ZMP
slc25a3l
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3, like [Source:RefSeq
Human Orthologue:
SLC25A3
Human Description:
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3 [Source:HGNC Symbol;Ac
Mouse Orthologue:
Slc25a3
Mouse Description:
solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3 Gene [Source:MGI Symbo
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20249 | Essential Splice Site | Available for shipment | Available now |
sa33436 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31392 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20249
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037949 | Essential Splice Site | 169 | 377 | 5 | 8 |
ENSDART00000125743 | Essential Splice Site | 164 | 372 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 4 (position 15917899)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16860739 |
GRCz11 | 4 | 16849715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTAAATTTAGCAGTAGATCACCCACTAACTGTTTGTGTTTGGCAAACA[G/T]GAGAATGCTTATTTGTGGAGGACATCCGTTTATCTGGCCGCCTCTGCCAG
Long Flanking Sequence:
GAAAATATTTATGATTTATTTACAATATAGTAAACATTGTACAATATTTACAATACAGTAAACATAAAATACAAGTTAAAAAGTTACTACTTTTTATTTCATATATTAAGGTTTTAGTTATGACACTCCAAAAATCATTTCGCATAAATCCGCAGATTTTACCAAAATTCTGTACAGAAATACCAAAAAATGTCTGCAGATTCCCTCTGGCCCTACCGAACACTCACAAACACACTGATCTTGTCTTCCAGGTGGACCCAGAGAAGTACAAGTCCATCTTCAATGGTTTCTCGGTCACTTTGAGAGAGGATGGTTTCAGAGGGCTGGGTAAAGGCTGGGCTCCTACATTCATCGGTTACTCCATGCAAGGGCTCTGCAAGTTTGGTTTCTATGAAATCTTTAAGGCGCTGTACAATGACATGCTCGGAGAGGTGAGCGTCGGCATCTTAATATTAAATTTAGCAGTAGATCACCCACTAACTGTTTGTGTTTGGCAAACA[G/T]GAGAATGCTTATTTGTGGAGGACATCCGTTTATCTGGCCGCCTCTGCCAGCGCTGAGTTTTTCGCTGATATTGCACTGGCTCCTATGGAAGCGTGCAAGGTGCGAATTCAGACGCAGCCCGGCTACGCCAACACCCTGAGAGAGTGCGCTCCAAAAATGCATGCCGAGGAGGGACTGAATGCGTGAGTCTCTGTCAAAATGGACACTTTATTATTATTAAAGTACTGTCATTATGTGCTCTTGTAGTTTTTAATGAAAAGAACTTCACCTCCTCTTTTGAAAATACATCTCTTCTTTGTGTACTGGTGAGAGGGCGGGACAACCTGTCAATCACATAAGACCGACCAATAGTAAGCCACAGTAATCCAGTCATTTCCAGAGGACAATATTCAAGTCATGTCCTGCATTTTTCGTATTTGAGAAGCTGTTTTAGCTGGGATGTACAGCACAAAAAGGAAGACAAAAGTAAAAGAGTGCACATTCTTAAAAGTGCTCACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33436
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037949 | Nonsense | 235 | 377 | 6 | 8 |
ENSDART00000125743 | Nonsense | 230 | 372 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 4 (position 15916880)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16859720 |
GRCz11 | 4 | 16848696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGTTTGCTAATGATGTTATTGTCTGTGCAGCTTCTATAAAGGTGTTTA[T/A]CCGCTGTGGCTGAGGCAGATTCCTTACACCATGATGAAGTTTGCTTGTTT
Long Flanking Sequence:
