ZMP

si:dkey-18p12.4

Ensembl ID:

ENSDARG00000079703

ZFIN ID:

ZDB-GENE-070912-408

Description:

hypothetical protein LOC794946 [Source:RefSeq peptide;Acc:NP_001116179]

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
sa34673	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34673

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112827	Nonsense	299	435	11	11

The following transcripts of ENSDARG00000079703 do not overlap with this mutation:

ENSDART00000141565

Genomic Location (Zv9):

Chromosome 9 (position 31425395)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	30581341
GRCz11	9	30392087

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAAGTCTAAAAAATATACCGGTCTCGATAACTGGGAAGGATTTCAAAGG[A/T]AGAAATGTAGGTTTGATGGCTGGGCGTGTGTTCAAGCTAAAGAGGGTTAC

Long Flanking Sequence:

TTTTCATGCTGGTAAATGTCTGACTCTGAATAATAACGAAGTGCACTCAATTATATGTTTAAAAGCTTGTCAAATGTGTTTTCTTGTCGTCTTTTCTCCTCATCTGTAGCTGGATTATGTATTCCTAAACCAGGTATTTTATTTAGATTCACTAACAACAAAAATAAGAAGAAAATGTTTCATCTTAAGAAAATTAAGTGGTCAGTCATCTTCTGACATATACAGTTTAATAATATTTTCATTTCTGCAGTTTGGAATTGGATTACAACATCAACAGGTAAAGCACCTCTGACTTAATTAAAGCTTTCATACAAGTGCAAATGTATTATAAACAGTTCAAGATTCAGAACTTAAGTACATTTTTTATTTTTTTATTTTTTGTAGATGTTGTTGTTCTAGATCCTAACACAGCCAACCCAGAACTCCTGGTCTCTGACGATGGAAAATATTTGAAGTCTAAAAAATATACCGGTCTCGATAACTGGGAAGGATTTCAAAGG[A/T]AGAAATGTAGGTTTGATGGCTGGGCGTGTGTTCAAGCTAAAGAGGGTTACAGCACAGGTCGTCATTACTGGGAGGTGGGTGTAAAAAAGAAACATGAGTGGCGAGTGGGAGTCGTGAAGGAATCTGCTCCTCGTAATGGATATGTCAACATGAACACAAAAGCAGGATACTGGAATCTGCGTCTGCAGCTGGGAACTGTGATGGCTTTGACTGAACCCGTTACTAAACTCAACGTGCAGTCTCCGTCCAAGATTGGAGTTTATCTAGATATAGAAGAAGGCCACGTCTCCTTTTATGATGCAGAAAAACAAAGACATATCTACACATTTAACACAGACTTTAATGAGACTGAAAACATTTACCCAATGTTTGGCACTGTCGAGACAGACAGGGCATTGGTCATTTTATCATAAAATGTATAGACGAATTACCATGTTTGTAAACATTCAGGATGTGCGCGCAGCGGGGTGGCAGAAAAAAAAACGGGAGCACTAGCATTT

Associated Phenotype:

Not determined