Busch Lab

ZMP

ehd3

Ensembl ID:
ENSDARG00000007869
ZFIN ID:
ZDB-GENE-041014-352
Description:
EH domain-containing protein 3 [Source:RefSeq peptide;Acc:NP_001038469]
Human Orthologue:
EHD3
Human Description:
EH-domain containing 3 [Source:HGNC Symbol;Acc:3244]
Mouse Orthologue:
Ehd3
Mouse Description:
EH-domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1928900]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa6644 Nonsense Mutation detected in F1 DNA Not yet available
sa6645 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6644
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022694 Nonsense 208 535 4 6
Genomic Location (Zv9):
Chromosome 20 (position 38257178)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 38329590
GRCz11 20 38232469
KASP Assay ID:
554-4089.1 (used for ordering genotyping assays)
KASP Sequence:
CCCACAAGCTGGACATCTCAGATGAGTTTTCAGAGGTCATCAAGGCCCTA[A/T]AGAACCATGAAGACAAGATCCGTGTGGTGCTCAACAAGGCCGACCAGATY
Long Flanking Sequence:
AATAATGTTTCCTTAATATTATACATAACGCAGTCTTTGTTTTAAATGAATCATCATTTTGCTGTTTACTTGAACGGTGGACTCTCTCTTTGACTTGCTACATCCCTGGAGAGAGAGAGTAAAGCTGAGCTGCAGAAGCCATTAACTGGCAGACATTAGATCATAAAAACCGCAACAGGCCCGAGCATTTTAACGATACTTGGAAGAGACTCAACATTTTCAGTTCTACTGAGCGCCAGGTCTAACAAGGTCATTTCGCCCATTCTGATTGGCCGACTGCCTCTCTGCTCTCATGTATCCGTTCATGCGGTGCAAAAGCTTTGTGAACCATAAACACTGAACAGAATATCAATCTCTTTTTTTTCCAATCTCTCCCTTCAGGCTATGACTTCGCTGCGGTGTTGGAGTGGTTCGCCGAGCGCGTAGACCGCATTATCCTCCTTTTCGACGCCCACAAGCTGGACATCTCAGATGAGTTTTCAGAGGTCATCAAGGCCCTA[A/T]AGAACCATGAAGACAAGATCCGTGTGGTGCTCAACAAGGCCGACCAGATCGAGACACAGCAGCTGATGCGAGTTTACGGCGCCCTCATGTGGTCACTGGGAAAGATCGTAAACACGCCGGAGGTGATTCGTGTCTACATTGGCTCTTTTTGGTCGCATCCATTGCTGATTCCAGACAATCGCAAGCTGTTCGAAGCAGAGGAGCAAGACCTGTTCAAGGATATACAATCACTTCCTCGCAATGCCGCTCTTCGCAAGCTCAACGATCTGATCAAGAGGGCCCGTCTGGCTAAGGTAAATTTGAATTTCTGTAGGCTAATCTTGTCAACGAATAACCCACCTGAGATTTCAGCAAAGTAAAGGCCTGTTTTCACCAAGGTCAATAGCTTAGTCCGGAAACTGTGACCATTTCTTCTTTTTCTTCCCATTGTGCCGCATTTCCAAGAGAAACTGAATACTAGATGAGGAAACAGTGGGTGTGGCTTGTTTTTTGACTGCGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6645
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022694 Nonsense 448 535 6 6
Genomic Location (Zv9):
Chromosome 20 (position 38265751)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 38338163
GRCz11 20 38241042
KASP Assay ID:
554-5444.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGGCATTGATGAAGTAGAATGGGTTGTGGCACGTGACAAACCCATGTA[T/A]GATGAAATCTTCTACACTCTCTCGCCTGTCAATGGCAAAGTGACTGGGGC
Long Flanking Sequence:
CATTTCAGACAAAATTTGGCCGGCTAGTTTGTATGTTTCTTCTCCGCCAATGAAACCATTTCCAAAAGAAGCCTTTTCATATTTTTCGAGCTGCAACACCCTGACACAGCCCTTCTGGAACTGAATATGTAAGGGGAGTGGAGCTGTTTTGCTCTTGCAGTATCAACAGATGTTGACAGGATCTTTTGTTACAACTTACAAGTGCTTCTTTCTCTTGGTTTCTTTCCCACTGAATAGGAGCAGCTTCAGGCACACGATCTAAACAAGTTCCAGCCTCTAAAAATGAAGCTTTTGGACACTGTGGATGATATGCTGGCCCATGACATCGCCCAACTTATGGTTCTGGTGCGCCAAGAAGAAACGCAGCGTCCTAACCAGGTGGTGAAGGGTGGTGCTTTTGAGGGCACCATGAACGGGCCGTTTGGACATGGATATGGTGAGGGAGCTGGAGAGGGCATTGATGAAGTAGAATGGGTTGTGGCACGTGACAAACCCATGTA[T/A]GATGAAATCTTCTACACTCTCTCGCCTGTCAATGGCAAAGTGACTGGGGCCAATGCCAAGAGGGAGATGGTGAAGTCCAAGCTGCCAAACACTGTGCTGGGAAAGATCTGGAAGCTGGCTGACATTGATAAAGACGGGATGCTCGATGACGAGGAGTTCGCCTTGGCCAACCATTTAATTAAGGTCAAACTTGAAGGTCACGAGCTGCCAAGTGATCTGCCCGGGCATCTCGTGCCTCCCTCCAAGAGGAAAGTTCCAGAGTAAGATTTCGGAGTGAATATAGTGGATTTAGATTGCTTTTAAATTGTGAATGATTGGACTTTATTATAGGAAAAGAACAAACAAACTTCCTTCAAATGTATGGTTTATGCTTCACTAGGAGGAATGGATTTGAAAATGATCCACCTTTTCAACTCTTTTGACCTGTGTATGTTTTTATTTTGATTTTGATTTTAGTTTTAGTTTCTTTTTTTATGAATGATATTCTTGTCAGCAGTGTG
Associated Phenotype:
Not determined