ZMP

LOC558824

Ensembl ID:

ENSDARG00000075906

Human Orthologue:

ADAD2

Human Description:

adenosine deaminase domain containing 2 [Source:HGNC Symbol;Acc:30714]

Mouse Orthologue:

Adad2

Mouse Description:

adenosine deaminase domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1923023]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9821	Essential Splice Site	Available for shipment	Available now
sa40884	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9821

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:

A > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108997	Essential Splice Site	139	517	2	8

Genomic Location (Zv9):

Chromosome 7 (position 26040459)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	24602211
GRCz11	7	24873368

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTTACATKATGCTKACTWTTACTTTTGTTTAAAACTCTCCTTGCTCTTAC[A/C]GTGAAGTTCGCAGACTGGCACAAAAATCGCGTAACAGCTTTGTGTACTGG

Long Flanking Sequence:

GATTTCTTACAACAGATAATGGCAAACCATGGTGTCAGCACAGAGGGGAAGCGGCTTCCACGAATGGCTGCCACCCTAATGATGCGCTTTGCCTCTGAAAGAGAGCCCACCTTTGGCATCCACAGGGCCAGCCTCAGACCGCTAACCCCTAACAGCGAGATTGAGGATTCCCGGTCTGCTGGAGAAGAGAGTCAGTCCACTAATCCAGAGTTACACTGCTTAGATGATGTTGAGGGACAATCTTCCGTAGGCCACCAAACCCAAGAGGTGCAGTCACCGGATTCCCCTCCCCAAATGGAAGACCTGGGCTCTTCCTCTGACGTTACTTCCCTATCTGGATGGAGCCTGAGCAGTGTTACGGCACCTGAAGCCACAGTAGATTTACTGGAAGATGCCACTGATGGCTCTCTCACGAGGGACCAGAGAACTGGAGGTACACTGACTGAAGATTTTACATTATGCTGACTTTTACTTTTGTTTAAAACTCTCCTTGCTCTTAC[A/C]GTGAAGTTCGCAGACTGGCACAAAAATCGCGTAACAGCTTTGTGTACTGGACGTTTTGACAAGCTACTCAGGGAATGCCCAGAATACCACAGCACTAAGAGCTGCTTTGCTGCTTTTGTACTGGAAAGAGGTGAGTGTGAGACAAGGTTATATTGTTAAATCATAAATAAAAGCAAATTCTTTATTTATTAGTATTTTTTAGTAATAATAACACATTTTTATTTATATAGCGCATTTCCAGAGCTCAAGAACACTTTACTATGAATTTAACAAAAAGAGATAGTACTGAAAATACAAAACAAGACCTAAGAGACAAATATGCAGACTACATTTAAAATAAAAAACTAATATATGCACTAAACTAAAATAAAAACAATAAACCTTTTTCACATTTACAAGTTTTTCAGCTGCGAAAGTCATCATAGTTCTGTAAAGTTAGATAGAAATGGATGGAAAAGTACCACATTATACATTATTTTGCATTCCAGTTTGCTCAAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40884

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
ENSDART00000108997	Nonsense	497	517	8	8

Genomic Location (Zv9):

Chromosome 7 (position 26030193)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	24591945
GRCz11	7	24863102

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTAGATGGCTGCCCAGTTGTATCAGGAGACAAAGACTCAAGTCAACATG[C/T]AATTCTTGACCAATAATGCTGGACCGTGGAACTCCAAACACTTGGTAGAT

Long Flanking Sequence:

TTATAGAATTTCTTTGTGTAGTTTTTCTGACAAATTTAATAGCCCGCTTTGTGTCGATAAAATTATTAAAAATTGTACTCAATTGACCGCCCTAATGGCATTTTTCAAATATACCAGTTGAGAAATTTAGCATTGTAGTTCTGGAGAACAGTGGCCCTCTACAATTAGACCCTAAATCCTTTTTATTGCTCTCTCTTACAGTTCTCCATTTGTAAGCGGTCCTGGGTCATCCAGCAGACTCTGTAAAAGAGCGTTGTACTTCTGCTTCAGAAAATTAGCGGGACTGGCAGGCCACCATGAGCTTCTGTCTTTCACCACGTATCGCAGTGCAAAAGTATGTGTACAGAGTTTTCACACTATCCACAAATATATATTATGAAATATTAGATAGAATGTATATAAATTTGCTGTAATTGACTGTTTATAACTGCTGATGTGCTTTACATTTTGTCTAGATGGCTGCCCAGTTGTATCAGGAGACAAAGACTCAAGTCAACATG[C/T]AATTCTTGACCAATAATGCTGGACCGTGGAACTCCAAACACTTGGTAGATTGCTTCAGCCGCTAAATGACAAGTTGAACAACCCTTGAAATACATCTAGGATTTCTAGTCATTTCAGGCTTTTGATGTTCAGGAAACGGCAACCTTTCTTTTTTAGTGTTTATTGATGTTTCAAGAATTACGTTCATATGCAAGTTCCTAGTTCATGATATATCTGGTAGATATAACTGCATATAATTGCACTTGTACTGAAAATATTCTGTTTGAAAATAGTGTTTTTTTTTTAGTGCTTGGCAGAGATTAATCATATCAAATAAAAGTTTGTTTTGACACATATATAATAAAAATAATAATATTAAAAAAATATCTAAATTAATATTTCCTCAAATATATGCACATCTGTGTGTATAATAAGTATCTACAATACACACACTTAAATTATGTCAAAACAGAATCTTATTTTGGATGTAATTAATTTTCTCCCAGCACTAGTATTTATTT

Associated Phenotype:

Not determined