ZMP

GPR37 (1 of 2)

Ensembl ID:

ENSDARG00000074563

Description:

G protein-coupled receptor 37 (endothelin receptor type B-like) [Source:HGNC Symbol;Acc:4494]

Human Orthologue:

GPR37

Human Description:

G protein-coupled receptor 37 (endothelin receptor type B-like) [Source:HGNC Symbol;Acc:4494]

Mouse Orthologue:

Gpr37

Mouse Description:

G protein-coupled receptor 37 Gene [Source:MGI Symbol;Acc:MGI:1313297]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18466	Nonsense	Available for shipment	Available now
sa6000	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18466

Status:

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

Availability:

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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112299	Nonsense	425	558	2	2

Genomic Location (Zv9):

Chromosome 25 (position 28366207)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	27056301
GRCz11	25	27499503

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCGCAYGTAAGATCCGCAAAGCCGAGCGTGCCAGTGTTCGGGGCAATCGC[A/T]AACAGATCCAACTTGAAAGCCAAATGAACTGCATTGTGGTCGCCTTAGCC

Long Flanking Sequence:

ATTTCTGTACTATATATACCCTGTGAAAGGATTTTCTAAAACTTTATTTGTAATGACCATACATTCCCTTTACCTTGCAGGTGGCATCTTTGGGAGTAACCACCTTCACTCTTTGTGCTTTGTGCATTGACCGTTTCCGTGCTGCGAGTAACGTCCAGATGTACTATGAAATGATTGAAAACTGCACGTCCACCACAGCCAAGCTAACCGTGATCTGGCTCGGTGCTTTGCTCCTCGCCCTTCCCGAGCTCCTCATCCGACAGTTGGTTAAAGAAGTGAGCGAGCCACCAGAGGTGACGCCTTGCGAACATTGTGTGGTTCGAATCTCCACAGATCTCCCTGACACTCTTTATGTTCTCGGACTCACATATAATAGTGCTCGTCTATGGTGGTACTTTGGCTGCTACTTCTGCCTTCCCACCCTCTTCACCATCATAAGCTCAGTGGTGACCGCACGTAAGATCCGCAAAGCCGAGCGTGCCAGTGTTCGGGGCAATCGC[A/T]AACAGATCCAACTTGAAAGCCAAATGAACTGCATTGTGGTCGCCTTAGCCATCCTTTATGGCTTTTGCGTCATTCCGGAAAACATCAGCAACATCGTATCTGTGTACATGGCTACAGGCGTGCCACGTCGCACACTAGATATCCTTCATCTAGTCAGTCAAATGATGCTGTTCTGCAAGTCTGCTGTCACACCCGTGCTGCTTCTTGCACTCTGTCGGCCATTTAGCAAAGCCTTTCTCGACTGCTGCTGCTGTTGCTTTGAGGAGTGTGGCCCACCAAAATCCTCTGAACCCAACAGTGATGACAACGATCAGGACGGCACAACAGATCTGGAGCTTTCACCCTACAGTACAGTAGGCCGCAGGGATGCATCTACCTTCCCAATAGCAGGAACGCACTGCTAAGGTTGTACCTTACCTAAGGGTTACTTGTCAACAAGGGCTTAGATTTGTGGAATAAACCAACCGAGAGATATTTTCGGAGGCTGTACAATTTTTTTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6000

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112299	Nonsense	483	558	2	2

Genomic Location (Zv9):

Chromosome 25 (position 28366383)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	27056477
GRCz11	25	27499679

KASP Assay ID:

554-3652.1 (used for ordering genotyping assays)

KASP Sequence:

CGTCGCACACTAGATATCCTTCATCTAGTCAGTCAAATGATGCTGTTCTG[C/A]AAGTCTGCTGTCACACCCGTGCTGCTTCTTGCACTCTGTCGGCCATTTAG

Long Flanking Sequence:

GAAAACTGCACGTCCACCACAGCCAAGCTAACCGTGATCTGGCTCGGTGCTTTGCTCCTCGCCCTTCCCGAGCTCCTCATCCGACAGTTGGTTAAAGAAGTGAGCGAGCCACCAGAGGTGACGCCTTGCGAACATTGTGTGGTTCGAATCTCCACAGATCTCCCTGACACTCTTTATGTTCTCGGACTCACATATAATAGTGCTCGTCTATGGTGGTACTTTGGCTGCTACTTCTGCCTTCCCACCCTCTTCACCATCATAAGCTCAGTGGTGACCGCACGTAAGATCCGCAAAGCCGAGCGTGCCAGTGTTCGGGGCAATCGCAAACAGATCCAACTTGAAAGCCAAATGAACTGCATTGTGGTCGCCTTAGCCATCCTTTATGGCTTTTGCGTCATTCCGGAAAACATCAGCAACATCGTATCTGTGTACATGGCTACAGGCGTGCCACGTCGCACACTAGATATCCTTCATCTAGTCAGTCAAATGATGCTGTTCTG[C/A]AAGTCTGCTGTCACACCCGTGCTGCTTCTTGCACTCTGTCGGCCATTTAGCAAAGCCTTTCTCGACTGCTGCTGCTGTTGCTTTGAGGAGTGTGGCCCACCAAAATCCTCTGAACCCAACAGTGATGACAACGATCAGGACGGCACAACAGATCTGGAGCTTTCACCCTACAGTACAGTAGGCCGCAGGGATGCATCTACCTTCCCAATAGCAGGAACGCACTGCTAAGGTTGTACCTTACCTAAGGGTTACTTGTCAACAAGGGCTTAGATTTGTGGAATAAACCAACCGAGAGATATTTTCGGAGGCTGTACAATTTTTTTCAGACTTCATGTCTGCTTTGTTTAGGGGAGATACCCACAAAGTGGATATTTTATGGAAATAGAGACAAAGAGCCACACTTTTATTACAGGATACTTGGTCTTAGGGATGACTGTTAATGTTTACAAAAAGAAGACATGTAGTTTCTTTGAAGTTCATACAAAGTTTAGAAGAATTAA

Associated Phenotype:

Not determined