ZMP

adamtsl2

Ensembl ID:

ENSDARG00000074033

ZFIN ID:

ZDB-GENE-070705-558

Human Orthologues:

AC002321.2, ADAMTSL2

Human Descriptions:

ADAMTS-like 2 [Source:HGNC Symbol;Acc:14631]
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A8MZ67]

Mouse Orthologue:

Adamtsl2

Mouse Description:

ADAMTS-like 2 Gene [Source:MGI Symbol;Acc:MGI:1925044]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7575	Missense	Mutation detected in F1 DNA	Not yet available
sa40592	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa38524	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7575

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 > G

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108729	Missense	50	617	2	14
ENSDART00000138816	None	None	396	None	8
ENSDART00000148064	Missense	200	362	6	8

Genomic Location (Zv9):

Chromosome 5 (position 68904652)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	65236874
GRCz11	5	65915989

KASP Assay ID:

554-4018.1 (used for ordering genotyping assays)

KASP Sequence:

TCCTAACTAAGTGAATTGCTTCTTTGAAGGCTATACTTTCATAACTCAAA[T/G]CCCCGAAGGATCATGGGACATCCAGGTYATTGAGAGGAAGAAGTCTGCAG

Long Flanking Sequence:

CGATTGGGCAAATGCTTAACATTTATTATTATTATTATTACTAGTATCATCATCATCATCATAATACTCATATCTCAAAAGAGATAAAAGCTGCCTGCATGTAAAACAATACATATAACAAACATTTTTTTTTTTTTTTAAATAGCTGACCGGCCCACATTTAAAGAATGGTCCGGCCCTTCTGGCATTTGCCAGAATTGCCAGATGGCCAGTCCGCCCCTGGTATAAGCTGATGTGTAATTTTGCAGCCCATAGGATGTGACGGTGTCCTCTTCTCCCCCAACACCCTGGATAAGTGTGGCGTGTGTCAGGGAGACGGGAGCAGCTGCAGTCGAGTTACTGGGAACTTTCGCCGCGGGGCCTCGAGTCTAGGTAACATCACTTCAGTGATTTGCAGAACTGCATTATAGTCAATGGTGCTGATTACATTCATCAAGTAGTCCACTAAAGTCCTAACTAAGTGAATTGCTTCTTTGAAGGCTATACTTTCATAACTCAAA[T/G]CCCCGAAGGATCATGGGACATCCAGGTTATTGAGAGGAAGAAGTCTGCAGATATCCTGGGTGAGCAACTGTACAGGGAGTTTTTAGACTGGTTTGCACGTATATTGGTAAAGCAATCCATAAACATTAAAGAAACAAATGGTCAAAAGCAAGGCCAGGCAAGACAAGGGAAACCACTTAGAAATGTTCACTACGATATAACAAGACTCAGCAAAGTGCTAGAGTGACTGGTTATATTTAGTGTGTACATGTGTGTATATTCAGTCCTAATAGTCTACAGCTGTGTGTAAACAGTGAGTCTATTGAAACAGCTGTGTGACTGGAGCACATGATGGGATTTGTAGTTGGGGTGAATGATACCACTGGCCATCATAATGCTGCGTTCACACCAGATGCGGCACGCACGTCAAGCGTGAGTGATTTACATGTTAAGTCAATGCAAACGAACGAATAGACATCCTGTGGCGCATTACGCGTGAATGGCGCAGCGGGAATGAGGCG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40592

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
ENSDART00000108729	Essential Splice Site	128	617	3	14
ENSDART00000138816	None	None	396	None	8
ENSDART00000148064	Essential Splice Site	278	362	7	8

Genomic Location (Zv9):

Chromosome 5 (position 68902030)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	65234252
GRCz11	5	65913367

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGAGTACATCGTGGCGAAAGGGCCCATCGATCAGCCCATCAATGTTCTGG[T/C]ACTGTAGCTGTGGTCCTCCCTTCGCCGCCAAGGGCTCATGGGTAATCTCA

Long Flanking Sequence:

