ZMP

hm:zehs0001

Ensembl ID:

ENSDARG00000002084

ZFIN IDs:

ZDB-GENE-030131-169, ZDB-GENE-030131-169, ZDB-GENE-081030-4

Description:

Novel protein similar to vertebrate laminin, beta 2 (Laminin S) (LAMB2) [Source:UniProtKB/TrEMBL;Acc

Human Orthologue:

LAMB2

Human Description:

laminin, beta 2 (laminin S) [Source:HGNC Symbol;Acc:6487]

Mouse Orthologue:

Lamb2

Mouse Description:

laminin, beta 2 Gene [Source:MGI Symbol;Acc:MGI:99916]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10763	Essential Splice Site	Available for shipment	Available now
sa43957	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10763

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012166	Essential Splice Site	330	1782	9	33
ENSDART00000147326	Essential Splice Site	330	1782	10	34

Genomic Location (Zv9):

Chromosome 23 (position 20502053)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	20287160
GRCz11	23	20213503

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATAGTGGCATAAATCTCTGATRTCATRGCTAATATATTTCTGTTTTTCCC[A/C]GAATGCAACTGTAATGGTCACTCCAACCAGTGTCATTTTGACATGGCGGT

Long Flanking Sequence:

AGCTGAAGATCACAAATCTTCGCCTGAATCTTACCAAGCTGCACACTCTGGGTGACAATCTGCTGGACTCACGGCCTGAGATCAAGGAGAAATACTACTATGCCATGTATGAGCTGGTCGTCAGGGGCAACTGCTTCTGCTATGGCCACGCCTCTGAGTGTGCGCCAATTGAGGGCATCAGGGATGACATTGAAGGCATGGTAAGTTAAGGAGTTGCTGGATAATTTTTTGTACCAAAATAGAGAAGTTGGTTAATATTACAAGAAACGCTGACGTTCAGCATTTTCATTCTTAGGTTCACGGGAGGTGTGTGTGCAAACACAACACTAAAGGACTGAACTGTGAACAGTGTGACGACTTCTACAATGATCTGCCCTGGAGACCAGCAGAAGGCCGGAACACTAATGCCTGCAAGAGTAATTATAGATTCTAATATAGATCACACCATACATAGTGGCATAAATCTCTGATATCATAGCTAATATATTTCTGTTTTTCCC[A/C]GAATGCAACTGTAATGGTCACTCCAACCAGTGTCATTTTGACATGGCGGTGTATTTGGCAACGGGGAACATCAGTGGAGGTGTGTGTGACAACTGCCTTCACAACACCATGGGCAGCAACTGTGAGAGCTGTAAACCTTTCTACTACCAGGATCCAACTAGAGATATTAGAGACCCTGGAGTCTGTGTAGGTAAGTGTGACTACTCACTTACTATCTTTCGGCTTAATCCCTGATTTATCGAGATATTTCCAGCTGCAGACCTACACACACACAATCTAGCACACACGTTCTAGGCAACCTCCTATTTGGTTAATGACAGATCAGTCTTGTTCTAATTTGTCTTGTATAACGACGACTAACTGCTTGGGAGCATTATCGCCACCTACTGAATTACACAAGTATGGCGATCAAGACCGCCCGTGCTATGATTGCCATTCATTAGACTGTGAACAGACTCCCATTTTAGGTATTATTTCATTATTACAGTATATCGCATCAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43957

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000012166	Nonsense	394	1782	10	33
ENSDART00000147326	Nonsense	394	1782	11	34

Genomic Location (Zv9):

Chromosome 23 (position 20500759)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	20285866
GRCz11	23	20212209

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCACTGGGGTATAATAAACAATTGGTTTTTGTCTGCCCTTTGTTAGCTTG[C/A]GATTGTGACCCAGATGGCTCTAAGAACGGTGGTGTTTGTGACGGCCATGA

Long Flanking Sequence:

GGGTACAATAAATTAAGTAAAAAATATATTTTTTGCTATTTAAATTTATTTATTGCAATTTCTCCTGGAGTTTCATTGGAGAACTGTGGAAAAAAATTGAAAACACTTCAGTCTATTTTATTTATCGGAAACAATTTTTCCCATTCGCCCATCACAATCACCATATTTGTAAAATAGTATACATTATTGATTATTGTGTACAATATTTATTTACAATATATATAAAATATATTGATGACGATGTCCGAGAAGACGTTAATAACATTAATATGCATTGTGACCATATATGGTTTGCCTAGATTGTGTGTGCTGGATTGTGTGTGCCTGAAACAAGTGTGGGTCTGCGGGTCTGCAGCTGGATATTATTGGATTTATCAGGGGTCACCACAATGGAACAAACCACTAAATACATATGTTTTACACGGCGGTTGCCCTTCCAGCTGCAACCCAGCACTGGGGTATAATAAACAATTGGTTTTTGTCTGCCCTTTGTTAGCTTG[C/A]GATTGTGACCCAGATGGCTCTAAGAACGGTGGTGTTTGTGACGGCCATGATGACCCTTCTCTGGGCATGATTGCTGGACAGTGCCGCTGTAAAGACAATGTTGAAGGTTCACGCTGTGATAAATGCAAGCCTGGTTTCTTTGGCCTGAGTGCTAGTGATCCACGTGGTTGTCAACGTAAGTACAAGCCTTAAAAACTCTTAAATTCACTGAAATAATTGTGTTGTAGGTCTTGAATAATTTTAAACAGGTCTTAATTTTCTTACCCATTTGGGCCGACATGCATCCAATCACAATCCATTTGGCCCAAAAGCCAACAAACATATAAAAAATAGTATAATAAAAATATAGTATAATAGTATAATAAAAATAGTGTATACAACTAGGTTTATTTATTTATTTATTTTTTTTGTGGCAAGCAAAAAAAAAAATCCATTGGCCCAATCGGGCCATTAGAAATAACCATTAGTGTTTAGCCCTGTATAAGTCAAAAATTTAATTC

Associated Phenotype:

Not determined