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