ZMP

si:dkey-98f17.3

Ensembl ID:

ENSDARG00000076137

ZFIN ID:

ZDB-GENE-060526-352

Description:

novel protein similar to human claudin 22 (CLDN22) [Source:RefSeq peptide;Acc:NP_001116178]

Human Orthologues:

CLDN22, CLDN24, CLDN25

Human Descriptions:

claudin 22 [Source:HGNC Symbol;Acc:2044]
claudin 24 [Source:HGNC Symbol;Acc:37200]
claudin 25 [Source:HGNC Symbol;Acc:37218]

Mouse Orthologues:

AC160137.1, Cldn22, Cldn24

Mouse Descriptions:

claudin 22 Gene [Source:MGI Symbol;Acc:MGI:1922927]
claudin 24 Gene [Source:MGI Symbol;Acc:MGI:3712484]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa7557	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7557

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 > T

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099749	Missense	26	220	1	1

Genomic Location (Zv9):

Chromosome 5 (position 13916191)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	12213628
GRCz11	5	12713845

KASP Assay ID:

554-4013.1 (used for ordering genotyping assays)

KASP Sequence:

TMCAGAGGRCTTCGCTCTTTGTGTCCTTCGGAGGTTTGGTCACAACGTTC[G/T]TCACAACCTTCTTGCCYCTATGGAAGACGATGAACTCCGATTTGAATGAA

Long Flanking Sequence:

TATTCAAATAAATCAAAAAAGGAATTGGAGTATTAATCATGTACGTATAATATATATCTTCCTTTATGGTCAACAGAAGAAACTCGAGTGAAGAGTGAATAATAATGGAAGGAATTTTATTGCCATTTAACTACTAAACAGATTTCTGTTTCCCCTCGATCTCAAAAAAGTCCAACCACACTCTGTTCAGGCTTCGTACGTCCAGACTTAAAACTAGACGTATCGTATTTCCTCTCAAAAAAGCAGTTATTGTCCTCGGCGAAGATATTCATCAGTTTGAAAAACAGTCCTGCCGTTGTGAAGGGCTCCAAGATTATCCAGCAGGAACAGGTGGGTTTTTATTAAAGCAAAGGAGGAGCCAGACGAAAACCAGAAGAGCTGAAAATCTCAGATGGACAGACAGACAAAATCAGACGAGAGGTAATATGGTGCTGTTCACCACCAAGTTTGTCCAGAGGGCTTCGCTCTTTGTGTCCTTCGGAGGTTTGGTCACAACGTTC[G/T]TCACAACCTTCTTGCCCCTATGGAAGACGATGAACTCCGATTTGAATGAAATGGAGAACTGGTACGAGGGTCTCTGGCACATGTGTATCTACACGGAGGAAGTTGGCATCCATTGCAAAGCCTTTGATTCTTTCTTAGCTCTTCCGCCGGACACTTTCGCTGGCCGGGTTCTCATGTGCATTTCCATCGCCACTGGAATTCTCGGTGTGGCGGCTGCTTTTTTCGGACTCCGCGGAGTTGAGATTGGCGCCAGTCGAGAGAGGATGAAGAGGAATCTGCTGATCCTCGGGGGAGTTTTTGTAGTTGTGTCTGGAGTCACGACTCTTGCGGCTGTTTCATTTATGGCGTATGTTATGGTTGTGAAATTCTGGGATGATGATCGTCCTGAAGTCATGCCCGGATGGGAGTATGGAGAAGCCATGTTTTCTGCCTGGTTTGCTGGACTTCTGTTAGTTGTCGGAGGGAGTTTTTTGTTTGTTGCAGTCTGCATGGGCGATCAT

Associated Phenotype:

Not determined