ZMP

cldn11a

Ensembl ID:

ENSDARG00000020031

ZFIN ID:

ZDB-GENE-040718-369

Description:

claudin-11 [Source:RefSeq peptide;Acc:NP_001002624]

Human Orthologue:

CLDN11

Human Description:

claudin 11 [Source:HGNC Symbol;Acc:8514]

Mouse Orthologue:

Cldn11

Mouse Description:

claudin 11 Gene [Source:MGI Symbol;Acc:MGI:106925]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa19766	Nonsense	Available for shipment	Available now
sa45104	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa19766

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000010615	Nonsense	161	215	3	3

Genomic Location (Zv9):

Chromosome 2 (position 26146238)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26342434
GRCz11	2	25998068

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGGCCCATCACGAGAAGGGTCTGATGTCCTTTGGCTTTTCTCTGTATTCA[G/T]GATGGGTGGGGACAGCTCTCTGTCTGCTGGGAGGCTGTATAATCAGCTGC

Long Flanking Sequence:

AATAAACAGCAAAAAACATCCCAAAGCACTCAAAACATGAGGAAAATATTTAAAAATATAGTTTTGTTTTTTAATATATTTTTTTCACTTTGTTTGAGTGCCCTGGACTGATTTTTGCTGGTTGTCCTTTATTTACACCAATGGTTTCTATAAGAACCTATAATATTCATAGAATCTATACTATACTATACTATACTATATATGTATATATATATATATATATATATATTGATTGATCCAACTGGACAATTATTCTGTCGGGAGTATCTGGCCTATTTTGCTAATATTAAAATTTACTTTGTTCAGTTATCAAGGTTTCAGTCAAAATATAGTAGGAAACTCTTTATTGCTCTCTCATTTAAGTCTTAATACAACATTAATGTGTATTTAATGTTGTCTTTACTTCCTCAGCTTTCTGTGGCATCGTCTCCACTGTGTGGTTTCCCATCGGGGCCCATCACGAGAAGGGTCTGATGTCCTTTGGCTTTTCTCTGTATTCA[G/T]GATGGGTGGGGACAGCTCTCTGTCTGCTGGGAGGCTGTATAATCAGCTGCTGTTCAGTGGACAGTCCTGCTACATACACTGAAAACAACCGATTCTACTACTCCAAACAAGGCCCTGCCCACACAGGCCCCACCTCCACCAACCACGCCAAAAGCGCTCACGTCTGAGCTTCTGGATTACAGATCAGATCTGATTTCCACTCCCTTTTTTCTCTCTCTTTCTTATTTCAGCCATGTTTCTTTATAGCGGTGTCTCTTTGGATAGTAATCATAAAGCTGAACTCACTCGAAACAAGGGACAATCGCTGGTGAAGGACCTGCACTGAAGGATTTGCTGTTCAAGAAGTCTTCTACTGATTCTGCTCATACAGTGTCATTTAAAGTTGTATTTTTGTAGTAAGAAATGTTTTTACGTTGCTATATGAATACTAACAGTATTTGCCAGTGTTGTTTTTCATTCTAAACTTCTCATGTTTGTACAGCTGTATTTTCATTTCAGAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45104

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000010615	Nonsense	168	215	3	3

Genomic Location (Zv9):

Chromosome 2 (position 26146215)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	26342411
GRCz11	2	25998045

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGTCCTTTGGCTTTTCTCTGTATTCAGGATGGGTGGGGACAGCTCTCTG[T/A]CTGCTGGGAGGCTGTATAATCAGCTGCTGTTCAGTGGACAGTCCTGCTAC

Long Flanking Sequence:

AAGCACTCAAAACATGAGGAAAATATTTAAAAATATAGTTTTGTTTTTTAATATATTTTTTTCACTTTGTTTGAGTGCCCTGGACTGATTTTTGCTGGTTGTCCTTTATTTACACCAATGGTTTCTATAAGAACCTATAATATTCATAGAATCTATACTATACTATACTATACTATATATGTATATATATATATATATATATATATTGATTGATCCAACTGGACAATTATTCTGTCGGGAGTATCTGGCCTATTTTGCTAATATTAAAATTTACTTTGTTCAGTTATCAAGGTTTCAGTCAAAATATAGTAGGAAACTCTTTATTGCTCTCTCATTTAAGTCTTAATACAACATTAATGTGTATTTAATGTTGTCTTTACTTCCTCAGCTTTCTGTGGCATCGTCTCCACTGTGTGGTTTCCCATCGGGGCCCATCACGAGAAGGGTCTGATGTCCTTTGGCTTTTCTCTGTATTCAGGATGGGTGGGGACAGCTCTCTG[T/A]CTGCTGGGAGGCTGTATAATCAGCTGCTGTTCAGTGGACAGTCCTGCTACATACACTGAAAACAACCGATTCTACTACTCCAAACAAGGCCCTGCCCACACAGGCCCCACCTCCACCAACCACGCCAAAAGCGCTCACGTCTGAGCTTCTGGATTACAGATCAGATCTGATTTCCACTCCCTTTTTTCTCTCTCTTTCTTATTTCAGCCATGTTTCTTTATAGCGGTGTCTCTTTGGATAGTAATCATAAAGCTGAACTCACTCGAAACAAGGGACAATCGCTGGTGAAGGACCTGCACTGAAGGATTTGCTGTTCAAGAAGTCTTCTACTGATTCTGCTCATACAGTGTCATTTAAAGTTGTATTTTTGTAGTAAGAAATGTTTTTACGTTGCTATATGAATACTAACAGTATTTGCCAGTGTTGTTTTTCATTCTAAACTTCTCATGTTTGTACAGCTGTATTTTCATTTCAGAGCATTTCAGAATAACCGATCAGAC

Associated Phenotype:

Not determined