ZMP

tmem22

Ensembl ID:

ENSDARG00000045447

ZFIN ID:

ZDB-GENE-050320-142

Description:

transmembrane protein 22 [Source:RefSeq peptide;Acc:NP_001013581]

Human Orthologue:

TMEM22

Human Description:

transmembrane protein 22 [Source:HGNC Symbol;Acc:28480]

Mouse Orthologue:

Tmem22

Mouse Description:

transmembrane protein 22 Gene [Source:MGI Symbol;Acc:MGI:2685365]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37809	Nonsense	Available for shipment	Available now
sa37808	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37809

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000066839	Nonsense	220	413	2	2

Genomic Location (Zv9):

Chromosome 24 (position 3492408)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	3382901
GRCz11	24	3414688

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTTTAGCGCAGTTCTGGCCTTTTTGCTTCTCGACGAACGCCTTGGTTA[T/A]ACTGATGTAGTGACTGTCGTCGGCAGCCTTTTCGGACTTTGTCTTGTAAT

Long Flanking Sequence:

AACAACCCCAGCAAGAGACTGGTGTCGGAGAGTGGTGGCAGGACTTTATTCGGCACTATGGATTCCCGTCCCAAAGCTGATCAGAAAGATAAAGGAGTGGGCAGCCAATTGGCCAGCTTCGGCGAAGCCAATGTGCTAGCTTCACGGGTCACCTGGGGTGCACTTTTTGGGGCGGCCATTGCTCATGGATGCGTAGCGCTCATCACACGCCTAGCAGCCGACCGCTCTAAAGTGCCCTCATTAGAGCTCATCTTCATCCGCTCCGTCATACAGGTGTTGTCAGTATTGGTGGTCCTCTACTATAAAGAGGCTCCCTTTGGGCCCAAGGGCTACCGACTGCGCTTGTTCTTCTACGGGGTTTGCAATGTCATCTCCATCACTTGTGCTTACACGTCCTTCGCGATTGTTCCACCCAGTAACGGCACCATCATGTGGCGGGCGACCACCACTGTCTTTAGCGCAGTTCTGGCCTTTTTGCTTCTCGACGAACGCCTTGGTTA[T/A]ACTGATGTAGTGACTGTCGTCGGCAGCCTTTTCGGACTTTGTCTTGTAATGATCCCGAACATCGCCGATGAGGAGAAATCTGCTTTGGGATTCTGGAAGGAAGCCTTTGGGTACACTATGACTGTAATGGCAGGTCTAACCGCCGCGCTGTCTATGATCGTGTACCGTGCCATTAAAGAGCGCGTCAGCATGTGGACGGCGCTCTTCACTTTCGGGTGGACCGGGACCGTTTGGGGAGCCTCCACCATGTTCATCATGCAAGAACCCATCATTCCTTTGGATGGCGAAACGTGGGGTTACCTAACAGGAATCTGCATATGCTCCACCGTTGCGTTTCTTGGCGTCTACTACGCCCTCAACAAGTTCCACCCGGCCTTGGTCAGCACCGTACAGCATCTGGAGATCGTGGTGGCCATGTTTCTTCAGCTTATCGTGCTGCGAATGATCCCGTCGGTGTATGACGTCTTTGGGGCGCTGGTTATCATGGTCAGCGTGTTCGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37808

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
ENSDART00000066839	Nonsense	337	413	2	2

Genomic Location (Zv9):

Chromosome 24 (position 3492057)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	3382550
GRCz11	24	3414337

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTAACAGGAATCTGCATATGCTCCACCGTTGCGTTTCTTGGCGTCTACTA[C/A]GCCCTCAACAAGTTCCACCCGGCCTTGGTCAGCACCGTACAGCATCTGGA

Long Flanking Sequence:

TACGGGGTTTGCAATGTCATCTCCATCACTTGTGCTTACACGTCCTTCGCGATTGTTCCACCCAGTAACGGCACCATCATGTGGCGGGCGACCACCACTGTCTTTAGCGCAGTTCTGGCCTTTTTGCTTCTCGACGAACGCCTTGGTTATACTGATGTAGTGACTGTCGTCGGCAGCCTTTTCGGACTTTGTCTTGTAATGATCCCGAACATCGCCGATGAGGAGAAATCTGCTTTGGGATTCTGGAAGGAAGCCTTTGGGTACACTATGACTGTAATGGCAGGTCTAACCGCCGCGCTGTCTATGATCGTGTACCGTGCCATTAAAGAGCGCGTCAGCATGTGGACGGCGCTCTTCACTTTCGGGTGGACCGGGACCGTTTGGGGAGCCTCCACCATGTTCATCATGCAAGAACCCATCATTCCTTTGGATGGCGAAACGTGGGGTTACCTAACAGGAATCTGCATATGCTCCACCGTTGCGTTTCTTGGCGTCTACTA[C/A]GCCCTCAACAAGTTCCACCCGGCCTTGGTCAGCACCGTACAGCATCTGGAGATCGTGGTGGCCATGTTTCTTCAGCTTATCGTGCTGCGAATGATCCCGTCGGTGTATGACGTCTTTGGGGCGCTGGTTATCATGGTCAGCGTGTTCGTCCTGACGGGTCTCAAGCTTTACAGGGTGAGCCGAGCCATAAGACAAGACTACCAGGAGATTCTGGACTCGCCCATTAAATGAACGCCGCAGATGTGTGTGGTTTTTTTGAGCGCATGAGGGGGCATGTATATGTGTGTCTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGCAGTGTTTCCCAGCCCCTCTTCTCTTACTAATGTGTGCAATCACTGAATGTCTGGATCTTCGGCATTTGTTTCCAATCGTGTCGTTGGAAGAGTGCCAATCGGTGTAATGTCTTTGCTAACTGTTGATGTGTGAAAATAAAAACGGTGATCCATAGAGCCCCCCTCTGATAGCA

Associated Phenotype:

Not determined