ZMP
zgc:92113
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC445054 [Source:RefSeq peptide;Acc:NP_001003448]
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 are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11993 | Nonsense | Available for shipment | Available now |
sa43898 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11993
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008177 | Nonsense | 25 | 331 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 23 (position 427353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 398344 |
GRCz11 | 23 | 411137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGCCAAGCTCATCAATGGCGGAGTTGCGGGACTGGTGGGCGTCACCTG[C/A]GTCTTTCCCATTGATCTGGCCAAAACCAGACTGCAGAACCAAAGAGGAAG
Long Flanking Sequence:
ACGGTGGCTCAGTGTTTGGCACTGTGGCCTCACAGCAAGAAGGTCTCTGGTTTGAGTCCCGGCTGGGTCAGTTGCTGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTAGCGAATTGATTAAATAAGTGTGTGTGTGAGTGTGTATGGGTGTTTCTCAGTACTGGGTTGCAGCTAGAAGGGTATCCACTGTGTAAAACCTGCCAGAATAGTTAGTGGTTCATTCCGCTGTGGTGACCCCTGATGAATAAGTGAATAAGCCGAAGGAAAATGAATGAATGAGTGAAAATAACATCATAAATGGTTTACGGAATAACACAAAGATGACGCTTACACAAAGCCATAACTATGAATTGTGAATCCAGAGAACTCTCAAGTGCCCTCTCTCTCTTATATTGTTCCATGTTTGCACATGCTTTTTCTCTCTCTCATGTGTTTTCCTTTAGCCTCCCTGCCAAGCTCATCAATGGCGGAGTTGCGGGACTGGTGGGCGTCACCTG[C/A]GTCTTTCCCATTGATCTGGCCAAAACCAGACTGCAGAACCAAAGAGGAAGCCAACGGGTGTACAAAAACATGTACGTCTGCATCCGTCATTTACTTCAGTCAAGCTGTTTTTGGTTCCTTTTCGAATCCCAATAAAAAAAAAAACCTTTAAACTGCACTAAAGAGTCGCCCAACCCTAAAGAGGAGAGGAGTTTCCTTAAAAGACAGTTGCTGAGGGAAAGTGAGATCATCAGCTGAAAACCCGTTTCTCTTTCTGCGACGGTGTGCATGAGTGACAGGGGTGCGGCGCTGTGTAGGGTTCATACTTGTGGTTTTGGGTCACATTTTATTTTAGGGTTGAGTTCTCACTGTTAACCACACATTAATCATGAGTTTTGCCTAATTAAACGACTAATTTCCTGCTTATTATTAATTATTAAGGTTTTAAGGGGTGTAGAATATGATTATGCAGAATATGTAGTGTATGTGTACTAATAAACAGTCAGTATCATACACGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43898
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008177 | Essential Splice Site | 279 | 331 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 23 (position 432544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 403535 |
GRCz11 | 23 | 416328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATAAAAGCGCAAACGAGGATACCTACAATGGCGTAGTGGACTGCATCAG[G/A]TACAGTAACAAAACATTCTCCTGGGGAAGAGAATCAGCAGGCATTAGCTC
Long Flanking Sequence:
GAGAACAATATGGTCAACAGTACTGTACTATACCGAACCATAAGACACAAGGCATTAGTAGCCTCTCATTCCTATCAAATCTTATGTGTAGGGTGGGGTGAAGGCTTTAATTATGTGCTAGGTATACATGTTAAAACAAGAAAGGTTGAGATATTAGTGCTACAGACCTTGGTTCTTCTTTTTACAGGGACATCCCCTTCTCTGTGGTTTACTTTCCATTGTTTGCCCACATCAACCAGTTGGGCAAGACCTCTGAGGACAGCGACGTGCCTTTTTACTGGTCGTTTATTTCGGGCTGTGTGGCTGGATGTACCGCGGCTGTGGCCGTCAGTCCATGTGATGGTGAGTGTGTATGTCTGGCTCCATAACACAAGCAGATGTTAGCATATGTGCAGAGTTTAAGCTTGATCCTCTCTCTTCACAGTTGTGAAAACCCGGCTGCAGTCGCTCAATAAAAGCGCAAACGAGGATACCTACAATGGCGTAGTGGACTGCATCAG[G/A]TACAGTAACAAAACATTCTCCTGGGGAAGAGAATCAGCAGGCATTAGCTCCTTTCACACAAACAGACTTTCTGGAAAATCACAGACAAAGAGATCATGTGTGAAGTAAAGTTGTTCCATCAATTTTCCATAAAGAGAAGTAATATTACGGGTAACAGACATCCCAAGTCTCCCGGAAGTTCCGTGAGTCTCACGCAAATGCATAGAGACTCCTGGATGCCCGCAATTAAATGATACTCTTCCAGAAGTCGCATGTCTCCCACCTGTGCTCAAATACCCCTCTGCACTGCATCCCTCCCTGCTCTTCAAATACGTCATGCACCCATCCCCACTGTTCAGAATCCTTGTGCCTTGATGTCTTTGGATAGTGGGAGGAAACCGGCGGAAACTCAAGCAAGCACGGGGAGAACATTTACACTCTACACAGAAACTTCAACTGACCTGGGAAAGACTTGAACCAGTGACATTCCTGCTGTGAGGCAACAGTGCTAACCACTGGGC
Associated Phenotype:
Not determined