Busch Lab

ZMP

LOC562999

Ensembl ID:
ENSDARG00000061194
Human Orthologue:
HECTD2
Human Description:
HECT domain containing 2 [Source:HGNC Symbol;Acc:26736]
Mouse Orthologue:
Hectd2
Mouse Description:
HECT domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2442663]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa6244 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6244
Status:
Mutation detected in F1 DNA
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Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086984 Nonsense 444 756 13 21
Genomic Location (Zv9):
Chromosome 12 (position 17430733)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16310443
GRCz11 12 16359253
KASP Assay ID:
554-5249.1 (used for ordering genotyping assays)
KASP Sequence:
ACGTTTGTTGGAGAAGCAGGATTGGACATGGGTGGACTCACGAAAGAGTG[G/A]TTTCTTCTCCTGATTCGACAGATTTTTCACACAGACTACGGTAAGACAGT
Long Flanking Sequence:
ATATTAATTAAGGAACTATTGTCTGACTACATGATGGTGCGCTTTATTAACCTCTCATGCAAGTGAAGGAAGTTAATAGAAAAAGTACCTTCCATCATGCAGATGCATGGCTCTTCATAGTAATGAGTTACACATTAAAAAATTCAAATCATGAATTGGTCAAACTTTAGGAAAAAATCTAGATTTTTATTTATTTGCCTTATCGCCCAGCCCTACTAGAATGATGGACGTTTGTATGAGCTGCATTGCTCTGTATAAAGTAGCTATAAAAATCTACATTTTGTTTTCCTAGTCTGAGGGGCTTTTCAGCCAAAAGCGTGTACATCATGTTCTGGAAAGTTCTAAGTCTGGCTAAGACTTAATTTGGAAAAATGGCCCCTCCATAAACGTGTTCCTTTTTTTTAATAGCTTTCAAGAAAGCGAGCAGACCTGAAGAAAAAACTGAAAGTGACGTTTGTTGGAGAAGCAGGATTGGACATGGGTGGACTCACGAAAGAGTG[G/A]TTTCTTCTCCTGATTCGACAGATTTTTCACACAGACTACGGTAAGACAGTCAGCACTAGTATTAAGACATTATGCAGCTGTTATATACTGCAAAAAAAGTATAATTATGTTTGCTTTTATTTCCCTATAAAATATGTAAGCATATAACAAAGATAATTCATTTATTGAGGTGAAAAGTTTAATATCAACTTATAACTTTTTTACATATACAATGGTTCATGTGTGCAAATTTCATCACCGGAAAAGTGTACATATCCTCACCACCAGCCTGAACTGTTCCATGATTTCATGTTGTTGACACCAAACTGACCCTACATCAGAGTGTCACAGCAAAAATCGAGACTCATTAGACAAGGCAACATTTTTCCAATCTTCTATTGTCCAATTTTGGTGAGCCTGTGAGAATTGTAGCCTTAGTTTCCCGTTCTTCGCTGACAGGAGTGGCGCTCGGTGTGGTCTTCTGCTGCTGTAGCCCATCCGTCTCAAGGTTGAACGTGTGC
Associated Phenotype:
Not determined