Busch Lab

ZMP

LOC100002437

Ensembl ID:
ENSDARG00000054218
Human Orthologue:
GLTPD2
Human Description:
glycolipid transfer protein domain containing 2 [Source:HGNC Symbol;Acc:33756]
Mouse Orthologue:
Gltpd2
Mouse Description:
glycolipid transfer protein domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2444527]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa11906 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11906
Status:
Available for shipment
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Availability:
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Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076381 Nonsense 150 212 3 3
Genomic Location (Zv9):
Chromosome 23 (position 45564361)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 45061615
GRCz11 23 44773671
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCTGTGTCGCGAGGCCTACCTGGAGGTTCTGGCTCCKCATCATCCCTG[G/A]CTGGTGCAGCGCGCCGCTGAACTRGTGTTTCACGCAATGCCCGACCGGAG
Long Flanking Sequence:
AAAATTACAACTAAATAACAAAAAACAGCACGGAGCAAAGTGCTCTGAATCAGACATGTTGATGAATGTGGAACTGTGCTTGTGGTGTGATGTTGTGTCCTGTGCTGCAGGTTCATGGAGGCTCTGGGTCCTCTGGTGGGATTTTTCACTCATAAAGTTGAAGAGAAGATCGCGCTCATCCGACAGCTCTCACTGGAGGAATCCACCAGACACAGTGTTACCGCTAGCAACAGTATGATGTATGGTGCTCAGCATGAAGCCCCGCCCCCTGGCCACGCCTACCATTCTGTGCATTCGATGCTGGAGGCGGAGCTGCAGAGGGGCGTGGTCTCCTTTGACCAACAGACGCCCTCTGGGAGTCGGACGTTGCTCCGCCTTCATCGTTCATTGCTGTGGTTACAGCTGCTGCTGGAGAAACTGGGGACTGAGCGTGAGGGGCGGAGCTTCGGTGAGCTGTGTCGCGAGGCCTACCTGGAGGTTCTGGCTCCTCATCATCCCTG[G/A]CTGGTGCAGCGCGCCGCTGAACTGGTGTTTCACGCAATGCCCGACCGGAGCGTCTTCCTGCAGCTGGTGTGCGTGCGGACACAGGAAGAGGCGGAGCCTGTGATGCGCATTGTTGTTGCAGCGATCCGAGAAATTCACCAAAGGACACAGAGAGAGCTGGAGATCAGAAACATGCTGGACCTGCCTTAAAGGGGCAGTTCACACAAATATTTAAATACGCTGTTTATCTCATCACCCTCTGCCACTGTAAAAAAAAAATCTGTAATTTTTCGGTTTATTTCTGGCAGCTAGGGTACCGGGAAAAAAATGAAAATAACAGCTGTTAAATTACAGAAACATAGTGTAAAATAATGGATATTAAATTACAGAATTTTGCTTAAATTAAAATTTCTGGTAAATTTCGATGATTTAATATCCGTTATTTTACAGTAAATTTCTGTAATTTAACGGTTGTTATTTTACGTTTATTTTCGGCACTCTAGCTGCTGGAAATAAACCAT
Associated Phenotype:
Not determined