ZMP
slc41a1
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC41A1
Human Description:
solute carrier family 41, member 1 [Source:HGNC Symbol;Acc:19429]
Mouse Orthologue:
Slc41a1
Mouse Description:
solute carrier family 41, member 1 Gene [Source:MGI Symbol;Acc:MGI:2444823]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44746 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44746
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102870 | Essential Splice Site | 483 | 544 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 39117977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37684996 |
GRCz11 | 11 | 37952201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCACTTACATCTTCATTGCTTTTTACCTGGCTGCTGCTCTACTACAGG[T/C]ACACCTGAACATCTGCTTATTATTACAAGGAAATAATCTGGGCTTCAAAA
Long Flanking Sequence:
TCTGACCGGATCATTTGAATCAGTGAGTCATTGCCTGTAGATTCACTTTGAATAGATCATTTGAATCTGTGAGTGTGTAACTTAGACTCAATATGACTGGATCATTAGAATCAGTGAGTCATTACCTGTAAATTCACTTTGAATAGATAATTTGAATCACTAAATCAATTTAACAAGTTATATAGCAAGAACCGTAACTGAAAGTTTCCAAAACCAGAAAGTACAGATCCTTAAATATGTACTTAAGTCCAACAGTGAAGTAGGAATACTGTAAGTTATTGTCCATCACTGCAGTGTACTGGTCAGTAGTGCCCTGTTCATGCTTCTGAAAGACTCTTTCTGTTCATCAGGTGTGAATTCTCGATCTGCCAAAGTGCTGTTTCTGCTGGTCGCTCCTGGTCATCTGGTCTTCCTCTACACTATTAACTCTATGCGGGGAGGACACACCACTCTCACTTACATCTTCATTGCTTTTTACCTGGCTGCTGCTCTACTACAGG[T/C]ACACCTGAACATCTGCTTATTATTACAAGGAAATAATCTGGGCTTCAAAAAACATGGGAGGGGGAATTTGGAGGAAATGTGTCGTCAAAGTTCAATGCAAATATATATATATTATATTATATAAATGTTATTCCTCGCATGAATATATGAACTTTTTTTTTAATGTTTTTGTGCATTGTGGCATTTTGTTCTTATAAATACACTACCATTAAAAGATTTAGGGTTTTAAAAAGTAGTTATATCAGAAATGGTGCATTAAATAGATATATAACATTAATAGGTAATATTTATAGATAGACAATATAGACATTTACGTAGATGTAAATGTAATAAATAGATATTTTTTGTATATACACTTCCTGACAAAAAATTTTTCACCTATTCAAGATTTAGGAACAACAAATATTAACTTGTCTTCAAGTTGATCATTTGGTATCAAAAGTGGCTTAAATGAAAGGCTAAGGCCTCTAGATTACGCTTATTTTAGCAAAATAAAACAT
Associated Phenotype:
Not determined