ZMP

relnl

Ensembl ID:

ENSDARG00000077935

ZFIN ID:

ZDB-GENE-040427-1

Description:

Reelin [Source:UniProtKB/TrEMBL;Acc:Q8AYT0]

Human Orthologue:

RELN

Human Description:

reelin [Source:HGNC Symbol;Acc:9957]

Mouse Orthologue:

Reln

Mouse Description:

reelin Gene [Source:MGI Symbol;Acc:MGI:103022]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43187	Nonsense	Mutation detected in F1 DNA	Not yet available
sa6540	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23393	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43187

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025746	Nonsense	97	308	3	7

Genomic Location (Zv9):

Chromosome 18 (position 49786406)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	50942335
GRCz11	18	50859971

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GACTCAGTTCCGCTGGATCCAGATGGAGGCTCCAGGCGAGCGCTACAGCT[G/A]GGCTGTGGACCAGGTCTACATCGGGGAGGCGTGCGCCGGACTGTGCAGTG

Long Flanking Sequence:

GCTGTGAGGCAGACAGGTGTGATGACCATCATTCAGTACTTCTGCAGTACAGGAAGGATGCCAGGTGAGTACAGACGACAGGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTCCACTTGCGTGTGTTGTTGTGACACATAAGCTATAAGATTGGGTTCCTCCGCAGGTCGGATGTGTGGCAGCTGGTTCAGTCTGCCTGTCTGCCGTCCTCCATCAATAACGTGGGCTGCTCACCATTCCAGTTCCACGAGTCCACCATCTACAGTCCAGTCAACAGCTCCGCCTGGACCAGGGTCACCATCCAGCTGCCGGACCACGTGTCCTCTGGGTACAGCTCACTCACGGCCCTTTATTAATGATATCTCGTGGAGACTGCAGGGTCACTGAGATCTGCTTGTTCTGTGGGTCGTGCTGAAGGCGTTACGCTTGTGTGTCCGCAGAGCGACTCAGTTCCGCTGGATCCAGATGGAGGCTCCAGGCGAGCGCTACAGCT[G/A]GGCTGTGGACCAGGTCTACATCGGGGAGGCGTGCGCCGGACTGTGCAGTGGGCACGGGTACTGCACCAGCGGGCCCGTCTGCATCTGTGACGAGGGACACCACGGTGAGCATCTCCTGCAGCTCTGAGTATTGCAGGAATTGACCGTGTTTTTAAGGTTCATCATAACTCTGCTGCTCCTTCTTTAAAACTCTTCATCAGTATAAAAACTCTCAATGATGCGCTCGAGGGCAAGAGGGGAGTGTATCTTCCCACACGTAAAACCTGATTTAGANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAGTCTTCTTTCTCCTATGCTTTATAACAGCAGTGTTTGTGTTCAGGTGATGACTGCTCCTTGTCCAGCACTGATCTGCCCAGCTCCATCAAGGATAACTTTGAGTCAGGCTGGGTGTCGGAGGAGAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6540

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025746	Essential Splice Site	271	308	6	7

Genomic Location (Zv9):

Chromosome 18 (position 49787781)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	50943710
GRCz11	18	50858596

KASP Assay ID:

554-5307.1 (used for ordering genotyping assays)

KASP Sequence:

GGTCTCCGTCATTACTGAACWGCAGGTAACGTGTGTGTTGTGTGTGCTGC[A/T]GTGAGGCGCGGGTCCGAGGCGTTCAGCTGCGGTGGTGGCAGSCGCGTCAC

Long Flanking Sequence:

