ZMP
gatm
Ensembl ID:
ZFIN ID:
Description:
Glycine amidinotransferase, mitochondrial [Source:UniProtKB/Swiss-Prot;Acc:Q6PH19]
Human Orthologue:
GATM
Human Description:
glycine amidinotransferase (L-arginine:glycine amidinotransferase) [Source:HGNC Symbol;Acc:4175]
Mouse Orthologue:
Gatm
Mouse Description:
glycine amidinotransferase (L-arginine:glycine amidinotransferase) Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa28947 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28948 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa28947
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 |
---|---|---|---|---|---|
ENSDART00000052641 | Essential Splice Site | 95 | 422 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 265057)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 40855 |
GRCz11 | 18 | 40855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGCCGAGCTGAAAACGCATGCGTGCCGCCGTTCACCGTGGAGGTGAAG[G/A]TGAGGATCTGCACACACACACACACACACACACACACACACACACACACA
Long Flanking Sequence:
CTCACGTGTTCCTCGATGAACATGAGCATCTCTGATCCTGCAGGTGATGGATGATCTGATCCAGTGTTCTTCTCCTCTCGGGATCGGGTCAGGTTTAGGAGTTTAGGGTTATGGGTTATAGGGTTGTGTGTGTGTGCAGATGAGGAGCTGTGTCATGTCCTCCACAGTTATATTACAGCTGGAGTCATTGATCATCTTATTGTAATATTGTGATACTCATTCGCTCTACATTGCTCTGGAGTGTTCTGGATATTCAAGTGCCGGTGTTCTGTGTGTGTGTTCAGGTGGGTCGCGCGCTCTCGGGAAGGCTGTCGCGCGCGTCCCGGAGCAGCTCGAGTTCCGCCGCCGCACAGCTCCCGCTGTCCGCGCACGAGCAGGTGCCCGAGCCCGCGGCCGAGGAGTGCCCCGTGTGCGCGCACAACGAGTGGGACCCGCTGGAGGAAGTGATCGTGGGCCGAGCTGAAAACGCATGCGTGCCGCCGTTCACCGTGGAGGTGAAG[G/A]TGAGGATCTGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATACACACACACCACTGCAGACTGAGGAGGACACGGTCAATAATGGGTGAACTGTCCCTTTAAGACCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGCAGGCCAACACCTATGAGAAGTACTGGCCCTTCTACCAGCAGTACGGCGGTCAGACATTCCCGAAGGAGCACGTGCAGAAGGCGGTGGCGGAGATCGAGGAGATGTGCAACATCCTGCAGCACGAGGGAGTGACGGTGCGGAGGCCAGAGCCGGTGGACTGGTCCCTGGAGTACCGCACACCTGACTTCAGCTCGACAGGTGACACACACACACACACACACCTGACTTCAGCTCGACAGGTGACACACACACACACACACACACACACACACACACACACACACACACACGCACATGACTTCAGCTTGACAGGTGACACACATACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28948
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052641 | Nonsense | 103 | 422 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 265253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 40659 |
GRCz11 | 18 | 40659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTCTGCAGGCCAACACCTATGAGAAGTACTG[G/A]CCCTTCTACCAGCAGTACGGCGGTCAGACATTCCCGAAGGAGCACGTGCA
Long Flanking Sequence:
TTATTGTAATATTGTGATACTCATTCGCTCTACATTGCTCTGGAGTGTTCTGGATATTCAAGTGCCGGTGTTCTGTGTGTGTGTTCAGGTGGGTCGCGCGCTCTCGGGAAGGCTGTCGCGCGCGTCCCGGAGCAGCTCGAGTTCCGCCGCCGCACAGCTCCCGCTGTCCGCGCACGAGCAGGTGCCCGAGCCCGCGGCCGAGGAGTGCCCCGTGTGCGCGCACAACGAGTGGGACCCGCTGGAGGAAGTGATCGTGGGCCGAGCTGAAAACGCATGCGTGCCGCCGTTCACCGTGGAGGTGAAGGTGAGGATCTGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATACACACACACCACTGCAGACTGAGGAGGACACGGTCAATAATGGGTGAACTGTCCCTTTAAGACCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGCAGGCCAACACCTATGAGAAGTACTG[G/A]CCCTTCTACCAGCAGTACGGCGGTCAGACATTCCCGAAGGAGCACGTGCAGAAGGCGGTGGCGGAGATCGAGGAGATGTGCAACATCCTGCAGCACGAGGGAGTGACGGTGCGGAGGCCAGAGCCGGTGGACTGGTCCCTGGAGTACCGCACACCTGACTTCAGCTCGACAGGTGACACACACACACACACACACCTGACTTCAGCTCGACAGGTGACACACACACACACACACACACACACACACACACACACACACACACACGCACATGACTTCAGCTTGACAGGTGACACACATACACACACACACACTCTTTCTTCTCTCTCTCTCACTCACTCTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGGCATGTACGCAGCGATGCCCAGGGATATCCTGATGGTGGTGGGGAATGAGATCATCGAGGCCCCGATGGCGTGGAGGGCTCGCTTCTTCGAGTACCGTGCGTACCGGCCCCTGATCAAAGAGTA
Associated Phenotype:
Not determined