ZMP

si:ch73-341p18.7

Ensembl ID:

ENSDARG00000075855

ZFIN ID:

ZDB-GENE-090313-152

Description:

Novel 7 transmembrane receptor (Secretin family) domain containing family [Source:UniProtKB/TrEMBL;A

Human Orthologues:

EMR1, EMR2, EMR3, EMR4P

Human Descriptions:

egf-like module containing, mucin-like, hormone receptor-like 1 [Source:HGNC Symbol;Acc:3336]
egf-like module containing, mucin-like, hormone receptor-like 2 [Source:HGNC Symbol;Acc:3337]
egf-like module containing, mucin-like, hormone receptor-like 3 [Source:HGNC Symbol;Acc:23647]
egf-like module containing, mucin-like, hormone receptor-like 4 pseudogene [Source:HGNC Symbol;Acc:1

Mouse Orthologues:

Emr1, Emr4

Mouse Descriptions:

EGF-like module containing, mucin-like, hormone receptor-like sequence 1 Gene [Source:MGI Symbol;Acc
EGF-like module containing, mucin-like, hormone receptor-like sequence 4 Gene [Source:MGI Symbol;Acc

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7415	Missense	Mutation detected in F1 DNA	Not yet available
sa6607	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7415

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110119	Missense	68	162	3	3
ENSDART00000148075	Missense	80	595	3	12

Genomic Location (Zv9):

Chromosome 1 (position 56278208)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	55060754
GRCz11	1	55738405

KASP Assay ID:

554-4005.1 (used for ordering genotyping assays)

KASP Sequence:

ACAACCCCCCATCATGTGTGATGCYTCAGTCTCCTGGAGCGGCTGGTATC[G/A]GCTCTTCATTAACGGTCTGAGYGCTCATRTCCCAGACACATGTGTTGAGG

Long Flanking Sequence:

AAAACTCAATTTAAAAAACTAAGTCTAGGGCAGCTGTATAAAAATAAGTAAATTGTTCATTAATTTTACTAGCAGTAATTCCCATAAAATATATTCCTAAGACATTTTTTTTAATAACAGGAAAAAACTTAGCATCTGTGGACACCCCTTCACATCTCAGTGAGTCACAGCTTCAGATGTCAACAAAACTGAGAGAAAAAAAAATGTTTCCATTATTATTATTTTTTTTAATGGAGTGTTCCTTTAATTTTTATGACTTACTCAAGATTCTCCTTCCCAATCATGATGTGTTTTTTAAATAATGCTTTGTAGTTCTCCCTGTATACATTATAGCAGTTTAAAACAATGTTTTGTAATGATTTTTCAAAATATTTTCCTAACAGCTAGTCTGACTGACCCCTGCAACAACTACACTGTGCTGAACGATTCATGGAGACACATTGGTAATTCACAACCCCCCATCATGTGTGATGCCTCAGTCTCCTGGAGCGGCTGGTATC[G/A]GCTCTTCATTAACGGTCTGAGCGCTCATATCCCAGACACATGTGTTGAGGTCTATAGCTGTGGCACTGCTGCCCCACTGTGGATTAGTGGTGGACACCCAGCAGTAGAGGATGGAGTCGTCACTCGAAATGTCTGCAGTCACTGGTGCGGGGACTGCTGCCTTAACGGCTCTTTTTCCATTCAAGTCAAAGCTTGTCCTGGAAATTATTCTGTCTATGAACTGATTAGTCCCTTAATTTGCTCAGCCTACTGTGCAGGTAAGTCTATTTACTTTCAGCTTTTTTAAACTCTTGAGTTTAGCATCACACCTTGCGTTGAAGCTTAATCAAGTAGTGATATTATTTAATTTACATGATCAATATACCCAATTTATACTCACAATCCAATAACTTTTACAAACCATCAAATTTTAACATCTAATCGAGTACATTTGAATGATTGCTAATTTATTTAGTGATATACTCCATCAGGATTTATTGGTTTTAACATACCACCGATAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6607

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110119	None	None	162	None	3
ENSDART00000148075	Essential Splice Site	567	595	12	12

Genomic Location (Zv9):

Chromosome 1 (position 56283355)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	55065901
GRCz11	1	55743552

KASP Assay ID:

554-5410.1 (used for ordering genotyping assays)

KASP Sequence:

CTTCATCCATMTTTTTTCAGTSTTTATTTGATTGTATCTTACTTYAAACA[G/C]ATGCTGGATTAAAATGGATAAAGGCTTCTTCTGGAGTTTTKTGGGACCTG

Long Flanking Sequence:

GGAGTCAATAATGTGGCTCGAATCAACATCTGCATCAGTCTGCTGTCGGCTCACCTTCTGTTGCTGCTCACACAACAGTTCCTGAGCCTCATTCGCCCTCAGCAGGTGAGAATGATGAAGGAGCTCTACAGCTCAGCACAGCCGCACTGAGAATCATCATAACCCTCTCTCATGCTCTCCAGGTGTTGTGTGTGGTGATAGCAGGCCTTCTGCACTTCCTCTTCCTCTCCGCCTTTGTGTGGATGTTCATTGAAGCTGTGCTGCTCTTCATCTGCGTCAAGAACCTATCACAGGTCAGCTCCAGAAAGAAGGAGGTGCTTAGCAATGGATTTCTGTGTGTGATTGGATATGTGGTTGCTTTGATTGGGGTGAGTGTGTCTATTGGGATGGTTCCAGAAGGATACGGCAGTGAACAGTGAGTTTACTTTTGAGTGATTCAACTCTCAACAGCTTCATCCATATTTTTTCAGTGTTTATTTGATTGTATCTTACTTCAAACA[G/C]ATGCTGGATTAAAATGGATAAAGGCTTCTTCTGGAGTTTTTTGGGACCTGTTTGCGTCATACTTGGAGTAAAGCTTTTTTTTCTATGACTTAAGTTTAGAAGAAAAACAATCTGATTAATACTGTTTTTTTTCCCTGCACAGTTGAACGTGATTCTCTTCATCAGCATCAGCATCTATCTGAACTCGGCACTCAAAAAGCTGAACGCTGAAGTTTCACAGTTGAAACAAACCAAGTAACAAACATTGGTTTAATTACTCTTTAGAATAACAAAATGTAAAAGTTAAAGATTAAATTTCAATTTCTCTGCAGGGTTATGGTGTTTAAAACACTGGGTCAGTTTGTGATTCTTGGTTGCCCTTGGATTCTGGGTTTCTTCGCTCATGTCAATATGGTGGTGGAGATCGTCTTCATCATCATAAACTCTCAGCAGGGAACCTTCATCTTCCTGATCTACTGTGTGCTCAGTACTGAGGTAAGGCATCACTCTGAGGCCCTGTT

Associated Phenotype:

Not determined