CCCAAAGACTTCATCAAAGCCCAGAGAGTGTCCTACAACATCCCGCTGTGAGTTTACACACATTTATCCCTGCCCTTAAGACAGTGAATGCTTGTCTGGAAGGAGGAGATGTTTATTGTATTTAGCAGAGAGCCCTTGGCATCTTCCGGACTGAGACAGCAGGTGAACTGTGTTACAATACTCAAACATGACCTTCAGGAGAACTGGGACCCTCCAGTGTTTACCTTGTGAGCCAGTGTTACCAGTGTCCGCTCTTCACCTTGTGAATGTTGTCCTGAGCAACAGAGCGCTGCTTCTCCAGCCCTCACGCTCTACAGATATTCCCACATCTCCGTTCTTCATCAAGGAGTCTTTAAGTGCCCTTAATTAAACAAGAGTCCTCCACCTTAACTGAAGAACCATAGTGTTAGGACTGAATGAATGTCTGAATGACCTGTGGACTGCTGTCCTGGTCTCCGTCATTACTGAACAGCAGGTAACGTGTGTGTTGTGTGTGCTGC[A/T]GTGAGGCGCGGGTCCGAGGCGTTCAGCTGCGGTGGTGGCAGCCGCGTCACGAGGGCACAGGCCACGACCAGTGGGCACTGGACCATGTGGAAGTCATTCTGTGAGTACTCCTGCCTACAGACACCGTATCACAGCTGTGTTTTCTCATTCCTCCATACATCTGTAAGGTCTCACAGCAGAACCAGCATAGCATAAAACTGGCAGATAATAGTTTAATACCAATCAAGGCCAAGCTGAAACAGGACTGACAGCGCTTAAGCGTCGTTCATCATTAATATCATAGTTTCTACACCGTGCTGCACTATCCTGCACACACACACACACACACACACACACACACACACAGTTTCTACACACAGGTCTGCCCCGTCCCGCTCTCTCTCTTGTCCTCACACTGCTCTCTCTCTCTCTCTCTCTCTCCTCCGTCTCCCCGTCTGCCCTCCACATCTCCTCTTCATCCTCTGCTTCTCCTCCTCCTCCTGTGTGTGTGTGTGTGTGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23393

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000025746	Essential Splice Site	304	308	6	7

Genomic Location (Zv9):

Chromosome 18 (position 49787882)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	50943811
GRCz11	18	50858495

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGGGCACAGGCCACGACCAGTGGGCACTGGACCATGTGGAAGTCATTCT[G/A]TGAGTACTCCTGCCTACAGACACCGTATCACAGCTGTGTTTTCTCATTCC

Long Flanking Sequence:

GGAGGAGATGTTTATTGTATTTAGCAGAGAGCCCTTGGCATCTTCCGGACTGAGACAGCAGGTGAACTGTGTTACAATACTCAAACATGACCTTCAGGAGAACTGGGACCCTCCAGTGTTTACCTTGTGAGCCAGTGTTACCAGTGTCCGCTCTTCACCTTGTGAATGTTGTCCTGAGCAACAGAGCGCTGCTTCTCCAGCCCTCACGCTCTACAGATATTCCCACATCTCCGTTCTTCATCAAGGAGTCTTTAAGTGCCCTTAATTAAACAAGAGTCCTCCACCTTAACTGAAGAACCATAGTGTTAGGACTGAATGAATGTCTGAATGACCTGTGGACTGCTGTCCTGGTCTCCGTCATTACTGAACAGCAGGTAACGTGTGTGTTGTGTGTGCTGCAGTGAGGCGCGGGTCCGAGGCGTTCAGCTGCGGTGGTGGCAGCCGCGTCACGAGGGCACAGGCCACGACCAGTGGGCACTGGACCATGTGGAAGTCATTCT[G/A]TGAGTACTCCTGCCTACAGACACCGTATCACAGCTGTGTTTTCTCATTCCTCCATACATCTGTAAGGTCTCACAGCAGAACCAGCATAGCATAAAACTGGCAGATAATAGTTTAATACCAATCAAGGCCAAGCTGAAACAGGACTGACAGCGCTTAAGCGTCGTTCATCATTAATATCATAGTTTCTACACCGTGCTGCACTATCCTGCACACACACACACACACACACACACACACACACACAGTTTCTACACACAGGTCTGCCCCGTCCCGCTCTCTCTCTTGTCCTCACACTGCTCTCTCTCTCTCTCTCTCTCTCCTCCGTCTCCCCGTCTGCCCTCCACATCTCCTCTTCATCCTCTGCTTCTCCTCCTCCTCCTGTGTGTGTGTGTGTGTGCACTGCTGGTTTGCTCCCTGTATCCCCCTGTTCTCCTGCACTGCCTGTTGCTCAGGTCAGGGTTCCTGCACCCTCAGACCCTCAGCAGCATCAGCCCTGTCCC

Associated Phenotype:

Not determined