ZMP

zgc:66447

Ensembl ID:

ENSDARG00000025577

ZFIN ID:

ZDB-GENE-030131-4748

Description:

SLAIN motif-containing protein-like [Source:UniProtKB/Swiss-Prot;Acc:Q7SXC6]

Human Orthologue:

SLAIN2

Human Description:

SLAIN motif family, member 2 [Source:HGNC Symbol;Acc:29282]

Mouse Orthologue:

Slain2

Mouse Description:

SLAIN motif family, member 2 Gene [Source:MGI Symbol;Acc:MGI:1923241]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35649	Nonsense	Available for shipment	Available now
sa7231	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35649

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029366	Nonsense	134	585	2	9

Genomic Location (Zv9):

Chromosome 14 (position 12308784)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	11744557
GRCz11	14	12050571

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTGACACCTCCAGGGTAGAGGAGCAGGATGGGTTTCTAAGCTTACCGTG[T/A]TCTTCTGGCTCCAAACAAACCATGGGATGGTTTGTCACAAGTAACTGTGA

Long Flanking Sequence:

ATTGCAATTGATCTATCTAAAAACATGTACATTATGTTGCAGTATATATTTGATTATCGAAACACATATGTTGTCACTGTACATTCATATTGCAGGAGAATGGTGGTCCCTGATAGTGGAAGTGATATTCAGCCAGCGGATAATGGTGATACAGACAAGGTGATGTCCAATTCTGAGCCTGAACTCGACCCAAACCTGACCACTGTGGAGCTTGAGGAAGTCCGTAAACTACAGGATCTGGTGCGGCAGCTGGAGGTCCAGAATCAAACCCTTCATAACAGAAGCAGAAAACAAGTGCTTGGAGGCACCAACAATAGCAACCTCAAAGCAGGAAGTAATATTAATAACCTGCACAAAGTCATGGACACTTCTCCCGGAGCAGAGGAGGCTGGGAACTTGGAGCTCTCTCCTCCAGCAGACAGCAGTGGCAGTGAAGACATGTCTCCACTACCTGACACCTCCAGGGTAGAGGAGCAGGATGGGTTTCTAAGCTTACCGTG[T/A]TCTTCTGGCTCCAAACAAACCATGGGATGGTTTGTCACAAGTAACTGTGATTCAGGCATGCTGGGAGCAAGTGAAGCAAGTAAGGACCAGTCCGCCCTGGATGAAGTCGATGTGCTTGACTTGGAGTTATGTGCTAAAGCTGAGGATGAAGACAGTTGGTGGGTTTTATTGATCTTTATACATGCAGTTGCAGTCAGGATTATTAGTCCCCTTGAATTATTAACCACCGTTTATTTTTTACCCAATTTCTGTTTAACGGAGAGAAGATTTTTTTTGAACACATTTCTAAATGTAATAGTTTTAATTACTCATTTCTAATAACTGATGTTTTTTTTGCCATGATGACAGCACATAATATTTTACTAGATATTTTTCATGACGCTAGTATTCAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTTGGCAGGTTAGGGTAATTAAGCAAGTTAATAAATAATGATGTTCTGTAGACTCTCGAAAAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7231

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029366	Essential Splice Site	321	585	5	9

Genomic Location (Zv9):

Chromosome 14 (position 12299470)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	11735243
GRCz11	14	12041257

KASP Assay ID:

554-4487.1 (used for ordering genotyping assays)

KASP Sequence:

CTTCAGGATCTGACTGATGTTCAGATAATGGCTCGCCTGCAAGAGGAGAG[T/G]AAGTATCATTCATGAGACACAATTCTTGACTAYAAGTGTTTTTTTACTTT

Long Flanking Sequence:

TACAACTCATGAACTTGCTAACACTAAAGCACACCATTTGGTAAAGAAGCTAATACGATTAAATAAACCACAAACCACAGAGCACCCGAAAGTTGCATTAAATGCTCATCGACTTATTTGAAGCTAATTGCACAGCTTTCTTATATTTAAGACGTGTGCATTTCCCCAAGCAATATGTGTATTTTATTATTTTCCAGAAGTGTTTTACATATAGAAATTCACTATTCACTTACTGAAGGAGAAAGGACATATTGTGTGCACAGATGTGGTTAATAATCTAATTGATTTCTATTGCTTATGATCAATTATTATCATTTTTATTAGTTATTTCATGCTGACTATTGCTTTCTGTTGTTTACAGGTTACATGGGGGTTTATTCTGCTCTCAGCTCACAGTCCTCTGTTGACAGTGAATTAAGCTCTGATGAATCCATCTCCATGGGCTATAAGCTTCAGGATCTGACTGATGTTCAGATAATGGCTCGCCTGCAAGAGGAGAG[T/G]AAGTATCATTCATGAGACACAATTCTTGACTATAAGTGTTTTTTTACTTTTTAATTTTATTCTAGGACTGTGCATCAACAAGAATCTGGTGATACCATACATATCACAAGACAGAGGTTGCATGTCTTATGCAGAGGACCATATGTGTTTACTTTAATTGCTTAAAAATTAGTCGTAAATTGTGCTTAGATACTTGTGCTCAGTATCAATGAAAAAGTGCTTTCAGGATTCTTTAATCAAATTGAATGGATGCAATATAAGCTGTTATAAACATACCAAGGTCTTGACATTAGGGATGTTGTCAGCAATGACAGATGCTGGAGGCTCAATTGGGTCAGTGCTGCCTCATCAGTAAATGTTTGGTAAAACTTTACTCGGAGGGTTGTTTAGTCTTGAAACATTTATAATCATGACACGTCATGAATGTGAATGAGGTTTTATGCATGCTTATGACCTCTGTTATTAAGTATGATTGTCTCAATTATGTCATTTTAAATGCA

Associated Phenotype:

Not determined