solute carrier family 47, member 2 Gene [Source:MGI Symbol;Acc:MGI:3588190]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14530 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14530
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046317 | Nonsense | 353 | 629 | 13 | 18 |
ENSDART00000133604 | Nonsense | 380 | 656 | 13 | 18 |
ENSDART00000135235 | None | None | 226 | None | 8 |
ENSDART00000137740 | None | None | 150 | None | 5 |
ENSDART00000144435 | Nonsense | 87 | 363 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 38803036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 39943101 |
GRCz11 | 21 | 39966654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTATCCAGRAGAAAAWATAACTTCAGNNNNNNTCKTTACTRTATTGCAGGGATTT[T/A]GGCTTTTGCACAGGGAATCGGGATCGCTYTGACAAARTCCAAATTAGGCT
Long Flanking Sequence:
CAATCCAATAGAGCACCTTTGGGATGTGGTGGAACGGGAGATTCACATCATGGTTTTGCAGCAGACAAACTTGCCGCAACTTTGTGATGCTATCATGTCAATATGGACCAAAATCTCTGAGGAACATTACCAGTACCATGTTGAATCTATGCCACGAAGGATTAAGGCAGTTCTGAAGGCAAAAGGAGGCCCAACCCGGTACTAGTAAGGTGTACCTAATAAAGTGGCCTGTGAGTGTACATCAAAAGCATTTATTTTGTTTTGGAGAATTTTGGGTTAATAGTCAGACTGGAAAAGACATTCTGATTTGAATCAAGAAGAAATATATCAAATTTGATATGTTTATTTGTTGTGTGCAAGATGATTAAATTGCTTGTGAGTTTGGAATGACATGACAGTGATTAAATGATATCAGTTTTTATTTTTGGATGAACTTTTTCCTCAATATCAAGTATCCAGAAGAAAAAATAACTTCAGTCTTTACTGTATTGCAGGGATTT[T/A]GGCTTTTGCACAGGGAATCGGGATCGCTTTGACAAAGTCCAAATTAGGCTACATCTTCACCTCTGATGAGTATGTACTCTTCTCTACTAATACTAGCTTATTACACTTTACAGATTTATTCATTATGTAATATAATGTGATATAATTATCTCATTTTAAGCCTTAGATAAATGAATGAGAACAAATATAAAGGCTGCTATCTAAAGCAACTCAGGCTCATTGTGGATATGTACCCGGGGCTACATTTCTGTGGCCCGTGAAATACATACCCAGAATAACAGTTGCTTGAAGTTTTTGTTTTTGCAAATCCAGCAGAGGCCACTGTGTACATTTTTGATGACGTCAAATTTCTCTCATACCTGACGTTTTGCATTCTCTTCTCGTCTAAATCCACCAGAAACTGCGATTCACATTTCATTAGGGATGTAACGGTATTGTAAATACTGTCATACCGCAATATTAATTTTTTTCGATATTACCGTAGTCGCATGACTCGGTAA
Associated Phenotype:
Not determined