ZMP

LOC563270

Ensembl ID:

ENSDARG00000055288

Human Orthologue:

SLMO1

Human Description:

slowmo homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:24639]

Mouse Orthologue:

Slmo1

Mouse Description:

slowmo homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2442865]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42724	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa10437	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa42724

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000077611	Essential Splice Site	11	175	1	6

Genomic Location (Zv9):

Chromosome 16 (position 27524718)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	25370405
GRCz11	16	25285437

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATAAACTGTGGCAAACATGAAGATTTGGAGCACGGAACACATATTCAG[G/A]TAGGCAAAGCCGCGTTTGGGATGAGTTGAGCGCGCGCGTGCACAGATTCC

Long Flanking Sequence:

TTTATTGAGTCATTCTGGCGAGCTGTTACCGCAACCTTTAATAATATGTAAATAATAACAACAACATATCAGAAAAAAACTTTTAAATATGTGCCTATCGATAAATTTATTGGCAACACATATTTTAAAGCACGTCGTTTATCAAATGAAATGTGAGATTAGTTTATATAGTCTTATAAATACAGACGCACGTTTGAACGAATTAAATCTTATTTACTAACTATAACATCGCCTTTGCTCGTTTGTAGCGCAACACTGATATTTCAAGCCCTCTCCAAGCGTCAGAGGCTCAGAGCTCGATCTCTATTGGCTCAGTTGGCAGTTGCTTTTGGGAAAGGGAGGATCCGCTGCACTTGATGAGATGAGGAGCATCCCAGAGCCGGTAAAATGGGAGCGGAGCTTGAAAATATGATTGTATGAGATGTACAGTCCACAGTTGTCTGGAGGCACGTATAAACTGTGGCAAACATGAAGATTTGGAGCACGGAACACATATTCAG[G/A]TAGGCAAAGCCGCGTTTGGGATGAGTTGAGCGCGCGCGTGCACAGATTCCAGCATCCTCTCTGTCGTTGCACCCCGTTTCGTTTTAGCTCTTGGAACGGGAAAGTCACATAATTTATTTAGACATTTTTTATATGTTTTTAACTATTAATTTCTATATGCTTGTAGATAACTCATTTTTCAACAATAGAGGTGAATAAGCATTTATTTGGGCCTAGCCGGTTGCTTTTCTGTCACATCTCTGCGCAGTGCACGACTGCTACTCATCATCACGCCTTTTAAAGGGATAGTTCAACCCCTTACACAGAAAACTCACCATGTACTGATCCTCAAGTCAAGTGGATCTGAAGAATTTTGAACCAGTTAACATTCACACCCATAGTATTCGGGGGAAAAAACAAACACAATGGAAAGCGATGGCTACCAGTTTCCAACAATCATTATAATATCTTCTTTTGTGTTCAACAGAAGAAAGCAGTTCAAACAGCTTGTGACTGAAGGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa10437

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000077611	Nonsense	103	175	4	6

Genomic Location (Zv9):

Chromosome 16 (position 27520483)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	25366170
GRCz11	16	25281202

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTAAACTGRACTAAATACATCTCTTTCCCTTCAGATAACCCTAACCAATT[T/A]AATATCAGTTGATGAAAGGCTTGTCTACAGGCCTCATCCAGACAATCCAG

Long Flanking Sequence:

GTACTTGAGTAGAGTAAGGATGTAGAATAAGATCATACTTTATAACTATTAATAAACAGTTAATAACATAATCATAATAACAAAATAATAGTCAACATGAAATAAGCCTGTAGTTAATAGTGGGAATTAGTACATATAGTAAAGTGTTACCAAATTTTCATTATAAACATTGTAATGGTGTTAAAAAGTCTTATTCGTTGACTTTCATCTACCTGGTTCTTTAAAAAGGCACCACTTACACAACTTATCTTAAATCTTTTTTTCTTTTCTTAGATTTTAGGGACAAGTCGAACTGTCACGTATGTAAAAGAACATTCTATTGTCGACCCCGAAGAAAAAAAAATGGAGCTTTGCTCAACAAACGTAAGTGTTTGCTTAGCTATTGACAACTGCAACAACTGTTATTGCAAAACAAATCTATGTTGTTTGATTACCGGAAAGTGCTTAATTTTAAACTGGACTAAATACATCTCTTTCCCTTCAGATAACCCTAACCAATT[T/A]AATATCAGTTGATGAAAGGCTTGTCTACAGGCCTCATCCAGACAATCCAGAAGTGTAAGTAAAGGATCATTTTATTACATTTATATGAATACACATAGAGTATAAATTGGCGCCAAGCCTAGGACAAATTGATATGTCACTCTTGATGTTTAAGCATTCTGCATAGTTGTGGTTGGAGATTGTATAACGTTTAGTATGTAAGTATAGTCTGTTCTAATGGTCTAATTTAAGTTGTTCGATCAATAAAGGCAAATATCTGCTCATCCCTTTTGGCCACTACTGTAAAGCCAACAAATAATATATCAATAAGTTCAATACCACATTGAAATGATGTTTGTTGTACTTTTTCAGCACTGTATTAACCCAGGAAGCAATCATCACGGTGAAGGGTGTCAGTCTGAGCAGCTACCTTGAAGGACTGATGGCTTTAACTATGTCAGCCAATGCAAGAAAGGTAGACTGCTGTTTTACTGGCAATTGTGGTTTCCAGAAGGATTGTA

Associated Phenotype:

Not determined