ZMP

zgc:194990

Ensembl ID:

ENSDARG00000069407

ZFIN ID:

ZDB-GENE-081022-171

Description:

hypothetical protein LOC568410 [Source:RefSeq peptide;Acc:NP_001124262]

Human Orthologues:

CTD-2611O12.2, CTD-2611O12.3, ERMAP, RFPL1, RFPL2, RFPL3, RFPL4A, RFPL4B

Human Descriptions:

erythroblast membrane-associated protein (Scianna blood group) [Source:HGNC Symbol;Acc:15743]
ret finger protein-like 1 [Source:HGNC Symbol;Acc:9977]
ret finger protein-like 2 [Source:HGNC Symbol;Acc:9979]
ret finger protein-like 3 [Source:HGNC Symbol;Acc:9980]
ret finger protein-like 4A [Source:HGNC Symbol;Acc:16449]
ret finger protein-like 4B [Source:HGNC Symbol;Acc:33264]

Mouse Orthologues:

Ermap, Rfpl4

Mouse Descriptions:

erythroblast membrane-associated protein Gene [Source:MGI Symbol;Acc:MGI:1349816]
ret finger protein-like 4 Gene [Source:MGI Symbol;Acc:MGI:2149590]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa34342	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34342

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100992	Essential Splice Site	189	410	5	9
ENSDART00000135738	Essential Splice Site	189	410	6	10

Genomic Location (Zv9):

Chromosome 8 (position 13683057)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	13128401
GRCz11	8	13166106

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGCTGTCGAGCTGCTTATAGGAGCCACTCTTGGAGAACATCTGGACAAG[G/A]TTTGATGCCTTTGGAAACATGCAAAGTCAAAATTACTGAAGTCAAAATTA

Long Flanking Sequence:

ATAGGGAGTAAATGTTCATTTTTTGGGTGAACTGACCCTTTAAGCCAGTCTTTCCACTCTTCGGGGAAGTCAACCTTCAAATGGCTAACTAATAGCTGTCACGCATTTAAACATCGATACAATTACACCATTAAATCTGTTAACACAGGTAACCTTACAAGGTAGCATTACCTTTCTAATGCCTGATCAATAATCCATGAAGTTCTCAGAGTTCCCTTTATTTTCTTAGGAGTGATTGTGTGGAACAAGATAGCGGTAAATACTGTTAGTGAAGTATCGCCTCGCTTTCTCACATAACAAACAACTCCAATGTCCGAGGCACGAAATGACACAAAAGGTCTGATTGTTGCTTGTTTCTCCAGCATGGCATCTGGCCGGGTGAGGCGGTGTTGATGATGCTGGATGACCTGGAGCTGCAATGGAAGCGAGGACTCCTGTCGCACCTGCAGTCTGCTGTCGAGCTGCTTATAGGAGCCACTCTTGGAGAACATCTGGACAAG[G/A]TTTGATGCCTTTGGAAACATGCAAAGTCAAAATTACTGAAGTCAAAATTATTAGCCCTCCTGAGAATTTTTTACTTTTTTCAAATATTTCCCAAAGTATGTTTAACAGAGCAAGGAAATTTTCACAGTATTTCTTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTATATTTCAGCTAGAGCAAAAGCAGTTTTTAATATTTAAAAAAAAAAAATTAAGGGTCAAAATTATAAGCCCCTTAATAAAGAAGGTGGTCCACTACAATATCATATTTTAAACTTTGTTTGTTGTGTAATGTAGCAGTGTGAACTTAAACAACGTCTCTGAATGTAATATGCTCAAAGTTCAAGGCAAAGAGAATTTGGCTTTTACAGAGTTAGCTTTGGCAAAGTTTGGGGACAACAAAAAAATATATCCAGGCTAGTGAGATCACAAGCGCTTCAAGTTACACACATACACCACACGCATACACCCCGCACAGAGCAGGGGCGTGGC

Associated Phenotype:

Not determined