Busch Lab

ZMP

psat1

Ensembl ID:
ENSDARG00000016733
ZFIN ID:
ZDB-GENE-030131-5723
Description:
phosphoserine aminotransferase isoform 1 [Source:RefSeq peptide;Acc:NP_956113]
Human Orthologue:
PSAT1
Human Description:
phosphoserine aminotransferase 1 [Source:HGNC Symbol;Acc:19129]
Mouse Orthologue:
Psat1
Mouse Description:
phosphoserine aminotransferase 1 Gene [Source:MGI Symbol;Acc:MGI:2183441]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa33776 Nonsense Mutation detected in F1 DNA Not yet available
sa40607 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33776
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023983 Nonsense 5 368 1 9
Genomic Location (Zv9):
Chromosome 5 (position 72365749)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 68727081
GRCz11 5 69499474
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATCTCACGGACGAACGAGACGGTTTTATTTACAACATGGAGAAGAAA[C/T]AAACCGTTAATTTTGGGGCAGGACCCGCTAAACTCCCACAGTCGGTAAGT
Long Flanking Sequence:
TAGGTTTGGAGCGATGTTATAGTGAGAAAATTAAAACTTTTTTATTTGTTTATTATTATTATTATTATTTTGATAGAACTAATACATAAACCATTGACATGTACGAGGGCCAGCGAACAGATTTTTGTTTTATAACCATTTATTCTCAATACTTTTCTGCGGTAGGCTAAGTTTAGATTCATTTACGTTTTTCCAAAGAGAAATTTTTATCCTCCGAAAAGAATCTCAAATATTTTCTGTCGTAAAATAAACGTCAATCACAGTGACGTCACATTTACATCATCCAATCACACAACAGATAAGCTGACTTTCGGATCCCGCCAGCCAATGAAAACCAGCAGGGAACTTCAACATTAGGTGCAATCATGTGGAAAGGGGGAATAATAGAAGCGGGTTGAAAGAAATCACTGACAGAAAAACTAGGTCAAGTGGAGGAGATTCAGAAAGGTTTACATCTCACGGACGAACGAGACGGTTTTATTTACAACATGGAGAAGAAA[C/T]AAACCGTTAATTTTGGGGCAGGACCCGCTAAACTCCCACAGTCGGTAAGTACATCCACAAGTAACGTTATCTGCATCCACAAACTGTTATTCGAAATATTATAGTGAGATATTGAACATTTATAATATTTTTTTCTTCTTTTACATTATATCTTCATTACATTTTTGTTTTTCTACGCGTTATCGTATTTACAGATGCCTAAATAATGCAGCGAGATCATCTTCATCACTGCGTTGTGTGATTACATCATCTGTTACAGCCACTAGTGTGCAAGAAAAGTCTGCATACACACATATATTGTGTCATACTGTAAAGTAAAAATGCTTTAAACACCATGCAGGAGTTTAAAGACTATATTGATGTGCTTTTTAGTGGTCGGTATGCGTGCAATGTTGCATCAGCCAAGTGAGCCAACTCGCCTTTTGAAGAGTGCCAAGTCCTCCAAGTCAACATTCAATTCAATAATACATTGAATAATATATTAAATCTGAGAGCATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40607
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
ENSDART00000023983 Nonsense 237 368 6 9
Genomic Location (Zv9):
Chromosome 5 (position 72358003)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 68719335
GRCz11 5 69491728
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGAATGCCCAATTATTCTGGACTATCAGGTGCAGGCTGGCAATAACT[C/A]GCTCTACAACACGCCTCCATGCTTCAGGTGCGGCTCCTCATTCTCCTCTC
Long Flanking Sequence:
TACATGAGGCCCCAAGTGATTATTAAATTATGAAGCCAACATTATTTTCTGCATTACAGAAATACCAGACAGCAGCACGTGGTCACTGAATCCTTCTGCGTCCTACGTTTACTACTGCTGCAATGAGACCGTGCACGGCGTGGAGTTTAACTTCATCCCGGACACCAAAGGAGTGATTCTGGTCAGCGATATGTCCTCCAACTTCCTCTCCAGACCAGTGGACGTGTCAAAGGTCAGTGATGCTTCTTTATGATCTAGCATTCATTAACAGACTTGTAAATACTATAAAATATGCAGGATATTACACTTATTTACTGTTAATTGTGGGCATTAAGTAACTGTGAGTGTGTGTCTTCAGTTTGGTCTGATATTTGCAGGCGCGCAGAAGAATGTGGGCTGCGCGGGTGTGACGGTTGTCATTGTCAGGGAGGATCTGATTGGCAAGGCTTTAAAGGAATGCCCAATTATTCTGGACTATCAGGTGCAGGCTGGCAATAACT[C/A]GCTCTACAACACGCCTCCATGCTTCAGGTGCGGCTCCTCATTCTCCTCTCCACTGTATTTACATTAGGAATGTGGTCGTGTGAAAAAGGTTAAGACACGCAGACGTCATGTGATGTTGTTCATCTTTCAAAATTGAAGACCTGCCAAGAACCATGTTGTATATTATGTCCTGAAACAGAAATCTGTGAAATTCCCTCCCCCTGCTCCTTTCTTCACTTCTGGTCACATGGTTTTCCTTTTAGGGCTGGCATATCAGTCCTTTAGTTCAAGGCTATCAGTCATTCACTGCAGGGCTGTCAGTCATTTAGGGCGGGGCTATTAGTCCTTTAGGGTGGCGCTATCAGTCGTCTAAGGGTGGGACTATCAGAAATTAGGGCATGGCTATCAGTCCTCTAGGGGCGGGGCTATCAGTCCTCTAGGGTGGTGCTATCAGTTCTCTTGGGCGGGGCTATCAGTCATTTAGTGTGGGGCTATCAGTCCTTTAGGGTGGCGCTATTAGT
Associated Phenotype:
Not determined