Busch Lab

ZMP

slc25a22

Ensembl ID:
ENSDARG00000020893
ZFIN ID:
ZDB-GENE-040426-2745
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
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

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.
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