ZMP

LOC571099

Ensembl ID:

ENSDARG00000005901

Human Orthologue:

AIM1L

Human Description:

absent in melanoma 1-like [Source:HGNC Symbol;Acc:17295]

Mouse Orthologue:

Aim1l

Mouse Description:

absent in melanoma 1-like Gene [Source:MGI Symbol;Acc:MGI:1334463]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa3003	Essential Splice Site	F2 line generated	Not yet available
sa11766	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa3003

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013972	Essential Splice Site	296	702	9	19

Genomic Location (Zv9):

Chromosome 19 (position 50051359)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	48617693
GRCz11	19	48277087

KASP Assay ID:

554-2512.1 (used for ordering genotyping assays)

KASP Sequence:

GTGGGGCGGAGTCAACTMTGAGCTGCGCTCCGTCAGAGTCATTCAGTCGG[T/G]AAGAAACATCTACRCTSAGCACATACACRCATTTCAGCAGCCATCAGGGG

Long Flanking Sequence:

ATGTGTGTGTGTACGTGGGTGCGTGCATGCGTGTCCACACCCTTTATAAATCTGATGTGTGTGTGTGAGTGCATGCACTTTTTCTGGATTTGCTGTGTGTGTGTGTGTCTGTGTGTGTGCGTGCGTCCGTGCATGTGTGTGTGTATATGTGTGTCCACACTCTTTATAAATCTGGTGTGTGTGTGTGTGTGTCTGTGTGTGTGCGTGCGTGTGTGCGTGCGTGCGTCCGTGCATGTGTGTGTATATAAGTGTGTCCACACTCTTTATAAATCTGGTGTGTGTGTGCGTGTGCGTGCACTTTTTCTGGATTTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCTGATGTGTGTGTCTGCTGTTCCTCCAGTTGGGTGGGTTATGAGAAGGAGGGTTTCCGTGGTAACCAGTATCTGCTAGAGGAGGGCGAGTATCATGATTGGCGGGTGTGGGGCGGAGTCAACTCTGAGCTGCGCTCCGTCAGAGTCATTCAGTCGG[T/G]AAGAAACATCTACACTCAGCACATACACGCATTTCAGCAGCCATCAGGGGGACATCTTAAATCGTCTGCAAGTTGAATAAATACACACTCCGTTGATGTATGATTGTTAAGATTAGACAATGTTCATCAACTAATCAAATATCTGCAATCTAAGAGAAAAAAAACACACATGTTGAGAAAAATGACAAAATTTCCAAATTGCATTTTTACCAATACACGTTATTAATTATAGAATAAGTTTAATATGTGTACAGTAATACATTTACTAAACATCTTCATGCACACGGGGTTTACTTTTTTCATAAAATTATAATAATTTTGACTCATACAATTTATTTTTGGCTATTTCTACAAATATACCCATGCTACATCAGACTGGCACTGTGCATCAGGGTCATATTTATATATAAATGATGTGTATCCATTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11766

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013972	Essential Splice Site	436	702	14	19

Genomic Location (Zv9):

Chromosome 19 (position 50047204)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	48621848
GRCz11	19	48281242

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTTTCAATGGAGCTGAATCCTAATTGTGATTGTAAACCTGTGTTTATTTC[A/G]GCTGGGTGCTGTAYGGAGAAGMGAAGTTCAGCGGCAGCATGTATGTYTTA

Long Flanking Sequence:

AATAAAAGAAGGGTGAATGATTTAGTCTTCAGTTGTATTTTATTAATAAGTCAGATGTTTATGTCTGCTAACTCACCTTCATATCCTGCAGGTGCTGCTGTACTCAGAGCCGGATTTCCTCGGCTCGTGTCGGGTTTGCCATCATAACCAGGACGCTTTGCCGGAGAGTCTGATGGTGAGGTCCTGCAGGGTGGTCGGAGGAAGGTTAGTGAGCGCACTGTTTACATGCAACATATACAGTGTGTGTGTGCAAATTCAGCATGCATTCAGACTGTGTGTGTATTTATGATTACAGCTGCACAACTCATCATTTCATTCAGTCAAATCAAGGCATTATATACATGCATCATTAAACATCATCTTTGCTTGTATTTTGTTTCAAAAATTGATGTATGATTCATAAATTAAATTTACAAACCGCACTATATATTGCAGAAAAAATAAACGTTATTTTCAATGGAGCTGAATCCTAATTGTGATTGTAAACCTGTGTTTATTTC[A/G]GCTGGGTGCTGTACGGAGAAGAGAAGTTCAGCGGCAGCATGTATGTTTTATCAGAAGGAGATTATCCTAACCTGAGCAGCATGGGTTTACCAGCAGACAGCAGAGTCCGCTCCGTTAGAGCTGTTCCTGTGGTGGGTGAAGTCTCTCCTTCAGATTCACTCTGACTTTCTGGATATAATGTAAATGTGCTGGAGAAATGATGTGCTTTAACACTGGAGCTACAGGAGTGACGCTAGCTGTCATTCACTACTCTGTACCCAGTGTCAGATTGAGTCAGCTCATATTTACATTTAATGGAGCTAATAAATGGAGGGGAGGAGTTTATTAAAAAGGGAGGGGCTGATTATTGAAGGGGAGGAGCTTAATAAATAGGGAGTGGCTGATTAGTGAAGAGGAGTAAATTGTCAGGGAGGGAAAAGTGACTGATTTATAAATGGGAGTGGCTTATTATGAAGGGGAGGAGCTGATTAATGAATGGGAGGAGCTGATTAATGAAGTTG

Associated Phenotype:

Not determined