TTCAATCTTTGACTAAAATTGTTTTAAAAATGTAATGCAATGGTTGTATTTTGTCCATATTTAATCCACCATATTTAAAACTTTTATTAAAACAACCCATAATTTTTAGAAAATAACAATACAATTCCTTGTACATTTCACAAATAATTACAAATTATTATTATTTGGTACTTTTATTATTATTCACTGAATGAAATATTACATATTGAAGTAGAAAAATAGAAAGTGTTCCTGCAAAGATCTCAAGTGATTATTAAACCTTTCTTAACACATTCATTAAATTTTTTATTTTTATATAGTTTCCTATTATTTTAGTTATATAAAATGTTTTCTTTTTTTAATAATGACTGGAGTTTACCAGTGATTTAAGACTGACCAAACTGTACAATATACAGTGCTGACTGCATTACCCATTAAACCCTTTTTTAAAGACTCTCTGACTGTGTGTTTAGTGTTTGCTAATGATGTTATTGTCTGTGCAGCTTCTATAAAGGTGTTTA[T/A]CCGCTGTGGCTGAGGCAGATTCCTTACACCATGATGAAGTTTGCTTGTTTCGAGCGAACGGTGGAAACTCTGTACAAGTACGTCGTACCCAAACCCCGCAGTGAGTGCTCCAAACCAGAGCAGCTGGTGGTCACGTTCGTCGCCGGTTACATTGGTAAGTTAACCGCAAACAGGCCTGAGCCTTTAGATGCGTAGATGTTTCTAACTCTGCAAGTTTGCATAGATATGGAGTCATGGTCAAAATTATTGGCACCCTTGGTAAATATGAAAAAAGAATGCTGTGAAAATTAATTGCATCTTTAATTCAGTGAAGTCACAAGAAAGCTAATCTTTTATTTAAATAAAACAATTGATTATAAATACAGTTGTAGTGAAATATATTTCAATATATTTTGGTTTGACAGGAGTATAAATATGAAACCCAATAGCCAAATTCCATTATTAATCTATCACAAATGAGTAAAGGCAAACAACACAGTTTTGATGCGCAGCAAAAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31392
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 |
---|---|---|---|---|---|
ENSDART00000037949 | Nonsense | 257 | 377 | 6 | 8 |
ENSDART00000125743 | Nonsense | 252 | 372 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 4 (position 15916816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 16859656 |
GRCz11 | 4 | 16848632 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGATTCCTTACACCATGATGAAGTTTGCTTGTTTCGAGCGAACGGTG[G/T]AAACTCTGTACAAGTACGTCGTACCCAAACCCCGCAGTGAGTGCTCCAAA
Long Flanking Sequence:
TCCACCATATTTAAAACTTTTATTAAAACAACCCATAATTTTTAGAAAATAACAATACAATTCCTTGTACATTTCACAAATAATTACAAATTATTATTATTTGGTACTTTTATTATTATTCACTGAATGAAATATTACATATTGAAGTAGAAAAATAGAAAGTGTTCCTGCAAAGATCTCAAGTGATTATTAAACCTTTCTTAACACATTCATTAAATTTTTTATTTTTATATAGTTTCCTATTATTTTAGTTATATAAAATGTTTTCTTTTTTTAATAATGACTGGAGTTTACCAGTGATTTAAGACTGACCAAACTGTACAATATACAGTGCTGACTGCATTACCCATTAAACCCTTTTTTAAAGACTCTCTGACTGTGTGTTTAGTGTTTGCTAATGATGTTATTGTCTGTGCAGCTTCTATAAAGGTGTTTATCCGCTGTGGCTGAGGCAGATTCCTTACACCATGATGAAGTTTGCTTGTTTCGAGCGAACGGTG[G/T]AAACTCTGTACAAGTACGTCGTACCCAAACCCCGCAGTGAGTGCTCCAAACCAGAGCAGCTGGTGGTCACGTTCGTCGCCGGTTACATTGGTAAGTTAACCGCAAACAGGCCTGAGCCTTTAGATGCGTAGATGTTTCTAACTCTGCAAGTTTGCATAGATATGGAGTCATGGTCAAAATTATTGGCACCCTTGGTAAATATGAAAAAAGAATGCTGTGAAAATTAATTGCATCTTTAATTCAGTGAAGTCACAAGAAAGCTAATCTTTTATTTAAATAAAACAATTGATTATAAATACAGTTGTAGTGAAATATATTTCAATATATTTTGGTTTGACAGGAGTATAAATATGAAACCCAATAGCCAAATTCCATTATTAATCTATCACAAATGAGTAAAGGCAAACAACACAGTTTTGATGCGCAGCAAAAGAATGTTGAACTTTACAAAATAGAGGCTTTACGAACATTAAAACATCCAGATAAAATGGAGATGTTCT
Associated Phenotype:
Not determined