ZMP

btr05

Ensembl ID:

ENSDARG00000074813

ZFIN ID:

ZDB-GENE-080219-8

Description:

Zgc:172119 protein [Source:UniProtKB/TrEMBL;Acc:A8WG13]

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 are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6075	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa2361	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa6075

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
ENSDART00000076300	Essential Splice Site	240	505	4	8

Genomic Location (Zv9):

Chromosome 7 (position 16967921)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	15950619
GRCz11	7	16202592

KASP Assay ID:

554-3754.1 (used for ordering genotyping assays)

KASP Sequence:

ACAGAAACAAGAAGATTCGAGACATCAAACACTTGGCAGAACTCAGAAAA[G/A]TGAGCTCAAGATATTCAATACTTAATAGATGGTGTTTAGATTTCTCGAAA

Long Flanking Sequence:

GTTGACTGTGCGAATATCTGAGGTTCTCTGTGACATCTGTGATGGGAGAAAGATGAAAGCTTTGAAGTCCTGTTTGACATGTCAGACTTCTTACTGTGAAACTCACTTAGAGCCTCATCGAAGAGTCCCGAACTTCAAGAAACACAAACTAATAGAGCCTGTGAAGAATATAAAGGACTACATATGCCAGAAACACGAGAGACCTCTGGAGCTGTTCTGTAGAGATGATCAGATGTGTGTTTGTGTGTTTTGCACTGATGGAGACCACAAGACTCACAACACTGTTCCTCTAGAGGAGGAGAGTAAAGTGAAAAAGGTGAGAGATACTGATAAAAATGTAACTTTTTTTCTTCAAAGCAAAGTTCTCATTGGGTGATCAAATGTGTTCGTGTTTCCTTCTGTAGACTCAGCTGATAGAAACTCAGAAAGACATGCAGAAGATGATTCAGGACAGAAACAAGAAGATTCGAGACATCAAACACTTGGCAGAACTCAGAAAA[G/A]TGAGCTCAAGATATTCAATACTTAATAGATGGTGTTTAGATTTCTCGAAAAGTAATTTCACTGTATATTTCAGAAGCAGGATGAAAAGCTGATTCAAGAGCTGCAGCAGGAAATCAATGAACTGAAGATAAGAAACTCAGAGCTGGATCATCTCTCACACACTAAGGATCACCTTCAGCTCCTACAGGTCAGTGACTTTCTATCTGTTCACATCACAGGACAACACTCAGACTCCTCCAGCTGAATGATTTCTCCTTTCTCATGTTGTAGCTTTACCCATCCATATGCAGCCCTTTAAATGGCAGGAACTGGTCTGATGTGAGCTTGGAGACTCTGAGGAGAGCTCTGACTCAACTGCAGGAAACCCCAGACCAGAAAGTCAGTCAAACTGGTTGGTTACTATCAAACACAACACAACACTATTTTAGGAATAAATTAAAAATTGAATCATAAATGAATCATATTTAAAATCAGCTTTCTTAATGACATAACCTACCAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa2361

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076300	Essential Splice Site	277	505	6	8

Genomic Location (Zv9):

Chromosome 7 (position 16967652)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	15950350
GRCz11	7	16202323

KASP Assay ID:

554-2840.1 (used for ordering genotyping assays)

KASP Sequence:

GACAACACTCAGACTCCTCCAGCTGAATGATTTCTCCTTTCTCATGTTGT[A/G]GCTTTACCCATCCATATGCAGCCCTTTAAATGGCAGGAACTGGTCTGATG

Long Flanking Sequence:

AGACTCACAACACTGTTCCTCTAGAGGAGGAGAGTAAAGTGAAAAAGGTGAGAGATACTGATAAAAATGTAACTTTTTTTCTTCAAAGCAAAGTTCTCATTGGGTGATCAAATGTGTTCGTGTTTCCTTCTGTAGACTCAGCTGATAGAAACTCAGAAAGACATGCAGAAGATGATTCAGGACAGAAACAAGAAGATTCGAGACATCAAACACTTGGCAGAACTCAGAAAAGTGAGCTCAAGATATTCAATACTTAATAGATGGTGTTTAGATTTCTCGAAAAGTAATTTCACTGTATATTTCAGAAGCAGGATGAAAAGCTGATTCAAGAGCTGCAGCAGGAAATCAATGAACTGAAGATAAGAAACTCAGAGCTGGATCATCTCTCACACACTAAGGATCACCTTCAGCTCCTACAGGTCAGTGACTTTCTATCTGTTCACATCACAGGACAACACTCAGACTCCTCCAGCTGAATGATTTCTCCTTTCTCATGTTGT[A/G]GCTTTACCCATCCATATGCAGCCCTTTAAATGGCAGGAACTGGTCTGATGTGAGCTTGGAGACTCTGAGGAGAGCTCTGACTCAACTGCAGGAAACCCCAGACCAGAAAGTCAGTCAAACTGGTTGGTTACTATCAAACACAACACAACACTATTTTAGGAATAAATTAAAAATTGAATCATAAATGAATCATATTTAAAATCAGCTTTCTTAATGACATAACCTACCAACGTGTATGCACTTTCATTTCAGTCAAATCCTAAAGGAGTAATGATAAATAAAATATGCATTCATTTTCCTTTAGTTTAGTCTCTTTATTCATCAGAGGTCGCCACAGTGGAATGAACCGCCAACTTATCCAGCTTATGTTTTGCATAAGATTGTCACGAGTGGGGGAGAATCACACAAAAGGCAAAAATCCATGTGCAGCAATTTATTAACAAAAAGACAAAGGTATCCAAAAAGACAGAGATTTCCAAGAGACAAAGGTTTCCAAATCT

Associated Phenotype:

Not determined