AATAATATATGTAATATATATAATTATGTTATAAATATATATATATATATTTGAAGTCAGAATTATTAGCCCCCCTCTGAATTATTAATATATACTATAAATATCTATTAAATATACGTTGTTAAACTATTATTTTTAAAATGTGTTGAAAAAGATAAAAAATTGGCAAATTATTTAGTTTTTAACAATATATTTTTAATATTTATACCATTTTAATCAAAATGCACAAAAAGACTTTAATACAATTTTGCTGAACAAGATCAAATGATAAAGAAATACTCACAATCCTCCCATCATTATATCTCCCCCTTGTCATTTTCCAGCTGTGACTGACCAAGCAGGGAACTTTTTCTTCAATGGGGCGTATAAGATGGACACCCCTCAGAACTTCCACGCCGCAGGGACCATTTTCAAATACCGGCGGCCCACCGATGTGTACGAGACGGGGATCGAGTACATCGTGGCGAAAGGGCCCATCGATCAGCCCATCAATGTTCTGG[T/C]ACTGTAGCTGTGGTCCTCCCTTCGCCGCCAAGGGCTCATGGGTAATCTCACTGGCTGGCTAACCATGGCTTTGACTTAGTGCAGGCCAAAGTCTAATGGTTCACTCTGATGCATTGTTCCAGGAGCAATGAATCTTATTATCGGTACTGTTGAATGCTCAGTTCTGTTTGGCTGATGGATATTTGTAGGCGTGTATTATTTTCTGATAATCACACTGTTAAAGTAGTTCCAGGAAGGCTTGACCACATCACTGTTCTGTATACACTGTAGAAAATGCAGGAATCCACACAATTCATTCATGTTTTCCTGTAACACAAGGTGATCATGTTAACTATTGACCAGTCATTGAACAGTTAAGTTGTCCCTAATAAATCAATTAAAAAGCTCATTTTAAATAAGTAGTAGCACAATTATTTCTTTGAGTGTAGAGTGATTTCACAGCAGACAACAGTCAAAAATCTCATGTTTAAGAAAGTCGAGGACACAATTTTCAACAGTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38524

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108729	Essential Splice Site	183	617	5	14
ENSDART00000138816	None	None	396	None	8
ENSDART00000148064	None	None	362	None	8

Genomic Location (Zv9):

Chromosome 5 (position 68891179)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	65223401
GRCz11	5	65902516

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGAATGGAATGTGCTGCAGACTCGAGGCTTTGCTTTTTTTTTTTGTTAA[C/T]GTTCTCCGAGACATTCAAAGAGCACAGAGGAGAGACGGCCAAGCAGAAGC

Long Flanking Sequence:

CTTATCATGCGTTGACACCAGTCGGCAAGAGTGTCAAAGTAGCCAGTAGTCATCCATGATGACACAAAAAAAAAATAAAAGAGAAAACATATAAACGATCCCTCACATGAGTGTAGATGCCATTTAAATTACAGTGTTTATGTCTACAGCATTCTAACAATCCTTTAGAGGGTTTGGATTTTAAAGTTATGCGTTTGTGTTTTATTTATATGCTAGTACAACTAGATGTCTTTAGTCTAGATTCAAACTCTATAGTTGAACAATTCAGCTCATTAGTTGCTCTGCTTGACCTACTGGTAACACTCTAAAGATCATGCCAAGGAACCAATTGATATATTGATTATTTGGCTTCACTGGTGGTTTTTGAATATTAGAAGCAGGGCCTAATCCTCAACACTGGCATGCCAAAGTGCTGCGGGATGGTCTCGGGTGGGACAGTCCTGATCATGGAGGAATGGAATGTGCTGCAGACTCGAGGCTTTGCTTTTTTTTTTTGTTAA[C/T]GTTCTCCGAGACATTCAAAGAGCACAGAGGAGAGACGGCCAAGCAGAAGCTGGCGGGATTGCATTCCATCATATTTATAATTCATGCTGGGTTCCCTCCGCTGCGTCCAAACACTGCTTTACCAGCCCCTCTGCCAGAGACCATAAAGAACATCTCATGCAATGCCCGTACACACAGTCAAAGACGAGGAGAAAGATTCCAGGTGGTGAGAAGAAAAAGCCTAGGCTGAGCCCAAGGAAGACGAACATAATTCATGATGTTTTGCTATTGGTTAAGGGAAAAAAAGCGCCATAGATCACTCGGGTACAGACTATGCTTGTCGCATCAGATAAATCCCAGGAATTTATCACGAGGAACAAATTTTATTGGCTCCTGTCTGGTTTGAGGGAATGTGCTGTTTTCCAGCCTTGACATTAAGGTAATGAGTGTGACCAGGAATGGTAAAAATGTTAGTGGTTTCATGGCTGGAGTGTCAGTCTGTGTCTCGGCGTCAACAAACG

Associated Phenotype:

Not determined