ZMP
glud1a
Ensembl ID:
ZFIN ID:
Description:
glutamate dehydrogenase 1a [Source:RefSeq peptide;Acc:NP_997741]
Human Orthologues:
GLUD1, GLUD2
Human Descriptions:
glutamate dehydrogenase 1 [Source:HGNC Symbol;Acc:4335]
glutamate dehydrogenase 2 [Source:HGNC Symbol;Acc:4336]
glutamate dehydrogenase 2 [Source:HGNC Symbol;Acc:4336]
Mouse Orthologues:
AC160930.1, Glud1
Mouse Descriptions:
glutamate dehydrogenase 1 Gene [Source:MGI Symbol;Acc:MGI:95753]
glutamate dehydrogenase 1, mitochondrial precursor [Source:RefSeq peptide;Acc:NP_032159]
glutamate dehydrogenase 1, mitochondrial precursor [Source:RefSeq peptide;Acc:NP_032159]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35471 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31925 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35471
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016946 | Essential Splice Site | 386 | 544 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 22826657)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22555995 |
GRCz11 | 13 | 22686445 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTAACAAATGTTAAAGAGAATATGAAAATAAAAAACTTGTTTTCATA[G/T]ATCATCGCTGAAGGAGCAAACGGCCCAACTACTCCTGAAGCAGACAAGAT
Long Flanking Sequence:
GCACTCCATGCGTTACCTACACCGCTACGGAGCGAAGTGTGTGGGTATTGGAGAACTGGATGGAAGCATCTGGAATCCCAATGGCATCGATCCAAAAGAGCTGGAAGACTATAAGCTGGTGAGTCAGACACTGAACTTTTCTTTTTTTTTTTTCCTTCACTAAACCTTCAGTGCGGGGTAAGAGAGCCACCTTGGGGCCACTTAGTTGCAATACATGCAATAACTCCAACCATAAAATGTGAATATATTCATTAAATATCACATATTCTTGTTTACCAGGCAAATGGCACTATTGTTGGCTACCCAGGGGCCACCGCGTATGAAGGCAACATTTTGGAAGCTGAGTGTGATATCCTGATCCCTGCTGCAAGTGAAAAACAGCTCACAAAGAAAAACGCCAACAATATCAAGGCCAAGGTCAGACATCAAAAGAGCCAAACCAAAGTGTGTTTTTTAACAAATGTTAAAGAGAATATGAAAATAAAAAACTTGTTTTCATA[G/T]ATCATCGCTGAAGGAGCAAACGGCCCAACTACTCCTGAAGCAGACAAGATATTCCTAGAGAGGAATATCATGGTGATCCCGGTACGGCTTCCTGTCACAAAAGTTCTTTTATGTTTAAATCTGAATTAACTTCTATACATGAGAATACACACTACCTGACAAAAGTATCTTCGCCTATCCAAGTTTTAGAAACAACAGATAATAACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTATATGAAAGACAAAGGCCTCTAGATTACGCTCATTTTACCAAAATAAAATATGATCATGCCTTGATTTTTAATTATTTAATTAGGATAGTAAAGTCTGACTTTGCTTAGAGAAAAGTCTAACTATGTACAGTCAATATAAAGTCATGGTGCAGTGGAAAAGAATGAATATTGTGTATGACTCTTATAAGCTTGGATGACTGCATCCATACATCTCTGCCATGACTCAAATAACTTATTAATAAAGTCAACTAGAATGGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31925
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 |
---|---|---|---|---|---|
ENSDART00000016946 | Essential Splice Site | 505 | 544 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 22823459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22552797 |
GRCz11 | 13 | 22683247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACATTGTGCATTCGGGATTGGCTTACACGATGGAACGATCGGCCAGA[G/T]TAAGTACATGTATAATAATAAGCAGTTTCATTTATCTGTTTATACAGGTA
Long Flanking Sequence:
AATTATGATTAATAAATGCTGCACAAAGAATACGAGTTCATGTTAGTAAATGCATTAACCAATGAATCCTTATTGTAAAATGTGAGCAAAAGGTTGAAATAAATAATTTAAATTCGTTTTAGTATATTCATATACTTGTTCCACTGCACTTTAAAAAATATTGCATACTTGGGACTCAATGTGGGTTTTCTTTCAGTAGAAATAAACAATGTTTTAAATTCACTGTCAGTATTGAATGGGAATCATGTATGTTTTTGGCAGTGTCTGTCCAGGAGAGTCTGGAGAGGAAATTTGGGAAACATGGTGGAGCCATACCCATTGTTCCCACTTCTGATTTTCAAGAAAGGATTTCTGTGAGTGCCAACACATTATTGTTGTATTTATTTCATTTGGAATAAGTGTGCTAGACATAAAAACTTGATTGGCTTGTCTCATAGGGGGCTTCTGAAAAGGACATTGTGCATTCGGGATTGGCTTACACGATGGAACGATCGGCCAGA[G/T]TAAGTACATGTATAATAATAAGCAGTTTCATTTATCTGTTTATACAGGTAGGTTATATAAAATAGACGTTTTGACTTATTTATATGGGTCTAAGATATATTTAGGATTTGTTTATGCAAAGTGTCTGTGTAAAGGTTTCATATAACTTTTTAATCTAACTTAATCTTCGTTTAAAGTAGCTGATATATTTATGCTTAGGTGAAACGTATGCTTGTTCTGACCTGCCCTTTTTACAATAAATTATATGAAAGAGTGATCATACTAAATGTTTCTATATTTTAAATGATTAACAAATTTATTGCTGACAAATGGGCTAAACCTAGTTTCAAGGGCAGTGGCAAAATTAAAAAAAATGTAAAATTACATTTAATGAACGTTAAATGCCTCAGCAGATCCTATCGAGTATCTTATTAAGTCAACAAATGATTCTTTTTGGTTGTTCCACTGAATGACATTTCAGTGGGTGTCTTCTGTAAATCGTATAGTTACAGGTTTTGTGC
Associated Phenotype:
Not determined