ZMP

LOC799840

Ensembl ID:

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12068	Nonsense	Available for shipment	Available now
sa5988	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12068

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000066816	Nonsense	315	532	5	7

Genomic Location (Zv9):

Chromosome 24 (position 7822675)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	7679967
GRCz11	24	7709286

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGAGRTGCCACACTGTAAAAGCTGGTCTYAGATCAGTGCTCACACCTGT[G/T]AGGGTCTGGAATTGYTGAGAGAAACCCTGAATGCAGCAGAAGAACTTCTG

Long Flanking Sequence:

AAATGCCCCGTTGCATTTGTCTTTCAGGAGAACACAGAAAGAGAGATGGCACACAGTGTTGAGGTGTTCACCACACTGCAGCAGATCATTGAAAAGAGTCAGAAGGAGCTGCTCAGAAAGATGAAACACAAGCAGAAAAGTGCTGAGAAACATGTAGAGCGCCTCATTAAAGAGCTGGAGGTGGAGATCGCTAAACTGAACACCAGAAACTCTGAGCTGGAGAGGCTTTCTAGTTCTGAAGACCACCTCTGCCTTATACAGGTGACTCTTTTCAGCCAGAAGAGCAAGTTGATTACCTCTAGTTTCAAACACCCTATCAAATAATAAATGATATTACAAATAAATAATAACTAATAATTAGTCGATCTTACAAGAAATTATCTGTTTGAAGACATACATTTTTTAACAAAACACTTTTTTTTGGACCTTTCCAGGCTTTCCCTACCCTAAGTGAGGTGCCACACTGTAAAAGCTGGTCTCAGATCAGTGCTCACACCTGT[G/T]AGGGTCTGGAATTGCTGAGAGAAACCCTGAATGCAGCAGAAGAACTTCTGAAAACACAAATACACTCAGCCACAAAGAGAGGTTACTAATGTTTCATTTAACAACTGAACTTAATGACCAAACATTCTAAGTGTTTTATTTTTTATTTTTTTATTTTCCCACAGAACTTGAGGCCATATCTCAGTATGCAGGTAATATAATATTTTTAAAAGACAGAATCTTTCATAAACTTACTATAACACACCTACTGGACAATTTACATTTTCGTTTGTTGTGTTTTACTCTGTGTGTTTAATGTATGTTTAACTTTATTTACTTTAATATTAACTTTATTGTGTGAAAATATTCTTTACTTGATTTTTTTAAACAGTTATATTCCATATTTACTTGGATCCCTAATATTCCTCAGTTTCTATTTAATTATGAGATTTAAATACTCACTATCACATTTTAAGCACTATATTTTAGCTGAATTATTTTGTCGGGTGATCCTCATAATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa5988

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000066816	Essential Splice Site	351	532	6	7

Genomic Location (Zv9):

Chromosome 24 (position 7822868)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	7680160
GRCz11	24	7709479

KASP Assay ID:

554-3899.1 (used for ordering genotyping assays)

KASP Sequence:

TTATTTTTTTATTTTCCCACAGAACTTGAGGCCWTATCTCAGTATGCAGG[T/C]AATATAATATTTTTAAAAGACAKAATCTTTCATAAACTTACTATAACACA

Long Flanking Sequence:

AACTGAACACCAGAAACTCTGAGCTGGAGAGGCTTTCTAGTTCTGAAGACCACCTCTGCCTTATACAGGTGACTCTTTTCAGCCAGAAGAGCAAGTTGATTACCTCTAGTTTCAAACACCCTATCAAATAATAAATGATATTACAAATAAATAATAACTAATAATTAGTCGATCTTACAAGAAATTATCTGTTTGAAGACATACATTTTTTAACAAAACACTTTTTTTTGGACCTTTCCAGGCTTTCCCTACCCTAAGTGAGGTGCCACACTGTAAAAGCTGGTCTCAGATCAGTGCTCACACCTGTGAGGGTCTGGAATTGCTGAGAGAAACCCTGAATGCAGCAGAAGAACTTCTGAAAACACAAATACACTCAGCCACAAAGAGAGGTTACTAATGTTTCATTTAACAACTGAACTTAATGACCAAACATTCTAAGTGTTTTATTTTTTATTTTTTTATTTTCCCACAGAACTTGAGGCCATATCTCAGTATGCAGG[T/C]AATATAATATTTTTAAAAGACAGAATCTTTCATAAACTTACTATAACACACCTACTGGACAATTTACATTTTCGTTTGTTGTGTTTTACTCTGTGTGTTTAATGTATGTTTAACTTTATTTACTTTAATATTAACTTTATTGTGTGAAAATATTCTTTACTTGATTTTTTTAAACAGTTATATTCCATATTTACTTGGATCCCTAATATTCCTCAGTTTCTATTTAATTATGAGATTTAAATACTCACTATCACATTTTAAGCACTATATTTTAGCTGAATTATTTTGTCGGGTGATCCTCATAATCACACTTTTTGATGTACCAAAAATATTTCCAAAAGATTCAAGATAAAGAAATTTTAAAAGAAAAAACACTTATTTTTAAAATAGGAATTTATTATATCACATATCATTAGAAAAAAATAGGAATCTGTTAAAGTTTTTAAATTAAACTGTAGCCTATTGTCATTTATTAGACAAATAACAAACTGGCCAGCACA

Associated Phenotype:

Not determined