ZMP

LOC100005485

Ensembl ID:

ENSDARG00000089698

Human Orthologue:

ATF7IP2

Human Description:

activating transcription factor 7 interacting protein 2 [Source:HGNC Symbol;Acc:20397]

Mouse Orthologue:

Atf7ip2

Mouse Description:

activating transcription factor 7 interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:1922579]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31332	Missense	Available for shipment	Available now
sa33181	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31332

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

Mutation:

C > T

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122841	Missense	17	369	1	11

Genomic Location (Zv9):

Chromosome 3 (position 27216545)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	26934584
GRCz11	3	27065426

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATGAAAAGGAGCAGATATGAAGATGATTCTGGAACGTTACAGTTGGCTC[C/T]AGGCAGTGGCCAGAAAGCGAGCAAGCTCCCCCGATCCGAGGCAAGTGGTA

Long Flanking Sequence:

TTCAACCATGGGAAGCCGGTGAGCTGTAAGAACAGTGTTTAAAAGTTATTAGTAAAGATAAGTAAAATGTCTGTTATTCTATATGTGAATTCCATTCATATGAAACAAATCGCTGATGGTTGCATTTACAATTTTACGAGGTATATCTAATTTGTTAACGTTATCTATTAATATGTAACTCCTGATCAAAGAAATAAAGCGAGATTTGCATCTCAGACTTTCCCCTTAATAATATAATTTCATAAAATTATTATTTGCAAACTCTAAATAGCGAAATCATATTAACAGCCAATGATTTTTAAAGTACAACGTTGTTCACAGTCAAATAAACAGTGGTAATGTTGATTTTAAGTCATACTTGCATGCTAATTCCAATCTAATATTCAAAGTTATCTTGGTAAACAAATGTGTGAATATAAAACCAACTTTACCTCTATCTCACCCCTCAGGTATGAAAAGGAGCAGATATGAAGATGATTCTGGAACGTTACAGTTGGCTC[C/T]AGGCAGTGGCCAGAAAGCGAGCAAGCTCCCCCGATCCGAGGCAAGTGGTATAATGAAGATGATAAACGACTTATCAAATGAGTTTACATCTTTGTTTTGATATGAGAAAACAGAGTATTTTGTTTGTTAGACTTGTTTTTTTGTTTGTTTGTTTGTTTGTTTGCTTTTTGCAAAATTCAGACTTCCTTCAGTTCATGAGCTGTGTTTAAAGTTAATGTGGCCACAGGTCCTATAATGTTGAATTTGAGTTTACATTACAGAAGTAATATTGACTTGCAATTCTGCAAAATCGTGGTTGCACAAAAGTCTTTAATGTAAATCTGTTTTTATCAATTTATCATCTGTAGTATATAAATGTGTACTTAGACGTTTATCTAAATCAAGTTCACTGGTAAAAAAAAAAGAAAGAAAATCTGTATTACAAAATATGCACTGCATCTCAGCATCTGAATATGCAGTAGGGCAGTATATGAGCCGATCAGTATGTTCAATGAAGTCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33181

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
ENSDART00000122841	Nonsense	103	369	3	11

Genomic Location (Zv9):

Chromosome 3 (position 27212876)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	26930915
GRCz11	3	27061757

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGTATTTGCATATATCAGAAAATGCAGGTCTCTGGGGATTTCTCATAGT[C/T]AGGTATGAACTGAGATTTTATTGTTAAAAAGCTGAATTGCATTTTTGTGT

Long Flanking Sequence:

TAAAAAAAAAAGTCATGTATTAAAATTTCCTTGTTGGCGGCGCAGTCAGTAGCACTGTTGCTTTACAGCAAAAAGGTCACTGGTTCGAGCCTCGGCTGGGTCAGTTGCCATTTCTGTATGGAGTTTGCATGTTCTGCCCGTGTTCGTGTGGGTATCCTCCGGGTGCCCTGGTTTCCCCCACACGTTTAAAGACATGATGCGCTATAGATGAATTGGGTAGGCTAAATGTTTTCAGTGTATGTGTACGAATGAGAGTGTATGGGTCTTTTCCAGTGATGGGTTGCAGCTGGAAGGGTTTCCACTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCTGCTGTAGCAACTCCTGATTAATATAAGGACTATGTATGCCATTGCTACCACTATATATTTTCTCTTTGCTTTTAGGCCCATGTAAGAAAAATAAAACGAAGAGGAGATGCTGTATTTGCATATATCAGAAAATGCAGGTCTCTGGGGATTTCTCATAGT[C/T]AGGTATGAACTGAGATTTTATTGTTAAAAAGCTGAATTGCATTTTTGTGTGTGCAACTCATCACTCTTGTGTTGTTTTTATCTTCTTAACAGTTTCTTCCTTCTTTAAGCCCTTCTTCTGGACAGCCACAGCGATGCATTTCTCCAGCTGAATCGCTAATTAATACCTCCAGGTATTTTGCAATATTTTATGCATGTTACAGTCTTGATTCATGAAACATCAGTGAATAAAATATAGCCTATGAAGGATTTTCGATTTTCTGTGTTAGTTTAGATGCATGTACTGCATAGGTTTTAATGCTGCAGTCTGATGCCTTTCCATTCTGTTTGGGAAATGGTGCAGTGGCTGTGTGCCTGCTGTTTGAATGACAATAGCTAAAATATTCCATTTACTGTTTAATCAGAACATATTCTAATAGAGTGATCAAAGTGAAATCATCTCAGTGCTCCCCTGTGGATCTTTTTCTTTTCAGTCGGTTGTTTTTTTAATTCAGTAATGAT

Associated Phenotype:

Not determined