ZMP

A8E7R8_DANRE

Ensembl ID:

ENSDARG00000071448

Description:

Novel protein similar to vertebrate leprecan-like 1 (LEPREL1) [Source:UniProtKB/TrEMBL;Acc:A8E7R8]

Human Orthologue:

LEPREL1

Human Description:

leprecan-like 1 [Source:HGNC Symbol;Acc:19317]

Mouse Orthologue:

Leprel1

Mouse Description:

leprecan-like 1 Gene [Source:MGI Symbol;Acc:MGI:2146663]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44988	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43842	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44988

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089827	Nonsense	202	678	3	15

Genomic Location (Zv9):

Chromosome 22 (position 23358269)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	24423587
GRCz11	22	24450151

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTCAGAGAGCCTTCTTCGCTGGCGTGAAGCTCTATGACAAAGGCCACTA[T/A]GAAGAGTCGGTGTCGCTGTTTGAGAAGGCTTTGAGCGAGTATTATCATGC

Long Flanking Sequence:

TTCACTATTTGCTAATGCTAATAGATGATTCGTAGTGTCTAGTTATTATAAACTGTTACCCAGTATTGCTCTCATGGTTCTTATAGCATGTCTTATAGTCATTATTTTTTTATATCTTGCTAATATTAGATGTAAAACATTTAGTTTGCAATAAAACAACCATGTTTGGATTTTATTATCATACTGGTGAAATATGAAAGCTGTGTGTCAAAAAAGAAAAAGCACAATATTGTGGAAATTGGATTTTAAATGCACTACAAATAATTCTTACTTAAAAAAATGTTCTCCAAAATGATTGTATATTAAAAATAACAACTTCACCATTCAAAATGGTTAAATAATCTCAATTGCCAGACTTTCCATGCATTACTACTAATTAGCTCCTCAAACCTTTAAAGACCCCACATTAAACTCTAAAATCACCAGATTTATTTTCATGCATCTTTATATTTTCAGAGAGCCTTCTTCGCTGGCGTGAAGCTCTATGACAAAGGCCACTA[T/A]GAAGAGTCGGTGTCGCTGTTTGAGAAGGCTTTGAGCGAGTATTATCATGCTGATGAGGATTGTCGGGCCCTTTGTGAAGGACCGCAGCACTTCGAGGAGCAGGATCACGTCTTGTACAAATACAGCCTGTACGAGCTCATCTCAGGTACAGATTTTGTATTCCGAGCTTTTCTGCTTGCTTTTAATGTGGTAAAGTGATCATATGCACTTTTGAGAAGGCCCTGGGAGTTTTCCATTGAGCTTCTCATGTTTCTAAAGCTATTTGTGTTTCCATCTTCCCGCTCTGACCTTTATATGAGCCTTGTTTGAGCAAGCAAGAGGCACAAATGTCTGACCTTCTTTTTTTTTTTTTTTGATGTACAGTTGTACAATTTGTTATTGTTGTGTCTGACAGGCAGTTCAGCAACGAACAGCTTGAAAGAGCATGACATACGATTGCCCTACACAAAGTTTTGCATATAAAACAAATCCAGGTGCATCCAAAGGACACTGCTTTTTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43842

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
ENSDART00000089827	Essential Splice Site	337	678	5	15

Genomic Location (Zv9):

Chromosome 22 (position 23348184)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	24433672
GRCz11	22	24460236

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTGGAGTTTTACAGAGAGGTGCTAGGACATGATGGCCAGCCACGTAAGG[T/C]GAGAAACATGGAAGGAGTCACCCAAAACCAAATGATTTCTCATGAATGTG

Long Flanking Sequence:

TCTTTAAAATAGGGTCTTTTGAGTTCATCCGATGAAAGAAACTGATTTGAAAAGACTTAAGATTGAGTAAAAATGGTGAGAAAATGTTTTACAGACGGTAATTCTTTATAAAGTGTCAGTTCATTTAGGTGTGTGTGAATGTTCATGTCTCACTTTTGTGTCTTTCCACTCGCTCAGCTCTGTGGTGTTTCTTCCATTGTGGTCACTGGCCTGGAATGTGAATGTTTCTGAGCGTTTAGGAAATAAACGTGACTCAAAAAAAAAAAAAAAATCACATGATGAATAATCTCCCAGATGAGCCGGAAAAACAGAGCCCTGGTGGCCTCATTAATGCTTAAAAACCTTTTTTTTTCTCTCTCTTTTGTGTTCAGCTGGGAGGTATGAAGAGGCATTGGACTGCGCATTGACTTATCTGTTGTTTCACGAAGGCGAAGAGTTCATGACGGAGAATGTGGAGTTTTACAGAGAGGTGCTAGGACATGATGGCCAGCCACGTAAGG[T/C]GAGAAACATGGAAGGAGTCACCCAAAACCAAATGATTTCTCATGAATGTGTGTGAAGGTTTTAATTTTAATTAAATTCATCTTAATTTCTATAGCTGTTTTACAATGTAGATTTTCAAAGCAGCTTAAGGTAGAAGTTATAGTAAATTGAAACTGTTCAGTTTAGTTCAGTGTGGTTTAATTTTCACTGCTGAAAGTACAAACACTGAAGAGCAAATCCATCAATGCGCAGCTCTACAAGTCCCAAACCAGGCGAGCCAGTGGCAACAGGGGTTAACAGGTTGTGTAAAATCTTCATTAATTTGATATGTTTATAGCAGCGTTTAGTGTGTCTTCAGTGCTTATATTACTGTACCCTTATCATAGAATAATATGGCTATGAAGATGGCAAAAAATCTGGGGTCATAGCTTATCAAATGCGTATTTACAAAACGAACCTTTTATTTCCGTTACAAAAACTTTTCTGGCCAACAATAAACCTTACTAAAGAATGTTCTGGGA

Associated Phenotype:

Not determined