ZMP

LOC100001408

Ensembl ID:

ENSDARG00000075557

Human Orthologue:

APCDD1L

Human Description:

adenomatosis polyposis coli down-regulated 1-like [Source:HGNC Symbol;Acc:26892]

Mouse Orthologue:

Apcdd1

Mouse Description:

adenomatosis polyposis coli down-regulated 1 Gene [Source:MGI Symbol;Acc:MGI:3513977]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7589	Missense	Mutation detected in F1 DNA	Not yet available
sa33964	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7589

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 > G

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112226	Missense	123	512	3	4

Genomic Location (Zv9):

Chromosome 6 (position 49607423)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	49657104
GRCz11	6	49655757

KASP Assay ID:

554-4212.1 (used for ordering genotyping assays)

KASP Sequence:

YAGGGCCCTCCAACACTATTACTCCGACAGCGAGTGCCAMGTCCCAACCT[A/G]CTCTCTTGTGATAAGGGGTAAACTGCGGCTCCGTCAGGCCTCGTGGATCA

Long Flanking Sequence:

ACACTTTGGGTCACTCAGAATCAGCTGACAATCATTTAAACAACACAACCTGCCAGGTGTACTCCTCTTTTGATGGCTATGTCAAACAGGATAGCACAACATATCACAAAGCTCAAATCATGTCAAACTGATTTGTAAATTAGTTCAATTTACTCAAATGTCTTTTAAAGACATCAGATCTCAATCCAACTAAGTATCTTTAGGAAGTGCTGGAAAATTATATAATCATCATGGATGTGCAGTCAACAAATAATTGTTAAAACCAGGGGTTTAAACAATGCTCAAAATTCCTAGAATTCCATCCCATTATAGAAGAAAATAGTTTTCAATTGCCAAGCTGACAAACCTATTGACTTGAATCCTTTATTTCCCACTCAGATGTGAAGTGCGGCCTGGTCCAGAATTCCTCACTCGATCCTACACACTCTACCAAAGCCCCACGCGTCTCTTCAGGGCCCTCCAACACTATTACTCCGACAGCGAGTGCCAAGTCCCAACCT[A/G]CTCTCTTGTGATAAGGGGTAAACTGCGGCTCCGTCAGGCCTCGTGGATCACCCGTGGAGCCACCGAAGCAGAGCACCACCTCCATAAAGTAGGGATGGTCATTCACAGTCAGAAGGCCATCCATCATCTTGCGACCCGCTTGCCCTCCTCCTGCCTGGGACTCAAAGCTGAAGGACACCTGGTGCTCCATCGCTTCTATGAACTCTTCAATGCCAAAGCAGAGAAAGATTGTCTGGGTGCTCTTGGGTTCTCCATGATGGAGCTGGAGTTGCTGCGGGTGGAGACGCATCATCATCCACACGGCAGACCGGCTCAGGAGCTGTTCTTAGGGGATGTTCACACAGAATGGAATGAAAGAGTGCACTATAGGCCAAGTGGTTACCAGGAGCCATTACAAAATGCAATGGTGAGAGTTAAGACTACTTTTTATTTGTTGCCTAAAAGTGCCTTTGGTATGCTAATATGATTGATATGATGGTTATACAAACTCCCTAGTTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33964

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
ENSDART00000112226	Nonsense	389	512	4	4

Genomic Location (Zv9):

Chromosome 6 (position 49604187)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	49653868
GRCz11	6	49652521

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCGTGTTCGACCGGGCGTTGTTAAGAGAACTGAATTCAACGCAAAATGGA[A/T]GATGTGGACAAGCAGGTGGATGGGAAGCAGGCATTGAGCAAGACATAACC

Long Flanking Sequence:

CACTACTCCCTATATTACTAATAATATGTAAAAATATATAATATGCTGTAATAATTATAATAAAAAAACATATTAATACAATCAATCAAAACATTGTTTTTTACTTTCAGCATCACATCCACCCATGCCCAGTGTGCGGCCTGGTATATCGAGCCTCAGAGCAGCATCCGCCCATTCTCCCTCCATCCCCTTCCATCCCTTTGAATCTAAATGGAAACTGGGTAAGCCAACGCTGCGAGTCTCGTCCCGCCGTCCTCTTCCTCACCCGCCTCTTTGTTTTCAACGAGGAGCAACACACATGGGAGGGCACATATCACCACTACTCTGACCCAACGTGCCGCCAGCCCAGCTTTACACTATCAGCATCAGGTAATTACGTTAAAGTGGGACAGTCCATAAAAGTACGTGGAGCCACCGAACTTGTCTTCAAAGTGACACACGCAAAAGTGATCGTGTTCGACCGGGCGTTGTTAAGAGAACTGAATTCAACGCAAAATGGA[A/T]GATGTGGACAAGCAGGTGGATGGGAAGCAGGCATTGAGCAAGACATAACCTGGACGAACGGTTGCGATGCATTGGGGATACGACTTCCACACAAAGAGTATGAGCTGTTTAAGATGGAGGTGGATCGTAAAGGTCATCCACTGTTATTCAATGGGGAAAGGCCAACGGATGGATCCAGCCCGGAACGACCTGCAAAAAGGCCAACGTCATTTCAGACACCAATGGTGCAATGCAGCACAAGCGTCAGGGTGGAGCCACACCACAGTCCCTACAGCGATCATTCAAAAGGACCCAAGAAAAGCTCTGCTAATGCACTGCACTCTTCGGTGATCCTGCTGTCGCTTCTAAACGCATGGATTATTCATCTTTTCTAAAATATGACAAGCCATTCACATGCATTGTTCAATTTTATGGACTTACAATCTAGAGGTGGAAAAACTAGAGAAGGATCATTGACTTAGGTGCTACGACAAAACGCTTGCTGCAAATGCTCTGAAATA

Associated Phenotype:

Not determined