Busch Lab

ZMP

DDHD1 (2 of 2)

Ensembl ID:
ENSDARG00000086808
Description:
DDHD domain containing 1 [Source:HGNC Symbol;Acc:19714]
Human Orthologue:
DDHD1
Human Description:
DDHD domain containing 1 [Source:HGNC Symbol;Acc:19714]
Mouse Orthologue:
Ddhd1
Mouse Description:
DDHD domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2150302]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa25048 Nonsense Mutation detected in F1 DNA Not yet available
sa31016 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25048
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
ENSDART00000127374 Nonsense 553 825 8 14
Genomic Location (Zv9):
Chromosome 17 (position 51209476)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 50600293
GRCz11 17 50679362
KASP Assay ID:
554-7629.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGCAGCTATGAAGAGCGACACCTGCTGGAGGAAGTGCAGCTCACCAGA[C/T]AAAGGTGTCTACAAACTATCCAAACCAAGGGTGTCCAAATTTGGTCCTGA
Long Flanking Sequence:
TAATGTTGAAAACACTTTTAAACAATTGGAAACCGTGCTTTTTAAGATTCTTGATGAGAATAAAGTTAAAAACAACAGCATTTAATTACAATAGAAGTGTTTTGTAACTACTGACACCTTTTAGAAATAAAATGTAGTAATAAGTTTTCAAACAGTAAACAGTCAAACAGTCTGTCTCTCCAGCTGACCAATGAGGTGTTTTGTAGAAATATCTATATATACTCCAGTGTTCATCTTTGCAGATCACTAAAGGGTTAACGCAGGAGCTCAACCGCCTCTACTCTCTCTTCTGCTCACGAAACCCCCAATTTGAGGGGGACGGCGGTAAAGTGTCCATCATCTCCCACTCTCTGGGCTGCGTGATCACCTTCGACATCATGACCGGCTGGGATCCTGTGCGCTTCTGCCTGCAGGAGCACCACGATCAGCTGGAAGCCGAAGATTCGCAGTGGAGCAGCTATGAAGAGCGACACCTGCTGGAGGAAGTGCAGCTCACCAGA[C/T]AAAGGTGTCTACAAACTATCCAAACCAAGGGTGTCCAAATTTGGTCCTGAAGGGCCGTTGTCCTGCATAGTTTAGTTCCAACCCCAGTTAGACACACCAGAACCAGCTAATCAAGCTTTTTCTAGGTATACTAGAAACTTCCAAGCAGGTGAAACTTGAAGGAAGTTGGAGCTAAACTATGTAGGACTCCGGCTCTCCAGGAAGGAGTTTAGACAAAGCCAAACAAAAGCATAGATTGATCTTCATAAGATACAATGATGATTCAGGATGGGAAAAAATGACATGTAAATGTAGTAACCGTGAGTTTTACATAGACAGGTAACACTCATCATTTAGAAATGAGTTTTGATGTATTAATCTGTGTTTGTAACAGGTTACACGAACTGCGAGATCAGCTTCACGGTCTGAAGGAGTCAAAACCTGCATCCTTCCCTACGCTAAAGTTTAAGGTAATGTAGTGCCTTTAACAGTGATATCAGCTCTCAAACAGTCTAGACCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31016
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
ENSDART00000127374 Nonsense 792 825 14 14
Genomic Location (Zv9):
Chromosome 17 (position 51218427)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 50609244
GRCz11 17 50688313
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCTGCGCGAGGGTATGGTGGAGAGCCGCTATTGGTCAGCGGTGACCT[C/A]ACACACAGCCTATTGGACGTCCCATGACGTGGCCCTGTTCCTCCTGACCT
Long Flanking Sequence:
GCATTGGCTTGTTTGACTCATGCTAGCAAATGGGACTTCCTGTGTACTATGCATGGTAACAATGATAATGGAAGCCAAGCGCTAATAACGATTAGCTACATGCTATGAATGATTATCTAAATGCAATAACATATGCTAGAAATGCCTATTAAGTATTAGCATTTGATCAAACATGTACACGAGCATTGCCATTTAGCAACTGCATAGCAACTACCTAACAATGCCATAATTGTTTTAGCAACTGCCTAGCAACCACTTAGCAACCGCCGCCGTGCTTCCTGCCAACTGCCATTCTTAGTCCTAGCACAGTCACGTTGGCTTTCTCAAGCCAACATCAAAGTTTATCAATAAACTTTAGGTTCTAGTTCATGTTGTGATTATTTTATCTCCATATGTCTGCTAATGCTCCTGCTGGTGTTTCGCAGTGGAGATGGAGCACCGCATTGACTTTGAGCTGCGCGAGGGTATGGTGGAGAGCCGCTATTGGTCAGCGGTGACCT[C/A]ACACACAGCCTATTGGACGTCCCATGACGTGGCCCTGTTCCTCCTGACCTTCATATACAAACAGCAGAGCACAGAGCAAACAGAAACCAGCACAGCCATGTAGCACAGGTGACGCAATACACACTGATCCATCCCTTAAATCAACACTTAGTGCCTCTGAGCTCCTTTCCTTAGGCCTTTCCTCATGGACAGAGGCCGGACTATGCAAAATCCTCCAGCACTGATCCTCATCATTAAGAAACGGCAATATTTTTGATATTTTTATATAGTCCAAAGAAGTCCGCCGATCCATAGAAAGCTCTTTATTTAGTTAACTATATAGAATAGTGTGGCTGCATCCGAAATCACCTACTGCTCGAGTACGTACTACATTTGATTTTACTACACGACCATTAAATAGTATAAATGTGAGGAGTATTGATGGAATTTGGACGTACTACATCAGCCATTTTGTCATGATCACATGACCTACACAACTCACTCGATTCACCCACATTCAT
Associated Phenotype:
Not determined