ZMP
si:dkey-204f11.59
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 25, member 23 [Source:RefSeq peptide;Acc:NP_001038417]
Human Orthologues:
SLC25A23, SLC25A41
Human Descriptions:
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 [Source:HGNC Symbol;A
solute carrier family 25, member 41 [Source:HGNC Symbol;Acc:28533]
solute carrier family 25, member 41 [Source:HGNC Symbol;Acc:28533]
Mouse Orthologues:
Slc25a23, Slc25a41
Mouse Descriptions:
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 Gene [Source:MGI Symb
solute carrier family 25, member 41 Gene [Source:MGI Symbol;Acc:MGI:2144215]
solute carrier family 25, member 41 Gene [Source:MGI Symbol;Acc:MGI:2144215]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20065 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20065
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030530 | Nonsense | 324 | 478 | 9 | 11 |
ENSDART00000145859 | Nonsense | 327 | 481 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 34312933)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34098129 |
GRCz11 | 3 | 34227637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTTCTGTTTCTCAGGTGTTGAAGACCCGTTTGACCCTTCGGAAGACT[G/T]GACAGTATTCTGGCATGGCAGACTGTGCCAAGCAGATACTGCGTAAAGAA
Long Flanking Sequence:
AATGAGAATCAGACCTGGCACATTTCTTTACTGATCTGACTCACATAATGTCTGTCTGAAAAGGTATCTGTCATCTCAAGTCGTGTGTAGTGTTCACAGATTTCAAACACCAGAGAATCATGTAACAGAGGAAGCTGTTAAACAAAGTTGTTCCTAATTTGTTTGCTTGTTAATTTATGCTATTCTAAATGCTCAAAGAGCCTGAAAATAAGCCGGGTCTGACTGTGAACATCTTCGATTGTCTACTCCTGGTAGGCTTCAATGCAAAAAACAAGCTTCTTTTCTGTCTTCGATTATTTATTCATTGAGCAGATCGGATTTTTAGAAGCCAAACACTTCATTTATTTATTTAAAGCACTTGATTAGACATGCTGAACAGAGCTGCTGATACTTACAGTTTCCTTGCAGGACCTCTAAGCTTTCTCTATATTTTCTGTATTGTTACTCTGTTCCTTTCTGTTTCTCAGGTGTTGAAGACCCGTTTGACCCTTCGGAAGACT[G/T]GACAGTATTCTGGCATGGCAGACTGTGCCAAGCAGATACTGCGTAAAGAAGGAGTGCGTGCGTTCTATAAGGGCTATGTGCCCAACACACTTGGCATCATCCCTTATGCTGGCATTGATCTGGCTGTCTATGAGGTATGGCTCTGTGTGTGTGTGTGTGTGTGTATGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTTTTACACATTAAAGTGTTTGTGAATGCTTTATGCCATTGACAAGCTCTGGGAATTCATCATTCTGAGTTGCTATGGTTTGTTAAACGATGTTATGTATTTACGTTGCTGTGTTCTGTCGTCTCTTCCCAACAACTCACAGATTATTTTTCAGCTGAACTCTATTAACCCCTTGTCATTCTTTACTTGGTGCCAAAAAACATCTTTTATTCAGCCAAGCATGCAATAAACTGATTAAAATTGT
Associated Phenotype:
Not determined