ZMP
slc25a22
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 25 (mitochondrial carrier: glutamate), member 22 [Source:RefSeq peptide;Acc:N
Human Orthologues:
SLC25A18, SLC25A22
Human Descriptions:
solute carrier family 25 (mitochondrial carrier), member 18 [Source:HGNC Symbol;Acc:10988]
solute carrier family 25 (mitochondrial carrier: glutamate), member 22 [Source:HGNC Symbol;Acc:19954
solute carrier family 25 (mitochondrial carrier: glutamate), member 22 [Source:HGNC Symbol;Acc:19954
Mouse Orthologues:
Slc25a18, Slc25a22
Mouse Descriptions:
solute carrier family 25 (mitochondrial carrier), member 18 Gene [Source:MGI Symbol;Acc:MGI:1919053]
solute carrier family 25 (mitochondrial carrier, glutamate), member 22 Gene [Source:MGI Symbol;Acc:M
solute carrier family 25 (mitochondrial carrier, glutamate), member 22 Gene [Source:MGI Symbol;Acc:M
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33961 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33961
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103385 | Nonsense | 241 | 329 | 8 | 10 |
The following transcripts of ENSDARG00000020893 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 49044828)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 49105575 |
GRCz11 | 6 | 49104228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGGCGGCGCCATTTTATTGGTCCTTCATCTCTGGATGTGTTGCAGGCT[C/A]AACAGCTGCTGTTGCTGTCAATCCATGTGATGGTAAGAGGATTTTTTTTT
Long Flanking Sequence:
CTTGGCTTTGTTCATAGTGGTAGTGTTTAGCCTTTACGGTTCTCACTGAGATGTGTTGAGTTACGCTAGAATAACTTTTGTGATCCTCATATTCCCAGCTGCCCAGCAGAGAAAGCCAGGCCTCATTCCTCCTACCAGACTGGCTGCGAACACTGTGCTGTGCCGCTCATACAACGTGGTTCCCAATTCATCAGCCAGAGCCGTATCTGCAACCCAGATCGCTAGAGAGCTGCTGCACACTCAGGGCATTCAGGGGCTCTATAAAGGCCTCGGAGCAACTCTGCTGAGGTGATGCATGCTAAAATCTCTGCTCTAAATGTCGACATGCACACTAATGACAGTGTAAATTAACATGTGGTCTTTTTTTCACTCTTTTAGAGATGTGCCTTTCTCGATCGTCTACTTCCCCCTCTTTGCAAATCTGAACAAGTTGGGCAAACCCTCCCCTGATGAGGCGGCGCCATTTTATTGGTCCTTCATCTCTGGATGTGTTGCAGGCT[C/A]AACAGCTGCTGTTGCTGTCAATCCATGTGATGGTAAGAGGATTTTTTTTTCTCTCCCTTTCGTATTTCGCTCTTTAGCAGTGAATTAAAGTGCCCATCCACTTAAAAGTTTTGTTTGGCTTTAACGTGTAATTTATTCAAAGAAATAATGTCAGCTTTCTTCATTTAACTCTTTAAAAAATAGTTTAAGTAAAATAAGATGAATTATTTAAAATGCAGAATAAAAGTTTCTGTGTTTGAATGTTAATAATGAGCTCTATCTATCTCTAAATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTTATTTTTTATATATATATTTATTTATTCATTATTATTGCTCTTTAGATTTTTAATTGTTTTTTATTTATGATTATTAAAAAATTTATTTATTATTTTTATTTGTTTTAATTTCTTTATTTTGTATTTTTATTTTTGTTTGTTCAGTTGTAAAAAAATTTATTGTTTTAATAAATTTTTC
Associated Phenotype:
Not determined