ZMP
LOC100148522
Ensembl ID:
Human Orthologue:
GPT
Human Description:
glutamic-pyruvate transaminase (alanine aminotransferase) [Source:HGNC Symbol;Acc:4552]
Mouse Orthologue:
Gpt
Mouse Description:
glutamic pyruvic transaminase, soluble Gene [Source:MGI Symbol;Acc:MGI:95802]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22057 | Essential Splice Site | Available for shipment | Available now |
sa31865 | Essential Splice Site | Available for shipment | Available now |
sa41987 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22057
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078033 | Essential Splice Site | 80 | 494 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 15196065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14051718 |
GRCz11 | 12 | 14090021 |
KASP Assay ID:
2260-5135.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTGACTGCCATGCAATGGGCCAGAAACCCATTACCTTCTTCAGACAGG[T/C]GTGTTTTTGAGCTATTGTGCATGTCTTGCTATTTTCTGAGCAGTAGTGTT
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAATGTTATTGTGTATGGAGGTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCTGCTGTGTAAAACAAATGCTGAATAAGTTGGTGGTTTACTCTACTGTGGCAACCCCTGATAAATAGGGGACTAAACCAAAGGAAAATGAATGGATAACAAATATTTATAATTTTTTATAATATTATCATTATTATAATCTAAAATGCAATATACAAAGTAAGATAACTTATTATTAATTTATAGAAAAGTTTTTAAATTATATTCTGCATTCTCTCTCTTGTTTCTTTGTCTCCTCTCTTTTTCTTTCTTCCATTCCCGCTGTCTTTGTGCTAAATCAACATAGGGCATAAAAAAACCATTTACAGAAGTCATTAAAGCCAACATCGGTGACTGCCATGCAATGGGCCAGAAACCCATTACCTTCTTCAGACAGG[T/C]GTGTTTTTGAGCTATTGTGCATGTCTTGCTATTTTCTGAGCAGTAGTGTTTGTACATACAGTGTGTATGCTTTATATATTTGTCAGGTGTTGGCATTGTGCTCTTATCCAGATCTTCTTGAAGACAACAAATTTCCAGAAGATGCCAAAAGTAGAGCACAGCGCATTCTAAAAGCTTGTGGTGGAGGAAGCCTTGGTACTGGAAAATGTTTTAATTAGATTTACATTACTAAGTAAACATGTATTTAAAAAAAAAAAAAAAATTTTATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGGGTACATACATATACACTTGTTTTTCTTCTTGCAGTGGAAGTTAAATGGTCCCATCAAACATTCTTCAAAAAGTCTTCTTTTTTTTATTAGGTAGTTGTTTGATTAAACATTACAATTCATTACAATCACAACTAAAACTTTAATTGGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31865
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078033 | Essential Splice Site | 119 | 494 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 15196268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14051921 |
GRCz11 | 12 | 14090224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCACAGCGCATTCTAAAAGCTTGTGGTGGAGGAAGCCTTGGTACTGG[A/T]AAATGTTTTAATTAGATTTACATTACTAAGTAAACATGTATTTAAAAAAA
Long Flanking Sequence:
