ZMP

A9JR91_DANRE

Ensembl ID:

Description:

Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A9JR91]

Human Orthologues:

EPB42, TGM2, TGM3, TGM5, TGM6, TGM7

Human Descriptions:

erythrocyte membrane protein band 4.2 [Source:HGNC Symbol;Acc:3381]
transglutaminase 2 (C polypeptide, protein-glutamine-gamma-glutamyltransferase) [Source:HGNC Symbol;
transglutaminase 3 (E polypeptide, protein-glutamine-gamma-glutamyltransferase) [Source:HGNC Symbol;
transglutaminase 5 [Source:HGNC Symbol;Acc:11781]
transglutaminase 6 [Source:HGNC Symbol;Acc:16255]
transglutaminase 7 [Source:HGNC Symbol;Acc:30790]

Mouse Orthologues:

Epb4.2, Tgm2, Tgm3, Tgm5, Tgm6, Tgm7

Mouse Descriptions:

erythrocyte protein band 4.2 Gene [Source:MGI Symbol;Acc:MGI:95402]
transglutaminase 2, C polypeptide Gene [Source:MGI Symbol;Acc:MGI:98731]
transglutaminase 3, E polypeptide Gene [Source:MGI Symbol;Acc:MGI:98732]
transglutaminase 5 Gene [Source:MGI Symbol;Acc:MGI:1921426]
transglutaminase 6 Gene [Source:MGI Symbol;Acc:MGI:3044321]
transglutaminase 7 Gene [Source:MGI Symbol;Acc:MGI:2151164]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa44381	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44381

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:

A > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109821	Essential Splice Site	77	699	3	15

Genomic Location (Zv9):

Chromosome Zv9_scaffold3522 (position 26494)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	2026859
GRCz11	6	2160525

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAACAATTGAATAATTAGTATGTGTATAATGTGTTTGTGCTGTGGTGTGC[A/C]GGTCCCCTGTCAGTGGAGGTGCCCGTCTCCTCATATGGACAGCCGTCTTC

Long Flanking Sequence:

GCTCCAGCACAGGACGGACGGTCTGAGCTCCGGCTCTCTGGTAGTGCGGAGAGGACAACCATTCACTGTGACAATCAACTATGCCGGACGACCATACGACCCACTGCGGGAAAAACTACAGTTCATATTCATTCTAGGTGTGTCTGTGTGTAATAATAACCCAACTTTCACAACACTCTCCCTGCATTAATCATCAGTACGCCTCTAATCAAGTCAGATCCAGAGTAACACTTTCACTACAAGATATTAAATCAAATTATATATTTATTAATTATATTATAAATTCTATCTTTAAAAATAAATGTATTAATTTAAATGTAAGATTTGTGTGTTTGAACTATATATATTTACACTGTCCTACTTATATTATACTTCTTGTCAACAAAATAGGTTTGATGCGCCTCGCGTTCTCAGAACAGCACATTAGGTCTATAAATATATATATTTTATAAACAATTGAATAATTAGTATGTGTATAATGTGTTTGTGCTGTGGTGTGC[A/C]GGTCCCCTGTCAGTGGAGGTGCCCGTCTCCTCATATGGACAGCCGTCTTCATCAAAGTGGTCTGCAGTTCTGGAGCGCGGTTTACCAAACCCCAGTGGCTCTCGAGCTCTGACTGTGTCACTAAGCAGCCCTGCGTCCTCCTCTATAGGAGTGTACACACTCCAACTGACAGTCCAGACTCGCTCCAGCACCAAAACACATCTACTGGGCCAGTTCACACTCCTCGCCAACCCCTGGTGCCAAGGTGAGCTGAAGAGACAAATACAGAGGGACAGTTCATGCAAAAATGGAGATTCTGTCATCATTTACCCATCTTGTACTGTCAACACTAATACGGTTTTGTTTAAAAAAATGCACATTTTTCTTTCCATTTTAGCCTTCCGTCTGTGCAGTTAATGGATCAAGGTGTTCATTTCTTGAACTTATCATAGGATTTTCATCAGAATTTTTTACTAACTATATACCTATTTTTATCTCTTTTTTGAGTGAATTTAAAGGGC

Associated Phenotype:

Not determined