ZMP

sla2

Ensembl ID:

ENSDARG00000020788

ZFIN ID:

ZDB-GENE-080204-98

Description:

src-like-adapter 2 [Source:RefSeq peptide;Acc:NP_001107907]

Human Orthologue:

SLA2

Human Description:

Src-like-adaptor 2 [Source:HGNC Symbol;Acc:17329]

Mouse Orthologue:

Sla2

Mouse Description:

Src-like-adaptor 2 Gene [Source:MGI Symbol;Acc:MGI:1925049]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32431	Essential Splice Site	Available for shipment	Available now
sa8830	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa32431

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000005072	Essential Splice Site	64	264	3	8
ENSDART00000134659	Essential Splice Site	64	264	4	9

The following transcripts of ENSDARG00000020788 do not overlap with this mutation:

ENSDART00000146900

Genomic Location (Zv9):

Chromosome 23 (position 14930238)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	15062171
GRCz11	23	14818248

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGGGCGACTGCGCCATTAGAGTCGGAGAACGCCTCAACATTCTGTCAGAG[T/C]AAGAGCACTGATACACAACACAACATGAGTCTGATCAGGGTTATACGTCT

Long Flanking Sequence:

ACCTCATAGATGTTTGCAGTAAAATTGTGTCAAATATGATGTTAAACTATTATGTCTACAGTCAATGTACAGGTAACTTTAAATAATGAGTTCATGTATTTACTTTATTAATAATCAGACATCAACTGTTTACATGTAACATTAGTGAATGCACTCAGTTAACAAGAACAAACTATGAACCACTTTACTTCCGTTACCGAACATCAACAAAGAATAATTAATACTGTGTAAATGTATTGTTGATGTTAGTAAATGCATCATCTTCCATGAGTTAATGTTAGTTATGGGGTTACCAATTGTCTGTGTAATCTTTATCTTAAATAAATGTTGAGATACCAATAGCTAATATGACTGACTGAAGTTGTGTGTGTGTATGTGTGTGTGTGTGTTTGTGTGTAGAAAGTATCAGATATGTGCTGGTGTCTCTGTATGACTATCCATCCAGAGGTCCGGGCGACTGCGCCATTAGAGTCGGAGAACGCCTCAACATTCTGTCAGAG[T/C]AAGAGCACTGATACACAACACAACATGAGTCTGATCAGGGTTATACGTCTGATAATATAACGTGTGTGTGTGTGTGTGTTACAGTGAGGGAGAGTGGTTTAAAGTCAGCTCATCAGCCACAGGAAACGAGAGCTACATCCCCAGCAACTACACCGCCAAACTCTACAACAGGTGAGTAATCACAATCAGACTGTTGTGCTCTTTCCAGATCATTCCTACACGTCTATGCTTTGCGTGAATTATGGGAGTTACTTCTGATTAGGGATTTTAATAAAAAAATAAAATGAAGTGTCTCTAAAAATTGGAAACGAGGGTTTCATTCTCCTCGATGCTAGCTAATCATTTAACTAATGTTATTTAGTCCCAGAACAAATGTCCAAAACCACAACAAACTGACTTAAAATTAACAGAAATTAAACAAACAAGCTTCAAATATACAGTCAAACATTAAAAGACCACTTATTACAATTGACAAGTTACTTTCGGAAACCTGAATAACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8830

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
ENSDART00000005072	Essential Splice Site	177	264	6	8
ENSDART00000134659	Essential Splice Site	177	264	7	9

The following transcripts of ENSDARG00000020788 do not overlap with this mutation:

ENSDART00000146900

Genomic Location (Zv9):

Chromosome 23 (position 14923969)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	15055902
GRCz11	23	14811979

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCCTGGACTCACCTTCAGGACCCTCTCAGACATGATCGCGCACTATTCAG[G/A]TACAGTACACACTAACACACACTTCATTGACACTTATTGSCTGGGTCATT

Long Flanking Sequence:

AAATAGCATTCTGAATACCATAGGAAAAGCACAGCAACATCCAGATCATCCTAGCAACTTGTTAACTAACATATTGATTGCCTCGAAAACAGCATAGAAACCAGCCACAACAATATAGAGAAACGTAACATTCTTAATACATTATCAGCTGCATACCAACCACCCAGAACACACTAGAAACTGCACATCTATGTATTAAATACCATTCTGAATACATTCTCAAAGCATTCACCCAGAACACCTTAAGAACAGCATAGCAACATGTTGAATACCATCCTGAACACATCAACAACTGGAAAGCAACCACCTAGAATACTCTAGCAACATTTGTCTTTATTTTCCCTCTCTAGGTAACTACACTCTGTCAGTGCGCAAAAGCGGCTCACAGGAGCGTGCATCTGTCAAACACTACCGTATCAGCTGTATCGACAACGGCTGGTTCTACATCTCTCCTGGACTCACCTTCAGGACCCTCTCAGACATGATCGCGCACTATTCAG[G/A]TACAGTACACACTAACACACACTTCATTGACACTTATTGCCTGGGTCATTGCTGGATGTGTGCATGACACTGATATAACGCAATACCAGTGGTGGACAGTGACAAAGTATTTTACTTTAGCTCAGATAAAACTCAGTGAATCTTCAGTTAGCAGCTCGCTGATACAGATGATTTGGTCTGAATGATGACGAGTCTTCCAGTTAATGACTCACTGATTCAATTAATATGGTTGGAACTAGTCTCCACTCAAGTTAATGATATACAGATTAAAATAATTCAACCAAAGTTAGTCTTCTAGTTAATGATTCAATGATTCAATCAATTCGGTAAGAACGAGTCTTCACTCCAGTTAATGACTCCCCGATTCAATCTATTTGGTAAGAGTTAGTCTTCCAGTTAATGACTCACTGATTCAATCAATTTGGTAGGAGCGAGTCTTCACTCCAGTTAATGACTCACTGATTCAATCTATTCAGTAAGAGCGAGTCTTCCAGTATATG

Associated Phenotype:

Not determined