ZMP

LOC100002201

Ensembl ID:

ENSDARG00000056057

Human Orthologue:

GREM2

Human Description:

gremlin 2 [Source:HGNC Symbol;Acc:17655]

Mouse Orthologue:

Grem2

Mouse Description:

gremlin 2 homolog, cysteine knot superfamily (Xenopus laevis) Gene [Source:MGI Symbol;Acc:MGI:134436

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42902	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36378	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42902

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078488	Nonsense	118	195	1	1

Genomic Location (Zv9):

Chromosome 17 (position 19578655)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	19728666
GRCz11	17	19748502

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCTGGAGGGCTGCCTAAGCCGAACCGTTATCAACCGGTTCTGTTACGGC[C/T]AGTGTAACTCCTTCTACATCCCACGCCACCTGACATCTCAAAGCTCACAT

Long Flanking Sequence:

TTTTAAAAACAGTGTTGTGTTGCTTGATTGTAAAATCATGACTACCGTGATAGGTTTAAAGTTAATTCAGCCTGAACGAGTATATCTACATATGACAATGTGTTTGCCTCTCTAACAGAAGTACTGAAGTTTTGTTCTATTTTGAATCTTTTCCCAGAATGTTCTGGAAGCTGGCAATACATGCCATTTTGGCATGGACCTTATTCGCATCTACAGAGACCAAGAAGCAACGTCCTCAAGGTTCCATCCCCTCCCCTTACAAGCTAAAGGGCAATGATTTATCATCGCCATCCCATGCACTAGCATCACTGCCTCAGCATACTGCATCAGCACGACGACAGAAGGGTAAACATGACATGCTGTCATCGAGTCGTGAGGCTCTGGTGGTCACCGAGCGCAAGTACCTGAAGAGTGACTGGTGTAAAACACAGCCGTTACGCCAAACTGTGAGCCTGGAGGGCTGCCTAAGCCGAACCGTTATCAACCGGTTCTGTTACGGC[C/T]AGTGTAACTCCTTCTACATCCCACGCCACCTGACATCTCAAAGCTCACATAGAAGTCGGAAAACAGCGTCCACACCAGACCACACCACTTCATTCCAGTCCTGTGCTTTCTGTCGACCGAGCCGGATAACCACAGTCACCGTCCGGCTTCACTGTCCTGGGCTGCAGCCGCCATACCGCCAACGGAAAGTGCAGCGGATCAAGCAGTGCAAATGTGTGTCTGTTAATGTCAATGCTGCATACTGAGATGAAACAATGATTTAGGGTGTTCCTTTCGGGGAAAAAAAGAACTGTGGCTGCCTGACAATCAGTGTGTGAAATGTGCCAAAGACAACAGCTAATCAGAGGCCTGGCCACCTTCATTATGTCTGGACTCTACCACAGAATGCTAAGCGGGAATACTTAATAGCTGCCGAGCAGCGTTCGAAACAAAGCTGGATTTTTTTCTTCTTTTCTTGACAATACGAAAGAGCTGAGAGTTGTTACATACAAAACCCAAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36378

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
ENSDART00000078488	Nonsense	123	195	1	1

Genomic Location (Zv9):

Chromosome 17 (position 19578672)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	19728683
GRCz11	17	19748519

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCCGAACCGTTATCAACCGGTTCTGTTACGGCCAGTGTAACTCCTTCTA[C/A]ATCCCACGCCACCTGACATCTCAAAGCTCACATAGAAGTCGGAAAACAGC

Long Flanking Sequence:

TGTTGCTTGATTGTAAAATCATGACTACCGTGATAGGTTTAAAGTTAATTCAGCCTGAACGAGTATATCTACATATGACAATGTGTTTGCCTCTCTAACAGAAGTACTGAAGTTTTGTTCTATTTTGAATCTTTTCCCAGAATGTTCTGGAAGCTGGCAATACATGCCATTTTGGCATGGACCTTATTCGCATCTACAGAGACCAAGAAGCAACGTCCTCAAGGTTCCATCCCCTCCCCTTACAAGCTAAAGGGCAATGATTTATCATCGCCATCCCATGCACTAGCATCACTGCCTCAGCATACTGCATCAGCACGACGACAGAAGGGTAAACATGACATGCTGTCATCGAGTCGTGAGGCTCTGGTGGTCACCGAGCGCAAGTACCTGAAGAGTGACTGGTGTAAAACACAGCCGTTACGCCAAACTGTGAGCCTGGAGGGCTGCCTAAGCCGAACCGTTATCAACCGGTTCTGTTACGGCCAGTGTAACTCCTTCTA[C/A]ATCCCACGCCACCTGACATCTCAAAGCTCACATAGAAGTCGGAAAACAGCGTCCACACCAGACCACACCACTTCATTCCAGTCCTGTGCTTTCTGTCGACCGAGCCGGATAACCACAGTCACCGTCCGGCTTCACTGTCCTGGGCTGCAGCCGCCATACCGCCAACGGAAAGTGCAGCGGATCAAGCAGTGCAAATGTGTGTCTGTTAATGTCAATGCTGCATACTGAGATGAAACAATGATTTAGGGTGTTCCTTTCGGGGAAAAAAAGAACTGTGGCTGCCTGACAATCAGTGTGTGAAATGTGCCAAAGACAACAGCTAATCAGAGGCCTGGCCACCTTCATTATGTCTGGACTCTACCACAGAATGCTAAGCGGGAATACTTAATAGCTGCCGAGCAGCGTTCGAAACAAAGCTGGATTTTTTTCTTCTTTTCTTGACAATACGAAAGAGCTGAGAGTTGTTACATACAAAACCCAAACTGTCAATTGTGTTTTAA

Associated Phenotype:

Not determined