AAGGAAAATGAATGGATAACAAATATTTATAATTTTTTATAATATTATCATTATTATAATCTAAAATGCAATATACAAAGTAAGATAACTTATTATTAATTTATAGAAAAGTTTTTAAATTATATTCTGCATTCTCTCTCTTGTTTCTTTGTCTCCTCTCTTTTTCTTTCTTCCATTCCCGCTGTCTTTGTGCTAAATCAACATAGGGCATAAAAAAACCATTTACAGAAGTCATTAAAGCCAACATCGGTGACTGCCATGCAATGGGCCAGAAACCCATTACCTTCTTCAGACAGGTGTGTTTTTGAGCTATTGTGCATGTCTTGCTATTTTCTGAGCAGTAGTGTTTGTACATACAGTGTGTATGCTTTATATATTTGTCAGGTGTTGGCATTGTGCTCTTATCCAGATCTTCTTGAAGACAACAAATTTCCAGAAGATGCCAAAAGTAGAGCACAGCGCATTCTAAAAGCTTGTGGTGGAGGAAGCCTTGGTACTGG[A/T]AAATGTTTTAATTAGATTTACATTACTAAGTAAACATGTATTTAAAAAAAAAAAAAAAATTTTATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGGGTACATACATATACACTTGTTTTTCTTCTTGCAGTGGAAGTTAAATGGTCCCATCAAACATTCTTCAAAAAGTCTTCTTTTTTTTATTAGGTAGTTGTTTGATTAAACATTACAATTCATTACAATCACAACTAAAACTTTAATTGGAATACTAAACAATAAAGTGAAAGCTAAACTTTTAGTCTTAACTTATATAATCTTAATCCAATTAAGTTATAGTTGTTTAACTTAATAATTTCAGTGTGTGTGCTTAAACCATGAACCTCTTGTTTGACCCAATTGGGAAACAATACAGATTTGGGAATAATAGAAAAAAGGCTAAATAATGATTTAAAAAAAAATAATAACATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41987
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 |
---|---|---|---|---|---|
ENSDART00000078033 | Essential Splice Site | 376 | 494 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 15234801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14090454 |
GRCz11 | 12 | 14128757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTATATAAAGAGTTTAGTAATTTAAAATTTGTAACTTTTTTTTTTTTA[G/T]GAACGCTCAGACACTTTGGCTGCTCTAGCAGAGAAAGCCAGCATGACGCA
Long Flanking Sequence:
AGCCTAAGAGGAAATGTTTATTTGCAAGAAAAGAGGTCTGATGGATTTAGAGGCTTTTGCATCTGAACTCTTCATATATTGCTGTCACTGTCCTTATCAGTTAAACAAAGTTTGTCAGATTGTTAAAATTATGAACATGATTAAACTAACACCAATAAGAGATATGTGAGATATCTGTAAGGATTGTCTGATTTTATCCAATTTAAAAAAATAATAATAATAATTTTAAACTGGGCTTCAGAATATGTGACTCATATTTTAAAAGTCTCCCATACTCTTTTAAGTACTTTAAATAGGACAAAGCAGTGAAGTAAATTTAAAACTTAAGAAATTGTAGGTCATTTTCTAAGTTTTATCTTTATTGTGTCTACTAGTCGTAGTTATTTAGATTTGTCTATAAACTTACTCAATTCATAGATTTATTTGTTGTTTCAAAATTCTTATTTTGTAAGGTATATAAAGAGTTTAGTAATTTAAAATTTGTAACTTTTTTTTTTTTA[G/T]GAACGCTCAGACACTTTGGCTGCTCTAGCAGAGAAAGCCAGCATGACGCAAGACATCTTAAATCAAGTACCTGGAATAAAATGTAACCCAGTGCAGGGTGCAATGTACACTTTCCCAAGGATCCACCTCCCACCGAAAGCCATATTGAAGGCCAAGGTAATAGTTAATCTCTTCACAGTTAAATCCAAGAAATGTAAATATTTTTATGGCCATCTTTAAATATGTGGTCACTTTTACTTTAGGTCTCATACGCAATTCATAGAGGGCCGCAGCTCTGCACATTTTTTGTTCCTAATCAGACACACCTGATCCAAATAATTAAGGTGTTCAAGAATAGTCTTCAACACCTTGATTTGTTGGATCAGCTGTAGACCCATGTATTACACAAAGTGTGCTGTATTAAAATATTTTGTTGCATTTTGTCCACAAAGCTACTCACTGGATATGTTCTCTTTTACTAAGCTTTCTTTGCAAAAAAGATTGTGATGCTTGAAAATTTA
Associated Phenotype:
Not determined