ZMP

ENSDARG00000075510

Ensembl ID:

Human Orthologues:

GTF2IRD2, GTF2IRD2B

Human Descriptions:

GTF2I repeat domain containing 2 [Source:HGNC Symbol;Acc:30775]
GTF2I repeat domain containing 2B [Source:HGNC Symbol;Acc:33125]

Mouse Orthologue:

Gtf2ird2

Mouse Description:

GTF2I repeat domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2149780]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa9827	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa9827

Status:

Available for shipment
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Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098919	Nonsense	176	594	2	2

Genomic Location (Zv9):

Chromosome 22 (position 27348551)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	26864025
GRCz11	22	26726477

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTATATGYCCAGCTGCAGGAGAAAGTGAAAGAATTTATTTATTTTGCTT[T/A]AGCTCTTGATGAGAGCAATGAMGTGCAGGACACGGCACWGCTGYTAATTT

Long Flanking Sequence:

GAGTGCAGGGTATTTAATCAAAAGTGGACAAGTGATTATTTTTTTTGTTTAGTGCAAAGAAGTGGCTGTTTGTCTCATCTGTCAAGAAACCGTGTCTGTGTTCAAAGAATACAATCTGCGCCGACACTATGAAACCCGCCACGGAGAGAAGTATGCAAGCTTGCAAGGCCAAATGAGAGCAGACAAAGTGTTGAAGCTAAAAGGTGTACAATCAGCTCAGCAGAGTGCATTTGTGCGCCAAACTCAGTTGAATCAGTCAGCCGTTCGAGCTAGCTTTCAGGTAGCTAAACTTATTGCAACCAGCGGTAGGCCGTTCAGTGATGGAGAGTTCGTCAGAAAATGTATGAATGCTGTTGTGGAGGAGGTGTGTCCCGATAAAAAAGTAGTCTTAAATGCGGTGAGTCTGTCAGCAAGTACAATAACCAGACGAATTGAAGAAATGGGGAATAATGTATATGCCCAGCTGCAGGAGAAAGTGAAAGAATTTATTTATTTTGCTT[T/A]AGCTCTTGATGAGAGCAATGACGTGCAGGACACGGCACAGCTGCTAATTTTTCTTTGCGGAGTTAACTCAAACTTTGAACTGTCTGAGGAGCTGGCAGCCCTACAAAGTCTAAAAGGCACAACGACAGGGGAGGATATTTTTGGTAAAGCGTGCCAAACGATGGAAGAGCTGGGTCTAGACTGGTCTAAGCTGGTCAGCATCACTACTGATGGGGCACCTAGTATAGTTGGCACATCAAGGGGACTTATAGGACACATGAACAGAGAAATGGAAGAAAGAGGTCTCACCCATCCGTTACAAGTGCACTGCCTGATTCACCAGCAAGCACTCTGCTGCAAAGTTTTAAAGTGGGAATCAATCATGAAGGTGGTGGTGTCATGTATAAACTTTATCAGAGCAAACGGACTTAAACACCAGCAGTTCCAAACCTTTCTTGCGGAGCTAGAATCTACTCACGGAGATGTGCTTTACCATACTGAAGTCCGATGGTTAAGCCGTG

Associated Phenotype:

Not determined