ZMP

si:dkey-189l3.1

Ensembl ID:

ENSDARG00000070467

ZFIN ID:

ZDB-GENE-061207-53

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:A2CF06]

Human Orthologue:

LACTBL1

Human Description:

lactamase, beta-like 1 [Source:HGNC Symbol;Acc:35445]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13718	Essential Splice Site	Available for shipment	Available now
sa7351	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13718

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103450	Essential Splice Site	48	653	None	8
ENSDART00000136061	Essential Splice Site	None	71	None	3

Genomic Location (Zv9):

Chromosome 11 (position 29033778)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	27909764
GRCz11	11	28156938

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACTCTTTCAACCATCAACGAAGAAAAGCGTTCCTAAACCAAACTAACAGG[T/A]AAGTTCATGWTAAAATAGATGYGTTTCTTGTGTTTTTGGTTCATGCGTTT

Long Flanking Sequence:

TTATTTTAATTTTATAGGATCTTTAAAGAGTTACTTTATAAAAGGTGTAATGTTTTATATGCAAAACTGAAGATTTTGCAAAGGTATAACAATTTACTTTCATAAAATATGCAGAACCTTATGTTGCAAATATAGTGTCATTGCTTTAGATACAAATATCTTGCATCTTGGTTTCATATTTGCAATATGTTTATGGCACTTTAAATTACAAAAGCCTGGCTACTAAAAAAAGCTTCCTTGTCTCTTAGGCCATATAGTGACACTCCTGTGTAACACTAGTGCTCAATCATCACTCTGCCTATTCTCCAGTGTTGACAGATGTTGCAGATGGCAGATAATCCAGAATCTTGGGTCTGATGCAAGCTGGATTTACCCATGGCCATGATACCAACATCTGTCGTGACTTCACAGTAAGCTACCCGAACACGAAAGAGCGTGCAGTGTGTGAATACTCTTTCAACCATCAACGAAGAAAAGCGTTCCTAAACCAAACTAACAGG[T/A]AAGTTCATGTTAAAATAGATGCGTTTCTTGTGTTTTTGGTTCATGCGTTTATATTAGACGAAATTATGTTTGGATATCAGTCATATTGTAGCCTACAGTACATGTGAATGCCAGTGCAGTGTACTGAACGTAACTGCTGTATTCGATTGTAAGTAAATTCTGCAGTGGAAAATGATACAAAAATGAGACAAAAATGTAACTTTCTCAGTTTAAAATGAAAGGACACAACGTGATGCAGAGAGAAAATGGACTAGCATTACTGAAGCCAGGGAAAAGCAAAGTCCATTTAATCTCACTAATACCCTGGATTCATATAGAATGCTTCATAACTGGATGAATTTTGCACTGGAGTATTGCACTTATGGAAAATGCTTTATTCCTTTACTTTTGCATGTCTTTTTTTCATAAAGCAGATGATGTTTTCTTTTTTCCTGGTAAAAATATGAGACATTTTTTGCTCATAAAAACGTTATATGGTTTATGCATTTGGATCCTGTTTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7351

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:

A > T

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103450	Missense	310	653	7	8
ENSDART00000136061	None	None	71	None	3

Genomic Location (Zv9):

Chromosome 11 (position 29008947)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	27884933
GRCz11	11	28132107

KASP Assay ID:

554-4073.1 (used for ordering genotyping assays)

KASP Sequence:

TCTACCTCGAAGACTCCGTGGGACTAACTTACTGTGGAAAGGCAAGACCA[A/T]GACTGCAATCAACCTCCTACAAGATGATGTGCTCGTAGCAGATCCGGGGA

Long Flanking Sequence:

TTTAAAATCCTCAATATCAGCTAAATTAGAAAAAGAAACACATTTCTGAAAGATATCAAAGGTTGTTATATCTGTTGTTTTGTTATTTCTAAACCTATGATAACCTTCTACAAAGGTCTATGCTAATATGTTGAACCACTTTTTTCACAAAGATTTTACAGTTTATGATGACATTCAGATTCACAATGACCTAAAGAATCGATAGATCATAGAATCAAGATCATGATTTCCTGACAAACTGTTTTCAAGCCACTTCCTTGTTGAAAGTTTGGTTTTCTGAACATTTATGCATAATTTGTTTGCTTTGACTTGTTTAAAAAAAGATCAATTTCCCTAAGCTGCAAACTTTCATATGACTAAAACAAATAGCTTTTTAAATGAGCAATAACATTCCTTTGGGCATAAAAACAACCTAATTATTCATTACTCTCCTACTGGATTGTCCCCAGGTCTACCTCGAAGACTCCGTGGGACTAACTTACTGTGGAAAGGCAAGACCA[A/T]GACTGCAATCAACCTCCTACAAGATGATGTGCTCGTAGCAGATCCGGGGACCAAGTACGTTTCTGCCAAATTTATTTTAGCTGGTTATCTGTTCTTGCCAGATACTTTAAATTATCCTTATCTCATGTATGCCCCATTGAAAAGCTTATAGACCATGATGATGATGATAATAGATTTTTTACTGTCTCTTAATAACATTCCTTTAAGGTACATTTGAGAAAAGAAGGGTAAAGTTTTATTTGGATGGTCTCTTTAAAGTGTCTCAAATGTGCATTATAAAATGTCATAGTTGGTTTTGGTGGTCCCCAACAATGGCCTGATATGCATACAAGGTCAAAAACACTTTCATAGTCTTAATACGCATTTATTTTTACCTAATTATCTCAACAACTGACATATGAATTGTTTAGCGATTCATTTCAAAACCCAAACCCCTCCTTTGTGGGATGCTAATTAGCAATGATTGGTCTGATGAGATCTGTTGTGATTGGTCGACTGTG

Associated Phenotype:

Not determined