ZMP

dennd3a

Ensembl ID:

ENSDARG00000078797

ZFIN ID:

ZDB-GENE-091230-6

Human Orthologue:

DENND3

Human Description:

DENN/MADD domain containing 3 [Source:HGNC Symbol;Acc:29134]

Mouse Orthologue:

Dennd3

Mouse Description:

DENN/MADD domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2146009]

Alleles

There are 7 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10213	Nonsense	Available for shipment	Available now
sa13522	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa10213

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115136	Nonsense	35	1270	2	23

Genomic Location (Zv9):

Chromosome 19 (position 1817932)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	1748887
GRCz11	19	1694357

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AACTTCTCTTGCTTTTTAACTTYTCGYACAGGGTAAAGAWGCAGATGTGT[T/A]RGTGGAGGCGGAGGTGCTGCAGGTTCACGCTCCACCGTTTATAACAAAGG

Long Flanking Sequence:

TTATGGGGTCTTTGTCGCCGTCTTGTGGCGTAACGTCAACAGTCTTTGCTCTGCTTAATGACATGCTGAATCTCCGAAATCATACATGTTTAAAATGGGCACTATCCTTTTAAATAAACTGCATAGTTGCAAACTAAACAACTATATTCTTACTAAAAACGACTCAAAAGTACATGATGTTGTCCAACAGCTGCAATATTTTTCAAAGTGAGTTTATTGATGTGCTGTCAGTCTATGTTGGCGGAGTAATACACAAGGTGCTGTAGGAGTGCTGTTATTGCAGAATATGGCACGGCTATCAGCCAGTCAGACTCGAGAACCAGACAGAACTGTTGTATATACATTAACTGTATATATAAATAGATTTTTTTACCATAAATTACTATTAGTTCTTAAAATATATAATGCATTTTGTATTTGCCATGAGTGAATGTGTATTTGCCGAATGCTAACTTCTCTTGCTTTTTAACTTTTCGCACAGGGTAAAGATGCAGATGTGT[T/A]GGTGGAGGCGGAGGTGCTGCAGGTTCACGCTCCACCGTTTATAACAAAGGATCGCTCTTGTAACGGCGGCGTAGACCAGGGCGTGGCTCCGGCCTTTAGCCGAGTCCAGAAGAGACGCTCCTTCAAGAAGAAGAAGAGAGAGCGGCCGGTGTCAACCCTCAGCAACTCCAGTCAAGCCAGTGAATCTGAAGAGCTGAGCGTCCCGCAGAACATTGATCTGATCGCCCTGCCACAGCTCTGCTTTCCTGGTAAAACACACATACACACACACACACACACACACACACACGCCTCGTTCTTACACACTCAATCTGACCGACACGCTCACACAGATGCTTTATCTTTAGTCAGATGCTGTGGTAAACAGTACCTAATTATTAATTTGAATTTGAAATGAATCAAATGATCAGTACAGAGTGAGTCTCCAGTAACTGATTCACTGATTCAAATGATCTGTTCGTAGTTTGTCTCCAGTAAATGATTCACTGATTCAAATAATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa13522

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115136	Essential Splice Site	970	1270	17	23

Genomic Location (Zv9):

Chromosome 19 (position 1845008)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	1775594
GRCz11	19	1721054

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGGACCAGACGAGTCCTCAAGCAGTGGACGTKCTGCTCTACACTCCWGG[T/C]GAGTCTCTCAGACACCKCCTCACAGCAAGAACGTCRCTGGTTCTAGTCCK

Long Flanking Sequence:

GAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGCTGGATAAGTTGTCGGTTCATTCTGCTGTGGCGACCCCGGATTAATAAAGGGACAAAGCCGACAAGAAAATGAATGAGTTTTAAACATAAACATTATTGCAGAATTAGTTTTACGGTTATGTTTATAGTGAATCTTTTGTTAAAGGTGTAGATTAAACCATCACATGCAGTGTTCGTTCGTTAGTTTGTTCGTTAGTTTGTTCGTTAGTTTGTTTGTTAGTTTGTTTGTTAGTTTGTTTGTTCGTTCACTCATTAAATGCATTCACATGTAAAGTGATTGCATTGGCCTGTGTTCTTCTGATTGCTGTAGTATTTGTTGACTGTATCTGTCTGTGGGTTTATTGTAGTGCCCATGATGGTCCCCAAAACCACCTCTGACACCCTGAAGCACAAGATCAACCCGTCTCTGGACCAGACGAGTCCTCAAGCAGTGGACGTTCTGCTCTACACTCCAGG[T/C]GAGTCTCTCAGACACCGCCTCACAGCAAGAACGTCGCTGGTTCTAGTCCTTACCAAGCCAGCCGACGTTTCTGTCTGGAGTTTACTTGTTACCCCTGTGCTTACGTGGGGGTTCCCTGGTTTCCTCCCACCATCCAAAAACATGCAACTTAAGTTAATTGACTAATCCAAATCAGCACCATAGACATGCTCCTGGTAAGCAGTTATCTCTTAAGAGCGATCACTATCTGTTCATTAGCTAGTTCTCCACATCTACCTGAGCTCAAACTCCCCTCTCGCCTTGCAAACAGGAAGGAGCCCCAGGCTCGAGGATCCTATGAGCTCAGGGCTTTCTCCCGGGACAGCATGCCTAACACTCTTTATAAACAATCATCAGCTAAGTGTGAACTCTTGAGTTGTATGCTATTCTATTGAGTTGAAGCGGTCTGACCTGGCATTTCCACAAGCGTGTCACTTCTGCGGTTGCTGCAGCAGTGTGTTGTGTAATGTGTATCTCCAGTG

Associated Phenotype:

Not determined